Publications:

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs878887

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites.

Frontiers In Genetics

de Almeida, Rodrigo C RC; Chagas, Vinícius S VS; Castro, Mauro A A MAA; Petzl-Erler, Maria L ML

Publication Date: 2018

Variant appearance in text: rs878887

PubMed Link: 29755505

Variant Present in the following documents:

• Main text
• fgene-09-00139.pdf

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What can time-frequency and phase coherence measures tell us about the genetic basis of P3 amplitude?

International Journal Of Psychophysiology : Official Journal Of The International Organization Of Psychophysiology

Malone, Stephen M SM; McGue, Matt M; Iacono, William G WG

Publication Date: 2017-05

Variant appearance in text: rs878887

PubMed Link: 27871913

Variant Present in the following documents:

• Main text

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A CRHR1 haplotype moderates the effect of adverse childhood experiences on lifetime risk of major depressive episode in African-American women.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Kranzler, Henry R HR; Feinn, Richard R; Nelson, Elliot C EC; Covault, Jonathan J; Anton, Raymond F RF; Farrer, Lindsay L; Gelernter, Joel J

Publication Date: 2011-12

Variant appearance in text: rs878887

PubMed Link: 21998007

Variant Present in the following documents:

• Main text

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Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal

Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV

Publication Date: 2012-12

Variant appearance in text: rs878887

PubMed Link: 21808284

Variant Present in the following documents:

• Main text
• nihms305090.pdf
• NIHMS305090-supplement-3.pdf

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Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

Nature Genetics

Hamza, Taye H TH; Zabetian, Cyrus P CP; Tenesa, Albert A; Laederach, Alain A; Montimurro, Jennifer J; Yearout, Dora D; Kay, Denise M DM; Doheny, Kimberly F KF; Paschall, Justin J; Pugh, Elizabeth E; Kusel, Victoria I VI; Collura, Randall R; Roberts, John J; Griffith, Alida A; Samii, Ali A; Scott, William K WK; Nutt, John J; Factor, Stewart A SA; Payami, Haydeh H

Publication Date: 2010-09

Variant appearance in text: rs878887

PubMed Link: 20711177

Variant Present in the following documents:

• NIHMS222438-supplement-1.pdf

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Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence.

Alcoholism, Clinical And Experimental Research

Chen, Andrew C H AC; Manz, Niklas N; Tang, Yongqiang Y; Rangaswamy, Madhavi M; Almasy, Laura L; Kuperman, Samuel S; Nurnberger, John J; O'Connor, Sean J SJ; Edenberg, Howard J HJ; Schuckit, Marc A MA; Tischfield, Jay J; Foroud, Tatiana T; Bierut, Laura J LJ; Rohrbaugh, John J; Rice, John P JP; Goate, Alison A; Hesselbrock, Victor V; Porjesz, Bernice B

Publication Date: 2010-06

Variant appearance in text: rs878887

PubMed Link: 20374216

Variant Present in the following documents:

• Main text

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High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts.

Journal Of Medical Genetics

Park, J W JW; Cai, J J; McIntosh, I I; Jabs, E W EW; Fallin, M D MD; Ingersoll, R R; Hetmanski, J B JB; Vekemans, M M; Attie-Bitach, T T; Lovett, M M; Scott, A F AF; Beaty, T H TH

Publication Date: 2006-07

Variant appearance in text: rs878887

PubMed Link: 16415175

Variant Present in the following documents:

• Main text

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