MTAP c.121-185A>G

Variant ID: 9-21816528-A-G

NM_002451.3(MTAP):c.121-185A>G

This variant was identified in 53 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: rs7023329
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Epidemiological Evidence for Associations Between Genetic Variants and Osteosarcoma Susceptibility: A Meta-Analysis.

Frontiers In Oncology
Yuan, Dechao D; Tian, Jie J; Fang, Xiang X; Xiong, Yan Y; Banskota, Nishant N; Kuang, Fuguo F; Zhang, Wenli W; Duan, Hong H
Publication Date: 2022

Variant appearance in text: rs7023329
PubMed Link: 35860595
Variant Present in the following documents:
  • Main text
  • fonc-12-912208.pdf
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The current state of genetic risk models for the development of kidney cancer: a review and validation.

Bju International
Harrison, Hannah H; Li, Nicole N; Saunders, Catherine L CL; Rossi, Sabrina H SH; Dennis, Joe J; Griffin, Simon J SJ; Stewart, Grant D GD; Usher-Smith, Juliet A JA
Publication Date: 2022-11

Variant appearance in text: rs7023329
PubMed Link: 35460182
Variant Present in the following documents:
  • BJU-130-550-s004.pdf
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Defining novel causal SNPs and linked phenotypes at melanoma-associated loci.

Human Molecular Genetics
Castaneda-Garcia, Carolina C; Iyer, Vivek V; Nsengimana, Jérémie J; Trower, Adam A; Droop, Alastair A; Brown, Kevin M KM; Choi, Jiyeon J; Zhang, Tongwu T; Harland, Mark M; Newton-Bishop, Julia A JA; Bishop, D Timothy DT; Adams, David J DJ; Iles, Mark M MM; Robles-Espinoza, Carla Daniela CD
Publication Date: 2022-08-25

Variant appearance in text: rs7023329
PubMed Link: 35357426
Variant Present in the following documents:
  • supplementary_table_1_ddac074.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: rs7023329
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: rs7023329
PubMed Link: 34898573
Variant Present in the following documents:
  • Main text
  • curroncol-28-00401.pdf
View BVdb publication page



The functional role of inherited CDKN2A variants in childhood acute lymphoblastic leukemia.

Pharmacogenetics And Genomics
Li, Chunjie C; Zhao, Xinying X; He, Yingyi Y; Li, Ziping Z; Qian, Jiabi J; Zhang, Li L; Ye, Qian Q; Qiu, Fei F; Lian, Peng P; Qian, Maoxiang M; Zhang, Hui H
Publication Date: 2022-02-01

Variant appearance in text: rs7023329
PubMed Link: 34369425
Variant Present in the following documents:
  • pgen-32-43-s001.pdf
View BVdb publication page



The functional role of inherited CDKN2A variants in childhood acute lymphoblastic leukemia.

Pharmacogenetics And Genomics
Li, Chunjie C; Zhao, Xinying X; He, Yingyi Y; Li, Ziping Z; Qian, Jiabi J; Zhang, Li L; Ye, Qian Q; Qiu, Fei F; Lian, Peng P; Qian, Maoxiang M; Zhang, Hui H
Publication Date: 2021-08-06

Variant appearance in text: rs7023329
PubMed Link: 34369425
Variant Present in the following documents:
  • pgen-32-43-s001.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: rs7023329
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



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: rs7023329
PubMed Link: 32856602
Variant Present in the following documents:
  • Main text
View BVdb publication page



Risk Prediction Models for Kidney Cancer: A Systematic Review.

European Urology Focus
Harrison, Hannah H; Thompson, Rachel E RE; Lin, Zhiyuan Z; Rossi, Sabrina H SH; Stewart, Grant D GD; Griffin, Simon J SJ; Usher-Smith, Juliet A JA
Publication Date: 2021-11

Variant appearance in text: rs7023329
PubMed Link: 32680829
Variant Present in the following documents:
  • Main text
View BVdb publication page



9p21.3 coronary artery disease risk locus and interferon alpha 21: Association study in an Asian Indian population.

Indian Heart Journal
Kalpana, Bellary B; Murthy, Dwarkanath K DK; Balakrishna, Nagalla N
Publication Date: 2019

Variant appearance in text: rs7023329
PubMed Link: 32248921
Variant Present in the following documents:
  • Main text
  • main.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: rs7023329
PubMed Link: 31568773
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.

Indian Heart Journal
Kalpana, Bellary B; Murthy, Dwarkanath K DK; Balakrishna, Nagalla N; Aiyengar, Mohini T MT
Publication Date: 2019

Variant appearance in text: rs7023329
PubMed Link: 31543200
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: MTAP: 121-185A>G; rs7023329
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



The digital age of melanoma management: detection and diagnostics.

Melanoma Management
Fogel, Alexander L AL; Sarin, Kavita K
Publication Date: 2015-11

Variant appearance in text: rs7023329
PubMed Link: 30190865
Variant Present in the following documents:
  • Main text
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: rs7023329
PubMed Link: 29753029
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Studies in Glioma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Kinnersley, Ben B; Houlston, Richard S RS; Bondy, Melissa L ML
Publication Date: 2018-04

Variant appearance in text: rs7023329
PubMed Link: 29382702
Variant Present in the following documents:
  • Main text
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: rs7023329
PubMed Link: 28667740
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs7023329
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Association of common variants in MTAP with susceptibility and overall survival of osteosarcoma: a two-stage population-based study in Han Chinese.

Journal Of Cancer
Zhi, Liqiang L; Liu, Dan D; Wu, Stephen G SG; Li, Tianqing T; Zhao, Guanghui G; Zhao, Bo B; Li, Meng M
Publication Date: 2016

Variant appearance in text: rs7023329
PubMed Link: 27994653
Variant Present in the following documents:
  • Main text
View BVdb publication page



Higher Nevus Count Exhibits a Distinct DNA Methylation Signature in Healthy Human Skin: Implications for Melanoma.

The Journal Of Investigative Dermatology
Roos, Leonie L; Sandling, Johanna K JK; Bell, Christopher G CG; Glass, Daniel D; Mangino, Massimo M; Spector, Tim D TD; Deloukas, Panos P; Bataille, Veronique V; Bell, Jordana T JT
Publication Date: 2017-04

Variant appearance in text: rs7023329
PubMed Link: 27993549
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population.

Cancer Science
Lin, Xiaoming X; Yan, Caiwang C; Gao, Yong Y; Du, Jiangbo J; Zhu, Xun X; Yu, Fei F; Huang, Tongtong T; Dai, Juncheng J; Ma, Hongxia H; Jiang, Yue Y; Yin, Rong R; Hu, Zhibin Z; Jin, Guangfu G; Xu, Lin L; Shen, Hongbing H
Publication Date: 2017-02

Variant appearance in text: rs7023329
PubMed Link: 27960044
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.

Cell
Chen, Lu L; Ge, Bing B; Casale, Francesco Paolo FP; Vasquez, Louella L; Kwan, Tony T; Garrido-Martín, Diego D; Watt, Stephen S; Yan, Ying Y; Kundu, Kousik K; Ecker, Simone S; Datta, Avik A; Richardson, David D; Burden, Frances F; Mead, Daniel D; Mann, Alice L AL; Fernandez, Jose Maria JM; Rowlston, Sophia S; Wilder, Steven P SP; Farrow, Samantha S; Shao, Xiaojian X; Lambourne, John J JJ; Redensek, Adriana A; Albers, Cornelis A CA; Amstislavskiy, Vyacheslav V; Ashford, Sofie S; Berentsen, Kim K; Bomba, Lorenzo L; Bourque, Guillaume G; Bujold, David D; Busche, Stephan S; Caron, Maxime M; Chen, Shu-Huang SH; Cheung, Warren W; Delaneau, Oliver O; Dermitzakis, Emmanouil T ET; Elding, Heather H; Colgiu, Irina I; Bagger, Frederik O FO; Flicek, Paul P; Habibi, Ehsan E; Iotchkova, Valentina V; Janssen-Megens, Eva E; Kim, Bowon B; Lehrach, Hans H; Lowy, Ernesto E; Mandoli, Amit A; Matarese, Filomena F; Maurano, Matthew T MT; Morris, John A JA; Pancaldi, Vera V; Pourfarzad, Farzin F; Rehnstrom, Karola K; Rendon, Augusto A; Risch, Thomas T; Sharifi, Nilofar N; Simon, Marie-Michelle MM; Sultan, Marc M; Valencia, Alfonso A; Walter, Klaudia K; Wang, Shuang-Yin SY; Frontini, Mattia M; Antonarakis, Stylianos E SE; Clarke, Laura L; Yaspo, Marie-Laure ML; Beck, Stephan S; Guigo, Roderic R; Rico, Daniel D; Martens, Joost H A JHA; Ouwehand, Willem H WH; Kuijpers, Taco W TW; Paul, Dirk S DS; Stunnenberg, Hendrik G HG; Stegle, Oliver O; Downes, Kate K; Pastinen, Tomi T; Soranzo, Nicole N
Publication Date: 2016-11-17

Variant appearance in text: rs7023329
PubMed Link: 27863251
Variant Present in the following documents:
  • main.pdf
View BVdb publication page



Characterization of the Methylthioadenosine Phosphorylase Polymorphism rs7023954 - Incidence and Effects on Enzymatic Function in Malignant Melanoma.

Plos One
Limm, Katharina K; Dettmer, Katja K; Reinders, Jörg J; Oefner, Peter J PJ; Bosserhoff, Anja-Katrin AK
Publication Date: 2016

Variant appearance in text: rs7023329
PubMed Link: 27479139
Variant Present in the following documents:
  • Main text
  • pone.0160348.pdf
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Genetic scores based on risk-associated single nucleotide polymorphisms (SNPs) can reveal inherited risk of renal cell carcinoma.

Oncotarget
Wu, Yishuo Y; Zhang, Ning N; Li, Kaiwen K; Chen, Haitao H; Lin, Xiaolin X; Yu, Yang Y; Gou, Yuancheng Y; Hou, Jiangang J; Jiang, Deke D; Na, Rong R; Wang, Xiang X; Ding, Qiang Q; Xu, Jianfeng J
Publication Date: 2016-04-05

Variant appearance in text: rs7023329
PubMed Link: 27229762
Variant Present in the following documents:
  • Main text
  • oncotarget-07-18631.pdf
View BVdb publication page



Genome-wide association studies and epigenome-wide association studies go together in cancer control.

Future Oncology (London, England)
Verma, Mukesh M
Publication Date: 2016-07

Variant appearance in text: rs7023329
PubMed Link: 27079684
Variant Present in the following documents:
  • Main text
View BVdb publication page



Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.

Human Molecular Genetics
Wang, Zhaoming Z; Seow, Wei Jie WJ; Shiraishi, Kouya K; Hsiung, Chao A CA; Matsuo, Keitaro K; Liu, Jie J; Chen, Kexin K; Yamji, Taiki T; Yang, Yang Y; Chang, I-Shou IS; Wu, Chen C; Hong, Yun-Chul YC; Burdett, Laurie L; Wyatt, Kathleen K; Chung, Charles C CC; Li, Shengchao A SA; Yeager, Meredith M; Hutchinson, Amy A; Hu, Wei W; Caporaso, Neil N; Landi, Maria T MT; Chatterjee, Nilanjan N; Song, Minsun M; Fraumeni, Joseph F JF; Kohno, Takashi T; Yokota, Jun J; Kunitoh, Hideo H; Ashikawa, Kyota K; Momozawa, Yukihide Y; Daigo, Yataro Y; Mitsudomi, Tetsuya T; Yatabe, Yasushi Y; Hida, Toyoaki T; Hu, Zhibin Z; Dai, Juncheng J; Ma, Hongxia H; Jin, Guangfu G; Song, Bao B; Wang, Zhehai Z; Cheng, Sensen S; Yin, Zhihua Z; Li, Xuelian X; Ren, Yangwu Y; Guan, Peng P; Chang, Jiang J; Tan, Wen W; Chen, Chien-Jen CJ; Chang, Gee-Chen GC; Tsai, Ying-Huang YH; Su, Wu-Chou WC; Chen, Kuan-Yu KY; Huang, Ming-Shyan MS; Chen, Yuh-Min YM; Zheng, Hong H; Li, Haixin H; Cui, Ping P; Guo, Huan H; Xu, Ping P; Liu, Li L; Iwasaki, Motoki M; Shimazu, Taichi T; Tsugane, Shoichiro S; Zhu, Junjie J; Jiang, Gening G; Fei, Ke K; Park, Jae Yong JY; Kim, Yeul Hong YH; Sung, Jae Sook JS; Park, Kyong Hwa KH; Kim, Young Tae YT; Jung, Yoo Jin YJ; Kang, Chang Hyun CH; Park, In Kyu IK; Kim, Hee Nam HN; Jeon, Hyo-Sung HS; Choi, Jin Eun JE; Choi, Yi Young YY; Kim, Jin Hee JH; Oh, In-Jae IJ; Kim, Young-Chul YC; Sung, Sook Whan SW; Kim, Jun Suk JS; Yoon, Ho-Il HI; Kweon, Sun-Seog SS; Shin, Min-Ho MH; Seow, Adeline A; Chen, Ying Y; Lim, Wei-Yen WY; Liu, Jianjun J; Wong, Maria Pik MP; Lee, Victor Ho Fun VH; Bassig, Bryan A BA; Tucker, Margaret M; Berndt, Sonja I SI; Chow, Wong-Ho WH; Ji, Bu-Tian BT; Wang, Junwen J; Xu, Jun J; Sihoe, Alan Dart Loon AD; Ho, James C M JC; Chan, John K C JK; Wang, Jiu-Cun JC; Lu, Daru D; Zhao, Xueying X; Zhao, Zhenhong Z; Wu, Junjie J; Chen, Hongyan H; Jin, Li L; Wei, Fusheng F; Wu, Guoping G; An, She-Juan SJ; Zhang, Xu-Chao XC; Su, Jian J; Wu, Yi-Long YL; Gao, Yu-Tang YT; Xiang, Yong-Bing YB; He, Xingzhou X; Li, Jihua J; Zheng, Wei W; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Klein, Robert R; Pao, William W; Lawrence, Charles C; Hosgood, H Dean HD; Hsiao, Chin-Fu CF; Chien, Li-Hsin LH; Chen, Ying-Hsiang YH; Chen, Chung-Hsing CH; Wang, Wen-Chang WC; Chen, Chih-Yi CY; Wang, Chih-Liang CL; Yu, Chong-Jen CJ; Chen, Hui-Ling HL; Su, Yu-Chun YC; Tsai, Fang-Yu FY; Chen, Yi-Song YS; Li, Yao-Jen YJ; Yang, Tsung-Ying TY; Lin, Chien-Chung CC; Yang, Pan-Chyr PC; Wu, Tangchun T; Lin, Dongxin D; Zhou, Baosen B; Yu, Jinming J; Shen, Hongbing H; Kubo, Michiaki M; Chanock, Stephen J SJ; Rothman, Nathaniel N; Lan, Qing Q
Publication Date: 2016-02-01

Variant appearance in text: rs7023329
PubMed Link: 26732429
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution.

Cancer Research
Walsh, Kyle M KM; de Smith, Adam J AJ; Hansen, Helen M HM; Smirnov, Ivan V IV; Gonseth, Semira S; Endicott, Alyson A AA; Xiao, Jianqiao J; Rice, Terri T; Fu, Cecilia H CH; McCoy, Lucie S LS; Lachance, Daniel H DH; Eckel-Passow, Jeanette E JE; Wiencke, John K JK; Jenkins, Robert B RB; Wrensch, Margaret R MR; Ma, Xiaomei X; Metayer, Catherine C; Wiemels, Joseph L JL
Publication Date: 2015-11-15

Variant appearance in text: rs7023329
PubMed Link: 26527286
Variant Present in the following documents:
  • Main text
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Genomic Study of Cardiovascular Continuum Comorbidity.

Acta Naturae
Makeeva, O A OA; Sleptsov, A A AA; Kulish, E V EV; Barbarash, O L OL; Mazur, A M AM; Prokhorchuk, E B EB; Chekanov, N N NN; Stepanov, V A VA; Puzyrev, V P VP
Publication Date: 2015

Variant appearance in text: rs7023329
PubMed Link: 26483964
Variant Present in the following documents:
  • Main text
  • AN20758251-26-089.pdf
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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: rs7023329
PubMed Link: 25837821
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Barón, Anna E AE; Asdigian, Nancy L NL; Gonzalez, Victoria V; Aalborg, Jenny J; Terzian, Tamara T; Stiegmann, Regan A RA; Torchia, Enrique C EC; Berwick, Marianne M; Dellavalle, Robert P RP; Morelli, Joseph G JG; Mokrohisky, Stefan T ST; Crane, Lori A LA; Box, Neil F NF
Publication Date: 2014-12

Variant appearance in text: rs7023329
PubMed Link: 25410285
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: rs7023329
PubMed Link: 25307738
Variant Present in the following documents:
  • Main text
  • bjd0172-1081-sd1.pdf
  • bjd0172-1081.pdf
View BVdb publication page



Bayesian variable selection for hierarchical gene-environment and gene-gene interactions.

Human Genetics
Liu, Changlu C; Ma, Jianzhong J; Amos, Christopher I CI
Publication Date: 2015-01

Variant appearance in text: rs7023329
PubMed Link: 25154630
Variant Present in the following documents:
  • Main text
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Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.

International Journal Of Cancer
Barrett, Jennifer H JH; Taylor, John C JC; Bright, Chloe C; Harland, Mark M; Dunning, Alison M AM; Akslen, Lars A LA; Andresen, Per A PA; Avril, Marie-Françoise MF; Azizi, Esther E; Bianchi Scarrà, Giovanna G; Brossard, Myriam M; Brown, Kevin M KM; Dębniak, Tadeusz T; Elder, David E DE; Friedman, Eitan E; Ghiorzo, Paola P; Gillanders, Elizabeth M EM; Gruis, Nelleke A NA; Hansson, Johan J; Helsing, Per P; Hočevar, Marko M; Höiom, Veronica V; Ingvar, Christian C; Landi, Maria Teresa MT; Lang, Julie J; Lathrop, G Mark GM; Lubiński, Jan J; Mackie, Rona M RM; Molven, Anders A; Novaković, Srdjan S; Olsson, Håkan H; Puig, Susana S; Puig-Butille, Joan Anton JA; van der Stoep, Nienke N; van Doorn, Remco R; van Workum, Wilbert W; Goldstein, Alisa M AM; Kanetsky, Peter A PA; Pharoah, Paul D P PD; Demenais, Florence F; Hayward, Nicholas K NK; Newton Bishop, Julia A JA; Bishop, D Timothy DT; Iles, Mark M MM; ,
Publication Date: 2015-03-15

Variant appearance in text: rs7023329
PubMed Link: 25077817
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Identification of a melanoma susceptibility locus and somatic mutation in TET2.

Carcinogenesis
Song, Fengju F; Amos, Christopher I CI; Lee, Jeffrey E JE; Lian, Christine G CG; Fang, Shenying S; Liu, Hongliang H; MacGregor, Stuart S; Iles, Mark M MM; Law, Matthew H MH; Lindeman, Neal I NI; Montgomery, Grant W GW; Duffy, David L DL; Cust, Anne E AE; Jenkins, Mark A MA; Whiteman, David C DC; Kefford, Richard F RF; Giles, Graham G GG; Armstrong, Bruce K BK; Aitken, Joanne F JF; Hopper, John L JL; Brown, Kevin M KM; Martin, Nicholas G NG; Mann, Graham J GJ; Bishop, D Timothy DT; Bishop, Julia A Newton JA; , ; Kraft, Peter P; Qureshi, Abrar A AA; Kanetsky, Peter A PA; Hayward, Nicholas K NK; Hunter, David J DJ; Wei, Qingyi Q; Han, Jiali J
Publication Date: 2014-09

Variant appearance in text: rs7023329
PubMed Link: 24980573
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Variants associated with susceptibility to pancreatic cancer and melanoma do not reciprocally affect risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Wu, Lang L; Goldstein, Alisa M AM; Yu, Kai K; Yang, Xiaohong Rose XR; Rabe, Kari G KG; Arslan, Alan A AA; Canzian, Federico F; Wolpin, Brian M BM; Stolzenberg-Solomon, Rachael R; Amundadottir, Laufey T LT; Petersen, Gloria M GM
Publication Date: 2014-06

Variant appearance in text: rs7023329
PubMed Link: 24642353
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Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.

The Journal Of Investigative Dermatology
Kocarnik, Jonathan M JM; Park, Sungshim Lani SL; Han, Jiali J; Dumitrescu, Logan L; Cheng, Iona I; Wilkens, Lynne R LR; Schumacher, Fredrick R FR; Kolonel, Laurence L; Carlson, Chris S CS; Crawford, Dana C DC; Goodloe, Robert J RJ; Dilks, Holli H; Baker, Paxton P; Richardson, Danielle D; Ambite, José Luis JL; Song, Fengju F; Quresh, Abrar A AA; Zhang, Mingfeng M; Duggan, David D; Hutter, Carolyn C; Hindorff, Lucia A LA; Bush, William S WS; Kooperberg, Charles C; Le Marchand, Loic L; Peters, Ulrike U
Publication Date: 2014-07

Variant appearance in text: rs7023329
PubMed Link: 24480881
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Joint effect of multiple common SNPs predicts melanoma susceptibility.

Plos One
Fang, Shenying S; Han, Jiali J; Zhang, Mingfeng M; Wang, Li-e LE; Wei, Qingyi Q; Amos, Christopher I CI; Lee, Jeffrey E JE
Publication Date: 2013

Variant appearance in text: rs7023329
PubMed Link: 24392023
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  • pone.0085642.pdf
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Variants at the 9p21 locus and melanoma risk.

Bmc Cancer
Maccioni, Livia L; Rachakonda, Panduranga Sivaramakrishna PS; Bermejo, Justo Lorenzo JL; Planelles, Dolores D; Requena, Celia C; Hemminki, Kari K; Nagore, Eduardo E; Kumar, Rajiv R
Publication Date: 2013-07-02

Variant appearance in text: rs7023329
PubMed Link: 23816148
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Update on the Epidemiology of Melanoma.

Current Dermatology Reports
Chen, Steven T ST; Geller, Alan C AC; Tsao, Hensin H
Publication Date: 2013-03-01

Variant appearance in text: rs7023329
PubMed Link: 23580930
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Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study.

Plos One
Stefanaki, Irene I; Panagiotou, Orestis A OA; Kodela, Elisavet E; Gogas, Helen H; Kypreou, Katerina P KP; Chatzinasiou, Foteini F; Nikolaou, Vasiliki V; Plaka, Michaela M; Kalfa, Iro I; Antoniou, Christina C; Ioannidis, John P A JP; Evangelou, Evangelos E; Stratigos, Alexander J AJ
Publication Date: 2013

Variant appearance in text: rs7023329
PubMed Link: 23393597
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Common genetic variants in the 9p21 region and their associations with multiple tumours.

British Journal Of Cancer
Gu, F F; Pfeiffer, R M RM; Bhattacharjee, S S; Han, S S SS; Taylor, P R PR; Berndt, S S; Yang, H H; Sigurdson, A J AJ; Toro, J J; Mirabello, L L; Greene, M H MH; Freedman, N D ND; Abnet, C C CC; Dawsey, S M SM; Hu, N N; Qiao, Y-L YL; Ding, T T; Brenner, A V AV; Garcia-Closas, M M; Hayes, R R; Brinton, L A LA; Lissowska, J J; Wentzensen, N N; Kratz, C C; Moore, L E LE; Ziegler, R G RG; Chow, W-H WH; Savage, S A SA; Burdette, L L; Yeager, M M; Chanock, S J SJ; Chatterjee, N N; Tucker, M A MA; Goldstein, A M AM; Yang, X R XR
Publication Date: 2013-04-02

Variant appearance in text: rs7023329
PubMed Link: 23361049
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  • bjc20137a.pdf
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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: rs7023329
PubMed Link: 21983787
Variant Present in the following documents:
  • Main text
  • NIHMS335189-supplement-1.pdf
  • nihms335189.pdf
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Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.

Twin Research And Human Genetics : The Official Journal Of The International Society For Twin Studies
Kvaskoff, Marina M; Whiteman, David C DC; Zhao, Zhen Z ZZ; Montgomery, Grant W GW; Martin, Nicholas G NG; Hayward, Nicholas K NK; Duffy, David L DL
Publication Date: 2011-10

Variant appearance in text: rs7023329
PubMed Link: 21962134
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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.

Human Molecular Genetics
Amos, Christopher I CI; Wang, Li-E LE; Lee, Jeffrey E JE; Gershenwald, Jeffrey E JE; Chen, Wei V WV; Fang, Shenying S; Kosoy, Roman R; Zhang, Mingfeng M; Qureshi, Abrar A AA; Vattathil, Selina S; Schacherer, Christopher W CW; Gardner, Julie M JM; Wang, Yuling Y; Bishop, D Tim DT; Barrett, Jennifer H JH; , ; MacGregor, Stuart S; Hayward, Nicholas K NK; Martin, Nicholas G NG; Duffy, David L DL; , ; Mann, Graham J GJ; Cust, Anne A; Hopper, John J; , ; Brown, Kevin M KM; Grimm, Elizabeth A EA; Xu, Yaji Y; Han, Younghun Y; Jing, Kaiyan K; McHugh, Caitlin C; Laurie, Cathy C CC; Doheny, Kim F KF; Pugh, Elizabeth W EW; Seldin, Michael F MF; Han, Jiali J; Wei, Qingyi Q
Publication Date: 2011-12-15

Variant appearance in text: rs7023329
PubMed Link: 21926416
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Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma.

Journal Of The National Cancer Institute
Chatzinasiou, Foteini F; Lill, Christina M CM; Kypreou, Katerina K; Stefanaki, Irene I; Nicolaou, Vasiliki V; Spyrou, George G; Evangelou, Evangelos E; Roehr, Johannes T JT; Kodela, Elizabeth E; Katsambas, Andreas A; Tsao, Hensin H; Ioannidis, John P A JP; Bertram, Lars L; Stratigos, Alexander J AJ
Publication Date: 2011-08-17

Variant appearance in text: rs7023329
PubMed Link: 21693730
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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: rs7023329
PubMed Link: 21219822
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  • zgfazz-14-1-C1.pdf
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Melanocytic nevi, nevus genes, and melanoma risk in a large case-control study in the United Kingdom.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Newton-Bishop, Julia A JA; Chang, Yu-Mei YM; Iles, Mark M MM; Taylor, John C JC; Bakker, Bert B; Chan, May M; Leake, Susan S; Karpavicius, Birute B; Haynes, Sue S; Fitzgibbon, Elaine E; Elliott, Faye F; Kanetsky, Peter A PA; Harland, Mark M; Barrett, Jennifer H JH; Bishop, D Timothy DT
Publication Date: 2010-08

Variant appearance in text: rs7023329
PubMed Link: 20647408
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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: rs7023329
PubMed Link: 20585100
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Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.

Familial Cancer
Yang, Xiaohong Rose XR; Liang, Xueying X; Pfeiffer, Ruth M RM; Wheeler, William W; Maeder, Dennis D; Burdette, Laurie L; Yeager, Meredith M; Chanock, Stephen S; Tucker, Margaret A MA; Goldstein, Alisa M AM
Publication Date: 2010-12

Variant appearance in text: rs7023329
PubMed Link: 20574843
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Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis.

Pigment Cell & Melanoma Research
Gerstenblith, Meg R MR; Shi, Jianxin J; Landi, Maria Teresa MT
Publication Date: 2010-10

Variant appearance in text: rs7023329
PubMed Link: 20546537
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Moderate- to low-risk variant alleles of cutaneous malignancies and nevi: lessons from genome-wide association studies.

Genome Medicine
Udayakumar, Durga D; Tsao, Hensin H
Publication Date: 2009-10-27

Variant appearance in text: rs7023329
PubMed Link: 19863770
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  • Main text
  • gm95.pdf
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Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.

Nature Genetics
Falchi, Mario M; Bataille, Veronique V; Hayward, Nicholas K NK; Duffy, David L DL; Bishop, Julia A Newton JA; Pastinen, Tomi T; Cervino, Alessandra A; Zhao, Zhen Z ZZ; Deloukas, Panos P; Soranzo, Nicole N; Elder, David E DE; Barrett, Jennifer H JH; Martin, Nicholas G NG; Bishop, D Timothy DT; Montgomery, Grant W GW; Spector, Timothy D TD
Publication Date: 2009-08

Variant appearance in text: rs7023329
PubMed Link: 19578365
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Genome-wide association study identifies three loci associated with melanoma risk.

Nature Genetics
Bishop, D Timothy DT; Demenais, Florence F; Iles, Mark M MM; Harland, Mark M; Taylor, John C JC; Corda, Eve E; Randerson-Moor, Juliette J; Aitken, Joanne F JF; Avril, Marie-Francoise MF; Azizi, Esther E; Bakker, Bert B; Bianchi-Scarrà, Giovanna G; Bressac-de Paillerets, Brigitte B; Calista, Donato D; Cannon-Albright, Lisa A LA; Chin-A-Woeng, Thomas T; Debniak, Tadeusz T; Galore-Haskel, Gilli G; Ghiorzo, Paola P; Gut, Ivo I; Hansson, Johan J; Hocevar, Marko M; Höiom, Veronica V; Hopper, John L JL; Ingvar, Christian C; Kanetsky, Peter A PA; Kefford, Richard F RF; Landi, Maria Teresa MT; Lang, Julie J; Lubiński, Jan J; Mackie, Rona R; Malvehy, Josep J; Mann, Graham J GJ; Martin, Nicholas G NG; Montgomery, Grant W GW; van Nieuwpoort, Frans A FA; Novakovic, Srdjan S; Olsson, Håkan H; Puig, Susana S; Weiss, Marjan M; van Workum, Wilbert W; Zelenika, Diana D; Brown, Kevin M KM; Goldstein, Alisa M AM; Gillanders, Elizabeth M EM; Boland, Anne A; Galan, Pilar P; Elder, David E DE; Gruis, Nelleke A NA; Hayward, Nicholas K NK; Lathrop, G Mark GM; Barrett, Jennifer H JH; Bishop, Julia A Newton JA
Publication Date: 2009-08

Variant appearance in text: rs7023329
PubMed Link: 19578364
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