| 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 | 336 | 2016 |
| 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 | 319 | 2018 |
| 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 | 251 | 2016 |
| 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 | 201 | 2002 |
| 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 | 159 | 2016 |
| 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 | 128 | 2007 |
| 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 | 97 | 2018 |
| 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 | 84 | 2007 |
| 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 | 82 | 2014 |
| 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 | 80 | 2007 |
| Personalized medicine and the power of electronic health records NS Abul-Husn, EE Kenny Cell 177 (1), 58-69, 2019 | 64 | 2019 |
| 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 | 55 | 2009 |
| 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 | 50 | 2011 |
| 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 | 47 | 2017 |
| Neuroproteomics of the synapse and drug addiction NS Abul-Husn, LA Devi Journal of Pharmacology and Experimental Therapeutics 318 (2), 461-468, 2006 | 46 | 2006 |
| 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 | 42 | 2014 |
| 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 | 37 | 2018 |
| 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 | 37 | 2009 |
| 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 | 33 | 2017 |
| 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 | 32 | 2019 |
