Showing results for "Schork"
Li Q, Wineinger NE, et al.
Genome-wide Association Study of Paliperidone Efficacy.
Pharmacogenetics and Genomics. 2017 Jan 01; 27: 7-18.
Benyamin B, Maihofer AX, et al.
Identification of Novel Loci Affecting Circulating Chromogranins and Related Peptides.
Human Molecular Genetics. 2016 Dec 22;
Aevermann B, McCorrison J, et al.
PRODUCTION OF A PRELIMINARY QUALITY CONTROL PIPELINE FOR SINGLE NUCLEI RNA-SEQ AND ITS APPLICATION IN THE ANALYSIS OF CELL TYPE DIVERSITY OF POST-MORTEM HUMAN BRAIN NEOCORTEX.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing. 2016 Dec 01; 22: 564-575.
Cui J, Chen CH, et al.
Shared Genetic Effects Between Hepatic Steatosis and Fibrosis: A Prospective Twin Study.
Hepatology (Baltimore, Md.). 2016 Nov 01; 64: 1547-1558.
Evans DS, Avery CL, et al.
Fine-mapping, Novel Loci Identification, and SNP Association Transferability in a Genome-wide Association Study of QRS Duration in African Americans.
Human Molecular Genetics. 2016 Aug 29;
Cayer DM, 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;
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;
Peng Q, Schork A, et al.
Conservation of Distinct Genetically-Mediated Human Cortical Pattern.
PLoS Genetics. 2016 Jul 01; 12: e1006143.
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.
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;