جستجوی استاد راهنمای دانشگاهی

Sunil Guharajanمشاهده پروفایل

پژوهشگر ارشد

• Transcription Factors
• Gene Regulation
• Developmental Biology
• +۳ مورد دیگر

Sunil Guharajan is a Research Fellow specializing in transcription factor (TF) biology and its implications for development, differentiation, and disease. He completed his PhD at UMass Chan Medical School under Robert Brewster, where he investigated promoter architecture in E. coli TFs using synthetic biology and thermodynamic modeling. His current research focuses on how TFs shape cellular decisions through contextual use of gene regulatory elements and how quantitative changes in TF dosage affect these processes across cell types. His educational background includes: PhD in Molecular Biology/Genetics from UMass Chan Medical School (advisor: Robert Brewster) Dr. Guharajan's research spans transcription factors, gene regulation, developmental biology, and craniofacial genetics. He employs chemical/genetic perturbations of TFs and high-resolution enhancer mapping to dissect dosage sensitivity mechanisms, with significant implications for understanding craniofacial development and disease. His work bridges quantitative modeling with experimental genomics to uncover fundamental principles of gene regulatory computation. Analysis of his 2022-2025 publications reveals dominant themes in craniofacial genetics using multi-ethnic GWAS and transcription factor dosage mechanics. Key contributions include identifying pleiotropic genetic architectures for cranial vault shape, developing transfer learning approaches for TF sequence determinants, and demonstrating DNA-guided TF cooperativity in mesenchymal development. His research consistently integrates population genetics with molecular mechanisms to address complex trait architecture. No scientific awards were mentioned in the provided text. No information regarding student advising or research grants was provided in the source materials. Details about laboratory affiliations or collaborative research teams were not specified in the given documentation.

Madelon Van de Kerkمشاهده پروفایل

استادیار

• Wildlife Ecology
• Quantitative Ecology
• Conservation Biology
• +۳ مورد دیگر

Dr. Madelon Van de Kerk serves as Director of the MS in Ecology program and Assistant Professor of Wildlife Ecology at Western Colorado University's Clark Family School of Environment & Sustainability. A Netherlands native who moved to the U.S. in 2011, she joined Western in summer 2021 after conducting wildlife research across diverse global ecosystems from Indonesia to Alaska. Her academic credentials include: PhD in Wildlife Ecology and Conservation from University of Florida (2016) MSc in Animal Ecology and Conservation from Radboud University Nijmegen (2009) BSc in Biology from Utrecht University (2007) Dr. Van de Kerk specializes in quantitative approaches to wildlife conservation, having studied species including mule deer, Dall's sheep, Florida panthers, black bears, and marine species across multiple continents. Her research integrates field data with advanced statistical modeling to address population dynamics, movement ecology, and conservation challenges. She teaches quantitative wildlife research methods and leads the Western Wildlife Lab, which focuses on Intermountain West ecology. Her publication record reveals expertise in movement ecology and population modeling, with research spanning terrestrial and marine systems. Her work frequently employs sophisticated statistical techniques to understand complex ecological relationships and inform management decisions. Scientific Recognition: The Wildlife Society Award Winner for research on Florida panther dynamics and persistence As Director of the MS in Ecology program, Dr. Van de Kerk advises graduate students while maintaining an active research program that bridges theoretical ecology with practical conservation applications. Her lab combines field studies with quantitative analysis to optimize wildlife management strategies in changing environments.

Valentina Peonaمشاهده پروفایل

پژوهشگر

• Comparative Genomics
• Speciation
• Transposable Elements
• +۱۷ مورد دیگر

Valentina Peona is a Visiting Researcher at the Department of Organismal Biology, Systematic Biology, Uppsala University, Sweden. She is actively engaged in research on comparative genomics, evolutionary biology, and genome dynamics, with a focus on transposable elements, sex chromosomes, and avian genomics, particularly in birds of paradise and other non-model organisms. Her research interests span a wide range of topics including: Comparative and population genomics Transposable elements and repeat annotation Sex chromosome evolution and neo-sex chromosomes Genome assembly using long-read technologies (PacBio, Hi-C) Structural variation and genome architecture Adaptive radiation and speciation mechanisms The analysis of her recent publications reveals a strong trend in utilizing cutting-edge genomic technologies to explore evolutionary processes in non-traditional model systems. Her work frequently involves multi-platform sequencing, manual curation of repetitive elements, and comparative analyses across diverse taxa such as birds, insects, and fungi. She has made significant contributions to understanding how transposable elements influence genome evolution, speciation, and sex chromosome dynamics. Valentina Peona has contributed to high-impact journals including Nature , Nature Communications , Molecular Ecology , and Mobile DNA . Her collaborative research spans international teams, reflecting a strong network in evolutionary genomics. She has not been explicitly listed as advising students, nor are any grants or scientific awards mentioned in the provided text. However, her role as a postdoctoral or visiting researcher suggests active participation in research projects and likely supervision of junior researchers. Her doctoral thesis, "The exploration and evolution of the avian genomic dark matter" (2021), highlights her deep expertise in avian genome complexity. Valentina Peona is associated with the Evolutionary Biology Centre (EBC) at Uppsala University, where she conducts research in a collaborative environment focused on systematics and organismal biology.

Alesha Hattonمشاهده پروفایل

پژوهشگر ارشد

• Statistical Genetics
• Genetic Epidemiology
• DNA Methylation
• +۵ مورد دیگر

Alesha Hatton is a Postdoctoral Research Fellow at the Institute for Molecular Bioscience, University of Queensland. Her research spans statistical genetics and orthopedic outcomes, utilizing large-scale registry data and advanced statistical methodologies to investigate complex biological questions. Dr. Hatton completed her PhD in systems genomics at the University of Queensland in 2024, focusing on quantitative genetics approaches to elucidate DNA methylation's role in complex trait variation. She holds a bachelor's degree in medical mathematics from the University of Wollongong (2016) and previously worked as a statistician at the South Australian Health and Medical Research Institute. Her research interests include statistical genetics, genetic epidemiology, DNA methylation, complex trait variation, and Mendelian randomization. In orthopedics, she specializes in analyzing joint replacement outcomes using Australian registry data. Her work bridges molecular genetics with clinical applications, demonstrating how genetic epidemiological methods can inform both basic science and clinical practice. Dr. Hatton has published 29 works including 25 journal articles in high-impact journals such as Nature Communications and The American Journal of Human Genetics. Her recent publications show increasing integration of genetic epidemiology with orthopedic outcomes research, reflecting her unique interdisciplinary approach. She is currently funded for 'Precision Brain Susceptibility Mapping for Large-Scale Neurogenetic Research' (2025-2026), indicating expansion into neurogenetics. Dr. Hatton is available for graduate student supervision and has expressed interest in mentoring in statistical genetics and orthopedic outcomes research.

Petar Zhelev Stoyanovمشاهده پروفایل

استاد

• Population Genetics
• Evolutionary Genetics
• Dendrology
• +۱ مورد دیگر

Prof. Petar Zhelev Stoyanov is a faculty member at the University of Forestry, Sofia, affiliated with the Faculty of Forestry and Department of Dendrology. His career spans over 25 years of research in population and evolutionary genetics of forest species. Education: M.Sc. (1985) and Ph.D. (1992) in Forestry/Forest Genetics from University of Forestry, Sofia Research focuses on genetic diversity , phylogeography , and conservation genetics of forest trees, including Pinus , Platanus , Quercus , and Sorbus species. His work employs allozymes, microsatellites, and morphological markers to study population structure and adaptation. Recent publications highlight trends in forest genetics (2011-2002), emphasizing phylogeography , gene conservation , and adaptive traits . Articles span journals like PLoS ONE , Canadian Journal of Forest Research , and Heredity , covering keywords such as population genetics, biodiversity, and tree systematics. He teaches courses in Forest Genetics and Tree Breeding , Natural Plant Resources , and Biodiversity Conservation , maintaining an active research presence in Balkan forest ecosystems.

Dietrich Oberمشاهده پروفایل

استاد

• Plant Secondary Metabolism
• Molecular Evolution
• Biochemical Ecology
• +۷ مورد دیگر

Dietrich Ober is a Professor at Kiel University, affiliated with the Institute of Botany within the Faculty of Mathematics and Natural Sciences. He leads the Research Group Biochemical Ecology and Molecular Evolution and also serves as Head of the Botanical Garden Kiel. His research integrates molecular biology, biochemistry, and evolutionary analysis to understand plant secondary metabolism, particularly focusing on pyrrolizidine alkaloids (PAs) and their ecological roles. His research interests center around the evolution of metabolic pathways in plants, especially how gene duplication leads to novel enzymatic functions in alkaloid biosynthesis. Using model systems such as Jacobaea vulgaris , Crotalaria , and Convolvulaceae species like morning glories, he investigates the genetic basis of chemical defense mechanisms in plants. His work explores how plants evolve new traits through mutations and gene duplications to survive herbivore pressure, exemplifying the 'plant-herbivore arms race.' The recent publications highlight a strong trend in evolutionary biochemistry, particularly in enzyme evolution, gene duplication dynamics, and plant-microbe interactions. Studies focus on key enzymes like homospermidine synthase (HSS) and putrescine-N-methyltransferase (PMT), analyzing their evolutionary trajectories and functional divergence. Methodologically, the research combines phylogenetics, heterologous protein expression, activity assays, and genomic analyses. Dietrich Ober actively supervises student research and offers bachelor’s and master’s thesis projects related to protein evolution and secondary metabolism. His group collaborates closely with Dr. Elisabeth Kaltenegger and is supported by resources from the Botanic Gardens Kiel. Though no specific awards are listed, his publication record in top journals such as PNAS , Plant Cell , and Trends in Plant Science reflects significant scientific impact. The research environment emphasizes training young scientists in diverse techniques including DNA/RNA isolation, PCR, cloning, protein purification, and bioinformatics. The group fosters interdisciplinary understanding by studying complex biological systems involving plants, insects, fungi, and bacteria.

Sarah Lessardمشاهده پروفایل

دانشیار

• Exercise Physiology
• Metabolism
• Diabetes
• +۷ مورد دیگر

Sarah Lessard, Ph.D., is an Associate Professor at the Fralin Biomedical Research Institute at VTC and in the Department of Human Foods, Nutrition, and Exercise within the College of Agriculture and Life Sciences at Virginia Tech. Her research is centered on the molecular mechanisms of exercise, particularly in the context of metabolic diseases such as diabetes. Associate Professor, Fralin Biomedical Research Institute at VTC Associate Professor, Department of Human Foods, Nutrition, and Exercise, College of Agriculture and Life Sciences, Virginia Tech Former Assistant Professor of Medicine, Harvard Medical School and Joslin Diabetes Center Education: Ph.D., Medical Sciences and Exercise Physiology, Royal Melbourne Institute of Technology (RMIT) University, Australia M.Sc., Human Biology and Nutritional Science, University of Guelph, Canada B.Sc., Biomedical Science and Biochemistry, University of Guelph, Canada Dr. Lessard’s research focuses on understanding why individuals respond differently to exercise, particularly those with metabolic disorders. Her work investigates the molecular signaling pathways that regulate muscle adaptation and aerobic capacity, especially under conditions of hyperglycemia. She aims to identify therapeutic strategies to enhance exercise benefits in populations with blunted responses, such as individuals with Type 1 and Type 2 diabetes. Her lab employs a multidisciplinary approach, including tissue culture, animal models, and human studies. Her recent publications reveal a strong trend in the molecular and metabolic responses to exercise, with a focus on insulin signaling, muscle remodeling, and the impact of hyperglycemia on training adaptation. She has published in top-tier journals such as Nature Metabolism , Nature Communications , and Diabetes , contributing to the understanding of exercise resistance and metabolic health. Scientific Awards: No awards listed in the provided text. Dr. Lessard leads the Lessard Lab, which is part of the Center for Exercise Medicine Research at the Fralin Biomedical Research Institute. Her research is funded by the National Institute of Diabetes, Digestive, and Kidney Diseases (NIDDK). She mentors a team of researchers and collaborates with experts in cardiovascular, cancer, and neuroscience fields to translate findings into clinical applications. Her work has significant implications for improving health outcomes in aging and chronic disease populations through optimized exercise regimens.

Marja Timmermansمشاهده پروفایل

استاد

• Plant Developmental Biology
• Molecular Genetics
• RNA Biology
• +۴ مورد دیگر

Prof. Marja Timmermans is a Professor at the University of Tübingen's Center for Plant Molecular Biology (ZMBP), leading the Developmental Genetics group within the Faculty of Science. Her research focuses on plant organogenesis, cell differentiation, and the role of mobile small RNAs as morphogens. She uses advanced techniques like single-cell RNA sequencing (scRNA-Seq) to study root and shoot stem cell niches, contributing to the development of the Arabidopsis root scRNA-Seq atlas. Her lab combines confocal imaging, genetic manipulations, and computational approaches to uncover mechanisms governing adaxial-abaxial polarity and meristem dynamics. Key projects include analyzing miRNA mobility via plasmodesmata and understanding threshold-based readouts of RNA gradients. Current positions include leading a vibrant research group with postdocs, PhD students, and technicians. Research interests emphasize small RNA regulation, epigenetic control, and developmental patterning. Her work bridges molecular mechanisms with organismal complexity, addressing questions like how stable cell fate boundaries form during leaf development. Technical innovations include the PscB browser for plant single-cell data interrogation. Collaborations span plant genetics, bioinformatics, and evolutionary biology. Lab members include postdocs like Tom Denyer and Cecilia Lara Mondragon, along with PhD students such as Aleksandar Parvanov. The group is supported by grants including the Alexander von Humboldt Foundation. Notable contributions include seminal papers on miRNA movement dynamics, developmental trajectories in roots, and the role of ancient trans-acting siRNAs in auxin response.

Todd Edwardsمشاهده پروفایل

دانشیار

• Genetic Epidemiology
• Human Genetics
• Complex Traits
• +۸ مورد دیگر

Todd Edwards is an Associate Professor in the Department of Medicine at Vanderbilt University School of of Medicine, with affiliations in the Division of Epidemiology and the Vanderbilt Institute for Global Health. He is also the Director of Graduate Studies for the Human Genetics PhD Program, playing a key leadership role in academic training. Education: BS in Biology, Middle Tennessee State University MS in Applied Statistics, Vanderbilt University PhD in Human Genetics, Vanderbilt University Dr. Edwards is a genetic epidemiologist whose research centers on identifying genetic determinants of complex human traits, particularly those exhibiting disparities across demographic groups. His work leverages electronic health records to build cohorts for large-scale genetic association studies. Key areas of investigation include cardiovascular traits (e.g., blood pressure, hypertension), diabetes, and women's health conditions such as uterine fibroids. His methodological expertise spans genetics, epidemiology, and statistical analysis. Although specific publications are not listed in the provided text, his research portfolio as reflected through his lab and program affiliations indicates a strong focus on translational genetic epidemiology, population health, and data-driven discovery using real-world clinical data. His work bridges computational methods with clinical insights to understand disease etiology. Scientific Awards and Recognition: No specific awards listed in the provided text. Dr. Edwards is deeply committed to mentoring and training future scientists. He previously served as Associate Director of Graduate Studies for the Epidemiology PhD Program and currently leads the Human Genetics PhD Program as Director of Graduate Studies. He developed a Coursera MOOC titled "Genetic Epidemiology Foundations," expanding educational access globally. He has mentored trainees who now hold faculty or equivalent positions in academia, industry, and the NIH, demonstrating significant impact on the next generation of researchers. He leads the Edwards Lab, which is engaged in collaborative reproductive and gynecological research, with active projects in pregnancy health and uterine fibroids. The lab works within a broader interdisciplinary framework involving epidemiology, genetics, and clinical medicine.

• Early Intervention in Psychosis
• Near-Psychotic States
• Suicide Prevention
• +۶ مورد دیگر

Inge Joa is an Associate Professor in Psychiatry at the University of Stavanger, affiliated with the Faculty of Health Sciences and the Department of Public Health. Her work is deeply rooted in clinical and translational psychiatry, with a focus on early intervention and mental health service improvement. Research Interests: Her primary areas of research include early intervention in psychosis and near-psychotic states, suicide prevention, quality register services, and implementation research. These interests are reflected in her extensive publication record, which bridges clinical practice with public health outcomes. Publication Trends: A review of her recent publications (2022–2025) reveals a strong emphasis on longitudinal, multicenter studies involving schizophrenia spectrum disorders. Her work frequently explores biological markers (e.g., cytokines, cellular adhesion molecules), treatment effectiveness of antipsychotics, and psychosocial determinants such as childhood trauma and help-seeking behavior. She is also deeply involved in implementation science, particularly regarding clinical guidelines and frontline leadership in mental health services. Scientific Contributions: While specific awards are not listed, her authorship in high-impact journals such as The Lancet Psychiatry , Nature Genetics , and Nature Communications underscores her significant contributions to psychiatric research. Advising and Grants: No information is available regarding students she may have advised or specific grants she has led. However, her involvement in large collaborative studies suggests active participation in funded research projects. Laboratories and Research Teams: Although no formal lab is mentioned, she is a key contributor to the TIPS (Treatment and Intervention in Psychosis) program, a long-standing initiative focused on early detection and intervention in psychosis, indicating strong team-based research collaboration.

• Plant Genomics
• Crop Improvement
• Wheat Genetics
• +۷ مورد دیگر

Anthony Hall is a Professor of Plant Genomics and Head of Plant Genomics at the Earlham Institute, affiliated with the School of Biological Sciences at the University of East Anglia. He leads cutting-edge research in wheat genomics, focusing on improving nutritional quality, stress resilience, and sustainable crop production through the integration of wild relative introgressions and advanced genomic technologies. His research interests span plant genomics , crop improvement , wheat genetics , and nutrient biofortification . He investigates how introgressions from wild relatives such as Amblyopyrum muticum and Aegilops comosa can enhance grain micronutrient content and abiotic stress tolerance in hexaploid wheat. His work combines high-throughput sequencing, transcriptomics, and marker development to accelerate breeding for climate-resilient and nutritionally enhanced crops. The recent trend in his publications reflects a strong focus on structural and functional genomics of wheat introgression lines , reference bias in RNA-seq , and molecular marker development . His studies integrate field-based phenotyping with genomic analysis to validate the impact of exotic alleles on agronomic traits under real-world conditions. While no scientific awards are listed in the provided text, his work has been widely recognized through citations and media coverage, including mentions in 12 news outlets and discussions on social media platforms like X (formerly Twitter). Anthony Hall actively supervises or collaborates with a research team focused on plant genomics, though specific student names are not listed. His lab at the Earlham Institute leverages state-of-the-art sequencing and bioinformatics infrastructure to analyze complex polyploid genomes. The group collaborates extensively with international partners to address global food security challenges.

Camron D. Bryantمشاهده پروفایل

استاد

• Addiction Genetics
• Neuropharmacology
• Behavioral Genetics
• +۵ مورد دیگر

Camron D. Bryant is a Professor in Pharmaceutical Sciences at Northeastern University's Bouvé College of Health Sciences. His research focuses on mapping genetic and neurobiological mechanisms underlying addiction, eating disorders, and pain through rodent forward genetic crosses, multi-omics, and gene editing. Key projects include validating Zhx2's role in opioid metabolism, developing near-isogenic substrains for genetic analysis, and applying machine learning to 'Big Behavior' datasets for opioid withdrawal studies. Dr. Bryant holds NIH BRLE study section membership (2021-2025) and is a past President of the International Behavioural and Neural Genetics Society (IBANGS). Education PhD in Neuroscience, UCLA Postdoc in Rodent Quantitative Genetics, University of Chicago BSc in Psychology, University of Illinois at Urbana-Champaign Research Interests Dr. Bryant's lab investigates the genetic basis of addiction model traits (opioids, psychostimulants), binge eating, and pain. Current projects include: Zhx2 validation in oxycodone metabolism and addiction Machine learning analysis of opioid withdrawal behavior Rat substrain comparisons for cocaine addiction genetics Awards Member, American College of Neuropsychopharmacology (2021) Early Career Scientist Award, International Behavioral and Neural Genetics Society (2014) Advising & Grants Dr. Bryant has supervised multiple postdocs and graduate students through NIH-funded projects. His lab employs 'Reduced Complexity Cross' strategies to accelerate gene discovery for complex traits. He also provides grant-writing training for NIH/NIDA initiatives. Lab Activities Current lab efforts focus on: Neonatal Opioid Withdrawal Syndrome (NOWS) hyperirritability studies Zhx2's role in opioid metabolism validation Rat substrain cocaine addiction genetics

Marie-Louise Schuttelaarمشاهده پروفایل

استاد

• Dermato-allergology
• Atopic Dermatitis
• Hand Eczema
• +۴ مورد دیگر

Marie-Louise Schuttelaar is a Professor in the Faculty of Medical Sciences at the University of Groningen, specializing in Dermatology and Allergy. Her work focuses on dermatological conditions such as atopic dermatitis, hand eczema, and occupational dermatology. She holds academic appointments and serves as an advisor, consultant, and speaker for pharmaceutical companies including Sanofi Genzyme, Regeneron, and Pfizer. Her research explores clinical assessment tools for skin conditions, drug efficacy in pediatric populations, and psychosocial impacts of dermatological diseases. She has contributed to studies on chemical allergens (e.g., hair dye reactions) and occupational exposures (e.g., wet work and hand eczema). Her recent work includes genetic analyses of hand eczema and validation of disease control metrics. Dr. Schuttelaar actively engages in public health initiatives, such as the European Dermato-Epidemiology Network, and provides expert commentary on skincare practices and product safety. Her interdisciplinary approach bridges clinical practice, epidemiology, and genetics to improve patient outcomes.

Tara Matiseمشاهده پروفایل

استاد

• Computational Human Genetics
• Statistical Genetics
• Bioinformatics
• +۷ مورد دیگر

Tara Matise is a Professor and Chair of the Department of Genetics at Rutgers University, where she leads a research program in computational human genetics. She co-directs the Rutgers University Genetics Coordinating Center (RUGCC), a hub for large-scale genomic research initiatives funded by the NIH. Research Interests: Her work spans computational genetics, statistical genetics, and bioinformatics, with a focus on identifying genes responsible for human diseases. Key areas include breast cancer genetics, inherited disorders of the central nervous system, reproductive health, and population-specific genetic variation. She emphasizes inclusive genomics by studying non-European populations to address health disparities. The articles reflect a consistent trajectory in genomic data coordination, statistical methodology development, and disease gene discovery. Her recent work centers on large cohort studies, genotype imputation, ancestry analysis, and cross-consortium collaboration, particularly through projects like The PAGE Study and the NHGRI Genome Sequencing Program. Scientific Leadership and Grants: Co-Director, Rutgers University Genetics Coordinating Center (RUGCC) Lead for NIH-funded PAGE Study (2008–2024) Coordinator, NHGRI Genome Sequencing Program (2015–2022) Principal Investigator, Breast Cancer Genetics Study (launched 2023) She advises graduate students and postdoctoral researchers through her lab and leadership roles, though specific advisees are not listed. Her team manages complex data workflows, facilitates multi-institutional collaborations, and develops analytical frameworks for genetic discovery.

• Genetics
• Diabetes
• Genomics
• +۷ مورد دیگر

Dr. Michael Weedon is a Professor at the University of Exeter's Clinical and Biomedical Sciences department, specializing in the genetics of diabetes and related traits. His work focuses on genome-wide association studies (GWAS) for Type 2 diabetes and whole genome sequencing to identify rare mutations in familial diabetes, particularly MODY. He is affiliated with the Genetics of Complex Traits Group and the Monogenic Diabetes Research Team, while also teaching Bioinformatics modules on the Genomics Medicine MSc program. Research Interests: Genetics of diabetes and metabolic diseases Genome-wide association studies (GWAS) Whole genome sequencing for rare mutations Bioinformatics and computational biology in genomics Public health implications of genetic research Collaborations: NIHR Exeter Biomedical Research Centre, Health Analytics @Exeter network.