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Editorial

RECOMB 2025 Special Issue

  • First Published December 3, 2025
Research

cis-regulatory variation modifies the penetrance of pathogenic SHROOM3 variants in craniofacial microsomia" > Common cis-regulatory variation modifies the penetrance of pathogenic SHROOM3 variants in craniofacial microsomia

  • First Published April 15, 2025
Method

A scalable adaptive quadratic kernel method for interpretable epistasis analysis in complex traits

  • First Published August 29, 2024
Method

Scalable summary-statistics-based heritability estimation method with individual genotype level accuracy

  • First Published July 22, 2024
Method

Leveraging family data to design Mendelian randomization that is provably robust to population stratification

  • First Published May 17, 2023
Perspective

Short arms of human acrocentric chromosomes and the completion of the human genome sequence

  • First Published March 31, 2022
In memoriam

Haig H. Kazazian, Jr. (1937–2022)

  • First Published March 21, 2022
Research

Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selection

  • First Published December 13, 2017
Research

APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication

  • First Published January 11, 2016
Research

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

  • First Published April 27, 2015
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