جست‌وجوی استاد و پژوهشگر

Holly Zimmermanمشاهده پروفایل

دانشیار

• Genetic Counseling
• Medical Genetics
• Pediatrics
• +۴ مورد دیگر

Holly Zimmerman is an Associate Professor in the Department of Medical Sciences at the University of Nebraska Medical Center (UNMC), serving as the inaugural Program Director for the Genetic Counseling Program. She holds dual affiliations with the College of Allied Health Professions and the School of Medicine. Zimmerman is a first-generation college graduate and a Certified Genetic Counselor (ABGC) with over a decade of clinical experience in pediatric genetic counseling in Mississippi. Education Bachelor of Science in Biology, University of Southern Mississippi (2004) Master of Science in Genetic Counseling, University of South Carolina (2007) Certified Genetic Counselor, American Board of Genetic Counseling (2009) Research & Teaching Her research focuses on holistic admissions processes in genetic counseling programs, psychosocial aspects of genetic counseling, and student mentorship. She is deeply involved in medical education, having contributed to teaching medical students, pediatric residents, and maternal-fetal medicine fellows. Her work emphasizes supportive approaches to teaching and mentorship, reflecting her belief in building strong interpersonal relationships in healthcare. Professional Engagement Zimmerman serves on the board of directors for the Genetic Counselor Educators Association (formerly the Association for Genetic Counseling Program Directors), advocating for standardized education and training in genetic counseling. Her clinical background in pediatric genetics has informed her advocacy for accessible and compassionate genetic services, including telehealth innovations during the pandemic. Labs & Initiatives As program director, she oversees the UNMC Genetic Counseling Program, which emphasizes interdisciplinary collaboration and student well-being. Her work bridges clinical practice, education, and research in medical genetics.

Omar Abdul-Rahmanمشاهده پروفایل

استاد

• Medical Genetics
• Pediatric Genetics
• Fetal Alcohol Spectrum Disorders (FASD)
• +۴ مورد دیگر

Omar Abdul-Rahman, M.D., is the Horace W. Goldsmith Foundation Professor of Pediatrics and Professor of Pediatrics at Weill Cornell Medical College, Cornell University. His clinical expertise spans fetal alcohol spectrum disorders, sexual development disorders, and adult genetics. He previously served as Director of the Department of Genetic Medicine at the Munroe-Meyer Institute (University of Nebraska Medical Center) and held leadership roles at the University of Mississippi Medical Center. Dr. Abdul-Rahman's academic journey includes an M.D. from the University of Mississippi School of Medicine (2000) and a B.S. from Millsaps College (1996). His research focuses on FASD epidemiology, genetic counseling program development, and molecular characterization of rare genetic syndromes. He has led studies in diverse populations, including global FASD prevalence assessments and genomic analyses of conditions like Cornelia de Lange syndrome. His honors include multiple 'Top Doctor' recognitions (2021–2022), Best Doctors in America listings, and awards for pediatric faculty excellence. He has authored over 150 peer-reviewed articles, emphasizing translational research linking genetic findings to clinical care. Dr. Abdul-Rahman's clinical practice spans general genetics, craniofacial anomalies, and prenatal counseling. He collaborates internationally on FASD interventions and advocates for multidisciplinary care models. His lab integrates genomic technologies to improve diagnostic pathways for rare diseases.

Sang H. Leeمشاهده پروفایل

استاد

• Neuropharmacology
• Synaptic Plasticity
• Neurodegenerative Diseases
• +۳ مورد دیگر

Sang H. Lee is a Professor in the Department of Pharmacology and Toxicology at the Medical College of Wisconsin. His research focuses on molecular mechanisms of synaptic plasticity, particularly synapse loss linked to neuropsychological and neurodegenerative diseases like Alzheimer’s. He employs multidisciplinary approaches including biochemistry, imaging, electrophysiology, and mouse genetics. Education: PhD in Biochemistry, Gyeongsang National University, South Korea (1998) Research Interests: Dynamic remodeling of synapses, secreted factors affecting excitatory and GABAergic synapses, and mechanisms of synapse loss. Key projects include studying PRR7’s role in excitatory synapse loss via exosomes and TAFA2’s impact on GABAergic synapses and anxiety-related behaviors. His work integrates activity-dependent signaling pathways and neurodegenerative disease models. Publications highlight contributions to understanding synaptic signaling, exosome-mediated communication, and molecular pathways in neurodegeneration. Recent work emphasizes Wnt inhibitors, chemokine-like proteins, and synaptic scaffolding molecules like S-SCAM. No scientific awards listed. Advising and grants: No formal advisee list provided. Labs/Teams: Utilizes advanced imaging techniques (confocal, super-resolution), electrophysiology, and genetic models to investigate synaptic mechanisms.

Troy Messickمشاهده پروفایل

استادیار

• Syntax
• Morphology
• Linguistic Agreement
• +۲ مورد دیگر

Troy Messick serves as Assistant Professor and Undergraduate Program Director in the Department of Linguistics within Rutgers University's School of Arts and Sciences. His primary academic appointment focuses on theoretical syntax and morphological phenomena. Research interests center on syntactic theory with specialized expertise in syntax , morphology , pronouns , agreement phenomena , and ellipsis . His work demonstrates particular depth in Dravidian languages (especially Telugu), exploring case-copying reflexives, shifty agreement patterns, and cross-clausal dependencies. Recent publications reveal a trajectory examining morphosyntactic interfaces through both theoretical and experimental approaches. Analysis of his 15 most recent publications (2012-2025) shows consistent focus on agreement anomalies, ellipsis mechanisms, and syntactic locality. Key trends include: investigation of hybrid noun phenomena in English and Telugu, experimental validation of gender asymmetries in ellipsis, and theoretical reevaluations of E-raising and case-matching reciprocals. His work bridges formal theory with cross-linguistic data, particularly from South Asian languages. No scientific awards or fellowships are documented in available sources. As Undergraduate Program Director, Messick oversees linguistics curriculum and student advising. Office hours are held Thursdays 9:00-11:00am (in-person) and 2:00-4:00pm (via Zoom), with primary contact through departmental email channels. No specific research grants or laboratory affiliations are mentioned in current materials.

Howard I. Scherمشاهده پروفایل

استاد

• Prostate Cancer Research
• Medical Oncology
• Biomarker Development
• +۵ مورد دیگر

Howard I. Scher, MD is a Professor of Medicine at Weill Cornell Medical College and holds the D. Wayne Calloway Chair in Urologic Oncology. He previously served as Chief of the Genitourinary Oncology Service at Memorial Sloan Kettering Cancer Center (MSKCC) for 25 years. His expertise lies in treating advanced prostate cancer and developing targeted therapies and biomarkers like circulating tumor cell analysis. He leads major initiatives including the Prostate Cancer Clinical Trials Consortium and the NCI-sponsored Prostate Cancer SPORE program. Scher has authored over 430 peer-reviewed articles and co-authored Principles and Practice of Genitourinary Oncology . His research focuses on androgen receptor signaling, novel imaging modalities, and clinical trial design. Awards include the Donald S. Coffey-Prostate Cancer Foundation Physician-Scientist Award and repeated recognition as a Top Doctor by Castle Connolly. He serves on editorial boards of journals like New England Journal of Medicine and Nature . Key contributions include standardizing phase II clinical trials for prostate cancer and developing the Clinical States Model to guide treatment. His work integrates basic science with clinical practice, emphasizing translational research to improve patient outcomes.

Samuel Singerمشاهده پروفایل

استاد

• Soft Tissue Sarcoma Research
• Genomics
• Molecular Biology
• +۳ مورد دیگر

Samuel Singer, MD, FACS, is a Professor and leader in sarcoma research at Memorial Sloan Kettering Cancer Center. He serves as Chief of the Gastric and Mixed Tumor Service, Vincent Astor Chair of Clinical Research, and Director of the Sarcoma Center. His research focuses on genomic and epigenetic alterations in soft tissue sarcomas to identify therapeutic targets and improve patient outcomes. Singer's work combines surgical oncology expertise with laboratory research, leading initiatives like the Sarcoma Genome Project and an NIH-funded SPORE grant. He received his MD from Harvard Medical School and has been recognized with multiple awards, including Castle Connolly’s Top Doctor distinctions. His research interests include sarcoma biology, targeted therapy development, and molecular diagnostics. Key projects include studying integrin-α10 as a therapeutic target and discovering novel agents for dedifferentiated liposarcoma. He leads a multidisciplinary team engaged in genomic profiling, drug screening, and preclinical models to advance precision medicine. Education: MD, Harvard Medical School Awards: Multiple Castle Connolly Top Doctor awards (2023–2025), and recognition in New York Magazine (2003–2020). Lab Affiliations: Memorial Hospital Research Laboratories, Department of Surgery, and Gerstner Sloan Kettering Graduate School. Publications highlight advancements in sarcoma genetics, therapeutic targets, and molecular pathways, with a focus on translational research to improve patient survival and quality of life.

• Cancer Research
• Genomics
• Immunotherapy
• +۴ مورد دیگر

Dr. Gyan Bhanot is a Professor at Rutgers, The State University of New Jersey, affiliated with the Department of Biological Physics. His research focuses on cancer genomics, immunotherapy biomarkers, pandemic modeling, and machine learning applications in biomedicine. He has advised students including Anshuman Panda (Ph.D. 2018) and Kshitij Wagh (Ph.D. 2013). His work integrates computational methods to study viral evolution, tumor recurrence, and genomic signatures in diseases like renal cell carcinoma and breast cancer. Education details are not explicitly provided in the text, but his extensive publications indicate advanced training in physics and computational biology. His research spans broad areas such as: Cancer immunotherapy response prediction using endogenous retrovirus expression Epidemiological models for SARS-CoV-2 transmission dynamics Machine learning platforms for genomics (e.g., PrismML) Analysis of ribosomal protein variations in malignancies Dr. Bhanot’s articles highlight innovations in predicting pandemic behaviors, identifying cancer biomarkers, and understanding genomic instability in tumors. His recent work addresses critical questions in public health and precision medicine.

• Parasitology
• Tropical Medicine
• Trypanosomiasis
• +۴ مورد دیگر

Nicolas Bebronne is a researcher at the Institute of Tropical Medicine Antwerp (ITG), Belgium, specializing in parasitology with a focus on Trypanosoma species. His work spans multiple continents, with significant research conducted in Algeria and the Democratic Republic of Congo. Bebronne has maintained a consistent research output from 2005 through 2024, demonstrating ongoing contributions to tropical medicine and parasitology. Bebronne's research interests encompass several critical areas in tropical disease research: Trypanosomiasis diagnostics and detection methodologies Genomic analysis of Trypanosoma species Epidemiology of animal trypanosomiasis (particularly surra) in North Africa Molecular characterization of Trypanosoma strains Development of improved diagnostic assays for human and animal African trypanosomiasis Capacity building for health research in endemic regions His publications reveal a strong emphasis on practical applications for disease detection and control, with numerous studies examining diagnostic test performance and epidemiological patterns in endemic areas. The research often involves collaborations with scientists from affected countries, particularly in Algeria and the Democratic Republic of Congo. Bebronne was a key collaborator in the DRC-FA4 project (2017-2021), funded by the Directorate-General for Development Cooperation and Humanitarian Aid, which focused on building health research capacity in three Democratic Republic of Congo institutions while strengthening efforts against Human African Trypanosomiasis (HAT). His scientific contributions include significant work on Trypanosoma brucei gambiense (74% of his research fingerprint), parasites (32%), Trypanosoma brucei brucei (29%), and related areas such as Pichia, genome analysis, routine diagnostic tests, and infections. His recent work demonstrates continued innovation in molecular diagnostics and epidemiological studies of trypanosomal diseases.

Nasrine Bendjilaliمشاهده پروفایل

دانشیار

• Biomedical Research
• Statistical Methods for Genetic Mapping
• Genetic Risk Factors
• +۳ مورد دیگر

Nasrine Bendjilali, Ph.D., is an Associate Professor in the Department of Mathematics at Rowan University's College of Science & Mathematics. Her affiliations include roles in academic advising and teaching graduate-level courses such as Master’s Thesis and Elements of Statistical Learning. She holds a Ph.D. in Applied Mathematics from Lehigh University, an M.S. in Mathematics from the same institution, and a B.S. in Applied Mathematics from the University of Petra. Her postdoctoral training was at the Center for Cerebrovascular Research, University of California-San Francisco. Dr. Bendjilali's research focuses on statistical methods applied to genetic and genomic data. Key interests include identifying genetic risk factors for complex diseases like cardiovascular and cerebrovascular disorders, developing statistical procedures for high-dimensional data analysis, and exploring gene-diet interactions. More recently, she has contributed to education research, leveraging item response theory to improve multiple-choice question analysis. Her work bridges biomedical research and quantitative methodologies. Her publications span topics from genetic associations in vascular diseases to statistical models in education. Notable contributions include genome-wide association studies on brain arteriovenous malformations and studies on Okinawan population genetics. She is actively involved in the Statistical Consulting Group at Rowan, assisting in collaborative research projects. Professional memberships include the American Statistical Association, Mathematical Association of America, American Society of Human Genetics, and European Society of Human Genetics. Her teaching and research roles reflect a commitment to both applied mathematics and interdisciplinary scientific inquiry.

Intiaz Chowdhuryمشاهده پروفایل

استادیار

• Nematology
• Plant Pathology
• Agricultural Science
• +۳ مورد دیگر

Intiaz Chowdhury is an Assistant Professor in the Department of Plant Pathology at the University of Georgia , affiliated with the College of Agricultural and Environmental Sciences . His work focuses on nematode management in cotton and vegetable crops to enhance grower profitability and sustainable agriculture. Ph.D. in Plant Pathology (2020), North Dakota State University B.S. in Microbiology (2015), North Dakota State University Chowdhury’s research targets plant-parasitic nematodes (PPN), particularly root-knot, reniform, and sting nematodes. He develops molecular diagnostics , evaluates non-fumigant nematicides , and studies host resistance mechanisms to create holistic management strategies for southeastern U.S. agriculture. His recent publications (2024–2025) highlight innovations in RPA assays for nematode detection, biochar and cover crops for soil health, and chemical-genetic integrated approaches for sustainable pest control across soybean, tomato, pepper, and cotton systems. Chowdhury has secured funding from USDA NIFA , Cotton Incorporated , and Georgia commodity commissions (2019–2027). Grants address threats like Pratylenchus dakotaensis and Meloidogyne species in tobacco, pecan, and Vidalia onion industries.

Albert Culbreathمشاهده پروفایل

استاد

• Plant Pathology
• Fungal Diseases
• Viral Diseases
• +۵ مورد دیگر

Albert Culbreath is a Professor in the Department of Plant Pathology at the University of Georgia's College of Agricultural and Environmental Sciences. His career spans decades of research on peanut diseases, with a focus on epidemiology and management of foliar fungal pathogens and Tomato Spotted Wilt Virus (TSWV). Education Ph.D. in Plant Pathology, North Carolina State University (1989) M.S. in Plant Pathology (Nematology), Auburn University (1985) B.S. in Botany, Auburn University (1982) Associate of Science in Science, Roane State Community College (1980) Dr. Culbreath's research emphasizes partial resistance mechanisms in peanut cultivars, fungicide resistance management, and integrated disease control systems applicable to both conventional and organic farming. His team investigates interactions between plant genetics and pathogen dynamics, particularly for Cercospora arachidicola , Nothopassalora personata , and TSWV. Recent publications highlight advancements in genomic mapping of TSWV resistance loci , fungicide combination trials, and MAGIC population-based studies for trait discovery. These works intersect with disciplines like virology, molecular genetics, and agricultural chemistry. Scientific Awards Outstanding contributions to peanut industry (2024) UGA Peanut Team Recognition (2023) Fellow of American Phytopathological Society (2020) D.W. Brooks Award for Research Excellence (2012) Current funded projects include collaborations with national peanut boards to develop resistant cultivars , refine fungicide application strategies , and explore genomic resources for thrips/TSWV management . His work supports sustainable practices through reduced pesticide inputs and organic system adaptations.

• Neurodegenerative Diseases
• Mitochondrial Genetics
• Genetic Disorders
• +۳ مورد دیگر

Dr. Michael Keogh is a Researcher at Newcastle University, contributing to neurogenetic and mitochondrial disease research. His work focuses on genetic mechanisms underlying neurodegenerative diseases, mitochondrial dysfunction, and brain iron accumulation. He has collaborated extensively with experts in neurology and genetics, publishing widely on topics such as Alzheimer's disease, Lewy body dementia, and genetic variants linked to neurological disorders. His research interests include understanding the role of genetic mutations (e.g., PLCG2, STXBP1, SCP2) in disease etiology, mitochondrial DNA variations, and the molecular pathways driving neurodegeneration. Recent studies have explored hereditary ferritinopathies, oligogenic genetic interactions, and the clinical implications of exome sequencing in undiagnosed ataxias. Dr. Keogh’s publications highlight a focus on translational research, including the development of diagnostic tools like the SVI variant interpretation system. His work bridges basic science and clinical applications, contributing to both mechanistic understanding and potential therapeutic avenues in neurodegenerative diseases.

• Pediatric Hematology
• Pediatric Oncology
• Neuro-Oncology
• +۳ مورد دیگر

Uwe Kordes is a Clinical Professor and Senior Physician specializing in Pediatric Hematology and Oncology at the University Medical Center Hamburg-Eppendorf (UKE), affiliated with the University of Hamburg Faculty of Medicine. He leads the Department of Pediatric Hematology and Oncology within the Center for Obstetrics and Pediatrics. His work focuses on neuro-oncological challenges, particularly choroid plexus tumors, rhabdoid tumors, and genetic syndromes such as Li-Fraumeni syndrome. He collaborates on multi-institutional trials and registries, including the CPT-SIOP registry for choroid plexus tumors. Research interests include molecular profiling of pediatric brain tumors, therapeutic strategies for high-risk malignancies, and genetic predisposition to cancer. Kordes has contributed to over 80 peer-reviewed publications, emphasizing translational research and clinical outcomes. Key collaborations involve institutions like the European Rhabdoid Registry (EU-RHAB) and the Mildred Scheel Foundation. Notable contributions include defining molecular subgroups in atypical teratoid/rhabdoid tumors (ATRT) and advancing targeted therapies for BRAF-mutant gliomas. He also investigates the role of germline mutations in cancer predisposition syndromes.

• Neuro-oncology
• Molecular Biology
• Cancer Genetics
• +۴ مورد دیگر

Ulrich Schüller is a Professor of Neuropathology and Medical Specialist in the Faculty of Medicine at the University of Hamburg. He holds dual roles as Senior Physician in the Institute of Neuropathology and Head of Research Group in the Department of Pediatric Hematology and Oncology at the University Medical Center Hamburg-Eppendorf (UKE). His research focuses on molecular profiling of brain tumors, including medulloblastoma, glioblastoma, and pediatric cancers, with expertise in DNA methylation-based classifications and nanopore sequencing technologies. He leads studies on tumor heterogeneity, therapeutic vulnerabilities, and clinical biomarkers. Key affiliations include the UKE’s Center for Molecular Neurobiology Hamburg (ZMNH) and collaborative networks like the European Liquid Biopsy Society (ELBS). He contributes to international trials (e.g., HIT-MED, P-HIT) and has pioneered work on extracellular vesicle-based diagnostics and targeted therapies for pediatric brain tumors. His interdisciplinary approach integrates genomics, proteomics, and clinical data to improve diagnosis and treatment stratification. Research interests span neuro-oncology, epigenetic profiling, and pediatric cancer biology, with publications emphasizing molecular mechanisms of tumor progression and novel therapeutic strategies. Collaborations include academic institutions globally, focusing on translational research to bridge basic science and clinical practice.

MO Yinمشاهده پروفایل

مدرس ارشد

• Antimicrobial Resistance
• Emerging Infectious Diseases
• Clinical Medicine
• +۳ مورد دیگر

Dr. MO Yin is a Senior Lecturer (Joint) at the Saw Swee Hock School of Public Health and Yong Loo Lin School of Medicine, National University of Singapore (NUS). She is affiliated with the National University Hospital (NUH) Division of Infectious Disease, Department of Medicine, and the Mahidol-Oxford Research Unit at the University of Oxford. Her career spans clinical research, medical education, and hospital administration, with a focus on translational research to influence health policies. Dr. Yin holds a DPhil in Clinical Medicine (University of Oxford, 2022), Master of Clinical Investigation (NUS, 2017), and American Board of Internal Medicine Certification (2013). She has been a Consultant in Infectious Diseases at NUH since 2019 and has held academic roles at NUS since 2017. Her research interests include Antimicrobial Resistance , Emerging Infectious Diseases , and Mathematical Modelling applied to public health. She actively contributes to clinical medicine and microbiology education. Her publications span molecular pathology of tumors, including sarcomas, vascular anomalies, and Epstein-Barr virus-associated tumors. Recent work emphasizes genetic profiling of pediatric cancers and diagnostic challenges in cytology. Awards: Gordon A Ransome Medal (2013), Seah Cheng Siang Medal (2013) Dr. Yin oversees research teams at the Mahidol-Oxford Tropical Medicine Research Unit and collaborates on global health initiatives. Her work bridges clinical practice and policy, addressing regional and global health challenges.