Skip to Main Content

Author Details

Daniel M Jordan
Icahn School of Medicine at Mount Sinai
2007
31
18
PMIDPaper TitleJournal TitlePublished Year
36563696Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.Lancet2023
36563696Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.Lancet2023
37169741A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.Nat Commun2023
36988189Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits.Elife2023
36988189Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits.Elife2023
37169741A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.Nat Commun2023
35076666Population-Based Penetrance of Deleterious Clinical Variants.JAMA2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35987940A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.Commun Biol2022
34951958Overcoming constraints on the detection of recessive selection in human genes from population frequency data.Am J Hum Genet2022
35076666Population-Based Penetrance of Deleterious Clinical Variants.JAMA2022
35987940A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.Commun Biol2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34951958Overcoming constraints on the detection of recessive selection in human genes from population frequency data.Am J Hum Genet2022
33499903Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.Genome Biol2021
33493176Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank.PLoS Genet2021
33483510An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease.Nat Commun2021
33499903Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.Genome Biol2021
33493176Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank.PLoS Genet2021
33483510An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease.Nat Commun2021
30645594No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study.PLoS Med2019
31653226HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases.Genome Biol2019
30478437Reply to 'Selective effects of heterozygous protein-truncating variants'.Nat Genet2019
30645594No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study.PLoS Med2019
30770844Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection.Nat Commun2019
31653226HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases.Genome Biol2019
30770844Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection.Nat Commun2019
30478437Reply to 'Selective effects of heterozygous protein-truncating variants'.Nat Genet2019
29388949A literature review at genome scale: improving clinical variant assessment.Genet Med2018
29388949A literature review at genome scale: improving clinical variant assessment.Genet Med2018
29641912Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.Annu Rev Genomics Hum Genet2018
29641912Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.Annu Rev Genomics Hum Genet2018
28746880TGF-β Signaling Is Necessary and Sufficient for Pharyngeal Arch Artery Angioblast Formation.Cell Rep2017
28487880When "<i>N</i> of 2" is not enough: integrating statistical and functional data in gene discovery.Cold Spring Harb Mol Case Stud2017
28369035Estimating the selective effects of heterozygous protein-truncating variants from human exome data.Nat Genet2017
28746880TGF-β Signaling Is Necessary and Sufficient for Pharyngeal Arch Artery Angioblast Formation.Cell Rep2017
28487880When "<i>N</i> of 2" is not enough: integrating statistical and functional data in gene discovery.Cold Spring Harb Mol Case Stud2017
28369035Estimating the selective effects of heterozygous protein-truncating variants from human exome data.Nat Genet2017
27436009Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection.Mol Biol Evol2016
27436009Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection.Mol Biol Evol2016
25910212Widespread macromolecular interaction perturbations in human genetic disorders.Cell2015
25910212Widespread macromolecular interaction perturbations in human genetic disorders.Cell2015
26509271Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.PLoS Genet2015
26123021Identification of cis-suppression of human disease mutations by comparative genomics.Nature2015
26378430Mitigating false-positive associations in rare disease gene discovery.Hum Mutat2015
26509271Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.PLoS Genet2015
26378430Mitigating false-positive associations in rare disease gene discovery.Hum Mutat2015
26123021Identification of cis-suppression of human disease mutations by comparative genomics.Nature2015
23315928Predicting functional effect of human missense mutations using PolyPhen-2.Curr Protoc Hum Genet2013
23818451Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals.Hum Mutat2013
  • 1 - 50 of 62

Recommended Authors

Kymberleigh A Pagel
The Institute for Computational Medicine, The Johns Hopkins University
Career Start Year 2016
Number of shared co-authors 1
Hao Hu
Aerospace Center Hospital
Career Start Year 2011
Number of shared co-authors 4
Max Schubach
Berlin Institute of Health of Health at Charite - Universitatsmedizin Berlin
Career Start Year 2010
Number of shared co-authors 8
Hilary C Martin
Wellcome Sanger Institute
Career Start Year 2010
Number of shared co-authors 12
Seung Hoan Choi
Broad Institute of MIT and Harvard
Career Start Year 2009
Number of shared co-authors 14
John D Overton
Regeneron Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 19
Graham R S Ritchie
Wellcome Sanger Institute
Career Start Year 2008
Number of shared co-authors 9
Zachary Zappala
Vertex Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 14
Manuel A Rivas
Stanford University School of Medicine
Career Start Year 2008
Number of shared co-authors 28
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Career Start Year 2007
Number of shared co-authors 9
William S Bush
Cleveland Institute for Computational Biology, Case Western Reserve University
Career Start Year 2006
Number of shared co-authors 11
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 8
Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
Career Start Year 2005
Number of shared co-authors 26
Tushar Bhangale
Genentech Inc.
Career Start Year 2004
Number of shared co-authors 19
Alicia Hawes
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 17
Joseph K Pickrell
Gencove Inc.
Career Start Year 2003
Number of shared co-authors 11
Fuli Yu
East China University of Science and Technology
Career Start Year 2002
Number of shared co-authors 20
Yufeng Shen
Columbia University
Career Start Year 2002
Number of shared co-authors 14
Andrew S Allen
Duke University School of Medicine
Career Start Year 2001
Number of shared co-authors 7
Sean D Mooney
University of Washington
Career Start Year 2001
Number of shared co-authors 5
Jessica M Maia
Institute for Genomic Medicine, Columbia University
Career Start Year 2001
Number of shared co-authors 2
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Career Start Year 2001
Number of shared co-authors 36
Paul I W de Bakker
Vertex Pharmaceuticals
Career Start Year 1999
Number of shared co-authors 36
Sebastian Z??llner
University of Michigan ann arbor
Career Start Year 1998
Number of shared co-authors 19
Sarah E Hunt
European Bioinformatics Institute
Career Start Year 1997
Number of shared co-authors 17
Andrew P Morris
The University of Manchester
Career Start Year 1997
Number of shared co-authors 34
David A Hinds
23andMe Inc.
Career Start Year 1992
Number of shared co-authors 22
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1992
Number of shared co-authors 35
Joel N Hirschhorn
Broad Institute of MIT and Harvard
Career Start Year 1988
Number of shared co-authors 35
Albert V Smith
University of Michigan School of Public Health ann arbor
Career Start Year 1987
Number of shared co-authors 40

Collaborators

Ron Do
Co-authored papers 14
Shamil R Sunyaev
Harvard Medical School
Co-authored papers 13
Ghislain Rocheleau
Co-authored papers 5
Marie Verbanck
Co-authored papers 5
Girish N Nadkarni
Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Hong-Hee Won
Co-authored papers 3
Noam D Beckmann
Icahn School of Medicine at Mount Sinai.
Co-authored papers 2
Kaitlin E Samocha
Co-authored papers 2
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers 2
Alexander W Charney
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
Carla Marquez-Luna
Co-authored papers 2
Eimear E Kenny
Icahn School of Medicine at Mount Sinai, NY Institute for Genomic Health
Co-authored papers 2
Mark J Daly
Massachusetts General Hospital
Co-authored papers 2
Ivan Adzhubei
Co-authored papers 2
Eric E Schadt
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
Anne O'Donnell-Luria
Broad Institute of MIT and Harvard
Co-authored papers 2
Birgit Funke
Partners Healthcare Center for Personalized Genetic Medicine
Co-authored papers 1
Mathieu Bourgey
McGill University
Co-authored papers 1
Albandari Binowayn
King Fahad Medical City and King Abdulaziz City for Science and Technology
Co-authored papers 1
Nattiya Hirankarn
Chulalongkorn University
Co-authored papers 1
Samantha Baxter
Broad Institute of MIT and Harvard
Co-authored papers 1
Carlos D Bustamante
Stanford University
Co-authored papers 1
Ho Namkoong
Keio University School of Medicine
Co-authored papers 1
Chiara Giannarelli
Co-authored papers 1
Mathieu Quinodoz
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
Co-authored papers 1
Antonio Salas
Instituto de Investigacion Sanitaria de Santiago
Co-authored papers 1
Timothy Sanders
David Geffen School of Medicine, University of California-Los Angeles
Co-authored papers 1
Nicole Simons
Icahn School of Medicine at Mount Sinai
Co-authored papers 1
Efren Sandoval
Co-authored papers 1
Carlo Rivolta
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
Co-authored papers 1
Release 1.2