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The nature of nurture: Effects of parental genotypes

Science (American Association for the Advancement of Science), 2018-01, Vol.359 (6374), p.424-428

2018

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A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

Nature genetics, 2019-02, Vol.51 (2), p.267-276

2019

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A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy

Scientific reports, 2021-02, Vol.11 (1), p.4188-4188, Article 4188

2021

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Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

Nature communications, 2017-02, Vol.8 (1), p.14265-14265, Article 14265

2017

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A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

Nature communications, 2019-04, Vol.10 (1), p.1777-1777, Article 1777

2019

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Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

Communications biology, 2023-07, Vol.6 (1), p.703-703, Article 703

2023

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Relatedness disequilibrium regression estimates heritability without environmental bias

Nature genetics, 2018-09, Vol.50 (9), p.1304-1310

2018

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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature genetics, 2019-02, Vol.51 (2), p.237-244

2019

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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Nature genetics, 2018-08, Vol.50 (8), p.1112-1121

2018

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Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Nature genetics, 2022-02, Vol.54 (2), p.152-160

2022

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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature genetics, 2022, Vol.54 (4), p.437-449

2022

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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Nature genetics, 2019-02, Vol.51 (2), p.245-257

2019

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Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

Cell, 2021-09, Vol.184 (18), p.4784-4818.e17

2021

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Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement

The nature of nurture: Effects of parental genotypes

CNVs conferring risk of autism or schizophrenia affect cognition in controls

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

A mutation in APP protects against Alzheimer's disease and age-related cognitive decline

A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

Genetics of gene expression and its effect on disease

Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy

Sequence variants at CYP1A1―CYP1A2 and AHR associate with coffee consumption

Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo

A sequence variant associating with educational attainment also affects childhood cognition

Relatedness disequilibrium regression estimates heritability without environmental bias

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

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