Quiat D, Kim S, Zhang Q, Morton S, Pereira A, DePalma S
Proc Natl Acad Sci U S A. 2022; 119(21):e2203928119.
PMID: 35584116
PMC: 9173816.
DOI: 10.1073/pnas.2203928119.
Makinde F, Tchamga M, Jafali J, Fatumo S, Chimusa E, Mulder N
Brief Bioinform. 2021; 22(6).
PMID: 34415019
PMC: 8575034.
DOI: 10.1093/bib/bbab324.
Shao S, Niu Y, Zhang X, Kong R, Wang J, Liu L
Sci Rep. 2016; 6:30454.
PMID: 27464509
PMC: 4964335.
DOI: 10.1038/srep30454.
Liu Y, Dai X, Wu W, Yuan F, Gu X, Chen J
Mol Neurobiol. 2016; 54(3):2189-2200.
PMID: 26941099
DOI: 10.1007/s12035-016-9810-9.
Zhao C, Fan Y, Huang J, Zhang H, Gao T, Wang C
Allergy Asthma Immunol Res. 2015; 7(2):175-85.
PMID: 25729625
PMC: 4341339.
DOI: 10.4168/aair.2015.7.2.175.
Alzheimer's disease and HLA-A2: linking neurodegenerative to immune processes through an in silico approach.
Cifuentes R, Murillo-Rojas J
Biomed Res Int. 2014; 2014:791238.
PMID: 25197660
PMC: 4150521.
DOI: 10.1155/2014/791238.
A genetic variant rs1801274 in FCGR2A as a potential risk marker for Kawasaki disease: a case-control study and meta-analysis.
Duan J, Lou J, Zhang Q, Ke J, Qi Y, Shen N
PLoS One. 2014; 9(8):e103329.
PMID: 25093412
PMC: 4122468.
DOI: 10.1371/journal.pone.0103329.
Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis.
Cai B, Zhang T, Zhong R, Zou L, Zhu B, Chen W
PLoS One. 2014; 9(3):e89609.
PMID: 24595101
PMC: 3942359.
DOI: 10.1371/journal.pone.0089609.
8p22-23-rs2254546 as a susceptibility locus for Kawasaki disease: a case-control study and a meta-analysis.
Wang W, Lou J, Lu X, Qi Y, Shen N, Zhong R
Sci Rep. 2014; 4:4247.
PMID: 24577620
PMC: 3937782.
DOI: 10.1038/srep04247.
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.
Tran C, Gagnon F, Wigg K, Feng Y, Gomez L, Cate-Carter T
Am J Med Genet B Neuropsychiatr Genet. 2013; 162B(2):146-56.
PMID: 23341075
PMC: 5381964.
DOI: 10.1002/ajmg.b.32123.
Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia.
Zhong R, Yang B, Tang H, Zou L, Song R, Zhu L
Mol Neurobiol. 2012; 47(1):435-42.
PMID: 23229871
DOI: 10.1007/s12035-012-8381-7.
A functional polymorphism, rs28493229, in ITPKC and risk of Kawasaki disease: an integrated meta-analysis.
Lou J, Xu S, Zou L, Zhong R, Zhang T, Sun Y
Mol Biol Rep. 2012; 39(12):11137-44.
PMID: 23065250
DOI: 10.1007/s11033-012-2022-0.
An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders.
Song R, Zou L, Zhong R, Zheng X, Zhu B, Chen W
PLoS One. 2011; 6(9):e25603.
PMID: 21980499
PMC: 3183057.
DOI: 10.1371/journal.pone.0025603.
Evaluation of genetic association between an ITGAM non-synonymous SNP (rs1143679) and multiple autoimmune diseases.
Anaya J, Kim-Howard X, Prahalad S, Chernavsky A, Canas C, Rojas-Villarraga A
Autoimmun Rev. 2011; 11(4):276-80.
PMID: 21840425
PMC: 3224188.
DOI: 10.1016/j.autrev.2011.07.007.
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.
Sharma S, Gao X, Londono D, Devroy S, Mauldin K, Frankel J
Hum Mol Genet. 2011; 20(7):1456-66.
PMID: 21216876
PMC: 3049353.
DOI: 10.1093/hmg/ddq571.
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers.
Zhang H, Zhai Y, Hu Z, Wu C, Qian J, Jia W
Nat Genet. 2010; 42(9):755-8.
PMID: 20676096
DOI: 10.1038/ng.638.
Association of CLU and PICALM variants with Alzheimer's disease.
Kamboh M, Minster R, Demirci F, Ganguli M, DeKosky S, Lopez O
Neurobiol Aging. 2010; 33(3):518-21.
PMID: 20570404
PMC: 3010357.
DOI: 10.1016/j.neurobiolaging.2010.04.015.
Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.
Maiti A, Kim-Howard X, Viswanathan P, Guillen L, Qian X, Rojas-Villarraga A
Rheumatology (Oxford). 2010; 49(7):1239-44.
PMID: 20338887
PMC: 2909799.
DOI: 10.1093/rheumatology/kep470.
Confirmation of an association between rs6822844 at the Il2-Il21 region and multiple autoimmune diseases: evidence of a general susceptibility locus.
Maiti A, Kim-Howard X, Viswanathan P, Guillen L, Rojas-Villarraga A, Deshmukh H
Arthritis Rheum. 2010; 62(2):323-9.
PMID: 20112382
PMC: 3028384.
DOI: 10.1002/art.27222.
Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).
Hellquist A, Zucchelli M, Lindgren C, Saarialho-Kere U, Jarvinen T, Koskenmies S
PLoS One. 2009; 4(12):e8037.
PMID: 19997561
PMC: 2785483.
DOI: 10.1371/journal.pone.0008037.