Artikel mit Open-Access-Mandaten - Mark DalyWeitere Informationen
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Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
WE Ek, A Reznichenko, S Ripke, B Niesler, M Zucchelli, NV Rivera, ...
Gut 64 (11), 1774-1782, 2015
Mandate: Research Foundation (Flanders), Swedish Research Council
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High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
C Tcheandjieu, K Xiao, H Tejeda, JA Lynch, S Ruotsalainen, T Bellomo, ...
Nature Genetics 54 (6), 772-782, 2022
Mandate: US National Institutes of Health, US Department of Veterans Affairs, UK …
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Thrombosis risk in single-and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
J Ryu, JT Rämö, SJ Jurgens, T Niiranen, S Sanna-Cherchi, KA Bauer, ...
Blood 143 (23), 2425-2432, 2024
Mandate: Business Finland
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High burden of ileus and pneumonia in clozapine-treated individuals with schizophrenia: a Finnish 25-year follow-up register study
JJ Partanen, P Häppölä, A Kämpe, A Ahola-Olli, A Hellsten, SM Rask, ...
American Journal of Psychiatry 181 (10), 879-892, 2024
Mandate: Academy of Finland, Business Finland
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153. A Novel Framework for Well-Calibrated Analysis of Complex Traits in Admixed Individuals
E Atkinson, A Maihofer, K Koenen, C Nievergelt, B Neale, M Daly
Biological Psychiatry 85 (10), S63-S64, 2019
Mandate: US National Institutes of Health
Verfügbar: 617
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The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
A McKenna, M Hanna, E Banks, A Sivachenko, K Cibulskis, A Kernytsky, ...
Genome research 20 (9), 1297-1303, 2010
Mandate: US National Institutes of Health
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A framework for variation discovery and genotyping using next-generation DNA sequencing data
MA DePristo, E Banks, R Poplin, KV Garimella, JR Maguire, C Hartl, ...
Nature genetics 43 (5), 491-498, 2011
Mandate: US National Institutes of Health
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Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
Mandate: US National Institutes of Health, Canadian Institutes of Health Research …
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A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung …
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An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Mandate: US National Institutes of Health, Howard Hughes Medical Institute, British …
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The mutational constraint spectrum quantified from variation in 141,456 humans
KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ...
Nature 581 (7809), 434-443, 2020
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung …
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Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
Mandate: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
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Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ...
Nature 491 (7422), 119-124, 2012
Mandate: US National Institutes of Health, National Health and Medical Research …
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
International Schizophrenia Consortium Manuscript preparation Purcell Shaun ...
Nature 460 (7256), 748-752, 2009
Mandate: US National Institutes of Health, Science Foundation Ireland, Chief …
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A haplotype map of the human genome
International HapMap Consortium
Nature 437 (7063), 1299, 2005
Mandate: Genome Canada
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
BK Bulik-Sullivan, PR Loh, HK Finucane, S Ripke, J Yang, ...
Nature genetics 47 (3), 291-295, 2015
Mandate: US National Institutes of Health, UK Medical Research Council
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The landscape of somatic copy-number alteration across human cancers
R Beroukhim, CH Mermel, D Porter, G Wei, S Raychaudhuri, J Donovan, ...
Nature 463 (7283), 899-905, 2010
Mandate: US National Institutes of Health, Howard Hughes Medical Institute
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An atlas of genetic correlations across human diseases and traits
B Bulik-Sullivan, HK Finucane, V Anttila, A Gusev, FR Day, PR Loh, ...
Nature genetics 47 (11), 1236-1241, 2015
Mandate: US National Institutes of Health, National Institute of Health and Medical …
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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
JC Barrett, S Hansoul, DL Nicolae, JH Cho, RH Duerr, JD Rioux, SR Brant, ...
Nature genetics 40 (8), 955-962, 2008
Mandate: US National Institutes of Health, Research Foundation (Flanders), National …
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Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung …
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