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Daniel Jordan
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Predicting functional effect of human missense mutations using PolyPhen‐2
I Adzhubei, DM Jordan, SR Sunyaev
Current protocols in human genetics 76 (1), 7.20. 1-7.20. 41, 2013
35842013
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ...
science 337 (6090), 64-69, 2012
18772012
Widespread macromolecular interaction perturbations in human genetic disorders
N Sahni, S Yi, M Taipale, JIF Bass, J Coulombe-Huntington, F Yang, ...
Cell 161 (3), 647-660, 2015
5612015
Genome analysis reveals insights into physiology and longevity of the Brandt’s bat Myotis brandtii
I Seim, X Fang, Z Xiong, AV Lobanov, Z Huang, S Ma, Y Feng, ...
Nature communications 4, 2212, 2013
3142013
Estimating the selective effects of heterozygous protein-truncating variants from human exome data
CA Cassa, D Weghorn, DJ Balick, DM Jordan, D Nusinow, KE Samocha, ...
Nature genetics 49 (5), 806, 2017
1512017
Identification of cis-suppression of human disease mutations by comparative genomics
DM Jordan, SG Frangakis, C Golzio, CA Cassa, J Kurtzberg, EE Davis, ...
Nature 524 (7564), 225, 2015
1112015
No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study
DM Jordan, HK Choi, M Verbanck, R Topless, HH Won, G Nadkarni, ...
PLoS medicine 16 (1), e1002725, 2019
1102019
Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection
AP Schoech, DM Jordan, PR Loh, S Gazal, LJ O’Connor, DJ Balick, ...
Nature communications 10 (1), 790, 2019
1042019
Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals
CA Cassa, MY Tong, DM Jordan
Human mutation 34 (9), 1216-1220, 2013
1012013
Disproportionate contributions of select genomic compartments and cell types to genetic risk for coronary artery disease
HH Won, P Natarajan, A Dobbyn, DM Jordan, P Roussos, K Lage, ...
PLoS genetics 11 (10), e1005622, 2015
972015
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy
DM Jordan, A Kiezun, SM Baxter, V Agarwala, RC Green, MF Murray, ...
The American Journal of Human Genetics 88 (2), 183-192, 2011
932011
Human allelic variation: perspective from protein function, structure, and evolution
DM Jordan, VE Ramensky, SR Sunyaev
Current opinion in structural biology 20 (3), 342-350, 2010
882010
Excess of deleterious mutations around HLA genes reveals evolutionary cost of balancing selection
TL Lenz, V Spirin, DM Jordan, SR Sunyaev
Molecular biology and evolution 33 (10), 2555-2564, 2016
612016
Mitigating false‐positive associations in rare disease gene discovery
S Akle, S Chun, DM Jordan, CA Cassa
Human mutation 36 (10), 998-1003, 2015
212015
Using full genomic information to predict disease: breaking down the barriers between complex and Mendelian diseases
DM Jordan, R Do
Annual review of genomics and human genetics 19, 289-301, 2018
162018
The landscape of pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases
DM Jordan, M Verbanck, R Do
Available at SSRN 3188410, 2018
142018
Parameterization of peptide 13C carbonyl chemical shielding anisotropy in molecular dynamics simulations
DM Jordan, KM Mills, I Andricioaei, A Bhattacharya, K Palmo, ...
ChemPhysChem 8 (9), 1375-1385, 2007
52007
Reply to ‘Selective effects of heterozygous protein-truncating variants’
CA Cassa, D Weghorn, DJ Balick, DM Jordan, D Nusinow, KE Samocha, ...
Nature genetics 51 (1), 3, 2019
32019
When “N of 2” is not enough: integrating statistical and functional data in gene discovery
CA Cassa, S Akle, DM Jordan, JA Rosenfeld
Molecular Case Studies 3 (3), a001099, 2017
22017
A literature review at genome scale: improving clinical variant assessment
CA Cassa, DM Jordan, I Adzhubei, S Sunyaev
Genetics in Medicine 20 (9), 936, 2018
12018
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