Turner
claire turner is an interdisciplinary scientist with a bsc in chemistry and biochemistry from the university of natal and a phd in biochemical engineering from ucl. her aim is to enable all our students to have an excellent education and student experience irrespective of their background and circumstances. she is very interested in innovations in pedagogy and how we can use these in improving the student experience. she was previously at the open university where she taught analytical science, and interdisciplinary science. her research is focussed around the analysis of volatile organic compounds, applied to diverse field as non-invasive disease dignosis and environmental monitoring.
Professor Claire Turner
Claire Turner is an interdisciplinary scientist with a BSc in Chemistry and Biochemistry from the University of Natal and a PhD in Biochemical Engineering from UCL. Her aim is to enable all our students to have an excellent education and student experience irrespective of their background and circumstances. She is very interested in innovations in pedagogy and how we can use these in improving the student experience. She was previously at The Open University where she taught Analytical Science, and interdisciplinary science. Her research is focussed around the analysis of volatile organic compounds, applied to diverse field as non-invasive disease dignosis and environmental monitoring.
Li
qualifications: · 1983 md, suzhou medical university, china. · 1994 ph.d, department of immunopathology, karolinska institute, stockholm, sweden. academic appointments · 1995-1996: post-doctor, department of clinical virology, karolinska institute, · 1996-2000: assistant professor, and then associate professor since 2000, institute of cell and molecular biology, lund university, sweden · 2001-2005: lecturer, division of biosciences, brunel university london · 2009-2014: division director of biosciences, brunel university london · 2005-present: reader in immunology, division of biosciences, brunel university london, immunology antigen presentation and vaccines autoimmune disease and inflammation regulation of adaptive immune response tumor immunology immunology teaching interests: adaptive immunology; cancer immunology; pathology; vaccine; biotechnologies, including microarray, rna seq, chip seq, transgenic mouse models, technology in drug discovery.
Dr Su-ling Li
Qualifications: · 1983 MD, Suzhou Medical University, China. · 1994 Ph.D, Department of Immunopathology, Karolinska Institute, Stockholm, Sweden. Academic Appointments · 1995-1996: Post-Doctor, Department of Clinical Virology, Karolinska Institute, · 1996-2000: Assistant Professor, and then Associate Professor since 2000, Institute of Cell and Molecular Biology, Lund University, Sweden · 2001-2005: Lecturer, Division of Biosciences, Brunel University London · 2009-2014: Division Director of Biosciences, Brunel University London · 2005-present: Reader in Immunology, Division of Biosciences, Brunel University London, Immunology Antigen presentation and vaccines Autoimmune disease and inflammation Regulation of adaptive immune response Tumor immunology Immunology Teaching interests: Adaptive immunology; Cancer Immunology; Pathology; Vaccine; Biotechnologies, including Microarray, RNA seq, Chip Seq, Transgenic mouse models, technology in drug discovery.
Mccarthy
ronan gained his bachelor of science in genetics with first class honours from university college cork, ireland in 2010 and was awarded the title of college scholar. in autumn 2010, ronan was awarded an irish research council phd scholarship to study novel biofilm inhibition strategies against the opportunistic pathogen pseudomonas aeruginosa in the lab of professor fergal o’gara. in 2014, ronan joined the research group of professor alain filloux at the mrc centre for bacteriology and infection at imperial college london. as a postdoctoral research associate, ronan interrogated the second messenger signalling cascades that govern the biofilm mode of growth in pseudomonas aeruginosa and agrobacterium tumefaciens. following on from his time at imperial college ronan joined the microbiology department at the animal and plant health agency where he used host transcriptomics and pathway analysis to profile the host response to infection. he joined the biosciences division in brunel university to continue his analysis of the regulatory networks that govern pathogenicity, antimicrobial resistance and biofilm formation in the gram negative opportunistic pathogens pseudomonas aeruginosa and acinetobacter baumannii. in 2021, ronan was awarded a bbsrc new investigator award to study the regulation of desiccation tolerance and biofilm formation in acinetobacter baumannii and to identify compounds that could disrupt these survival mechanisms. he has also expanded into the field of biofilm engineering, using synthetic biology approaches to give control over bacterial biofilm formation and using these tools to tackle environmental challenges such as plastic waste. as a pi he has secured funding from the bbsrc, nc3rs, academy of medical sciences, horizon 2020, british society for antimicrobial chemotherapy, innovate uk, nerc and the medical research council. my research focuses on profiling key signalling pathways that play a role in chronic bacterial infection and antibiotic resistance. studying interactions that occur at the host-pathogen interface using integrated ‘omics approaches. understanding the protective role of the microbiome in an infection setting. assessing the ability of old drugs to be repurposed to inhibit bacterial infection opportunities for phd study enquires are welcome from those who are keen to pursue phd and msc degrees. joint supervision, industry partnerships and collaborative research opportunities are also very welcome.
Professor Ronan Mccarthy
Ronan gained his Bachelor of Science in Genetics with first class honours from University College Cork, Ireland in 2010 and was awarded the title of College Scholar. In autumn 2010, Ronan was awarded an Irish Research Council PhD Scholarship to study novel biofilm inhibition strategies against the opportunistic pathogen Pseudomonas aeruginosa in the lab of Professor Fergal O’Gara. In 2014, Ronan joined the research group of Professor Alain Filloux at the MRC Centre for Bacteriology and Infection at Imperial College London. As a Postdoctoral Research Associate, Ronan interrogated the second messenger signalling cascades that govern the biofilm mode of growth in Pseudomonas aeruginosa and Agrobacterium tumefaciens. Following on from his time at Imperial College Ronan joined the Microbiology Department at the Animal and Plant Health Agency where he used host transcriptomics and pathway analysis to profile the host response to infection. He joined the Biosciences Division in Brunel University to continue his analysis of the regulatory networks that govern pathogenicity, antimicrobial resistance and biofilm formation in the Gram negative opportunistic pathogens Pseudomonas aeruginosa and Acinetobacter baumannii. In 2021, Ronan was awarded a BBSRC New Investigator Award to study the regulation of desiccation tolerance and biofilm formation in Acinetobacter baumannii and to identify compounds that could disrupt these survival mechanisms. He has also expanded into the field of biofilm engineering, using synthetic biology approaches to give control over bacterial biofilm formation and using these tools to tackle environmental challenges such as plastic waste. As a PI he has secured funding from the BBSRC, NC3Rs, Academy of Medical Sciences, Horizon 2020, British Society for Antimicrobial Chemotherapy, Innovate UK, NERC and the Medical Research Council. My research focuses on Profiling key signalling pathways that play a role in chronic bacterial infection and antibiotic resistance. Studying interactions that occur at the host-pathogen interface using integrated ‘omics approaches. Understanding the protective role of the microbiome in an infection setting. Assessing the ability of old drugs to be repurposed to inhibit bacterial infection Opportunities for PhD Study Enquires are welcome from those who are keen to pursue PhD and MSc degrees. Joint supervision, industry partnerships and collaborative research opportunities are also very welcome.
Pazoki
raha pazok md phd fhea is a medical doctor and an epidemiologist. she studied epidemiology at the netherlands institute for health sciences (nihes) and in the university of amsterdam. she worked with various cohort and case control studies such as the arrhythmia genetics in the netherlands (agnes), the rotterdam study, the airwave health monitoring study and the uk bio bank. in 2016, she joined the department of epidemiology and bio-statistics at imperial college london as a research associate. in 2020, she started a teaching & research academic position at brunel university london. dr pazoki specializes in the field of health data research, with a primary focus on the epidemiology of cardiometabolic diseases. she holds a particular interest in exploring causal inference and precision medicine by leveraging genomics and extensive health data sets with sample sizes exceeding 500,000 individuals. her expertise spans various domains, including precision medicine, global health, interventions, and the application of artificial intelligence for predicting health outcomes. she harbors a keen interest in identification of the relationship between circulating molecules and biomarkers, nutrition, lifestyle choices, genetic factors, and their collective contribution to the modulation of health risk factors and outcomes. she was the first to identify 517 novel genetic loci associated with liver enzymes and the first to show the causal effect of liver dysfunction on cardiovascular diseases. in addition, she is the first to show the effect of the alcohol consumption wdpcp gene in lipid metabolism, and liver cirrhosis. (genetic) epidemiology of cardiovascular diseases big data genome-wide association studies genetic risk scores mendelian randomization machine learning dr paozki is a founder and director of the cardiovascular and metabolic research group hosting researchers and academics across brunel university with direct or indirect research interest involving cardiometabolic aetiology, prevention, and health. we work in various areas to identify causes of cardiometabolic diseases (environmental, lifestyle, molecular, and clinical) and provide insight into how they interplay. we use the information for better prevention of cardiometabolic diseases in the community. if you are a msc graduates (with upper second class degree or higher) in the relevant field to the above research area, please contact dr raha pazoki (raha.pazoki@brunel.ac.uk). postgraduate fees and funding | brunel university london or scholarships and bursaries | brunel university london and other funding | brunel university london dr. raha pazoki's research is centered around health data science, with a strong emphasis on cardiometabolic diseases. 🔬 key research themes cardiometabolic epidemiology investigating the genetic and environmental determinants of cardiovascular and metabolic disorders. studying conditions like hypertension, diabetes, liver dysfunction, and lipid metabolism. genomics and precision medicine utilizing large-scale genomic data (e.g., uk biobank) to identify genetic loci associated with disease. she was the first to identify 517 novel genetic loci linked to liver enzymes and demonstrated their causal role in cardiovascular disease. causal inference in epidemiology applying mendelian randomization and other causal inference techniques to understand the relationships between biomarkers, lifestyle factors, and disease outcomes. lifestyle, nutrition, and biomarkers exploring how diet, alcohol consumption, and other lifestyle factors interact with genetic predispositions to influence health. artificial intelligence in health prediction leveraging ai and machine learning to predict health outcomes using large datasets. global health and interventions engaging in research that informs public health interventions and policies, especially in the context of global health disparities. dr. raha pazoki is addressing several critical problems in public health and biomedical science, particularly in the context of cardiometabolic diseases. here's a breakdown of the problems she's tackling and why they matter: 🧩 problems she’s solving understanding genetic and environmental risk factors problem: cardiovascular and metabolic diseases (like heart disease, diabetes, and liver dysfunction) are influenced by a complex interplay of genetic and lifestyle factors. her work: she identifies both genetic variants and non-genetic contributors (e.g., diet, alcohol, physical activity) that increase disease risk. causal inference in epidemiology problem: observational studies often show associations, but not causation. her work: she uses mendelian randomization to determine whether certain biomarkers or behaviors cause disease, rather than just correlate with it. improving disease prediction and prevention problem: current risk prediction models often lack precision, especially across diverse populations. her work: by integrating genomic data with clinical and lifestyle information, she helps build more accurate, personalized prediction tools. bridging the gap between big data and clinical practice problem: despite the explosion of health data, translating it into actionable insights remains a challenge. her work: she applies ai and machine learning to large datasets (e.g., uk biobank) to uncover patterns that can inform public health interventions and clinical guidelines. 🌍 why it matters public health impact: cardiometabolic diseases are leading causes of death globally. understanding their root causes can lead to better prevention strategies and reduced healthcare costs. equity in healthcare: her work helps ensure that genetic research benefits diverse populations. scientific rigor: by focusing on causal relationships, her research improves the reliability of health recommendations. policy and practice: her findings can inform national health policies, especially around lifestyle interventions and early screening. dr. raha pazoki’s research has significant clinical and societal applications, particularly in the prevention, early detection, and personalized treatment of cardiometabolic diseases. here's how her work translates into real-world impact: 🏥 clinical applications personalized risk prediction by integrating genetic data with lifestyle factors, her research helps develop precision medicine tools that can predict an individual’s risk for conditions like hypertension, liver disease, and cardiovascular disease. example: her work on genetic liabilities and hypertension using machine learning improves how clinicians classify and manage high blood pressure. causal insights for treatment using mendelian randomization, she identifies causal relationships between biomarkers (like liver enzymes or alcohol-related genes) and diseases. this helps clinicians target the right pathways for intervention. improved screening and diagnostics her findings on gene-diet interactions and biomarker profiles can inform screening guidelines, especially for at-risk populations, enabling earlier and more accurate diagnoses . 🌍 societal applications public health policy her research supports evidence-based policies on alcohol consumption, nutrition, and physical activity by showing how these factors interact with genetics to influence disease risk. health equity by analyzing large, diverse datasets like the uk biobank, she contributes to more inclusive health research, ensuring that findings are applicable across different ethnic and socioeconomic groups. ai in healthcare her use of artificial intelligence to analyze complex health data helps automate and scale health risk assessments, making them more accessible in both high- and low-resource settings . education and capacity building as a senior lecturer and research leader, she trains the next generation of scientists in data-driven, ethical, and impactful health research. dr. raha pazoki’s research is already showing real-world outcomes and holds strong near-future potential in both clinical and public health domains. ✅ real-world outcomes stroke risk prediction using genetics and ai in a recent study, dr. pazoki and her team demonstrated that incorporating genetic liability scores into machine learning models significantly improves the prediction of stroke risk. this model, using uk biobank data, showed that individuals with higher genetic risk had a 14% increased risk of stroke. the best-performing model achieved an auc of 69.5, indicating strong predictive power. discovery of genetic loci for liver enzymes she was the first to identify 517 novel genetic loci associated with liver enzymes, and showed their causal role in cardiovascular disease .this discovery is already influencing how researchers and clinicians understand liver function as a predictive biomarker for heart disease. alcohol-related genetic insights her work on the wdpcp gene revealed its role in alcohol metabolism and its link to liver cirrhosis and lipid disorders, which could inform personalized lifestyle recommendations and early intervention. 🔮 near-future potential precision medicine tools her research is paving the way for genetically-informed clinical decision-making, where a patient’s genetic profile could guide personalized prevention and treatment plans for cardiometabolic diseases. ai-driven health risk platforms by combining ai with genomics, her models could be integrated into clinical software to help gps and specialists identify high-risk patients earlier, especially for stroke, liver disease, and hypertension. public health interventions her findings on the interaction between lifestyle and genetic risk can inform targeted public health campaigns, especially in populations with high genetic susceptibility to certain diseases. global health equity her use of large, diverse datasets ensures that these tools and insights are applicable across ethnicities, helping reduce health disparities in genomic medicine. dr. raha pazoki’s work significantly advances our understanding of health, ageing, and wellbeing, particularly through the lens of genomics, lifestyle, and precision medicine. here's how her research contributes to these areas: 🧠 improving understanding genetic and lifestyle interactions her studies reveal how genetic predispositions interact with lifestyle factors like physical activity, diet, and alcohol consumption to influence ageing-related conditions such as hypertension, liver dysfunction, and cardiovascular disease . causal pathways in ageing diseases by applying mendelian randomization, she identifies causal relationships between biomarkers (e.g., liver enzymes, lipid levels) and age-related diseases, helping to clarify which factors are true drivers of decline in health . 🩺 enhancing treatment and prevention precision medicine for ageing populations her work supports the development of personalized treatment strategies by integrating genetic risk scores with clinical and lifestyle data. this is especially valuable for older adults, who often have complex, multi-factorial health profiles. early detection of age-related conditions her research on biomarkers and genetic loci enables earlier identification of individuals at risk for diseases like stroke, liver cirrhosis, and metabolic syndrome—conditions that become more prevalent with age . lifestyle-based interventions she has shown that physical activity can mitigate genetic risk for conditions like hypertension, offering actionable insights for public health and individual prevention strategies . 🌍 promoting wellbeing and healthy ageing data-driven public health her findings inform public health campaigns that promote healthy behaviours tailored to genetic risk, supporting longer, healthier lives. reducing health inequities by using large, diverse datasets, her work ensures that genomic insights are inclusive, helping to close gaps in health outcomes across different populations. ai for ageing research she applies machine learning to predict health outcomes in ageing populations, enabling scalable, cost-effective tools for monitoring and intervention
Dr Raha Pazoki
Raha Pazok MD PhD FHEA is a medical doctor and an epidemiologist. She studied Epidemiology at the Netherlands Institute for Health Sciences (NIHES) and in the University of Amsterdam. She worked with various cohort and case control studies such as the Arrhythmia Genetics in the Netherlands (AGNES), the Rotterdam Study, the Airwave Health Monitoring Study and the UK Bio bank. In 2016, she joined the Department of Epidemiology and Bio-statistics at Imperial College London as a Research Associate. In 2020, she started a Teaching & Research academic position at Brunel University London. Dr Pazoki specializes in the field of health data research, with a primary focus on the epidemiology of cardiometabolic diseases. She holds a particular interest in exploring causal inference and precision medicine by leveraging genomics and extensive health data sets with sample sizes exceeding 500,000 individuals. Her expertise spans various domains, including precision medicine, global health, interventions, and the application of artificial intelligence for predicting health outcomes. She harbors a keen interest in identification of the relationship between circulating molecules and biomarkers, nutrition, lifestyle choices, genetic factors, and their collective contribution to the modulation of health risk factors and outcomes. She was the first to identify 517 novel genetic loci associated with liver enzymes and the first to show the causal effect of liver dysfunction on cardiovascular diseases. In addition, she is the first to show the effect of the alcohol consumption WDPCP gene in lipid metabolism, and liver cirrhosis. (Genetic) Epidemiology of Cardiovascular Diseases Big Data Genome-wide Association Studies Genetic risk scores Mendelian Randomization Machine Learning Dr Paozki is a founder and director of the Cardiovascular and Metabolic Research Group hosting researchers and academics across Brunel university with direct or indirect research interest involving cardiometabolic aetiology, prevention, and health. We work in various areas to identify causes of cardiometabolic diseases (environmental, lifestyle, molecular, and clinical) and provide insight into how they interplay. We use the information for better prevention of cardiometabolic diseases in the community. If you are a MSc graduates (with upper second class degree or higher) in the relevant field to the above research area, please contact Dr Raha Pazoki (raha.pazoki@brunel.ac.uk). Postgraduate fees and funding | Brunel University London or Scholarships and Bursaries | Brunel University London and Other funding | Brunel University London Dr. Raha Pazoki's research is centered around health data science, with a strong emphasis on cardiometabolic diseases. 🔬 Key Research Themes Cardiometabolic Epidemiology Investigating the genetic and environmental determinants of cardiovascular and metabolic disorders. Studying conditions like hypertension, diabetes, liver dysfunction, and lipid metabolism. Genomics and Precision Medicine Utilizing large-scale genomic data (e.g., UK Biobank) to identify genetic loci associated with disease. She was the first to identify 517 novel genetic loci linked to liver enzymes and demonstrated their causal role in cardiovascular disease. Causal Inference in Epidemiology Applying Mendelian randomization and other causal inference techniques to understand the relationships between biomarkers, lifestyle factors, and disease outcomes. Lifestyle, Nutrition, and Biomarkers Exploring how diet, alcohol consumption, and other lifestyle factors interact with genetic predispositions to influence health. Artificial Intelligence in Health Prediction Leveraging AI and machine learning to predict health outcomes using large datasets. Global Health and Interventions Engaging in research that informs public health interventions and policies, especially in the context of global health disparities. Dr. Raha Pazoki is addressing several critical problems in public health and biomedical science, particularly in the context of cardiometabolic diseases. Here's a breakdown of the problems she's tackling and why they matter: 🧩 Problems She’s Solving Understanding Genetic and Environmental Risk Factors Problem: Cardiovascular and metabolic diseases (like heart disease, diabetes, and liver dysfunction) are influenced by a complex interplay of genetic and lifestyle factors. Her Work: She identifies both genetic variants and non-genetic contributors (e.g., diet, alcohol, physical activity) that increase disease risk. Causal Inference in Epidemiology Problem: Observational studies often show associations, but not causation. Her Work: She uses Mendelian randomization to determine whether certain biomarkers or behaviors cause disease, rather than just correlate with it. Improving Disease Prediction and Prevention Problem: Current risk prediction models often lack precision, especially across diverse populations. Her Work: By integrating genomic data with clinical and lifestyle information, she helps build more accurate, personalized prediction tools. Bridging the Gap Between Big Data and Clinical Practice Problem: Despite the explosion of health data, translating it into actionable insights remains a challenge. Her Work: She applies AI and machine learning to large datasets (e.g., UK Biobank) to uncover patterns that can inform public health interventions and clinical guidelines. 🌍 Why It Matters Public Health Impact: Cardiometabolic diseases are leading causes of death globally. Understanding their root causes can lead to better prevention strategies and reduced healthcare costs. Equity in Healthcare: Her work helps ensure that genetic research benefits diverse populations. Scientific Rigor: By focusing on causal relationships, her research improves the reliability of health recommendations. Policy and Practice: Her findings can inform national health policies, especially around lifestyle interventions and early screening. Dr. Raha Pazoki’s research has significant clinical and societal applications, particularly in the prevention, early detection, and personalized treatment of cardiometabolic diseases. Here's how her work translates into real-world impact: 🏥 Clinical Applications Personalized Risk Prediction By integrating genetic data with lifestyle factors, her research helps develop precision medicine tools that can predict an individual’s risk for conditions like hypertension, liver disease, and cardiovascular disease. Example: Her work on genetic liabilities and hypertension using machine learning improves how clinicians classify and manage high blood pressure. Causal Insights for Treatment Using Mendelian randomization, she identifies causal relationships between biomarkers (like liver enzymes or alcohol-related genes) and diseases. This helps clinicians target the right pathways for intervention. Improved Screening and Diagnostics Her findings on gene-diet interactions and biomarker profiles can inform screening guidelines, especially for at-risk populations, enabling earlier and more accurate diagnoses . 🌍 Societal Applications Public Health Policy Her research supports evidence-based policies on alcohol consumption, nutrition, and physical activity by showing how these factors interact with genetics to influence disease risk. Health Equity By analyzing large, diverse datasets like the UK Biobank, she contributes to more inclusive health research, ensuring that findings are applicable across different ethnic and socioeconomic groups. AI in Healthcare Her use of artificial intelligence to analyze complex health data helps automate and scale health risk assessments, making them more accessible in both high- and low-resource settings . Education and Capacity Building As a senior lecturer and research leader, she trains the next generation of scientists in data-driven, ethical, and impactful health research. Dr. Raha Pazoki’s research is already showing real-world outcomes and holds strong near-future potential in both clinical and public health domains. ✅ Real-World Outcomes Stroke Risk Prediction Using Genetics and AI In a recent study, Dr. Pazoki and her team demonstrated that incorporating genetic liability scores into machine learning models significantly improves the prediction of stroke risk. This model, using UK Biobank data, showed that individuals with higher genetic risk had a 14% increased risk of stroke. The best-performing model achieved an AUC of 69.5, indicating strong predictive power. Discovery of Genetic Loci for Liver Enzymes She was the first to identify 517 novel genetic loci associated with liver enzymes, and showed their causal role in cardiovascular disease .This discovery is already influencing how researchers and clinicians understand liver function as a predictive biomarker for heart disease. Alcohol-Related Genetic Insights Her work on the WDPCP gene revealed its role in alcohol metabolism and its link to liver cirrhosis and lipid disorders, which could inform personalized lifestyle recommendations and early intervention. 🔮 Near-Future Potential Precision Medicine Tools Her research is paving the way for genetically-informed clinical decision-making, where a patient’s genetic profile could guide personalized prevention and treatment plans for cardiometabolic diseases. AI-Driven Health Risk Platforms By combining AI with genomics, her models could be integrated into clinical software to help GPs and specialists identify high-risk patients earlier, especially for stroke, liver disease, and hypertension. Public Health Interventions Her findings on the interaction between lifestyle and genetic risk can inform targeted public health campaigns, especially in populations with high genetic susceptibility to certain diseases. Global Health Equity Her use of large, diverse datasets ensures that these tools and insights are applicable across ethnicities, helping reduce health disparities in genomic medicine. Dr. Raha Pazoki’s work significantly advances our understanding of health, ageing, and wellbeing, particularly through the lens of genomics, lifestyle, and precision medicine. Here's how her research contributes to these areas: 🧠 Improving Understanding Genetic and Lifestyle Interactions Her studies reveal how genetic predispositions interact with lifestyle factors like physical activity, diet, and alcohol consumption to influence ageing-related conditions such as hypertension, liver dysfunction, and cardiovascular disease . Causal Pathways in Ageing Diseases By applying Mendelian randomization, she identifies causal relationships between biomarkers (e.g., liver enzymes, lipid levels) and age-related diseases, helping to clarify which factors are true drivers of decline in health . 🩺 Enhancing Treatment and Prevention Precision Medicine for Ageing Populations Her work supports the development of personalized treatment strategies by integrating genetic risk scores with clinical and lifestyle data. This is especially valuable for older adults, who often have complex, multi-factorial health profiles. Early Detection of Age-Related Conditions Her research on biomarkers and genetic loci enables earlier identification of individuals at risk for diseases like stroke, liver cirrhosis, and metabolic syndrome—conditions that become more prevalent with age . Lifestyle-Based Interventions She has shown that physical activity can mitigate genetic risk for conditions like hypertension, offering actionable insights for public health and individual prevention strategies . 🌍 Promoting Wellbeing and Healthy Ageing Data-Driven Public Health Her findings inform public health campaigns that promote healthy behaviours tailored to genetic risk, supporting longer, healthier lives. Reducing Health Inequities By using large, diverse datasets, her work ensures that genomic insights are inclusive, helping to close gaps in health outcomes across different populations. AI for Ageing Research She applies machine learning to predict health outcomes in ageing populations, enabling scalable, cost-effective tools for monitoring and intervention
Cliff
jackie read physiological sciences at the university of oxford, followed by an msc in the immunology of infectious diseases at the london school of hygiene & tropical medicine. she then moved to the national institute for medical research for her phd, where she investigated the role of cytokines in b cell activation and differentiation with dr gerry klaus. jackie worked with prof hazel dockrell at lshtm (1999-2022), mainly studying immune responses in tuberculosis and how these could be utilised to assess responses to antibiotic treatment. more recently, her research has also encompassed comorbidities such as diabetes in tuberculosis, and expanded to include the role of the infection and immunity in myalgic encephalomyelitis/ chronic fatigue syndrome. jackie joined brunel university in march 2022, combining her research in the biosciences division with her teaching within the medical school. myalgic encephalomyelitis / chronic fatigue syndrome long covid tuberculosis type 2 diabetes treatment-response biomarkers jackie’s main research interests are in infectious diseases, and particularly how chronic conditions affect immune responses to pathogens. a substantial part of jackie’s research has been investigating immune responses in people with tuberculosis, and specifically how altered blood gene expression can be utilised for tuberculosis diagnosis and drug treatment monitoring: this is beneficial for clinical management and for the development of new drugs. in a multicentre study, her research group also found that people with type 2 diabetes have excessive inflammatory responses in tuberculosis but suppressed specific protective immune responses, which may underpin their recognised enhanced susceptibility to tuberculosis disease. we are currently using macrophage in vitro models to further understand protective immunity to mycobacterium tuberculosis, and how this is affected in diabetes. this could lead to host-directed therapy in this group of people, alongside conventional antibiotic treatment. jackie has also been investigating immunological changes in people living with myalgic encephalomyelitis / chronic fatigue syndrome (me/cfs), a poorly understood condition estimated to affect around 125,000 people in the uk, often leading to severe disability. it is frequently triggered by viral infection, and there are substantial overlaps in symptomology with people with long covid, including severe fatigue, post-exertional symptom exacerbation and brain fog. we have found alterations in the t cell compartment in people with me/cfs, and also preliminary evidence of enhanced reactivation of some human herpesviruses, which are highly prevalent in the adult population but usually well-controlled. medicine mbbs academic lead year 2 student selected component medicine mbbs academic content expert immunology y1 and y2 medicine mbbs house tutor – elizabeth garrett anderson
Dr Jacqueline Cliff
Jackie read Physiological Sciences at the University of Oxford, followed by an MSc in the Immunology of Infectious Diseases at the London School of Hygiene & Tropical Medicine. She then moved to the National Institute for Medical Research for her PhD, where she investigated the role of cytokines in B cell activation and differentiation with Dr Gerry Klaus. Jackie worked with Prof Hazel Dockrell at LSHTM (1999-2022), mainly studying immune responses in tuberculosis and how these could be utilised to assess responses to antibiotic treatment. More recently, her research has also encompassed comorbidities such as diabetes in tuberculosis, and expanded to include the role of the infection and immunity in Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome. Jackie joined Brunel University in March 2022, combining her research in the Biosciences Division with her teaching within the Medical School. Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Long COVID Tuberculosis Type 2 diabetes Treatment-response Biomarkers Jackie’s main research interests are in infectious diseases, and particularly how chronic conditions affect immune responses to pathogens. A substantial part of Jackie’s research has been investigating immune responses in people with tuberculosis, and specifically how altered blood gene expression can be utilised for tuberculosis diagnosis and drug treatment monitoring: this is beneficial for clinical management and for the development of new drugs. In a multicentre study, her research group also found that people with type 2 diabetes have excessive inflammatory responses in tuberculosis but suppressed specific protective immune responses, which may underpin their recognised enhanced susceptibility to tuberculosis disease. We are currently using macrophage in vitro models to further understand protective immunity to Mycobacterium tuberculosis, and how this is affected in diabetes. This could lead to host-directed therapy in this group of people, alongside conventional antibiotic treatment. Jackie has also been investigating immunological changes in people living with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS), a poorly understood condition estimated to affect around 125,000 people in the UK, often leading to severe disability. It is frequently triggered by viral infection, and there are substantial overlaps in symptomology with people with Long COVID, including severe fatigue, post-exertional symptom exacerbation and brain fog. We have found alterations in the T cell compartment in people with ME/CFS, and also preliminary evidence of enhanced reactivation of some human herpesviruses, which are highly prevalent in the adult population but usually well-controlled. Medicine MBBS Academic Lead Year 2 Student Selected Component Medicine MBBS Academic Content Expert Immunology Y1 and Y2 Medicine MBBS House Tutor – Elizabeth Garrett Anderson
Tsolaki
qualifications: dphil, university of oxford, 1999 msc, london school of hygiene and tropical medicine, 1994 bsc (hons), biochemistry, university of north london, 1993 academic appointments september 2006 - present lecturer, brunel university london september 2004 - august 2006, post doctoral fellow, imperial college london may 2000 - july 2004 post doctoral fellow, stanford university may 1999 - may 2000 university of california, berkeley molecular epidemiology of tuberculosis host-pathogen interactions in tuberculosis molecular evolution of mycobacterium tuberculosis mechanisms of genomic variability in mycobacterium tuberculosis microbial genomics innate immunity in tuberculosis infection teaching responsibilities: bb2716 medical microbiology bb3716 microbial pathogenesis bb2805 biomedical sciences
Dr Anthony Tsolaki
Qualifications: DPhil, University of Oxford, 1999 MSc, London School of Hygiene and Tropical Medicine, 1994 BSc (Hons), Biochemistry, University of North London, 1993 Academic Appointments September 2006 - Present Lecturer, Brunel University London September 2004 - August 2006, Post Doctoral Fellow, Imperial College London May 2000 - July 2004 Post Doctoral Fellow, Stanford University May 1999 - May 2000 University of California, Berkeley Molecular epidemiology of tuberculosis Host-pathogen interactions in tuberculosis Molecular evolution of Mycobacterium tuberculosis Mechanisms of genomic variability in Mycobacterium tuberculosis Microbial genomics Innate Immunity in tuberculosis Infection Teaching Responsibilities: BB2716 Medical Microbiology BB3716 Microbial Pathogenesis BB2805 Biomedical Sciences
Smith
steven obtained a b.sc. in medical sciences from the university of leeds and received a ph.d. for a project at the cancer medicine research unit at st. james's university hospital, leeds, investigating the cd8 t-cell stimulating properties of a dna vaccine encoding multiple, melanoma-associated epitopes. following a post-doctoral position at the edward jenner institute for vaccine research in which he examined the role of auto-reactive cd8 t-cells and t-cell regulation in the context of joint inflammation, he joined the group of prof. hazel dockrell at the london school of hygiene and tropical medicine where he investigated the cellular immune response to bcg vaccination and more generally with immune mechanisms that might provide protection against tuberculosis infection and disease. steven joined the division of biosciences in january 2020. i am is interested in understanding which immune response elements are responsible for protection against infection with mycobacterium tuberculosis, the causative agent of tb, as well as those which prevent the development of active tb disease. although it provides incomplete protection against tb, there is much to be learnt from the immune response to the bcg vaccine which in certain circumstances, may be effective. although traditionally seen as t-cell-mediated, recent times have seen an increased interested in the role of b-cells and antibodies as well as potentially long-lived innate cells in immune protection against tb. as bcg is known to impact upon each of these immune compartments, each or all could have a role in protection. in collaboration with teams at the mrc/uvri & lshtm unit in uganda, the international tuberculosis research center, korea and institut politecnico nacional, mexico, i use samples from bcg-vaccinated individuals, a variety of in vitro cellular models of innate and adaptive immune responses and analytical methods such as functional bacterial inhibition assays, multiparameter flow cytomtry, elisa/luminex and dna methylation analysis to probe questions such as: the phenotype and function of bcg-vaccine-induced t-cells the potential for bcg-"trained" monocytes to protect against tb the role of metabolic intermediates in bcg-induced trained immunity and the potential for these to enhance vaccine effectiveness the use of immunological biomarker assays to monitor responses in patients and in vaccine trials against tb in different settings immunological biomarkers of protection against tuberculosis bcg vaccination innate/adaptive immunity
Dr Steven Smith
Steven obtained a B.Sc. in Medical Sciences from the University of Leeds and received a Ph.D. for a project at the Cancer Medicine Research Unit at St. James's University Hospital, Leeds, investigating the CD8 T-cell stimulating properties of a DNA vaccine encoding multiple, melanoma-associated epitopes. Following a post-doctoral position at the Edward Jenner Institute for Vaccine Research in which he examined the role of auto-reactive CD8 T-cells and T-cell regulation in the context of joint inflammation, he joined the group of Prof. Hazel Dockrell at the London School of Hygiene and Tropical Medicine where he investigated the cellular immune response to BCG vaccination and more generally with immune mechanisms that might provide protection against tuberculosis infection and disease. Steven joined the Division of Biosciences in January 2020. I am is interested in understanding which immune response elements are responsible for protection against infection with Mycobacterium tuberculosis, the causative agent of TB, as well as those which prevent the development of active TB disease. Although it provides incomplete protection against TB, there is much to be learnt from the immune response to the BCG vaccine which in certain circumstances, may be effective. Although traditionally seen as T-cell-mediated, recent times have seen an increased interested in the role of B-cells and antibodies as well as potentially long-lived innate cells in immune protection against TB. As BCG is known to impact upon each of these immune compartments, each or all could have a role in protection. In collaboration with teams at the MRC/UVRI & LSHTM Unit in Uganda, the International Tuberculosis Research Center, Korea and Institut Politecnico Nacional, Mexico, I use samples from BCG-vaccinated individuals, a variety of in vitro cellular models of innate and adaptive immune responses and analytical methods such as functional bacterial inhibition assays, multiparameter flow cytomtry, ELISA/Luminex and DNA methylation analysis to probe questions such as: the phenotype and function of BCG-vaccine-induced T-cells the potential for BCG-"trained" monocytes to protect against TB the role of metabolic intermediates in BCG-induced trained immunity and the potential for these to enhance vaccine effectiveness the use of immunological biomarker assays to monitor responses in patients and in vaccine trials against TB in different settings Immunological biomarkers of protection against tuberculosis BCG vaccination Innate/adaptive immunity
Sala
trained in biochemistry and cellular biology at the university of rome and the italian national institute of health, i completed a phd in biochemistry at the university of rome “la sapienza” on the topic of dna and rna methylation in relation to muscle cell differentiation. after a short postdoctoral training in the national institute of health in rome, i won an international post-doctoral fellowship from the italian association for cancer research (airc) and moved to the kimmel cancer institute, thomas jefferson university philadelphia. working in the laboratory of prof. bruno calabretta, i was the first to characterize the transcription factor and oncoprotein b-myb and establish its relationship with key tumour suppressor genes, such as p53 and retinoblastoma family members. in 2001 i was recruited by the ucl institute of child health as senior lecturer and later promoted to reader. in ucl i continued to pursue the study of oncogenic transcription factors in the context of neuroblastoma, a childhood tumour affecting the peripheral nervous system. i was appointed professor of translational cancer research and deputy director of the brunel institute of cancer genetics and pharmacogenomics in september 2011. in 2016 i joined the synthetic biology theme in the institute of environment, health and societes. neuroblastoma, adenoid cystic carcinoma, friedreich's ataxia rare cancers; neurodegenerative diseases; gene and cell therapy coordinator of the masters' cancer module
Professor Arturo Sala
Trained in Biochemistry and Cellular Biology at the University of Rome and the Italian National Institute of Health, I completed a PhD in Biochemistry at the University of Rome “La Sapienza” on the topic of DNA and RNA methylation in relation to muscle cell differentiation. After a short postdoctoral training in the National Institute of Health in Rome, I won an international post-doctoral fellowship from the Italian Association for Cancer Research (AIRC) and moved to the Kimmel Cancer Institute, Thomas Jefferson University Philadelphia. Working in the laboratory of Prof. Bruno Calabretta, I was the first to characterize the transcription factor and oncoprotein B-MYB and establish its relationship with key tumour suppressor genes, such as p53 and retinoblastoma family members. In 2001 I was recruited by the UCL Institute of Child Health as Senior Lecturer and later promoted to Reader. In UCL I continued to pursue the study of oncogenic transcription factors in the context of neuroblastoma, a childhood tumour affecting the peripheral nervous system. I was appointed Professor of Translational Cancer Research and Deputy Director of the Brunel Institute of Cancer Genetics and Pharmacogenomics in September 2011. In 2016 I joined the Synthetic Biology Theme in the Institute of Environment, Health and Societes. Neuroblastoma, adenoid cystic carcinoma, Friedreich's ataxia Rare cancers; neurodegenerative diseases; Gene and cell therapy Coordinator of the masters' cancer module
Houlden
i am a microbial ecologist in the division of biosciences, within the college of health and life sciences at the university of brunel london. my research interests lie in the assessment of microbial community structure and function using high throughput sequencing and molecular microbiological techniques. focusing on the host microbiome their interaction with one another in this community and changes as a result of disease or injury, this characterisation of the communities allows the identification of functionally important changes in microbial assemblages and detection of antimicrobial resistance. my research has included work on the impact of stroke, brain injury, parasitic intestinal infections, and dementia on the interactions with the host and its microbiome. one of my current research focus areas is women's health, i am studying bacterial vaginosis, the interaction of microbes present in the vagina, detection of potential pathogens, and the development of an in-house in vitro model system using organ on a chip technology for 3d tissue culture to simulate the vaginal environment. linked to this i am interested in the impact that space travel and microgravity has on microbial populations and implications for health. i am also interested in antimicrobial resistance (amr) and detection of amr in bacterial communities with a focus on the environmental impact and ecological implications of this. it is becoming increasing an issue that amr organisms are colonising animal populations and if these pathogens are accumulated in apex predators via food chain acquisition. my doctorial training was in soil microbial ecology carrying out risk assessments and the efficacy of using bacterial biological control agents against fungi diseases of crops in laboratory, glass house and field experiments while at ceh-oxford/cardiff university. i then undertook postdoctoral research at the university of sheffield followed by the university of manchester continuing research into environmental microbiology looking a biogeochemical cycling of nitrogen and sulphur. while at manchester i moved into medical microbiome research as researcher co-investigator on a grant on t. muris and the impact on the microbiome and host. as a result of this i have formed a number of collaborations involving microbiome research. bb2716 medical microbiology (second year)
Dr Ashley Houlden
I am a Microbial Ecologist in the Division of Biosciences, within the College of Health and Life Sciences at the University of Brunel London. My research interests lie in the assessment of microbial community structure and function using high throughput sequencing and molecular microbiological techniques. Focusing on the Host microbiome their interaction with one another in this community and changes as a result of disease or injury, this characterisation of the communities allows the identification of functionally important changes in microbial assemblages and detection of Antimicrobial Resistance. My research has included work on the impact of stroke, brain injury, parasitic intestinal infections, and dementia on the interactions with the host and its microbiome. One of my Current research focus areas is women's health, I am studying bacterial vaginosis, the interaction of microbes present in the vagina, detection of potential pathogens, and the development of an in-house in vitro model system using Organ on a Chip technology for 3D tissue culture to simulate the vaginal environment. Linked to this I am interested in the impact that space travel and microgravity has on microbial populations and implications for health. I am also interested in antimicrobial resistance (AMR) and detection of AMR in bacterial communities with a focus on the environmental impact and ecological implications of this. It is becoming increasing an issue that AMR organisms are colonising animal populations and if these pathogens are accumulated in Apex predators via food chain acquisition. My Doctorial training was in soil microbial ecology carrying out risk assessments and the efficacy of using bacterial biological control agents against fungi diseases of crops in laboratory, glass house and field experiments while at CEH-Oxford/Cardiff University. I then undertook postdoctoral research at The University of Sheffield followed by The University of Manchester continuing research into environmental microbiology looking a biogeochemical cycling of Nitrogen and sulphur. While at Manchester I moved into medical microbiome research as Researcher Co-Investigator on a grant on T. Muris and the impact on the microbiome and host. As a result of this I have formed a number of collaborations involving microbiome research. BB2716 Medical Microbiology (Second Year)
Redpath
keith graduated with a bsc (hons) in biomedical sciences, physiology from the university of aberdeen, scotland, 2009. he then moved straight into a phd in the lab of prof graeme nixon at the university of aberdeen, investigating how zinc deficiency affects vascular smooth muscle cell signalling within the aorta and carotid arteries. this phd was part funded by the national research foundation of korea (nrf). he graduated with his phd in 2013. keith then moved to cardiff, wales to take up a 5-year bhf funded research associate position in the lab of prof valerie o'donnell investigating specfically how oxidized phospholipids participate in abdominal aortic aneurysms (aaa). in 2018, keith then took up a senior research fellow position at the university of reading, england in the lab of prof parveen yaqoob, it was here that he developed a keen interest in extracellular vesicles and how they signal in vascular diseases such as ischemic heart disease (ihd) and aaa. in january 2023, keith became a lecturer in vascular biology at brunel university london, england where he aims to develop further his research into extracellular vesicles and vascular diseases. ischemic heart disease abdominal aortic aneurysms coagulation extracellular vesicles nutrition and zinc deficiency inflammation vascular smooth muscle cell physiology coagulation and thrombosis ageing and vascular senescence bb1724- career planning & innovation (block lead) bb1822- biomedical sciences examinations (block lead) bb1721- the human body: principles of anatomy & physiology bb2555- work placement bb1700- tutoring bb1601- biomedical science training ls1807- biochemistry and molecular and cellular biology examinations
Dr Keith Redpath
Keith graduated with a BSc (Hons) in Biomedical Sciences, Physiology from the University of Aberdeen, Scotland, 2009. He then moved straight into a PhD in the lab of Prof Graeme Nixon at the University of Aberdeen, investigating how zinc deficiency affects vascular smooth muscle cell signalling within the aorta and carotid arteries. This PhD was part funded by the National Research Foundation of Korea (NRF). He graduated with his PhD in 2013. Keith then moved to Cardiff, Wales to take up a 5-year BHF funded research associate position in the lab of Prof Valerie O'Donnell investigating specfically how oxidized phospholipids participate in abdominal aortic aneurysms (AAA). In 2018, Keith then took up a senior research fellow position at the University of Reading, England in the lab of Prof Parveen Yaqoob, it was here that he developed a keen interest in extracellular vesicles and how they signal in vascular diseases such as ischemic heart disease (IHD) and AAA. In January 2023, Keith became a lecturer in vascular biology at Brunel University London, England where he aims to develop further his research into extracellular vesicles and vascular diseases. Ischemic heart disease Abdominal aortic aneurysms Coagulation Extracellular vesicles Nutrition and zinc deficiency Inflammation Vascular smooth muscle cell physiology Coagulation and thrombosis Ageing and vascular senescence BB1724- Career Planning & Innovation (Block Lead) BB1822- Biomedical Sciences Examinations (Block Lead) BB1721- The Human Body: Principles of Anatomy & Physiology BB2555- Work Placement BB1700- Tutoring BB1601- Biomedical Science Training LS1807- Biochemistry and Molecular and Cellular Biology Examinations
Willcocks
sam joined brunel university london as a lecturer in biosciences in 2022 from the london school of hygiene and tropical medicine (lshtm), where he worked as assistant professor in the department of infection biology. he previously received his phd in innate immunology at the royal veterinary college, london in 2008. in 2018, sam received an mrc confidence in concept award for the development of a novel class of antimicrobials against mycobacterium tuberculosis and in 2020 was awarded the wellcome translational accelerator award to determine their mechanism of action. sam also holds an honorary fellowship at birkbeck university london and retains strong links with the antimicrobial resistance centre at lshtm where he was previously head of biological and pharmacological sciences. my research interests are focussed on: developing new antimicrobials against mycobacterial species, and using molecular approaches to understand their targets, mechanisms of action and resistance exploring the repurposing of existing drugs for use as antimicrobials modelling the role of the host immune system on drug-target interactions in vivo
Dr Sam Willcocks
Sam joined Brunel University London as a Lecturer in Biosciences in 2022 from the London School of Hygiene and Tropical Medicine (LSHTM), where he worked as Assistant Professor in the Department of Infection Biology. He previously received his PhD in Innate Immunology at the Royal Veterinary College, London in 2008. In 2018, Sam received an MRC Confidence in Concept Award for the development of a novel class of antimicrobials against Mycobacterium tuberculosis and in 2020 was awarded the Wellcome Translational Accelerator Award to determine their mechanism of action. Sam also holds an Honorary Fellowship at Birkbeck University London and retains strong links with the Antimicrobial Resistance Centre at LSHTM where he was previously Head of Biological and Pharmacological Sciences. My research interests are focussed on: Developing new antimicrobials against mycobacterial species, and using molecular approaches to understand their targets, mechanisms of action and resistance Exploring the repurposing of existing drugs for use as antimicrobials Modelling the role of the host immune system on drug-target interactions in vivo
Cerutti
dr camilla cerutti is a lecturer in inflammation, ageing and cancer biology at brunel university london and visiting researcher at the european institute of oncology since 2023. her research focuses on vascular and cancer cell biology in particular on cell-cell interaction and cancer metastasis. camilla graduated in medical biotechnology (bsc) at the university of milan bicocca in italy. at the same university she completed a msc in industrial biotechnology-pharmacogenomic- in 2009 with an erasmus final project placement of one year at complutense university in madrid, spain. here, she investigated the anti-tumoral effects of cannabinoids on breast cancer via jund in vitro and via akt in vivo (caffarel et al. 2008 and 2010). she completed her phd in neuro-vascular immunology in 2014 at the open university in milton keynes, uk, studying the role of human brain endothelial micrornas in leukocyte adhesion in neurodegenerative disorder such as multiple sclerosis. she developed an microfluidic system to model the interaction of human leukocyte with brain endothelial cells under hemodynamic shear forces in vitro (cerutti et al 2022). she found that human brain endothelial mir-155, mir-126 and mir-126* regulate leukocyte trafficking at the blood-brain barrier in inflammatory conditions (cerutti et al 2016 and 2017, wu 2015). dr cerutti joined the ridley`s lab at kcl, london, as research associate postdoc, where she investigated the role of rhogtpases in human breast and prostate cancer cells in the interaction with endothelial cells and during metastasis formation (cerutti et al 2021;and cerutti et al 2024). this cruk funded project in collaboration with prof muschel lab at the university of oxford (lucotti et al 2019) was further developed as senior research associate postdoc at the university of bristol leading to find that iqgap1 and nwasp promote human cancer cell dissemination and metastasis by regulating β1-integrin via fak and mrtf/srf. in 2018 she won a global research development fund from kcl to join peter searson nanobiotechnology lab at the john hopkins university (baltimore, usa) to learn the fabrication of 3d perfusable vascular microvessels. in 2020 camilla was awarded the icare-2 msca h2020 fellowship as principal investigator of the project -single-cell epigenetic and molecular signatures in human breast cancer metastasis formation - reintegration fellowship in the host lab of professor pier giuseppe pelicci at the european institute of oncology. currently, dr cerutti lab at brunel university london investigates cancer metastasis mechanisms with 2d and 3d vascular models to study cell-cell interactions by high-content live-cell imaging. 📣msca postdoctoral fellow welcome! apply here: cancer metastasis organ-specific vasculatures microfluidic 2d and 3d human vascular models cell adhesion and migration cell signaling breast and prostate cancer; endothelial cells blood-brain-barrier vascular inflammation signalling shear stress high-content live-cell imaging we are interested to unravel the molecular mechanisms of cell:cell interaction with particular focus on cancer metastasis formation. grants: 2025 diabetes uk early career small grant (co-pi) 2025 royal society international exchanges 2024 global round 3 (pi) 2024 brief award brunel university of london, uk (pi) 2024 bhf non-clinical phd-fellowship british heart fundation uk (co-pi) teaching: bb3091-final year projects (trimester 1) bb2704-molecular and cellular biology (trimester 2) bb2708-clonogenic lecture and praticals (week 19) bb3733-molecular pharmacology and toxicology (week 25) bb5715 & bb5715 cancer biology machanism and treatments (week 25) lead assessment block bb2804 data analysis on a study case (mcqs and poster presentation) assessments: bb2802&ls2800-primary literature interrogation and synthesis (trimester 1) bb2555 work placement bb2803- data evaluation and reporting bb2804-data analysis, interpretation and presentation. bb3801-scientific communication bb3091-final year projects ls2808_cn - cell biology data evaluation and reporting - a scientific report
Dr Camilla Cerutti
Dr Camilla Cerutti is a Lecturer in Inflammation, Ageing and Cancer Biology at Brunel University London and visiting researcher at the European Institute of Oncology since 2023. Her research focuses on Vascular and Cancer cell biology in particular on cell-cell interaction and cancer metastasis. Camilla graduated in medical Biotechnology (BSc) at the University of Milan Bicocca in Italy. At the same university she completed a MSc in Industrial Biotechnology-Pharmacogenomic- in 2009 with an ERASMUS final project placement of one year at Complutense University in Madrid, Spain. Here, she investigated the anti-tumoral effects of cannabinoids on breast cancer via JunD in vitro and via Akt in vivo (Caffarel et al. 2008 and 2010). She completed her PhD in neuro-vascular immunology in 2014 at The Open University in Milton Keynes, UK, studying the role of human brain endothelial microRNAs in leukocyte adhesion in neurodegenerative disorder such as multiple sclerosis. She developed an microfluidic system to model the interaction of human leukocyte with brain endothelial cells under hemodynamic shear forces in vitro (Cerutti et al 2022). She found that human brain endothelial mir-155, mir-126 and mir-126* regulate leukocyte trafficking at the blood-brain barrier in inflammatory conditions (Cerutti et al 2016 and 2017, Wu 2015). Dr Cerutti joined the Ridley`s Lab at KCL, London, as research associate postdoc, where she investigated the role of RhoGTPases in human breast and prostate cancer cells in the interaction with endothelial cells and during metastasis formation (Cerutti et al 2021;and Cerutti et al 2024). This CRUK funded project in collaboration with Prof Muschel Lab at the University of Oxford (Lucotti et al 2019) was further developed as senior research associate postdoc at the University of Bristol leading to find that IQGAP1 and NWASP promote human cancer cell dissemination and metastasis by regulating β1-integrin via FAK and MRTF/SRF. In 2018 she won a Global Research Development Fund from KCL to join Peter Searson Nanobiotechnology Lab at the John Hopkins University (Baltimore, USA) to learn the fabrication of 3D perfusable vascular microvessels. In 2020 Camilla was awarded the iCARE-2 MSCA H2020 fellowship as principal investigator of the project -Single-cell epigenetic and molecular signatures in human breast cancer metastasis formation - reintegration fellowship in the host lab of Professor Pier Giuseppe Pelicci at the European Institute of Oncology. Currently, Dr Cerutti lab at Brunel University London investigates cancer metastasis mechanisms with 2D and 3D vascular models to study cell-cell interactions by high-content live-cell imaging. 📣MSCA Postdoctoral fellow welcome! Apply here: Cancer metastasis Organ-specific vasculatures Microfluidic 2D and 3D human vascular models Cell adhesion and migration cell signaling breast and prostate cancer; Endothelial cells blood-brain-barrier vascular inflammation signalling Shear stress High-content Live-cell imaging We are interested to unravel the molecular mechanisms of cell:cell interaction with particular focus on cancer metastasis formation. GRANTS: 2025 DIABETES UK Early career small grant (co-PI) 2025 Royal Society International Exchanges 2024 Global Round 3 (PI) 2024 BRIEF award Brunel University of London, UK (PI) 2024 BHF Non-clinical PhD-fellowship British Heart Fundation UK (co-PI) Teaching: BB3091-Final Year Projects (trimester 1) BB2704-Molecular and Cellular Biology (trimester 2) BB2708-Clonogenic lecture and praticals (week 19) BB3733-Molecular Pharmacology and Toxicology (week 25) BB5715 & BB5715 Cancer Biology Machanism and Treatments (week 25) LEAD Assessment BLOCK BB2804 Data analysis on a study case (MCQs and Poster presentation) Assessments: BB2802&LS2800-Primary Literature Interrogation and Synthesis (trimester 1) BB2555 Work PLacement BB2803- Data Evaluation and Reporting BB2804-Data analysis, Interpretation and Presentation. BB3801-Scientific communication BB3091-Final Year Projects LS2808_CN - Cell Biology Data Evaluation and Reporting - A scientific report
Lau
dr doreen lau is a lecturer at brunel university of london and a visiting researcher at the university of cambridge. she earned a phd from the university of cambridge as a cancer research uk and cambridge trust scholar, specialising in cancer immunology and the clinical translation of molecular imaging techniques and biomarkers for cancer immunotherapy in both patients and preclinical models. she received postgraduate training in cancer imaging and pharmacology at imperial college london, and previously worked as a scientist at the university of oxford and the agency for science, technology and research (a*star) in singapore. she was also a visiting scientist at astrazeneca, where she collaborated on tissue-based imaging biomarkers in immuno-oncology. dr lau served as a part-time lecturer in oxford previously, where she taught imaging, disease and treatment mechanisms in cancer, and was the module co-lead for cancer immunology. dr lau has received multiple international awards for her contributions to cancer immunology and imaging research. these include the 1st place william g. negendank young investigator award from the international society for magnetic resonance in medicine for cancer imaging (2018); the women in molecular imaging network scholar award from the world molecular imaging society (2019); a top 3 phd award from the european society for molecular imaging (2021); the merit travel grant and best poster award in immuno-oncology biomarker development from the european society for medical oncology (2023); and the best flash talk in cancer immunology from the chinese academy of medical sciences oxford institute network (2023). in recognition of her achievements as an early-career scientist, she was awarded a junior research fellowship in sciences from wolfson college, university of oxford, in 2022. dr lau's research group focuses on immuno-oncology imaging and experimental medicine. using state-of-the-art platforms for immune cell tracking, whole-body imaging, preclinical models, immuno-profiling and bioinformatics, the team investigates the biological mechanisms underlying anti-tumour immunity, treatment resistance and immune-related adverse events. the ultimate goal is to translate these findings into clinical practice for patient stratification, immunotherapy monitoring, and improved drug delivery. additionally, this research supports early-phase drug discovery by facilitating the screening and target validation of novel immunotherapeutics. these approaches have broader implications for studying chronic inflammation, infection, autoimmune diseases, and aging-related disorders including cancer. research collaboration open to academic collaboration, industry partnerships and joint phd supervision. cancer immunology, immunotherapy, biomarkers, imaging science, biomedical engineering
Dr Doreen Lau
Dr Doreen Lau is a Lecturer at Brunel University of London and a Visiting Researcher at the University of Cambridge. She earned a PhD from the University of Cambridge as a Cancer Research UK and Cambridge Trust Scholar, specialising in cancer immunology and the clinical translation of molecular imaging techniques and biomarkers for cancer immunotherapy in both patients and preclinical models. She received postgraduate training in cancer imaging and pharmacology at Imperial College London, and previously worked as a scientist at the University of Oxford and the Agency for Science, Technology and Research (A*STAR) in Singapore. She was also a Visiting Scientist at AstraZeneca, where she collaborated on tissue-based imaging biomarkers in immuno-oncology. Dr Lau served as a part-time Lecturer in Oxford previously, where she taught imaging, disease and treatment mechanisms in cancer, and was the Module Co-Lead for Cancer Immunology. Dr Lau has received multiple international awards for her contributions to cancer immunology and imaging research. These include the 1st Place William G. Negendank Young Investigator Award from the International Society for Magnetic Resonance in Medicine for cancer imaging (2018); the Women in Molecular Imaging Network Scholar Award from the World Molecular Imaging Society (2019); a Top 3 PhD Award from the European Society for Molecular Imaging (2021); the Merit Travel Grant and Best Poster Award in Immuno-oncology Biomarker Development from the European Society for Medical Oncology (2023); and the Best Flash Talk in Cancer Immunology from the Chinese Academy of Medical Sciences Oxford Institute Network (2023). In recognition of her achievements as an early-career scientist, she was awarded a Junior Research Fellowship in Sciences from Wolfson College, University of Oxford, in 2022. Dr Lau's research group focuses on immuno-oncology imaging and experimental medicine. Using state-of-the-art platforms for immune cell tracking, whole-body imaging, preclinical models, immuno-profiling and bioinformatics, the team investigates the biological mechanisms underlying anti-tumour immunity, treatment resistance and immune-related adverse events. The ultimate goal is to translate these findings into clinical practice for patient stratification, immunotherapy monitoring, and improved drug delivery. Additionally, this research supports early-phase drug discovery by facilitating the screening and target validation of novel immunotherapeutics. These approaches have broader implications for studying chronic inflammation, infection, autoimmune diseases, and aging-related disorders including cancer. Research Collaboration Open to academic collaboration, industry partnerships and joint PhD supervision. Cancer immunology, immunotherapy, biomarkers, imaging science, biomedical engineering