Publications:

Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans.

Scientific Reports

Nakatsuka, Nathan N; Patterson, Nick N; Patsopoulos, Nikolaos A NA; Altemose, Nicolas N; Tandon, Arti A; Beecham, Ashley H AH; McCauley, Jacob L JL; Isobe, Noriko N; Hauser, Stephen S; De Jager, Philip L PL; Hafler, David A DA; Oksenberg, Jorge R JR; Reich, David D

Publication Date: 2020-10-09

Variant appearance in text: rs6681271

PubMed Link: 33037294

Variant Present in the following documents:

• Main text
• 41598_2020_Article_74035.pdf

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Transcript specific regulation of expression influences susceptibility to multiple sclerosis.

European Journal Of Human Genetics : Ejhg

Ban, Maria M; Liao, Wenjia W; Baker, Amie A; Compston, Alastair A; Thorpe, John J; Molyneux, Paul P; Fraser, Mary M; Khadake, Jyoti J; Jones, Joanne J; Coles, Alasdair A; Sawcer, Stephen S

Publication Date: 2020-06

Variant appearance in text: rs6681271

PubMed Link: 31932686

Variant Present in the following documents:

• Main text

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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: FCRL3: 844+286A>G; rs6681271

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1

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A refined study of FCRL genes from a genome-wide association study for Graves' disease.

Plos One

Zhao, Shuang-Xia SX; Liu, Wei W; Zhan, Ming M; Song, Zhi-Yi ZY; Yang, Shao-Ying SY; Xue, Li-Qiong LQ; Pan, Chun-Ming CM; Gu, Zhao-Hui ZH; Liu, Bing-Li BL; Wang, Hai-Ning HN; Liang, Liming L; Liang, Jun J; Zhang, Xiao-Mei XM; Yuan, Guo-Yue GY; Li, Chang-Gui CG; Chen, Ming-Dao MD; Chen, Jia-Lun JL; Gao, Guan-Qi GQ; Song, Huai-Dong HD; ,

Publication Date: 2013

Variant appearance in text: rs6681271

PubMed Link: 23505439

Variant Present in the following documents:

• Main text
• pone.0057758.pdf

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