FCRL3 c.52+204G>T

Variant ID: 1-157669278-C-A

NM_052939.3(FCRL3):c.52+204G>T

This variant was identified in 38 publications

View GRCh38 version.




Publications:


Identification of multiple novel susceptibility genes associated with autoimmune thyroid disease.

Frontiers In Immunology
Liu, Xueying X; Miao, Yahu Y; Liu, Chao C; Lu, Wan W; Feng, Qing Q; Zhang, Qiu Q
Publication Date: 2023

Variant appearance in text: rs3761959
PubMed Link: 37197658
Variant Present in the following documents:
  • Main text
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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs3761959
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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The longitudinal loss of islet autoantibody responses from diagnosis of type 1 diabetes occurs progressively over follow-up and is determined by low autoantibody titres, early-onset, and genetic variants.

Clinical And Experimental Immunology
Williams, C L CL; Fareed, R R; Mortimer, G L M GLM; Aitken, R J RJ; Wilson, I V IV; George, G G; Gillespie, K M KM; Williams, A J K AJK; , ; Long, A E AE
Publication Date: 2022-10-01

Variant appearance in text: rs3761959
PubMed Link: 36181724
Variant Present in the following documents:
  • Main text
  • uxac087.pdf
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Genetics behind Cerebral Disease with Ocular Comorbidity: Finding Parallels between the Brain and Eye Molecular Pathology.

International Journal Of Molecular Sciences
Chang, Kao-Jung KJ; Wu, Hsin-Yu HY; Yarmishyn, Aliaksandr A AA; Li, Cheng-Yi CY; Hsiao, Yu-Jer YJ; Chi, Yi-Chun YC; Lo, Tzu-Chen TC; Dai, He-Jhen HJ; Yang, Yi-Chiang YC; Liu, Ding-Hao DH; Hwang, De-Kuang DK; Chen, Shih-Jen SJ; Hsu, Chih-Chien CC; Kao, Chung-Lan CL
Publication Date: 2022-08-26

Variant appearance in text: rs3761959
PubMed Link: 36077104
Variant Present in the following documents:
  • ijms-23-09707.pdf
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Natural Killer cells demonstrate distinct eQTL and transcriptome-wide disease associations, highlighting their role in autoimmunity.

Nature Communications
Gilchrist, James J JJ; Makino, Seiko S; Naranbhai, Vivek V; Sharma, Piyush K PK; Koturan, Surya S; Tong, Orion O; Taylor, Chelsea A CA; Watson, Robert A RA; de Los Aires, Alba Verge AV; Cooper, Rosalin R; Lau, Evelyn E; Danielli, Sara S; Hameiri-Bowen, Dan D; Lee, Wanseon W; Ng, Esther E; Whalley, Justin J; Knight, Julian C JC; Fairfax, Benjamin P BP
Publication Date: 2022-07-14

Variant appearance in text: rs3761959
PubMed Link: 35835762
Variant Present in the following documents:
  • Main text
  • 41467_2022_Article_31626.pdf
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A Comprehensive Review on the Role of Genetic Factors in Neuromyelitis Optica Spectrum Disorder.

Frontiers In Immunology
Ghafouri-Fard, Soudeh S; Azimi, Tahereh T; Taheri, Mohammad M
Publication Date: 2021

Variant appearance in text: rs3761959
PubMed Link: 34675927
Variant Present in the following documents:
  • Main text
  • fimmu-12-737673.pdf
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Fc receptor-like 1, 3, and 6 variants are associated with rheumatoid arthritis risk in the Chinese Han population.

Genes And Environment : The Official Journal Of The Japanese Environmental Mutagen Society
Yang, Yonghui Y; Li, Dandan D; He, Chunjuan C; Peng, Linna L; Xing, Shishi S; Bai, Mei M; Rong, Hao H; Yuan, Dongya D; He, Yongjun Y; He, Xue X; Wang, Li L; Jin, Tianbo T
Publication Date: 2021-10-07

Variant appearance in text: rs3761959
PubMed Link: 34620245
Variant Present in the following documents:
  • Main text
  • 41021_2021_Article_213.pdf
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Characterization of Rheumatoid Arthritis Risk-Associated SNPs and Identification of Novel Therapeutic Sites Using an In-Silico Approach.

Biology
Akhtar, Mehran M; Ali, Yasir Y; Islam, Zia-Ul ZU; Arshad, Maria M; Rauf, Mamoona M; Ali, Muhammad M; Maodaa, Saleh N SN; Al-Farraj, Saleh A SA; El-Serehy, Hamed A HA; Jalil, Fazal F
Publication Date: 2021-06-04

Variant appearance in text: rs3761959
PubMed Link: 34199962
Variant Present in the following documents:
  • Main text
  • biology-10-00501.pdf
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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs3761959
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
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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: rs3761959
PubMed Link: 33037294
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_74035.pdf
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Dysregulated Antibody, Natural Killer Cell and Immune Mediator Profiles in Autoimmune Thyroid Diseases.

Cells
Martin, Tiphaine C TC; Ilieva, Kristina M KM; Visconti, Alessia A; Beaumont, Michelle M; Kiddle, Steven J SJ; Dobson, Richard J B RJB; Mangino, Massimo M; Lim, Ee Mun EM; Pezer, Marija M; Steves, Claire J CJ; Bell, Jordana T JT; Wilson, Scott G SG; Lauc, Gordan G; Roederer, Mario M; Walsh, John P JP; Spector, Tim D TD; Karagiannis, Sophia N SN
Publication Date: 2020-03-09

Variant appearance in text: rs3761959
PubMed Link: 32182948
Variant Present in the following documents:
  • Main text
  • cells-09-00665.pdf
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Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

Physiological Genomics
Shepard, C Joy CJ; Cline, Sara G SG; Hinds, David D; Jahanbakhsh, Seyedehameneh S; Prokop, Jeremy W JW
Publication Date: 2019-11-01

Variant appearance in text: rs3761959
PubMed Link: 31482761
Variant Present in the following documents:
  • Main text
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Single Nucleotide Polymorphisms of FCRL3 in Iranian Patients with Behcet's Disease.

Iranian Journal Of Public Health
Shahram, Farhad F; Kazemi, Javad J; Mahmoudi, Mahmoud M; Jadali, Zohreh Z
Publication Date: 2019-06

Variant appearance in text: rs3761959
PubMed Link: 31341856
Variant Present in the following documents:
  • Main text
  • IJPH-48-1133.pdf
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Fc receptor-like 3 (-169T>C) polymorphism increases the risk of tendinopathy in volleyball athletes: a case control study.

Bmc Medical Genetics
Salles, José Inácio JI; Lopes, Lucas Rafael LR; Duarte, Maria Eugenia Leite MEL; Morrissey, Dylan D; Martins, Marilena Bezerra MB; Machado, Daniel Escorsim DE; Guimarães, João Antonio Matheus JAM; Perini, Jamila Alessandra JA
Publication Date: 2018-07-18

Variant appearance in text: rs3761959
PubMed Link: 30021560
Variant Present in the following documents:
  • 12881_2018_Article_633.pdf
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Association of Optic Neuritis with CYP4F2 Gene Single Nucleotide Polymorphism and IL-17A Concentration.

Journal Of Ophthalmology
Banevicius, Mantas M; Vilkeviciute, Alvita A; Glebauskiene, Brigita B; Kriauciuniene, Loresa L; Liutkeviciene, Rasa R
Publication Date: 2018

Variant appearance in text: rs3761959
PubMed Link: 29736281
Variant Present in the following documents:
  • Main text
  • JOPH2018-1686297.pdf
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Inflammation-Related Gene Polymorphisms Associated With Primary Immune Thrombocytopenia.

Frontiers In Immunology
Li, Ju J; Ma, Sai S; Shao, Linlin L; Ma, Chunhong C; Gao, Chengjiang C; Zhang, Xiao-Hui XH; Hou, Ming M; Peng, Jun J
Publication Date: 2017

Variant appearance in text: rs3761959
PubMed Link: 28702029
Variant Present in the following documents:
  • Main text
  • fimmu-08-00744.pdf
View BVdb publication page



Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.

Bmc Genomics
Khong, Jwu Jin JJ; Burdon, Kathryn P KP; Lu, Yi Y; Laurie, Kate K; Leonardos, Lefta L; Baird, Paul N PN; Sahebjada, Srujana S; Walsh, John P JP; Gajdatsy, Adam A; Ebeling, Peter R PR; Hamblin, Peter Shane PS; Wong, Rosemary R; Forehan, Simon P SP; Fourlanos, Spiros S; Roberts, Anthony P AP; Doogue, Matthew M; Selva, Dinesh D; Montgomery, Grant W GW; Macgregor, Stuart S; Craig, Jamie E JE
Publication Date: 2016-11-18

Variant appearance in text: rs3761959
PubMed Link: 27863461
Variant Present in the following documents:
  • Main text
  • 12864_2016_Article_3276.pdf
View BVdb publication page



Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.

Multiple Sclerosis (Houndmills, Basingstoke, England)
Wang, Yunpeng Y; Bos, Steffan D SD; Harbo, Hanne F HF; Thompson, Wesley K WK; Schork, Andrew J AJ; Bettella, Francesco F; Witoelar, Aree A; Lie, Benedicte A BA; Li, Wen W; McEvoy, Linda K LK; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; Andreassen, Ole A OA
Publication Date: 2016-12

Variant appearance in text: rs3761959
PubMed Link: 26920376
Variant Present in the following documents:
  • Main text
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Genetic associations of FCRL3 polymorphisms with the susceptibility of Graves ophthalmopathy in a Chinese population.

International Journal Of Clinical And Experimental Medicine
Wu, Shanshan S; Cai, Ting T; Chen, Feng F; He, Xuefei X; Cui, Zhihua Z
Publication Date: 2015

Variant appearance in text: rs3761959
PubMed Link: 26629249
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population.

Medicine
Lan, Wenjing W; Fang, Shaokuan S; Zhang, Huimao H; Wang, Dan Tong Jianmeng DTJ; Wu, Jiang J
Publication Date: 2015-09

Variant appearance in text: rs3761959
PubMed Link: 26402798
Variant Present in the following documents:
  • Main text
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Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk: An Independent Study in Han Chinese.

Medicine
Zhang, Haiyan H; Zhang, Zhen Z; Li, Guang G; Wang, Surong S; Zhang, Shiqian S; Xie, Beibei B
Publication Date: 2015-09

Variant appearance in text: rs3761959
PubMed Link: 26334889
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes.

Diabetes
Brorsson, Caroline A CA; Onengut, Suna S; Chen, Wei-Min WM; Wenzlau, Janet J; Yu, Liping L; Baker, Peter P; Williams, Alistair J K AJ; Bingley, Polly J PJ; Hutton, John C JC; Eisenbarth, George S GS; Concannon, Patrick P; Rich, Stephen S SS; Pociot, Flemming F; ,
Publication Date: 2015-08

Variant appearance in text: rs3761959
PubMed Link: 25829454
Variant Present in the following documents:
  • Main text
View BVdb publication page



FCRL3 gene polymorphisms confer autoimmunity risk for allergic rhinitis in a Chinese Han population.

Plos One
Gu, Zheng Z; Hong, Su-Ling SL; Ke, Xia X; Shen, Yang Y; Wang, Xiao-Qiang XQ; Hu, Di D; Hu, Guo-Hua GH; Kang, Hou-Yong HY
Publication Date: 2015

Variant appearance in text: rs3761959
PubMed Link: 25594855
Variant Present in the following documents:
  • Main text
  • pone.0116419.pdf
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A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis.

Arthritis Research & Therapy
van Steenbergen, Hanna W HW; Rodríguez-Rodríguez, Luis L; Berglin, Ewa E; Zhernakova, Alexandra A; Knevel, Rachel R; Ivorra-Cortés, Jose J; Huizinga, Tom W J TW; Fernández-Gutiérrez, Benjamin B; Gregersen, Peter K PK; Rantapää-Dahlqvist, Solbritt S; van der Helm-van Mil, Annette H M AH
Publication Date: 2015-01-08

Variant appearance in text: rs3761959
PubMed Link: 25566937
Variant Present in the following documents:
  • Main text
View BVdb publication page



Replication of association of nine susceptibility loci with Graves' disease in the Chinese Han population.

International Journal Of Clinical And Experimental Medicine
Du, Wenhua W; Liang, Cuige C; Che, Fengyuan F; Liu, Xiaomeng X; Pan, Chunming C; Zhao, Shuangxia S; Dong, Qingyu Q; Li, Wenxia W; Wang, Yueli Y; Pan, Zhenyu Z; Gong, Qian Q; Li, Lanxia L; Song, Huaidong H; Gao, Guanqi G
Publication Date: 2014

Variant appearance in text: rs3761959
PubMed Link: 25550959
Variant Present in the following documents:
  • Main text
View BVdb publication page



Heritability and genomics of gene expression in peripheral blood.

Nature Genetics
Wright, Fred A FA; Sullivan, Patrick F PF; Brooks, Andrew I AI; Zou, Fei F; Sun, Wei W; Xia, Kai K; Madar, Vered V; Jansen, Rick R; Chung, Wonil W; Zhou, Yi-Hui YH; Abdellaoui, Abdel A; Batista, Sandra S; Butler, Casey C; Chen, Guanhua G; Chen, Ting-Huei TH; D'Ambrosio, David D; Gallins, Paul P; Ha, Min Jin MJ; Hottenga, Jouke Jan JJ; Huang, Shunping S; Kattenberg, Mathijs M; Kochar, Jaspreet J; Middeldorp, Christel M CM; Qu, Ani A; Shabalin, Andrey A; Tischfield, Jay J; Todd, Laura L; Tzeng, Jung-Ying JY; van Grootheest, Gerard G; Vink, Jacqueline M JM; Wang, Qi Q; Wang, Wei W; Wang, Weibo W; Willemsen, Gonneke G; Smit, Johannes H JH; de Geus, Eco J EJ; Yin, Zhaoyu Z; Penninx, Brenda W J H BW; Boomsma, Dorret I DI
Publication Date: 2014-05

Variant appearance in text: rs3761959
PubMed Link: 24728292
Variant Present in the following documents:
  • NIHMS576016-supplement-1.pdf
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The new perspectives on genetic studies of type 2 diabetes and thyroid diseases.

Current Genomics
Xu, Min M; Bi, Yufang Y; Cui, Bin B; Hong, Jie J; Wang, Weiqing W; Ning, Guang G
Publication Date: 2013-03

Variant appearance in text: rs3761959
PubMed Link: 23997649
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs3761959
PubMed Link: 23505439
Variant Present in the following documents:
  • Main text
View BVdb publication page



Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.

Plos One
Ragnedda, Giammario G; Disanto, Giulio G; Giovannoni, Gavin G; Ebers, George C GC; Sotgiu, Stefano S; Ramagopalan, Sreeram V SV
Publication Date: 2012

Variant appearance in text: rs3761959
PubMed Link: 23094030
Variant Present in the following documents:
  • Main text
  • pone.0046730.pdf
View BVdb publication page



The genetic basis of graves' disease.

Current Genomics
Płoski, Rafał R; Szymański, Konrad K; Bednarczuk, Tomasz T
Publication Date: 2011-12

Variant appearance in text: rs3761959
PubMed Link: 22654555
Variant Present in the following documents:
  • Main text
View BVdb publication page



Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians.

Plos One
Prasad, Pushplata P; Kumar, Ashok A; Gupta, Rajiva R; Juyal, Ramesh C RC; Thelma, B K BK
Publication Date: 2012

Variant appearance in text: rs3761959
PubMed Link: 22355377
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic factors of autoimmune thyroid diseases in Japanese.

Autoimmune Diseases
Ban, Yoshiyuki Y
Publication Date: 2012

Variant appearance in text: rs3761959
PubMed Link: 22242199
Variant Present in the following documents:
  • Main text
  • AD2012-236981.pdf
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Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.

Clinical Endocrinology
Simmonds, Matthew J MJ; Brand, Oliver J OJ; Barrett, Jeffrey C JC; Newby, Paul R PR; Franklyn, Jayne A JA; Gough, Stephen C L SC
Publication Date: 2010-11

Variant appearance in text: rs3761959
PubMed Link: 20626413
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.

Nature Genetics
Stahl, Eli A EA; Raychaudhuri, Soumya S; Remmers, Elaine F EF; Xie, Gang G; Eyre, Stephen S; Thomson, Brian P BP; Li, Yonghong Y; Kurreeman, Fina A S FA; Zhernakova, Alexandra A; Hinks, Anne A; Guiducci, Candace C; Chen, Robert R; Alfredsson, Lars L; Amos, Christopher I CI; Ardlie, Kristin G KG; , ; Barton, Anne A; Bowes, John J; Brouwer, Elisabeth E; Burtt, Noel P NP; Catanese, Joseph J JJ; Coblyn, Jonathan J; Coenen, Marieke J H MJ; Costenbader, Karen H KH; Criswell, Lindsey A LA; Crusius, J Bart A JB; Cui, Jing J; de Bakker, Paul I W PI; De Jager, Philip L PL; Ding, Bo B; Emery, Paul P; Flynn, Edward E; Harrison, Pille P; Hocking, Lynne J LJ; Huizinga, Tom W J TW; Kastner, Daniel L DL; Ke, Xiayi X; Lee, Annette T AT; Liu, Xiangdong X; Martin, Paul P; Morgan, Ann W AW; Padyukov, Leonid L; Posthumus, Marcel D MD; Radstake, Timothy R D J TR; Reid, David M DM; Seielstad, Mark M; Seldin, Michael F MF; Shadick, Nancy A NA; Steer, Sophia S; Tak, Paul P PP; Thomson, Wendy W; van der Helm-van Mil, Annette H M AH; van der Horst-Bruinsma, Irene E IE; van der Schoot, C Ellen CE; van Riel, Piet L C M PL; Weinblatt, Michael E ME; Wilson, Anthony G AG; Wolbink, Gert Jan GJ; Wordsworth, B Paul BP; , ; Wijmenga, Cisca C; Karlson, Elizabeth W EW; Toes, Rene E M RE; de Vries, Niek N; Begovich, Ann B AB; Worthington, Jane J; Siminovitch, Katherine A KA; Gregersen, Peter K PK; Klareskog, Lars L; Plenge, Robert M RM
Publication Date: 2010-06

Variant appearance in text: rs3761959
PubMed Link: 20453842
Variant Present in the following documents:
  • Main text
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Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.

Molecular Vision
Li, Ke K; Yang, Peizeng P; Zhao, Min M; Hou, Shengping S; Du, Liping L; Zhou, Hongyan H; Kijlstra, Aize A
Publication Date: 2009-05-11

Variant appearance in text: rs3761959
PubMed Link: 19452015
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations.

Molecular Vision
Li, Ke K; Zhao, Min M; Hou, Shengping S; Du, Liping L; Kijlstra, Aize A; Yang, Peizeng P
Publication Date: 2008

Variant appearance in text: rs3761959
PubMed Link: 19050767
Variant Present in the following documents:
  • Main text
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

Nature Genetics
, ; , ; Burton, Paul R PR; Clayton, David G DG; Cardon, Lon R LR; Craddock, Nick N; Deloukas, Panos P; Duncanson, Audrey A; Kwiatkowski, Dominic P DP; McCarthy, Mark I MI; Ouwehand, Willem H WH; Samani, Nilesh J NJ; Todd, John A JA; Donnelly, Peter P; Barrett, Jeffrey C JC; Davison, Dan D; Easton, Doug D; Evans, David M DM; Leung, Hin-Tak HT; Marchini, Jonathan L JL; Morris, Andrew P AP; Spencer, Chris C A CC; Tobin, Martin D MD; Attwood, Antony P AP; Boorman, James P JP; Cant, Barbara B; Everson, Ursula U; Hussey, Judith M JM; Jolley, Jennifer D JD; Knight, Alexandra S AS; Koch, Kerstin K; Meech, Elizabeth E; Nutland, Sarah S; Prowse, Christopher V CV; Stevens, Helen E HE; Taylor, Niall C NC; Walters, Graham R GR; Walker, Neil M NM; Watkins, Nicholas A NA; Winzer, Thilo T; Jones, Richard W RW; McArdle, Wendy L WL; Ring, Susan M SM; Strachan, David P DP; Pembrey, Marcus M; Breen, Gerome G; St Clair, David D; Caesar, Sian S; Gordon-Smith, Katharine K; Jones, Lisa L; Fraser, Christine C; Green, Elaine K EK; Grozeva, Detelina D; Hamshere, Marian L ML; Holmans, Peter A PA; Jones, Ian R IR; Kirov, George G; Moskivina, Valentina V; Nikolov, Ivan I; O'Donovan, Michael C MC; Owen, Michael J MJ; Collier, David A DA; Elkin, Amanda A; Farmer, Anne A; Williamson, Richard R; McGuffin, Peter P; Young, Allan H AH; Ferrier, I Nicol IN; Ball, Stephen G SG; Balmforth, Anthony J AJ; Barrett, Jennifer H JH; Bishop, Timothy D TD; Iles, Mark M MM; Maqbool, Azhar A; Yuldasheva, Nadira N; Hall, Alistair S AS; Braund, Peter S PS; Dixon, Richard J RJ; Mangino, Massimo M; Stevens, Suzanne S; Thompson, John R JR; Bredin, Francesca F; Tremelling, Mark M; Parkes, Miles M; Drummond, Hazel H; Lees, Charles W CW; Nimmo, Elaine R ER; Satsangi, Jack J; Fisher, Sheila A SA; Forbes, Alastair A; Lewis, Cathryn M CM; Onnie, Clive M CM; Prescott, Natalie J NJ; Sanderson, Jeremy J; Matthew, Christopher G CG; Barbour, Jamie J; Mohiuddin, M Khalid MK; Todhunter, Catherine E CE; Mansfield, John C JC; Ahmad, Tariq T; Cummings, Fraser R FR; Jewell, Derek P DP; Webster, John J; Brown, Morris J MJ; Lathrop, Mark G MG; Connell, John J; Dominiczak, Anna A; Marcano, Carolina A Braga CA; Burke, Beverley B; Dobson, Richard R; Gungadoo, Johannie J; Lee, Kate L KL; Munroe, Patricia B PB; Newhouse, Stephen J SJ; Onipinla, Abiodun A; Wallace, Chris C; Xue, Mingzhan M; Caulfield, Mark M; Farrall, Martin M; Barton, Anne A; , ; Bruce, Ian N IN; Donovan, Hannah H; Eyre, Steve S; Gilbert, Paul D PD; Hilder, Samantha L SL; Hinks, Anne M AM; John, Sally L SL; Potter, Catherine C; Silman, Alan J AJ; Symmons, Deborah P M DP; Thomson, Wendy W; Worthington, Jane J; Dunger, David B DB; Widmer, Barry B; Frayling, Timothy M TM; Freathy, Rachel M RM; Lango, Hana H; Perry, John R B JR; Shields, Beverley M BM; Weedon, Michael N MN; Hattersley, Andrew T AT; Hitman, Graham A GA; Walker, Mark M; Elliott, Kate S KS; Groves, Christopher J CJ; Lindgren, Cecilia M CM; Rayner, Nigel W NW; Timpson, Nicolas J NJ; Zeggini, Eleftheria E; Newport, Melanie M; Sirugo, Giorgio G; Lyons, Emily E; Vannberg, Fredrik F; Hill, Adrian V S AV; Bradbury, Linda A LA; Farrar, Claire C; Pointon, Jennifer J JJ; Wordsworth, Paul P; Brown, Matthew A MA; Franklyn, Jayne A JA; Heward, Joanne M JM; Simmonds, Matthew J MJ; Gough, Stephen C L SC; Seal, Sheila S; , ; Stratton, Michael R MR; Rahman, Nazneen N; Ban, Maria M; Goris, An A; Sawcer, Stephen J SJ; Compston, Alastair A; Conway, David D; Jallow, Muminatou M; Newport, Melanie M; Sirugo, Giorgio G; Rockett, Kirk A KA; Bumpstead, Suzannah J SJ; Chaney, Amy A; Downes, Kate K; Ghori, Mohammed J R MJ; Gwilliam, Rhian R; Hunt, Sarah E SE; Inouye, Michael M; Keniry, Andrew A; King, Emma E; McGinnis, Ralph R; Potter, Simon S; Ravindrarajah, Rathi R; Whittaker, Pamela P; Widden, Claire C; Withers, David D; Cardin, Niall J NJ; Davison, Dan D; Ferreira, Teresa T; Pereira-Gale, Joanne J; Hallgrimsdo'ttir, Ingeleif B IB; Howie, Bryan N BN; Su, Zhan Z; Teo, Yik Ying YY; Vukcevic, Damjan D; Bentley, David D; Brown, Matthew A MA; Compston, Alastair A; Farrall, Martin M; Hall, Alistair S AS; Hattersley, Andrew T AT; Hill, Adrian V S AV; Parkes, Miles M; Pembrey, Marcus M; Stratton, Michael R MR; Mitchell, Sarah L SL; Newby, Paul R PR; Brand, Oliver J OJ; Carr-Smith, Jackie J; Pearce, Simon H S SH; McGinnis, R R; Keniry, A A; Deloukas, P P; Reveille, John D JD; Zhou, Xiaodong X; Sims, Anne-Marie AM; Dowling, Alison A; Taylor, Jacqueline J; Doan, Tracy T; Davis, John C JC; Savage, Laurie L; Ward, Michael M MM; Learch, Thomas L TL; Weisman, Michael H MH; Brown, Mathew M
Publication Date: 2007-11

Variant appearance in text: rs3761959
PubMed Link: 17952073
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?

Arthritis Research & Therapy
Eyre, Stephen S; Bowes, John J; Potter, Catherine C; Worthington, Jane J; Barton, Anne A
Publication Date: 2006

Variant appearance in text: rs3761959
PubMed Link: 16859508
Variant Present in the following documents:
  • Main text
  • ar2006.pdf
View BVdb publication page