Nicholas Schork
Affiliations: | 1994-2000 | Case Western Reserve University, Cleveland Heights, OH, United States | |
2000-2007 | University of California, San Diego, La Jolla, CA | ||
2007- | Scripps Research Institute, La Jolla, La Jolla, CA, United States |
Area:
statistical genetics of neuropschiatric disordersWebsite:
https://www.scripps.edu/schork/Google:
"Nicholas Schork"Mean distance: 15.03 (cluster 11)
Cross-listing: GenetiTree - Epi Tree
Children
Sign in to add traineeM Daniele Fallin | grad student | 2001 | Case Western (Epi Tree) |
Coleman A. Mosley | grad student | 2006 | UCSD |
Martin L. Jirout | grad student | 2007 | UCSD |
Matthew A. Zapala | grad student | 2007 | UCSD |
Ali Torkamani | grad student | 2008 | UCSD |
Maggie L. Chow | grad student | 2011 | UCSD |
Alexander H. Joyner | grad student | 2011 | UCSD |
Trygve E. Bakken | grad student | 2007-2011 | UCSD |
Ryan S. Tewhey | grad student | 2012 | UCSD |
Qian Peng | post-doc | Scripps Research Institute |
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Publications
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Yoo D, Rhie A, Hebbar P, et al. (2024) Complete sequencing of ape genomes. Biorxiv : the Preprint Server For Biology |
Bae H, Gurinovich A, Karagiannis TT, et al. (2022) A Genome-Wide Association Study of 2304 Extreme Longevity Cases Identifies Novel Longevity Variants. International Journal of Molecular Sciences. 24 |
Hodge RD, Miller JA, Novotny M, et al. (2020) Transcriptomic evidence that von Economo neurons are regionally specialized extratelencephalic-projecting excitatory neurons. Nature Communications. 11: 1172 |
Deacon DC, Happe CL, Chen C, et al. (2019) Combinatorial interactions of genetic variants in human cardiomyopathy. Nature Biomedical Engineering. 3: 147-157 |
Fan X, Wang H, Sun L, et al. (2019) Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population. Epigenomics |
Bergen A, Shih PB, Zeeland AS, et al. (2019) Whole Genome Sequence Analysis Of A Cousin Pair With Restricting Anorexia Nervosa European Neuropsychopharmacology. 29 |
Bakken TE, Hodge RD, Miller JA, et al. (2018) Single-nucleus and single-cell transcriptomes compared in matched cortical cell types. Plos One. 13: e0209648 |
Budde M, Friedrichs S, Alliey-Rodriguez N, et al. (2018) Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology |
Breuer R, Mattheisen M, Frank J, et al. (2018) Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. International Journal of Bipolar Disorders. 6: 24 |
Ligthart S, Vaez A, Võsa U, et al. (2018) Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706 |