| Year |
Citation |
Score |
| 2023 |
Zhao J, Wei K, Shi Y, Jiang P, Xu L, Chang C, Xu L, Zheng Y, Shan Y, Liu J, Li L, Guo S, Schrodi SJ, Wang R, He D. Identification of immunological characterization and Anoikis-related molecular clusters in rheumatoid arthritis. Frontiers in Molecular Biosciences. 10: 1202371. PMID 38046810 DOI: 10.3389/fmolb.2023.1202371 |
0.599 |
|
| 2023 |
Zheng Y, Zhao J, Zhou M, Wei K, Jiang P, Xu L, Chang C, Shan Y, Xu L, Shi Y, Schrodi SJ, Guo S, He D. Role of signaling lymphocytic activation molecule family of receptors in the pathogenesis of rheumatoid arthritis: insights and application. Frontiers in Pharmacology. 14: 1306584. PMID 38027031 DOI: 10.3389/fphar.2023.1306584 |
0.629 |
|
| 2023 |
Shan Y, Zhao J, Wei K, Jiang P, Xu L, Chang C, Xu L, Shi Y, Zheng Y, Bian Y, Zhou M, Schrodi SJ, Guo S, He D. A comprehensive review of hook. f. in the treatment of rheumatic and autoimmune diseases: Bioactive compounds, mechanisms of action, and future directions. Frontiers in Pharmacology. 14: 1282610. PMID 38027004 DOI: 10.3389/fphar.2023.1282610 |
0.579 |
|
| 2023 |
Zhao M, Zhang R, Chang C, Jin Y, Xu L, Guo S, Schrodi S, He Y, He D. Case report: Whole exome sequencing and genome-wide methylation profiling of Czech dysplasia in a Chinese pedigree. Frontiers in Medicine. 10: 1244888. PMID 38020103 DOI: 10.3389/fmed.2023.1244888 |
0.554 |
|
| 2023 |
Zhang F, Zhang X, Zhang H, Lin D, Fan H, Guo S, An F, Zhao Y, Li J, Schrodi SJ, Zhang D. Pan-precancer and cancer DNA methylation profiles revealed significant tissue specificity of interrupted biological processes in tumorigenesis. Epigenetics. 18: 2231222. PMID 37393582 DOI: 10.1080/15592294.2023.2231222 |
0.543 |
|
| 2023 |
Zhang H, Dong P, Fan H, Liang H, Zhang K, Zhao Y, Guo S, Schrodi SJ, Fan Y, Zhang D. Gene body hypomethylation of pyroptosis-related genes NLRP7, NLRP2, and NLRP3 facilitate non-invasive surveillance of hepatocellular carcinoma. Functional & Integrative Genomics. 23: 198. PMID 37273114 DOI: 10.1007/s10142-023-01114-z |
0.548 |
|
| 2023 |
Singhal P, Veturi Y, Dudek SM, Lucas A, Frase A, van Steen K, Schrodi SJ, Fasel D, Weng C, Pendergrass R, Schaid DJ, Kullo IJ, Dikilitas O, Sleiman PMA, Hakonarson H, et al. Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets. American Journal of Human Genetics. 110: 575-591. PMID 37028392 DOI: 10.1016/j.ajhg.2023.03.007 |
0.3 |
|
| 2023 |
Li X, Fan H, Song X, Song B, Liu W, Dong R, Zhang H, Guo S, Liang H, Schrodi SJ, Fu X, Kaushal S, Ren Y, Zhang D. DNA methylome and transcriptome profiling reveal key electrophysiology and immune dysregulation in hypertrophic cardiomyopathy. Epigenetics. 18: 2195307. PMID 37005704 DOI: 10.1080/15592294.2023.2195307 |
0.58 |
|
| 2023 |
Zheng Y, Zhao J, Shan Y, Guo S, Schrodi SJ, He D. Role of the granzyme family in rheumatoid arthritis: Current Insights and future perspectives. Frontiers in Immunology. 14: 1137918. PMID 36875082 DOI: 10.3389/fimmu.2023.1137918 |
0.622 |
|
| 2023 |
Shan Y, Zhao J, Zheng Y, Guo S, Schrodi SJ, He D. Understanding the function of the GABAergic system and its potential role in rheumatoid arthritis. Frontiers in Immunology. 14: 1114350. PMID 36825000 DOI: 10.3389/fimmu.2023.1114350 |
0.599 |
|
| 2022 |
Zhao J, Xu L, Chang C, Jiang P, Wei K, Shi Y, Xu L, Zheng Y, Shan Y, Bian Y, Li L, Guo S, Schrodi SJ, Wang R, He D. Circulating methylation level of is associated with inflammation and disease activity in rheumatoid arthritis. Frontiers in Immunology. 13: 1054451. PMID 36561742 DOI: 10.3389/fimmu.2022.1054451 |
0.63 |
|
| 2022 |
Zhao J, Guo S, Schrodi SJ, He D. Absent in melanoma 2 (AIM2) in rheumatoid arthritis: novel molecular insights and implications. Cellular & Molecular Biology Letters. 27: 108. PMID 36476420 DOI: 10.1186/s11658-022-00402-z |
0.633 |
|
| 2022 |
Zhao J, Guo S, Schrodi SJ, He D. Cuproptosis and cuproptosis-related genes in rheumatoid arthritis: Implication, prospects, and perspectives. Frontiers in Immunology. 13: 930278. PMID 35990673 DOI: 10.3389/fimmu.2022.930278 |
0.638 |
|
| 2022 |
Zhao J, Guo S, Schrodi SJ, He D. Trends in the Contribution of Genetic Susceptibility Loci to Hyperuricemia and Gout and Associated Novel Mechanisms. Frontiers in Cell and Developmental Biology. 10: 937855. PMID 35813212 DOI: 10.3389/fcell.2022.937855 |
0.602 |
|
| 2022 |
Jiang P, Wei K, Chang C, Zhao J, Zhang R, Xu L, Jin Y, Xu L, Shi Y, Guo S, Schrodi SJ, He D. SFRP1 Negatively Modulates Pyroptosis of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis: A Review. Frontiers in Immunology. 13: 903475. PMID 35795672 DOI: 10.3389/fimmu.2022.903475 |
0.626 |
|
| 2022 |
Zhang R, Jin Y, Chang C, Xu L, Bian Y, Shen Y, Sun Y, Sun S, Schrodi SJ, Guo S, He D. RNA-seq and Network Analysis Reveal Unique Chemokine Activity Signatures in the Synovial Tissue of Patients With Rheumatoid Arthritis. Frontiers in Medicine. 9: 799440. PMID 35602512 DOI: 10.3389/fmed.2022.799440 |
0.611 |
|
| 2022 |
Zhao J, Wei K, Chang C, Xu L, Jiang P, Guo S, Schrodi SJ, He D. DNA Methylation of T Lymphocytes as a Therapeutic Target: Implications for Rheumatoid Arthritis Etiology. Frontiers in Immunology. 13: 863703. PMID 35309322 DOI: 10.3389/fimmu.2022.863703 |
0.605 |
|
| 2021 |
Zhao J, Jiang P, Guo S, Schrodi SJ, He D. Apoptosis, Autophagy, NETosis, Necroptosis, and Pyroptosis Mediated Programmed Cell Death as Targets for Innovative Therapy in Rheumatoid Arthritis. Frontiers in Immunology. 12: 809806. PMID 35003139 DOI: 10.3389/fimmu.2021.809806 |
0.629 |
|
| 2021 |
Zhao J, Guo S, Schrodi SJ, He D. Molecular and Cellular Heterogeneity in Rheumatoid Arthritis: Mechanisms and Clinical Implications. Frontiers in Immunology. 12: 790122. PMID 34899757 DOI: 10.3389/fimmu.2021.790122 |
0.615 |
|
| 2021 |
Deng L, Xu J, Chen W, Guo S, Steiner RD, Chen Q, Cheng Z, Xu Y, Yao B, Li X, Wang X, Deng K, Schrodi SJ, Zhang D, Xin H. Remediation of -Linked Macrothrombocytopenia With Ezetimibe Therapy. Frontiers in Genetics. 12: 769699. PMID 34880906 DOI: 10.3389/fgene.2021.769699 |
0.553 |
|
| 2021 |
Guo S, Jin Y, Zhou J, Zhu Q, Jiang T, Bian Y, Zhang R, Chang C, Xu L, Shen J, Zheng X, Shen Y, Qin Y, Chen J, Tang X, ... ... Schrodi SJ, et al. MicroRNA Variants and HLA-miRNA Interactions are Novel Rheumatoid Arthritis Susceptibility Factors. Frontiers in Genetics. 12: 747274. PMID 34777472 DOI: 10.3389/fgene.2021.747274 |
0.579 |
|
| 2021 |
Zhang D, Guo S, Schrodi SJ. Mechanisms of DNA Methylation in Virus-Host Interaction in Hepatitis B Infection: Pathogenesis and Oncogenetic Properties. International Journal of Molecular Sciences. 22. PMID 34576022 DOI: 10.3390/ijms22189858 |
0.562 |
|
| 2020 |
Zhang H, Dong P, Guo S, Tao C, Chen W, Zhao W, Wang J, Cheung R, Villanueva A, Fan J, Ding H, Schrodi SJ, Zhang D, Zeng C. Hypomethylation in HBV integration regions aids non-invasive surveillance to hepatocellular carcinoma by low-pass genome-wide bisulfite sequencing. Bmc Medicine. 18: 200. PMID 32741373 DOI: 10.1186/S12916-020-01667-X |
0.578 |
|
| 2019 |
Guo S, Liu J, Jiang T, Lee D, Wang R, Zhou X, Jin Y, Shen Y, Wang Y, Bai F, Ding Q, Wang G, Zhang J, Zhou X, Schrodi SJ, et al. (5R)-5-Hydroxytriptolide (LLDT-8) induces substantial epigenetic mediated immune response network changes in fibroblast-like synoviocytes from rheumatoid arthritis patients. Scientific Reports. 9: 11155. PMID 31371761 DOI: 10.1038/S41598-019-47411-1 |
0.63 |
|
| 2019 |
Mergaert AM, Bawadekar M, Nguyen TQ, Massarenti L, Holmes CL, Rebernick R, Schrodi SJ, Shelef MA. Reduced Anti-Histone Antibodies and Increased Risk of Rheumatoid Arthritis Associated with a Single Nucleotide Polymorphism in PADI4 in North Americans. International Journal of Molecular Sciences. 20. PMID 31242568 DOI: 10.3390/Ijms20123093 |
0.397 |
|
| 2019 |
Guo S, Jiang S, Epperla N, Ma Y, Maadooliat M, Ye Z, Olson B, Wang M, Kitchner T, Joyce J, Strenn R, Mazza JJ, Meece JK, Wu W, Jin L, ... ... Schrodi SJ, et al. A gene-based recessive diplotype exome scan discovers , a novel hepcidin-regulating iron metabolism gene. Blood. PMID 30814063 DOI: 10.1182/Blood-2018-10-879585 |
0.678 |
|
| 2017 |
Liu Y, Ye Z, Li X, Anderson JL, Khan M, DaSilva D, Baron M, Wilson D, Bocoun V, Ivacic LC, Schrodi SJ, Smith JA. Genetic and Functional Associations with Decreased Anti-inflammatory Tumor Necrosis Factor Alpha Induced Protein 3 in Macrophages from Subjects with Axial Spondyloarthritis. Frontiers in Immunology. 8: 860. PMID 28791018 DOI: 10.3389/Fimmu.2017.00860 |
0.313 |
|
| 2016 |
Maadooliat M, Bansal NK, Upadhya J, Farazi MR, Li X, He MM, Hebbring SJ, Ye Z, Schrodi SJ. The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem. Frontiers in Genetics. 7: 217. PMID 28018425 DOI: 10.3389/Fgene.2016.00217 |
0.326 |
|
| 2016 |
Schrodi SJ. Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory. Frontiers in Genetics. 7: 106. PMID 27375680 DOI: 10.3389/Fgene.2016.00106 |
0.342 |
|
| 2016 |
Tokarz SA, DeValk J, Luo W, Pattnaik BR, Schrodi SJ, Pillers DA. Cell line donor genotype and its influence on experimental phenotype: Toll-like receptor SNPs and potential variability in innate immunity. Molecular Genetics and Metabolism. 118: 147-52. PMID 27324283 DOI: 10.1016/J.Ymgme.2016.04.011 |
0.35 |
|
| 2015 |
Shukla SK, Rose W, Schrodi SJ. Complex host genetic susceptibility to Staphylococcus aureus infections. Trends in Microbiology. 23: 529-36. PMID 26112911 DOI: 10.1016/J.Tim.2015.05.008 |
0.311 |
|
| 2015 |
Schrodi SJ, DeBarber A, He M, Ye Z, Peissig P, Van Wormer JJ, Haws R, Brilliant MH, Steiner RD. Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data. Human Genetics. 134: 659-69. PMID 25893794 DOI: 10.1007/S00439-015-1551-8 |
0.322 |
|
| 2015 |
Ye Z, Mayer J, Ivacic L, Zhou Z, He M, Schrodi SJ, Page D, Brilliant MH, Hebbring SJ. Phenome-wide association studies (PheWASs) for functional variants. European Journal of Human Genetics : Ejhg. 23: 523-9. PMID 25074467 DOI: 10.1038/Ejhg.2014.123 |
0.371 |
|
| 2014 |
Mayer J, Kitchner T, Ye Z, Zhou Z, He M, Schrodi SJ, Hebbring SJ. Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort. Genetic Epidemiology. 38: 692-8. PMID 25250975 DOI: 10.1002/Gepi.21855 |
0.329 |
|
| 2014 |
Schrodi SJ, Mukherjee S, Shan Y, Tromp G, Sninsky JJ, Callear AP, Carter TC, Ye Z, Haines JL, Brilliant MH, Crane PK, Smelser DT, Elston RC, Weeks DE. Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Frontiers in Genetics. 5: 162. PMID 24917882 DOI: 10.3389/Fgene.2014.00162 |
0.323 |
|
| 2014 |
Ye Z, Vasco DA, Carter TC, Brilliant MH, Schrodi SJ, Shukla SK. Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Frontiers in Genetics. 5: 125. PMID 24847357 DOI: 10.3389/Fgene.2014.00125 |
0.384 |
|
| 2013 |
Hebbring SJ, Schrodi SJ, Ye Z, Zhou Z, Page D, Brilliant MH. A PheWAS approach in studying HLA-DRB1*1501. Genes and Immunity. 14: 187-91. PMID 23392276 DOI: 10.1038/Gene.2013.2 |
0.345 |
|
| 2009 |
Feng BJ, Sun LD, Soltani-Arabshahi R, Bowcock AM, Nair RP, Stuart P, Elder JT, Schrodi SJ, Begovich AB, Abecasis GR, Zhang XJ, Callis-Duffin KP, Krueger GG, Goldgar DE. Multiple Loci within the major histocompatibility complex confer risk of psoriasis. Plos Genetics. 5: e1000606. PMID 19680446 DOI: 10.1371/Journal.Pgen.1000606 |
0.336 |
|
| 2009 |
Nair RP, Duffin KC, Helms C, Ding J, Stuart PE, Goldgar D, Gudjonsson JE, Li Y, Tejasvi T, Feng BJ, Ruether A, Schreiber S, Weichenthal M, Gladman D, Rahman P, ... Schrodi SJ, et al. Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nature Genetics. 41: 199-204. PMID 19169254 DOI: 10.1038/Ng.311 |
0.378 |
|
| 2009 |
Li Y, Liao W, Chang M, Schrodi SJ, Bui N, Catanese JJ, Poon A, Matsunami N, Callis-Duffin KP, Leppert MF, Bowcock AM, Kwok PY, Krueger GG, Begovich AB. Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. The Journal of Investigative Dermatology. 129: 629-34. PMID 18923449 DOI: 10.1038/Jid.2008.297 |
0.331 |
|
| 2008 |
Schrodi SJ. Genome-wide association scan in psoriasis: new insights into chronic inflammatory disease. Expert Review of Clinical Immunology. 4: 565-71. PMID 20476959 DOI: 10.1586/1744666X.4.5.565 |
0.424 |
|
| 2008 |
Garcia VE, Chang M, Brandon R, Li Y, Matsunami N, Callis-Duffin KP, Civello D, Rowland CM, Bui N, Catanese JJ, Krueger GG, Leppert MF, Begovich AB, Schrodi SJ. Detailed genetic characterization of the interleukin-23 receptor in psoriasis. Genes and Immunity. 9: 546-55. PMID 18650833 DOI: 10.1038/Gene.2008.55 |
0.39 |
|
| 2008 |
Chang M, Rowland CM, Garcia VE, Schrodi SJ, Catanese JJ, van der Helm-van Mil AH, Ardlie KG, Amos CI, Criswell LA, Kastner DL, Gregersen PK, Kurreeman FA, Toes RE, Huizinga TW, Seldin MF, et al. A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2. Plos Genetics. 4: e1000107. PMID 18648537 DOI: 10.1371/Journal.Pgen.1000107 |
0.426 |
|
| 2008 |
Li Y, Rowland C, Xiromerisiou G, Lagier RJ, Schrodi SJ, Dradiotis E, Ross D, Bui N, Catanese J, Aggelakis K, Grupe A, Hadjigeorgiou G. Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease. Plos One. 3: e2707. PMID 18628988 DOI: 10.1371/Journal.Pone.0002707 |
0.311 |
|
| 2008 |
Li Y, Chang M, Schrodi SJ, Callis-Duffin KP, Matsunami N, Civello D, Bui N, Catanese JJ, Leppert MF, Krueger GG, Begovich AB. The 5q31 variants associated with psoriasis and Crohn's disease are distinct. Human Molecular Genetics. 17: 2978-85. PMID 18614543 DOI: 10.1093/Hmg/Ddn196 |
0.342 |
|
| 2008 |
Chang M, Saiki RK, Cantanese JJ, Lew D, van der Helm-van Mil AH, Toes RE, Huizinga TW, Ardlie KG, Criswell LA, Seldin MF, Amos CI, Kastner DL, Gregersen PK, Schrodi SJ, Begovich AB. The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritis. Arthritis and Rheumatism. 58: 1877-81. PMID 18512797 DOI: 10.1002/Art.23492 |
0.465 |
|
| 2008 |
Chang M, Li Y, Yan C, Callis-Duffin KP, Matsunami N, Garcia VE, Cargill M, Civello D, Bui N, Catanese JJ, Leppert MF, Krueger GG, Begovich AB, Schrodi SJ. Variants in the 5q31 cytokine gene cluster are associated with psoriasis. Genes and Immunity. 9: 176-81. PMID 18075513 DOI: 10.1038/Sj.Gene.6364451 |
0.373 |
|
| 2007 |
Kurreeman FA, Padyukov L, Marques RB, Schrodi SJ, Seddighzadeh M, Stoeken-Rijsbergen G, van der Helm-van Mil AH, Allaart CF, Verduyn W, Houwing-Duistermaat J, Alfredsson L, Begovich AB, Klareskog L, Huizinga TW, Toes RE. A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis. Plos Medicine. 4: e278. PMID 17880261 DOI: 10.1371/Journal.Pmed.0040278 |
0.469 |
|
| 2007 |
Begovich AB, Chang M, Schrodi SJ. Meta-analysis evidence of a differential risk of the FCRL3 -169T-->C polymorphism in white and East Asian rheumatoid arthritis patients. Arthritis and Rheumatism. 56: 3168-71. PMID 17763442 DOI: 10.1002/Art.22857 |
0.351 |
|
| 2007 |
Cargill M, Schrodi SJ, Chang M, Garcia VE, Brandon R, Callis KP, Matsunami N, Ardlie KG, Civello D, Catanese JJ, Leong DU, Panko JM, McAllister LB, Hansen CB, Papenfuss J, et al. A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes. American Journal of Human Genetics. 80: 273-90. PMID 17236132 DOI: 10.1086/511051 |
0.347 |
|
| 2007 |
Schrodi SJ, Garcia VE, Rowland C, Jones HB. Pairwise linkage disequilibrium under disease models. European Journal of Human Genetics : Ejhg. 15: 212-20. PMID 17106449 DOI: 10.1038/Sj.Ejhg.5201731 |
0.339 |
|
| 2007 |
Kurreeman FAS, Padyukov L, Marques RB, Schrodi SJ, Seddighzadeh M, Stoeken-Rijsbergen G, Van Der Helm-Van Mil AHM, Allaart CF, Verduyn W, Houwing-Duistermaat J, Alfredsson L, Begovich AB, Klareskog L, Huizinga TWJ, Toes REM. A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis (PLos Medicine (2007) 4, 9, DOI: 10.1371/journal.pmed. 0040278) Plos Medicine. 4: 2013. DOI: 10.1371/Journal.Pmed.0040358 |
0.335 |
|
| 2007 |
Begovich A, Chang M, Leppert M, Schrodi S, Krueger G. Characterization of the Psoriasis-associated IL12B and IL23R Genes Clinical Immunology. 123: S126. DOI: 10.1016/J.Clim.2007.03.537 |
0.337 |
|
| 2006 |
Li Y, Schrodi S, Rowland C, Tacey K, Catanese J, Grupe A. Genetic evidence for ubiquitin-specific proteases USP24 and USP40 as candidate genes for late-onset Parkinson disease. Human Mutation. 27: 1017-23. PMID 16917932 DOI: 10.1002/Humu.20382 |
0.347 |
|
| 2005 |
Schrodi SJ. A probabilistic approach to large-scale association scans: a semi-Bayesian method to detect disease-predisposing alleles. Statistical Applications in Genetics and Molecular Biology. 4: Article31. PMID 16646850 DOI: 10.2202/1544-6115.1168 |
0.352 |
|
| 2005 |
Carlton VE, Hu X, Chokkalingam AP, Schrodi SJ, Brandon R, Alexander HC, Chang M, Catanese JJ, Leong DU, Ardlie KG, Kastner DL, Seldin MF, Criswell LA, Gregersen PK, Beasley E, et al. PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. American Journal of Human Genetics. 77: 567-81. PMID 16175503 DOI: 10.1086/468189 |
0.465 |
|
| 2004 |
Li Y, Nowotny P, Holmans P, Smemo S, Kauwe JS, Hinrichs AL, Tacey K, Doil L, van Luchene R, Garcia V, Rowland C, Schrodi S, Leong D, Gogic G, Chan J, et al. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences of the United States of America. 101: 15688-93. PMID 15507493 DOI: 10.1073/Pnas.0403535101 |
0.383 |
|
| 2004 |
Hu X, Schrodi SJ, Ross DA, Cargill M. Selecting tagging SNPs for association studies using power calculations from genotype data. Human Heredity. 57: 156-70. PMID 15297809 DOI: 10.1159/000079246 |
0.342 |
|
| 2004 |
Li Y, Tacey K, Doil L, van Luchene R, Garcia V, Rowland C, Schrodi S, Leong D, Lau K, Catanese J, Sninsky J, Nowotny P, Holmans P, Hardy J, Powell J, et al. Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study. Neuroscience Letters. 366: 268-71. PMID 15288432 DOI: 10.1016/J.Neulet.2004.05.047 |
0.331 |
|
| 2004 |
Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, Chokkalingam AP, Alexander HC, Ardlie KG, Huang Q, Smith AM, Spoerke JM, Conn MT, Chang M, Chang SY, Saiki RK, Catanese JJ, et al. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. American Journal of Human Genetics. 75: 330-7. PMID 15208781 DOI: 10.1086/422827 |
0.465 |
|
| 2004 |
Li Y, Nowotny P, Holmans P, Smemo S, Kawe K, Tacey K, Doil L, Luchene Rv, Garcia V, Rowland C, Schrodi S, Leong D, Chan J, Lau K, Chang S, et al. P4-046 Association of late onset Alzheimer's disease with genetic variation in multiple members of a gene family involved in neuronal apoptosis Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81604-X |
0.321 |
|
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