Noura Abul-Husn
Noura Abul-Husn
Unknown affiliation
Verified email at mssm.edu
Title
Cited by
Cited by
Year
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ...
Science 354 (6319), 2016
3362016
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
NS Abul-Husn, X Cheng, AH Li, Y Xin, C Schurmann, P Stevis, Y Liu, ...
New England Journal of Medicine 378 (12), 1096-1106, 2018
3192018
Genetic identification of familial hypercholesterolemia within a single US health care system
NS Abul-Husn, K Manickam, LK Jones, EA Wright, DN Hartzel, ...
Science 354 (6319), 2016
2512016
Paradoxical effects of the opioid antagonist naltrexone on morphine analgesia, tolerance, and reward in rats
KJ Powell, NS Abul-Husn, A Jhamandas, MC Olmstead, RJ Beninger, ...
Journal of Pharmacology and Experimental Therapeutics 300 (2), 588-596, 2002
2012002
Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records
SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ...
Jama 315 (1), 47-57, 2016
1592016
Morphine administration alters the profile of hippocampal postsynaptic density-associated proteins: a proteomics study focusing on endocytic proteins
JA Morón, NS Abul-Husn, R Rozenfeld, G Dolios, R Wang, LA Devi
Molecular & Cellular Proteomics 6 (1), 29-42, 2007
1282007
Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants
K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ...
JAMA Network Open 1 (5), e182140-e182140, 2018
972018
Augmentation of spinal morphine analgesia and inhibition of tolerance by low doses of μ‐ and δ‐opioid receptor antagonists
NS Abul‐Husn, M Sutak, B Milne, K Jhamandas
British journal of pharmacology 151 (6), 877-887, 2007
842007
Implementation and utilization of genetic testing in personalized medicine
NS Abul-Husn, AO Obeng, SC Sanderson, O Gottesman, SA Scott
Pharmacogenomics and personalized medicine 7, 227, 2014
822014
An emerging role for the delta opioid receptor in the regulation of mu opioid receptor function
R Rozenfeld, NS Abul-Husn, I Gomez, LA Devi
TheScientificWorldJOURNAL 7, 64-73, 2007
802007
Personalized medicine and the power of electronic health records
NS Abul-Husn, EE Kenny
Cell 177 (1), 58-69, 2019
642019
Systems approach to explore components and interactions in the presynapse
NS Abul‐Husn, I Bushlin, JA Morón, SL Jenkins, G Dolios, R Wang, ...
Proteomics 9 (12), 3303-3315, 2009
552009
Chronic morphine alters the presynaptic protein profile: identification of novel molecular targets using proteomics and network analysis
NS Abul-Husn, SP Annangudi, A Ma'Ayan, DL Ramos-Ortolaza, ...
PLoS One 6 (10), e25535, 2011
502011
Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system
GM Belbin, J Odgis, EP Sorokin, MC Yee, S Kohli, BS Glicksberg, ...
Elife 6, e25060, 2017
472017
Neuroproteomics of the synapse and drug addiction
NS Abul-Husn, LA Devi
Journal of Pharmacology and Experimental Therapeutics 318 (2), 461-468, 2006
462006
Physician attitudes toward adopting genome-guided prescribing through clinical decision support
CL Overby, AL Erwin, NS Abul-Husn, SB Ellis, SA Scott, AO Obeng, ...
Journal of personalized medicine 4 (1), 35-49, 2014
422014
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
AH Buchanan, K Manickam, MN Meyer, JK Wagner, MLG Hallquist, ...
Genetics in Medicine 20 (5), 554-558, 2018
372018
SNAVI: Desktop application for analysis and visualization of large-scale signaling networks
A Ma'ayan, SL Jenkins, RL Webb, SI Berger, SP Purushothaman, ...
BMC systems biology 3 (1), 1-11, 2009
372009
Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience
CR Rohrer Vitek, NS Abul-Husn, JJ Connolly, AL Hartzler, T Kitchner, ...
Pharmacogenomics 18 (10), 1013-1025, 2017
332017
Association of the V122I hereditary transthyretin amyloidosis genetic variant with heart failure among individuals of African or Hispanic/Latino ancestry
SM Damrauer, K Chaudhary, JH Cho, LW Liang, E Argulian, L Chan, ...
Jama 322 (22), 2191-2202, 2019
322019
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