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Reference-based phasing using the Haplotype Reference Consortium panel

Nature genetics, 2016-11, Vol.48 (11), p.1443-1448

2016

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Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits

Nature genetics, 2018-07, Vol.50 (7), p.1041-1047

2018

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Functionally informed fine-mapping and polygenic localization of complex trait heritability

Nature genetics, 2020-12, Vol.52 (12), p.1355-1363

2020

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Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Nature genetics, 2018-04, Vol.50 (4), p.621-629

2018

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Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature genetics, 2015-11, Vol.47 (11), p.1228-1235

2015

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Detecting Novel Associations in Large Data Sets

Science (American Association for the Advancement of Science), 2011-12, Vol.334 (6062), p.1518-1524

2011

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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Nature genetics, 2018-04, Vol.50 (4), p.538-548

2018

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Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Nature genetics, 2021-02, Vol.53 (2), p.195-204

2021

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Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

Nature genetics, 2018-11, Vol.50 (11), p.1600-1607

2018

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Reconciling S-LDSC and LDAK functional enrichment estimates

Nature genetics, 2019-08, Vol.51 (8), p.1202-1204

2019

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An atlas of genetic correlations across human diseases and traits

Nature genetics, 2015-11, Vol.47 (11), p.1236-1241

2015

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Nature genetics, 2015-12, Vol.47 (12), p.1385-1392

2015

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Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations

Nature (London), 2018-07, Vol.559 (7714), p.350-355

2018

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Linkage disequilibrium–dependent architecture of human complex traits shows action of negative selection

Nature genetics, 2017-10, Vol.49 (10), p.1421-1427

2017

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Efficient Bayesian mixed-model analysis increases association power in large cohorts

Nature genetics, 2015-03, Vol.47 (3), p.284-290

2015

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Misuse of the term ‘trans-ethnic’ in genomics research

Nature genetics, 2021-11, Vol.53 (11), p.1520-1521

2021

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LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Bioinformatics (Oxford, England), 2017-01, Vol.33 (2), p.272-279

2017

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Interrogation of human hematopoiesis at single-cell and single-variant resolution

Nature genetics, 2019-04, Vol.51 (4), p.683-693

2019

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Genome-wide enhancer maps link risk variants to disease genes

Nature (London), 2021-05, Vol.593 (7858), p.238-243

2021

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Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection

Nature communications, 2019-02, Vol.10 (1), p.790-790, Article 790

2019

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Nature genetics, 2015-03, Vol.47 (3), p.291-295

2015

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Estimating heritability and its enrichment in tissue-specific gene sets in admixed populations

Human molecular genetics, 2021-07, Vol.30 (16), p.1521-1534

2021

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Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

American journal of human genetics, 2017-04, Vol.100 (4), p.605-616

2017

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Estimating cross‐population genetic correlations of causal effect sizes

Genetic epidemiology, 2019-03, Vol.43 (2), p.180-188

2019

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Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH

Nature genetics, 2021-08, Vol.53 (8), p.1166-1176

2021

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Reference-based phasing using the Haplotype Reference Consortium panel

Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits

Functionally informed fine-mapping and polygenic localization of complex trait heritability

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Partitioning heritability by functional annotation using genome-wide association summary statistics

Detecting Novel Associations in Large Data Sets

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

Reconciling S-LDSC and LDAK functional enrichment estimates

An atlas of genetic correlations across human diseases and traits

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations

Linkage disequilibrium–dependent architecture of human complex traits shows action of negative selection

Efficient Bayesian mixed-model analysis increases association power in large cohorts

Misuse of the term ‘trans-ethnic’ in genomics research

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Interrogation of human hematopoiesis at single-cell and single-variant resolution

Genome-wide enhancer maps link risk variants to disease genes

Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Estimating heritability and its enrichment in tissue-specific gene sets in admixed populations

Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

Estimating cross‐population genetic correlations of causal effect sizes

Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH

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