Nature genetics Journal

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Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.. 54:1564-1571. 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.. 54:1320-1331. 2022
New insights into the genetic etiology of Alzheimer's disease and related dementias.. 54:412-436. 2022
Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.. 51:1423-1424. 2019
Recessive gene disruptions in autism spectrum disorder.. 51:1092-1098. 2019
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.. 51:636-648. 2019
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.. 51:414-430. 2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.. 51:237-244. 2019
An atlas of genetic influences on osteoporosis in humans and mice.. 51:258-266. 2018
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.. 50:912-919. 2018
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.. 49:1373-1384. 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.. 49:993-1004. 2017
The complex genetics of hypoplastic left heart syndrome.. 49:1152-1159. 2017
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.. 48:1162-70. 2016
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.. 48:624-33. 2016
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.. 48:189-94. 2016
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.. 47:1294-1303. 2015
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.. 46:826-36. 2014
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.. 45:1452-8. 2013
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.. 45:690-6. 2013
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.. 44:1349-54. 2012
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.. 44:886-9. 2012
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.. 44:916-21. 2012
Common variants at 12q14 and 12q24 are associated with hippocampal volume.. 44:545-51. 2012
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.. 44:491-501. 2012
Identification of common variants associated with human hippocampal and intracranial volumes.. 44:552-61. 2012
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.. 44:260-8. 2012
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.. 43:1005-11. 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.. 43:940-7. 2011
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.. 43:753-60. 2011
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.. 42:1077-85. 2010
Common variants in KCNN3 are associated with lone atrial fibrillation.. 42:240-4. 2010
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.. 42:142-8. 2010
Genome-wide association identifies multiple ulcerative colitis susceptibility loci.. 42:332-7. 2010
Genome-wide association study of PR interval.. 42:153-9. 2010
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.. 42:949-60. 2010
New loci associated with kidney function and chronic kidney disease.. 42:376-84. 2010
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.. 41:1199-206. 2009
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.. 41:648-50. 2009
Genome-wide association study of blood pressure and hypertension.. 41:677-87. 2009
Multiple loci associated with indices of renal function and chronic kidney disease.. 41:712-7. 2009
The genome of the cucumber, Cucumis sativus L.. 41:1275-81. 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.. 41:879-81. 2009
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.. 38:644-51. 2006
Dynamic mutations on the move in Banff.. 36:667-70. 2004
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions.. 22:110-4. 1999
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.. 2:301-4. 1992