Artikel mit Open-Access-Mandaten - Yun LiWeitere Informationen
Nicht verfügbar: 3
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Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images
B Zhao, T Li, Z Fan, Y Yang, J Shu, X Yang, X Wang, T Luo, J Tang, ...
Science 380 (6648), abn6598, 2023
Mandate: US National Institutes of Health
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Machine learning and deep learning in genetics and genomics
D Wu, DS Karhade, M Pillai, MZ Jiang, L Huang, G Li, H Cho, J Roach, ...
Machine Learning in Dentistry, 163-181, 2021
Mandate: US National Institutes of Health
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GMEPS: a fast and efficient likelihood approach for genome-wide mediation analysis under extreme phenotype sequencing
JSS Liyanage, JH Estepp, K Srivastava, Y Li, M Mori, G Kang
Statistical Applications in Genetics and Molecular Biology 21 (1), 20210071, 2022
Mandate: US National Institutes of Health
Verfügbar: 261
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A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Mandate: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
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The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
Mandate: US National Institutes of Health, British Heart Foundation
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A map of human genome variation from population scale sequencing
DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ...
Nature 467 (7319), 1061-1073, 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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METAL: fast and efficient meta-analysis of genomewide association scans
CJ Willer, Y Li, GR Abecasis
Bioinformatics 26 (17), 2190-2191, 2010
Mandate: US National Institutes of Health
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Rare-variant association testing for sequencing data with the sequence kernel association test
MC Wu, S Lee, T Cai, Y Li, M Boehnke, X Lin
The American Journal of Human Genetics 89 (1), 82-93, 2011
Mandate: US National Institutes of Health
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
Mandate: US National Institutes of Health, UK Medical Research Council, Wellcome …
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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
J Dupuis, C Langenberg, I Prokopenko, R Saxena, N Soranzo, ...
Nature genetics 42 (2), 105-116, 2010
Mandate: US National Institutes of Health, British Heart Foundation, Dunhill Medical …
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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini, LJ Scott, R Saxena, BF Voight, JL Marchini, T Hu, ...
Nature genetics 40 (5), 638-645, 2008
Mandate: US National Institutes of Health
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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
Y Li, CJ Willer, J Ding, P Scheet, GR Abecasis
Genetic epidemiology 34 (8), 816-834, 2010
Mandate: US National Institutes of Health
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An epigenetic biomarker of aging for lifespan and healthspan
ME Levine, AT Lu, A Quach, BH Chen, TL Assimes, S Bandinelli, L Hou, ...
Aging (albany NY) 10 (4), 573, 2018
Mandate: US National Institutes of Health, Government of Italy
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Newly identified loci that influence lipid concentrations and risk of coronary artery disease
CJ Willer, S Sanna, AU Jackson, A Scuteri, LL Bonnycastle, R Clarke, ...
Nature genetics 40 (2), 161-169, 2008
Mandate: British Heart Foundation
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Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
RP Nair, KC Duffin, C Helms, J Ding, PE Stuart, D Goldgar, ...
Nature genetics 41 (2), 199-204, 2009
Mandate: US National Institutes of Health, Canadian Institutes of Health Research
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Common variants at 30 loci contribute to polygenic dyslipidemia
S Kathiresan, CJ Willer, GM Peloso, S Demissie, K Musunuru, EE Schadt, ...
Nature genetics 41 (1), 56-65, 2009
Mandate: US National Institutes of Health, British Heart Foundation, Cancer Research UK
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Mandate: US National Institutes of Health, US Department of Veterans Affairs
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DNA methylation GrimAge strongly predicts lifespan and healthspan
AT Lu, A Quach, JG Wilson, AP Reiner, A Aviv, K Raj, L Hou, ...
Aging (albany NY) 11 (2), 303, 2019
Mandate: US National Institutes of Health
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A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung …
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