Nicholas Schork

Affiliations: 
TSRI, San Diego, CA, United States 
Area:
statistical genetics of neuropschiatric disorders
Google:
"Nicholas Schork"
Mean distance: 15.03 (cluster 11)
 

Children

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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
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Publications

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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
Stahl EA, Breen G, Forstner AJ, et al. (2019) Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics
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
Boldog E, Bakken TE, Hodge RD, et al. (2018) Transcriptomic and morphophysiological evidence for a specialized human cortical GABAergic cell type. Nature Neuroscience
Boeldt DL, Cheung C, Ariniello L, et al. (2017) Patient perspectives on whole-genome sequencing for undiagnosed diseases. Personalized Medicine. 14: 17-25
Bakken T, Cowell L, Aevermann BD, et al. (2017) Cell type discovery and representation in the era of high-content single cell phenotyping. Bmc Bioinformatics. 18: 559
Peng Q, Schork A, Bartsch H, et al. (2016) Conservation of Distinct Genetically-Mediated Human Cortical Pattern. Plos Genetics. 12: e1006143
Bhutani K, Nazor KL, Williams R, et al. (2016) Whole-genome mutational burden analysis of three pluripotency induction methods. Nature Communications. 7: 10536
Libiger O, Schork NJ. (2015) Partial Least Squares Regression Can Aid in Detecting Differential Abundance of Multiple Features in Sets of Metagenomic Samples. Frontiers in Genetics. 6: 350
Standish KA, Carland TM, Lockwood GK, et al. (2015) Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies. Bmc Bioinformatics. 16: 304
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