Publications:

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In silico prioritisation of microRNA-associated common variants in multiple sclerosis.

Human Genomics

Fashina, Ifeolutembi A IA; McCoy, Claire E CE; Furney, Simon J SJ

Publication Date: 2023-03-30

Variant appearance in text: rs1414273

PubMed Link: 36991503

Variant Present in the following documents:

• Main text
• 40246_2023_Article_478.pdf

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Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications

Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C

Publication Date: 2023-03-29

Variant appearance in text: rs1414273

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

View BVdb publication page

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JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research

Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K

Publication Date: 2022-11-21

Variant appearance in text: CD58: 70+10876G>A; rs1414273

PubMed Link: 36409824

Variant Present in the following documents:

• can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: rs1414273

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

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Implication of genetic variants in primary microRNA processing sites in the risk of multiple sclerosis.

Ebiomedicine

Hecker, Michael M; Fitzner, Brit B; Putscher, Elena E; Schwartz, Margit M; Winkelmann, Alexander A; Meister, Stefanie S; Dudesek, Ales A; Koczan, Dirk D; Lorenz, Peter P; Boxberger, Nina N; Zettl, Uwe Klaus UK

Publication Date: 2022-06

Variant appearance in text: rs1414273

PubMed Link: 35561450

Variant Present in the following documents:

• Main text
• main.pdf

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MicroRNA Variants and HLA-miRNA Interactions are Novel Rheumatoid Arthritis Susceptibility Factors.

Frontiers In Genetics

Guo, Shicheng S; Jin, Yehua Y; Zhou, Jieru J; Zhu, Qi Q; Jiang, Ting T; Bian, Yanqin Y; Zhang, Runrun R; Chang, Cen C; Xu, Lingxia L; Shen, Jie J; Zheng, Xinchun X; Shen, Yi Y; Qin, Yingying Y; Chen, Jihong J; Tang, Xiaorong X; Cheng, Peng P; Ding, Qin Q; Zhang, Yuanyuan Y; Liu, Jia J; Cheng, Qingqing Q; Guo, Mengru M; Liu, Zhaoyi Z; Qiu, Weifang W; Qian, Yi Y; Sun, Yang Y; Shen, Yu Y; Nie, Hong H; Schrodi, Steven J SJ; He, Dongyi D

Publication Date: 2021

Variant appearance in text: rs1414273

PubMed Link: 34777472

Variant Present in the following documents:

• Main text
• fgene-12-747274.pdf

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CD58 Immunobiology at a Glance.

Frontiers In Immunology

Zhang, Yalu Y; Liu, Qiaofei Q; Yang, Sen S; Liao, Quan Q

Publication Date: 2021

Variant appearance in text: rs1414273

PubMed Link: 34168659

Variant Present in the following documents:

• Main text
• fimmu-12-705260.pdf

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Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports

Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R

Publication Date: 2020-04-30

Variant appearance in text: rs1414273

PubMed Link: 32355262

Variant Present in the following documents:

• Main text
• 41598_2020_64432_MOESM1_ESM.pdf
• 41598_2020_Article_64432.pdf

View BVdb publication page

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Reworking GWAS Data to Understand the Role of Nongenetic Factors in MS Etiopathogenesis.

Genes

Mechelli, Rosella R; Umeton, Renato R; Manfrè, Grazia G; Romano, Silvia S; Buscarinu, Maria Chiara MC; Rinaldi, Virginia V; Bellucci, Gianmarco G; Bigi, Rachele R; Ferraldeschi, Michela M; Salvetti, Marco M; Ristori, Giovanni G

Publication Date: 2020-01-14

Variant appearance in text: rs1414273

PubMed Link: 31947683

Variant Present in the following documents:

• Main text
• genes-11-00097.pdf

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A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.

Plos Genetics

Hecker, Michael M; Boxberger, Nina N; Illner, Nicole N; Fitzner, Brit B; Schröder, Ina I; Winkelmann, Alexander A; Dudesek, Ales A; Meister, Stefanie S; Koczan, Dirk D; Lorenz, Peter P; Thiesen, Hans-Jürgen HJ; Zettl, Uwe Klaus UK

Publication Date: 2019-02

Variant appearance in text: rs1414273

PubMed Link: 30730892

Variant Present in the following documents:

• Main text
• pgen.1007961.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: CD58: 70+10876G>A; rs1414273

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

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: rs1414273

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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A genome-wide association study identifies six novel risk loci for primary biliary cholangitis.

Nature Communications

Qiu, Fang F; Tang, Ruqi R; Zuo, Xianbo X; Shi, Xingjuan X; Wei, Yiran Y; Zheng, Xiaodong X; Dai, Yaping Y; Gong, Yuhua Y; Wang, Lan L; Xu, Ping P; Zhu, Xiang X; Wu, Jian J; Han, Chongxu C; Gao, Yueqiu Y; Zhang, Kui K; Jiang, Yuzhang Y; Zhou, Jianbo J; Shao, Youlin Y; Hu, Zhigang Z; Tian, Ye Y; Zhang, Haiyan H; Dai, Na N; Liu, Lei L; Wu, Xudong X; Zhao, Weifeng W; Zhang, Xiaomin X; Zang, Zhidong Z; Nie, Jinshan J; Sun, Weihao W; Zhao, Yi Y; Mao, Yuan Y; Jiang, Po P; Ji, Hualiang H; Dong, Qing Q; Li, Junming J; Li, Zhenzhong Z; Bai, Xinli X; Li, Li L; Lin, Maosong M; Dong, Ming M; Li, Jinxin J; Zhu, Ping P; Wang, Chan C; Zhang, Yanqiu Y; Jiang, Peng P; Wang, Yujue Y; Jawed, Rohil R; Xu, Jing J; Zhang, Yu Y; Wang, Qixia Q; Yang, Yue Y; Yang, Fan F; Lian, Min M; Jiang, Xiang X; Xiao, Xiao X; Li, Yanmei Y; Fang, Jingyuan J; Qiu, Dekai D; Zhu, Zhen Z; Qiu, Hong H; Zhang, Jianqiong J; Tian, Wenyan W; Chen, Sufang S; Jiang, Ling L; Ji, Bing B; Li, Ping P; Chen, Guochang G; Wu, Tianxue T; Sun, Yan Y; Yu, Jianjiang J; Tang, Huijun H; He, Michun M; Xia, Min M; Pei, Hao H; Huang, Lihua L; Qing, Zhuye Z; Wu, Jianfang J; Huang, Qinghai Q; Han, Junhai J; Xie, Wei W; Sun, Zhongsheng Z; Guo, Jian J; He, Gengsheng G; Eric Gershwin, M M; Lian, Zhexiong Z; Liu, Xiang X; Seldin, Michael F MF; Liu, Xiangdong X; Chen, Weichang W; Ma, Xiong X

Publication Date: 2017-04-20

Variant appearance in text: rs1414273

PubMed Link: 28425483

Variant Present in the following documents:

• ncomms14828-s1.pdf

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