School of Medicine
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Assistant Professor of Pathology at the Stanford University Medical Center
Bio Dr. Merker is co-director of the Stanford Medicine Clinical Genomics Service, a joint effort between Stanford Children’s Health, Stanford Health Care, and the Stanford School of Medicine. The Clinical Genomics Service is clinical and laboratory service that uses genome sequencing and other advanced molecular testing to assist in the diagnosis of genetic disease. Dr. Merker received his M.D. and Ph.D. in Genetics from the University of North Carolina at Chapel Hill. He then completed residency training in Clinical Pathology and fellowship training in Molecular Genetic Pathology and Clinical Cytogenetics at Stanford Hospital and Clinics, followed post-doctoral training in cancer genomics at Stanford University. Dr. Merker also directs a research group that focuses on two areas. First, the laboratory uses classical genetics, genomics, and functional studies to identify and characterize acquired and heritable genetic variants important for the development of hematologic disorders and other malignancies. Second, the laboratory evaluates the clinical utility of genomic and other omics-based approaches for translation into clinical care.
Professor of Pathology
Current Research and Scholarly Interests Lymphocyte/endothelial cell adhesion mechanisms involved in lymphocyte migration to sites of inflammation; regulation of expression of endothelial cell adhesion molecules.
Assistant Professor of Neurology and, by courtesy, of Neurosurgery, of Pediatrics and of Pathology
Current Research and Scholarly Interests The Monje Lab studies the molecular and cellular mechanisms of postnatal neurodevelopment. This includes microenvironmental influences on neural precursor cell fate choice in normal neurodevelopment and in disease states.
Stephen B. Montgomery
Assistant Professor of Pathology, Genetics and, by courtesy, of Computer Science
Current Research and Scholarly Interests We focus on understanding the effects of genome variation on cellular phenotypes and cellular modeling of disease through genomic approaches such as next generation RNA sequencing in combination with developing and utilizing state-of-the-art bioinformatics and statistical genetics approaches. See our website at http://montgomerylab.stanford.edu/