| Year |
Citation |
Score |
| 2024 |
Adams C, Manouchehrinia A, Quach HL, Quach DL, Olsson T, Kockum I, Schaefer C, Ponting CP, Alfredsson L, Barcellos LF. Evidence supports a causal association between allele-specific vitamin D receptor binding and multiple sclerosis among Europeans. Proceedings of the National Academy of Sciences of the United States of America. 121: e2302259121. PMID 38346204 DOI: 10.1073/pnas.2302259121 |
0.331 |
|
| 2024 |
Ziaei A, Solomon O, Casper TC, Waltz M, Weinstock-Guttman B, Aaen G, Wheeler Y, Graves J, Benson L, Gorman M, Rensel M, Mar S, Lotze T, Greenberg B, Chitnis T, ... ... Barcellos LF, et al. Gene-environment interactions: Epstein-Barr virus infection and risk of pediatric-onset multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 13524585231224685. PMID 38332747 DOI: 10.1177/13524585231224685 |
0.345 |
|
| 2023 |
Horton MK, Shim JE, Wallace A, Graves JS, Aaen G, Greenberg B, Mar S, Wheeler Y, Weinstock-Guttman B, Waldman A, Schreiner T, Rodriguez M, Tillema JM, Chitnis T, Krupp L, ... ... Barcellos LF, et al. Rare and low-frequency coding genetic variants contribute to pediatric-onset multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 13524585221150736. PMID 36755464 DOI: 10.1177/13524585221150736 |
0.329 |
|
| 2023 |
Horton MK, Robinson SC, Shao X, Quach H, Quach D, Choudhary V, Bellesis KH, Dorin P, Mei J, Chinn T, Meyers TJ, Bakshi N, Marcus JF, Waubant E, Schaefer CA, ... Barcellos LF, et al. A Cross-Trait, Mendelian Randomization Study to Investigate Whether Migraine Is a Risk Factor for Multiple Sclerosis. Neurology. PMID 36631270 DOI: 10.1212/WNL.0000000000206791 |
0.374 |
|
| 2022 |
Shams H, Shao X, Santaniello A, Kirkish G, Harroud A, Ma Q, Isobe N, Schaefer C, McCauley JL, Cree BAC, Didonna A, Baranzini SE, Patsopoulos NA, Hauser SL, Barcellos LF, et al. Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans. Brain : a Journal of Neurology. PMID 35253861 DOI: 10.1093/brain/awac092 |
0.364 |
|
| 2022 |
Horton MK, McCurdy S, Shao X, Bellesis K, Chinn T, Schaefer C, Barcellos LF. Case-control study of adverse childhood experiences and multiple sclerosis risk and clinical outcomes. Plos One. 17: e0262093. PMID 35025951 DOI: 10.1371/journal.pone.0262093 |
0.31 |
|
| 2022 |
Ziaei A, Lavery AM, Shao XM, Adams C, Casper TC, Rose J, Candee M, Weinstock-Guttman B, Aaen G, Harris Y, Graves J, Benson L, Gorman M, Rensel M, Mar S, ... ... Barcellos LF, et al. Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollution. Multiple Sclerosis (Houndmills, Basingstoke, England). 13524585211069926. PMID 35000467 DOI: 10.1177/13524585211069926 |
0.328 |
|
| 2022 |
Sebastian P, Cherbuin N, Barcellos LF, Roalstad S, Casper C, Hart J, Aaen GS, Krupp L, Benson L, Gorman M, Candee M, Chitnis T, Goyal M, Greenberg B, Mar S, et al. Association Between Time Spent Outdoors and Risk of Multiple Sclerosis. Neurology. 98: e267-e278. PMID 34880094 DOI: 10.1212/WNL.0000000000013045 |
0.304 |
|
| 2021 |
Roostaei T, Klein HU, Ma Y, Felsky D, Kivisäkk P, Connor SM, Kroshilina A, Yung C, Kaskow BJ, Shao X, Rhead B, Ordovás JM, Absher DM, Arnett DK, Liu J, ... ... Barcellos LF, et al. Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome. Nature Communications. 12: 7078. PMID 34873174 DOI: 10.1038/s41467-021-27427-w |
0.345 |
|
| 2021 |
Chi C, Taylor KE, Quach H, Quach D, Criswell LA, Barcellos LF. Hypomethylation mediates genetic association with the major histocompatibility complex genes in Sjögren's syndrome. Plos One. 16: e0248429. PMID 33886574 DOI: 10.1371/journal.pone.0248429 |
0.32 |
|
| 2020 |
Langer-Gould A, Black LJ, Waubant E, Smith JB, Wu J, Gonzales EG, Shao X, Koebnick C, Lucas RM, Xiang A, Barcellos LF. Seafood, fatty acid biosynthesis genes, and multiple sclerosis susceptibility. Multiple Sclerosis (Houndmills, Basingstoke, England). 26: 1476-1485. PMID 33063621 DOI: 10.25384/Sage.C.4657781.V1 |
0.374 |
|
| 2020 |
Adams CJ, Wu SL, Shao X, Bradshaw PT, Gonzales E, Smith JB, Xiang AH, Bellesis KH, Chinn T, Bos SD, Wendel-Haga M, Olsson T, Kockum I, Langer-Gould AM, Schaefer C, ... ... Barcellos LF, et al. Pregnancy does not modify the risk of MS in genetically susceptible women. Neurology(R) Neuroimmunology & Neuroinflammation. 7. PMID 33037103 DOI: 10.1212/NXI.0000000000000898 |
0.329 |
|
| 2020 |
Barcellos LF, Horton M, Shao X, Bellesis KH, Chinn T, Waubant E, Bakshi N, Marcus J, Benedict RH, Schaefer C. A validation study for remote testing of cognitive function in multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 1352458520937385. PMID 32662747 DOI: 10.1177/1352458520937385 |
0.336 |
|
| 2020 |
Rhead B, Shao X, Quach H, Ghai P, Barcellos LF, Bowcock AM. Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs. Plos One. 15: e0230884. PMID 32231389 DOI: 10.1371/Journal.Pone.0230884 |
0.346 |
|
| 2020 |
Lanata CM, Paranjpe I, Nititham J, Taylor KE, Gianfrancesco M, Paranjpe M, Andrews S, Chung SA, Rhead B, Barcellos LF, Trupin L, Katz P, Dall'Era M, Yazdany J, Sirota M, et al. Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus. Nature Communications. 11: 1164. PMID 32109229 DOI: 10.1038/S41467-020-15097-Z |
0.61 |
|
| 2019 |
Lanata CM, Paranjpe I, Nititham J, Taylor KE, Gianfrancesco M, Paranjpe M, Andrews S, Chung SA, Rhead B, Barcellos LF, Trupin L, Katz P, Dall'Era M, Yazdany J, Sirota M, et al. A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus. Nature Communications. 10: 3902. PMID 31467281 DOI: 10.1038/S41467-019-11845-Y |
0.664 |
|
| 2019 |
Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, ... ... Barcellos LF, et al. Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. Blood. PMID 31350265 DOI: 10.1182/Blood.2018890764 |
0.405 |
|
| 2019 |
de Smith AJ, Walsh KM, Morimoto LM, Francis SS, Hansen HM, Jeon S, Gonseth S, Chen M, Sun H, Luna-Fineman S, Antillón F, Girón V, Kang AY, Smirnov I, Shao X, ... ... Barcellos LF, et al. Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. Leukemia. PMID 31296947 DOI: 10.1038/S41375-019-0514-9 |
0.305 |
|
| 2019 |
Brorson IS, Eriksson A, Leikfoss IS, Celius EG, Berg-Hansen P, Barcellos LF, Berge T, Harbo HF, Bos SD. No differential gene expression for CD4 T cells of MS patients and healthy controls. Multiple Sclerosis Journal - Experimental, Translational and Clinical. 5: 2055217319856903. PMID 31223483 DOI: 10.1177/2055217319856903 |
0.374 |
|
| 2019 |
Rhead B, Shao X, Graves JS, Chitnis T, Waldman AT, Lotze T, Schreiner T, Belman A, Krupp L, Greenberg BM, Weinstock-Guttman B, Aaen G, Tillema JM, Rodriguez M, Hart J, ... ... Barcellos LF, et al. miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS. Annals of Clinical and Translational Neurology. 6: 1053-1061. PMID 31211169 DOI: 10.1002/Acn3.786 |
0.398 |
|
| 2019 |
Graves JS, Barcellos LF, Krupp L, Belman A, Shao X, Quach H, Hart J, Chitnis T, Weinstock-Guttman B, Aaen G, Benson L, Gorman M, Greenberg B, Lotze T, Soe M, et al. Vitamin D genes influence MS relapses in children. Multiple Sclerosis (Houndmills, Basingstoke, England). 1352458519845842. PMID 31081484 DOI: 10.1177/1352458519845842 |
0.368 |
|
| 2019 |
Chi C, Shao X, Rhead B, Gonzales E, Smith JB, Xiang AH, Graves J, Waldman A, Lotze T, Schreiner T, Weinstock-Guttman B, Aaen G, Tillema JM, Ness J, Candee M, ... ... Barcellos LF, et al. Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry. Plos Genetics. 15: e1007808. PMID 30653506 DOI: 10.1371/Journal.Pgen.1007808 |
0.541 |
|
| 2019 |
Cruz GI, Shao X, Quach H, Quach D, Ho KA, Sterba K, Noble JA, Patsopoulos NA, Busch MP, Triulzi DJ, Ladas N, Blasczyk R, Wong WSW, Solomon BD, Niederhuber JE, ... ... Barcellos LF, et al. Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers. Genes and Immunity. PMID 30635658 DOI: 10.1038/S41435-018-0055-7 |
0.372 |
|
| 2019 |
Paranjpe I, Lanata C, Nititham J, Taylor K, Gianfrancesco MA, Paranjpe M, Andrews S, Chung S, Rhead B, Barcellos L, Trupin L, Katz P, DallEra MC, Yazdany J, Sirota M, et al. 149 Network-based analysis of clinical and molecular data in a multiethnic lupus cohort identifies molecular associations with serological manifestations Lupus Science & Medicine. 6. DOI: 10.1136/Lupus-2019-Lsm.149 |
0.681 |
|
| 2018 |
Mar S, Liang S, Waltz M, Casper TC, Goyal M, Greenberg B, Weinstock-Guttman B, Rodriguez M, Aaen G, Belman A, Barcellos LF, Rose J, Gorman M, Benson L, Candee M, et al. Several household chemical exposures are associated with pediatric-onset multiple sclerosis. Annals of Clinical and Translational Neurology. 5: 1513-1521. PMID 30564618 DOI: 10.1002/Acn3.663 |
0.415 |
|
| 2018 |
Rhead B, Brorson IS, Berge T, Adams C, Quach H, Moen SM, Berg-Hansen P, Celius EG, Sangurdekar DP, Bronson PG, Lea RA, Burnard S, Maltby VE, Scott RJ, Lechner-Scott J, ... ... Barcellos LF, et al. Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients. Plos One. 13: e0206511. PMID 30379917 DOI: 10.1371/Journal.Pone.0206511 |
0.734 |
|
| 2018 |
Nourbakhsh B, Rutatangwa A, Waltz M, Rensel M, Moodley M, Graves J, Casper TC, Waldman A, Belman A, Greenberg B, Goyal M, Harris Y, Kahn I, Lotze T, Mar S, ... ... Barcellos L, et al. Heterogeneity in association of remote herpesvirus infections and pediatric MS. Annals of Clinical and Translational Neurology. 5: 1222-1228. PMID 30349857 DOI: 10.1002/Acn3.636 |
0.411 |
|
| 2018 |
Jackman RP, Cruz GI, Nititham J, Triulzi DJ, Barcellos LF, Criswell LA, Norris PJ, Busch MP. Increased alloreactive and autoreactive antihuman leucocyte antigen antibodies associated with systemic lupus erythematosus and rheumatoid arthritis. Lupus Science & Medicine. 5: e000278. PMID 30305912 DOI: 10.1136/Lupus-2018-000278 |
0.305 |
|
| 2018 |
Wallace AD, Wendt GA, Barcellos LF, de Smith AJ, Walsh KM, Metayer C, Costello JF, Wiemels JL, Francis SS. To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes. Frontiers in Genetics. 9: 298. PMID 30154825 DOI: 10.3389/Fgene.2018.00298 |
0.356 |
|
| 2018 |
Mowry EM, Hedström AK, Gianfrancesco MA, Shao X, Schaefer CA, Shen L, Bellesis KH, Briggs FBS, Olsson T, Alfredsson L, Barcellos LF. Incorporating machine learning approaches to assess putative environmental risk factors for multiple sclerosis. Multiple Sclerosis and Related Disorders. 24: 135-141. PMID 30005356 DOI: 10.1016/j.msard.2018.06.009 |
0.673 |
|
| 2018 |
de Smith AJ, Walsh KM, Francis SS, Zhang C, Hansen HM, Smirnov I, Morimoto L, Whitehead TP, Kang A, Shao X, Barcellos LF, McKean-Cowdin R, Zhang L, Fu C, Wang R, et al. BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia. International Journal of Cancer. PMID 29923177 DOI: 10.1002/Ijc.31622 |
0.384 |
|
| 2018 |
Langer-Gould A, Lucas R, Xiang AH, Chen LH, Wu J, Gonzalez E, Haraszti S, Smith JB, Quach H, Barcellos LF. MS Sunshine Study: Sun Exposure But Not Vitamin D Is Associated with Multiple Sclerosis Risk in Blacks and Hispanics. Nutrients. 10. PMID 29495467 DOI: 10.3390/Nu10030268 |
0.44 |
|
| 2018 |
Langer-Gould A, Lucas RM, Xiang AH, Wu J, Chen LH, Gonzales E, Haraszti S, Smith JB, Quach H, Barcellos LF. Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis. Nutrients. 10. PMID 29414925 DOI: 10.3390/Nu10020184 |
0.424 |
|
| 2018 |
Graves JS, Barcellos LF, Simpson S, Belman A, Lin R, Taylor BV, Ponsonby AL, Dwyer T, Krupp L, Waubant E, van der Mei IAF. The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults. Multiple Sclerosis and Related Disorders. 19: 161-165. PMID 29409597 DOI: 10.1016/J.Msard.2017.10.008 |
0.516 |
|
| 2018 |
Wiemels JL, Walsh KM, de Smith AJ, Metayer C, Gonseth S, Hansen HM, Francis SS, Ojha J, Smirnov I, Barcellos L, Xiao X, Morimoto L, McKean-Cowdin R, Wang R, Yu H, et al. GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Nature Communications. 9: 286. PMID 29348612 DOI: 10.1038/S41467-017-02596-9 |
0.342 |
|
| 2018 |
Brown AL, Smith AJd, Scheurer ME, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Zwick ME, Winick N, Maloney K, Angiolillo AL, Schore R, Burke MM, Salzer WL, Heerema NA, ... ... Barcellos LF, et al. Abstract 222: Genome-wide association study of acute lymphoblastic leukemia in children with Down syndrome Cancer Research. 78: 222-222. DOI: 10.1158/1538-7445.Am2018-222 |
0.344 |
|
| 2018 |
Lanata C, Paranjpe I, Nititham J, Taylor K, Rhead B, Gianfrancesco M, Barcellos L, Murphy L, Katz P, Dall’Era M, Yazdany J, Sirota M, Criswell L. GG-06 Integrative analysis of multi-omics data in an ethnically diverse lupus cohort identifies distinct molecular subtypes of SLE Lupus Science & Medicine. 5. DOI: 10.1136/Lupus-2018-Lsm.93 |
0.649 |
|
| 2017 |
Mok A, Rhead B, Holingue C, Shao X, Quach HL, Quach D, Sinclair E, Graf J, Imboden J, Link T, Harrison R, Chernitskiy V, Barcellos LF, Criswell LA. Hypomethylation of CYP2E1 and DUSP22 promoters associated with disease activity and erosive disease among rheumatoid arthritis patients. Arthritis & Rheumatology (Hoboken, N.J.). PMID 29287311 DOI: 10.1002/Art.40408 |
0.63 |
|
| 2017 |
Seielstad M, Page GP, Gaddis N, Lanteri M, Lee TH, Kakaiya R, Barcellos LF, Criswell LA, Triulzi D, Norris PJ, Busch MP. Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Transfusion. PMID 29168253 DOI: 10.1111/Trf.14402 |
0.322 |
|
| 2017 |
Sharp GC, Salas LA, Monnereau C, Allard C, Yousefi P, Everson TM, Bohlin J, Xu Z, Huang RC, Reese SE, Xu CJ, Baïz N, Hoyo C, Agha G, Roy R, ... ... Barcellos LF, et al. Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium. Human Molecular Genetics. 26: 4067-4085. PMID 29016858 DOI: 10.1093/Hmg/Ddx290 |
0.543 |
|
| 2017 |
Marshall DA, MacDonald KV, Robinson JO, Barcellos LF, Gianfrancesco M, Helm M, McGuire A, Green RC, Douglas MP, Goldman MA, Phillips KA. The price of whole-genome sequencing may be decreasing, but who will be sequenced? Personalized Medicine. 14: 203-211. PMID 28993792 DOI: 10.2217/Pme-2016-0075 |
0.583 |
|
| 2017 |
Azary S, Schreiner T, Graves J, Waldman A, Belman A, Guttman BW, Aaen G, Tillema JM, Mar S, Hart J, Ness J, Harris Y, Krupp L, Gorman M, Benson L, ... ... Barcellos LF, et al. Contribution of dietary intake to relapse rate in early paediatric multiple sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28993476 DOI: 10.1136/Jnnp-2017-315936 |
0.384 |
|
| 2017 |
Gianfrancesco MA, Stridh P, Shao X, Rhead B, Graves JS, Chitnis T, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, ... ... Barcellos LF, et al. Genetic risk factors for pediatric-onset multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 1352458517733551. PMID 28980494 DOI: 10.1177/1352458517733551 |
0.659 |
|
| 2017 |
Langer-Gould A, Wu J, Lucas R, Smith J, Gonzales E, Amezcua L, Haraszti S, Chen LH, Quach H, James JA, Barcellos LF, Xiang AH. Epstein-Barr virus, cytomegalovirus, and multiple sclerosis susceptibility: A multiethnic study. Neurology. PMID 28855411 DOI: 10.1212/Wnl.0000000000004412 |
0.427 |
|
| 2017 |
Zhou Y, Graves JS, Simpson S, Charlesworth JC, Mei IV, Waubant E, Barcellos LF, Belman A, Krupp L, Lucas R, Ponsonby AL, Taylor BV. Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28739605 DOI: 10.1136/Jnnp-2017-315971 |
0.461 |
|
| 2017 |
Hedström AK, Katsoulis M, Hössjer O, Bomfim IL, Oturai A, Sondergaard HB, Sellebjerg F, Ullum H, Thørner LW, Gustavsen MW, Harbo HF, Obradovic D, Gianfrancesco MA, Barcellos LF, Schaefer CA, et al. The interaction between smoking and HLA genes in multiple sclerosis: replication and refinement. European Journal of Epidemiology. PMID 28597127 DOI: 10.1007/S10654-017-0250-2 |
0.711 |
|
| 2017 |
Solomon O, Yousefi P, Huen K, Gunier RB, Escudero-Fung M, Barcellos LF, Eskenazi B, Holland N. Prenatal phthalate exposure and altered patterns of DNA methylation in cord blood. Environmental and Molecular Mutagenesis. PMID 28556291 DOI: 10.1002/Em.22095 |
0.302 |
|
| 2017 |
Gianfrancesco MA, Stridh P, Rhead B, Shao X, Xu E, Graves JS, Chitnis T, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, ... ... Barcellos LF, et al. Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS. Neurology. PMID 28356466 DOI: 10.1212/Wnl.0000000000003849 |
0.645 |
|
| 2017 |
Galarza-Muñoz G, Briggs FB, Evsyukova I, Schott-Lerner G, Kennedy EM, Nyanhete T, Wang L, Bergamaschi L, Widen SG, Tomaras GD, Ko DC, Bradrick SS, Barcellos LF, Gregory SG, Garcia-Blanco MA. Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk. Cell. 169: 72-84.e13. PMID 28340352 DOI: 10.1016/J.Cell.2017.03.007 |
0.733 |
|
| 2017 |
Bourne T, Waltz M, Casper TC, Kavak K, Aaen G, Belman A, Benson L, Candee M, Chitnis T, Graves J, Greenberg B, Gorman M, Harris Y, Krupp L, Lotze T, ... ... Barcellos L, et al. Evaluating the association of allergies with multiple sclerosis susceptibility risk and disease activity in a pediatric population. Journal of the Neurological Sciences. 375: 371-375. PMID 28320170 DOI: 10.1016/J.Jns.2017.02.041 |
0.439 |
|
| 2017 |
Gianfrancesco MA, Glymour MM, Walter S, Rhead B, Shao X, Shen L, Quach H, Hubbard A, Jónsdóttir I, Stefánsson K, Strid P, Hillert J, Hedström A, Olsson T, Kockum I, ... ... Barcellos LF, et al. Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility. American Journal of Epidemiology. PMID 28073764 DOI: 10.1093/aje/kww120 |
0.697 |
|
| 2016 |
George MF, Holingue CB, Briggs FB, Shao X, Bellesis KH, Whitmer RA, Schaefer C, Benedict RH, Barcellos LF. Feasibility study for remote assessment of cognitive function in multiple sclerosis. Journal of Neurology & Neuromedicine. 1: 10-18. PMID 28255581 |
0.768 |
|
| 2016 |
Mok A, Solomon O, Nayak RR, Coit P, Quach HL, Nititham J, Sawalha AH, Barcellos LF, Criswell LA, Chung SA. Genome-wide profiling identifies associations between lupus nephritis and differential methylation of genes regulating tissue hypoxia and type 1 interferon responses. Lupus Science & Medicine. 3: e000183. PMID 28074145 DOI: 10.1136/Lupus-2016-000183 |
0.325 |
|
| 2016 |
Gianfrancesco MA, Barcellos LF. Obesity and Multiple Sclerosis Susceptibility: A Review. Journal of Neurology & Neuromedicine. 1: 1-5. PMID 27990499 |
0.661 |
|
| 2016 |
Olsson T, Barcellos LF, Alfredsson L. Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis. Nature Reviews. Neurology. PMID 27934854 DOI: 10.1038/nrneurol.2016.187 |
0.356 |
|
| 2016 |
Antel J, Ban M, Baranzini S, Barcellos L, Barizzone N, Beecham A, Berge T, Bernardinelli L, Booth D, Bos S, Buck D, Butkiewicz M, Celius EG, Comabella M, Compston A, et al. NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk Neuron. 92: 333-335. PMID 27764667 DOI: 10.1016/J.Neuron.2016.09.052 |
0.34 |
|
| 2016 |
Rhead B, Holingue C, Cole M, Shao X, Quach HL, Quach D, Shah K, Sinclair E, Graf J, Link T, Harrison R, Rahmani E, Halperin E, Wang W, Firestein GS, ... Barcellos LF, et al. Rheumatoid arthritis naïve T cells share hypermethylation sites with synoviocytes. Arthritis & Rheumatology (Hoboken, N.J.). PMID 27723282 DOI: 10.1002/Art.39952 |
0.637 |
|
| 2016 |
Rhead B, Bäärnhielm M, Gianfrancesco M, Mok A, Shao X, Quach H, Shen L, Schaefer C, Link J, Gyllenberg A, Hedström AK, Olsson T, Hillert J, Kockum I, Glymour MM, ... ... Barcellos LF, et al. Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk. Neurology. Genetics. 2: e97. PMID 27652346 DOI: 10.1212/Nxg.0000000000000097 |
0.645 |
|
| 2016 |
George MF, Briggs FB, Shao X, Gianfrancesco MA, Kockum I, Harbo HF, Celius EG, Bos SD, Hedström A, Shen L, Bernstein A, Alfredsson L, Hillert J, Olsson T, Patsopoulos NA, ... ... Barcellos LF, et al. Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies. Neurology. Genetics. 2: e87. PMID 27540591 DOI: 10.1212/Nxg.0000000000000087 |
0.813 |
|
| 2016 |
Nourbakhsh B, Graves J, Casper TC, Lulu S, Waldman A, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Ness J, Rubin J, Krupp L, Gorman M, ... ... Barcellos L, et al. Dietary salt intake and time to relapse in paediatric multiple sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 27343226 DOI: 10.1136/Jnnp-2016-313410 |
0.388 |
|
| 2016 |
McDonald J, Graves J, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Lulu S, Ness J, Harris Y, Rubin J, ... ... Barcellos LF, et al. A case-control study of dietary salt intake in pediatric-onset multiple sclerosis. Multiple Sclerosis and Related Disorders. 6: 87-92. PMID 27063630 DOI: 10.1016/J.Msard.2016.02.011 |
0.334 |
|
| 2016 |
Joubert BR, Felix JF, Yousefi P, Bakulski KM, Just AC, Breton C, Reese SE, Markunas CA, Richmond RC, Xu CJ, Küpers LK, Oh SS, Hoyo C, Gruzieva O, Söderhäll C, ... ... Barcellos LF, et al. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis. American Journal of Human Genetics. PMID 27040690 DOI: 10.1016/J.Ajhg.2016.02.019 |
0.537 |
|
| 2016 |
Hsu LI, Briggs F, Shao X, Metayer C, Wiemels JL, Chokkalingam AP, Barcellos LF. Pathway analysis of genome-wide association study in childhood leukemia among Hispanics. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 26941364 DOI: 10.1158/1055-9965.Epi-15-0528 |
0.693 |
|
| 2016 |
Hedström AK, Mowry EM, Gianfrancesco MA, Shao X, Schaefer CA, Shen L, Olsson T, Barcellos LF, Alfredsson L. High consumption of coffee is associated with decreased multiple sclerosis risk; results from two independent studies. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 26940586 DOI: 10.1136/Jnnp-2015-312176 |
0.71 |
|
| 2016 |
Elboudwarej E, Cole M, Briggs FB, Fouts A, Fain PR, Quach H, Quach D, Sinclair E, Criswell LA, Lane JA, Steck AK, Barcellos LF, Noble JA. Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins. Journal of Autoimmunity. PMID 26782299 DOI: 10.1016/J.Jaut.2015.12.003 |
0.678 |
|
| 2016 |
Graves JS, Barcellos LF, Shao X, Noble J, Mowry EM, Quach H, Belman A, Casper TC, Krupp LB, Waubant E. Genetic predictors of relapse rate in pediatric MS. Multiple Sclerosis (Houndmills, Basingstoke, England). PMID 26769066 DOI: 10.1177/1352458515624269 |
0.381 |
|
| 2016 |
Lanata CM, Nititham J, Taylor K, Nayak R, Barcellos L, Chung SA, Galanter J, Criswell LA. CE-48 Residential proximity to highways, DNA methylation and systemic lupus erythematosus Lupus Science & Medicine. 3. DOI: 10.1136/Lupus-2016-000179.126 |
0.392 |
|
| 2015 |
Yousefi P, Huen K, Davé V, Barcellos L, Eskenazi B, Holland N. Sex differences in DNA methylation assessed by 450 K BeadChip in newborns. Bmc Genomics. 16: 911. PMID 26553366 DOI: 10.1186/S12864-015-2034-Y |
0.322 |
|
| 2015 |
Chung SA, Nititham J, Elboudwarej E, Quach HL, Taylor KE, Barcellos LF, Criswell LA. Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus. Plos One. 10: e0129813. PMID 26192630 DOI: 10.1371/Journal.Pone.0129813 |
0.358 |
|
| 2015 |
Hsu LI, Chokkalingam AP, Briggs FB, Walsh K, Crouse V, Fu C, Metayer C, Wiemels JL, Barcellos LF, Buffler PA. Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children. Cancer Causes & Control : Ccc. 26: 609-19. PMID 25761407 DOI: 10.1007/S10552-015-0550-3 |
0.669 |
|
| 2015 |
Bos SD, Page CM, Andreassen BK, Elboudwarej E, Gustavsen MW, Briggs F, Quach H, Leikfoss IS, Bjølgerud A, Berge T, Harbo HF, Barcellos LF. Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis. Plos One. 10: e0117403. PMID 25734800 DOI: 10.1371/Journal.Pone.0117403 |
0.657 |
|
| 2015 |
Lisak RP, Barcellos L. New insights into the genetics of autoimmune myasthenia gravis: an evolving story. Jama Neurology. 72: 386-387. PMID 25643244 DOI: 10.1001/Jamaneurol.2014.4493 |
0.308 |
|
| 2015 |
Morris DL, Taylor KE, Fernando MMA, Nititham J, Alarcón-Riquelme ME, Barcellos LF, Behrens TW, Cotsapas C, Gaffney PM, Graham RR, Pons-Estel BA, Gregersen PK, Harley JB, Hauser SL, Hom G, et al. Erratum: Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans (The American Journal of Human Genetics (2012) 91 (778-793)) American Journal of Human Genetics. 97. DOI: 10.1016/J.Ajhg.2015.08.005 |
0.402 |
|
| 2014 |
Hedström AK, Bomfim IL, Barcellos LF, Briggs F, Schaefer C, Kockum I, Olsson T, Alfredsson L. Interaction between passive smoking and two HLA genes with regard to multiple sclerosis risk. International Journal of Epidemiology. 43: 1791-8. PMID 25324153 DOI: 10.1093/Ije/Dyu195 |
0.687 |
|
| 2014 |
Gianfrancesco MA, Acuna B, Shen L, Briggs FB, Quach H, Bellesis KH, Bernstein A, Hedstrom AK, Kockum I, Alfredsson L, Olsson T, Schaefer C, Barcellos LF. Obesity during childhood and adolescence increases susceptibility to multiple sclerosis after accounting for established genetic and environmental risk factors. Obesity Research & Clinical Practice. 8: e435-47. PMID 25263833 DOI: 10.1016/j.orcp.2014.01.002 |
0.771 |
|
| 2014 |
Pittock SJ, Lennon VA, Bakshi N, Shen L, McKeon A, Quach H, Briggs FB, Bernstein AL, Schaefer CA, Barcellos LF. Seroprevalence of aquaporin-4-IgG in a northern California population representative cohort of multiple sclerosis. Jama Neurology. 71: 1433-6. PMID 25178362 DOI: 10.1001/jamaneurol.2014.1581 |
0.624 |
|
| 2014 |
Briggs FB, Leung LJ, Barcellos LF. Annotation of functional variation within non-MHC MS susceptibility loci through bioinformatics analysis. Genes and Immunity. 15: 466-76. PMID 25030428 DOI: 10.1038/gene.2014.37 |
0.718 |
|
| 2014 |
Walsh KM, de Smith AJ, Welch TC, Smirnov I, Cunningham MJ, Ma X, Chokkalingam AP, Dahl GV, Roberts W, Barcellos LF, Buffler PA, Metayer C, Wiemels JL. Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia. American Journal of Hematology. 89: 721-5. PMID 24753091 DOI: 10.1002/Ajh.23727 |
0.319 |
|
| 2014 |
Briggs FB, Acuna B, Shen L, Ramsay P, Quach H, Bernstein A, Bellesis KH, Kockum IS, Hedström AK, Alfredsson L, Olsson T, Schaefer C, Barcellos LF. Smoking and risk of multiple sclerosis: evidence of modification by NAT1 variants. Epidemiology (Cambridge, Mass.). 25: 605-14. PMID 24625537 DOI: 10.1097/EDE.0000000000000089 |
0.649 |
|
| 2014 |
Morris DL, Fernando MM, Taylor KE, Chung SA, Nititham J, Alarcón-Riquelme ME, Barcellos LF, Behrens TW, Cotsapas C, Gaffney PM, Graham RR, Pons-Estel BA, Gregersen PK, Harley JB, Hauser SL, et al. MHC associations with clinical and autoantibody manifestations in European SLE. Genes and Immunity. 15: 210-7. PMID 24598797 DOI: 10.1038/Gene.2014.6 |
0.398 |
|
| 2014 |
Briggs FB, Acuña BS, Shen L, Bellesis KH, Ramsay PP, Quach H, Bernstein A, Schaefer C, Barcellos LF. Adverse socioeconomic position during the life course is associated with multiple sclerosis. Journal of Epidemiology and Community Health. 68: 622-9. PMID 24577137 DOI: 10.1136/jech-2013-203184 |
0.681 |
|
| 2014 |
Hedström AK, Lima Bomfim I, Barcellos L, Gianfrancesco M, Schaefer C, Kockum I, Olsson T, Alfredsson L. Interaction between adolescent obesity and HLA risk genes in the etiology of multiple sclerosis. Neurology. 82: 865-72. PMID 24500647 DOI: 10.1212/Wnl.0000000000000203 |
0.674 |
|
| 2014 |
de Smith AJ, Walsh KM, Hansen HM, Barcellos LF, Chokkalingam AP, Jenkins RB, Wrensch MR, Wiencke JK, Metayer C, Wiemels JL. Missense SNP rs3731249 Explains the CDKN2A Association with Childhood ALL and Shows Risk Allele Selection in Tumors with Somatic CDKN2A Alterations Blood. 124: 129-129. DOI: 10.1182/Blood.V124.21.129.129 |
0.399 |
|
| 2014 |
Bos SD, Page CM, Andreassen BK, Elboudwarej E, Gustavsen MW, Briggs F, Quach H, Leikfoss I, Bjølgerud A, Berge T, Harbo HF, Barcellos L. Methylation profiles of untreated MS patients and controls for whole blood, CD4 + and CD8 + T cells show no consistent change of methylation levels in MS Journal of Neuroimmunology. 275: 49-50. DOI: 10.1016/J.Jneuroim.2014.08.132 |
0.661 |
|
| 2013 |
Patsopoulos NA, Barcellos LF, Hintzen RQ, Schaefer C, van Duijn CM, Noble JA, Raj T, Gourraud PA, Stranger BE, Oksenberg J, Olsson T, Taylor BV, Sawcer S, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. Plos Genetics. 9: e1003926. PMID 24278027 DOI: 10.1371/Journal.Pgen.1003926 |
0.381 |
|
| 2013 |
Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Roberts W, Barcellos LF, Wiemels JL, Buffler PA. GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL. Blood. 122: 3385-7. PMID 24203929 DOI: 10.1182/Blood-2013-08-524124 |
0.352 |
|
| 2013 |
Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, ... ... Barcellos LF, et al. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics. 45: 1353-60. PMID 24076602 DOI: 10.1038/Ng.2770 |
0.363 |
|
| 2013 |
Urayama KY, Chokkalingam AP, Metayer C, Hansen H, May S, Ramsay P, Wiemels JL, Wiencke JK, Trachtenberg E, Thompson P, Ishida Y, Brennan P, Jolly KW, Termuhlen AM, Taylor M, ... Barcellos LF, et al. SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children. Plos One. 8: e72557. PMID 23991122 DOI: 10.1371/Journal.Pone.0072557 |
0.423 |
|
| 2013 |
Chokkalingam AP, Hsu LI, Metayer C, Hansen HM, Month SR, Barcellos LF, Wiemels JL, Buffler PA. Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics. Cancer Causes & Control : Ccc. 24: 1789-95. PMID 23836053 DOI: 10.1007/S10552-013-0256-3 |
0.416 |
|
| 2013 |
Walsh KM, de Smith AJ, Chokkalingam AP, Metayer C, Dahl GV, Hsu LI, Barcellos LF, Wiemels JL, Buffler PA. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype. Blood. 121: 4808-9. PMID 23744494 DOI: 10.1182/Blood-2013-04-495390 |
0.366 |
|
| 2013 |
Walsh KM, Chokkalingam AP, Hsu LI, Metayer C, de Smith AJ, Jacobs DI, Dahl GV, Loh ML, Smirnov IV, Bartley K, Ma X, Wiencke JK, Barcellos LF, Wiemels JL, Buffler PA. Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children. Leukemia. 27: 2416-9. PMID 23615557 DOI: 10.1038/Leu.2013.130 |
0.364 |
|
| 2012 |
Urayama KY, Chokkalingam AP, Metayer C, Ma X, Selvin S, Barcellos LF, Wiemels JL, Wiencke JK, Taylor M, Brennan P, Dahl GV, Moonsamy P, Erlich HA, Trachtenberg E, Buffler PA. HLA-DP genetic variation, proxies for early life immune modulation and childhood acute lymphoblastic leukemia risk. Blood. 120: 3039-47. PMID 22923493 DOI: 10.1182/Blood-2012-01-404723 |
0.424 |
|
| 2012 |
Chokkalingam AP, Metayer C, Scelo G, Chang JS, Schiffman J, Urayama KY, Ma X, Hansen HM, Feusner JH, Barcellos LF, Wiencke JK, Wiemels JL, Buffler PA. Fetal growth and body size genes and risk of childhood acute lymphoblastic leukemia. Cancer Causes & Control : Ccc. 23: 1577-85. PMID 22878902 DOI: 10.1007/S10552-012-0035-6 |
0.364 |
|
| 2012 |
Chokkalingam AP, Metayer C, Scelo GA, Chang JS, Urayama KY, Aldrich MC, Guha N, Hansen HM, Dahl GV, Barcellos LF, Wiencke JK, Wiemels JL, Buffler PA. Variation in xenobiotic transport and metabolism genes, household chemical exposures, and risk of childhood acute lymphoblastic leukemia. Cancer Causes & Control : Ccc. 23: 1367-75. PMID 22674224 DOI: 10.1007/S10552-012-9947-4 |
0.359 |
|
| 2011 |
Chokkalingam AP, Aldrich MC, Bartley K, Hsu LI, Metayer C, Barcellos LF, Wiemels JL, Wiencke JK, Buffler PA, Selvin S. Matching on Race and Ethnicity in Case-Control Studies as a Means of Control for Population Stratification. Epidemiology (Sunnyvale, Calif.). 1: 101. PMID 24683503 DOI: 10.4172/2161-1165.1000101 |
0.352 |
|
| 2011 |
Chokkalingam AP, Bartley K, Wiemels JL, Metayer C, Barcellos LF, Hansen HM, Aldrich MC, Guha N, Urayama KY, Scélo G, Chang JS, Month SR, Wiencke JK, Buffler PA. Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia. Cancer Causes & Control : Ccc. 22: 1721-30. PMID 21987080 DOI: 10.1007/S10552-011-9848-Y |
0.352 |
|
| 2011 |
Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, ... ... Barcellos LF, et al. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature. 476: 214-9. PMID 21833088 DOI: 10.1038/Nature10251 |
0.403 |
|
| 2011 |
Metayer C, Scélo G, Chokkalingam AP, Barcellos LF, Aldrich MC, Chang JS, Guha N, Urayama KY, Hansen HM, Block G, Kiley V, Wiencke JK, Wiemels JL, Buffler PA. Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia. Cancer Causes & Control : Ccc. 22: 1243-58. PMID 21748308 DOI: 10.1007/S10552-011-9795-7 |
0.433 |
|
| 2011 |
Briggs FBS, Shao X, Goldstein BA, Oksenberg JR, Barcellos LF, De Jager PL. Genome-wide association study of severity in multiple sclerosis Genes and Immunity. 12: 615-625. PMID 21654844 DOI: 10.1038/gene.2011.34 |
0.391 |
|
| 2011 |
Zuvich RL, Bush WS, McCauley JL, Beecham AH, De Jager PL, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Sawcer SJ, Pericak-Vance MA, Barcellos LF, Mortlock DP, Haines JL. Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Human Molecular Genetics. 20: 3517-24. PMID 21653641 DOI: 10.1093/Hmg/Ddr250 |
0.489 |
|
| 2011 |
Bronson PG, Goldstein BA, Ramsay PP, Beckman KB, Noble JA, Lane JA, Seldin MF, Kelly JA, Harley JB, Moser KL, Gaffney PM, Behrens TW, Criswell LA, Barcellos LF. The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus. Genes and Immunity. 12: 667-71. PMID 21614020 DOI: 10.1038/Gene.2011.36 |
0.728 |
|
| 2011 |
Bloch EM, Reed WF, Lee TH, Montalvo L, Shiboski S, Custer B, Barcellos LF. Male microchimerism in peripheral blood leukocytes from women with multiple sclerosis. Chimerism. 2: 6-10. PMID 21547029 DOI: 10.4161/Chim.2.1.15151 |
0.364 |
|
| 2011 |
McLaren CE, Garner CP, Constantine CC, McLachlan S, Vulpe CD, Snively BM, Gordeuk VR, Nickerson DA, Cook JD, Leiendecker-Foster C, Beckman KB, Eckfeldt JH, Barcellos LF, Murray JA, Adams PC, et al. Genome-wide association study identifies genetic loci associated with iron deficiency. Plos One. 6: e17390. PMID 21483845 DOI: 10.1182/Blood.V114.22.4048.4048 |
0.348 |
|
| 2011 |
Bronson PG, Ramsay PP, Seldin MF, Gregersen PK, Criswell LA, Barcellos LF. CIITA is not associated with risk of developing rheumatoid arthritis. Genes and Immunity. 12: 235-8. PMID 21248776 DOI: 10.1038/Gene.2010.67 |
0.73 |
|
| 2011 |
Huen K, Barcellos L, Beckman K, Rose S, Eskenazi B, Holland N. Effects of PON polymorphisms and haplotypes on molecular phenotype in Mexican-American mothers and children. Environmental and Molecular Mutagenesis. 52: 105-16. PMID 20839225 DOI: 10.1002/Em.20567 |
0.375 |
|
| 2010 |
Chang JS, Wiemels JL, Chokkalingam AP, Metayer C, Barcellos LF, Hansen HM, Aldrich MC, Guha N, Urayama KY, Scélo G, Green J, May SL, Kiley VA, Wiencke JK, Buffler PA. Genetic polymorphisms in adaptive immunity genes and childhood acute lymphoblastic leukemia. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 2152-63. PMID 20716621 DOI: 10.1158/1055-9965.Epi-10-0389 |
0.394 |
|
| 2010 |
Briggs FB, Bartlett SE, Goldstein BA, Wang J, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR, Sawcer SJ, Pericak-Vance MA, ... ... Barcellos LF, et al. Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals. Human Molecular Genetics. 19: 4286-95. PMID 20699326 DOI: 10.1093/Hmg/Ddq328 |
0.742 |
|
| 2010 |
Ban M, McCauley JL, Zuvich R, Baker A, Bergamaschi L, Cox M, Kemppinen A, D'Alfonso S, Guerini FR, Lechner-Scott J, Dudbridge F, Wason J, Robertson NP, De Jager PL, Hafler DA, ... Barcellos LF, et al. A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis. Genes and Immunity. 11: 660-4. PMID 20574445 DOI: 10.1038/Gene.2010.36 |
0.44 |
|
| 2010 |
Goldstein BA, Hubbard AE, Cutler A, Barcellos LF. An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings. Bmc Genetics. 11: 49. PMID 20546594 DOI: 10.1186/1471-2156-11-49 |
0.323 |
|
| 2010 |
Briggs FB, Goldstein BA, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR, Sawcer SJ, Pericak-Vance MA, Haines JL, Barcellos LF, et al. Variation within DNA repair pathway genes and risk of multiple sclerosis. American Journal of Epidemiology. 172: 217-24. PMID 20522537 DOI: 10.1093/Aje/Kwq086 |
0.738 |
|
| 2010 |
Bronson PG, Ramsay PP, Seldin MF, Gregersen PK, Criswell LA, Barcellos LF. A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis. Genes and Immunity. 11: 504-8. PMID 20220768 DOI: 10.1038/Gene.2010.7 |
0.717 |
|
| 2010 |
Bronson PG, Caillier S, Ramsay PP, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Sawcer SJ, Pericak-Vance MA, Haines JL, Hauser SL, ... ... Barcellos LF, et al. CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis. Human Molecular Genetics. 19: 2331-40. PMID 20211854 DOI: 10.1093/Hmg/Ddq101 |
0.763 |
|
| 2010 |
Bronson PG, Komorowski LK, Ramsay PP, May SL, Noble J, Lane JA, Thomson G, Claas FH, Seldin MF, Kelly JA, Harley JB, Moser KL, Gaffney PM, Behrens T, Criswell LA, ... Barcellos LF, et al. Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus. Arthritis and Rheumatism. 62: 1712-7. PMID 20191587 DOI: 10.1002/Art.27426 |
0.757 |
|
| 2010 |
Briggs FB, Ramsay PP, Madden E, Norris JM, Holers VM, Mikuls TR, Sokka T, Seldin MF, Gregersen PK, Criswell LA, Barcellos LF. Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis. Genes and Immunity. 11: 199-208. PMID 20090771 DOI: 10.1038/Gene.2009.110 |
0.659 |
|
| 2010 |
Valdes AM, Thomson G, Barcellos LF. Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes Genes and Immunity. 11: 209-218. PMID 20054343 DOI: 10.1038/Gene.2009.104 |
0.602 |
|
| 2009 |
Barcellos LF, May SL, Ramsay PP, Quach HL, Lane JA, Nititham J, Noble JA, Taylor KE, Quach DL, Chung SA, Kelly JA, Moser KL, Behrens TW, Seldin MF, Thomson G, et al. High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. Plos Genetics. 5: e1000696. PMID 19851445 DOI: 10.1371/Journal.Pgen.1000696 |
0.591 |
|
| 2009 |
Shaw GM, Lu W, Zhu H, Yang W, Briggs FB, Carmichael SL, Barcellos LF, Lammer EJ, Finnell RH. 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects. Bmc Medical Genetics. 10: 49. PMID 19493349 DOI: 10.1186/1471-2350-10-49 |
0.657 |
|
| 2009 |
Aldrich MC, Selvin S, Hansen HM, Barcellos LF, Wrensch MR, Sison JD, Kelsey KT, Buffler PA, Quesenberry CP, Seldin MF, Wiencke JK. CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification. Cancer Research. 69: 2340-8. PMID 19276377 DOI: 10.1158/0008-5472.Can-08-2576 |
0.308 |
|
| 2009 |
De Jager PL, Baecher-Allan C, Maier LM, Arthur AT, Ottoboni L, Barcellos L, McCauley JL, Sawcer S, Goris A, Saarela J, Yelensky R, Price A, Leppa V, Patterson N, de Bakker PI, et al. The role of the CD58 locus in multiple sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 106: 5264-9. PMID 19237575 DOI: 10.1073/Pnas.0813310106 |
0.395 |
|
| 2009 |
Bronson PG, Ramsay PP, Thomson G, Barcellos LF. Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes. Diabetes, Obesity & Metabolism. 11: 74-83. PMID 19143818 DOI: 10.1111/J.1463-1326.2008.01006.X |
0.764 |
|
| 2008 |
Caillier SJ, Briggs F, Cree BA, Baranzini SE, Fernandez-Viña M, Ramsay PP, Khan O, Royal W, Hauser SL, Barcellos LF, Oksenberg JR. Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis. Journal of Immunology (Baltimore, Md. : 1950). 181: 5473-80. PMID 18832704 DOI: 10.4049/Jimmunol.181.8.5473 |
0.735 |
|
| 2008 |
Aldrich MC, Selvin S, Hansen HM, Barcellos LF, Wrensch MR, Sison JD, Quesenberry CP, Kittles RA, Silva G, Buffler PA, Seldin MF, Wiencke JK. Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos. American Journal of Epidemiology. 168: 1035-46. PMID 18791191 DOI: 10.1093/Aje/Kwn224 |
0.318 |
|
| 2008 |
Barcellos LF, Ramsay PP, Caillier SJ, Sawcer S, Haines J, Schmidt S, Pericak-Vance M, Compston DA, Gabatto P, Hauser SL, Oksenberg JR. Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis. Genes and Immunity. 9: 493-500. PMID 18580885 DOI: 10.1038/Gene.2008.41 |
0.52 |
|
| 2008 |
Thomson G, Barcellos LF, Valdes AM. Searching for additional disease loci in a genomic region. Advances in Genetics. 60: 253-92. PMID 18358324 DOI: 10.1016/S0065-2660(07)00411-7 |
0.584 |
|
| 2008 |
Byun E, Caillier SJ, Montalban X, Villoslada P, Fernández O, Brassat D, Comabella M, Wang J, Barcellos LF, Baranzini SE, Oksenberg JR. Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis. Archives of Neurology. 65: 337-44. PMID 18195134 DOI: 10.1001/Archneurol.2008.47 |
0.317 |
|
| 2008 |
Fontaine B, Barcellos LF. Evidence for a complex interaction between HLA-DRB1 and environmental factors in MS. Neurology. 70: 97-8. PMID 18180438 DOI: 10.1212/01.Wnl.0000296821.72466.D3 |
0.488 |
|
| 2008 |
Bronson PG, Criswell LA, Barcellos LF. The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association. Annals of the Rheumatic Diseases. 67: 933-6. PMID 17875550 DOI: 10.1136/Ard.2007.077099 |
0.729 |
|
| 2008 |
Urayama K, Wiemels J, Chokkalingam A, Wiencke J, Barcellos L, Metayer C, Buffler P. Membrane transporter gene (MDR1 and MRP1) polymorphisms and haplotyp4es and risk of childhood acute lymphoblastic leukemia European Journal of Cancer Supplements. 6: 208. DOI: 10.1016/S1359-6349(08)71915-3 |
0.31 |
|
| 2008 |
Scelo G, Chokkalingam AP, Metayer C, Guha N, Barcellos LF, Wiemels JL, Wiencke JK, Buffler PA. Genetic polymorphisms in the cytochrome gene family and the risk of childhood acute lymphoblastic leukemia Ejc Supplements. 6: 207. DOI: 10.1016/S1359-6349(08)71912-8 |
0.364 |
|
| 2008 |
De Jager P, Baecher-Allan C, Maier L, Sawcer S, Goris A, Saarela J, Barcellos L, Dubois B, Peltonen L, Palotie A, Weiner H, Booth D, Stewart G, Pericak-Vance M, Haines J, et al. OR.102. The CD58 Pathway is Implicated in MS Susceptibility Clinical Immunology. 127: S40-S41. DOI: 10.1016/J.Clim.2008.03.109 |
0.361 |
|
| 2007 |
Gregory SG, Schmidt S, Seth P, Oksenberg JR, Hart J, Prokop A, Caillier SJ, Ban M, Goris A, Barcellos LF, Lincoln R, McCauley JL, Sawcer SJ, Compston DA, Dubois B, et al. Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nature Genetics. 39: 1083-91. PMID 17660817 DOI: 10.1038/Ng2103 |
0.45 |
|
| 2007 |
Hafler DA, Compston A, Sawcer S, Lander ES, Daly MJ, De Jager PL, de Bakker PI, Gabriel SB, Mirel DB, Ivinson AJ, Pericak-Vance MA, Gregory SG, Rioux JD, McCauley JL, ... ... Barcellos LF, et al. Risk alleles for multiple sclerosis identified by a genomewide study. The New England Journal of Medicine. 357: 851-62. PMID 17660530 DOI: 10.1056/Nejmoa073493 |
0.449 |
|
| 2007 |
Hensiek AE, Seaman SR, Barcellos LF, Oturai A, Eraksoi M, Cocco E, Vecsei L, Stewart G, Dubois B, Bellman-Strobl J, Leone M, Andersen O, Bencsik K, Booth D, Celius EG, et al. Familial effects on the clinical course of multiple sclerosis. Neurology. 68: 376-83. PMID 17261686 DOI: 10.1212/01.Wnl.0000252822.53506.46 |
0.396 |
|
| 2007 |
Yeo TW, De Jager PL, Gregory SG, Barcellos LF, Walton A, Goris A, Fenoglio C, Ban M, Taylor CJ, Goodman RS, Walsh E, Wolfish CS, Horton R, Traherne J, Beck S, et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Annals of Neurology. 61: 228-36. PMID 17252545 DOI: 10.1002/Ana.21063 |
0.459 |
|
| 2007 |
Motsinger AA, Brassat D, Caillier SJ, Erlich HA, Walker K, Steiner LL, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes. Neurogenetics. 8: 11-20. PMID 17024427 DOI: 10.1007/S10048-006-0058-9 |
0.447 |
|
| 2007 |
Hauser SL, Barcellos LF, Pericak-Vance M, Haines JL, Oksenberg JR. Clustering of autoimmune disease in families at high risk for multiple sclerosis? - Authors' reply Lancet Neurology. 6: 207. DOI: 10.1016/S1474-4422(07)70044-3 |
0.346 |
|
| 2007 |
Barcellos L, Shen L, Herrinton L, Bernstein AL, Allison JE, Citron J, Shoor S, Karter A, Li D, Schaefer C, Gunderson E, Selby J, Croen L, Risch N. Population-based Studies of Risk Factors in Autoimmunity: The Kaiser Permanente Autoimmune Disease Research Group (KPADRG) Clinical Immunology. 123: S126-S127. DOI: 10.1016/J.Clim.2007.03.539 |
0.314 |
|
| 2006 |
Barcellos LF, Sawcer S, Ramsay PP, Baranzini SE, Thomson G, Briggs F, Cree BC, Begovich AB, Villoslada P, Montalban X, Uccelli A, Savettieri G, Lincoln RR, DeLoa C, Haines JL, et al. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis. Human Molecular Genetics. 15: 2813-24. PMID 16905561 DOI: 10.1093/Hmg/Ddl223 |
0.772 |
|
| 2006 |
Schmidt S, Pericak-Vance MA, Sawcer S, Barcellos LF, Hart J, Sims J, Prokop AM, van der Walt J, DeLoa C, Lincoln RR, Oksenberg JR, Compston A, Hauser SL, Haines JL, Gregory SG, et al. Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis. Genes and Immunity. 7: 384-92. PMID 16738668 DOI: 10.1038/Sj.Gene.6364311 |
0.493 |
|
| 2006 |
Burwick RM, Ramsay PP, Haines JL, Hauser SL, Oksenberg JR, Pericak-Vance MA, Schmidt S, Compston A, Sawcer S, Cittadella R, Savettieri G, Quattrone A, Polman CH, Uitdehaag BM, Zwemmer JN, ... ... Barcellos LF, et al. APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers. Neurology. 66: 1373-83. PMID 16682670 DOI: 10.1212/01.Wnl.0000210531.19498.3F |
0.401 |
|
| 2006 |
Brassat D, Motsinger AA, Caillier SJ, Erlich HA, Walker K, Steiner LL, Cree BA, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans. Genes and Immunity. 7: 310-5. PMID 16625214 DOI: 10.1038/Sj.Gene.6364299 |
0.475 |
|
| 2006 |
Kenealy SJ, Herrel LA, Bradford Y, Schnetz-Boutaud N, Oksenberg JR, Hauser SL, Barcellos LF, Schmidt S, Gregory SG, Pericak-Vance MA, Haines JL. Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44. Genes and Immunity. 7: 73-6. PMID 16341055 DOI: 10.1038/Sj.Gene.6364275 |
0.331 |
|
| 2006 |
Traherne JA, Barcellos LF, Sawcer SJ, Compston A, Ramsay PP, Hauser SL, Oksenberg JR, Trowsdale J. Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15. Human Molecular Genetics. 15: 155-61. PMID 16321988 DOI: 10.1093/Hmg/Ddi436 |
0.534 |
|
| 2005 |
Oksenberg JR, Barcellos LF. Multiple sclerosis genetics: Leaving no stone unturned Genes and Immunity. 6: 375-387. PMID 15973459 DOI: 10.1038/Sj.Gene.6364237 |
0.457 |
|
| 2005 |
Brassat D, Salemi G, Barcellos LF, McNeill G, Proia P, Hauser SL, Oksenberg JR, Savettieri G. The HLA locus and multiple sclerosis in Sicily. Neurology. 64: 361-3. PMID 15668443 DOI: 10.1212/01.Wnl.0000149765.71212.0A |
0.456 |
|
| 2005 |
Begovich AB, Caillier SJ, Alexander HC, Penko JM, Hauser SL, Barcellos LF, Oksenberg JR. The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis. American Journal of Human Genetics. 76: 184-7. PMID 15580548 DOI: 10.1086/427244 |
0.388 |
|
| 2004 |
Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, et al. A second-generation genomic screen for multiple sclerosis. American Journal of Human Genetics. 75: 1070-8. PMID 15494893 DOI: 10.1086/426459 |
0.371 |
|
| 2004 |
Sawcer SJ, Maranian M, Singlehurst S, Yeo T, Compston A, Daly MJ, De Jager PL, Gabriel S, Hafler DA, Ivinson AJ, Lander ES, Rioux JD, Walsh E, Gregory SG, Schmidt S, ... ... Barcellos L, et al. Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping. Human Molecular Genetics. 13: 1943-9. PMID 15238506 DOI: 10.1093/Hmg/Ddh202 |
0.312 |
|
| 2004 |
Barcellos LF, Begovich AB, Reynolds RL, Caillier SJ, Brassat D, Schmidt S, Grams SE, Walker K, Steiner LL, Cree BA, Stillman A, Lincoln RR, Pericak-Vance MA, Haines JL, Erlich HA, et al. Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis. Annals of Neurology. 55: 793-800. PMID 15174013 DOI: 10.1002/Ana.20092 |
0.468 |
|
| 2004 |
Mirel DB, Barcellos LF, Wang J, Hauser SL, Oksenberg JR, Erlich HA. Analysis of IL4R haplotypes in predisposition to multiple sclerosis. Genes and Immunity. 5: 138-41. PMID 14712310 DOI: 10.1038/Sj.Gene.6364048 |
0.522 |
|
| 2004 |
Oksenberg JR, Barcellos LF, Cree BA, Baranzini SE, Bugawan TL, Khan O, Lincoln RR, Swerdlin A, Mignot E, Lin L, Goodin D, Erlich HA, Schmidt S, Thomson G, Reich DE, et al. Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. American Journal of Human Genetics. 74: 160-7. PMID 14669136 DOI: 10.1086/380997 |
0.663 |
|
| 2004 |
Pericak-Vance MA, Rimmler JB, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL, Cournu-Rebeix I, Azoulay-Cayla A, Lyon-Caen O, Fontaine B, Duhamel E, Coppin H, Brassat D, et al. Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study. Neurogenetics. 5: 45-8. PMID 14595552 DOI: 10.1007/S10048-003-0163-Y |
0.414 |
|
| 2003 |
Barcellos LF, Thomson G. Genetic analysis of multiple sclerosis in Europeans. Journal of Neuroimmunology. 143: 1-6. PMID 14575906 DOI: 10.1016/J.Jneuroim.2003.08.004 |
0.597 |
|
| 2003 |
Caillier S, Barcellos LF, Baranzini SE, Swerdlin A, Lincoln RR, Steinman L, Martin E, Haines JL, Pericak-Vance M, Hauser SL, Oksenberg JR. Osteopontin polymorphisms and disease course in multiple sclerosis. Genes and Immunity. 4: 312-5. PMID 12761568 DOI: 10.1038/Sj.Gene.6363952 |
0.45 |
|
| 2003 |
Sriram U, Barcellos LF, Villoslada P, Rio J, Baranzini SE, Caillier S, Stillman A, Hauser SL, Montalban X, Oksenberg JR. Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis. Genes and Immunity. 4: 147-52. PMID 12618863 DOI: 10.1038/Sj.Gene.6363946 |
0.445 |
|
| 2003 |
Barcellos LF, Oksenberg JR, Begovich AB, Martin ER, Schmidt S, Vittinghoff E, Goodin DS, Pelletier D, Lincoln RR, Bucher P, Swerdlin A, Pericak-Vance MA, Haines JL, Hauser SL. HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course. American Journal of Human Genetics. 72: 710-6. PMID 12557126 DOI: 10.1086/367781 |
0.506 |
|
| 2003 |
Hoglund B, Bugawan TL, Barcellos L, Oksenberg J, Klitz W, Erlich HA. AbstractThe influence of HLA-C alleles on multiple sclerosis in African Americans Human Immunology. 64. DOI: 10.1016/J.Humimm.2003.08.017 |
0.381 |
|
| 2002 |
Villoslada P, Barcellos LF, Rio J, Begovich AB, Tintore M, Sastre-Garriga J, Baranzini SE, Casquero P, Hauser SL, Montalban X, Oksenberg JR. The HLA locus and multiple sclerosis in Spain. Role in disease susceptibility, clinical course and response to interferon-beta. Journal of Neuroimmunology. 130: 194-201. PMID 12225902 DOI: 10.1016/S0165-5728(02)00215-1 |
0.471 |
|
| 2002 |
Haines JL, Bradford Y, Garcia ME, Reed AD, Neumeister E, Pericak-Vance MA, Rimmler JB, Menold MM, Martin ER, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL. Multiple susceptibility loci for multiple sclerosis. Human Molecular Genetics. 11: 2251-6. PMID 12217953 DOI: 10.1093/Hmg/11.19.2251 |
0.399 |
|
| 2002 |
Schmidt S, Barcellos LF, DeSombre K, Rimmler JB, Lincoln RR, Bucher P, Saunders AM, Lai E, Martin ER, Vance JM, Oksenberg JR, Hauser SL, Pericak-Vance MA, Haines JL. Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis. American Journal of Human Genetics. 70: 708-17. PMID 11836653 DOI: 10.1086/339269 |
0.393 |
|
| 2002 |
Barcellos LF, Oksenberg JR, Green AJ, Bucher P, Rimmler JB, Schmidt S, Garcia ME, Lincoln RR, Pericak-Vance MA, Haines JL, Hauser SL. Genetic basis for clinical expression in multiple sclerosis. Brain : a Journal of Neurology. 125: 150-8. PMID 11834600 DOI: 10.1093/Brain/Awf009 |
0.416 |
|
| 2001 |
Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics. 3: 195-201. PMID 11714099 DOI: 10.1007/S100480100119 |
0.506 |
|
| 2001 |
Barcellos LF, Caillier S, Dragone L, Elder M, Vittinghoff E, Bucher P, Lincoln RR, Pericak-Vance M, Haines JL, Weiss A, Hauser SL, Oksenberg JR. PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients. Nature Genetics. 29: 23-4. PMID 11528386 DOI: 10.1038/Ng722 |
0.46 |
|
| 2001 |
Green AJ, Barcellos LF, Rimmler JB, Garcia ME, Caillier S, Lincoln RR, Bucher P, Pericak-Vance MA, Haines JL, Hauser SL, Oksenberg JR. Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility. Journal of Neuroimmunology. 116: 116-24. PMID 11311337 DOI: 10.1016/S0165-5728(01)00283-1 |
0.453 |
|
| 2001 |
Oksenberg JR, Baranzini SE, Barcellos LF, Hauser SL. Multiple sclerosis: genomic rewards. Journal of Neuroimmunology. 113: 171-84. PMID 11164900 DOI: 10.1016/S0165-5728(00)00444-6 |
0.503 |
|
| 2000 |
Oksenberg JR, Barcellos LF. The complex genetic aetiology of multiple sclerosis Journal of Neurovirology. 6. PMID 10871777 |
0.404 |
|
| 2000 |
Barcellos LF, Schito AM, Rimmler JB, Vittinghoff E, Shih A, Lincoln R, Callier S, Elkins MK, Goodkin DE, Haines JL, Pericak-Vance MA, Hauser SL, Oksenberg JR. CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group. Immunogenetics. 51: 281-8. PMID 10803840 DOI: 10.1007/S002510050621 |
0.487 |
|
| 1999 |
Oksenberg JR, Barcellos LF, Hauser SL. Genetic aspects of multiple sclerosis. Seminars in Neurology. 19: 281-8. PMID 12194384 DOI: 10.1055/S-2008-1040844 |
0.503 |
|
| 1999 |
Karni A, Kohn Y, Safirman C, Abramsky O, Barcellos L, Oksenberg JR, Kahana E, Karussis D, Chapman J, Brautbar C. Evidence for the genetic role of human leukocyte antigens in low frequency DRB1*1501 multiple sclerosis patients in Israel Multiple Sclerosis. 5: 410-415. PMID 10618697 DOI: 10.1177/135245859900500I607 |
0.505 |
|
| 1997 |
Barcellos LF, Thomson G, Carrington M, Schafer J, Begovich AB, Lin P, Xu XH, Min BQ, Marti D, Klitz W. Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis: Evidence of a new susceptibility locus in caucasian and chinese patients Journal of the American Medical Association. 278: 1256-1261. PMID 9333267 |
0.583 |
|
| 1997 |
Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G. Association mapping of disease loci, by use of a pooled DNA genomic screen American Journal of Human Genetics. 61: 734-747. PMID 9326338 DOI: 10.1086/515512 |
0.547 |
|
| 1996 |
Thomson G, Barcellos L, Klitz W, Field L, Tobias R, Bowcock A, Wilson R, Gilbert S. Association mapping with a pooled DNA genomic screen of the non-HLA genes in IDDM, RA and MS Human Immunology. 47: 152. DOI: 10.1016/0198-8859(96)85525-X |
0.595 |
|
| 1996 |
Hollenbach J, Barcellos L, Thomson G, Winkler C, Winter M, Klitz W. HLA differentiation among Mesoamerican natives Human Immunology. 47: 62. DOI: 10.1016/0198-8859(96)85024-5 |
0.513 |
|
| 1996 |
Calandro L, Grote M, Roth M, Barcellos L, Baer D, Sensabaugh G, Thomson G, Klitz W. Hemochromatosis and HLA: New evidence and methods Human Immunology. 47: 40. DOI: 10.1016/0198-8859(96)84897-X |
0.495 |
|
| 1996 |
Barcellos L, Lin P, Schafer J, Thomson G, Klitz W. Gene partnerships with HLA in multiple sclerosis: DR2 and APOE Human Immunology. 47: 30. DOI: 10.1016/0198-8859(96)84837-3 |
0.594 |
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