| Year |
Citation |
Score |
| 2023 |
Liu D, Meyer D, Fennessy B, Feng C, Cheng E, Johnson JS, Park YJ, Rieder MK, Ascolillo S, de Pins A, Dobbyn A, Lebovitch D, Moya E, Nguyen TH, Wilkins L, ... ... Stahl EA, et al. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature Genetics. 55: 369-376. PMID 36914870 DOI: 10.1038/s41588-023-01305-1 |
0.371 |
|
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Stahl EA, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.32 |
|
| 2022 |
Highland HM, Wojcik GL, Graff M, Nishimura KK, Hodonsky CJ, Baldassari AR, Cote AC, Cheng I, Gignoux CR, Tao R, Li Y, Boerwinkle E, Fornage M, Haessler J, Hindorff LA, ... ... Stahl EA, et al. Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits. American Journal of Human Genetics. PMID 35263625 DOI: 10.1016/j.ajhg.2022.02.013 |
0.344 |
|
| 2021 |
Backman JD, Li AH, Marcketta A, Sun D, Mbatchou J, Kessler MD, Benner C, Liu D, Locke AE, Balasubramanian S, Yadav A, Banerjee N, Gillies C, Damask A, Liu S, ... ... Stahl E, et al. Exome sequencing and analysis of 454,787 UK Biobank participants. Nature. PMID 34662886 DOI: 10.1038/s41586-021-04103-z |
0.329 |
|
| 2021 |
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Stahl EA, et al. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33483695 DOI: 10.1038/s41380-020-01006-9 |
0.311 |
|
| 2020 |
Coombes BJ, Markota M, Mann JJ, Colby C, Stahl E, Talati A, Pathak J, Weissman MM, McElroy SL, Frye MA, Biernacka JM. Dissecting clinical heterogeneity of bipolar disorder using multiple polygenic risk scores. Translational Psychiatry. 10: 314. PMID 32948743 DOI: 10.1038/S41398-020-00996-Y |
0.358 |
|
| 2020 |
Nguyen TH, Dobbyn A, Brown RC, Riley BP, Buxbaum JD, Pinto D, Purcell SM, Sullivan PF, He X, Stahl EA. mTADA is a framework for identifying risk genes from de novo mutations in multiple traits. Nature Communications. 11: 2929. PMID 32522981 DOI: 10.1038/S41467-020-16487-Z |
0.419 |
|
| 2020 |
Huckins LM, Chatzinakos C, Breen MS, Hartmann J, Klengel T, da Silva Almeida AC, Dobbyn A, Girdhar K, Hoffman GE, Klengel C, Logue MW, Lori A, Maihofer AX, Morrison FG, Nguyen HT, ... ... Stahl EA, et al. Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts. Cell Reports. 31: 107716. PMID 32492425 DOI: 10.1016/J.Celrep.2020.107716 |
0.372 |
|
| 2020 |
Zhang Z, Menon MC, Zhang W, Stahl E, Loza BL, Rosales IA, Yi Z, Banu K, Garzon F, Sun Z, Wei C, Huang W, Lin Q, Israni A, Keating BJ, et al. Genome-wide non-HLA donor-recipient genetic differences influence renal allograft survival via early allograft fibrosis. Kidney International. PMID 32454123 DOI: 10.1016/J.Kint.2020.04.039 |
0.31 |
|
| 2020 |
Byrne EM, Zhu Z, Qi T, Skene NG, Bryois J, Pardinas AF, Stahl E, Smoller JW, Rietschel M, Owen MJ, Walters JTR, O'Donovan MC, McGrath JG, et al. Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry. PMID 32398722 DOI: 10.1038/S41380-020-0705-9 |
0.37 |
|
| 2020 |
Stahl E, Roda G, Dobbyn A, Hu J, Zhang Z, Westerlind H, Bonfiglio F, Raj T, Torres J, Chen A, Petras R, Pardi DS, Iuga AC, Levi GS, Cao W, et al. COLLAGENOUS COLITIS IS ASSOCIATED WITH HLA SIGNATURE AND SHARES GENETIC RISKS WITH OTHER IMMUNE-MEDIATED DISEASES. Gastroenterology. PMID 32371109 DOI: 10.1053/J.Gastro.2020.04.063 |
0.387 |
|
| 2020 |
Boocock J, Leask M, Okada Y, Matsuo H, Kawamura Y, Shi Y, Li C, Mount DB, Mandal AK, Wang W, Cadzow M, Gosling AL, Major TJ, Horsfield JA, ... ... Stahl EA, et al. Genomic dissection of 43 serum urate-associated loci provides multiple insights into molecular mechanisms of urate control. Human Molecular Genetics. PMID 31985003 DOI: 10.1093/Hmg/Ddaa013 |
0.42 |
|
| 2020 |
Biernacka J, Moscati A, Coombes B, Charney A, Huckins L, McElroy S, Frye M, Stahl E. Multiple Polygenic Risk Score Analysis Reveals Genetic Contributions to Psychiatric Traits in Research and Electronic Health Records Data Biological Psychiatry. 87. DOI: 10.1016/J.Biopsych.2020.02.197 |
0.347 |
|
| 2020 |
Dobbyn A, Feng C, Cheng E, Moya E, Rieder MK, Johnson J, Pins Ad, O'Donovan M, Sullivan P, Sklar P, Huckins L, Charney A, Stahl E. Targeted Sequencing of Genes Most Likely to Harbor Rare Causal Variants in Schizophrenia Biological Psychiatry. 87. DOI: 10.1016/J.Biopsych.2020.02.1135 |
0.332 |
|
| 2020 |
Huckins L, Pietrzak R, Yehuda R, Stahl E, Feder A. Genetic Regulation of PTSD and Resilience Among World Trade Center Responders Biological Psychiatry. 87. DOI: 10.1016/J.Biopsych.2020.02.091 |
0.307 |
|
| 2019 |
Szatkiewicz JP, Fromer M, Nonneman RJ, Ancalade N, Johnson JS, Stahl EA, Rees E, Bergen SE, Hultman CM, Kirov G, O'Donovan M, Owen M, Holmans P, Sklar P, Sullivan PF, et al. Characterization of Single Gene Copy Number Variants in Schizophrenia. Biological Psychiatry. PMID 31767120 DOI: 10.1016/J.Biopsych.2019.09.023 |
0.41 |
|
| 2019 |
Peterson RE, Kuchenbaecker K, Walters RK, Chen CY, Popejoy AB, Periyasamy S, Lam M, Iyegbe C, Strawbridge RJ, Brick L, Carey CE, Martin AR, Meyers JL, Su J, Chen J, ... ... Stahl EA, et al. Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations. Cell. PMID 31607513 DOI: 10.1016/J.Cell.2019.08.051 |
0.402 |
|
| 2019 |
Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Molecular Psychiatry. PMID 31591465 DOI: 10.1038/S41380-019-0517-Y |
0.435 |
|
| 2019 |
Schrode N, Ho SM, Yamamuro K, Dobbyn A, Huckins L, Matos MR, Cheng E, Deans PJM, Flaherty E, Barretto N, Topol A, Alganem K, Abadali S, Gregory J, Hoelzli E, ... ... Stahl EA, et al. Synergistic effects of common schizophrenia risk variants. Nature Genetics. PMID 31548722 DOI: 10.1038/S41588-019-0497-5 |
0.458 |
|
| 2019 |
Breen MS, Dobbyn A, Li Q, Roussos P, Hoffman GE, Stahl E, Chess A, Sklar P, Li JB, Devlin B, Buxbaum JD. Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia. Nature Neuroscience. 22: 1402-1412. PMID 31455887 DOI: 10.1016/J.Euroneuro.2019.07.236 |
0.317 |
|
| 2019 |
Zheutlin AB, Dennis J, Karlsson Linnér R, Moscati A, Restrepo N, Straub P, Ruderfer D, Castro VM, Chen CY, Ge T, Huckins LM, Charney A, Kirchner HL, Stahl EA, Chabris CF, et al. Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems. The American Journal of Psychiatry. appiajp201918091085. PMID 31416338 DOI: 10.1176/Appi.Ajp.2019.18091085 |
0.338 |
|
| 2019 |
Lam M, Hill WD, Trampush JW, Yu J, Knowles E, Davies G, Stahl E, Huckins L, Liewald DC, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, et al. Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. American Journal of Human Genetics. 105: 334-350. PMID 31374203 DOI: 10.1016/J.Ajhg.2019.06.012 |
0.348 |
|
| 2019 |
Wojcik GL, Graff M, Nishimura KK, Tao R, Haessler J, Gignoux CR, Highland HM, Patel YM, Sorokin EP, Avery CL, Belbin GM, Bien SA, Cheng I, Cullina S, Hodonsky CJ, ... ... Stahl EA, et al. Genetic analyses of diverse populations improves discovery for complex traits. Nature. PMID 31217584 DOI: 10.1038/S41586-019-1310-4 |
0.433 |
|
| 2019 |
Demontis D, Rajagopal VM, Thorgeirsson TE, Als TD, Grove J, Leppälä K, Gudbjartsson DF, Pallesen J, Hjorthøj C, Reginsson GW, Tyrfingsson T, Runarsdottir V, Qvist P, Christensen JH, Bybjerg-Grauholm J, ... ... Stahl EA, et al. Genome-wide association study implicates CHRNA2 in cannabis use disorder. Nature Neuroscience. PMID 31209380 DOI: 10.1038/S41593-019-0416-1 |
0.452 |
|
| 2019 |
Mullins N, Bigdeli TB, Børglum AD, Coleman JRI, Demontis D, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A, Corvin A, Sanders AR, Forstner AJ, et al. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. The American Journal of Psychiatry. appiajp201918080957. PMID 31164008 DOI: 10.1176/Appi.Ajp.2019.18080957 |
0.33 |
|
| 2019 |
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, ... ... Stahl EA, et al. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. PMID 31160808 DOI: 10.1038/S41588-019-0450-7 |
0.331 |
|
| 2019 |
Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Stahl EA, et al. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 31086353 DOI: 10.1038/S41588-019-0435-6 |
0.316 |
|
| 2019 |
Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. PMID 31043756 DOI: 10.1038/S41588-019-0397-8 |
0.416 |
|
| 2019 |
Kim S, Jang HJ, Myung W, Kim K, Cha S, Lee H, Cho SK, Kim B, Ha TH, Kim JW, Kim DK, Stahl EA, Won HH. Heritability estimates of individual psychological distress symptoms from genetic variation. Journal of Affective Disorders. 252: 413-420. PMID 31003110 DOI: 10.1016/J.Jad.2019.04.011 |
0.34 |
|
| 2019 |
Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Stahl EA, et al. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 30911161 DOI: 10.1038/S41588-019-0364-4 |
0.414 |
|
| 2019 |
Charney A, Feng C, O'Donovan M, Sullivan P, Sklar P, Stahl E. 39 Targeted Sequencing Of Genes Most Likely To Harbor Rare Causal Variants In Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.180 |
0.332 |
|
| 2019 |
Nguyen T, Charney A, He X, Kendler K, Sullivan P, Bacanu S, Riley B, Stahl E. 13 INTEGRATED ANALYSIS OF RARE VARIANTS AND SINGLE-CELL EXPRESSION DATA PROVIDES INSIGHTS INTO SCHIZOPHRENIA RISK European Neuropsychopharmacology. 29: S65-S66. DOI: 10.1016/J.Euroneuro.2019.07.154 |
0.333 |
|
| 2019 |
Huckins L, Breen M, van Rooij S, Hartmann J, Girdhar K, Jovanovic T, Nievergelt C, Im HK, Buxbaum J, Sklar P, Ressler K, Stahl E, Daskalakis N. GENETICALLY REGULATED GENE EXPRESSION IN BRAIN AND PERIPHERAL TISSUES IN PTSD European Neuropsychopharmacology. 29: S1056. DOI: 10.1016/J.Euroneuro.2018.07.072 |
0.317 |
|
| 2019 |
Huckins L, Girdhar K, Dobbyn A, Jovanovic T, Nievergelt C, Hoffman G, Maihofer A, Stein M, Sklar P, Ressler K, Buxbaum J, Stahl E, Daskalakis N. Genetically Predicted Gene Expression In The Brain And Peripheral Tissues Associates With Ptsd European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.200 |
0.356 |
|
| 2019 |
Mullins N, Bigdeli T, Power R, McQuillin A, Stahl E, Mehta D, Lewis C. Genome-Wide Association Study Of Suicide Attempt In Major Psychiatric Disorders European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.068 |
0.34 |
|
| 2019 |
Huckins L, Dobbyn A, Thornton L, Devlin B, Sieberts S, Cox N, Im HK, Breen G, Sklar P, Bulik C, Stahl E. Transcriptomic Imputation Analysis In Anorexia Nervosa Identifies Both Metabolic And Psychiatric Aetiologies European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.064 |
0.37 |
|
| 2019 |
Stahl E. Genome-Wide Association Study Identifies Twenty New Loci Associated With Bipolar Disorder European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.061 |
0.419 |
|
| 2018 |
Charney AW, Stahl EA, Green EK, Chen CY, Moran JL, Chambert K, Belliveau RA, Forty L, Gordon-Smith K, Lee PH, Bromet EJ, Buckley PF, Escamilla MA, Fanous AH, Fochtmann LJ, et al. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases. Biological Psychiatry. PMID 30686506 DOI: 10.1016/J.Biopsych.2018.12.009 |
0.347 |
|
| 2018 |
Velthorst E, Froudist-Walsh S, Stahl E, Ruderfer D, Ivanov I, Buxbaum J. Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis. Translational Psychiatry. 8: 204. PMID 30258131 DOI: 10.1038/S41398-018-0229-0 |
0.328 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Stahl E, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.355 |
|
| 2018 |
Dobbyn A, Huckins LM, Boocock J, Sloofman LG, Glicksberg BS, Giambartolomei C, Hoffman GE, Perumal TM, Girdhar K, Jiang Y, Raj T, Ruderfer DM, Kramer RS, Pinto D, ... ... Stahl EA, et al. Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS. American Journal of Human Genetics. PMID 29805045 DOI: 10.1016/J.Ajhg.2018.04.011 |
0.426 |
|
| 2018 |
Rangan AV, McGrouther CC, Kelsoe J, Schork N, Stahl E, Zhu Q, Krishnan A, Yao V, Troyanskaya O, Bilaloglu S, Raghavan P, Bergen S, Jureus A, Landen M. A loop-counting method for covariate-corrected low-rank biclustering of gene-expression and genome-wide association study data. Plos Computational Biology. 14: e1006105. PMID 29758032 DOI: 10.1371/Journal.Pcbi.1006105 |
0.3 |
|
| 2018 |
Major TJ, Dalbeth N, Stahl EA, Merriman TR. An update on the genetics of hyperuricaemia and gout. Nature Reviews. Rheumatology. PMID 29740155 DOI: 10.1038/S41584-018-0004-X |
0.446 |
|
| 2018 |
Barbeira AN, Dickinson SP, Bonazzola R, Zheng J, Wheeler HE, Torres JM, Torstenson ES, Shah KP, Garcia T, Edwards TL, Stahl EA, Huckins LM, Nicolae DL, Cox NJ, et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nature Communications. 9: 1825. PMID 29739930 DOI: 10.1038/S41467-018-03621-1 |
0.414 |
|
| 2018 |
Chen CY, Lee PH, Castro VM, Minnier J, Charney AW, Stahl EA, Ruderfer DM, Murphy SN, Gainer V, Cai T, Jones I, Pato CN, Pato MT, Landén M, Sklar P, et al. Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records. Translational Psychiatry. 8: 86. PMID 29666432 DOI: 10.1038/S41398-018-0133-7 |
0.371 |
|
| 2018 |
Maier RM, Zhu Z, Lee SH, Trzaskowski M, Ruderfer DM, Stahl EA, Ripke S, Wray NR, Yang J, Visscher PM, Robinson MR. Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Nature Communications. 9: 989. PMID 29515099 DOI: 10.1038/S41467-017-02769-6 |
0.408 |
|
| 2018 |
Baillie JK, Bretherick A, Haley CS, Clohisey S, Gray A, Neyton LPA, Barrett J, Stahl EA, Tenesa A, Andersson R, Brown JB, Faulkner GJ, Lizio M, Schaefer U, Daub C, et al. Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease. Plos Computational Biology. 14: e1005934. PMID 29494619 DOI: 10.1371/Journal.Pcbi.1005934 |
0.435 |
|
| 2018 |
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, ... ... Stahl EA, et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. PMID 29483656 DOI: 10.1038/S41588-018-0059-2 |
0.448 |
|
| 2017 |
Hoffman GE, Hartley BJ, Flaherty E, Ladran I, Gochman P, Ruderfer DM, Stahl EA, Rapoport J, Sklar P, Brennand KJ. Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains. Nature Communications. 8: 2225. PMID 29263384 DOI: 10.1038/S41467-017-02330-5 |
0.332 |
|
| 2017 |
Nguyen HT, Bryois J, Kim A, Dobbyn A, Huckins LM, Munoz-Manchado AB, Ruderfer DM, Genovese G, Fromer M, Xu X, Pinto D, Linnarsson S, Verhage M, Smit AB, Hjerling-Leffler J, ... ... Stahl EA, et al. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders. Genome Medicine. 9: 114. PMID 29262854 DOI: 10.1186/S13073-017-0497-Y |
0.378 |
|
| 2017 |
Gosling AL, Boocock J, Dalbeth N, Harré Hindmarsh J, Stamp LK, Stahl EA, Choi HK, Matisoo-Smith EA, Merriman TR. Mitochondrial genetic variation and gout in Māori and Pacific people living in Aotearoa New Zealand. Annals of the Rheumatic Diseases. PMID 29247128 DOI: 10.1136/Annrheumdis-2017-212416 |
0.319 |
|
| 2017 |
Tanner C, Boocock J, Stahl EA, Dobbyn A, Mandal AK, Cadzow M, Phipps-Green AJ, Topless RK, Harré Hindmarsh J, Stamp LK, Dalbeth N, Choi HK, Mount DB, Merriman TR. Population specific resequencing associates the ATP Binding Cassette Subfamily C Member 4 (ABCC4) gene with gout in New Zealand Māori and Pacific men. Arthritis & Rheumatology (Hoboken, N.J.). PMID 28371506 DOI: 10.1002/Art.40110 |
0.423 |
|
| 2017 |
Webb TR, Erdmann J, Stirrups KE, Stitziel NO, Masca NG, Jansen H, Kanoni S, Nelson CP, Ferrario PG, König IR, Eicher JD, Johnson AD, Hamby SE, Betsholtz C, Ruusalepp A, ... ... Stahl E, et al. Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology. 69: 823-836. PMID 28209224 DOI: 10.1016/J.Jacc.2016.11.056 |
0.326 |
|
| 2017 |
Charney AW, Ruderfer DM, Stahl EA, Moran JL, Chambert K, Belliveau RA, Forty L, Gordon-Smith K, Di Florio A, Lee PH, Bromet EJ, Buckley PF, Escamilla MA, Fanous AH, Fochtmann LJ, et al. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder. Translational Psychiatry. 7: e993. PMID 28072414 DOI: 10.1038/Tp.2016.242 |
0.43 |
|
| 2017 |
Merriman T, Cadzow M, Merriman M, Phipps-Green A, Topless R, Abhishek A, Andres M, Bradbury L, Buchanan R, Cremin K, Guzman Ed, Zoysa Jd, Doherty M, Hill C, Huizinga T, ... ... Stahl E, et al. A Genome-Wide Association Study of Gout in People of European Ancestry Annals of the Rheumatic Diseases. 76: 383-383. DOI: 10.1136/Annrheumdis-2017-Eular.5634 |
0.383 |
|
| 2017 |
Merriman T, Cadzow M, Topless R, Mount D, Choi H, Okada Y, Boocock J, Stahl E. OP0263 Trans-ancestral meta-analysis identifies 13 new loci associated with serum urate levels Annals of the Rheumatic Diseases. 76: 165-165. DOI: 10.1136/Annrheumdis-2017-Eular.4611 |
0.417 |
|
| 2017 |
Roda G, Dobbyn A, Hu J, Zhang Z, Torres J, Chen A, Petras RE, Pardi DS, Iuga A, Levy G, cao W, Rieder F, Gordon I, Harpaz N, Cho JH, ... ... Stahl E, et al. Immunochip Analysis Revealed HLA Mechanism in Collagenous Colitis and Overlapping Genes with Immunomediated Diseases Gastroenterology. 152: S1306. DOI: 10.1016/S0016-5085(17)34352-4 |
0.313 |
|
| 2017 |
Huckins L, Dobbyn A, Ruderfer D, Fromer M, CommonMind Consortium CC, Cox N, Im HK, Sieberts S, Devlin B, Roussos P, Purcell S, Sklar P, Stahl E. Novel Bipolar And Schizophrenia Risk Genes Identified Through Genic Associations In Transcriptome Imputation European Neuropsychopharmacology. 27: S487. DOI: 10.1016/J.Euroneuro.2016.09.577 |
0.447 |
|
| 2017 |
Genovese G, Fromer M, Stahl E, Ruderfer D, Chambert K, Landen M, Moran J, Purcell S, Sklar P, Sullivan P, Hultman C, McCarroll S. Ultra-Rare Protein-Altering Variants Among 4,877 Swedish Individuals with Schizophrenia European Neuropsychopharmacology. 27: S426-S427. DOI: 10.1016/J.Euroneuro.2016.09.480 |
0.306 |
|
| 2016 |
Zubair N, Graff M, Luis Ambite J, Bush WS, Kichaev G, Lu Y, Manichaikul A, Sheu WH, Absher D, Assimes TL, Bielinski SJ, Bottinger EP, Buzkova P, Chuang LM, Chung RH, ... ... Stahl E, et al. Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci. Human Molecular Genetics. 25: 5500-5512. PMID 28426890 DOI: 10.1093/Hmg/Ddw358 |
0.352 |
|
| 2016 |
Johnson EC, Bjelland DW, Howrigan DP, Abdellaoui A, Breen G, Borglum A, Cichon S, Degenhardt F, Forstner AJ, Frank J, Genovese G, Heilmann-Heimbach S, Herms S, Hoffman P, Maier W, ... ... Stahl E, et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. Plos Genetics. 12: e1006343. PMID 27792727 DOI: 10.1371/Journal.Pgen.1006343 |
0.357 |
|
| 2016 |
Cui J, Diogo D, Stahl EA, Canhao H, Mariette X, Greenberg JD, Okada Y, Pappas DA, Fulton RS, Tak PP, Nurmohamed MT, Lee A, Larson DE, Kurreeman F, Deluca TL, et al. The role of rare protein-coding variants to anti-TNF treatment response in rheumatoid arthritis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 27788309 DOI: 10.1002/Art.39966 |
0.358 |
|
| 2016 |
Genovese G, Fromer M, Stahl EA, Ruderfer DM, Chambert K, Landén M, Moran JL, Purcell SM, Sklar P, Sullivan PF, Hultman CM, McCarroll SA. Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia. Nature Neuroscience. PMID 27694994 DOI: 10.1038/Nn.4402 |
0.369 |
|
| 2016 |
Fromer M, Roussos P, Sieberts SK, Johnson JS, Kavanagh DH, Perumal TM, Ruderfer DM, Oh EC, Topol A, Shah HR, Klei LL, Kramer R, Pinto D, Gümüş ZH, Cicek AE, ... ... Stahl EA, et al. Gene expression elucidates functional impact of polygenic risk for schizophrenia. Nature Neuroscience. PMID 27668389 DOI: 10.1038/Nn.4399 |
0.392 |
|
| 2016 |
Sieberts SK, Zhu F, García-García J, Stahl E, Pratap A, Pandey G, Pappas D, Aguilar D, Anton B, Bonet J, Eksi R, Fornés O, Guney E, Li H, Marín MA, et al. Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis. Nature Communications. 7: 12460. PMID 27549343 DOI: 10.1038/Ncomms12460 |
0.349 |
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| 2016 |
Han B, Pouget JG, Slowikowski K, Stahl E, Lee CH, Diogo D, Hu X, Park YR, Kim E, Gregersen PK, Dahlqvist SR, Worthington J, Martin J, Eyre S, Klareskog L, et al. A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases. Nature Genetics. PMID 27182969 DOI: 10.1038/Ng.3572 |
0.415 |
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| 2016 |
Goes FS, Pirooznia M, Parla JS, Kramer M, Ghiban E, Mavruk S, Chen YC, Monson ET, Willour VL, Karchin R, Flickinger M, Locke AE, Levy SE, Scott LJ, Boehnke M, ... Stahl E, et al. Exome Sequencing of Familial Bipolar Disorder. Jama Psychiatry. PMID 27120077 DOI: 10.1001/Jamapsychiatry.2016.0251 |
0.328 |
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| 2016 |
Rasheed H, McKinney C, Stamp LK, Dalbeth N, Topless RK, Day R, Kannangara D, Williams K, Smith M, Janssen M, Jansen TL, Joosten LA, Radstake TR, Riches PL, Tausche AK, ... ... Stahl EA, et al. The Toll-Like Receptor 4 (TLR4) Variant rs2149356 and Risk of Gout in European and Polynesian Sample Sets. Plos One. 11: e0147939. PMID 26808548 DOI: 10.1371/Journal.Pone.0147939 |
0.391 |
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| 2016 |
Merriman T, Gosling A, Boocock J, Dalbeth N, Stamp L, Stahl E, Choi H, Matisoo-Smith L. OP0158 Mitochondrial Genetic Variation and Susceptibility To Gout in Polynesians Annals of the Rheumatic Diseases. 75: 115-116. DOI: 10.1136/Annrheumdis-2016-Eular.4476 |
0.368 |
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| 2016 |
Merriman T, Boocock J, Stahl E, Cadzow M, Phipps-Green A, Topless R, Hindmarsh JH, Mount D, Stamp L, Dalbeth N, Choi H, Tanner C. THU0539 Population-Specific Resequencing Reveals Association of The ABCC4/MRP4 Gene with Gout in New Zealand Māori and Pacific Men Annals of the Rheumatic Diseases. 75: 387-387. DOI: 10.1136/Annrheumdis-2016-Eular.4365 |
0.42 |
|
| 2015 |
Won HH, Natarajan P, Dobbyn A, Jordan DM, Roussos P, Lage K, Raychaudhuri S, Stahl E, Do R. Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease. Plos Genetics. 11: e1005622. PMID 26509271 DOI: 10.1371/Journal.Pgen.1005622 |
0.426 |
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| 2015 |
Song J, Bergen SE, Di Florio A, Karlsson R, Charney A, Ruderfer DM, Stahl EA, Chambert KD, Moran JL, Gordon-Smith K, Forty L, Green EK, Jones I, Jones L, ... ... Stahl EA, et al. Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Molecular Psychiatry. PMID 26503763 DOI: 10.1038/Mp.2015.165 |
0.424 |
|
| 2015 |
Vilhjálmsson BJ, Yang J, Finucane HK, Gusev A, Lindström S, Ripke S, Genovese G, Loh PR, Bhatia G, Do R, Hayeck T, Won HH, Kathiresan S, ... ... Stahl E, et al. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. American Journal of Human Genetics. 97: 576-592. PMID 26430803 DOI: 10.1016/J.Ajhg.2015.09.001 |
0.322 |
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| 2015 |
Finucane HK, Bulik-Sullivan B, Gusev A, Trynka G, Reshef Y, Loh PR, Anttila V, Xu H, Zang C, Farh K, Ripke S, Day FR, ... ... Stahl E, et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nature Genetics. PMID 26414678 DOI: 10.1038/Ng.3404 |
0.374 |
|
| 2015 |
Lee SH, Byrne EM, Hultman CM, Kähler A, Vinkhuyzen AA, Ripke S, Andreassen OA, Frisell T, Gusev A, Hu X, Karlsson R, Mantzioris VX, McGrath JJ, Mehta D, Stahl EA, et al. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology. PMID 26286434 DOI: 10.1093/Ije/Dyv136 |
0.395 |
|
| 2015 |
Diogo D, Bastarache L, Liao KP, Graham RR, Fulton RS, Greenberg JD, Eyre S, Bowes J, Cui J, Lee A, Pappas DA, Kremer JM, Barton A, Coenen MJ, Franke B, ... ... Stahl EA, et al. TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. Plos One. 10: e0122271. PMID 25849893 DOI: 10.1371/Journal.Pone.0122271 |
0.408 |
|
| 2015 |
Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert MF, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, ... ... Stahl EA, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897. PMID 25631608 DOI: 10.1038/Ncomms6897 |
0.31 |
|
| 2014 |
Chhibber A, Kroetz DL, Tantisira KG, McGeachie M, Cheng C, Plenge R, Stahl E, Sadee W, Ritchie MD, Pendergrass SA. Genomic architecture of pharmacological efficacy and adverse events. Pharmacogenomics. 15: 2025-48. PMID 25521360 DOI: 10.2217/Pgs.14.144 |
0.411 |
|
| 2014 |
Roussos P, Mitchell AC, Voloudakis G, Fullard JF, Pothula VM, Tsang J, Stahl EA, Georgakopoulos A, Ruderfer DM, Charney A, Okada Y, Siminovitch KA, Worthington J, Padyukov L, Klareskog L, et al. A role for noncoding variation in schizophrenia. Cell Reports. 9: 1417-29. PMID 25453756 DOI: 10.1016/J.Celrep.2014.10.015 |
0.412 |
|
| 2014 |
Gusev A, Lee SH, Trynka G, Finucane H, Vilhjálmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E, Kähler AK, Hultman CM, Purcell SM, et al. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics. 95: 535-52. PMID 25439723 DOI: 10.1016/J.Ajhg.2014.10.004 |
0.423 |
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| 2014 |
Hutchinson JN, Raj T, Fagerness J, Stahl E, Viloria FT, Gimelbrant A, Seddon J, Daly M, Chess A, Plenge R. Allele-specific methylation occurs at genetic variants associated with complex disease. Plos One. 9: e98464. PMID 24911414 DOI: 10.1371/Journal.Pone.0098464 |
0.437 |
|
| 2014 |
Okada Y, Diogo D, Greenberg JD, Mouassess F, Achkar WA, Fulton RS, Denny JC, Gupta N, Mirel D, Gabriel S, Li G, Kremer JM, Pappas DA, Carroll RJ, Eyler AE, ... ... Stahl EA, et al. Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. Plos One. 9: e87645. PMID 24520335 DOI: 10.1371/Journal.Pone.0087645 |
0.435 |
|
| 2014 |
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, ... ... Stahl EA, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. American Journal of Human Genetics. 94: 233-45. PMID 24507775 DOI: 10.1016/J.Ajhg.2014.01.010 |
0.358 |
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| 2014 |
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O'Dushlaine C, Chambert K, Bergen SE, Kähler A, Duncan L, Stahl E, Genovese G, Fernández E, Collins MO, et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 506: 185-90. PMID 24463508 DOI: 10.1038/Nature12975 |
0.424 |
|
| 2014 |
Okada Y, Wu D, Trynka G, Raj T, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Yoshida S, Graham RR, Manoharan A, Ortmann W, Bhangale T, Denny JC, ... ... Stahl EA, et al. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature. 506: 376-81. PMID 24390342 DOI: 10.1038/Nature12873 |
0.426 |
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| 2013 |
Gusev A, Bhatia G, Zaitlen N, Vilhjalmsson BJ, Diogo D, Stahl EA, Gregersen PK, Worthington J, Klareskog L, Raychaudhuri S, Plenge RM, Pasaniuc B, Price AL. Quantifying missing heritability at known GWAS loci. Plos Genetics. 9: e1003993. PMID 24385918 DOI: 10.1371/Journal.Pgen.1003993 |
0.395 |
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| 2013 |
Lee SH, Yang J, Chen GB, Ripke S, Stahl EA, Hultman CM, Sklar P, Visscher PM, Sullivan PF, Goddard ME, Wray NR. Estimation of SNP heritability from dense genotype data. American Journal of Human Genetics. 93: 1151-5. PMID 24314550 DOI: 10.1016/J.Ajhg.2013.10.015 |
0.308 |
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| 2013 |
Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics. 45: 1150-9. PMID 23974872 DOI: 10.1038/Ng.2742 |
0.421 |
|
| 2013 |
Li G, Diogo D, Wu D, Spoonamore J, Dancik V, Franke L, Kurreeman F, Rossin EJ, Duclos G, Hartland C, Zhou X, Li K, Liu J, De Jager PL, Siminovitch KA, ... ... Stahl E, et al. Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. Plos Genetics. 9: e1003487. PMID 23696745 DOI: 10.1371/Journal.Pgen.1003487 |
0.322 |
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| 2013 |
Plenge RM, Greenberg JD, Mangravite LM, Derry JM, Stahl EA, Coenen MJ, Barton A, Padyukov L, Klareskog L, Gregersen PK, Mariette X, Moreland LW, Bridges SL, de Vries N, Huizinga TW, et al. Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge. Nature Genetics. 45: 468-9. PMID 23619782 DOI: 10.1038/Ng.2623 |
0.328 |
|
| 2013 |
Trouw LA, Daha N, Kurreeman FA, Böhringer S, Goulielmos GN, Westra HJ, Zhernakova A, Franke L, Stahl EA, Levarht EW, Stoeken-Rijsbergen G, Verduijn W, Roos A, Li Y, Houwing-Duistermaat JJ, et al. Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis. Clinical and Experimental Immunology. 173: 76-83. PMID 23607884 DOI: 10.1111/Cei.12097 |
0.437 |
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| 2013 |
Cui J, Stahl EA, Saevarsdottir S, Miceli C, Diogo D, Trynka G, Raj T, Mirkov MU, Canhao H, Ikari K, Terao C, Okada Y, Wedrén S, Askling J, Yamanaka H, et al. Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Plos Genetics. 9: e1003394. PMID 23555300 DOI: 10.1371/Journal.Pgen.1003394 |
0.355 |
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| 2013 |
McGeachie MJ, Stahl EA, Himes BE, Pendergrass SA, Lima JJ, Irvin CG, Peters SP, Ritchie MD, Plenge RM, Tantisira KG. Polygenic heritability estimates in pharmacogenetics: focus on asthma and related phenotypes. Pharmacogenetics and Genomics. 23: 324-8. PMID 23532052 DOI: 10.1097/Fpc.0B013E3283607Acf |
0.348 |
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| 2013 |
Diogo D, Kurreeman F, Stahl EA, Liao KP, Gupta N, Greenberg JD, Rivas MA, Hickey B, Flannick J, Thomson B, Guiducci C, Ripke S, Adzhubey I, Barton A, Kremer JM, et al. Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. American Journal of Human Genetics. 92: 15-27. PMID 23261300 DOI: 10.1016/J.Ajhg.2012.11.012 |
0.386 |
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| 2013 |
Umiċeviċ Mirkov M, Cui J, Vermeulen SH, Stahl EA, Toonen EJ, Makkinje RR, Lee AT, Huizinga TW, Allaart R, Barton A, Mariette X, Miceli CR, Criswell LA, Tak PP, de Vries N, et al. Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis. Annals of the Rheumatic Diseases. 72: 1375-81. PMID 23233654 DOI: 10.1136/Annrheumdis-2012-202405 |
0.389 |
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| 2013 |
Eyre S, Bowes J, Diogo D, Raychaudhuri S, Stahl E, Zhernakova A, Padyukov L, Amos C, Plenge R, Klareskog L, Gregersen P, Worthington J. OP0208 High density fine mapping in rheumatoid arthritis indentifies 14 new loci: Annals of the Rheumatic Diseases. 71: 126.1-126. DOI: 10.1136/Annrheumdis-2012-Eular.1891 |
0.436 |
|
| 2012 |
Eyre S, Bowes J, Diogo D, Lee A, Barton A, Martin P, Zhernakova A, Stahl E, Viatte S, McAllister K, Amos CI, Padyukov L, Toes RE, Huizinga TW, Wijmenga C, et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics. 44: 1336-40. PMID 23143596 DOI: 10.1038/Ng.2462 |
0.457 |
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| 2012 |
Stahl EA, Raychaudhuri S. Rheumatoid arthritis. Evidence for a genetic component to disease severity in RA. Nature Reviews. Rheumatology. 8: 312-3. PMID 22647779 DOI: 10.1038/Nrrheum.2012.74 |
0.338 |
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| 2012 |
Okada Y, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Kawaguchi T, Stahl EA, Kurreeman FA, Nishida N, Ohmiya H, Myouzen K, Takahashi M, Sawada T, Nishioka Y, et al. Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Nature Genetics. 44: 511-6. PMID 22446963 DOI: 10.1038/Ng.2231 |
0.399 |
|
| 2012 |
Stahl EA, Wegmann D, Trynka G, Gutierrez-Achury J, Do R, Voight BF, Kraft P, Chen R, Kallberg HJ, Kurreeman FA, Kathiresan S, Wijmenga C, Gregersen PK, et al. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nature Genetics. 44: 483-9. PMID 22446960 DOI: 10.1038/Ng.2232 |
0.44 |
|
| 2012 |
Kurreeman FA, Stahl EA, Okada Y, Liao K, Diogo D, Raychaudhuri S, Freudenberg J, Kochi Y, Patsopoulos NA, Gupta N, Sandor C, Bang SY, Lee HS, Padyukov L, et al. Use of a multiethnic approach to identify rheumatoid- arthritis-susceptibility loci, 1p36 and 17q12. American Journal of Human Genetics. 90: 524-32. PMID 22365150 DOI: 10.1016/J.Ajhg.2012.01.010 |
0.41 |
|
| 2012 |
Raychaudhuri S, Sandor C, Stahl EA, Freudenberg J, Lee HS, Jia X, Alfredsson L, Padyukov L, Klareskog L, Worthington J, Siminovitch KA, Bae SC, Plenge RM, Gregersen PK, de Bakker PI. Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis. Nature Genetics. 44: 291-6. PMID 22286218 DOI: 10.1038/Ng.1076 |
0.342 |
|
| 2011 |
Trouw LA, Böhringer S, Daha NA, Stahl EA, Raychaudhuri S, Kurreeman FA, Stoeken-Rijsbergen G, Houwing-Duistermaat JJ, Huizinga TW, Toes RE. The major risk alleles of age-related macular degeneration (AMD) in CFH do not play a major role in rheumatoid arthritis (RA). Clinical and Experimental Immunology. 166: 333-7. PMID 22059990 DOI: 10.1111/J.1365-2249.2011.04482.X |
0.366 |
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| 2011 |
Hu X, Kim H, Stahl E, Plenge R, Daly M, Raychaudhuri S. Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets. American Journal of Human Genetics. 89: 496-506. PMID 21963258 DOI: 10.1016/J.Ajhg.2011.09.002 |
0.404 |
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| 2011 |
Chen R, Stahl EA, Kurreeman FA, Gregersen PK, Siminovitch KA, Worthington J, Padyukov L, Raychaudhuri S, Plenge RM. Fine mapping the TAGAP risk locus in rheumatoid arthritis. Genes and Immunity. 12: 314-8. PMID 21390051 DOI: 10.1038/Gene.2011.8 |
0.414 |
|
| 2011 |
Zhernakova A, Stahl EA, Trynka G, Raychaudhuri S, Festen EA, Franke L, Westra HJ, Fehrmann RS, Kurreeman FA, Thomson B, Gupta N, Romanos J, McManus R, Ryan AW, Turner G, et al. Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. Plos Genetics. 7: e1002004. PMID 21383967 DOI: 10.1371/Journal.Pgen.1002004 |
0.425 |
|
| 2011 |
Kurreeman F, Liao K, Chibnik L, Hickey B, Stahl E, Gainer V, Li G, Bry L, Mahan S, Ardlie K, Thomson B, Szolovits P, Churchill S, Murphy SN, Cai T, et al. Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records. American Journal of Human Genetics. 88: 57-69. PMID 21211616 DOI: 10.1016/J.Ajhg.2010.12.007 |
0.424 |
|
| 2011 |
Stranger BE, Stahl EA, Raj T. Progress and promise of genome-wide association studies for human complex trait genetics. Genetics. 187: 367-83. PMID 21115973 DOI: 10.1534/Genetics.110.120907 |
0.438 |
|
| 2011 |
Shi J, Bohringer S, Stahl EA, Raychaudhuri S, Kurreeman FA, Houwing-Duistermaat JJ, Huizinga TW, Toes RE, Trouw LA. The major risk alleles of age related macular degeneration in CFH, do not play a major role in rheumatoid arthritis Annals of the Rheumatic Diseases. 70: A17-A18. DOI: 10.1136/Ard.2010.148965.12 |
0.397 |
|
| 2010 |
Stahl EA, Raychaudhuri S, Remmers EF, Xie G, Eyre S, Thomson BP, Li Y, Kurreeman FA, Zhernakova A, Hinks A, Guiducci C, Chen R, Alfredsson L, Amos CI, Ardlie KG, et al. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nature Genetics. 42: 508-14. PMID 20453842 DOI: 10.1038/Ng.582 |
0.431 |
|
| 2010 |
Juenger TE, Sen S, Bray E, Stahl E, Wayne T, McKay J, Richards JH. Exploring genetic and expression differences between physiologically extreme ecotypes: comparative genomic hybridization and gene expression studies of Kas-1 and Tsu-1 accessions of Arabidopsis thaliana. Plant, Cell & Environment. 33: 1268-84. PMID 20302603 DOI: 10.1111/J.1365-3040.2010.02146.X |
0.408 |
|
| 2009 |
Raychaudhuri S, Thomson BP, Remmers EF, Eyre S, Hinks A, Guiducci C, Catanese JJ, Xie G, Stahl EA, Chen R, Alfredsson L, Amos CI, Ardlie KG, Barton A, et al. Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. Nature Genetics. 41: 1313-8. PMID 19898481 DOI: 10.1038/Ng.479 |
0.344 |
|
| 2008 |
McKay JK, Richards JH, Nemali KS, Sen S, Mitchell-Olds T, Boles S, Stahl EA, Wayne T, Juenger TE. Genetics of drought adaptation in Arabidopsis thaliana II. QTL analysis of a new mapping population, KAS-1 x TSU-1. Evolution; International Journal of Organic Evolution. 62: 3014-26. PMID 18691264 DOI: 10.1111/J.1558-5646.2008.00474.X |
0.38 |
|
| 2008 |
Christman MA, Richards JH, McKay JK, Stahl EA, Juenger TE, Donovan LA. Genetic variation in Arabidopsis thaliana for night-time leaf conductance. Plant, Cell & Environment. 31: 1170-8. PMID 18510710 DOI: 10.1111/J.1365-3040.2008.01833.X |
0.319 |
|
| 2007 |
Hickerson MJ, Stahl E, Takebayashi N. msBayes: pipeline for testing comparative phylogeographic histories using hierarchical approximate Bayesian computation. Bmc Bioinformatics. 8: 268. PMID 17655753 DOI: 10.1186/1471-2105-8-268 |
0.327 |
|
| 2006 |
Hickerson MJ, Stahl EA, Lessios HA. Test for simultaneous divergence using approximate Bayesian computation. Evolution; International Journal of Organic Evolution. 60: 2435-53. PMID 17263107 DOI: 10.1554/05-578.1 |
0.316 |
|
| 2006 |
Bakker EG, Stahl EA, Toomajian C, Nordborg M, Kreitman M, Bergelson J. Distribution of genetic variation within and among local populations of Arabidopsis thaliana over its species range. Molecular Ecology. 15: 1405-18. PMID 16626462 DOI: 10.1111/J.1365-294X.2006.02884.X |
0.738 |
|
| 2005 |
Real LA, Henderson JC, Biek R, Snaman J, Jack TL, Childs JE, Stahl E, Waller L, Tinline R, Nadin-Davis S. Unifying the spatial population dynamics and molecular evolution of epidemic rabies virus. Proceedings of the National Academy of Sciences of the United States of America. 102: 12107-11. PMID 16103358 DOI: 10.1073/Pnas.0500057102 |
0.333 |
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| 2003 |
Mauricio R, Stahl EA, Korves T, Tian D, Kreitman M, Bergelson J. Natural selection for polymorphism in the disease resistance gene Rps2 of Arabidopsis thaliana. Genetics. 163: 735-46. PMID 12618410 |
0.58 |
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| 2002 |
Tian D, Araki H, Stahl E, Bergelson J, Kreitman M. Signature of balancing selection in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America. 99: 11525-30. PMID 12172007 DOI: 10.1073/Pnas.172203599 |
0.635 |
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| 2002 |
Nordborg M, Borevitz JO, Bergelson J, Berry CC, Chory J, Hagenblad J, Kreitman M, Maloof JN, Noyes T, Oefner PJ, Stahl EA, Weigel D. The extent of linkage disequilibrium in Arabidopsis thaliana. Nature Genetics. 30: 190-3. PMID 11780140 DOI: 10.1038/Ng813 |
0.634 |
|
| 2001 |
Bergelson J, Kreitman M, Stahl EA, Tian D. Evolutionary dynamics of plant R-genes. Science (New York, N.Y.). 292: 2281-5. PMID 11423651 DOI: 10.1126/Science.1061337 |
0.574 |
|
| 1999 |
Stahl EA, Dwyer G, Mauricio R, Kreitman M, Bergelson J. Dynamics of disease resistance polymorphism at the Rpm1 locus of Arabidopsis. Nature. 400: 667-71. PMID 10458161 DOI: 10.1038/23260 |
0.616 |
|
| 1998 |
Bergelson J, Stahl E, Dudek S, Kreitman M. Genetic variation within and among populations of Arabidopsis thaliana. Genetics. 148: 1311-23. PMID 9539444 |
0.607 |
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