TP53 c.672+62A>C

Variant ID: 17-7578115-T-G

NM_000546.5(TP53):c.672+62A>C

This variant was identified in 67 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: rs1625895
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome.

Acta Neuropathologica Communications
Perez-Rivas, Luis Gustavo LG; Simon, Julia J; Albani, Adriana A; Tang, Sicheng S; Roeber, Sigrun S; Assié, Guillaume G; Deutschbein, Timo T; Fassnacht, Martin M; Gadelha, Monica R MR; Hermus, Ad R AR; Stalla, Günter K GK; Tichomirowa, Maria A MA; Rotermund, Roman R; Flitsch, Jörg J; Buchfelder, Michael M; Nasi-Kordhishti, Isabella I; Honegger, Jürgen J; Thorsteinsdottir, Jun J; Saeger, Wolfgang W; Herms, Jochen J; Reincke, Martin M; Theodoropoulou, Marily M
Publication Date: 2022-09-19

Variant appearance in text: rs1625895
PubMed Link: 36123588
Variant Present in the following documents:
  • 40478_2022_1437_MOESM1_ESM.pdf
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs1625895
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Impact on breast cancer susceptibility and clinicopathological traits of common genetic polymorphisms in TP53, MDM2 and ATM genes in Sardinian women.

Oncology Letters
Floris, Matteo M; Pira, Giovanna G; Castiglia, Paolo P; Idda, Maria Laura ML; Steri, Maristella M; De Miglio, Maria Rosaria MR; Piana, Andrea A; Cossu, Andrea A; Azara, Antonio A; Arru, Caterina C; Deiana, Giovanna G; Putzu, Carlo C; Sanna, Valeria V; Carru, Ciriaco C; Serra, Antonello A; Bisail, Marco M; Muroni, Maria Rosaria MR
Publication Date: 2022-10

Variant appearance in text: rs1625895
PubMed Link: 36039053
Variant Present in the following documents:
  • Main text
  • ol-24-04-13451.pdf
View BVdb publication page



The Association Between Polymorphisms in Cell-Cycle Genes and Mitochondrial DNA Copy Number in Coke Oven Workers.

Frontiers In Public Health
Wang, Yuping Y; Tan, Jiebing J; Wang, Wei W; Duan, Xiaoran X; Lappe, Brooke B; Shi, Liuhua L; Yang, Yongli Y; Shi, Xuezhong X
Publication Date: 2022

Variant appearance in text: rs1625895
PubMed Link: 35865244
Variant Present in the following documents:
  • Main text
  • fpubh-10-904856.pdf
View BVdb publication page



Association Between the TP53 Polymorphisms and Breast Cancer Risk: An Updated Meta-Analysis.

Frontiers In Genetics
Zhao, Lin L; Yin, Xiang-Xiongyi XX; Qin, Jun J; Wang, Wei W; He, Xiao-Feng XF
Publication Date: 2022

Variant appearance in text: rs1625895
PubMed Link: 35571038
Variant Present in the following documents:
  • Main text
  • fgene-13-807466.pdf
View BVdb publication page



TP53 common variants and interaction with PPP1R13L and CD3EAP SNPs and lung cancer risk and smoking behavior in a Chinese population.

Biomedical Journal
Yin, Jiaoyang J; Hou, Wei W; Vogel, Ulla U; Li, Xinxin X; Ma, Yegang Y; Wang, Chunhong C; Wang, Huiwen H; Sun, Zhenxiang Z
Publication Date: 2022-02

Variant appearance in text: rs1625895
PubMed Link: 35351459
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Monitoring of Leukemia Clones in B-cell Acute Lymphoblastic Leukemia at Diagnosis and During Treatment by Single-cell DNA Amplicon Sequencing.

Hemasphere
Meyers, Sarah S; Alberti-Servera, Llucia L; Gielen, Olga O; Erard, Margot M; Swings, Toon T; De Bie, Jolien J; Michaux, Lucienne L; Dewaele, Barbara B; Boeckx, Nancy N; Uyttebroeck, Anne A; De Keersmaecker, Kim K; Maertens, Johan J; Segers, Heidi H; Cools, Jan J; Demeyer, Sofie S
Publication Date: 2022-04

Variant appearance in text: rs1625895
PubMed Link: 35291210
Variant Present in the following documents:
  • hs9-6-e700-s004.xlsx, sheet 8
  • hs9-6-e700-s004.xlsx, sheet 12
  • hs9-6-e700-s004.xlsx, sheet 11
  • hs9-6-e700-s004.xlsx, sheet 9
  • hs9-6-e700-s004.xlsx, sheet 6
  • hs9-6-e700-s004.xlsx, sheet 7
  • hs9-6-e700-s004.xlsx, sheet 10
  • hs9-6-e700-s004.xlsx, sheet 13
  • hs9-6-e700-s004.xlsx, sheet 4
  • hs9-6-e700-s004.xlsx, sheet 3
  • hs9-6-e700-s004.xlsx, sheet 2
  • hs9-6-e700-s004.xlsx, sheet 5
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Importance of TP53 codon 72 and intron 3 duplication 16 bp polymorphisms and their haplotypes in susceptibility to sarcopenia in Iranian older adults.

Bmc Geriatrics
Montazeri-Najafabady, Nima N; Dabbaghmanesh, Mohammad Hossein MH; Nasimi, Nasrin N; Sohrabi, Zahra Z; Estedlal, Alireza A; Asmarian, Naeimehossadat N
Publication Date: 2022-02-05

Variant appearance in text: rs1625895
PubMed Link: 35123410
Variant Present in the following documents:
  • Main text
  • 12877_2022_Article_2765.pdf
View BVdb publication page



Importance of TP53 codon 72 and intron 3 duplication 16 bp polymorphisms and their haplotypes in susceptibility to sarcopenia in Iranian older adults.

Bmc Geriatrics
Montazeri-Najafabady, Nima N; Dabbaghmanesh, Mohammad Hossein MH; Nasimi, Nasrin N; Sohrabi, Zahra Z; Estedlal, Alireza A; Asmarian, Naeimehossadat N
Publication Date: 2022-02-05

Variant appearance in text: rs1625895
PubMed Link: 35123410
Variant Present in the following documents:
  • Main text
  • 12877_2022_Article_2765.pdf
View BVdb publication page



Genetically predicted sex hormone binding globulin and ischemic heart disease in men and women: a univariable and multivariable Mendelian randomization study.

Scientific Reports
Zhao, Jie V JV; Schooling, C Mary CM
Publication Date: 2021-11-30

Variant appearance in text: rs1625895
PubMed Link: 34848757
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_2510.pdf
View BVdb publication page



Genetic determination of the ovarian reserve: a literature review.

Journal Of Ovarian Research
Moiseeva, Aleksandra V AV; Kudryavtseva, Varvara A VA; Nikolenko, Vladimir N VN; Gevorgyan, Marine M MM; Unanyan, Ara L AL; Bakhmet, Anastassia A AA; Sinelnikov, Mikhail Y MY
Publication Date: 2021-08-06

Variant appearance in text: rs1625895
PubMed Link: 34362406
Variant Present in the following documents:
  • 13048_2021_Article_850.pdf
View BVdb publication page



The effects of genetic polymorphisms on benzene-exposed workers: A systematic review.

Health Science Reports
Ramírez-Lopera, Verónica V; Uribe-Castro, Daniel D; Bautista-Amorocho, Henry H; Silva-Sayago, Jorge Alexander JA; Mateus-Sánchez, Enrique E; Ardila-Barbosa, Wilman Yesid WY; Pérez-Cala, Tania Liseth TL
Publication Date: 2021-09

Variant appearance in text: rs1625895
PubMed Link: 34295994
Variant Present in the following documents:
  • Main text
  • HSR2-4-e327.pdf
View BVdb publication page



The association between TP53 rs1625895 polymorphism and the risk of sarcopenic obesity in Iranian older adults: a case-control study.

Bmc Musculoskeletal Disorders
Montazeri-Najababady, Nima N; Dabbaghmanesh, Mohammad Hossein MH; Nasimi, Nasrin N; Sohrabi, Zahra Z; Chatrabnous, Nazanin N
Publication Date: 2021-05-13

Variant appearance in text: rs1625895
PubMed Link: 33985476
Variant Present in the following documents:
  • Main text
View BVdb publication page



Male and female breast cancer: the two faces of the same genetic susceptibility coin.

Breast Cancer Research And Treatment
Silva, Susana Nunes SN; Gomes, Bruno Costa BC; André, Saudade S; Félix, Ana A; Rodrigues, António Sebastião AS; Rueff, José J
Publication Date: 2021-07

Variant appearance in text: rs1625895
PubMed Link: 33942220
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of TP53 gene and particular infrastructural alterations in invasive ductal mammary carcinoma.

Romanian Journal Of Morphology And Embryology = Revue Roumaine De Morphologie Et Embryologie
Mihalcea, Corina Elena CE; Moroşanu, Ana Maria AM; Murăraşu, Daniela D; Puiu, Liliana L; Cinca, Sabin Aurel SA; Voinea, Silviu Cristian SC; Mirancea, Nicolae N
Publication Date: 2020

Variant appearance in text: rs1625895
PubMed Link: 33544795
Variant Present in the following documents:
  • Main text
  • RJME-61-2-441.pdf
View BVdb publication page



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

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

Variant appearance in text: rs1625895
PubMed Link: 33420045
Variant Present in the following documents:
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs1625895
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs1625895
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



The rs78378222 prevalence and the copy loss of the protective allele A in the tumor tissue of diffuse large B-cell lymphoma.

Peerj
Voropaeva, Elena N EN; Orlov, Yuriy L YL; Pospelova, Tatiana I TI; Gurageva, Anna A AA; Voevoda, Mikhail I MI; Maksimov, Vladimir N VN; Seregina, Olga B OB; Churkina, Maria I MI
Publication Date: 2020

Variant appearance in text: rs1625895
PubMed Link: 33240649
Variant Present in the following documents:
  • peerj-08-10335.pdf
View BVdb publication page



Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.

Breast Cancer (Tokyo, Japan)
Rogoża-Janiszewska, Emilia E; Malińska, Karolina K; Górski, Bohdan B; Scott, Rodney J RJ; Cybulski, Cezary C; Kluźniak, Wojciech W; Lener, Marcin M; Jakubowska, Anna A; Gronwald, Jacek J; Huzarski, Tomasz T; Lubiński, Jan J; Dębniak, Tadeusz T
Publication Date: 2021-01

Variant appearance in text: rs1625895
PubMed Link: 32888145
Variant Present in the following documents:
  • Main text
  • 12282_2020_Article_1151.pdf
View BVdb publication page



A novel hotspot and rare somatic mutation p.A138V, at TP53 is associated with poor survival of pancreatic ductal and periampullary adenocarcinoma patients.

Molecular Medicine (Cambridge, Mass.)
Saha, Gourab G; Singh, Richa R; Mandal, Argha A; Das, Subrata S; Chattopadhyay, Esita E; Panja, Prasun P; Roy, Paromita P; DeSarkar, Navonil N; Gulati, Sumit S; Ghatak, Supriyo S; Ghosh, Shibajyoti S; Banerjee, Sudeep S; Roy, Bidyut B; Ghosh, Saurabh S; Chaudhuri, Dipankar D; Arora, Neeraj N; Biswas, Nidhan K NK; Sikdar, Nilabja N
Publication Date: 2020-06-17

Variant appearance in text: rs1625895
PubMed Link: 32552660
Variant Present in the following documents:
  • Main text
  • 10020_2020_183_MOESM4_ESM.xlsx, sheet 3
  • 10020_2020_Article_183.pdf
View BVdb publication page



Environmental exposures and breast cancer risk in the context of underlying susceptibility: A systematic review of the epidemiological literature.

Environmental Research
Zeinomar, Nur N; Oskar, Sabine S; Kehm, Rebecca D RD; Sahebzeda, Shamin S; Terry, Mary Beth MB
Publication Date: 2020-08

Variant appearance in text: rs1625895
PubMed Link: 32445942
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sex hormone-binding globulin and arthritis: a Mendelian randomization study.

Arthritis Research & Therapy
Qu, Zihao Z; Huang, Jiawei J; Yang, Fangkun F; Hong, Jianqiao J; Wang, Wei W; Yan, Shigui S
Publication Date: 2020-05-18

Variant appearance in text: rs1625895
PubMed Link: 32423484
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of XRCC1, XRCC2 and XRCC3 Gene Polymorphism with Esophageal Cancer Risk.

Clinical And Experimental Gastroenterology
Kaur, Jagjeet J; Sambyal, Vasudha V; Guleria, Kamlesh K; Singh, Neeti Rajan NR; Uppal, Manjit Singh MS; Manjari, Mridu M; Sudan, Meena M
Publication Date: 2020

Variant appearance in text: rs1625895
PubMed Link: 32214837
Variant Present in the following documents:
  • Main text
  • ceg-13-73.pdf
View BVdb publication page



p53 protein expression affected by TP53 polymorphism is associated with the biological behavior and prognosis of low rectal cancer.

Oncology Letters
Zhang, Guangzhe G; Xu, Qian Q; Wang, Zeyang Z; Sun, Liping L; Lv, Zhi Z; Liu, Jingwei J; Xing, Chengzhong C; Yuan, Yuan Y
Publication Date: 2019-12

Variant appearance in text: rs1625895
PubMed Link: 31788124
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic dynamics in untreated CLL patients with either stable or progressive disease: a longitudinal study.

Journal Of Hematology & Oncology
Ramassone, Alice A; D'Argenio, Andrea A; Veronese, Angelo A; Basti, Alessio A; Soliman, Shimaa Hassan AbdelAziz SHA; Volinia, Stefano S; Bassi, Cristian C; Pagotto, Sara S; Ferracin, Manuela M; Lupini, Laura L; Saccenti, Elena E; Balatti, Veronica V; Pepe, Felice F; Rassenti, Laura Z LZ; Innocenti, Idanna I; Autore, Francesco F; Marzetti, Laura L; Mariani-Costantini, Renato R; Kipps, Thomas J TJ; Negrini, Massimo M; Laurenti, Luca L; Visone, Rosa R
Publication Date: 2019-11-19

Variant appearance in text: rs1625895
PubMed Link: 31744508
Variant Present in the following documents:
  • 13045_2019_802_MOESM7_ESM.xlsx, sheet 1
  • 13045_2019_802_MOESM4_ESM.pdf
View BVdb publication page



TP53 rs1625895 is Related to Breast Cancer Incidence and Early Death in Iranian Population.

Indian Journal Of Clinical Biochemistry : Ijcb
Assad Samani, Leila L; Javadirad, Seyed-Morteza SM; Parsafar, Soha S; Tabatabaeian, Hossein H; Ghaedi, Kamran K; Azadeh, Mansoureh M
Publication Date: 2019-10

Variant appearance in text: rs1625895
PubMed Link: 31686737
Variant Present in the following documents:
  • Main text
View BVdb publication page



[Relationship between p53 rs1625895 polymorphism and prognosis in diffuse large B-cell lymphoma].

Beijing Da Xue Xue Bao. Yi Xue Ban = Journal Of Peking University. Health Sciences
Tian, Y Y; Zhu, J J
Publication Date: 2019-10-18

Variant appearance in text: rs1625895
PubMed Link: 31624379
Variant Present in the following documents:
  • Main text
View BVdb publication page



Clonal Evolution and Changes in Two AML Patients Detected with A Novel Single-Cell DNA Sequencing Platform.

Scientific Reports
Xu, Liwen L; Durruthy-Durruthy, Robert R; Eastburn, Dennis J DJ; Pellegrino, Maurizio M; Shah, Omid O; Meyer, Everett E; Zehnder, James J
Publication Date: 2019-07-31

Variant appearance in text: rs1625895
PubMed Link: 31366893
Variant Present in the following documents:
  • 41598_2019_47297_MOESM1_ESM.pdf
View BVdb publication page



Five P53 SNPs Involved in Low Rectal Cancer Risk and Prognosis in a Chinese Population.

Journal Of Cancer
Zhang, Guangzhe G; Xu, Qian Q; Liu, Jingwei J; Lv, Zhi Z; Lu, Youzhu Y; Yang, Huaiwei H; Sun, Liping L; Xing, Chengzhong C; Yuan, Yuan Y
Publication Date: 2019

Variant appearance in text: rs1625895
PubMed Link: 31205533
Variant Present in the following documents:
  • Main text
  • jcav10p1772.pdf
View BVdb publication page



Sex hormone binding globulin and risk of breast cancer: a Mendelian randomization study.

International Journal Of Epidemiology
Dimou, Niki L NL; Papadimitriou, Nikos N; Gill, Dipender D; Christakoudi, Sofia S; Murphy, Neil N; Gunter, Marc J MJ; Travis, Ruth C RC; Key, Tim J TJ; Fortner, Renee T RT; Haycock, Philip C PC; Lewis, Sarah J SJ; Muir, Kenneth K; Martin, Richard M RM; Tsilidis, Konstantinos K KK
Publication Date: 2019-06-01

Variant appearance in text: rs1625895
PubMed Link: 31143958
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between TP53 genetic polymorphisms and the methylation and expression of miR-34a, 34b/c in colorectal cancer tissues.

Oncology Letters
Jun, Hak Hoon HH; Kwack, Kyubum K; Lee, Keun Hee KH; Kim, Jung Oh JO; Park, Han Sung HS; Ryu, Chang Soo CS; Lee, Jeong Yong JY; Ko, Daeun D; Kim, Jong Woo JW; Kim, Nam Keun NK
Publication Date: 2019-05

Variant appearance in text: rs1625895
PubMed Link: 30944658
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germline TP53 mutation spectrum in Sudanese premenopausal breast cancer patients: correlations with reproductive factors.

Breast Cancer Research And Treatment
Aceto, Gitana Maria GM; Awadelkarim, Khalid Dafaallah KD; Di Nicola, Marta M; Moscatello, Carmelo C; Pantalone, Mattia Russel MR; Verginelli, Fabio F; Elwali, Nasr Eldin NE; Mariani-Costantini, Renato R
Publication Date: 2019-06

Variant appearance in text: rs1625895
PubMed Link: 30796655
Variant Present in the following documents:
  • Main text
  • 10549_2019_Article_5168.pdf
View BVdb publication page



Genetic Variations and Cisplatin Nephrotoxicity: A Systematic Review.

Frontiers In Pharmacology
Zazuli, Zulfan Z; Vijverberg, Susanne S; Slob, Elise E; Liu, Geoffrey G; Carleton, Bruce B; Veltman, Joris J; Baas, Paul P; Masereeuw, Rosalinde R; Maitland-van der Zee, Anke-Hilse AH
Publication Date: 2018

Variant appearance in text: rs1625895
PubMed Link: 30319427
Variant Present in the following documents:
  • Main text
  • fphar-09-01111.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs1625895
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Interaction between polymorphisms in cell-cycle genes and environmental factors in regulating cholinesterase activity in people with exposure to omethoate.

Royal Society Open Science
Duan, Xiaoran X; Yang, Yongli Y; Wang, Sihua S; Feng, Xiaolei X; Wang, Tuanwei T; Wang, Pengpeng P; Yao, Wu W; Cui, Liuxin L; Wang, Wei W
Publication Date: 2018-05

Variant appearance in text: rs1625895
PubMed Link: 29892419
Variant Present in the following documents:
  • Main text
  • rsos172357.pdf
View BVdb publication page



TP53 Gene Polymorphisms and Occupational Skin Cancer Risks for Workers of Glass Fiber Manufacture.

Iranian Journal Of Public Health
Mukhammadiyeva, Guzel F GF; Karimov, Denis O DO; Bakirov, Akhat B AB; Karimova, Liliya K LK
Publication Date: 2017-11

Variant appearance in text: rs1625895
PubMed Link: 29167767
Variant Present in the following documents:
  • Main text
  • IJPH-46-1495.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs1625895
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Identifying novel genes and biological processes relevant to the development of cancer therapy-induced mucositis: An informative gene network analysis.

Plos One
Reyes-Gibby, Cielito C CC; Melkonian, Stephanie C SC; Wang, Jian J; Yu, Robert K RK; Shelburne, Samuel A SA; Lu, Charles C; Gunn, Gary Brandon GB; Chambers, Mark S MS; Hanna, Ehab Y EY; Yeung, Sai-Ching J SJ; Shete, Sanjay S
Publication Date: 2017

Variant appearance in text: rs1625895
PubMed Link: 28678827
Variant Present in the following documents:
  • Main text
  • pone.0180396.pdf
View BVdb publication page



Relevance of DNA repair gene polymorphisms to gastric cancer risk and phenotype.

Oncotarget
Carrera-Lasfuentes, Patricia P; Lanas, Angel A; Bujanda, Luis L; Strunk, Mark M; Quintero, Enrique E; Santolaria, Santos S; Benito, Rafael R; Sopeña, Federico F; Piazuelo, Elena E; Thomson, Concha C; Pérez-Aisa, Angeles A; Nicolás-Pérez, David D; Hijona, Elizabeth E; Espinel, Jesús J; Campo, Rafael R; Manzano, Marisa M; Geijo, Fernando F; Pellise, María M; Zaballa, Manuel M; González-Huix, Ferrán F; Espinós, Jorge J; Titó, Llúcia L; Barranco, Luis L; D'Amato, Mauro M; García-González, María Asunción MA
Publication Date: 2017-05-30

Variant appearance in text: rs1625895
PubMed Link: 28415781
Variant Present in the following documents:
  • Main text
View BVdb publication page



Low statistical power in biomedical science: a review of three human research domains.

Royal Society Open Science
Dumas-Mallet, Estelle E; Button, Katherine S KS; Boraud, Thomas T; Gonon, Francois F; Munafò, Marcus R MR
Publication Date: 2017-02

Variant appearance in text: rs1625895
PubMed Link: 28386409
Variant Present in the following documents:
  • rsos160254supp3.xlsx, sheet 1
  • rsos160254supp3.xlsx, sheet 10
View BVdb publication page