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Paola G. Bronson, Ph.D. - Publications

Affiliations: 
2010 Epidemiology University of California, Berkeley, Berkeley, CA, United States 
Area:
Epidemiology, Immunology, Genetics
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Misicka E, Huang Y, Loomis S, Sadhu N, Fisher E, Gafson A, Runz H, Tsai E, Jia X, Herman A, Bronson PG, Bhangale T, Briggs FB. Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple Sclerosis. Neurology. Genetics. 10: e200159. PMID 38817245 DOI: 10.1212/NXG.0000000000200159  0.607
2023 Loomis SJ, Sadhu N, Fisher E, Gafson AR, Huang Y, Yang C, Hughes EE, Marshall E, Herman A, John S, Runz H, Jia X, Bhangale T, Bronson PG. Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials. Scientific Reports. 13: 14313. PMID 37652990 DOI: 10.1038/s41598-023-41099-0  0.368
2022 Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-Gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, ... ... Bronson PG, et al. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics. 2: 100168. PMID 36778668 DOI: 10.1016/j.xgen.2022.100168  0.307
2021 Lim CK, Bronson PG, Varade J, Behrens TW, Hammarström L. and Genes are Associated With Selective IgA Deficiency. Frontiers in Genetics. 12: 736235. PMID 34976003 DOI: 10.3389/fgene.2021.736235  0.422
2021 Misicka E, Davis MF, Kim W, Brugger SW, Beales J, Loomis S, Bronson PG, Briggs FB. A higher burden of multiple sclerosis genetic risk confers an earlier onset. Multiple Sclerosis (Houndmills, Basingstoke, England). 13524585211053155. PMID 34709090 DOI: 10.1177/13524585211053155  0.593
2019 Sangurdekar D, Sun C, McLaughlin H, Ayling-Rouse K, Allaire NE, Penny MA, Bronson PG. Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate. Frontiers in Genetics. 10: 1039. PMID 31749835 DOI: 10.3389/Fgene.2019.01039  0.44
2019 Soskic B, Cano-Gamez E, Smyth DJ, Rowan WC, Nakic N, Esparza-Gordillo J, Bossini-Castillo L, Tough DF, Larminie CGC, Bronson PG, Willé D, Trynka G. Chromatin activity at GWAS loci identifies T cell states driving complex immune diseases. Nature Genetics. PMID 31548716 DOI: 10.1038/S41588-019-0493-9  0.318
2019 Kawabata E, Lessard S, Paul D, Bronson PG, Peters R, Krishnamoorthy S, Astle W, Butterworth A. Identification of Novel Variants Associated with Fetal Hemoglobin Levels in Healthy Donors (the INTERVAL study) Blood. 134: 2243-2243. DOI: 10.1182/Blood-2019-123977  0.342
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, 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  0.542
2018 Estrada K, Whelan CW, Zhao F, Bronson P, Handsaker RE, Sun C, Carulli JP, Harris T, Ransohoff RM, McCarroll SA, Day-Williams AG, Greenberg BM, MacArthur DG. A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Nature Communications. 9: 1929. PMID 29769526 DOI: 10.1038/S41467-018-04332-3  0.451
2016 Bronson PG, Chang D, Bhangale T, Seldin MF, Ortmann W, Ferreira RC, Urcelay E, Pereira LF, Martin J, Plebani A, Lougaris V, Friman V, Freiberger T, Litzman J, Thon V, et al. Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. Nature Genetics. PMID 27723758 DOI: 10.1038/Ng.3675  0.4
2013 Bronson PG, Mack SJ, Erlich HA, Slatkin M. A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric. Human Molecular Genetics. 22: 252-61. PMID 23065702 DOI: 10.1093/Hmg/Dds424  0.402
2012 Bronson PG, Chaivorapol C, Ortmann W, Behrens TW, Graham RR. The genetics of type I interferon in systemic lupus erythematosus. Current Opinion in Immunology. 24: 530-7. PMID 22889593 DOI: 10.1016/J.Coi.2012.07.008  0.357
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  0.609
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  0.615
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  0.583
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, 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  0.623
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, 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  0.644
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  0.655
2008 Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3. Annals of Human Genetics. 72: 725-31. PMID 18761660 DOI: 10.1111/J.1469-1809.2008.00474.X  0.391
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  0.612
2006 Lin PI, Martin ER, Bronson PG, Browning-Large C, Small GW, Schmechel DE, Welsh-Bohmer KA, Haines JL, Gilbert JR, Pericak-Vance MA. Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease. Neurology. 67: 64-8. PMID 16832079 DOI: 10.1212/01.Wnl.0000223438.90113.4E  0.408
2006 Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, Welsh-Bohmer KA, Gilbert JR, Haines JL, Pericak-Vance MA. Lack of association between UBQLN1 and Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 208-13. PMID 16526030 DOI: 10.1002/Ajmg.B.30298  0.356
2006 Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Molecular Psychiatry. 11: 280-5. PMID 16222332 DOI: 10.1038/Sj.Mp.4001766  0.336
2006 Zuchner S, Xu P, Browning C, Bronson PG, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. P1-362: Genetic evaluation of the Alzheimer’s disease locus on chromosome 9p21.3 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.740  0.339
2006 Bronson PG, Wall NN, Haines JL, Schmechel DE, Gilbert JR, Pericak-Vance MA, Martin ER. P1-345: Evidence for association between late-onset Alzheimer's disease and MTHFR on chromosome 1 Alzheimer's & Dementia. 2: S198-S198. DOI: 10.1016/J.Jalz.2006.05.723  0.34
2005 Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of Medical Genetics. 42: 787-92. PMID 16199552 DOI: 10.1136/Jmg.2004.029553  0.424
2004 Martin E, Bronson P, Jiang L, Welsh-Bohmer K, Schmechel D, Small G, Haines J, Gilbert J, Pericak-Vance M, Moore J. P4-134 A multilocus association analysis of APOE, LRP1 and A2M in Alzheimer disease Neurobiology of Aging. 25: S513. DOI: 10.1016/S0197-4580(04)81692-0  0.348
2004 Pericak-Vance MA, Bronson P, Martin ER, Browning C, Rayner M, Xu P, Small GW, Roses AD, Schmechel DE, Doraiswamy PM, Welsh-Bohmer KA, Haines JL, Gilbert JR. P4-080 Genetic studies of Alzheimer disease on chromosome 9P Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81638-5  0.342
2004 Browning C, Vance DD, Bronson PG, Schmechel D, Welsh-Bohmer K, Scott W, Haines JL, Vance JM, Pericak-Vance MA. P4-072 Follow-up analysis of chromosome 2 linkage in early-onset Alzheimer disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81630-0  0.323
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