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Showing results for "Schork"

Cayer D, Nazor KL, et al.
Mission Critical: The Need for Proteomics in the Era of Next-Generation Sequencing and Precision Medicine.

Human Molecular Genetics. 2016 Jul 20;[more]

Song Y, Shi Y, et al.
P53-Dependent DNA Damage Response Sensitive to Editing-defective TRNA Synthetase in Zebrafish.

Proceedings of the National Academy of Sciences of the United States of America. 2016 Jul 08;[more]

Buscot MJ, Magnussen CG, et al.
The Combined Effect of Common Genetic Risk Variants on Circulating Lipoproteins Is Evident in Childhood: A Longitudinal Analysis of the Cardiovascular Risk in Young Finns Study.

PloS One. 2016 Jul 01; 11: e0146081.[more]

Cui J, Chen CH, et al.
Shared Genetic Effects Between Hepatic Steatosis and Fibrosis: A Prospective Twin Study.

Hepatology (Baltimore, Md.). 2016 Jun 17;[more]

Ehlers CL, Gizer IR, et al.
Single Nucleotide Polymorphisms in the REG-CTNNA2 Region of chromosome 2 and NEIL3 Associated With Impulsivity in a Native American Sample.

Genes, Brain, and Behavior. 2016 May 11;[more]

Krishnaswami SR, Grindberg RV, et al.
Using Single Nuclei for RNA-seq to Capture the Transcriptome of Postmortem Neurons.

Nature Protocols. 2016 Mar 01; 11: 499-524.[more]

Jernigan TL, Brown TT, et al.
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.

NeuroImage. 2016 Jan 01; 124: 1149-54.[more]

Loomba R, Schork N, et al.
Heritability of Hepatic Fibrosis and Steatosis Based on a Prospective Twin Study.

Gastroenterology. 2015 Aug 20;[more]

Fan CC, Bartsch H, et al.
Modeling the 3D Geometry of the Cortical Surface With Genetic Ancestry.

Current Biology : CB. 2015 Aug 03; 25: 1988-92.[more]

Coombes B, Basu S, et al.
Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.

PloS One. 2015 Jun 01; 10: e0139355.[more]

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