Publications:

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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: ATM: 3576+687C>T; rs1003623

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

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The association between early-onset cardiac events caused by neoadjuvant or adjuvant chemotherapy in triple-negative breast cancer patients and some novel autophagy-related polymorphisms in their genomic DNA: a real-world study.

Cancer Communications (London, England)

Liu, Binliang B; An, Tao T; Li, Meiying M; Yi, Zongbi Z; Li, Chunxiao C; Sun, Xiaoying X; Guan, Xiuwen X; Li, Lixi L; Wang, Yanfeng Y; Zhang, Yuhui Y; Xu, Binghe B; Ma, Fei F; Zeng, Yixin Y

Publication Date: 2018-12-04

Variant appearance in text: rs1003623

PubMed Link: 30514381

Variant Present in the following documents:

• Main text
• 40880_2018_Article_343.pdf

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Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Human Genomics

Karageorgos, Ioannis I; Mizzi, Clint C; Giannopoulou, Efstathia E; Pavlidis, Cristiana C; Peters, Brock A BA; Zagoriti, Zoi Z; Stenson, Peter D PD; Mitropoulos, Konstantinos K; Borg, Joseph J; Kalofonos, Haralabos P HP; Drmanac, Radoje R; Stubbs, Andrew A; van der Spek, Peter P; Cooper, David N DN; Katsila, Theodora T; Patrinos, George P GP

Publication Date: 2015-06-20

Variant appearance in text: rs1003623

PubMed Link: 26092435

Variant Present in the following documents:

• 40246_2015_34_MOESM1_ESM.xlsx, sheet 2

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Hereditary breast cancer in the Han Chinese population.

Journal Of Epidemiology

Cao, Wenming W; Wang, Xiaojia X; Li, Ji-Cheng JC

Publication Date: 2013

Variant appearance in text: rs1003623

PubMed Link: 23318652

Variant Present in the following documents:

• Main text
• je-23-075.pdf

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Evaluation of functional genetic variants for breast cancer risk: results from the Shanghai breast cancer study.

American Journal Of Epidemiology

Zhang, Ben B; Beeghly-Fadiel, Alicia A; Lu, Wei W; Cai, Qiuyin Q; Xiang, Yong-Bing YB; Zheng, Ying Y; Long, Jirong J; Ye, Chuanzhong C; Gu, Kai K; Shu, Xiao-Ou XO; Gao, Yutang Y; Zheng, Wei W

Publication Date: 2011-05-15

Variant appearance in text: rs1003623

PubMed Link: 21454829

Variant Present in the following documents:

• Main text

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Comprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.

Breast Cancer Research : Bcr

Einarsdóttir, Kristjana K; Rosenberg, Lena U LU; Humphreys, Keith K; Bonnard, Carine C; Palmgren, Juni J; Li, Yuqing Y; Li, Yi Y; Chia, Kee S KS; Liu, Edison T ET; Hall, Per P; Liu, Jianjun J; Wedrén, Sara S

Publication Date: 2006

Variant appearance in text: rs1003623

PubMed Link: 17132159

Variant Present in the following documents:

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Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes.

Bmc Cancer

Allen-Brady, Kristina K; Camp, Nicola J NJ

Publication Date: 2005-08-09

Variant appearance in text: rs1003623

PubMed Link: 16091150

Variant Present in the following documents:

• Main text
• 1471-2407-5-99.pdf

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