Publications:

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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: rs4919686

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Association Between the Polymorphism of Steroid Hormone Metabolism Genes and High-Altitude Pulmonary Edema in the Chinese Han Population.

International Journal Of General Medicine

Gao, Hui H; Xu, Jin J; Ma, Qiang Q; Tang, Feng F; Ga, Qin Q; Li, Yuhong Y; Guan, Wei W; Ge, Ri-Li RL; Yang, Ying-Zhong YZ

Publication Date: 2022

Variant appearance in text: rs4919686

PubMed Link: 35087285

Variant Present in the following documents:

• Main text
• ijgm-15-787.pdf

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Aromatase Inhibitors-Induced Musculoskeletal Disorders: Current Knowledge on Clinical and Molecular Aspects.

International Journal Of Molecular Sciences

Tenti, Sara S; Correale, Pierpaolo P; Cheleschi, Sara S; Fioravanti, Antonella A; Pirtoli, Luigi L

Publication Date: 2020-08-06

Variant appearance in text: rs4919686

PubMed Link: 32781535

Variant Present in the following documents:

• Main text
• ijms-21-05625.pdf

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Genetic Underpinnings of Musculoskeletal Pain During Treatment With Aromatase Inhibitors for Breast Cancer: A Biological Pathway Analysis.

Biological Research For Nursing

Zhu, Yehui Y; Koleck, Theresa A TA; Bender, Catherine M CM; Conley, Yvette P YP

Publication Date: 2020-04

Variant appearance in text: rs4919686

PubMed Link: 31847542

Variant Present in the following documents:

• Main text

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: CYP17A1: 1139+19T>G; rs4919686

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: rs4919686

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1

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Genetic Variants Associated with Cancer Pain and Response to Opioid Analgesics: Implications for Precision Pain Management.

Seminars In Oncology Nursing

Yang, Gee Su GS; Barnes, Natalie M NM; Lyon, Debra E DE; Dorsey, Susan G SG

Publication Date: 2019-06

Variant appearance in text: rs4919686

PubMed Link: 31085105

Variant Present in the following documents:

• Main text

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Interaction between CYP1A1/CYP17A1 polymorphisms and parental risk factors in the risk of hypospadias in a Chinese population.

Scientific Reports

Mao, Yaping Y; Zhang, Kang K; Ma, Lin L; Yun, Xiaoyun X; Ou, Fengrong F; Liu, Ge G; Yang, Yi Y; Zhang, Yumin Y; Pei, Xiucong X; Duan, Zhiwen Z; Ma, Mingyue M

Publication Date: 2019-03-11

Variant appearance in text: rs4919686

PubMed Link: 30858503

Variant Present in the following documents:

• Main text
• 41598_2019_Article_40755.pdf

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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: CYP17A1: 1139+19T>G; rs4919686

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1

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Association of CYP17A1 Genetic Polymorphisms and Susceptibility to Essential Hypertension in the Southwest Han Chinese Population.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research

Li, Qian Q; Gao, Tangxin T; Yuan, Yuncang Y; Wu, Yanrui Y; Huang, Qionglin Q; Xie, Fei F; Ran, Pengzhan P; Sun, Lijuan L; Xiao, Chunjie C

Publication Date: 2017-05-24

Variant appearance in text: rs4919686

PubMed Link: 28537227

Variant Present in the following documents:

• Main text
• medscimonit-23-2488.pdf

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Relationship between CYP17A1 Genetic Polymorphism and Essential Hypertension in a Chinese Population.

Aging And Disease

Dai, Chuan-Fang CF; Xie, Xiang X; Ma, Yi-Tong YT; Yang, Yi-Ning YN; Li, Xiao-Mei XM; Fu, Zhen-Yan ZY; Liu, Fen F; Chen, Bang-Dang BD; Gai, Min-Tao MT

Publication Date: 2015-11

Variant appearance in text: rs4919686

PubMed Link: 26618050

Variant Present in the following documents:

• Main text

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Polymorphisms in genes in the androgen pathway and risk of Barrett's esophagus and esophageal adenocarcinoma.

International Journal Of Cancer

Ek, Weronica E WE; Lagergren, Katarina K; Cook, Michael M; Wu, Anna H AH; Abnet, Christian C CC; Levine, David D; Chow, Wong-Ho WH; Bernstein, Leslie L; Risch, Harvey A HA; Shaheen, Nicholas J NJ; Bird, Nigel C NC; Corley, Douglas A DA; Hardie, Laura J LJ; Fitzgerald, Rebecca C RC; Gammon, Marilie D MD; Romero, Yvonne Y; Liu, Geoffrey G; Ye, Weimin W; Vaughan, Thomas L TL; MacGregor, Stuart S; Whiteman, David C DC; Westberg, Lars L; Lagergren, Jesper J

Publication Date: 2016-03-01

Variant appearance in text: rs4919686

PubMed Link: 26414697

Variant Present in the following documents:

• Main text

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Relationship between CYP17A1 genetic polymorphism and coronary artery disease in a Chinese Han population.

Lipids In Health And Disease

Dai, Chuan-Fang CF; Xie, Xiang X; Yang, Yi-Ning YN; Li, Xiao-Mei XM; Zheng, Ying-Ying YY; Fu, Zhen-Yan ZY; Liu, Fen F; Chen, Bang-Dang BD; Gai, Min-Tao MT; Ma, Yi-Tong YT

Publication Date: 2015-03-07

Variant appearance in text: rs4919686

PubMed Link: 25889125

Variant Present in the following documents:

• Main text
• 12944_2015_Article_7.pdf

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Association between cytochrome CYP17A1, CYP3A4, and CYP3A43 polymorphisms and prostate cancer risk and aggressiveness in a Korean study population.

Asian Journal Of Andrology

Han, Jun Hyun JH; Lee, Yong Seong YS; Kim, Hae Jong HJ; Lee, Shin Young SY; Myung, Soon Chul SC

Publication Date: 2015

Variant appearance in text: rs4919686

PubMed Link: 25337833

Variant Present in the following documents:

• AJA-17-285.pdf

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Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.

Cancer Discovery

Shi, Jianxin J; Chatterjee, Nilanjan N; Rotunno, Melissa M; Wang, Yufei Y; Pesatori, Angela C AC; Consonni, Dario D; Li, Peng P; Wheeler, William W; Broderick, Peter P; Henrion, Marc M; Eisen, Timothy T; Wang, Zhaoming Z; Chen, Wei W; Dong, Qiong Q; Albanes, Demetrius D; Thun, Michael M; Spitz, Margaret R MR; Bertazzi, Pier Alberto PA; Caporaso, Neil E NE; Chanock, Stephen J SJ; Amos, Christopher I CI; Houlston, Richard S RS; Landi, Maria Teresa MT

Publication Date: 2012-02

Variant appearance in text: rs4919686

PubMed Link: 22585858

Variant Present in the following documents:

• Main text

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Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.

Plos Genetics

Zhai, Guangju G; Teumer, Alexander A; Stolk, Lisette L; Perry, John R B JR; Vandenput, Liesbeth L; Coviello, Andrea D AD; Koster, Annemarie A; Bell, Jordana T JT; Bhasin, Shalender S; Eriksson, Joel J; Eriksson, Anna A; Ernst, Florian F; Ferrucci, Luigi L; Frayling, Timothy M TM; Glass, Daniel D; Grundberg, Elin E; Haring, Robin R; Hedman, Asa K AK; Hofman, Albert A; Kiel, Douglas P DP; Kroemer, Heyo K HK; Liu, Yongmei Y; Lunetta, Kathryn L KL; Maggio, Marcello M; Lorentzon, Mattias M; Mangino, Massimo M; Melzer, David D; Miljkovic, Iva I; , ; Nica, Alexandra A; Penninx, Brenda W J H BW; Vasan, Ramachandran S RS; Rivadeneira, Fernando F; Small, Kerrin S KS; Soranzo, Nicole N; Uitterlinden, André G AG; Völzke, Henry H; Wilson, Scott G SG; Xi, Li L; Zhuang, Wei Vivian WV; Harris, Tamara B TB; Murabito, Joanne M JM; Ohlsson, Claes C; Murray, Anna A; de Jong, Frank H FH; Spector, Tim D TD; Wallaschofski, Henri H

Publication Date: 2011-04

Variant appearance in text: rs4919686

PubMed Link: 21533175

Variant Present in the following documents:

• Main text
• pgen.1002025.pdf

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