Publications:

---

Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: rs6058896

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

View BVdb publication page

---

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: rs6058896

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

---

MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine

Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM

Publication Date: 2019-12

Variant appearance in text: rs6058896

PubMed Link: 31637880

Variant Present in the following documents:

• Main text
• CAM4-8-7477.pdf

View BVdb publication page

---

Polymorphisms in maternal folate pathway genes interact with arsenic in drinking water to influence risk of myelomeningocele.

Birth Defects Research. Part A, Clinical And Molecular Teratology

Mazumdar, Maitreyi M; Valeri, Linda L; Rodrigues, Ema G EG; Ibne Hasan, Md Omar Sharif MO; Hamid, Rezina R; Paul, Ligi L; Selhub, Jacob J; Silva, Fareesa F; Mostofa, Md Golam MG; Quamruzzaman, Quazi Q; Rahman, Mahmuder M; Christiani, David C DC

Publication Date: 2015-09

Variant appearance in text: rs6058896

PubMed Link: 26250961

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.

Bmc Medical Genetics

Pangilinan, Faith F; Molloy, Anne M AM; Mills, James L JL; Troendle, James F JF; Parle-McDermott, Anne A; Kay, Denise M DM; Browne, Marilyn L ML; McGrath, Emily C EC; Abaan, Hatice Ozel HO; Sutton, Marie M; Kirke, Peadar N PN; Caggana, Michele M; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC

Publication Date: 2014-10-08

Variant appearance in text: rs6058896

PubMed Link: 25293959

Variant Present in the following documents:

• Main text
• 12881_2014_Article_102.pdf

View BVdb publication page

---

DNMT1 genetic polymorphisms affect breast cancer risk in the central European Caucasian population.

Clinical Epigenetics

Kullmann, Kathrin K; Deryal, Mustafa M; Ong, Mei Fang MF; Schmidt, Werner W; Mahlknecht, Ulrich U

Publication Date: 2013-05-02

Variant appearance in text: rs6058896

PubMed Link: 23638630

Variant Present in the following documents:

• Main text

View BVdb publication page

---

MirSNP, a database of polymorphisms altering miRNA target sites, identifies miRNA-related SNPs in GWAS SNPs and eQTLs.

Bmc Genomics

Liu, Chenxing C; Zhang, Fuquan F; Li, Tingting T; Lu, Ming M; Wang, Lifang L; Yue, Weihua W; Zhang, Dai D

Publication Date: 2012-11-23

Variant appearance in text: rs6058896

PubMed Link: 23173617

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.

Bmc Medical Genetics

Pangilinan, Faith F; Molloy, Anne M AM; Mills, James L JL; Troendle, James F JF; Parle-McDermott, Anne A; Signore, Caroline C; O'Leary, Valerie B VB; Chines, Peter P; Seay, Jessica M JM; Geiler-Samerotte, Kerry K; Mitchell, Adam A; VanderMeer, Julia E JE; Krebs, Kristine M KM; Sanchez, Angelica A; Cornman-Homonoff, Joshua J; Stone, Nicole N; Conley, Mary M; Kirke, Peadar N PN; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC

Publication Date: 2012-08-02

Variant appearance in text: rs6058896

PubMed Link: 22856873

Variant Present in the following documents:

• Main text
• 1471-2350-13-62.pdf

View BVdb publication page

---

Two-stage case-control study of DNMT-1 and DNMT-3B gene variants and breast cancer risk.

Breast Cancer Research And Treatment

Ye, Chuanzhong C; Beeghly-Fadiel, Alicia A; Lu, Wei W; Long, Jirong J; Shu, Xiao Ou XO; Gao, Yu-Tang YT; Zheng, Wei W; Cai, Qiuyin Q

Publication Date: 2010-06

Variant appearance in text: rs6058896

PubMed Link: 19798569

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Genetic variation in healthy oldest-old.

Plos One

Halaschek-Wiener, Julius J; Amirabbasi-Beik, Mahsa M; Monfared, Nasim N; Pieczyk, Markus M; Sailer, Christian C; Kollar, Anita A; Thomas, Ruth R; Agalaridis, Georgios G; Yamada, So S; Oliveira, Lisa L; Collins, Jennifer A JA; Meneilly, Graydon G; Marra, Marco A MA; Madden, Kenneth M KM; Le, Nhu D ND; Connors, Joseph M JM; Brooks-Wilson, Angela R AR

Publication Date: 2009-08-14

Variant appearance in text: rs6058896

PubMed Link: 19680556

Variant Present in the following documents:

• pone.0006641.s001.xls, sheet 1

View BVdb publication page

---