جست‌وجوی استاد و پژوهشگر

Alexis Battleمشاهده پروفایل

دانشیار

• Genomics
• Machine Learning
• Computational Biology
• +۳ مورد دیگر

Alexis Battle is an Associate Professor at Johns Hopkins University with appointments in Biomedical Engineering , Computer Science , and Genetic Medicine (secondary). She directs the Malone Center for Engineering in Healthcare and serves as Deputy Director of the Data Science and AI Institute . Educated at Stanford University (PhD in Computer Science, 2013), Battle transitioned to academia after leadership roles at Google. Research Focus: Battle’s work bridges genomics and machine learning , emphasizing the impact of genetic variation on human health. Her lab develops tools like Watershed to predict functional effects of rare variants, aiming to enhance rare disease diagnosis. Key themes include non-coding DNA analysis , personalized genomics , and systems biology , with applications in cardiovascular disease and neurodegenerative disorders . Publications & Awards: Over 60 peer-reviewed articles in journals like Nature , Science , and Genome Biology , with recent emphasis on single-cell transcriptomics , multiomics integration , and telomere biology . Recipient of the President’s Frontier Award (2022), Microsoft Investigator Fellowship (2019), and Searle Scholar (2016). Scientific Awards: 2022 President’s Frontier Award 2019 Microsoft Investigator Fellowship 2019 Johns Hopkins Discovery Award 2017 Johns Hopkins Catalyst Award 2016 Searle Scholar Advising & Funding: Mentors 11 PhD students, 3 undergraduates, and postdoctoral fellows. Her research is funded by NIH, Searle Scholars, and institutional grants. The Battle Lab collaborates on projects like the GTEx Consortium , focusing on gene regulation and clinical genomics .

Bertram Müller-Myhsokمشاهده پروفایل

استاد پژوهشی

• Psychiatric Genetics
• Statistical Genetics
• Transcriptomics
• +۳ مورد دیگر

Bertram Müller-Myhsok is a Research Professor and Research Group Leader at the Max Planck Institute of Psychiatry in Munich, Germany. His research focuses on statistical genetics and transcriptomic data analysis in psychiatric disorders, particularly major depression, PTSD, schizophrenia, and their treatment responses. He integrates machine learning with genetic and clinical data to develop predictive models and stratified treatment approaches. Professional activities include leadership roles in the International Max Planck Research School for Translational Psychiatry and collaborations with institutions like the Institut du Cerveau (Paris) and Bernhard Nocht Institute (Hamburg). His work spans genetic epidemiology, psychiatric genomics, and precision medicine, with over 400 publications in high-impact journals. Key research areas include identifying genetic risk factors for mental disorders, developing polygenic scores, and leveraging omics data to uncover disease mechanisms. He leads projects like Psych-STRATA, a Horizon Europe-funded initiative advancing personalized psychiatry through pharmacogenomics.

Chiara Sabattiمشاهده پروفایل

استاد

• Statistical Genetics
• Computational Biology
• Bayesian Statistics
• +۲ مورد دیگر

Chiara Sabatti is a Professor of Biomedical Data Science and Statistics at Stanford University, with affiliations to the Stanford Center for Computational, Evolutionary and Human Genomics (CEHG), Bio-X, and the Stanford Cancer Institute. She serves as Associate Director for Stanford Data Science and has led the development of the Data Science Major curriculum since 2012. Research Focus: Statistical models for high-throughput genomics data, causal inference in genetic studies, false discovery rate control, and knockoff methods for variable selection. Key Leadership: Associate Chair for Education and Training (2020-present), Vice Chair of Biomedical Data Science (2018-2019). Her work bridges statistical genetics with data science education, emphasizing robustness and interpretability in scientific findings. Recent publications highlight innovations in genome-wide association studies (GWAS), causal variant localization, and cost-effective sequencing techniques for underrepresented populations. Current projects include developing knockoff-based methods to address population structure and multi-resolution hypothesis testing. Scientific Awards: Institute of Mathematical Statistics (IMS) Fellow (2022) NSF CAREER Award (2003-2008) She mentors doctoral and graduate students in Biomedical Data Science, collaborates with the Data Studio on interdisciplinary projects, and actively recruits curious researchers to her lab. Her outreach efforts focus on expanding data science education and increasing research participation from underrepresented groups.

• Archaeology
• Mesolithic Studies
• Biomolecular Analysis
• +۴ مورد دیگر

Birgitte Skar is an Associate Professor and Collection Manager for the Stone Age and Bronze Age at the Department of Archaeology and Cultural History, NTNU Science Museum. Her research focuses on Mesolithic and Neolithic adaptations, biomolecular studies, submerged landscapes, and cultural heritage protection. She leads the SCAPES project (2025-2028), funded by RCN FRIPRO, exploring social complexity through biomolecular data. Her work integrates archaeology with genetics and isotopic analysis, addressing topics such as migration patterns, dietary practices, and social stratification in prehistoric societies. Key contributions include studies on Scandinavian Neolithic pathogens, Viking Age genetic diversity, and Mesolithic mobility in Fennoscandia. She advises numerous master’s students and collaborates with institutions like the University of Bergen and the Swedish Museum of Natural History. Publications span high-impact journals like Nature and Cell , alongside museum exhibitions and policy-oriented reports on heritage management. Her research often bridges natural sciences and humanities, emphasizing interdisciplinary approaches to understanding human-environment interactions.

Albert Erivesمشاهده پروفایل

دانشیار

• Regulatory Genomics
• Evolutionary Genomics
• Evolution of Metazoa
• +۶ مورد دیگر

Albert Erives is an Associate Professor in the Department of Biology at the University of Iowa , specializing in regulatory genomics, evolutionary genomics, and the evolution of metazoans. His research focuses on decoding gene regulatory logic in DNA sequences, particularly during animal embryogenesis, using comparative genomics to identify regulatory modules driving phylogenetic transitions. PhD from University of California, Berkeley His work spans eukaryotic gene regulation, integrating biochemistry, molecular genetics, and computational biology to uncover principles of organismal evolution. Recent studies include viral nucleosome structure, Notch signaling pathway evolution, and enhancer organization in model organisms like Drosophila and Ciona . Notable scientific awards include the NSF CAREER Award (2012, 2010) . He actively seeks graduate students and postdoctoral researchers for his laboratory, which utilizes core facilities such as the Carver Center for Genomics.

• Genome Evolution
• Comparative Genomics
• Organelle Evolution
• +۳ مورد دیگر

Andrew J. Roger is a Professor in the Department of Biochemistry and Molecular Biology at Dalhousie University, Faculty of Medicine. His primary roles include academic research and leadership as the Founding Director of the Institute for Comparative Genomics (ICG) and Canada Research Chair in Comparative Genomics. He has been a department member since 2001. Education: PhD in Biochemistry from Dalhousie University Affiliations: Dalhousie University, Department of Biochemistry and Molecular Biology; Institute for Comparative Genomics (ICG) His research focuses on genome evolution, particularly in eukaryotic protists. Key interests include: Phylogenomics of eukaryotic super-kingdoms like Excavata Comparative genomics of anaerobic protists and lateral gene transfer (LGT) Evolution of mitochondria, hydrogenosomes, and mitosomes Modeling molecular evolution with computational tools Recent publications (2021–2023) highlight studies on protist organelle evolution, genomic adaptation mechanisms, and novel phylogenetic methods. His lab includes graduate students and postdocs actively researching these areas. He collaborates extensively with statisticians and computational biologists. Lab Members: Tugba Nur Atalay, Min Cho, Marlena Dlutek, Katherine Dunn, Ryo Harada, Joran Martijn, Charley McCarthy, Greg Seaton, Jason Shao, Kelsey Williamson, and others.

Fulai Jinمشاهده پروفایل

دانشیار

• 3D Genome Architecture
• Computational Biology
• Genomics
• +۳ مورد دیگر

Fulai Jin, PhD, is an Associate Professor in the Department of Genetics and Genome Sciences at Case Western Reserve University School of Medicine, with joint appointments in the Department of Population and Quantitative Health Sciences and the Department of Computer and Data Sciences. He is also Co-Leader of the Cancer Genomics and Epigenomics Program at the Case Comprehensive Cancer Center. Dr. Jin holds a PhD in Molecular and Medical Pharmacology from UCLA and bachelor’s degrees in Biology and Computer Science from USTC. His postdoctoral training at the Ludwig Institute for Cancer Research focused on genomics and epigenetics. His research focuses on 3D genome architecture, computational tools for genomic data integration, and single-cell technologies applied to health and disease. Key areas include cancer, diabetes, and neurological disorders, with a focus on chromatin structure, enhancer function, and ancestry-related disease mechanisms. His lab develops low-input 3D genome mapping methods and employs CRISPR tools, scRNA-seq, and multi-omic integration. Research is funded by NIH grants. Dr. Jin seeks motivated students/postdocs with experimental or computational expertise. The lab’s work is detailed on their website, and publications are listed on PubMed.

Emile Rugamika Chimusaمشاهده پروفایل

استاد

• Computational Population Genomics
• Bioinformatics
• Genome-Wide Association Studies
• +۵ مورد دیگر

Prof. Emile Rugamika Chimusa is a Professor at Northumbria University , College of Engineering and Science, specializing in Computational Population Genomics and Bioinformatics . Previously, he served as Associate Professor and Programme Director at the University of Cape Town for postgraduate programs in Computational Health Informatics and Human Genetics. His research focuses on genomic methodologies for analyzing large-scale genomic data, including Genome-wide association studies Admixture mapping in mixed-ancestry populations Pharmacogenetics of disease treatments Multi-omics integration for disease-drug associations Development of bioinformatics tools Population-specific disease risk prediction He has received over £17.7 million in research funding from organizations like the NIH , Wellcome Trust , and National Research Foundation . His work spans translational genomics in both non-communicable and infectious diseases .

Laura Raffieldمشاهده پروفایل

استادیار

• Genetic Epidemiology
• Human Genetics
• Genome-wide Association Studies
• +۷ مورد دیگر

Laura Raffield, PhD, is an Assistant Professor in the Department of Genetics at the UNC School of Medicine, University of North Carolina at Chapel Hill. Her research focuses on genetic epidemiology and human genomics, particularly in understudied populations, to understand inherited and environmental risk factors for cardiometabolic diseases, Alzheimer’s disease, and related quantitative traits. She co-leads collaborative efforts such as the Jackson Heart Study Genetics Working Group and the NHLBI TOPMed Multi-Omics working group. Dr. Raffield’s work emphasizes multi-omics integration (transcriptomic, epigenomic, proteomic, metabolomic) to link genetic variants to molecular function. She has received grants including a U01 from the NIA to study racial disparities in Alzheimer’s disease mechanisms and a subcontract from UTSW Medical Center for proteomic profiling in the Jackson Heart Study. Her lab actively publishes on topics like polygenic risk scores, clonal hematopoiesis, and inflammation-cardiovascular links. Recent studies include characterizing Duffy-null genotype effects and proteomic associations with cognitive impairment. Key collaborations involve TOPMed, CHARGE, and PAGE consortia. Dr. Raffield advises students like Micah Hysong (Blood Advances publication) and Madeline Gillman (proteomic trajectory research). Her lab focuses on improving genomic representativeness for precision medicine equity, including leadership in the PRIMED consortium for polygenic risk scores in diverse populations.

Rana Özbalمشاهده پروفایل

دانشیار

• Anatolian Archaeology
• Near Eastern Archaeology
• Neolithization
• +۵ مورد دیگر

Rana Özbal is an Associate Professor of Archaeology and History of Art at Koç University. She is affiliated with the Faculty of Archaeology and History of Art and specializes in the archaeology of Anatolia and the Near East, focusing on Neolithization processes, microarchaeology, and cultural interaction. Her research integrates interdisciplinary methods including geochemical analysis, ancient DNA studies, and ceramic technology. Özbal holds a PhD from Northwestern University and a Bachelor’s degree from Bates College. Her research interests center on understanding early complex societies, particularly Neolithic Anatolia’s social, economic, and technological developments. She has led excavations at critical sites like Barcın Höyük and Aşıklı Höyük, advancing knowledge of settlement patterns, domestic architecture, and subsistence strategies. Her work bridges micro-scale analyses (e.g., floor sediments, footprints) with macro-scale perspectives on regional interaction and migration. Key projects include studies on ancient kinship structures through genomic data, the Neolithization of Northwest Anatolia, and the analysis of Ubaid-related settlements. Özbal collaborates internationally, contributing to journals like Current Biology , Scientific Reports , and Journal of Archaeological Science . Her recent publications explore topics such as Neolithic sheep domestication, Y-chromosome studies, and the social implications of prehistoric architectural choices. While no scientific awards are explicitly mentioned, her extensive publications and leadership in major excavations (e.g., Barcın Höyük since 2012) highlight her scholarly impact. She advises students on archaeological fieldwork and lab-based analyses, though specific student names are not listed in the provided texts.

• Acute Lymphoblastic Leukemia
• Pediatric Brain Tumors
• Genetic Heterogeneity
• +۵ مورد دیگر

Stephen E. Sallan, MD , is a Professor of Pediatrics at Harvard Medical School and a Physician at Dana-Farber Cancer Institute and Children's Hospital . His career spans over five decades in pediatric hematology/oncology , with a focus on acute lymphoblastic leukemia (ALL) and pediatric brain tumors . Education : MD, Wayne State University School of Medicine (1967) Residencies : Boston Floating Hospital (1968), Children's Hospital of Philadelphia (1969), Hospital for Sick Children, London (1970) Fellowship : Pediatric Oncology, Children's Hospital/DFCI (1972) Leadership Roles : Chief of Staff (1995), Chairman of Medical Staff Executive Committee (1995), Chief of Staff Emeritus (2012) Dr. Sallan's research integrates genetic heterogeneity , disease recurrence , and drug resistance in ALL, with efforts to develop targeted therapies like tumor vaccines and antiangiogenesis agents. His work addresses long-term treatment toxicities (cardiac, skeletal, neurocognitive), particularly in survivors of childhood cancers. His 15 most recent publications (2024–2018) demonstrate ongoing engagement with pharmacogenomics, thrombosis risk models, dietary interventions, and molecular markers in brain tumors. Key subfields include TRK-C in medulloblastoma , asparaginase complications , and DFCI ALL Consortium Protocols . Scientific Awards : Distinguished Alumni Award, Wayne State University School of Medicine (1997) James Carreras Prize for International Pediatrician of the Year (1987) As a leader in pediatric leukemia research , Dr. Sallan has shaped treatment protocols that minimize late effects while improving survival. He collaborates with multidisciplinary teams in neuro-oncology and pharmacogenomics, maintaining active roles in clinical trials and laboratory investigations.

Torsten Güntherمشاهده پروفایل

پژوهشگر

• Population Genomics
• Ancient DNA
• Human Evolution
• +۵ مورد دیگر

Torsten Günther is a Researcher at Uppsala University's Department of Organismal Biology, holding a PhD and the Swedish academic title of Docent. His work bridges evolutionary biology, archaeology, and genomics through cutting-edge analysis of ancient DNA from human and animal specimens across Europe, Africa, and the Middle East. His research focuses on reconstructing population histories using paleogenomic data, with particular expertise in human migration patterns, domestication processes of livestock (especially sheep and cattle), and methodological innovations in archaeogenomics. Recent work examines vanished hybrid zones in Saharan rock doves, genomic legacies of aurochs hybridization in Iberian cattle, and Neolithic transitions in Northwest Africa. His interdisciplinary approach integrates archaeological context with high-resolution genomic analysis to address fundamental questions about human prehistory and evolutionary adaptation. Analysis of his 15 most recent publications (2023-2025) reveals three dominant research strands: 1) Livestock domestication genomics (sheep, cattle, mouflon), 2) Human population dynamics during critical transitions (Neolithic, Bronze Age), and 3) Methodological advances in ancient DNA analysis. His collaborative network spans over 20 institutions across Europe and North America, with fieldwork concentrated in Mediterranean and Atlantic European regions. Günther frequently publishes in high-impact journals including Nature , Science , and eLIFE , demonstrating significant influence in archaeogenomics. He maintains active research leadership through methodological software development (READv2) and participation in major international consortia studying ancient human and animal genomes. His work consistently addresses how historical demographic processes shaped modern biodiversity and human genetic variation, with implications for conservation biology and understanding human adaptation.

• Evolutionary Genomics
• Endosymbiosis
• Phylogenomics
• +۳ مورد دیگر

Professor Thomas Richards is a Professor of Evolutionary Genomics at the University of Oxford and a Royal Society University Research Fellow. His research focuses on understanding the origins and diversification of eukaryotic cellular complexity through phylogenomic, cell biological, and molecular approaches. Current research themes include phylogenomic analysis of gene ancestry, endosymbiosis mechanisms, and environmental DNA studies of microbial diversity. His work spans disciplines such as evolutionary genomics, microbial ecology, and systems biology, addressing questions like how endosymbioses form and how uncultured protists contribute to biodiversity. Key projects include studies on pathogen evolution, transporter proteins, and the genetic networks governing symbiotic interactions. Prof. Richards has published extensively on topics like membrane permeability, genetic code reassignments, and the evolution of eukaryotic microbes. His awards include the Royal Society University Research Fellowship, recognizing his contributions to understanding microbial and eukaryotic evolution.

• Molecular Biology
• Developmental Biology
• Evolutionary Biology
• +۳ مورد دیگر

Tatjana Haitina is a Researcher at the Department of Organismal Biology; Evolution and Development at Uppsala University. She holds a PhD and Docent title, with an ORCID identifier 0000-0002-8754-5534. Her research focuses on the regulatory mechanisms and 3D organization of skeletal tissues during vertebrate development and evolution, particularly studying skeletal joints, connective tissues, and mineralized structures using zebrafish as a primary model. Her academic background includes a doctoral thesis on 'Function, Pharmacology, Evolution and Anatomical Localization of G Protein-Coupled Receptors and Solute Carriers' (2009). She has contributed chapters to books such as 'Odontodes' (2023) and 'Evolving Neural Crest Cells' (2020). Research interests span molecular evolution of genes and regulatory sequences, CRISPR-Cas9 genome editing, and 3D microstructure analysis of mineralized tissues. Recent work includes studies on craniofacial development, sensory organ evolution in sharks, and cis-regulatory elements in lymphatic vascular beds. Her publications highlight collaboration with institutions globally, with notable contributions to journals like Nature Communications and Molecular Biology and Evolution. No scientific awards are explicitly listed, though her work has been cited widely. Dr. Haitina's lab employs cutting-edge imaging techniques such as synchrotron X-ray microtomography and optical projection tomography (zOPT) to study developmental defects in zebrafish mutants. She investigates ancestral features of skeletal mineralization and the evolutionary origins of enamel.

• Clinical Oncology
• Translational Research
• Prostate Cancer
• +۷ مورد دیگر

Dr. Eric Small is a Professor in the Department of Medicine at the University of California, San Francisco (UCSF), School of Medicine. He is a leading clinical and translational researcher in advanced prostate cancer. B.S. in Biology, Stanford University (1980) M.D., Case Western Reserve University (1985) Residency and Fellowship in Internal Medicine and Cancer Research at Beth Israel Hospital and UCSF Dr. Small's research focuses on clinical and translational aspects of advanced prostate cancer, including the development of novel agents targeting the androgen receptor (e.g., abiraterone, apalutamide) and immunotherapies (e.g., sipuleucel-T, ipilimumab). His work emphasizes understanding resistance mechanisms, particularly through genomic and epigenomic studies of metastatic disease. He has led major initiatives such as the Stand Up to Cancer/Prostate Cancer Foundation Dream Team. His extensive publication record, particularly in high-impact journals from 2023–2025, reflects a strong focus on resistance mechanisms, lineage plasticity, genomic characterization, and clinical trial outcomes in metastatic and castration-resistant prostate cancer. His work integrates genomics, transcriptomics, and clinical data to advance precision oncology. Scientific Awards: Alpha Omega Alpha Honor Medical Society (1984) UCSF Division of Hematology-Oncology Faculty Research Award (2001) Richard L. Schilsky CALGB Award for Clinical Research (2011) UCSF Academic Senate Faculty Research Lecture in Clinical Science (2011) Fellow of the American Society of Clinical Oncology (FASCO) (2015) Dr. Small holds significant leadership roles, including Co-Leader of the UCSF Prostate Cancer Program and Chief Scientific Officer of the UCSF Helen Diller Family Comprehensive Cancer Center. He serves on the ASCO Board of Directors and chairs multiple external advisory boards. He has been Principal Investigator on major grants, including a $10 million SU2C/PCF award, and has mentored numerous collaborators and trainees through large multi-institutional research teams. He is actively involved in national and international consensus efforts, such as the Advanced Prostate Cancer Consensus Conference (APCCC), shaping clinical guidelines and identifying future research directions.