Causal inference in genetic trio studies

Hierarchical inference for genome-wide association studies: a view on methodology with software

(2020) Claude Renaux et al.   COMPUTATIONAL STATISTICS

Metropolized Knockoff Sampling

(2020) Stephen Bates et al.   JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION

Multi-resolution localization of causal variants across the genome

(2020) Matteo Sesia et al.   Nature Communications

Identification of common genetic risk variants for autism spectrum disorder

(2019) Jakob Grove et al.   NATURE GENETICS

OUP accepted manuscript

(2018)   BIOMETRIKA

Panning for gold: ‘model-X’ knockoffs for high dimensional controlled variable selection

(2018) Emmanuel Candès et al.   JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY

Mixed-model association for biobank-scale datasets

(2018) Po-Ru Loh et al.   NATURE GENETICS

The UK Biobank resource with deep phenotyping and genomic data

(2018) Clare Bycroft et al.   NATURE

Rejoinder: ‘Gene hunting with hidden Markov model knockoffs’

(2018) M Sesia et al.   BIOMETRIKA

Accumulation Tests for FDR Control in Ordered Hypothesis Testing

(2017) Ang Li et al.   JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION

Refined genetic maps reveal sexual dimorphism in human meiotic recombination at multiple scales

(2017) Claude Bhérer et al.   Nature Communications

Gene Mapping in Admixed Families: A Cautionary Note on the Interpretation of the Transmission Disequilibrium Test and a Possible Solution

(2016) Xuexia Wang et al.   HUMAN HEREDITY

Controlling the false discovery rate via knockoffs

(2015) Rina Foygel Barber et al.   ANNALS OF STATISTICS

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

(2014) Jared O'Connell et al.   PLoS Genetics

NCBI’s Database of Genotypes and Phenotypes: dbGaP

(2013) Kimberly A. Tryka et al.   NUCLEIC ACIDS RESEARCH

Individual common variants exert weak effects on the risk for autism spectrum disorders

(2012) Richard Anney et al.   HUMAN MOLECULAR GENETICS

The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders

(2012) Joseph D. Buxbaum et al.   NEURON

Family-based designs for genome-wide association studies

(2011) Jurg Ott et al.   NATURE REVIEWS GENETICS

Haplotype phasing: existing methods and new developments

(2011) Sharon R. Browning et al.   NATURE REVIEWS GENETICS

Do common variants play a role in risk for autism? Evidence and theoretical musings

(2010) Bernie Devlin et al.   BRAIN RESEARCH

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

Genome-Wide Significance Levels and Weighted Hypothesis Testing

(2010) Kathryn Roeder et al.   STATISTICAL SCIENCE

The Role of Family-Based Designs in Genome-Wide Association Studies

(2010) Nan M. Laird et al.   STATISTICAL SCIENCE

Estimating high-dimensional intervention effects from observational data

(2009) Marloes H. Maathuis et al.   ANNALS OF STATISTICS

FBAT-SNP-PC: An Approach for Multiple Markers and Single Trait in Family-Based Association Tests

(2008) Cyril S. Rakovski et al.   HUMAN HEREDITY

Haplotype Mapping of a Diploid Non-Meiotic Organism Using Existing and Induced Aneuploidies

(2007) Melanie Legrand et al.   PLoS Genetics