Year |
Citation |
Score |
2019 |
MULTHAUP ML, KITA R, ERIKSSON N, ASLIBEKYAN S, SHELTON J, TENNEN RI, KIM E, KOELSCH B. 304-OR: Polygenic Risk Score Predicts Type 2 Diabetes Susceptibility in a Diverse Consumer Genetic Database Diabetes. 68: 304-OR. DOI: 10.2337/Db19-304-Or |
0.353 |
|
2018 |
Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics. PMID 30478444 DOI: 10.1038/S41588-018-0269-7 |
0.315 |
|
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, ... ... Eriksson N, 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 |
0.305 |
|
2018 |
Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Eriksson N, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3 |
0.328 |
|
2017 |
Tian C, Hromatka BS, Kiefer AK, Eriksson N, Noble SM, Tung JY, Hinds DA. Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Nature Communications. 8: 599. PMID 28928442 DOI: 10.1038/S41467-017-00257-5 |
0.34 |
|
2017 |
Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S, Zawistowski M, Ellinghaus E, Barker JN, Chandran V, Dand N, Duffin KC, Enerbäck C, Esko T, Franke A, Gladman DD, ... ... Eriksson N, et al. Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nature Communications. 8: 15382. PMID 28537254 DOI: 10.1038/Ncomms15382 |
0.391 |
|
2016 |
Barban N, Jansen R, de Vlaming R, Vaez A, Mandemakers JJ, Tropf FC, Shen X, Wilson JF, Chasman DI, Nolte IM, Tragante V, van der Laan SW, Perry JR, Kong A, ... ... Eriksson N, et al. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nature Genetics. PMID 27798627 DOI: 10.1038/Ng.3698 |
0.412 |
|
2016 |
Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Eriksson N, et al. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. 48: 1296. PMID 27681292 DOI: 10.1038/Ng1016-1296C |
0.344 |
|
2016 |
Hinds DA, Barnholt KE, Mesa RA, Kiefer AK, Do CB, Eriksson N, Mountain JL, Francke U, Tung JY, Nguyen HM, Zhang H, Gojenola L, Zehnder JL, Gotlib J. Germline variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms. Blood. PMID 27365426 DOI: 10.1182/Blood-2015-06-652941 |
0.421 |
|
2016 |
Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Eriksson N, et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. PMID 27322543 DOI: 10.1038/Ng.3598 |
0.41 |
|
2016 |
Hu Y, Shmygelska A, Tran D, Eriksson N, Tung JY, Hinds DA. GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. Nature Communications. 7: 10448. PMID 26835600 DOI: 10.1038/Ncomms10448 |
0.367 |
|
2015 |
Chang AL, Raber I, Xu J, Li R, Spitale R, Chen J, Kiefer AK, Tian C, Eriksson NK, Hinds DA, Tung JY. Assessment of the genetic basis of rosacea by genome-wide association study. The Journal of Investigative Dermatology. 135: 1548-55. PMID 25695682 DOI: 10.1038/Jid.2015.53 |
0.358 |
|
2015 |
Hromatka BS, Tung JY, Kiefer AK, Do CB, Hinds DA, Eriksson N. Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. Human Molecular Genetics. 24: 2700-8. PMID 25628336 DOI: 10.1093/Hmg/Ddv028 |
0.339 |
|
2015 |
Nalls MA, Bras J, Hernandez DG, Keller MF, Majounie E, Renton AE, Saad M, Jansen I, Guerreiro R, Lubbe S, Plagnol V, Gibbs JR, Schulte C, Pankratz N, Sutherland M, ... ... Eriksson N, et al. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiology of Aging. 36: 1605.e7-12. PMID 25444595 DOI: 10.1016/J.Neurobiolaging.2014.07.028 |
0.381 |
|
2014 |
Rietveld CA, Conley D, Eriksson N, Esko T, Medland SE, Vinkhuyzen AA, Yang J, Boardman JD, Chabris CF, Dawes CT, Domingue BW, Hinds DA, Johannesson M, Kiefer AK, Laibson D, et al. Replicability and robustness of genome-wide-association studies for behavioral traits. Psychological Science. 25: 1975-86. PMID 25287667 DOI: 10.1177/0956797614545132 |
0.409 |
|
2014 |
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, ... ... Eriksson N, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043 |
0.438 |
|
2014 |
Durand EY, Eriksson N, McLean CY. Reducing pervasive false positive identical-by-descent segments detected by large-scale pedigree analysis Molecular Biology and Evolution. 31: 2212-2222. PMID 24784137 DOI: 10.1093/Molbev/Msu151 |
0.307 |
|
2014 |
Ferreira MA, Matheson MC, Tang CS, Granell R, Ang W, Hui J, Kiefer AK, Duffy DL, Baltic S, Danoy P, Bui M, Price L, Sly PD, Eriksson N, Madden PA, et al. Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. The Journal of Allergy and Clinical Immunology. 133: 1564-71. PMID 24388013 DOI: 10.1016/J.Jaci.2013.10.030 |
0.359 |
|
2013 |
Lubke G, Laurin C, Walters R, Eriksson N, Hysi P, Spector T, Montgomery G, Martin N, Medland S, Boomsma D. Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data. Journal of Data Mining in Genomics & Proteomics. 4. PMID 24404405 DOI: 10.4172/2153-0602.1000143 |
0.38 |
|
2013 |
Hinds DA, McMahon G, Kiefer AK, Do CB, Eriksson N, Evans DM, St Pourcain B, Ring SM, Mountain JL, Francke U, Davey-Smith G, Timpson NJ, Tung JY. A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. Nature Genetics. 45: 907-11. PMID 23817569 DOI: 10.1038/Ng.2686 |
0.367 |
|
2013 |
Tung JY, Kiefer AK, Mullins M, Francke U, Eriksson N. Genome-wide association analysis implicates elastic microfibrils in the development of nonsyndromic striae distensae. The Journal of Investigative Dermatology. 133: 2628-31. PMID 23633020 DOI: 10.1038/Jid.2013.196 |
0.365 |
|
2013 |
Kiefer AK, Tung JY, Do CB, Hinds DA, Mountain JL, Francke U, Eriksson N. Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia. Plos Genetics. 9: e1003299. PMID 23468642 DOI: 10.1371/Journal.Pgen.1003299 |
0.323 |
|
2013 |
Heilmann S, Kiefer AK, Fricker N, Drichel D, Hillmer AM, Herold C, Tung JY, Eriksson N, Redler S, Betz RC, Li R, Kárason A, Nyholt DR, Song K, Vermeulen SH, et al. Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. The Journal of Investigative Dermatology. 133: 1489-96. PMID 23358095 DOI: 10.1038/Jid.2013.43 |
0.453 |
|
2012 |
Do CB, Hinds DA, Francke U, Eriksson N. Comparison of family history and SNPs for predicting risk of complex disease. Plos Genetics. 8: e1002973. PMID 23071447 DOI: 10.1371/Journal.Pgen.1002973 |
0.362 |
|
2012 |
Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Glass D, Medland SE, Dimitriou M, Waterworth D, Tung JY, Geller F, Heilmann S, ... ... Eriksson N, et al. Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. Plos Genetics. 8: e1002746. PMID 22693459 DOI: 10.1371/Journal.Pgen.1002746 |
0.402 |
|
2012 |
Henn BM, Hon L, Macpherson JM, Eriksson N, Saxonov S, Pe'er I, Mountain JL. Cryptic distant relatives are common in both isolated and cosmopolitan genetic samples. Plos One. 7: e34267. PMID 22509285 DOI: 10.1371/Journal.Pone.0034267 |
0.378 |
|
2012 |
Eriksson N, Tung JY, Kiefer AK, Hinds DA, Francke U, Mountain JL, Do CB. Novel associations for hypothyroidism include known autoimmune risk loci. Plos One. 7: e34442. PMID 22493691 DOI: 10.1038/Npre.2011.6055.1 |
0.42 |
|
2012 |
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Eriksson N, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548 |
0.415 |
|
2012 |
Panagiotou OA, Ioannidis JPA, Hirschhorn JN, Abecasis GR, Frayling TM, McCarthy MI, Lindgren CM, Beaty TH, Eriksson N, Polychronakos C, Kathirensan S, Plenge RM, Spritz R, Payami H, Martin ER, et al. What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations International Journal of Epidemiology. 41: 273-286. PMID 22253303 DOI: 10.1093/Ije/Dyr178 |
0.402 |
|
2012 |
Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Glass D, Medland SE, Dimitriou M, Waterworth D, Tung JY, Geller F, Heilmann S, ... ... Eriksson N, et al. Genotype score associated with the risk of androgenetic alopecia. Plos Genetics. DOI: 10.1371/Journal.Pgen.1002746.T003 |
0.335 |
|
2012 |
Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Glass D, Medland SE, Dimitriou M, Waterworth D, Tung JY, Geller F, Heilmann S, ... ... Eriksson N, et al. Genome-wide meta-analysis results for AGA in MAAN. Plos Genetics. DOI: 10.1371/Journal.Pgen.1002746.G001 |
0.324 |
|
2012 |
Eriksson N, Wu S, Do CB, Kiefer AK, Tung JY, Mountain JL, Hinds DA, Francke U. A genetic variant near olfactory receptor genes influences cilantro preference Flavour. 1: 22. DOI: 10.1186/2044-7248-1-22 |
0.342 |
|
2012 |
Hinds DA, Barnholt KE, Zehnder JL, Kiefer AK, Do CB, Eriksson N, Mountain JL, Francke U, Tung JA, Nguyen H(, Levine RL, Mesa RA, Gotlib J. A Germline Variant in the TERT Gene Is a Novel Predisposition Allele Associated with Myeloproliferative Neoplasms Blood. 120: 707-707. DOI: 10.1182/Blood.V120.21.707.707 |
0.414 |
|
2012 |
Barnholt KE, Hinds DA, Kiefer AK, Do CB, Eriksson N, Mountain JL, Francke U, Tung JA, Nguyen H(, Levine RL, Mesa RA, Gotlib J, Zehnder JL. Estimation of JAK2 V617F Prevalence by Detection of the Mutation in Saliva Samples From Online MPN and General Population Cohorts Blood. 120: 1737-1737. DOI: 10.1182/Blood.V120.21.1737.1737 |
0.338 |
|
2011 |
Tung JY, Do CB, Hinds DA, Kiefer AK, Macpherson JM, Chowdry AB, Francke U, Naughton BT, Mountain JL, Wojcicki A, Eriksson N. Efficient replication of over 180 genetic associations with self-reported medical data. Plos One. 6: e23473. PMID 21858135 DOI: 10.1371/Journal.Pone.0023473 |
0.367 |
|
2011 |
Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. Plos Genetics. 7: e1002141. PMID 21738487 DOI: 10.1371/Journal.Pgen.1002141 |
0.403 |
|
2011 |
Zagordi O, Bhattacharya A, Eriksson N, Beerenwinkel N. ShoRAH: estimating the genetic diversity of a mixed sample from next-generation sequencing data. Bmc Bioinformatics. 12: 119. PMID 21521499 DOI: 10.1186/1471-2105-12-119 |
0.303 |
|
2010 |
Eriksson N, Macpherson JM, Tung JY, Hon LS, Naughton B, Saxonov S, Avey L, Wojcicki A, Pe'er I, Mountain J. Web-based, participant-driven studies yield novel genetic associations for common traits. Plos Genetics. 6: e1000993. PMID 20585627 DOI: 10.1371/Journal.Pgen.1000993 |
0.391 |
|
2007 |
Beerenwinkel N, Eriksson N, Sturmfels B. Conjunctive Bayesian networks Bernoulli. 13: 893-909. DOI: 10.3150/07-Bej6133 |
0.494 |
|
2006 |
Beerenwinkel N, Eriksson N, Sturmfels B. Evolution on distributive lattices. Journal of Theoretical Biology. 242: 409-20. PMID 16650439 DOI: 10.1016/J.Jtbi.2006.03.013 |
0.509 |
|
2006 |
Eriksson N, Fienberg SE, Rinaldo A, Sullivant S. Polyhedral conditions for the nonexistence of the MLE for hierarchical log-linear models Journal of Symbolic Computation. 41: 222-233. DOI: 10.1016/J.Jsc.2005.04.003 |
0.576 |
|
Show low-probability matches. |