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Lista de obras de Daniel M. Jordan

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

artículo científico publicado en 2018

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

artículo científico publicado en 2022

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

artículo científico publicado en 2021

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Mitigating false-positive associations in rare disease gene discovery

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2013

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

artículo científico publicado en 2019

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.

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Widespread macromolecular interaction perturbations in human genetic disorders

scientific journal article

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