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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

Nature communications, 2021-05, Vol.12 (1), p.3152-3152, Article 3152

2021

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Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

Nature communications, 2022-02, Vol.13 (1), p.800-800, Article 800

2022

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A spectral approach integrating functional genomic annotations for coding and noncoding variants

Nature genetics, 2016-02, Vol.48 (2), p.214-220

2016

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Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

American journal of human genetics, 2013-06, Vol.92 (6), p.841-853

2013

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De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

Nature genetics, 2012-12, Vol.44 (12), p.1365-1369

2012

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A genome-wide scan statistic framework for whole-genome sequence data analysis

Nature communications, 2019-07, Vol.10 (1), p.3018-11, Article 3018

2019

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Differences in plasma metabolites related to Alzheimer's disease, APOE ε4 status, and ethnicity

Alzheimer's & dementia : translational research & clinical interventions, 2020, Vol.6 (1), p.e12025-n/a

2020

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De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia

Neuron (Cambridge, Mass.), 2016-03, Vol.89 (5), p.940-947

2016

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A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

Nature communications, 2018-12, Vol.9 (1), p.5199-12, Article 5199

2018

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Genome-wide discovery for biomarkers using quantile regression at biobank scale

Nature communications, 2024-07, Vol.15 (1), p.6460-13, Article 6460

2024

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Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies

NPJ digital medicine, 2021-07, Vol.4 (1), p.116-116, Article 116

2021

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Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene

Neuron (Cambridge, Mass.), 2014-05, Vol.82 (4), p.773-780

2014

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FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications

American journal of human genetics, 2018-05, Vol.102 (5), p.920-942

2018

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BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data

Genome Biology, 2023-02, Vol.24 (1), p.24-24, Article 24

2023

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Rare variant analysis for family-based design

PloS one, 2013-01, Vol.8 (1), p.e48495-e48495

2013

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Disease Heritability Inferred from Familial Relationships Reported in Medical Records

Cell, 2018-06, Vol.173 (7), p.1692-1704.e11

2018

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A new testing strategy to identify rare variants with either risk or protective effect on disease

PLoS genetics, 2011-02, Vol.7 (2), p.e1001289-e1001289

2011

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GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Nature communications, 2022-11, Vol.13 (1), p.7209-16, Article 7209

2022

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GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

PLoS genetics, 2017-02, Vol.13 (2), p.e1006609-e1006609

2017

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Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders

Frontiers in genetics, 2020-12, Vol.11, p.575928-575928

2020

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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

American journal of human genetics, 2017-11, Vol.101 (5), p.789-802

2017

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On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

Genetic epidemiology, 2008-04, Vol.32 (3), p.273-284

2008

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Multitrait GWAS to connect disease variants and biological mechanisms

PLoS genetics, 2021-08, Vol.17 (8), p.e1009713

2021

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Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

Genomics (San Diego, Calif.), 2009-01, Vol.93 (1), p.22-26

2009

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Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (1), p.343-348

2014

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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

A spectral approach integrating functional genomic annotations for coding and noncoding variants

Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

A genome-wide scan statistic framework for whole-genome sequence data analysis

Differences in plasma metabolites related to Alzheimer's disease, APOE ε4 status, and ethnicity

De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia

A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

Genome-wide discovery for biomarkers using quantile regression at biobank scale

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies

Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene

FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications

BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data

Rare variant analysis for family-based design

Disease Heritability Inferred from Familial Relationships Reported in Medical Records

A new testing strategy to identify rare variants with either risk or protective effect on disease

GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

Multitrait GWAS to connect disease variants and biological mechanisms

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism

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