جست‌وجوی استاد و پژوهشگر

Saroj Aryalمشاهده پروفایل

دانشیار

• Sparse Moment Problem
• Applied Analysis
• Control Systems
• +۳ مورد دیگر

Dr. Saroj Aryal is an Associate Professor of Mathematics at Georgian Court University (2024–present), previously serving as Assistant Professor there (2020–2024) and at Montana State University Billings (2013–2019). He holds a PhD in Mathematics (University of Wyoming, 2013), an MS (2011), and a BS from Trinity College (2009). His research focuses on sparse moment problems, applied analysis, control systems, finance mathematics, and mathematics education. Notable projects include undergraduate collaborations on Fibonacci sequence properties, circulant matrices, and stability of polynomials. He emphasizes involving students in research, with grants from the New Jersey Space Grant Consortium. Publications span diverse topics like NCLEX-RN success indicators, moment sequences, and ETF volatility analysis. His work bridges theoretical mathematics with practical applications in healthcare, engineering, and finance.

Jean-Philippe Gourdineمشاهده پروفایل

استادیار

• Glycobiology
• Genomics
• Computational Biology
• +۳ مورد دیگر

Jean-Philippe Gourdine is an Assistant Professor of Chemistry at Lewis & Clark College , located in Portland, Oregon. His work bridges glycobiology, computational biology, and clinical genomics, focusing on molecular mechanisms of genetic disorders and glycophenotype classification. He is affiliated with the Chemistry Department and actively participates in interdisciplinary initiatives like the Monarch Initiative and Human Phenotype Ontology (HPO) expansion. Research Interests: Role of glycans in disease diagnostics Genetic mutations affecting GPI-anchor biosynthesis Semantic integration of clinical data for biomarker discovery Urobiome dynamics in health and disease Key Contributions: Developed computational platforms for phenotype-genotype mapping Advanced methods for diagnosing undiagnosed genetic conditions Explored host-microbial interactions via glycan microarrays Professional Activities: Collaborates with the Undiagnosed Diseases Network and contributes to international efforts in genomic data standardization.

• ALS Genetics
• Neurodegenerative Disorders
• Genomic Analysis
• +۲ مورد دیگر

John Landers is Professor of Neurology at UMass Chan Medical School, where he directs ALS genetics research. His laboratory uses high-throughput genomics to identify genes associated with familial and sporadic amyotrophic lateral sclerosis (ALS), including the discovery of KIFAP3 as a survival modifier. Dr. Landers' work bridges basic science and clinical applications, developing diagnostic approaches and investigating disease mechanisms. He previously served as Chief Scientific Officer at PolyGenyx and holds appointments in multiple graduate programs.

• Molecular Pathology
• Genetic Diagnostics
• Pediatric Oncology
• +۵ مورد دیگر

Jianling Ji, MD is a Clinical Associate Professor of Clinical Pathology at the University of Southern California. Her work focuses on molecular diagnostics, genomic analysis, and pediatric oncology. She is actively involved in translational research bridging genetic findings with clinical applications. Her research emphasizes improving diagnostic accuracy through advanced genomic techniques like optical genome mapping and RNA sequencing. Her publications span topics including pediatric tumor characterization, genomic variant interpretation, and clinical trial outcomes for surgical oncology interventions. She collaborates on multi-institutional studies and contributes to guideline development for molecular pathology practices. Dr. Ji's work frequently addresses challenges in pediatric malignancies, including diagnostic yield optimization and resistance mechanisms in targeted therapies. Key areas of contribution include: (1) Development of clinical sequencing assays for fusion gene detection in tumors, (2) Validation of liquid biopsy approaches for disease monitoring, (3) Standardization of genomic testing protocols through professional society collaboration, and (4) Analysis of rare genetic syndromes with complex phenotypic presentations. Her research demonstrates a strong focus on actionable genomic insights for clinical decision-making.

Christoforos Charalambousمشاهده پروفایل

مدرس

• Video Analytics
• Computer Vision
• Human Motion Analysis
• +۵ مورد دیگر

Dr. Christoforos Charalambous is a Lecturer in Data Analytics and Course Leader of the MSc Data Analytics (Distance Learning) at the University of Central Lancashire Cyprus (UCLan Cyprus), part of the School of Business & Management . He holds a PhD in Computer Vision from Imperial College London (2017), an MSc in Biomedical Engineering (Imperial College London, 2012), and a BSc/MEng in Electrical and Computer Engineering from the National Technical University of Athens (2011). His research focuses on multi-disciplinary applications of video analytics, computer vision, and human motion analysis , with emphasis on security, healthcare, sports, and smart city projects. He has published in areas such as gait recognition, crime forensics, and biomedical imaging. Notable awards include 2nd place in the DASA Real-World Incident Response Hackathon 2018 and a prestigious PhD scholarship from Imperial College London. Teaching responsibilities include modules such as Enterprise Data Management, Business Intelligence, and Knowledge Discovery. He previously served as a Research Scientist and Manager at SeeQuestor Ltd (2016–2023), contributing to industry-driven research projects. He is an Associate Fellow of the Higher Education Academy (UK).

Paul Lewisمشاهده پروفایل

استاد

• Environmental Health
• Public Health Policy
• Environmental Monitoring
• +۵ مورد دیگر

Professor Paul Lewis holds a joint Chair in the School of Management and School of Medicine at Swansea University. He is Director of the Centre for Health and Environmental Management Research and Innovation (CHEMRI) and leads the Respiratory Diagnostics Group. His research focuses on environmental data modeling, air quality monitoring, and optical diagnostics for respiratory diseases. He collaborates with Welsh health boards and industry to address particulate pollution impacts, securing over £6 million in grants. Lewis is a member of Welsh Government clean air advisory panels and has led clinical trials, filing three patents and founding spin-off companies in diagnostics and environmental analytics. Education: PhD and first degree in Genetics. Previously a lecturer at Cardiff University. Research Interests: Environmental health impacts, pollutant modeling, big data analytics, optical technologies, respiratory disease management. Recent work includes studies on lung cancer biomarkers, air pollution exposure in youth, and antimicrobial peptide cytotoxicity. Grants & Impact: Over £6M external funding. Patents and spin-offs in diagnostics and air quality. Collaborations with Swansea Bay UHB, Cwm Taf UHB, and Cardiff and Vale UHB. Labs/Teams: CHEMRI and Respiratory Diagnostics Group, with industry and local authority partnerships.

• Genetics
• Epigenetics
• Genomic Disorders
• +۳ مورد دیگر

Emily Niemitz Forrest is an Associate Research Scientist in the Department of Genetics at Yale University's Yale School of Medicine. She also serves as a Scientific Manager in the Office of Strategic Research Development, focusing on enhancing research competitiveness within the department. Her academic background includes a PhD from Johns Hopkins University's McKusick-Nathans Institute of Genetic Medicine and a BS in Biochemistry (Honors) from the University of Massachusetts Amherst. Education : PhD: Johns Hopkins University, 2000 BS (Honors): University of Massachusetts Amherst, 1998 Her research focuses on genetics, epigenetics, and genomic disorders such as Beckwith-Wiedemann syndrome and Wilms tumors. She has contributed to understanding the molecular mechanisms underlying imprinting disorders and the impact of assisted reproductive technologies. Her work also extends to stem cell biology and neurodevelopmental disorders, with recent studies exploring autism-associated genes like SHANK. Her publications reflect expertise in genetic analysis, epigenetic regulation, and translational research. Notable contributions include investigations into microarray technologies and protein evolution. Collaborations with researchers like Mark Gerstein and Yong-Hui Jiang highlight interdisciplinary efforts in genomics and clinical genetics. Dr. Forrest previously served as an editor at Nature Genetics (2004–2015), where she handled manuscripts across genetic and genomic research. Her current role emphasizes strategic research development and program management to advance scientific initiatives within the department.

• Genetics
• Molecular Biology
• Biomedical Data Science
• +۳ مورد دیگر

Dejian Zhao is an Associate Research Scientist in the Department of Genetics at Yale School of Medicine, with affiliations to the Keck Microarray Shared Resource and Yale Center for Genome Analysis. His research spans molecular biology, immunology, and biomedical data science, focusing on mechanisms of cellular aging, cancer immune evasion, and neuroimmune interactions in disease. Education: Postdoctoral Research Fellow, Albert Einstein College of Medicine (2018) PhD in Eco-genomics, Institute of Zoology, Chinese Academy of Sciences (2010) BS in Bioscience, Ocean University of China (2004) Research Interests: Dr. Zhao's work investigates protein sumoylation in aging, alternative RNA processing in atherosclerosis, epigenetic regulation in endometriosis, and tumor microenvironment dynamics. His interdisciplinary approach combines genomics, bioinformatics, and translational medicine to address fundamental mechanisms in cancer, metabolic disorders, and neurological conditions. Collaborations: Frequent collaborators include James Knight (Genetics), Ellen F Foxman (Immunobiology), Francesc Lopez-Giraldez (Genomics), and Marie-Louise Landry (Virology). His research is supported by Yale's state-of-the-art facilities, including the Yale Center for Genome Analysis. Professional Activities: Dr. Zhao serves on the editorial board of Cancer and acts as a reviewer for journals including Frontiers in Immunology and Wellcome Open Research .

Kelly Williamsمشاهده پروفایل

دانشیار

• Genetic Basis of Motor Neuron Disease (MND)
• Genomics
• Bioinformatics
• +۵ مورد دیگر

Kelly Williams is an Associate Professor at the Macquarie Medical School , Macquarie University, and leads the Advanced Gene Discovery Team as Head of Genomics & Bioinformatics within the Centre for Motor Neuron Disease (MND) Research. She holds a PhD from the University of Sydney and a BSc (Honours I) from Macquarie University . Education: PhD, University of Sydney (2013) BSc (Honours I), Macquarie University (2007) Research Interests : Genetic basis of MND and frontotemporal dementia (FTD) Identification of causal mutations and disease-modifying factors in neurodegenerative diseases Bioinformatic and biostatistical analysis of RNA-seq, exome sequencing, and methylation microarrays Translational genomics for clinical diagnostics, including PGD and pre-symptomatic testing Recent Publications focus on transcriptomic alterations in ALS, cerebellum involvement, and UBQLN2 pathology in ALS-FTD. Her work also includes global collaborations on MND genetics and biobank infrastructure development. Scientific Awards : MNDRA Bill Gole Postdoctoral Fellowship NHMRC Early Career Research Fellowship FightMND Bill Guest Mid-Career Research Fellowship NHMRC EL2 Investigator Fellowship Teaching : Co-instructor for the LaTeX and Overleaf training course (MEDI2201) for HDR students and supervisors. External Positions : Visiting Scholar, University of Utah (2024-2025) Visiting Research Fellow, Garvan Institute of Medical Research (2016) Visiting Research Fellow, University of Queensland (2015-2016) Research Residency, University of Montréal (2010)

• Cytogenomics
• Molecular Diagnostics
• Prenatal Genetics
• +۳ مورد دیگر

Shashirekha Shetty, PhD, serves as Associate Professor in the Department of Pathology at Case Western Reserve University School of Medicine. Externally, she holds dual leadership roles at University Hospitals: Director of the Cytogenetics Laboratory at the Center for Human Genetics Laboratory and Associate Director of the Laboratory Genetics and Genomics (LGG) Fellowship Program. Her office is located on the 6th floor of the Walker Building. As a board-certified clinical cytogeneticist and molecular geneticist, Dr. Shetty specializes in cytogenomics and molecular diagnostics for both germline and somatic conditions. Her primary clinical focus involves developing non-invasive prenatal screening (NIPS) assays using panel-based testing to evaluate genes linked to ultrasound-detected fetal structural abnormalities. Research collaborations center on characterizing human model cell lines to decipher disease mechanisms. The cytogenomics laboratory under her direction employs chromosome karyotyping, fluorescence in situ hybridization (FISH), and genomic chromosomal microarrays to detect balanced structural and unbalanced copy number changes, while the molecular laboratory utilizes next-generation sequencing (NGS) for comprehensive genomic profiling. Analysis of her publication record reveals a strong emphasis on cancer genomics, with research spanning acute myeloid leukemia, breast cancer, mantle cell lymphoma, and multiple myeloma. Her work consistently bridges diagnostic cytogenetics with molecular pathology to address clinical challenges in oncology and prenatal genetics, demonstrating translational applications of genomic technologies in disease characterization and biomarker discovery. No scientific awards were mentioned in the provided text. The text does not specify any graduate students, postdoctoral advisees, or research grants under Dr. Shetty's direct supervision. Her laboratory infrastructure at University Hospitals serves as a critical resource for genomic characterization, providing clinically validated data that supports both diagnostic operations and collaborative research initiatives. Dr. Shetty's laboratory ecosystem integrates cytogenomics and molecular diagnostics workflows, featuring dedicated facilities for karyotyping, FISH analysis, chromosomal microarray processing, and NGS-based testing. This infrastructure enables comprehensive genomic characterization that informs clinical decision-making while generating high-quality data for translational research partnerships across oncology and prenatal medicine domains.

• Bioinformatics
• Transcriptomics
• Gene Expression Analysis
• +۴ مورد دیگر

David Philip Kreil is an Associate Professor at the Institute of Molecular Biotechnology within the Department of Biotechnology and Food Science at the University of Natural Resources and Life Sciences, Vienna (BOKU) . He holds a joint appointment as Chair of Bioinformatics at the University of Warwick (2012-2014) and has held research positions at the European Bioinformatics Institute (EBI) and the University of Cambridge . His work bridges computational biology, transcriptomics, and plant-nematode interactions. 2012-2014: Chair of Bioinformatics, University of Warwick 2005: WWTF Vienna Science Chair at BOKU 2001-2004: MRC Research Fellow, University of Cambridge 1997-2001: EMBL PhD Programme, EBI Kreil's research focuses on transcriptomic analysis of plant-pathogen interactions (e.g., Fusarium resistance in wheat, nematode-induced syncytia) and computational methods for microarray calibration, data normalization, and statistical modeling. He has applied machine learning to weather forecasting and biomedical data. Scientific Awards : Research Fellow, Darwin College, University of Cambridge (2002-2005) His 15 most recent articles emphasize bioinformatics tools, plant immunity, and interdisciplinary applications of machine learning in biology and climate science. He has supervised theses on wheat transcriptomics and nematode-induced gene expression.

Daniel G. Malufمشاهده پروفایل

استاد

• Transplant Surgery
• Hepatology
• Immunology
• +۷ مورد دیگر

Dr. Daniel G. Maluf is a Professor of Surgery at the University of Maryland School of Medicine, where he serves as Vice Chair for System Integration Education and Training and Director of the Program in Transplantation. With over 19 years of experience in clinical and translational research, he specializes in transplant surgery and immunology, managing transplant patients and advancing therapeutic interventions for ischemia-reperfusion injury. Education: MD, Universidad Nacional de Cordoba Facultad de Ciencias Medicas, 1994 MD, Universidad Nacional de Cordoba Facultad de Ciencias Medicas, 1993 Residency, Hospital Privado Catholic University, 2000 Fellowship, Virginia Commonwealth University School of Medicine (Transplant Surgery), 2002 Research Interests: Dr. Maluf’s work focuses on liver transplantation, ischemia-reperfusion injury, and biomarker validation. His research integrates immunology, microarray data analysis, and machine perfusion to improve outcomes in kidney, liver, pancreas, and renal transplantation. He also investigates RNA/DNA isolation techniques for molecular-level insights. Scientific Awards: David Hume Young Investigator Award, South-Eastern Organ Procurement Foundation (2001) International Liver Transplant Society Young Investigator and Mentor Award (2007) Grants and Leadership: As a principal investigator in pharmaceutical clinical trials and co-investigator on NIH-funded grants, Dr. Maluf bridges clinical practice with translational research. His leadership in the Program in Transplantation emphasizes education, training, and innovation in transplantation science.

Thomas LaFramboiseمشاهده پروفایل

استاد

• Cancer Genomics
• Bioinformatics
• Computational Biology
• +۳ مورد دیگر

Dr. Thomas LaFramboise is a Professor in the Department of Genetics and Genome Sciences at Case Western Reserve University School of Medicine . He serves as a member of the Cancer Genomics and Epigenomics Program within the Case Comprehensive Cancer Center. His research focuses on computational oncogenomics and bioinformatics methodology for identifying molecular variants in cancer. Key areas include: Development of R software packages for genomic data analysis Statistical modeling of SNP microarray data in tumors Investigation of germline-somatic interactions in myeloid malignancies Exploration of mitochondrial DNA dynamics in cancer progression Recent publication trends show interdisciplinary work spanning hematologic malignancies , solid tumors , and neurodegenerative disease models . His group integrates high-dimensional data mining with experimental validation in human cancer cells. Contact: thomas.laframboise@case.edu

Subhash C. Baguiمشاهده پروفایل

استاد

• Nonparametric Classification
• Statistical Pattern Recognition
• Cluster Analysis
• +۹ مورد دیگر

Dr. Subhash C. Bagui is a Distinguished University Professor in the Department of Mathematics and Statistics at the University of West Florida, part of the Hal Marcus College of Science and Engineering. He has been a faculty member at UWF since 1990 and holds a Ph.D. in Statistics from the University of Alberta, Canada. His educational background includes a B.Sc. in Statistics (Honors) from the University of Calcutta, a Master’s in Statistics, and a Post-Graduate Diploma in Statistical Quality Control and Operations Research from the Indian Statistical Institute. Dr. Bagui's research centers on nonparametric classification, statistical pattern recognition, and cluster analysis , with significant applications in cancer detection, gene identification, and DNA microarray data analysis . He also works in data mining, biostatistics, experimental design, statistical computing, and K-12 statistics education. His work bridges theoretical statistics and real-world biomedical applications. His research has been published in journals such as the International Journal of Science and Research and the Journal of Statistical Theory and Applications , and he authored the book Handbook of Percentiles in the Non-Central t-distributions . Scientific Awards: UWF Faculty Catalyst Initiative Award (2013–14) Dr. Bagui has served as an editor and editorial board member for several peer-reviewed journals and has reviewed manuscripts for academic publications. He aims to establish a research program that supports student recruitment and improves STEM enrollment and graduation rates. He is actively involved in promoting mathematics education through initiatives like AMC 8 and AMC 10/12. His lab and research group focus on statistical methodologies with applications in biomedical sciences, though specific lab names are not mentioned.

Pavlos Antoniouمشاهده پروفایل

استاد آموزشی

• Networked Systems Design
• Nature-Inspired Algorithms
• Swarm Intelligence
• +۵ مورد دیگر

Pavlos Antoniou is a Teaching Professor at the Department of Computer Science, University of Cyprus since 2009 and a member of the Networks Research Laboratory (NetRL). He holds a Ph.D. (2012) and a Dip.Ing. (2005) in Electrical and Computer Engineering from the National Technical University of Athens. His research focuses on nature-inspired algorithms for networked systems, including swarm intelligence, bio-inspired congestion control, and machine learning applications in complex systems. He has contributed to projects like the EU-funded GINSENG and the SEnDIng IoT initiative, and co-founded the energy-intelligent startup Viridom. Education: Ph.D. in Computer Science, University of Cyprus (2012) Dip.Ing. in Electrical and Computer Engineering, National Technical University of Athens (2005) Research Interests: Design/analysis of networked systems using bio-inspired models (e.g., Lotka-Volterra, bird flocking) Machine learning for complex system optimization Energy-efficient IoT and smart home technologies Self-organizing wireless sensor networks Service Roles: Departmental Webmaster for Computer Science Logipaignion Competition Webmaster (annual computer game competition for students) Awards: Top 3% graduate student at NTUA (2000s) IKY Scholarship for academic excellence Special awards for academic excellence in high school Labs/Teams: Networks Research Laboratory (NetRL) at University of Cyprus.