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Hanmin Guo
Postdoctoral Scholar, Psychiatry
Print Profile
Email Profile
Bio
Bio
Publications
Contact
hmguo@stanford.edu
All Publications
Publications (8)
All Publications
(8)
Journal Articles
(8)
Profiles With Related Publications
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Themistocles (Tim) Assimes
Associate Professor of Medicine (Cardiovascular Medicine) and, by courtesy, of Epidemiology and Population Health
Research Interests
Genetic Epidemiology, Genetic Determinants of Complex Traits related to Cardiovasular Medicine, Coronary Artery Disease related pathway analyses and integrative genomics, Mendelian randomization studies, risk prediction for major adverse cardiovascular events, cardiovascular medicine related pharmacogenomics, ethnic differences in the determinants of Insulin Mediated Glucose Uptake, pharmacoepidemiology of cardiovascular drugs & outcomes
352
Total Publications
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Lisa W Chu
Senior Research Scientist, Medicine - Med/Stanford Prevention Research Center
24
Total Publications
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Shoa L. Clarke, MD, PhD
Assistant Professor of Medicine (Stanford Prevention Research Center) and of Pediatrics (Cardiology)
Clinical Focus
Preventive Cardiology, Genetics, Familial Hypercholesterolemia, Lipoprotein-a, Lipids, Coronary Artery Disease, Coronary Artery Calcification, Pediatrics, Cardiovascular Disease
54
Total Publications
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Ben Domingue
Associate Professor of Education and, by courtesy, of Sociology
Research Interests
I'm interested in models for psychological measurement and their uses alongside applied statistical projects of all kinds.
130
Total Publications
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Jesse Engreitz
Assistant Professor of Genetics
Research Interests
Regulatory elements in the human genome harbor thousands of genetic risk variants for common diseases and could reveal targets for therapeutics — if only we could map the complex regulatory wiring that connects 2 million regulatory elements with 21,000 genes in thousands of cell types in the human body.
We combine experimental and computational genomics, biochemistry, molecular biology, and genetics to assemble regulatory maps of the human genome and uncover biological mechanisms of disease.
73
Total Publications
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Shreyas Gopalakrishnan
Postdoctoral Scholar, Biology
2
Total Publications
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Tamar Green
Associate Professor of Psychiatry and Behavioral Sciences (Interdisciplinary Brain Sciences) and, by courtesy, of Pediatrics
Clinical Focus
Child and Adolescent Psychiatry, ADHD, Neurogenetic syndromes
Research Interests
The Brain Imaging, Development, and Genetic (BRIDGE) Lab focuses on disorders associated with child development, such as attention deficits, hyperactivity, and autism spectrum disorders. we aim to uncover biological principles of how genetic variation and its associated downstream pathways affect children's neurodevelopmental disorders.
68
Total Publications
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Joachim Hallmayer
Professor of Psychiatry and Behavioral Sciences (Child and Adolescent Psychiatry and Child Development)
243
Total Publications
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Esther M. John
Professor (Research) of Epidemiology and Population Health and of Medicine (Oncology)
612
Total Publications
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Daniel Kim
Postdoctoral Medical Fellow, Cardiovascular Medicine
21
Total Publications
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Stephen B. Montgomery
Stanford Medicine Professor of Pathology, Professor of Genetics and of Biomedical Data Science
Research 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/
200
Total Publications
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Jack O'Sullivan
Fellow in Medicine - Med/Cardiovascular Medicine
31
Total Publications
Publication Topics For This Person
Algorithms
CRISPR-Cas Systems
Chromosome Breakpoints
Chromosome Deletion
Chromosomes, Human, Pair 22
Computational Biology
DiGeorge Syndrome
Exome
Gene Rearrangement
Genetic Predisposition to Disease
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Linkage Disequilibrium
Multifactorial Inheritance
Mutation
Phenotype
Polymorphism, Single Nucleotide
Reproducibility of Results
Risk Factors
Sequence Analysis, DNA
Whole Exome Sequencing