Publications by authors named "Joseph DeYoung"

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D
DNA methylation networks underlying mammalian traits.
Amin Haghani, Caesar Z Li, Todd R Robeck, Joshua Zhang, Ake T Lu, Joseph DeYoung

Science· August 2023

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Effect of menopausal hormone therapy on methylation levels in early and late postmenopausal women.
James R Hilser, Jaana A Hartiala, Intira Sriprasert, Naoko Kono, Zhiheng Cai, Joseph DeYoung

Clin Epigenetics· July 2022

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Epigenetic clock and methylation studies in vervet monkeys.
Anna J Jasinska, Amin Haghani, Joseph A Zoller, Caesar Z Li, Adriana Arneson, Joseph DeYoung

Geroscience· April 2022

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Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate.
Anna J Jasinska, Ivette Zelaya, Susan K Service, Christine B Peterson, Rita M Cantor, Joseph DeYoung

Nat Genet· December 2017

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Genome-wide burden of deleterious coding variants increased in schizophrenia.
Loes M Olde Loohuis, Jacob A S Vorstman, Anil P Ori, Kim A Staats, Tina Wang, Joseph DeYoung

Nat Commun· July 2015

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A non-human primate system for large-scale genetic studies of complex traits.
Anna J Jasinska, Michelle K Lin, Susan Service, Oi-Wa Choi, Joseph DeYoung

Hum Mol Genet· August 2012

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Development and implementation of high-throughput SNP genotyping in barley.
Timothy J Close, Prasanna R Bhat, Stefano Lonardi, Yonghui Wu, Nils Rostoks, Joseph DeYoung

BMC Genomics· December 2009

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Identification of brain transcriptional variation reproduced in peripheral blood: an approach for mapping brain expression traits.
Anna J Jasinska, Susan Service, Oi-wa Choi, Joseph DeYoung, Olivera Grujic

Hum Mol Genet· November 2009

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Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients.
Christiaan G J Saris, Steve Horvath, Paul W J van Vught, Michael A van Es, Hylke M Blauw, Joseph DeYoung

BMC Genomics· August 2009

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Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder.
Berit Kerner, Anna J Jasinska, Joseph DeYoung, Maricel Almonte, Oi-Wa Choi

Am J Med Genet B Neuropsychiatr Genet· January 2009

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Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder.
Susan Service, Julio Molina, Joseph Deyoung, Damini Jawaheer, Ileana Aldana

Am J Med Genet B Neuropsychiatr Genet· June 2006

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Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
Susan Service, Joseph DeYoung, Maria Karayiorgou, J Louw Roos, Herman Pretorious

Nat Genet· May 2006

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Characterization of mutations in ATP8B1 associated with hereditary cholestasis.
Leo W J Klomp, Julie C Vargas, Saskia W C van Mil, Ludmila Pawlikowska, Sandra S Strautnieks, Joseph A DeYoung

Hepatology· July 2004

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PharmGKB update: III. Genetic variants of SLC22A1, solute carrier family 22 (organic cation transporter), member 1.
Yan Shu, Maya K Leabman, Bo Feng, Lara M Mangravite, Conrad C Huang, Joseph DeYoung

Pharmacol Rev· June 2004

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PharmGKB update: I. Genetic variants of the organic cation transporter 2 (OCT2, SLC22A2).
Maya K Leabman, Conrad C Huang, Doug Stryke, Susan J Johns, Michiko Kawamoto, Joseph DeYoung

Pharmacol Rev· September 2003

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SNP analysis and presentation in the Pharmacogenetics of Membrane Transporters Project.
Doug Stryke, Conrad C Huang, Michiko Kawamoto, Susan J Johns, Elaine J Carlson, Joseph A Deyoung

Pac Symp Biocomput· August 2003

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Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene.
Deanna L Kroetz, Christiane Pauli-Magnus, Laura M Hodges, Conrad C Huang, Michiko Kawamoto, Joseph DeYoung

Pharmacogenetics· August 2003

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Natural variation in human membrane transporter genes reveals evolutionary and functional constraints.
Maya K Leabman, Conrad C Huang, Joseph DeYoung, Elaine J Carlson, Travis R Taylor

Proc Natl Acad Sci U S A· May 2003

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Evolutionary conservation predicts function of variants of the human organic cation transporter, OCT1.
Yan Shu, Maya K Leabman, Bo Feng, Lara M Mangravite, Conrad C Huang, Joseph DeYoung

Proc Natl Acad Sci U S A· May 2003

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Polymorphisms in a human kidney xenobiotic transporter, OCT2, exhibit altered function.
Maya K Leabman, Conrad C Huang, Michiko Kawamoto, Susan J Johns, Douglas Stryke, Joseph DeYoung

Pharmacogenetics· July 2002

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