ABO c.28+748C>T

Variant ID: 9-136149830-G-A

NM_020469.2(ABO):c.28+748C>T

This variant was identified in 26 publications

View GRCh38 version.




Publications:


Dissecting the genetic heterogeneity of gastric cancer.

Ebiomedicine
Hess, Timo T; Maj, Carlo C; Gehlen, Jan J; Borisov, Oleg O; Haas, Stephan L SL; Gockel, Ines I; Vieth, Michael M; Piessen, Guillaume G; Alakus, Hakan H; Vashist, Yogesh Y; Pereira, Carina C; Knapp, Michael M; Schüller, Vitalia V; Quaas, Alexander A; Grabsch, Heike I HI; Trautmann, Jessica J; Malecka-Wojciesko, Ewa E; Mokrowiecka, Anna A; Speller, Jan J; Mayr, Andreas A; Schröder, Julia J; Hillmer, Axel M AM; Heider, Dominik D; Lordick, Florian F; Pérez-Aísa, Ángeles Á; Campo, Rafael R; Espinel, Jesús J; Geijo, Fernando F; Thomson, Concha C; Bujanda, Luis L; Sopeña, Federico F; Lanas, Ángel Á; Pellisé, María M; Pauligk, Claudia C; Goetze, Thorsten Oliver TO; Zelck, Carolin C; Reingruber, Julian J; Hassanin, Emadeldin E; Elbe, Peter P; Alsabeah, Sandra S; Lindblad, Mats M; Nilsson, Magnus M; Kreuser, Nicole N; Thieme, René R; Tavano, Francesca F; Pastorino, Roberta R; Arzani, Dario D; Persiani, Roberto R; Jung, Jin-On JO; Nienhüser, Henrik H; Ott, Katja K; Schumann, Ralf R RR; Kumpf, Oliver O; Burock, Susen S; Arndt, Volker V; Jakubowska, Anna A; Ławniczak, Małgorzta M; Moreno, Victor V; Martín, Vicente V; Kogevinas, Manolis M; Pollán, Marina M; Dąbrowska, Justyna J; Salas, Antonio A; Cussenot, Olivier O; Boland-Auge, Anne A; Daian, Delphine D; Deleuze, Jean-Francois JF; Salvi, Erika E; Teder-Laving, Maris M; Tomasello, Gianluca G; Ratti, Margherita M; Senti, Chiara C; De Re, Valli V; Steffan, Agostino A; Hölscher, Arnulf H AH; Messerle, Katharina K; Bruns, Christiane Josephine CJ; Sīviņš, Armands A; Bogdanova, Inga I; Skieceviciene, Jurgita J; Arstikyte, Justina J; Moehler, Markus M; Lang, Hauke H; Grimminger, Peter P PP; Kruschewski, Martin M; Vassos, Nikolaos N; Schildberg, Claus C; Lingohr, Philipp P; Ridwelski, Karsten K; Lippert, Hans H; Fricker, Nadine N; Krawitz, Peter P; Hoffmann, Per P; Nöthen, Markus M MM; Veits, Lothar L; Izbicki, Jakob R JR; Mostowska, Adrianna A; Martinón-Torres, Federico F; Cusi, Daniele D; Adolfsson, Rolf R; Cancel-Tassin, Geraldine G; Höblinger, Aksana A; Rodermann, Ernst E; Ludwig, Monika M; Keller, Gisela G; Metspalu, Andres A; Brenner, Hermann H; Heller, Joerg J; Neef, Markus M; Schepke, Michael M; Dumoulin, Franz Ludwig FL; Hamann, Lutz L; Cannizzaro, Renato R; Ghidini, Michele M; Plaßmann, Dominik D; Geppert, Michael M; Malfertheiner, Peter P; Gehlen, Olivier O; Skoczylas, Tomasz T; Majewski, Marek M; Lubiński, Jan J; Palmieri, Orazio O; Boccia, Stefania S; Latiano, Anna A; Aragones, Nuria N; Schmidt, Thomas T; Dinis-Ribeiro, Mário M; Medeiros, Rui R; Al-Batran, Salah-Eddin SE; Leja, Mārcis M; Kupcinskas, Juozas J; García-González, María A MA; Venerito, Marino M; Schumacher, Johannes J
Publication Date: 2023-05-18

Variant appearance in text: rs532436
PubMed Link: 37209533
Variant Present in the following documents:
  • Main text
  • main.pdf
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Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.

Journal Of The American Heart Association
Shi, Mengyao M; Kelly, Tanika N TN; Zhu, Zhengbao Z; Li, Changwei C; Shen, Chong C; Sun, Yingxian Y; Wang, Aili A; Shan, Guangliang G; Bu, Xiaoqing X; Guo, Daoxia D; Zhao, Jingbo J; Xu, Tan T; Peng, Hao H; Xu, Tian T; Zhong, Chongke C; Sun, Xiao X; Chen, Jing J; Zhang, Yonghong Y; He, Jiang J
Publication Date: 2022-10-04

Variant appearance in text: rs532436
PubMed Link: 36193932
Variant Present in the following documents:
  • JAH3-11-e025245.pdf
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Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.

Blood Advances
Gueuning, Morgan M; Thun, Gian Andri GA; Wittig, Michael M; Galati, Anna-Lena AL; Meyer, Stefan S; Trost, Nadine N; Gourri, Elise E; Fuss, Janina J; Sigurdardottir, Sonja S; Merki, Yvonne Y; Neuenschwander, Kathrin K; Busch, Yannik Y; Trojok, Peter P; Schäfer, Marco M; Gottschalk, Jochen J; Franke, Andre A; Gassner, Christoph C; Peter, Wolfgang W; Frey, Beat M BM; Mattle-Greminger, Maja Patricia MP
Publication Date: 2022-09-21

Variant appearance in text: rs532436
PubMed Link: 36129841
Variant Present in the following documents:
  • Main text
  • BLOODA_ADV-2022-007133-mmc1.pdf
  • main.pdf
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Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.

Jci Insight
Li, Yong Y; Cheng, Yurong Y; Consolato, Francesco F; Schiano, Guglielmo G; Chong, Michael R MR; Pietzner, Maik M; Nguyen, Ngoc Quynh H NQH; Scherer, Nora N; Biggs, Mary L ML; Kleber, Marcus E ME; Haug, Stefan S; Göçmen, Burulça B; Pigeyre, Marie M; Sekula, Peggy P; Steinbrenner, Inga I; Schlosser, Pascal P; Joseph, Christina B CB; Brody, Jennifer A JA; Grams, Morgan E ME; Hayward, Caroline C; Schultheiss, Ulla T UT; Krämer, Bernhard K BK; Kronenberg, Florian F; Peters, Annette A; Seissler, Jochen J; Steubl, Dominik D; Then, Cornelia C; Wuttke, Matthias M; März, Winfried W; Eckardt, Kai-Uwe KU; Gieger, Christian C; Boerwinkle, Eric E; Psaty, Bruce M BM; Coresh, Josef J; Oefner, Peter J PJ; Pare, Guillaume G; Langenberg, Claudia C; Scherberich, Jürgen E JE; Yu, Bing B; Akilesh, Shreeram S; Devuyst, Olivier O; Rampoldi, Luca L; Köttgen, Anna A
Publication Date: 2022-05-23

Variant appearance in text: rs532436
PubMed Link: 35446786
Variant Present in the following documents:
  • jciinsight-7-157035-s129.xlsx, sheet 13
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Circulating α-Klotho Levels in Relation to Cardiovascular Diseases: A Mendelian Randomization Study.

Frontiers In Endocrinology
Sun, Xingang X; Chen, Lu L; He, Yuxian Y; Zheng, Liangrong L
Publication Date: 2022

Variant appearance in text: rs532436
PubMed Link: 35197934
Variant Present in the following documents:
  • Main text
  • fendo-13-842846.pdf
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Mendelian randomization study updates the effect of 25-hydroxyvitamin D levels on the risk of multiple sclerosis.

Journal Of Translational Medicine
Wang, Renxi R
Publication Date: 2022-01-03

Variant appearance in text: rs532436
PubMed Link: 34980161
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian randomization study updates the effect of 25-hydroxyvitamin D levels on the risk of multiple sclerosis.

Journal Of Translational Medicine
Wang, Renxi R
Publication Date: 2022-01-03

Variant appearance in text: rs532436
PubMed Link: 34980161
Variant Present in the following documents:
  • Main text
View BVdb publication page



Stroke and Myocardial Infarction: A Bidirectional Mendelian Randomization Study.

International Journal Of General Medicine
Sun, Wenxian W; Zhang, Luyang L; Liu, Weishi W; Tian, Mengke M; Wang, Xin X; Liang, Jing J; Wang, Yuying Y; Ding, Lan L; Pei, Lulu L; Lu, Jie J; Xu, Yuming Y; Song, Bo B
Publication Date: 2021

Variant appearance in text: rs532436
PubMed Link: 34916835
Variant Present in the following documents:
  • Main text
  • ijgm-14-9537.pdf
View BVdb publication page



GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating α-Klotho levels.

Human Molecular Genetics
Gergei, Ingrid I; Zheng, Jie J; Andlauer, Till F M TFM; Brandenburg, Vincent V; Mirza-Schreiber, Nazanin N; Müller-Myhsok, Bertram B; Krämer, Bernhard K BK; Richard, Daniel D; Falk, Louise L; Movérare-Skrtic, Sofia S; Ohlsson, Claes C; Davey Smith, George G; März, Winfried W; Voelkl, Jakob J; Tobias, Jonathan H JH
Publication Date: 2022-03-03

Variant appearance in text: rs532436
PubMed Link: 34542150
Variant Present in the following documents:
  • Main text
  • ddab263.pdf
View BVdb publication page



Is vitamin D a modifiable risk factor for dental caries?

Wellcome Open Research
Dodhia, Serena A SA; West, Nicola X NX; Thomas, Steven J SJ; Timpson, Nicholas J NJ; Johansson, Ingegerd I; Lif Holgerson, Pernilla P; Dudding, Tom T; Haworth, Simon S
Publication Date: 2020

Variant appearance in text: rs532436
PubMed Link: 34386609
Variant Present in the following documents:
  • Main text
  • wellcomeopenres-5-18849.pdf
View BVdb publication page



Using genetic variants to evaluate the causal effect of serum vitamin D concentration on COVID-19 susceptibility, severity and hospitalization traits: a Mendelian randomization study.

Journal Of Translational Medicine
Cui, Zhiyong Z; Tian, Yun Y
Publication Date: 2021-07-10

Variant appearance in text: rs532436
PubMed Link: 34246301
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs532436
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
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GWAS-linked hot loci predict short-term functional outcome and recurrence of ischemic stroke in Chinese population.

American Journal Of Translational Research
Zhu, Ruixia R; Zhao, Yating Y; Tian, Dandan D; Guo, Na N; Zhang, Chenguang C; Liu, Xu X
Publication Date: 2021

Variant appearance in text: rs532436
PubMed Link: 34150032
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Implications of ncRNAs in the Development of Human Diseases.

Non-Coding Rna
López-Jiménez, Elena E; Andrés-León, Eduardo E
Publication Date: 2021-02-24

Variant appearance in text: rs532436
PubMed Link: 33668203
Variant Present in the following documents:
  • Main text
  • ncrna-07-00017.pdf
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The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study.

Plos Medicine
Johnson, Kelsey E KE; Siewert, Katherine M KM; Klarin, Derek D; Damrauer, Scott M SM; , ; Chang, Kyong-Mi KM; Tsao, Philip S PS; Assimes, Themistocles L TL; Maxwell, Kara N KN; Voight, Benjamin F BF
Publication Date: 2020-09

Variant appearance in text: rs532436
PubMed Link: 32915777
Variant Present in the following documents:
  • Main text
  • pmed.1003302.pdf
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Multi-Omics Analysis Reveals MicroRNAs Associated With Cardiometabolic Traits.

Frontiers In Genetics
Mens, Michelle M J MMJ; Maas, Silvana C E SCE; Klap, Jaco J; Weverling, Gerrit Jan GJ; Klatser, Paul P; Brakenhoff, Just P J JPJ; van Meurs, Joyce B J JBJ; Uitterlinden, André G AG; Ikram, M Arfan MA; Kavousi, Maryam M; Ghanbari, Mohsen M
Publication Date: 2020

Variant appearance in text: rs532436
PubMed Link: 32174972
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integrating Multi-Omics Data to Identify Novel Disease Genes and Single-Neucleotide Polymorphisms.

Frontiers In Genetics
Zhao, Sheng S; Jiang, Huijie H; Liang, Zong-Hui ZH; Ju, Hong H
Publication Date: 2019

Variant appearance in text: rs532436
PubMed Link: 32038707
Variant Present in the following documents:
  • Main text
  • fgene-10-01336.pdf
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Adhesion molecule gene variants and plasma protein levels in patients with suspected obstructive sleep apnea.

Plos One
Sandford, Andrew J AJ; Ha, Amanda A; Ngan, David A DA; Akhabir, Loubna L; Saferali, Aabida A; Fox, Nurit N; Hirsch Allen, A J AJ; Warby, Simon C SC; van Eeden, Stephan F SF; Ayas, Najib T NT
Publication Date: 2019

Variant appearance in text: rs532436
PubMed Link: 30653588
Variant Present in the following documents:
  • pone.0210732.s001.pdf
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Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.

Nature Communications
Yao, Chen C; Chen, George G; Song, Ci C; Keefe, Joshua J; Mendelson, Michael M; Huan, Tianxiao T; Sun, Benjamin B BB; Laser, Annika A; Maranville, Joseph C JC; Wu, Hongsheng H; Ho, Jennifer E JE; Courchesne, Paul P; Lyass, Asya A; Larson, Martin G MG; Gieger, Christian C; Graumann, Johannes J; Johnson, Andrew D AD; Danesh, John J; Runz, Heiko H; Hwang, Shih-Jen SJ; Liu, Chunyu C; Butterworth, Adam S AS; Suhre, Karsten K; Levy, Daniel D
Publication Date: 2018-08-15

Variant appearance in text: rs532436
PubMed Link: 30111768
Variant Present in the following documents:
  • 41467_2018_5512_MOESM2_ESM.pdf
View BVdb publication page



Monogenic, Polygenic, and MicroRNA Markers for Ischemic Stroke.

Molecular Neurobiology
Chen, Wu W; Sinha, Bharati B; Li, Yi Y; Benowitz, Larry L; Chen, Qinhua Q; Zhang, Zhenghong Z; Patel, Nirav J NJ; Aziz-Sultan, Ali M AM; Chiocca, Antonio E AE; Wang, Xin X
Publication Date: 2019-02

Variant appearance in text: rs532436
PubMed Link: 29948938
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia.

Scientific Reports
Han, Yi Y; Dorajoo, Rajkumar R; Chang, Xuling X; Wang, Ling L; Khor, Chiea-Chuen CC; Sim, Xueling X; Cheng, Ching-Yu CY; Shi, Yuan Y; Tham, Yih Chung YC; Zhao, Wanting W; Chee, Miao Ling ML; Sabanayagam, Charumathi C; Chee, Miao Li ML; Tan, Nicholas N; Wong, Tien Yin TY; Tai, E-Shyong ES; Liu, Jianjun J; Goh, Daniel Y T DYT; Yuan, Jian-Min JM; Koh, Woon-Puay WP; van Dam, Rob M RM; Low, Adrian F AF; Chan, Mark Yan-Yee MY; Friedlander, Yechiel Y; Heng, Chew-Kiat CK
Publication Date: 2017-12-20

Variant appearance in text: rs532436
PubMed Link: 29263402
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_18214.pdf
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Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study.

Neurology. Genetics
Traylor, Matthew M; Rutten-Jacobs, Loes L; Curtis, Charles C; Patel, Hamel H; Breen, Gerome G; Newhouse, Stephen S; Lewis, Cathryn M CM; Markus, Hugh S HS
Publication Date: 2017-04

Variant appearance in text: rs532436
PubMed Link: 28349126
Variant Present in the following documents:
  • NG2016003749.pdf
View BVdb publication page



Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.

Plos One
McLachlan, Stela S; Giambartolomei, Claudia C; White, Jon J; Charoen, Pimphen P; Wong, Andrew A; Finan, Chris C; Engmann, Jorgen J; Shah, Tina T; Hersch, Micha M; Podmore, Clara C; Cavadino, Alana A; Jefferis, Barbara J BJ; Dale, Caroline E CE; Hypponen, Elina E; Morris, Richard W RW; Casas, Juan P JP; Kumari, Meena M; Ben-Shlomo, Yoav Y; Gaunt, Tom R TR; Drenos, Fotios F; Langenberg, Claudia C; Kuh, Diana D; Kivimaki, Mika M; Rueedi, Rico R; Waeber, Gerard G; Hingorani, Aroon D AD; Price, Jacqueline F JF; Walker, Ann P AP; ,
Publication Date: 2016

Variant appearance in text: rs532436
PubMed Link: 27280446
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population.

Human Genome Variation
Masuda, Masatoshi M; Okuda, Kayo K; Ikeda, Daisuke D DD; Hishigaki, Haretsugu H; Fujiwara, Tsutomu T
Publication Date: 2015

Variant appearance in text: rs532436
PubMed Link: 27081532
Variant Present in the following documents:
  • Main text
  • hgv201519.pdf
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Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

Neurology
Malik, Rainer R; Traylor, Matthew M; Pulit, Sara L SL; Bevan, Steve S; Hopewell, Jemma C JC; Holliday, Elizabeth G EG; Zhao, Wei W; Abrantes, Patricia P; Amouyel, Philippe P; Attia, John R JR; Battey, Thomas W K TW; Berger, Klaus K; Boncoraglio, Giorgio B GB; Chauhan, Ganesh G; Cheng, Yu-Ching YC; Chen, Wei-Min WM; Clarke, Robert R; Cotlarciuc, Ioana I; Debette, Stephanie S; Falcone, Guido J GJ; Ferro, Jose M JM; Gamble, Dale M DM; Ilinca, Andreea A; Kittner, Steven J SJ; Kourkoulis, Christina E CE; Lemmens, Robin R; Levi, Christopher R CR; Lichtner, Peter P; Lindgren, Arne A; Liu, Jingmin J; Meschia, James F JF; Mitchell, Braxton D BD; Oliveira, Sofia A SA; Pera, Joana J; Reiner, Alex P AP; Rothwell, Peter M PM; Sharma, Pankaj P; Slowik, Agnieszka A; Sudlow, Cathie L M CL; Tatlisumak, Turgut T; Thijs, Vincent V; Vicente, Astrid M AM; Woo, Daniel D; Seshadri, Sudha S; Saleheen, Danish D; Rosand, Jonathan J; Markus, Hugh S HS; Worrall, Bradford B BB; Dichgans, Martin M; , ; , ; , ; ,
Publication Date: 2016-03-29

Variant appearance in text: rs532436
PubMed Link: 26935894
Variant Present in the following documents:
  • Main text
View BVdb publication page



Which Genetics Variants in DNase-Seq Footprints Are More Likely to Alter Binding?

Plos Genetics
Moyerbrailean, Gregory A GA; Kalita, Cynthia A CA; Harvey, Chris T CT; Wen, Xiaoquan X; Luca, Francesca F; Pique-Regi, Roger R
Publication Date: 2016-02

Variant appearance in text: rs532436
PubMed Link: 26901046
Variant Present in the following documents:
  • Main text
  • pgen.1005875.pdf
View BVdb publication page



Identification of six new susceptibility loci for invasive epithelial ovarian cancer.

Nature Genetics
Kuchenbaecker, Karoline B KB; Ramus, Susan J SJ; Tyrer, Jonathan J; Lee, Andrew A; Shen, Howard C HC; Beesley, Jonathan J; Lawrenson, Kate K; McGuffog, Lesley L; Healey, Sue S; Lee, Janet M JM; Spindler, Tassja J TJ; Lin, Yvonne G YG; Pejovic, Tanja T; Bean, Yukie Y; Li, Qiyuan Q; Coetzee, Simon S; Hazelett, Dennis D; Miron, Alexander A; Southey, Melissa M; Terry, Mary Beth MB; Goldgar, David E DE; Buys, Saundra S SS; Janavicius, Ramunas R; Dorfling, Cecilia M CM; van Rensburg, Elizabeth J EJ; Neuhausen, Susan L SL; Ding, Yuan Chun YC; Hansen, Thomas V O TV; Jønson, Lars L; Gerdes, Anne-Marie AM; Ejlertsen, Bent B; Barrowdale, Daniel D; Dennis, Joe J; Benitez, Javier J; Osorio, Ana A; Garcia, Maria Jose MJ; Komenaka, Ian I; Weitzel, Jeffrey N JN; Ganschow, Pamela P; Peterlongo, Paolo P; Bernard, Loris L; Viel, Alessandra A; Bonanni, Bernardo B; Peissel, Bernard B; Manoukian, Siranoush S; Radice, Paolo P; Papi, Laura L; Ottini, Laura L; Fostira, Florentia F; Konstantopoulou, Irene I; Garber, Judy J; Frost, Debra D; Perkins, Jo J; Platte, Radka R; Ellis, Steve S; , ; Godwin, Andrew K AK; Schmutzler, Rita Katharina RK; Meindl, Alfons A; Engel, Christoph C; Sutter, Christian C; Sinilnikova, Olga M OM; , ; Damiola, Francesca F; Mazoyer, Sylvie S; Stoppa-Lyonnet, Dominique D; Claes, Kathleen K; De Leeneer, Kim K; Kirk, Judy J; Rodriguez, Gustavo C GC; Piedmonte, Marion M; O'Malley, David M DM; de la Hoya, Miguel M; Caldes, Trinidad T; Aittomäki, Kristiina K; Nevanlinna, Heli H; Collée, J Margriet JM; Rookus, Matti A MA; Oosterwijk, Jan C JC; , ; Tihomirova, Laima L; Tung, Nadine N; Hamann, Ute U; Isaccs, Claudine C; Tischkowitz, Marc M; Imyanitov, Evgeny N EN; Caligo, Maria A MA; Campbell, Ian G IG; Hogervorst, Frans B L FB; , ; Olah, Edith E; Diez, Orland O; Blanco, Ignacio I; Brunet, Joan J; Lazaro, Conxi C; Pujana, Miquel Angel MA; Jakubowska, Anna A; Gronwald, Jacek J; Lubinski, Jan J; Sukiennicki, Grzegorz G; Barkardottir, Rosa B RB; Plante, Marie M; Simard, Jacques J; Soucy, Penny P; Montagna, Marco M; Tognazzo, Silvia S; Teixeira, Manuel R MR; , ; Pankratz, Vernon S VS; Wang, Xianshu X; Lindor, Noralane N; Szabo, Csilla I CI; Kauff, Noah N; Vijai, Joseph J; Aghajanian, Carol A CA; Pfeiler, Georg G; Berger, Andreas A; Singer, Christian F CF; Tea, Muy-Kheng MK; Phelan, Catherine M CM; Greene, Mark H MH; Mai, Phuong L PL; Rennert, Gad G; Mulligan, Anna Marie AM; Tchatchou, Sandrine S; Andrulis, Irene L IL; Glendon, Gord G; Toland, Amanda Ewart AE; Jensen, Uffe Birk UB; Kruse, Torben A TA; Thomassen, Mads M; Bojesen, Anders A; Zidan, Jamal J; Friedman, Eitan E; Laitman, Yael Y; Soller, Maria M; Liljegren, Annelie A; Arver, Brita B; Einbeigi, Zakaria Z; Stenmark-Askmalm, Marie M; Olopade, Olufunmilayo I OI; Nussbaum, Robert L RL; Rebbeck, Timothy R TR; Nathanson, Katherine L KL; Domchek, Susan M SM; Lu, Karen H KH; Karlan, Beth Y BY; Walsh, Christine C; Lester, Jenny J; , ; , ; Hein, Alexander A; Ekici, Arif B AB; Beckmann, Matthias W MW; Fasching, Peter A PA; Lambrechts, Diether D; Van Nieuwenhuysen, Els E; Vergote, Ignace I; Lambrechts, Sandrina S; Dicks, Ed E; Doherty, Jennifer A JA; Wicklund, Kristine G KG; Rossing, Mary Anne MA; Rudolph, Anja A; Chang-Claude, Jenny J; Wang-Gohrke, Shan S; Eilber, Ursula U; Moysich, Kirsten B KB; Odunsi, Kunle K; Sucheston, Lara L; Lele, Shashi S; Wilkens, Lynne R LR; Goodman, Marc T MT; Thompson, Pamela J PJ; Shvetsov, Yurii B YB; Runnebaum, Ingo B IB; Dürst, Matthias M; Hillemanns, Peter P; Dörk, Thilo T; Antonenkova, Natalia N; Bogdanova, Natalia N; Leminen, Arto A; Pelttari, Liisa M LM; Butzow, Ralf R; Modugno, Francesmary F; Kelley, Joseph L JL; Edwards, Robert P RP; Ness, Roberta B RB; du Bois, Andreas A; Heitz, Florian F; Schwaab, Ira I; Harter, Philipp P; Matsuo, Keitaro K; Hosono, Satoyo S; Orsulic, Sandra S; Jensen, Allan A; Kjaer, Susanne Kruger SK; Hogdall, Estrid E; Hasmad, Hanis Nazihah HN; Azmi, Mat Adenan Noor MA; Teo, Soo-Hwang SH; Woo, Yin-Ling YL; Fridley, Brooke L BL; Goode, Ellen L EL; Cunningham, Julie M JM; Vierkant, Robert A RA; Bruinsma, Fiona F; Giles, Graham G GG; Liang, Dong D; Hildebrandt, Michelle A T MA; Wu, Xifeng X; Levine, Douglas A DA; Bisogna, Maria M; Berchuck, Andrew A; Iversen, Edwin S ES; Schildkraut, Joellen M JM; Concannon, Patrick P; Weber, Rachel Palmieri RP; Cramer, Daniel W DW; Terry, Kathryn L KL; Poole, Elizabeth M EM; Tworoger, Shelley S SS; Bandera, Elisa V EV; Orlow, Irene I; Olson, Sara H SH; Krakstad, Camilla C; Salvesen, Helga B HB; Tangen, Ingvild L IL; Bjorge, Line L; van Altena, Anne M AM; Aben, Katja K H KK; Kiemeney, Lambertus A LA; Massuger, Leon F A G LF; Kellar, Melissa M; Brooks-Wilson, Angela A; Kelemen, Linda E LE; Cook, Linda S LS; Le, Nhu D ND; Cybulski, Cezary C; Yang, Hannah H; Lissowska, Jolanta J; Brinton, Louise A LA; Wentzensen, Nicolas N; Hogdall, Claus C; Lundvall, Lene L; Nedergaard, Lotte L; Baker, Helen H; Song, Honglin H; Eccles, Diana D; McNeish, Ian I; Paul, James J; Carty, Karen K; Siddiqui, Nadeem N; Glasspool, Rosalind R; Whittemore, Alice S AS; Rothstein, Joseph H JH; McGuire, Valerie V; Sieh, Weiva W; Ji, Bu-Tian BT; Zheng, Wei W; Shu, Xiao-Ou XO; Gao, Yu-Tang YT; Rosen, Barry B; Risch, Harvey A HA; McLaughlin, John R JR; Narod, Steven A SA; Monteiro, Alvaro N AN; Chen, Ann A; Lin, Hui-Yi HY; Permuth-Wey, Jenny J; Sellers, Thomas A TA; Tsai, Ya-Yu YY; Chen, Zhihua Z; Ziogas, Argyrios A; Anton-Culver, Hoda H; Gentry-Maharaj, Aleksandra A; Menon, Usha U; Harrington, Patricia P; Lee, Alice W AW; Wu, Anna H AH; Pearce, Celeste L CL; Coetzee, Gerry G; Pike, Malcolm C MC; Dansonka-Mieszkowska, Agnieszka A; Timorek, Agnieszka A; Rzepecka, Iwona K IK; Kupryjanczyk, Jolanta J; Freedman, Matt M; Noushmehr, Houtan H; Easton, Douglas F DF; Offit, Kenneth K; Couch, Fergus J FJ; Gayther, Simon S; Pharoah, Paul P PP; Antoniou, Antonis C AC; Chenevix-Trench, Georgia G; ,
Publication Date: 2015-02

Variant appearance in text: rs532436
PubMed Link: 25581431
Variant Present in the following documents:
  • NIHMS647338-supplement-1.pdf
View BVdb publication page