Publications:

---

Identifying the Potential Mechanism of Action of SNPs Associated With Breast Cancer Susceptibility With GVITamIN.

Frontiers In Bioengineering And Biotechnology

Nguyen, An-Phi AP; Nicoletti, Paola P; Arnol, Damien D; Califano, Andrea A; Rodríguez Martínez, María M

Publication Date: 2020

Variant appearance in text: rs10510102

PubMed Link: 32850701

Variant Present in the following documents:

• Main text
• fbioe-08-00798.pdf

View BVdb publication page

---

Evaluation of significant genome-wide association studies risk - SNPs in young breast cancer patients.

Plos One

Rath, Michelle M; Li, Qiyuan Q; Li, Huili H; Lindström, Sara S; Miron, Alexander A; Miron, Penelope P; Dowton, Anne E AE; Meyer, Meghan E ME; Larson, Bryce G BG; Pomerantz, Mark M; Seo, Ji-Heui JH; Collins, Laura C LC; Vardeh, Hilde H; Brachtel, Elena E; Come, Steven E SE; Borges, Virginia V; Schapira, Lidia L; Tamimi, Rulla M RM; Partridge, Ann H AH; Freedman, Matthew M; Ruddy, Kathryn J KJ

Publication Date: 2019

Variant appearance in text: rs10510102

PubMed Link: 31125336

Variant Present in the following documents:

• Main text
• pone.0216997.pdf

View BVdb publication page

---

FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population.

American Journal Of Cancer Research

Xia, Peng P; Li, Bin B; Geng, Tingting T; Deng, Zhiping Z; Dang, Chengxue C; Chang, Dongmin D; Kang, Longli L; Jin, Tianbo T; Chen, Chao C

Publication Date: 2015

Variant appearance in text: rs10510102

PubMed Link: 26175953

Variant Present in the following documents:

• Main text

View BVdb publication page

---

A powerful association test of multiple genetic variants using a random-effects model.

Statistics In Medicine

Cheng, K F KF; Lee, J Y JY; Zheng, W W; Li, C C

Publication Date: 2014-05-20

Variant appearance in text: rs10510102

PubMed Link: 24338936

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Hereditary breast cancer: ever more pieces to the polygenic puzzle.

Hereditary Cancer In Clinical Practice

Bogdanova, Natalia N; Helbig, Sonja S; Dörk, Thilo T

Publication Date: 2013-09-11

Variant appearance in text: rs10510102

PubMed Link: 24025454

Variant Present in the following documents:

• Main text
• 1897-4287-11-12.pdf

View BVdb publication page

---

A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.

Breast Cancer Research : Bcr

Kim, Hyung-cheol HC; Lee, Ji-Young JY; Sung, Hyuna H; Choi, Ji-Yeob JY; Park, Sue K SK; Lee, Kyoung-Mu KM; Kim, Young Jin YJ; Go, Min Jin MJ; Li, Lian L; Cho, Yoon Shin YS; Park, Miey M; Kim, Dong-Joon DJ; Oh, Ji Hee JH; Kim, Jun-Woo JW; Jeon, Jae-Pil JP; Jeon, Soon-Young SY; Min, Haesook H; Kim, Hyo Mi HM; Park, Jaekyung J; Yoo, Keun-Young KY; Noh, Dong-Young DY; Ahn, Sei-Hyun SH; Lee, Min Hyuk MH; Kim, Sung-Won SW; Lee, Jong Won JW; Park, Byeong-Woo BW; Park, Woong-Yang WY; Kim, Eun-Hye EH; Kim, Mi Kyung MK; Han, Wonshik W; Lee, Sang-Ah SA; Matsuo, Keitaro K; Shen, Chen-Yang CY; Wu, Pei-Ei PE; Hsiung, Chia-Ni CN; Lee, Jong-Young JY; Kim, Hyung-Lae HL; Han, Bok-Ghee BG; Kang, Daehee D

Publication Date: 2012-03-27

Variant appearance in text: rs10510102

PubMed Link: 22452962

Variant Present in the following documents:

• Main text
• bcr3158.pdf

View BVdb publication page

---