List of works - Donald F Conrad

A de novo paradigm for male infertility

scientific article published on 10 January 2022

A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse

scientific article published on 04 April 2020

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

scientific article

Genome-wide significance testing of variation from single case exomes

scientific article published on 24 October 2016

Global variation in copy number in the human genome

scientific article

Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia

scientific article published on 21 October 2019

Mapping copy number variation by population-scale genome sequencing

scientific article

Multiplex shRNA Screening of Germ Cell Development by in Vivo Transfection of Mouse Testis

scientific article

Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia

scientific article published on 07 August 2020

Origins and functional impact of copy number variation in the human genome

scientific article (publication date: April 2010)

Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility

scientific article published on 11 October 2019

The impact of structural variation on human gene expression

scientific article published on 3 April 2017

The population genetics of structural variation

scientific article (publication date: July 2007)

Towards a comprehensive structural variation map of an individual human genome

scientific article

Unified single-cell analysis of testis gene regulation and pathology in five mouse strains

scientific article published on 25 June 2019

Variation in genome-wide mutation rates within and between human families

scientific article

List of works by Donald F Conrad

A de novo paradigm for male infertility

A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide significance testing of variation from single case exomes

Global variation in copy number in the human genome

Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia

Mapping copy number variation by population-scale genome sequencing

Multiplex shRNA Screening of Germ Cell Development by in Vivo Transfection of Mouse Testis

Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia

Origins and functional impact of copy number variation in the human genome

Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility

The impact of structural variation on human gene expression

The population genetics of structural variation

Towards a comprehensive structural variation map of an individual human genome

Unified single-cell analysis of testis gene regulation and pathology in five mouse strains

Variation in genome-wide mutation rates within and between human families