Publications:

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: rs1396862

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2

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Association and Genetic Expression between Genes Involved in HPA Axis and Suicide Behavior: A Systematic Review.

Genes

Hernández-Díaz, Yazmín Y; Genis-Mendoza, Alma Delia AD; González-Castro, Thelma Beatriz TB; Tovilla-Zárate, Carlos Alfonso CA; Juárez-Rojop, Isela Esther IE; López-Narváez, María Lilia ML; Nicolini, Humberto H

Publication Date: 2021-10-13

Variant appearance in text: rs1396862

PubMed Link: 34681002

Variant Present in the following documents:

• Main text
• genes-12-01608.pdf

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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: rs1396862

PubMed Link: 32879140

Variant Present in the following documents:

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

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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: rs1396862

PubMed Link: 27871913

Variant Present in the following documents:

• Main text

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Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions.

Frontiers In Psychiatry

Mirkovic, Bojan B; Laurent, Claudine C; Podlipski, Marc-Antoine MA; Frebourg, Thierry T; Cohen, David D; Gerardin, Priscille P

Publication Date: 2016

Variant appearance in text: rs1396862

PubMed Link: 27721799

Variant Present in the following documents:

• Main text
• fpsyt-07-00158.pdf

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Epidemiological support for genetic variability at hypothalamic-pituitary-adrenal axis and serotonergic system as risk factors for major depression.

Neuropsychiatric Disease And Treatment

Ching-López, Ana A; Cervilla, Jorge J; Rivera, Margarita M; Molina, Esther E; McKenney, Kathryn K; Ruiz-Perez, Isabel I; Rodríguez-Barranco, Miguel M; Gutiérrez, Blanca B

Publication Date: 2015

Variant appearance in text: rs1396862

PubMed Link: 26543368

Variant Present in the following documents:

• Main text

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Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome.

Human Genomics

Bhattacharjee, Madhuchhanda M; Rajeevan, Mangalathu S MS; Sillanpää, Mikko J MJ

Publication Date: 2015-06-11

Variant appearance in text: rs1396862

PubMed Link: 26063326

Variant Present in the following documents:

• Main text

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Ethnic-specific genetic association of variants in the corticotropin-releasing hormone receptor 1 gene with nicotine dependence.

Biomed Research International

Tang, Xiujun X; Zhan, Shumin S; Yang, Liping L; Cui, Wenyan W; Ma, Jennie Z JZ; Payne, Thomas J TJ; Li, Ming D MD

Publication Date: 2015

Variant appearance in text: rs1396862

PubMed Link: 25802844

Variant Present in the following documents:

• Main text
• BMRI2015-263864.pdf

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The CRHR1 gene, trauma exposure, and alcoholism risk: a test of G × E effects.

Genes, Brain, And Behavior

Ray, L A LA; Sehl, M M; Bujarski, S S; Hutchison, K K; Blaine, S S; Enoch, M-A MA

Publication Date: 2013-06

Variant appearance in text: rs1396862

PubMed Link: 23473364

Variant Present in the following documents:

• Main text

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Structural diversity and African origin of the 17q21.31 inversion polymorphism.

Nature Genetics

Steinberg, Karyn Meltz KM; Antonacci, Francesca F; Sudmant, Peter H PH; Kidd, Jeffrey M JM; Campbell, Catarina D CD; Vives, Laura L; Malig, Maika M; Scheinfeldt, Laura L; Beggs, William W; Ibrahim, Muntaser M; Lema, Godfrey G; Nyambo, Thomas B TB; Omar, Sabah A SA; Bodo, Jean-Marie JM; Froment, Alain A; Donnelly, Michael P MP; Kidd, Kenneth K KK; Tishkoff, Sarah A SA; Eichler, Evan E EE

Publication Date: 2012-07-01

Variant appearance in text: rs1396862

PubMed Link: 22751100

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: rs1396862

PubMed Link: 21998007

Variant Present in the following documents:

• Main text

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Identification of significant genes in genomics using Bayesian variable selection methods.

Advances And Applications In Bioinformatics And Chemistry : Aabc

Lin, Eugene E; Huang, Lung-Cheng LC

Publication Date: 2008

Variant appearance in text: rs1396862

PubMed Link: 21918603

Variant Present in the following documents:

• Main text
• aabc-1-13.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: rs1396862

PubMed Link: 20711177

Variant Present in the following documents:

• NIHMS222438-supplement-1.pdf

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Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.

Human Molecular Genetics

Briggs, Farren B S FB; Bartlett, Selena E SE; Goldstein, Benjamin A BA; Wang, Joanne J; McCauley, Jacob L JL; Zuvich, Rebecca L RL; De Jager, Philip L PL; Rioux, John D JD; Ivinson, Adrian J AJ; Compston, Alastair A; Hafler, David A DA; Hauser, Stephen L SL; Oksenberg, Jorge R JR; Sawcer, Stephen J SJ; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; , ; Barcellos, Lisa F LF

Publication Date: 2010-11-01

Variant appearance in text: rs1396862

PubMed Link: 20699326

Variant Present in the following documents:

• Main text

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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: rs1396862

PubMed Link: 20374216

Variant Present in the following documents:

• Main text

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The distribution and most recent common ancestor of the 17q21 inversion in humans.

American Journal Of Human Genetics

Donnelly, Michael P MP; Paschou, Peristera P; Grigorenko, Elena E; Gurwitz, David D; Mehdi, Syed Qasim SQ; Kajuna, Sylvester L B SL; Barta, Csaba C; Kungulilo, Selemani S; Karoma, N J NJ; Lu, Ru-Band RB; Zhukova, Olga V OV; Kim, Jong-Jin JJ; Comas, David D; Siniscalco, Marcello M; New, Maria M; Li, Peining P; Li, Hui H; Manolopoulos, Vangelis G VG; Speed, William C WC; Rajeevan, Haseena H; Pakstis, Andrew J AJ; Kidd, Judith R JR; Kidd, Kenneth K KK

Publication Date: 2010-02-12

Variant appearance in text: rs1396862

PubMed Link: 20116045

Variant Present in the following documents:

• Main text

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H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence.

Addiction Biology

Nelson, Elliot C EC; Agrawal, Arpana A; Pergadia, Michele L ML; Wang, Jen C JC; Whitfield, John B JB; Saccone, F Scott FS; Kern, Jason J; Grant, Julia D JD; Schrage, Andrew J AJ; Rice, John P JP; Montgomery, Grant W GW; Heath, Andrew C AC; Goate, Alison M AM; Martin, Nicholas G NG; Madden, Pamela A F PA

Publication Date: 2010-01

Variant appearance in text: rs1396862

PubMed Link: 19878140

Variant Present in the following documents:

• Main text

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A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.

Journal Of Translational Medicine

Huang, Lung-Cheng LC; Hsu, Sen-Yen SY; Lin, Eugene E

Publication Date: 2009-09-22

Variant appearance in text: rs1396862

PubMed Link: 19772600

Variant Present in the following documents:

• Main text
• 1479-5876-7-81.pdf

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Chromosome 17: association of a large inversion polymorphism with corticosteroid response in asthma.

Pharmacogenetics And Genomics

Tantisira, Kelan G KG; Lazarus, Ross R; Litonjua, Augusto A AA; Klanderman, Barbara B; Weiss, Scott T ST

Publication Date: 2008-08

Variant appearance in text: rs1396862

PubMed Link: 18622266

Variant Present in the following documents:

• Main text

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