IRF4 c.*3466A>T

Variant ID: 6-411064-A-T

NM_002460.3(IRF4):c.*3466A>T

This variant was identified in 68 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs872071
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection.

Nature Communications
Pankratov, Vasili V; Yunusbaeva, Milyausha M; Ryakhovsky, Sergei S; Zarodniuk, Maksym M; , ; Yunusbayev, Bayazit B
Publication Date: 2022-11-18

Variant appearance in text: rs872071
PubMed Link: 36400766
Variant Present in the following documents:
  • 41467_2022_Article_34461.pdf
View BVdb publication page



Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.

Nature Communications
Stackpole, Mary L ML; Zeng, Weihua W; Li, Shuo S; Liu, Chun-Chi CC; Zhou, Yonggang Y; He, Shanshan S; Yeh, Angela A; Wang, Ziye Z; Sun, Fengzhu F; Li, Qingjiao Q; Yuan, Zuyang Z; Yildirim, Asli A; Chen, Pin-Jung PJ; Winograd, Paul P; Tran, Benjamin B; Lee, Yi-Te YT; Li, Paul Shize PS; Noor, Zorawar Z; Yokomizo, Megumi M; Ahuja, Preeti P; Zhu, Yazhen Y; Tseng, Hsian-Rong HR; Tomlinson, James S JS; Garon, Edward E; French, Samuel S; Magyar, Clara E CE; Dry, Sarah S; Lajonchere, Clara C; Geschwind, Daniel D; Choi, Gina G; Saab, Sammy S; Alber, Frank F; Wong, Wing Hung WH; Dubinett, Steven M SM; Aberle, Denise R DR; Agopian, Vatche V; Han, Steven-Huy B SB; Ni, Xiaohui X; Li, Wenyuan W; Zhou, Xianghong Jasmine XJ
Publication Date: 2022-09-29

Variant appearance in text: rs872071
PubMed Link: 36175411
Variant Present in the following documents:
  • 41467_2022_32995_MOESM9_ESM.xlsx, sheet 1
View BVdb publication page



Association of Melanoma-Risk Variants with Primary Melanoma Tumor Prognostic Characteristics and Melanoma-Specific Survival in the GEM Study.

Current Oncology (Toronto, Ont.)
Davari, Danielle R DR; Orlow, Irene I; Kanetsky, Peter A PA; Luo, Li L; Busam, Klaus J KJ; Sharma, Ajay A; Kricker, Anne A; Cust, Anne E AE; Anton-Culver, Hoda H; Gruber, Stephen B SB; Gallagher, Richard P RP; Zanetti, Roberto R; Rosso, Stefano S; Sacchetto, Lidia L; Dwyer, Terence T; Gibbs, David C DC; Ollila, David W DW; Begg, Colin B CB; Berwick, Marianne M; Thomas, Nancy E NE
Publication Date: 2021-11-16

Variant appearance in text: rs872071
PubMed Link: 34898573
Variant Present in the following documents:
  • Main text
  • curroncol-28-00401.pdf
View BVdb publication page



Association of Melanoma-Risk Variants with Primary Melanoma Tumor Prognostic Characteristics and Melanoma-Specific Survival in the GEM Study.

Current Oncology (Toronto, Ont.)
Davari, Danielle R DR; Orlow, Irene I; Kanetsky, Peter A PA; Luo, Li L; Busam, Klaus J KJ; Sharma, Ajay A; Kricker, Anne A; Cust, Anne E AE; Anton-Culver, Hoda H; Gruber, Stephen B SB; Gallagher, Richard P RP; Zanetti, Roberto R; Rosso, Stefano S; Sacchetto, Lidia L; Dwyer, Terence T; Gibbs, David C DC; Ollila, David W DW; Begg, Colin B CB; Berwick, Marianne M; Thomas, Nancy E NE
Publication Date: 2021-11-16

Variant appearance in text: rs872071
PubMed Link: 34898573
Variant Present in the following documents:
  • Main text
  • curroncol-28-00401.pdf
View BVdb publication page



Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes.

Nature Genetics
Robertson, Catherine C CC; Inshaw, Jamie R J JRJ; Onengut-Gumuscu, Suna S; Chen, Wei-Min WM; Santa Cruz, David Flores DF; Yang, Hanzhi H; Cutler, Antony J AJ; Crouch, Daniel J M DJM; Farber, Emily E; Bridges, S Louis SL; Edberg, Jeffrey C JC; Kimberly, Robert P RP; Buckner, Jane H JH; Deloukas, Panos P; Divers, Jasmin J; Dabelea, Dana D; Lawrence, Jean M JM; Marcovina, Santica S; Shah, Amy S AS; Greenbaum, Carla J CJ; Atkinson, Mark A MA; Gregersen, Peter K PK; Oksenberg, Jorge R JR; Pociot, Flemming F; Rewers, Marian J MJ; Steck, Andrea K AK; Dunger, David B DB; , ; Wicker, Linda S LS; Concannon, Patrick P; Todd, John A JA; Rich, Stephen S SS
Publication Date: 2021-07

Variant appearance in text: rs872071
PubMed Link: 34127860
Variant Present in the following documents:
  • EMS123940-supplement-Supplementary_Tables.xlsx, sheet 14
View BVdb publication page



Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes.

Nature Genetics
Robertson, Catherine C CC; Inshaw, Jamie R J JRJ; Onengut-Gumuscu, Suna S; Chen, Wei-Min WM; Santa Cruz, David Flores DF; Yang, Hanzhi H; Cutler, Antony J AJ; Crouch, Daniel J M DJM; Farber, Emily E; Bridges, S Louis SL; Edberg, Jeffrey C JC; Kimberly, Robert P RP; Buckner, Jane H JH; Deloukas, Panos P; Divers, Jasmin J; Dabelea, Dana D; Lawrence, Jean M JM; Marcovina, Santica S; Shah, Amy S AS; Greenbaum, Carla J CJ; Atkinson, Mark A MA; Gregersen, Peter K PK; Oksenberg, Jorge R JR; Pociot, Flemming F; Rewers, Marian J MJ; Steck, Andrea K AK; Dunger, David B DB; , ; Wicker, Linda S LS; Concannon, Patrick P; Todd, John A JA; Rich, Stephen S SS
Publication Date: 2021-07

Variant appearance in text: rs872071
PubMed Link: 34127860
Variant Present in the following documents:
  • EMS123940-supplement-Supplementary_Tables.xlsx, sheet 14
View BVdb publication page



Identification of methylation changes associated with positive and negative growth deviance in Gambian infants using a targeted methyl sequencing approach of genomic DNA.

Faseb Bioadvances
Quilter, Claire R CR; Harvey, Kerry M KM; Bauer, Julien J; Skinner, Benjamin M BM; Gomez, Maria M; Shrivastava, Manu M; Doel, Andrew M AM; Drammeh, Saikou S; Dunger, David B DB; Moore, Sophie E SE; Ong, Ken K KK; Prentice, Andrew M AM; Bernstein, Robin M RM; Sargent, Carole A CA; Affara, Nabeel A NA
Publication Date: 2021-04

Variant appearance in text: rs872071
PubMed Link: 33842847
Variant Present in the following documents:
  • FBA2-3-205-s004.xlsx, sheet 4
View BVdb publication page



Common genetic polymorphisms contribute to the association between chronic lymphocytic leukaemia and non-melanoma skin cancer.

International Journal Of Epidemiology
Besson, Caroline C; Moore, Amy A; Wu, Wenting W; Vajdic, Claire M CM; de Sanjose, Silvia S; Camp, Nicola J NJ; Smedby, Karin E KE; Shanafelt, Tait D TD; Morton, Lindsay M LM; Brewer, Jerry D JD; Zablotska, Lydia L; Engels, Eric A EA; Cerhan, James R JR; Slager, Susan L SL; Han, Jiali J; Berndt, Sonja I SI; ,
Publication Date: 2021-08-30

Variant appearance in text: rs872071
PubMed Link: 33748835
Variant Present in the following documents:
  • Main text
View BVdb publication page



Blood cancer health disparities in the United States Hispanic population.

Cold Spring Harbor Molecular Case Studies
Bencomo-Alvarez, Alfonso E AE; Rubio, Andres J AJ; Gonzalez, Mayra A MA; Eiring, Anna M AM
Publication Date: 2021-04

Variant appearance in text: rs872071
PubMed Link: 33593728
Variant Present in the following documents:
  • Main text
  • MCS005967Ben.pdf
View BVdb publication page



Germline variants are associated with increased primary melanoma tumor thickness at diagnosis.

Human Molecular Genetics
Mangantig, Ernest E; MacGregor, Stuart S; Iles, Mark M MM; Scolyer, Richard A RA; Cust, Anne E AE; Hayward, Nicholas K NK; Montgomery, Grant W GW; Duffy, David L DL; Thompson, John F JF; Henders, Anjali A; Bowdler, Lisa L; Rowe, Casey C; Cadby, Gemma G; Mann, Graham J GJ; Whiteman, David C DC; Long, Georgina V GV; Ward, Sarah V SV; Khosrotehrani, Kiarash K; Barrett, Jennifer H JH; Law, Matthew H MH
Publication Date: 2021-01-06

Variant appearance in text: rs872071
PubMed Link: 33410475
Variant Present in the following documents:
  • hmg-2020-ez-00182_law_supplementary_table_clean_ddaa222.xlsx, sheet 1
View BVdb publication page



Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association Studies.

International Journal Of Molecular Sciences
Hernández-Verdin, Isaias I; Labreche, Karim K; Benazra, Marion M; Mokhtari, Karima K; Hoang-Xuan, Khê K; Alentorn, Agusti A
Publication Date: 2020-12-24

Variant appearance in text: rs872071
PubMed Link: 33374413
Variant Present in the following documents:
  • Main text
  • ijms-22-00122.pdf
View BVdb publication page



Association between brown eye colour in rs12913832:GG individuals and SNPs in TYR, TYRP1, and SLC24A4.

Plos One
Meyer, Olivia S OS; Lunn, Maja M B MMB; Garcia, Sara L SL; Kjærbye, Anne B AB; Morling, Niels N; Børsting, Claus C; Andersen, Jeppe D JD
Publication Date: 2020

Variant appearance in text: rs872071
PubMed Link: 32915910
Variant Present in the following documents:
  • Main text
  • pone.0239131.pdf
View BVdb publication page



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: rs872071
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Association of Known Melanoma Risk Factors with Primary Melanoma of the Scalp and Neck.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Wood, Renee P RP; Heyworth, Jane S JS; McCarthy, Nina S NS; Mauguen, Audrey A; Berwick, Marianne M; Thomas, Nancy E NE; Millward, Michael J MJ; Anton-Culver, Hoda H; Cust, Anne E AE; Dwyer, Terence T; Gallagher, Richard P RP; Gruber, Stephen B SB; Kanetsky, Peter A PA; Orlow, Irene I; Rosso, Stefano S; Moses, Eric K EK; Begg, Colin B CB; Ward, Sarah V SV
Publication Date: 2020-11

Variant appearance in text: rs872071
PubMed Link: 32856602
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chronic lymphocytic leukemia (CLL) risk is mediated by multiple enhancer variants within CLL risk loci.

Human Molecular Genetics
Yan, Huihuang H; Tian, Shulan S; Kleinstern, Geffen G; Wang, Zhiquan Z; Lee, Jeong-Heon JH; Boddicker, Nicholas J NJ; Cerhan, James R JR; Kay, Neil E NE; Braggio, Esteban E; Slager, Susan L SL
Publication Date: 2020-09-29

Variant appearance in text: rs872071
PubMed Link: 32744316
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.

Nature Communications
Xie, Jingyuan J; Liu, Lili L; Mladkova, Nikol N; Li, Yifu Y; Ren, Hong H; Wang, Weiming W; Cui, Zhao Z; Lin, Li L; Hu, Xiaofan X; Yu, Xialian X; Xu, Jing J; Liu, Gang G; Caliskan, Yasar Y; Sidore, Carlo C; Balderes, Olivia O; Rosen, Raphael J RJ; Bodria, Monica M; Zanoni, Francesca F; Zhang, Jun Y JY; Krithivasan, Priya P; Mehl, Karla K; Marasa, Maddalena M; Khan, Atlas A; Ozay, Fatih F; Canetta, Pietro A PA; Bomback, Andrew S AS; Appel, Gerald B GB; Sanna-Cherchi, Simone S; Sampson, Matthew G MG; Mariani, Laura H LH; Perkowska-Ptasinska, Agnieszka A; Durlik, Magdalena M; Mucha, Krzysztof K; Moszczuk, Barbara B; Foroncewicz, Bartosz B; Pączek, Leszek L; Habura, Ireneusz I; Ars, Elisabet E; Ballarin, Jose J; Mani, Laila-Yasmin LY; Vogt, Bruno B; Ozturk, Savas S; Yildiz, Abdülmecit A; Seyahi, Nurhan N; Arikan, Hakki H; Koc, Mehmet M; Basturk, Taner T; Karahan, Gonca G; Akgul, Sebahat Usta SU; Sever, Mehmet Sukru MS; Zhang, Dan D; Santoro, Domenico D; Bonomini, Mario M; Londrino, Francesco F; Gesualdo, Loreto L; Reiterova, Jana J; Tesar, Vladimir V; Izzi, Claudia C; Savoldi, Silvana S; Spotti, Donatella D; Marcantoni, Carmelita C; Messa, Piergiorgio P; Galliani, Marco M; Roccatello, Dario D; Granata, Simona S; Zaza, Gianluigi G; Lugani, Francesca F; Ghiggeri, GianMarco G; Pisani, Isabella I; Allegri, Landino L; Sprangers, Ben B; Park, Jin-Ho JH; Cho, BeLong B; Kim, Yon Su YS; Kim, Dong Ki DK; Suzuki, Hitoshi H; Amoroso, Antonio A; Cattran, Daniel C DC; Fervenza, Fernando C FC; Pani, Antonello A; Hamilton, Patrick P; Harris, Shelly S; Gupta, Sanjana S; Cheshire, Chris C; Dufek, Stephanie S; Issler, Naomi N; Pepper, Ruth J RJ; Connolly, John J; Powis, Stephen S; Bockenhauer, Detlef D; Stanescu, Horia C HC; Ashman, Neil N; Loos, Ruth J F RJF; Kenny, Eimear E EE; Wuttke, Matthias M; Eckardt, Kai-Uwe KU; Köttgen, Anna A; Hofstra, Julia M JM; Coenen, Marieke J H MJH; Kiemeney, Lambertus A LA; Akilesh, Shreeram S; Kretzler, Matthias M; Beck, Lawrence H LH; Stengel, Benedicte B; Debiec, Hanna H; Ronco, Pierre P; Wetzels, Jack F M JFM; Zoledziewska, Magdalena M; Cucca, Francesco F; Ionita-Laza, Iuliana I; Lee, Hajeong H; Hoxha, Elion E; Stahl, Rolf A K RAK; Brenchley, Paul P; Scolari, Francesco F; Zhao, Ming-Hui MH; Gharavi, Ali G AG; Kleta, Robert R; Chen, Nan N; Kiryluk, Krzysztof K
Publication Date: 2020-03-30

Variant appearance in text: rs872071
PubMed Link: 32231244
Variant Present in the following documents:
  • 41467_2020_15383_MOESM1_ESM.pdf
View BVdb publication page



Inherited Melanoma Risk Variants Associated with Histopathologically Amelanotic Melanoma.

The Journal Of Investigative Dermatology
Gibbs, David Corley DC; Orlow, Irene I; Vernali, Steven S; Powell, Helen B HB; Kanetsky, Peter A PA; Luo, Li L; Busam, Klaus J KJ; Sharma, Ajay A; Kricker, Anne A; Armstrong, Bruce K BK; Cust, Anne E AE; Anton-Culver, Hoda H; Gruber, Stephen B SB; Gallagher, Richard P RP; Zanetti, Roberto R; Rosso, Stefano S; Sacchetto, Lidia L; Dwyer, Terence T; Ollila, David W DW; Begg, Colin B CB; Berwick, Marianne M; Thomas, Nancy E NE; ,
Publication Date: 2020-04

Variant appearance in text: rs872071
PubMed Link: 31568773
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evidence of a Causal Association Between Cancer and Alzheimer's Disease: a Mendelian Randomization Analysis.

Scientific Reports
Seddighi, Sahba S; Houck, Alexander L AL; Rowe, James B JB; Pharoah, Paul D P PDP
Publication Date: 2019-09-19

Variant appearance in text: rs872071
PubMed Link: 31537833
Variant Present in the following documents:
  • 41598_2019_49795_MOESM1_ESM.pdf
View BVdb publication page



Direct Inhibition of IRF-Dependent Transcriptional Regulatory Mechanisms Associated With Disease.

Frontiers In Immunology
Antonczyk, Aleksandra A; Krist, Bart B; Sajek, Malgorzata M; Michalska, Agata A; Piaszyk-Borychowska, Anna A; Plens-Galaska, Martyna M; Wesoly, Joanna J; Bluyssen, Hans A R HAR
Publication Date: 2019

Variant appearance in text: rs872071
PubMed Link: 31178872
Variant Present in the following documents:
  • Main text
  • fimmu-10-01176.pdf
View BVdb publication page



Modeling Gene-Environment Interaction for the Risk of Non-hodgkin Lymphoma.

Frontiers In Oncology
Zhang, Jiahui J; Ye, Xibiao X; Wu, Cuie C; Fu, Hua H; Xu, Wei W; Hu, Pingzhao P
Publication Date: 2018

Variant appearance in text: rs872071
PubMed Link: 30693270
Variant Present in the following documents:
  • Main text
  • fonc-08-00657.pdf
View BVdb publication page



Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology.

Blood Cancer Journal
Went, Molly M; Sud, Amit A; Speedy, Helen H; Sunter, Nicola J NJ; Försti, Asta A; Law, Philip J PJ; Johnson, David C DC; Mirabella, Fabio F; Holroyd, Amy A; Li, Ni N; Orlando, Giulia G; Weinhold, Niels N; van Duin, Mark M; Chen, Bowang B; Mitchell, Jonathan S JS; Mansouri, Larry L; Juliusson, Gunnar G; Smedby, Karin E KE; Jayne, Sandrine S; Majid, Aneela A; Dearden, Claire C; Allsup, David J DJ; Bailey, James R JR; Pratt, Guy G; Pepper, Chris C; Fegan, Chris C; Rosenquist, Richard R; Kuiper, Rowan R; Stephens, Owen W OW; Bertsch, Uta U; Broderick, Peter P; Einsele, Hermann H; Gregory, Walter M WM; Hillengass, Jens J; Hoffmann, Per P; Jackson, Graham H GH; Jöckel, Karl-Heinz KH; Nickel, Jolanta J; Nöthen, Markus M MM; da Silva Filho, Miguel Inacio MI; Thomsen, Hauke H; Walker, Brian A BA; Broyl, Annemiek A; Davies, Faith E FE; Hansson, Markus M; Goldschmidt, Hartmut H; Dyer, Martin J S MJS; Kaiser, Martin M; Sonneveld, Pieter P; Morgan, Gareth J GJ; Hemminki, Kari K; Nilsson, Björn B; Catovsky, Daniel D; Allan, James M JM; Houlston, Richard S RS
Publication Date: 2018-12-21

Variant appearance in text: rs872071
PubMed Link: 30602759
Variant Present in the following documents:
  • Main text
  • 41408_2018_Article_162.pdf
View BVdb publication page



Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.

Nature
Loh, Po-Ru PR; Genovese, Giulio G; Handsaker, Robert E RE; Finucane, Hilary K HK; Reshef, Yakir A YA; Palamara, Pier Francesco PF; Birmann, Brenda M BM; Talkowski, Michael E ME; Bakhoum, Samuel F SF; McCarroll, Steven A SA; Price, Alkes L AL
Publication Date: 2018-07

Variant appearance in text: rs872071
PubMed Link: 29995854
Variant Present in the following documents:
  • NIHMS968664-supplement-Supplementary_Notes_and_Tables.pdf
View BVdb publication page



Inherited Genetic Variants Associated with Melanoma BRAF/NRAS Subtypes.

The Journal Of Investigative Dermatology
Thomas, Nancy E NE; Edmiston, Sharon N SN; Orlow, Irene I; Kanetsky, Peter A PA; Luo, Li L; Gibbs, David C DC; Parrish, Eloise A EA; Hao, Honglin H; Busam, Klaus J KJ; Armstrong, Bruce K BK; Kricker, Anne A; Cust, Anne E AE; Anton-Culver, Hoda H; Gruber, Stephen B SB; Gallagher, Richard P RP; Zanetti, Roberto R; Rosso, Stefano S; Sacchetto, Lidia L; Dwyer, Terence T; Ollila, David W DW; Begg, Colin B CB; Berwick, Marianne M; Conway, Kathleen K; ,
Publication Date: 2018-11

Variant appearance in text: rs872071
PubMed Link: 29753029
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.

Nature Genetics
Hysi, Pirro G PG; Valdes, Ana M AM; Liu, Fan F; Furlotte, Nicholas A NA; Evans, David M DM; Bataille, Veronique V; Visconti, Alessia A; Hemani, Gibran G; McMahon, George G; Ring, Susan M SM; Smith, George Davey GD; Duffy, David L DL; Zhu, Gu G; Gordon, Scott D SD; Medland, Sarah E SE; Lin, Bochao D BD; Willemsen, Gonneke G; Jan Hottenga, Jouke J; Vuckovic, Dragana D; Girotto, Giorgia G; Gandin, Ilaria I; Sala, Cinzia C; Concas, Maria Pina MP; Brumat, Marco M; Gasparini, Paolo P; Toniolo, Daniela D; Cocca, Massimiliano M; Robino, Antonietta A; Yazar, Seyhan S; Hewitt, Alex W AW; Chen, Yan Y; Zeng, Changqing C; Uitterlinden, Andre G AG; Ikram, M Arfan MA; Hamer, Merel A MA; van Duijn, Cornelia M CM; Nijsten, Tamar T; Mackey, David A DA; Falchi, Mario M; Boomsma, Dorret I DI; Martin, Nicholas G NG; , ; Hinds, David A DA; Kayser, Manfred M; Spector, Timothy D TD
Publication Date: 2018-05

Variant appearance in text: rs872071
PubMed Link: 29662168
Variant Present in the following documents:
  • NIHMS76542-supplement-Supplementary_notes_and_tables.pdf
View BVdb publication page



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: rs872071
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Functional melanoma-risk variant IRF4 rs12203592 associated with Breslow thickness: a pooled international study of primary melanomas.

The British Journal Of Dermatology
Gibbs, D C DC; Ward, S V SV; Orlow, I I; Cadby, G G; Kanetsky, P A PA; Luo, L L; Busam, K J KJ; Kricker, A A; Armstrong, B K BK; Cust, A E AE; Anton-Culver, H H; Gallagher, R P RP; Zanetti, R R; Rosso, S S; Sacchetto, L L; Ollila, D W DW; Begg, C B CB; Berwick, M M; Thomas, N E NE; ,
Publication Date: 2017-11

Variant appearance in text: rs872071
PubMed Link: 28667740
Variant Present in the following documents:
  • Main text
View BVdb publication page



Molecular cytogenetic characterisation of a novel de novo ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosome.

Molecular Cytogenetics
Pace, Nikolai Paul NP; Maggouta, Frideriki F; Twigden, Melissa M; Borg, Isabella I
Publication Date: 2017

Variant appearance in text: rs872071
PubMed Link: 28344652
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cereblon and IRF4 Variants Affect Risk and Response to Treatment in Multiple Myeloma.

Archivum Immunologiae Et Therapiae Experimentalis
Butrym, Aleksandra A; Łacina, Piotr P; Rybka, Justyna J; Chaszczewska-Markowska, Monika M; Mazur, Grzegorz G; Bogunia-Kubik, Katarzyna K
Publication Date: 2016-12

Variant appearance in text: rs872071
PubMed Link: 28083618
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between genetic variants in immunoregulatory genes and risk of non-Hodgkin lymphoma in a Chinese population.

Oncotarget
Ye, Xibiao X; Zhao, Kaiqiong K; Wu, Cuie C; Hu, Pingzhao P; Fu, Hua H
Publication Date: 2017-02-07

Variant appearance in text: rs872071
PubMed Link: 28060727
Variant Present in the following documents:
  • Main text
  • oncotarget-08-10450.pdf
View BVdb publication page



Common Genetic Polymorphisms within NFκB-Related Genes and the Risk of Developing Invasive Aspergillosis.

Frontiers In Microbiology
Lupiañez, Carmen B CB; Villaescusa, María T MT; Carvalho, Agostinho A; Springer, Jan J; Lackner, Michaela M; Sánchez-Maldonado, José M JM; Canet, Luz M LM; Cunha, Cristina C; Segura-Catena, Juana J; Alcazar-Fuoli, Laura L; Solano, Carlos C; Fianchi, Luana L; Pagano, Livio L; Potenza, Leonardo L; Aguado, José M JM; Luppi, Mario M; Cuenca-Estrella, Manuel M; Lass-Flörl, Cornelia C; Einsele, Hermann H; Vázquez, Lourdes L; , ; Ríos-Tamayo, Rafael R; Loeffler, Jurgen J; Jurado, Manuel M; Sainz, Juan J
Publication Date: 2016

Variant appearance in text: rs872071
PubMed Link: 27570521
Variant Present in the following documents:
  • Main text
  • fmicb-07-01243.pdf
View BVdb publication page



Human Cytokine Genetic Variants Associated With HBsAg Reverse Seroconversion in Rituximab-Treated Non-Hodgkin Lymphoma Patients.

Medicine
Hsiao, Liang-Tsai LT; Wang, Hao-Yuan HY; Yang, Ching-Fen CF; Chiou, Tzeon-Jye TJ; Gau, Jyh-Pyng JP; Yu, Yuan-Bin YB; Liu, Hsiao-Ling HL; Chang, Wen-Chun WC; Chen, Po-Min PM; Tzeng, Cheng-Hwai CH; Chan, Yu-Jiun YJ; Yang, Muh-Hwa MH; Liu, Jin-Hwang JH; Huang, Yi-Hsiang YH
Publication Date: 2016-03

Variant appearance in text: rs872071
PubMed Link: 26986131
Variant Present in the following documents:
  • medi-95-e3064-s001.pdf
View BVdb publication page



Familial predisposition and genetic risk factors for lymphoma.

Blood
Cerhan, James R JR; Slager, Susan L SL
Publication Date: 2015-11-12

Variant appearance in text: rs872071
PubMed Link: 26405224
Variant Present in the following documents:
  • Main text
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Monoclonal B-cell lymphocytosis and early-stage chronic lymphocytic leukemia: diagnosis, natural history, and risk stratification.

Blood
Strati, Paolo P; Shanafelt, Tait D TD
Publication Date: 2015-07-23

Variant appearance in text: rs872071
PubMed Link: 26065657
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  • Main text
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Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis.

Hematological Oncology
Sud, Amit A; Hemminki, Kari K; Houlston, Richard S RS
Publication Date: 2017-03

Variant appearance in text: rs872071
PubMed Link: 26053036
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  • Main text
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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs872071
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
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Inherited genetic variants associated with occurrence of multiple primary melanoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Gibbs, David C DC; Orlow, Irene I; Kanetsky, Peter A PA; Luo, Li L; Kricker, Anne A; Armstrong, Bruce K BK; Anton-Culver, Hoda H; Gruber, Stephen B SB; Marrett, Loraine D LD; Gallagher, Richard P RP; Zanetti, Roberto R; Rosso, Stefano S; Dwyer, Terence T; Sharma, Ajay A; La Pilla, Emily E; From, Lynn L; Busam, Klaus J KJ; Cust, Anne E AE; Ollila, David W DW; Begg, Colin B CB; Berwick, Marianne M; Thomas, Nancy E NE; ,
Publication Date: 2015-06

Variant appearance in text: rs872071
PubMed Link: 25837821
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  • Main text
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The oncogenic transcription factor IRF4 is regulated by a novel CD30/NF-κB positive feedback loop in peripheral T-cell lymphoma.

Blood
Boddicker, Rebecca L RL; Kip, N Sertac NS; Xing, Xiaoming X; Zeng, Yu Y; Yang, Zhi-Zhang ZZ; Lee, Jeong-Heon JH; Almada, Luciana L LL; Elsawa, Sherine F SF; Knudson, Ryan A RA; Law, Mark E ME; Ketterling, Rhett P RP; Cunningham, Julie M JM; Wu, Yanhong Y; Maurer, Matthew J MJ; O'Byrne, Megan M MM; Cerhan, James R JR; Slager, Susan L SL; Link, Brian K BK; Porcher, Julie C JC; Grote, Deanna M DM; Jelinek, Diane F DF; Dogan, Ahmet A; Ansell, Stephen M SM; Fernandez-Zapico, Martin E ME; Feldman, Andrew L AL
Publication Date: 2015-05-14

Variant appearance in text: rs872071
PubMed Link: 25833963
Variant Present in the following documents:
  • Main text
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Genetic factors associated with naevus count and dermoscopic patterns: preliminary results from the Study of Nevi in Children (SONIC).

The British Journal Of Dermatology
Orlow, I I; Satagopan, J M JM; Berwick, M M; Enriquez, H L HL; White, K A M KA; Cheung, K K; Dusza, S W SW; Oliveria, S A SA; Marchetti, M A MA; Scope, A A; Marghoob, A A AA; Halpern, A C AC
Publication Date: 2015-04

Variant appearance in text: rs872071
PubMed Link: 25307738
Variant Present in the following documents:
  • Main text
  • bjd0172-1081-sd1.pdf
  • bjd0172-1081.pdf
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Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.

Nature Genetics
Cerhan, James R JR; Berndt, Sonja I SI; Vijai, Joseph J; Ghesquières, Hervé H; McKay, James J; Wang, Sophia S SS; Wang, Zhaoming Z; Yeager, Meredith M; Conde, Lucia L; de Bakker, Paul I W PI; Nieters, Alexandra A; Cox, David D; Burdett, Laurie L; Monnereau, Alain A; Flowers, Christopher R CR; De Roos, Anneclaire J AJ; Brooks-Wilson, Angela R AR; Lan, Qing Q; Severi, Gianluca G; Melbye, Mads M; Gu, Jian J; Jackson, Rebecca D RD; Kane, Eleanor E; Teras, Lauren R LR; Purdue, Mark P MP; Vajdic, Claire M CM; Spinelli, John J JJ; Giles, Graham G GG; Albanes, Demetrius D; Kelly, Rachel S RS; Zucca, Mariagrazia M; Bertrand, Kimberly A KA; Zeleniuch-Jacquotte, Anne A; Lawrence, Charles C; Hutchinson, Amy A; Zhi, Degui D; Habermann, Thomas M TM; Link, Brian K BK; Novak, Anne J AJ; Dogan, Ahmet A; Asmann, Yan W YW; Liebow, Mark M; Thompson, Carrie A CA; Ansell, Stephen M SM; Witzig, Thomas E TE; Weiner, George J GJ; Veron, Amelie S AS; Zelenika, Diana D; Tilly, Hervé H; Haioun, Corinne C; Molina, Thierry Jo TJ; Hjalgrim, Henrik H; Glimelius, Bengt B; Adami, Hans-Olov HO; Bracci, Paige M PM; Riby, Jacques J; Smith, Martyn T MT; Holly, Elizabeth A EA; Cozen, Wendy W; Hartge, Patricia P; Morton, Lindsay M LM; Severson, Richard K RK; Tinker, Lesley F LF; North, Kari E KE; Becker, Nikolaus N; Benavente, Yolanda Y; Boffetta, Paolo P; Brennan, Paul P; Foretova, Lenka L; Maynadie, Marc M; Staines, Anthony A; Lightfoot, Tracy T; Crouch, Simon S; Smith, Alex A; Roman, Eve E; Diver, W Ryan WR; Offit, Kenneth K; Zelenetz, Andrew A; Klein, Robert J RJ; Villano, Danylo J DJ; Zheng, Tongzhang T; Zhang, Yawei Y; Holford, Theodore R TR; Kricker, Anne A; Turner, Jenny J; Southey, Melissa C MC; Clavel, Jacqueline J; Virtamo, Jarmo J; Weinstein, Stephanie S; Riboli, Elio E; Vineis, Paolo P; Kaaks, Rudolph R; Trichopoulos, Dimitrios D; Vermeulen, Roel C H RC; Boeing, Heiner H; Tjonneland, Anne A; Angelucci, Emanuele E; Di Lollo, Simonetta S; Rais, Marco M; Birmann, Brenda M BM; Laden, Francine F; Giovannucci, Edward E; Kraft, Peter P; Huang, Jinyan J; Ma, Baoshan B; Ye, Yuanqing Y; Chiu, Brian C H BC; Sampson, Joshua J; Liang, Liming L; Park, Ju-Hyun JH; Chung, Charles C CC; Weisenburger, Dennis D DD; Chatterjee, Nilanjan N; Fraumeni, Joseph F JF; Slager, Susan L SL; Wu, Xifeng X; de Sanjose, Silvia S; Smedby, Karin E KE; Salles, Gilles G; Skibola, Christine F CF; Rothman, Nathaniel N; Chanock, Stephen J SJ
Publication Date: 2014-11

Variant appearance in text: rs872071
PubMed Link: 25261932
Variant Present in the following documents:
  • Main text
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The interferon regulatory factors as novel potential targets in the treatment of cardiovascular diseases.

British Journal Of Pharmacology
Zhang, Xiao-Jing XJ; Jiang, Ding-Sheng DS; Li, Hongliang H
Publication Date: 2015-12

Variant appearance in text: rs872071
PubMed Link: 25131895
Variant Present in the following documents:
  • Main text
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Association of interferon regulatory factor 4 gene polymorphisms rs12203592 and rs872071 with skin cancer and haematological malignancies susceptibility: a meta-analysis of 19 case-control studies.

Bmc Cancer
Wang, Songtao S; Yan, Qing Q; Chen, Pin P; Zhao, Peng P; Gu, Aihua A
Publication Date: 2014-06-06

Variant appearance in text: rs872071
PubMed Link: 24906573
Variant Present in the following documents:
  • Main text
  • 1471-2407-14-410.pdf
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A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.

Cell
Praetorius, Christian C; Grill, Christine C; Stacey, Simon N SN; Metcalf, Alexander M AM; Gorkin, David U DU; Robinson, Kathleen C KC; Van Otterloo, Eric E; Kim, Reuben S Q RS; Bergsteinsdottir, Kristin K; Ogmundsdottir, Margret H MH; Magnusdottir, Erna E; Mishra, Pravin J PJ; Davis, Sean R SR; Guo, Theresa T; Zaidi, M Raza MR; Helgason, Agnar S AS; Sigurdsson, Martin I MI; Meltzer, Paul S PS; Merlino, Glenn G; Petit, Valerie V; Larue, Lionel L; Loftus, Stacie K SK; Adams, David R DR; Sobhiafshar, Ulduz U; Emre, N C Tolga NC; Pavan, William J WJ; Cornell, Robert R; Smith, Aaron G AG; McCallion, Andrew S AS; Fisher, David E DE; Stefansson, Kari K; Sturm, Richard A RA; Steingrimsson, Eirikur E
Publication Date: 2013-11-21

Variant appearance in text: rs872071
PubMed Link: 24267888
Variant Present in the following documents:
  • Main text
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Genetic susceptibility to chronic lymphocytic leukemia.

Seminars In Hematology
Slager, Susan L SL; Caporaso, Neil E NE; de Sanjose, Silvia S; Goldin, Lynn R LR
Publication Date: 2013-10

Variant appearance in text: rs872071
PubMed Link: 24246697
Variant Present in the following documents:
  • Main text
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Non-Hodgkin lymphoma risk and variants in genes controlling lymphocyte development.

Plos One
Schuetz, Johanna M JM; Daley, Denise D; Leach, Stephen S; Conde, Lucia L; Berry, Brian R BR; Gallagher, Richard P RP; Connors, Joseph M JM; Gascoyne, Randy D RD; Bracci, Paige M PM; Skibola, Christine F CF; Spinelli, John J JJ; Brooks-Wilson, Angela R AR
Publication Date: 2013

Variant appearance in text: rs872071
PubMed Link: 24098683
Variant Present in the following documents:
  • pone.0075170.s001.xls, sheet 1
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Inherited susceptibility to chronic lymphocytic leukemia: evidence and prospects for the future.

Therapeutic Advances In Hematology
Brown, Jennifer R JR
Publication Date: 2013-08

Variant appearance in text: rs872071
PubMed Link: 23926461
Variant Present in the following documents:
  • Main text
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Personalized medicine in CLL: current status and future perspectives.

Cancer Letters
Rozovski, Uri U; Hazan-Halevy, Inbal I; Keating, Michael J MJ; Estrov, Zeev Z
Publication Date: 2014-09-28

Variant appearance in text: rs872071
PubMed Link: 23879961
Variant Present in the following documents:
  • Main text
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Genetic differences between Asian and Caucasian chronic lymphocytic leukemia.

International Journal Of Oncology
Kawamata, Norihiko N; Moreilhon, Chimene C; Saitoh, Takayuki T; Karasawa, Masamitsu M; Bernstein, Brian K BK; Sato-Otsubo, Aiko A; Ogawa, Seishi S; Raynaud, Sophie S; Koeffler, H Phillip HP
Publication Date: 2013-08

Variant appearance in text: rs872071
PubMed Link: 23708256
Variant Present in the following documents:
  • Main text
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Genomic approaches to chronic lymphocytic leukemia.

Hematology/Oncology Clinics Of North America
Improgo, Ma Reina MR; Brown, Jennifer R JR
Publication Date: 2013-04

Variant appearance in text: rs872071
PubMed Link: 23561468
Variant Present in the following documents:
  • Main text
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Current understanding of lifestyle and environmental factors and risk of non-hodgkin lymphoma: an epidemiological update.

Journal Of Cancer Epidemiology
Bassig, Bryan A BA; Lan, Qing Q; Rothman, Nathaniel N; Zhang, Yawei Y; Zheng, Tongzhang T
Publication Date: 2012

Variant appearance in text: rs872071
PubMed Link: 23008714
Variant Present in the following documents:
  • Main text
  • JCE2012-978930.pdf
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Single nucleotide polymorphisms and inherited risk of chronic lymphocytic leukemia among African Americans.

Blood
Coombs, Catherine C CC; Rassenti, Laura Z LZ; Falchi, Lorenzo L; Slager, Susan L SL; Strom, Sara S SS; Ferrajoli, Alessandra A; Weinberg, J Brice JB; Kipps, Thomas J TJ; Lanasa, Mark C MC
Publication Date: 2012-08-23

Variant appearance in text: rs872071
PubMed Link: 22745306
Variant Present in the following documents:
  • Main text
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A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits.

American Journal Of Human Genetics
Bhattacharjee, Samsiddhi S; Rajaraman, Preetha P; Jacobs, Kevin B KB; Wheeler, William A WA; Melin, Beatrice S BS; Hartge, Patricia P; , ; Yeager, Meredith M; Chung, Charles C CC; Chanock, Stephen J SJ; Chatterjee, Nilanjan N
Publication Date: 2012-05-04

Variant appearance in text: rs872071
PubMed Link: 22560090
Variant Present in the following documents:
  • Main text
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Post-GWAS functional characterization of susceptibility variants for chronic lymphocytic leukemia.

Plos One
Sillé, Fenna C M FC; Thomas, Reuben R; Smith, Martyn T MT; Conde, Lucia L; Skibola, Christine F CF
Publication Date: 2012

Variant appearance in text: rs872071
PubMed Link: 22235315
Variant Present in the following documents:
  • Main text
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Genome-wide association study identifies three new melanoma susceptibility loci.

Nature Genetics
Barrett, Jennifer H JH; Iles, Mark M MM; Harland, Mark M; Taylor, John C JC; Aitken, Joanne F JF; Andresen, Per Arne PA; Akslen, Lars A LA; Armstrong, Bruce K BK; Avril, Marie-Francoise MF; Azizi, Esther E; Bakker, Bert B; Bergman, Wilma W; Bianchi-Scarrà, Giovanna G; Bressac-de Paillerets, Brigitte B; Calista, Donato D; Cannon-Albright, Lisa A LA; Corda, Eve E; Cust, Anne E AE; Dębniak, Tadeusz T; Duffy, David D; Dunning, Alison M AM; Easton, Douglas F DF; Friedman, Eitan E; Galan, Pilar P; Ghiorzo, Paola P; Giles, Graham G GG; Hansson, Johan J; Hocevar, Marko M; Höiom, Veronica V; Hopper, John L JL; Ingvar, Christian C; Janssen, Bart B; Jenkins, Mark A MA; Jönsson, Göran G; Kefford, Richard F RF; Landi, Giorgio G; Landi, Maria Teresa MT; Lang, Julie J; Lubiński, Jan J; Mackie, Rona R; Malvehy, Josep J; Martin, Nicholas G NG; Molven, Anders A; Montgomery, Grant W GW; van Nieuwpoort, Frans A FA; Novakovic, Srdjan S; Olsson, Håkan H; Pastorino, Lorenza L; Puig, Susana S; Puig-Butille, Joan Anton JA; Randerson-Moor, Juliette J; Snowden, Helen H; Tuominen, Rainer R; Van Belle, Patricia P; van der Stoep, Nienke N; Whiteman, David C DC; Zelenika, Diana D; Han, Jiali J; Fang, Shenying S; Lee, Jeffrey E JE; Wei, Qingyi Q; Lathrop, G Mark GM; Gillanders, Elizabeth M EM; Brown, Kevin M KM; Goldstein, Alisa M AM; Kanetsky, Peter A PA; Mann, Graham J GJ; Macgregor, Stuart S; Elder, David E DE; Amos, Christopher I CI; Hayward, Nicholas K NK; Gruis, Nelleke A NA; Demenais, Florence F; Bishop, Julia A Newton JA; Bishop, D Timothy DT; ,
Publication Date: 2011-10-09

Variant appearance in text: rs872071
PubMed Link: 21983787
Variant Present in the following documents:
  • NIHMS335189-supplement-1.pdf
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Interferon-signaling pathway: associations with colon and rectal cancer risk and subsequent survival.

Carcinogenesis
Slattery, Martha L ML; Lundgreen, Abbie A; Bondurant, Kristina L KL; Wolff, Roger K RK
Publication Date: 2011-11

Variant appearance in text: rs872071
PubMed Link: 21859832
Variant Present in the following documents:
  • Main text
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Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.

Haematologica
Wade, Rachel R; Di Bernardo, Maria Chiara MC; Richards, Sue S; Rossi, Davide D; Crowther-Swanepoel, Dalemari D; Gaidano, Gianluca G; Oscier, David G DG; Catovsky, Daniel D; Houlston, Richard S RS
Publication Date: 2011-10

Variant appearance in text: rs872071
PubMed Link: 21659360
Variant Present in the following documents:
  • Main text
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What are genome-wide association studies telling us about B-cell tumor development?

Oncotarget
Sherborne, Amy L AL; Houlston, Richard S RS
Publication Date: 2010-09

Variant appearance in text: rs872071
PubMed Link: 21307401
Variant Present in the following documents:
  • Main text
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[Recent progress in genetic variants associated with cancer and their implications in diagnostics development].

Zhongguo Fei Ai Za Zhi = Chinese Journal Of Lung Cancer
Cho, William C S WC
Publication Date: 2011-01

Variant appearance in text: rs872071
PubMed Link: 21219822
Variant Present in the following documents:
  • Main text
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Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.

Blood
Slager, Susan L SL; Rabe, Kari G KG; Achenbach, Sara J SJ; Vachon, Celine M CM; Goldin, Lynn R LR; Strom, Sara S SS; Lanasa, Mark C MC; Spector, Logan G LG; Rassenti, Laura Z LZ; Leis, Jose F JF; Camp, Nicola J NJ; Glenn, Martha M; Kay, Neil E NE; Cunningham, Julie M JM; Hanson, Curtis A CA; Marti, Gerald E GE; Weinberg, J Brice JB; Morrison, Vicki A VA; Link, Brian K BK; Call, Timothy G TG; Caporaso, Neil E NE; Cerhan, James R JR
Publication Date: 2011-02-10

Variant appearance in text: rs872071
PubMed Link: 21131588
Variant Present in the following documents:
  • Main text
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Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

Nature Genetics
Conde, Lucia L; Halperin, Eran E; Akers, Nicholas K NK; Brown, Kevin M KM; Smedby, Karin E KE; Rothman, Nathaniel N; Nieters, Alexandra A; Slager, Susan L SL; Brooks-Wilson, Angela A; Agana, Luz L; Riby, Jacques J; Liu, Jianjun J; Adami, Hans-Olov HO; Darabi, Hatef H; Hjalgrim, Henrik H; Low, Hui-Qi HQ; Humphreys, Keith K; Melbye, Mads M; Chang, Ellen T ET; Glimelius, Bengt B; Cozen, Wendy W; Davis, Scott S; Hartge, Patricia P; Morton, Lindsay M LM; Schenk, Maryjean M; Wang, Sophia S SS; Armstrong, Bruce B; Kricker, Anne A; Milliken, Sam S; Purdue, Mark P MP; Vajdic, Claire M CM; Boyle, Peter P; Lan, Qing Q; Zahm, Shelia H SH; Zhang, Yawei Y; Zheng, Tongzhang T; Becker, Nikolaus N; Benavente, Yolanda Y; Boffetta, Paolo P; Brennan, Paul P; Butterbach, Katja K; Cocco, Pierluigi P; Foretova, Lenka L; Maynadié, Marc M; de Sanjosé, Silvia S; Staines, Anthony A; Spinelli, John J JJ; Achenbach, Sara J SJ; Call, Timothy G TG; Camp, Nicola J NJ; Glenn, Martha M; Caporaso, Neil E NE; Cerhan, James R JR; Cunningham, Julie M JM; Goldin, Lynn R LR; Hanson, Curtis A CA; Kay, Neil E NE; Lanasa, Mark C MC; Leis, Jose F JF; Marti, Gerald E GE; Rabe, Kari G KG; Rassenti, Laura Z LZ; Spector, Logan G LG; Strom, Sara S SS; Vachon, Celine M CM; Weinberg, J Brice JB; Holly, Elizabeth A EA; Chanock, Stephen S; Smith, Martyn T MT; Bracci, Paige M PM; Skibola, Christine F CF
Publication Date: 2010-08

Variant appearance in text: rs872071
PubMed Link: 20639881
Variant Present in the following documents:
  • Main text
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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

American Journal Of Human Genetics
Duffy, David L DL; Iles, Mark M MM; Glass, Dan D; Zhu, Gu G; Barrett, Jennifer H JH; Höiom, Veronica V; Zhao, Zhen Z ZZ; Sturm, Richard A RA; Soranzo, Nicole N; Hammond, Chris C; Kvaskoff, Marina M; Whiteman, David C DC; Mangino, Massimo M; Hansson, Johan J; Newton-Bishop, Julia A JA; , ; Bataille, Veronique V; Hayward, Nicholas K NK; Martin, Nicholas G NG; Bishop, D Timothy DT; Spector, Timothy D TD; Montgomery, Grant W GW
Publication Date: 2010-07-09

Variant appearance in text: rs872071
PubMed Link: 20602913
Variant Present in the following documents:
  • Main text
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Web-based, participant-driven studies yield novel genetic associations for common traits.

Plos Genetics
Eriksson, Nicholas N; Macpherson, J Michael JM; Tung, Joyce Y JY; Hon, Lawrence S LS; Naughton, Brian B; Saxonov, Serge S; Avey, Linda L; Wojcicki, Anne A; Pe'er, Itsik I; Mountain, Joanna J
Publication Date: 2010-06-24

Variant appearance in text: rs872071
PubMed Link: 20585627
Variant Present in the following documents:
  • Main text
  • pgen.1000993.s007.pdf
  • pgen.1000993.pdf
View BVdb publication page



Genome-wide association studies of cancer.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Stadler, Zsofia K ZK; Thom, Peter P; Robson, Mark E ME; Weitzel, Jeffrey N JN; Kauff, Noah D ND; Hurley, Karen E KE; Devlin, Vincent V; Gold, Bert B; Klein, Robert J RJ; Offit, Kenneth K
Publication Date: 2010-09-20

Variant appearance in text: rs872071
PubMed Link: 20585100
Variant Present in the following documents:
  • Main text
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Familial chronic lymphocytic leukemia.

Current Opinion In Hematology
Goldin, Lynn R LR; Slager, Susan L SL; Caporaso, Neil E NE
Publication Date: 2010-07

Variant appearance in text: rs872071
PubMed Link: 20389242
Variant Present in the following documents:
  • Main text
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Genetic susceptibility variants for chronic lymphocytic leukemia.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Slager, Susan L SL; Goldin, Lynn R LR; Strom, Sara S SS; Lanasa, Mark C MC; Spector, Logan G LG; Rassenti, Laura L; Leis, Jose F JF; Camp, Nicola J NJ; Kay, Neil E NE; Vachon, Celine M CM; Glenn, Martha M; Weinberg, J Brice JB; Rabe, Kari G KG; Cunningham, Julie M JM; Achenbach, Sara J SJ; Hanson, Curtis A CA; Marti, Gerald E GE; Call, Timothy G TG; Caporaso, Neil E NE; Cerhan, James R JR
Publication Date: 2010-04

Variant appearance in text: rs872071
PubMed Link: 20332261
Variant Present in the following documents:
  • Main text
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Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.

Nature Genetics
Crowther-Swanepoel, Dalemari D; Broderick, Peter P; Di Bernardo, Maria Chiara MC; Dobbins, Sara E SE; Torres, María M; Mansouri, Mahmoud M; Ruiz-Ponte, Clara C; Enjuanes, Anna A; Rosenquist, Richard R; Carracedo, Angel A; Jurlander, Jesper J; Campo, Elias E; Juliusson, Gunnar G; Montserrat, Emilio E; Smedby, Karin E KE; Dyer, Martin J S MJ; Matutes, Estella E; Dearden, Claire C; Sunter, Nicola J NJ; Hall, Andrew G AG; Mainou-Fowler, Tryfonia T; Jackson, Graham H GH; Summerfield, Geoffrey G; Harris, Robert J RJ; Pettitt, Andrew R AR; Allsup, David J DJ; Bailey, James R JR; Pratt, Guy G; Pepper, Chris C; Fegan, Chris C; Parker, Anton A; Oscier, David D; Allan, James M JM; Catovsky, Daniel D; Houlston, Richard S RS
Publication Date: 2010-02

Variant appearance in text: rs872071
PubMed Link: 20062064
Variant Present in the following documents:
  • Main text
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Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.

Nature Genetics
Skibola, Christine F CF; Bracci, Paige M PM; Halperin, Eran E; Conde, Lucia L; Craig, David W DW; Agana, Luz L; Iyadurai, Kelly K; Becker, Nikolaus N; Brooks-Wilson, Angela A; Curry, John D JD; Spinelli, John J JJ; Holly, Elizabeth A EA; Riby, Jacques J; Zhang, Luoping L; Nieters, Alexandra A; Smith, Martyn T MT; Brown, Kevin M KM
Publication Date: 2009-08

Variant appearance in text: rs872071
PubMed Link: 19620980
Variant Present in the following documents:
  • Main text
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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Hindorff, Lucia A LA; Sethupathy, Praveen P; Junkins, Heather A HA; Ramos, Erin M EM; Mehta, Jayashri P JP; Collins, Francis S FS; Manolio, Teri A TA
Publication Date: 2009-06-09

Variant appearance in text: rs872071
PubMed Link: 19474294
Variant Present in the following documents:
  • Main text
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The molecular basis of familial chronic lymphocytic leukemia.

Haematologica
Crowther-Swanepoel, Dalemari D; Houlston, Richard S RS
Publication Date: 2009-05

Variant appearance in text: rs872071
PubMed Link: 19407315
Variant Present in the following documents:
  • Main text
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Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.

Plos One
Wang, Sophia S SS; Purdue, Mark P MP; Cerhan, James R JR; Zheng, Tongzhang T; Menashe, Idan I; Armstrong, Bruce K BK; Lan, Qing Q; Hartge, Patricia P; Kricker, Anne A; Zhang, Yawei Y; Morton, Lindsay M LM; Vajdic, Claire M CM; Holford, Theodore R TR; Severson, Richard K RK; Grulich, Andrew A; Leaderer, Brian P BP; Davis, Scott S; Cozen, Wendy W; Yeager, Meredith M; Chanock, Stephen J SJ; Chatterjee, Nilanjan N; Rothman, Nathaniel N
Publication Date: 2009

Variant appearance in text: rs872071
PubMed Link: 19390683
Variant Present in the following documents:
  • Main text
  • pone.0005360.pdf
View BVdb publication page