List of works - Daniel M. Jordan

A literature review at genome scale: improving clinical variant assessment.

scientific article published in February 2018

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

scientific article published in 2022

An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease

scientific article published on 22 January 2021

Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy

scientific article

Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

scientific article published on 28 October 2015

Estimating the selective effects of heterozygous protein-truncating variants from human exome data.

scientific article

Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection.

scientific article published on 28 June 2016

Genome analysis reveals insights into physiology and longevity of the Brandt's bat Myotis brandtii

scientific article

Human allelic variation: perspective from protein function, structure, and evolution

scientific article

Identification of cis-suppression of human disease mutations by comparative genomics

scientific article

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals

scientific article published on 05 August 2013

Mitigating false-positive associations in rare disease gene discovery

scientific article

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study

scientific article published on 15 January 2019

Parameterization of Peptide13C Carbonyl Chemical Shielding Anisotropy in Molecular Dynamics Simulations

scientific article published on 01 June 2007

Predicting functional effect of human missense mutations using PolyPhen-2.

scientific article published on January 2013

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

scientific article published in Nature Communications

Reply to 'Selective effects of heterozygous protein-truncating variants'

scientific article published on 01 January 2019

Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases

scientific article published on 11 April 2018

When "N of 2" is not enough: integrating statistical and functional data in gene discovery.

scientific article

Widespread macromolecular interaction perturbations in human genetic disorders

scientific journal article

List of works by Daniel M. Jordan

A literature review at genome scale: improving clinical variant assessment.

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease

Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy

Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

Estimating the selective effects of heterozygous protein-truncating variants from human exome data.

Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection.

Genome analysis reveals insights into physiology and longevity of the Brandt's bat Myotis brandtii

Human allelic variation: perspective from protein function, structure, and evolution

Identification of cis-suppression of human disease mutations by comparative genomics

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals

Mitigating false-positive associations in rare disease gene discovery

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study

Parameterization of Peptide13C Carbonyl Chemical Shielding Anisotropy in Molecular Dynamics Simulations

Predicting functional effect of human missense mutations using PolyPhen-2.

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

Reply to 'Selective effects of heterozygous protein-truncating variants'

Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases

When "N of 2" is not enough: integrating statistical and functional data in gene discovery.

Widespread macromolecular interaction perturbations in human genetic disorders