Nicole L Washington
TitleCited byYear
Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project
MB Gerstein, ZJ Lu, EL Van Nostrand, C Cheng, BI Arshinoff, T Liu, ...
Science 330 (6012), 1775-1787, 2010
8242010
Identification of functional elements and regulatory circuits by Drosophila modENCODE
S Roy, J Ernst, PV Kharchenko, P Kheradpour, N Negre, ML Eaton, ...
Science 330 (6012), 1787, 2010
7502010
Linking human diseases to animal models using ontology-based phenotype annotation
NL Washington, MA Haendel, CJ Mungall, M Ashburner, M Westerfield, ...
PLoS biology 7 (11), e1000247, 2009
2432009
The matchmaker exchange: a platform for rare disease gene discovery
AA Philippakis, DR Azzariti, S Beltran, AJ Brookes, CA Brownstein, ...
Human Mutation 36 (10), 915-921, 2015
2062015
Improved exome prioritization of disease genes through cross-species phenotype comparison
PN Robinson, S Köhler, A Oellrich, K Wang, CJ Mungall, SE Lewis, ...
Genome research 24 (2), 340-348, 2014
2022014
FER-1 regulates Ca2+-mediated membrane fusion during C. elegans spermatogenesis
NL Washington, S Ward
Journal of cell science 119 (12), 2552-2562, 2006
1252006
modMine: flexible access to modENCODE data
S Contrino, RN Smith, D Butano, A Carr, F Hu, R Lyne, K Rutherford, ...
Nucleic Acids Research, 2011
1172011
The human phenotype ontology: semantic unification of common and rare disease
T Groza, S Köhler, D Moldenhauer, N Vasilevsky, G Baynam, T Zemojtel, ...
The American Journal of Human Genetics 97 (1), 111-124, 2015
1102015
A whole-genome analysis framework for effective identification of pathogenic regulatory variants in Mendelian disease
D Smedley, M Schubach, JOB Jacobsen, S Köhler, T Zemojtel, ...
The American Journal of Human Genetics 99 (3), 595-606, 2016
982016
Next-generation diagnostics and disease-gene discovery with the Exomiser
D Smedley, JOB Jacobsen, M Jäger, S Köhler, M Holtgrewe, M Schubach, ...
Nature protocols 10 (12), 2004-2015, 2015
902015
Deletions of chromosomal regulatory boundaries are associated with congenital disease
J Ibn-Salem, S Köhler, MI Love, HR Chung, N Huang, ME Hurles, ...
Genome Biology 15, 423, 2014
892014
Patterns of molecular evolution in Caenorhabditis preclude ancient origins of selfing
AD Cutter, JD Wasmuth, NL Washington
Genetics 178 (4), 2093-2104, 2008
892008
The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species
CJ Mungall, JA McMurry, S Köhler, JP Balhoff, C Borromeo, M Brush, ...
Nucleic Acids Research 45 (D1), D712-D722, 2017
862017
Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research [version 2; referees: 3 approved]
S Köhler, SC Doelken, BJ Ruef, S Bauer, N Washington, M Westerfield, ...
69*
The Resource Identification Initiative: A cultural shift in publishing
A Bandrowski, M Brush, JS Grethe, MA Haendel, DN Kennedy, S Hill, ...
Journal of Comparative Neurology 524 (1), 8-22, 2016
672016
The Resource Identification Initiative: A cultural shift in publishing
A Bandrowski, M Brush, JS Grethe, MA Haendel, DN Kennedy, S Hill, ...
Brain and Behavior, 2015
672015
PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases
OJ Buske, M Girdea, S Dumitriu, B Gallinger, T Hartley, H Trang, ...
Human Mutation 36 (10), 931-940, 2015
652015
Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research
S Köhler, SC Doelken, BJ Ruef, S Bauer, N Washington, M Westerfield, ...
F1000Research 2, 2013
652013
Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency
WP Bone, NL Washington, OJ Buske, DR Adams, J Davis, D Draper, ...
Genetics in Medicine, 2015
542015
Representing Phenotypes in OWL.
C Mungall, G Gkoutos, N Washington, S Lewis
OWLED, 2007
402007
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Articles 1–20