CRHR1 c.*656G>A

Variant ID: 17-43912786-G-A

NM_004382.4(CRHR1):c.*656G>A

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08

Variant appearance in text: rs4640231
PubMed Link: 33420045
Variant Present in the following documents:
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 2
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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: rs4640231
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



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: rs4640231
PubMed Link: 29755505
Variant Present in the following documents:
  • Main text
  • fgene-09-00139.pdf
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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs4640231
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.

Bmc Genomics
Zhang, Xiaoling X; Gierman, Hinco J HJ; Levy, Daniel D; Plump, Andrew A; Dobrin, Radu R; Goring, Harald H H HH; Curran, Joanne E JE; Johnson, Matthew P MP; Blangero, John J; Kim, Stuart K SK; O'Donnell, Christopher J CJ; Emilsson, Valur V; Johnson, Andrew D AD
Publication Date: 2014-06-27

Variant appearance in text: rs4640231
PubMed Link: 24973796
Variant Present in the following documents:
  • 12864_2013_6258_MOESM17_ESM.xlsx, sheet 1
View BVdb publication page



Genomic markers of ovarian reserve.

Seminars In Reproductive Medicine
Wood, Michelle A MA; Rajkovic, Aleksandar A
Publication Date: 2013-11

Variant appearance in text: rs4640231
PubMed Link: 24101221
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

Nature Communications
Permuth-Wey, Jennifer J; Lawrenson, Kate K; Shen, Howard C HC; Velkova, Aneliya A; Tyrer, Jonathan P JP; Chen, Zhihua Z; Lin, Hui-Yi HY; Chen, Y Ann YA; Tsai, Ya-Yu YY; Qu, Xiaotao X; Ramus, Susan J SJ; Karevan, Rod R; Lee, Janet J; Lee, Nathan N; Larson, Melissa C MC; Aben, Katja K KK; Anton-Culver, Hoda H; Antonenkova, Natalia N; Antoniou, Antonis C AC; Armasu, Sebastian M SM; , ; , ; Bacot, François F; Baglietto, Laura L; Bandera, Elisa V EV; Barnholtz-Sloan, Jill J; Beckmann, Matthias W MW; Birrer, Michael J MJ; Bloom, Greg G; Bogdanova, Natalia N; Brinton, Louise A LA; Brooks-Wilson, Angela A; Brown, Robert R; Butzow, Ralf R; Cai, Qiuyin Q; Campbell, Ian I; Chang-Claude, Jenny J; Chanock, Stephen S; Chenevix-Trench, Georgia G; Cheng, Jin Q JQ; Cicek, Mine S MS; Coetzee, Gerhard A GA; , ; Cook, Linda S LS; Couch, Fergus J FJ; Cramer, Daniel W DW; Cunningham, Julie M JM; Dansonka-Mieszkowska, Agnieszka A; Despierre, Evelyn E; Doherty, Jennifer A JA; Dörk, Thilo T; du Bois, Andreas A; Dürst, Matthias M; Easton, Douglas F DF; Eccles, Diana D; Edwards, Robert R; Ekici, Arif B AB; Fasching, Peter A PA; Fenstermacher, David A DA; Flanagan, James M JM; Garcia-Closas, Montserrat M; Gentry-Maharaj, Aleksandra A; Giles, Graham G GG; Glasspool, Rosalind M RM; Gonzalez-Bosquet, Jesus J; Goodman, Marc T MT; Gore, Martin M; Górski, Bohdan B; Gronwald, Jacek J; Hall, Per P; Halle, Mari K MK; Harter, Philipp P; Heitz, Florian F; Hillemanns, Peter P; Hoatlin, Maureen M; Høgdall, Claus K CK; Høgdall, Estrid E; Hosono, Satoyo S; Jakubowska, Anna A; Jensen, Allan A; Jim, Heather H; Kalli, Kimberly R KR; Karlan, Beth Y BY; Kaye, Stanley B SB; Kelemen, Linda E LE; Kiemeney, Lambertus A LA; Kikkawa, Fumitaka F; Konecny, Gottfried E GE; Krakstad, Camilla C; Kjaer, Susanne Krüger SK; Kupryjanczyk, Jolanta J; Lambrechts, Diether D; Lambrechts, Sandrina S; Lancaster, Johnathan M JM; Le, Nhu D ND; Leminen, Arto A; Levine, Douglas A DA; Liang, Dong D; Lim, Boon Kiong BK; Lin, Jie J; Lissowska, Jolanta J; Lu, Karen H KH; Lubiński, Jan J; Lurie, Galina G; Massuger, Leon F A G LF; Matsuo, Keitaro K; McGuire, Valerie V; McLaughlin, John R JR; Menon, Usha U; Modugno, Francesmary F; Moysich, Kirsten B KB; Nakanishi, Toru T; Narod, Steven A SA; Nedergaard, Lotte L; Ness, Roberta B RB; Nevanlinna, Heli H; Nickels, Stefan S; Noushmehr, Houtan H; Odunsi, Kunle K; Olson, Sara H SH; Orlow, Irene I; Paul, James J; Pearce, Celeste L CL; Pejovic, Tanja T; Pelttari, Liisa M LM; Pike, Malcolm C MC; Poole, Elizabeth M EM; Raska, Paola P; Renner, Stefan P SP; Risch, Harvey A HA; Rodriguez-Rodriguez, Lorna L; Rossing, Mary Anne MA; Rudolph, Anja A; Runnebaum, Ingo B IB; Rzepecka, Iwona K IK; Salvesen, Helga B HB; Schwaab, Ira I; Severi, Gianluca G; Shridhar, Viji V; Shu, Xiao-Ou XO; Shvetsov, Yurii B YB; Sieh, Weiva W; Song, Honglin H; Southey, Melissa C MC; Spiewankiewicz, Beata B; Stram, Daniel D; Sutphen, Rebecca R; Teo, Soo-Hwang SH; Terry, Kathryn L KL; Tessier, Daniel C DC; Thompson, Pamela J PJ; Tworoger, Shelley S SS; van Altena, Anne M AM; Vergote, Ignace I; Vierkant, Robert A RA; Vincent, Daniel D; Vitonis, Allison F AF; Wang-Gohrke, Shan S; Palmieri Weber, Rachel R; Wentzensen, Nicolas N; Whittemore, Alice S AS; Wik, Elisabeth E; Wilkens, Lynne R LR; Winterhoff, Boris B; Woo, Yin Ling YL; Wu, Anna H AH; Xiang, Yong-Bing YB; Yang, Hannah P HP; Zheng, Wei W; Ziogas, Argyrios A; Zulkifli, Famida F; Phelan, Catherine M CM; Iversen, Edwin E; Schildkraut, Joellen M JM; Berchuck, Andrew A; Fridley, Brooke L BL; Goode, Ellen L EL; Pharoah, Paul D P PD; Monteiro, Alvaro N A AN; Sellers, Thomas A TA; Gayther, Simon A SA
Publication Date: 2013

Variant appearance in text: rs4640231
PubMed Link: 23535648
Variant Present in the following documents:
  • Main text
  • nihms447293.pdf
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A genome-wide association study of early menopause and the combined impact of identified variants.

Human Molecular Genetics
Perry, John R B JR; Corre, Tanguy T; Esko, Tõnu T; Chasman, Daniel I DI; Fischer, Krista K; Franceschini, Nora N; He, Chunyan C; Kutalik, Zoltan Z; Mangino, Massimo M; Rose, Lynda M LM; Vernon Smith, Albert A; Stolk, Lisette L; Sulem, Patrick P; Weedon, Michael N MN; Zhuang, Wei V WV; Arnold, Alice A; Ashworth, Alan A; Bergmann, Sven S; Buring, Julie E JE; Burri, Andrea A; Chen, Constance C; Cornelis, Marilyn C MC; Couper, David J DJ; Goodarzi, Mark O MO; Gudnason, Vilmundur V; Harris, Tamara T; Hofman, Albert A; Jones, Michael M; Kraft, Peter P; Launer, Lenore L; Laven, Joop S E JS; Li, Guo G; McKnight, Barbara B; Masciullo, Corrado C; Milani, Lili L; Orr, Nicholas N; Psaty, Bruce M BM; , ; Ridker, Paul M PM; Rivadeneira, Fernando F; Sala, Cinzia C; Salumets, Andres A; Schoemaker, Minouk M; Traglia, Michela M; Waeber, Gérard G; Chanock, Stephen J SJ; Demerath, Ellen W EW; Garcia, Melissa M; Hankinson, Susan E SE; Hu, Frank B FB; Hunter, David J DJ; Lunetta, Kathryn L KL; Metspalu, Andres A; Montgomery, Grant W GW; Murabito, Joanne M JM; Newman, Anne B AB; Ong, Ken K KK; Spector, Tim D TD; Stefansson, Kari K; Swerdlow, Anthony J AJ; Thorsteinsdottir, Unnur U; Van Dam, Rob M RM; Uitterlinden, André G AG; Visser, Jenny A JA; Vollenweider, Peter P; Toniolo, Daniela D; Murray, Anna A
Publication Date: 2013-04-01

Variant appearance in text: rs4640231
PubMed Link: 23307926
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4640231
PubMed Link: 20711177
Variant Present in the following documents:
  • NIHMS222438-supplement-1.pdf
View BVdb publication page



Genetic analysis of variation in human meiotic recombination.

Plos Genetics
Chowdhury, Reshmi R; Bois, Philippe R J PR; Feingold, Eleanor E; Sherman, Stephanie L SL; Cheung, Vivian G VG
Publication Date: 2009-09

Variant appearance in text: rs4640231
PubMed Link: 19763160
Variant Present in the following documents:
  • Main text
  • pgen.1000648.pdf
View BVdb publication page