Publications:

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Genetic Variants and Their Associations to Type 2 Diabetes Mellitus Complications in the United Arab Emirates.

Frontiers In Endocrinology

ElHajj Chehadeh, Sarah S; Sayed, Noura S NS; Abdelsamad, Hanin S HS; Almahmeed, Wael W; Khandoker, Ahsan H AH; Jelinek, Herbert F HF; Alsafar, Habiba S HS

Publication Date: 2021

Variant appearance in text: rs3024998

PubMed Link: 35069435

Variant Present in the following documents:

• Main text
• fendo-12-751885.pdf

View BVdb publication page

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Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)

Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S

Publication Date: 2021-06

Variant appearance in text: VEGFA: 855+175C>T; rs3024998

PubMed Link: 33503336

Variant Present in the following documents:

• CNR2-4-e1335-s003.xlsx, sheet 2

View BVdb publication page

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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: rs3024998

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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Multilocus genetic risk score for diabetic retinopathy in the Han Chinese population of Taiwan.

Scientific Reports

Liao, Wen-Ling WL; Lin, Jang-Ming JM; Chen, Wen-Lu WL; Hsieh, Ming-Chia MC; Wu, Chia-Ming CM; Chang, Ya-Wen YW; Huang, Yu-Chuen YC; Tsai, Fuu-Jen FJ

Publication Date: 2018-09-28

Variant appearance in text: rs3024998

PubMed Link: 30266984

Variant Present in the following documents:

• 41598_2018_32916_MOESM1_ESM.pdf

View BVdb publication page

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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: rs3024998

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms.

Plos One

Ruggiero, Daniela D; Dalmasso, Cyril C; Nutile, Teresa T; Sorice, Rossella R; Dionisi, Laura L; Aversano, Mario M; Bröet, Philippe P; Leutenegger, Anne-Louise AL; Bourgain, Catherine C; Ciullo, Marina M

Publication Date: 2011-02-09

Variant appearance in text: rs3024998

PubMed Link: 21347390

Variant Present in the following documents:

• Main text
• pone.0016982.pdf

View BVdb publication page

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Large-scale evaluation of candidate genes identifies associations between VEGF polymorphisms and bladder cancer risk.

Plos Genetics

García-Closas, Montserrat M; Malats, Núria N; Real, Francisco X FX; Yeager, Meredith M; Welch, Robert R; Silverman, Debra D; Kogevinas, Manolis M; Dosemeci, Mustafa M; Figueroa, Jonine J; Chatterjee, Nilanjan N; Tardón, Adonina A; Serra, Consol C; Carrato, Alfredo A; García-Closas, Reina R; Murta-Nascimento, Cristiane C; Rothman, Nathaniel N; Chanock, Stephen J SJ

Publication Date: 2007-02-23

Variant appearance in text: rs3024998

PubMed Link: 17319747

Variant Present in the following documents:

• Main text
• pgen.0030029.pdf

View BVdb publication page

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