Publications:

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Association analysis of polymorphisms of the CRHR1 gene with infantile spasms.

Molecular Medicine Reports

Yang, Guang G; Zou, Li-Ping LP; Wang, Jing J; Shi, Xiu-Yu XY; Yang, Xiao-Fan XF; Wang, Bin B; Liu, Yu-Jie YJ; Sun, Yan-Hong YH; Jia, Fei-Yong FY

Publication Date: 2015-08

Variant appearance in text: rs171440

PubMed Link: 25954915

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: rs171440

PubMed Link: 25802844

Variant Present in the following documents:

• Main text
• BMRI2015-263864.pdf

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Investigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) study.

Plos One

Anderson, Laura N LN; Briollais, Laurent L; Atkinson, Helen C HC; Marsh, Julie A JA; Xu, Jingxiong J; Connor, Kristin L KL; Matthews, Stephen G SG; Pennell, Craig E CE; Lye, Stephen J SJ

Publication Date: 2014

Variant appearance in text: rs171440

PubMed Link: 24691024

Variant Present in the following documents:

• Main text
• pone.0092957.pdf

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HPA axis genetic variation, cortisol and psychosis in major depression.

Molecular Psychiatry

Schatzberg, A F AF; Keller, J J; Tennakoon, L L; Lembke, A A; Williams, G G; Kraemer, F B FB; Sarginson, J E JE; Lazzeroni, L C LC; Murphy, G M GM

Publication Date: 2014-02

Variant appearance in text: rs171440

PubMed Link: 24166410

Variant Present in the following documents:

• Main text

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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: rs171440

PubMed Link: 23473364

Variant Present in the following documents:

• Main text

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Common variants at 12q15 and 12q24 are associated with infant head circumference.

Nature Genetics

Taal, H Rob HR; Pourcain, Beate St BS; Thiering, Elisabeth E; Das, Shikta S; Mook-Kanamori, Dennis O DO; Warrington, Nicole M NM; Kaakinen, Marika M; Kreiner-Møller, Eskil E; Bradfield, Jonathan P JP; Freathy, Rachel M RM; Geller, Frank F; Guxens, Mònica M; Cousminer, Diana L DL; Kerkhof, Marjan M; Timpson, Nicholas J NJ; Ikram, M Arfan MA; Beilin, Lawrence J LJ; Bønnelykke, Klaus K; Buxton, Jessica L JL; Charoen, Pimphen P; Chawes, Bo Lund Krogsgaard BLK; Eriksson, Johan J; Evans, David M DM; Hofman, Albert A; Kemp, John P JP; Kim, Cecilia E CE; Klopp, Norman N; Lahti, Jari J; Lye, Stephen J SJ; McMahon, George G; Mentch, Frank D FD; Müller, Martina M; O'Reilly, Paul F PF; Prokopenko, Inga I; Rivadeneira, Fernando F; Steegers, Eric A P EAP; Sunyer, Jordi J; Tiesler, Carla C; Yaghootkar, Hanieh H; , ; Breteler, Monique M B MMB; Debette, Stephanie S; Fornage, Myriam M; Gudnason, Vilmundur V; Launer, Lenore J LJ; van der Lugt, Aad A; Mosley, Thomas H TH; Seshadri, Sudha S; Smith, Albert V AV; Vernooij, Meike W MW; , ; Blakemore, Alexandra If AI; Chiavacci, Rosetta M RM; Feenstra, Bjarke B; Fernandez-Benet, Julio J; Grant, Struan F A SFA; Hartikainen, Anna-Liisa AL; van der Heijden, Albert J AJ; Iñiguez, Carmen C; Lathrop, Mark M; McArdle, Wendy L WL; Mølgaard, Anne A; Newnham, John P JP; Palmer, Lyle J LJ; Palotie, Aarno A; Pouta, Annneli A; Ring, Susan M SM; Sovio, Ulla U; Standl, Marie M; Uitterlinden, Andre G AG; Wichmann, H-Erich HE; Vissing, Nadja Hawwa NH; DeCarli, Charles C; van Duijn, Cornelia M CM; McCarthy, Mark I MI; Koppelman, Gerard H GH; Estivill, Xavier X; Hattersley, Andrew T AT; Melbye, Mads M; Bisgaard, Hans H; Pennell, Craig E CE; Widen, Elisabeth E; Hakonarson, Hakon H; Smith, George Davey GD; Heinrich, Joachim J; Jarvelin, Marjo-Riitta MR; , ; Jaddoe, Vincent W V VWV

Publication Date: 2012-04-15

Variant appearance in text: rs171440

PubMed Link: 22504419

Variant Present in the following documents:

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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: rs171440

PubMed Link: 20116045

Variant Present in the following documents:

• Main text

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Linkage disequilibrium and association of MAPT H1 in Parkinson disease.

American Journal Of Human Genetics

Skipper, Lisa L; Wilkes, Kristen K; Toft, Mathias M; Baker, Matthew M; Lincoln, Sarah S; Hulihan, Mary M; Ross, Owen A OA; Hutton, Mike M; Aasly, Jan J; Farrer, Matthew M

Publication Date: 2004-10

Variant appearance in text: rs171440

PubMed Link: 15297935

Variant Present in the following documents:

• Main text

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