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| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8593 | 2012 |
| Reduced ventricular volumes and improved systolic function with cardiac resynchronization therapy: a randomized trial comparing simultaneous biventricular pacing, sequential … RK Rao, UN Kumar, J Schafer, E Viloria, D De Lurgio, E Foster Circulation 115 (16), 2136-2144, 2007 | 555* | 2007 |
| Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014 | 466 | 2014 |
| Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ... Nature genetics 48 (6), 593-599, 2016 | 376 | 2016 |
| Reconstructing Native American migrations from whole-genome and whole-exome data S Gravel, F Zakharia, A Moreno-Estrada, JK Byrnes, M Muzzio, ... PLoS genetics 9 (12), e1004023, 2013 | 222 | 2013 |
| RNA-Seq quantification of the human small airway epithelium transcriptome NR Hackett, MW Butler, R Shaykhiev, J Salit, L Omberg, ... BMC genomics 13, 1-31, 2012 | 139 | 2012 |
| Point-of-care whole-exome sequencing of idiopathic male infertility KA Fakhro, H Elbardisi, M Arafa, A Robay, JL Rodriguez-Flores, ... Genetics in Medicine 20 (11), 1365-1373, 2018 | 133 | 2018 |
| The Qatar genome: a population-specific tool for precision medicine in the Middle East KA Fakhro, MR Staudt, MD Ramstetter, A Robay, JA Malek, R Badii, ... Human genome variation 3 (1), 1-7, 2016 | 129 | 2016 |
| Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations JL Rodriguez-Flores, K Fakhro, F Agosto-Perez, MD Ramstetter, L Arbiza, ... Genome research 26 (2), 151-162, 2016 | 114 | 2016 |
| Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk L Zhang, F Rao, K Zhang, S Khandrika, M Das, SM Vaingankar, X Bao, ... The Journal of clinical investigation 117 (9), 2658-2671, 2007 | 105 | 2007 |
| Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations L Omberg, J Salit, N Hackett, J Fuller, R Matthew, L Chouchane, ... BMC genetics 13, 1-10, 2012 | 83 | 2012 |
| Cathepsin L colocalizes with chromogranin a in chromaffin vesicles to generate active peptides N Biswas, JL Rodriguez-Flores, M Courel, JR Gayen, SM Vaingankar, ... Endocrinology 150 (8), 3547-3557, 2009 | 80 | 2009 |
| Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population NA Yousri, KA Fakhro, A Robay, JL Rodriguez-Flores, RP Mohney, ... Nature communications 9 (1), 333, 2018 | 75 | 2018 |
| Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure Y Chen, G Wen, F Rao, K Zhang, L Wang, JL Rodriguez-Flores, ... Journal of hypertension 28 (1), 76-86, 2010 | 70 | 2010 |
| Naturally occurring human genetic variation in the 3′-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and … Y Chen, F Rao, JL Rodriguez-Flores, M Mahata, MM Fung, M Stridsberg, ... Journal of the American College of Cardiology 52 (18), 1468-1481, 2008 | 56 | 2008 |
| Pro-hormone secretogranin II regulates dense core secretory granule biogenesis in catecholaminergic cells M Courel, A Soler-Jover, JL Rodriguez-Flores, SK Mahata, S Elias, ... Journal of Biological Chemistry 285 (13), 10030-10043, 2010 | 52 | 2010 |
| Exome Sequencing Identifies Potential Risk Variants for M endelian Disorders at High Prevalence in Q atar JL Rodriguez‐Flores, K Fakhro, NR Hackett, J Salit, J Fuller, ... Human mutation 35 (1), 105-116, 2014 | 51 | 2014 |
| Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure Y Chen, F Rao, JL Rodriguez-Flores, NR Mahapatra, M Mahata, G Wen, ... Kidney international 74 (1), 115-125, 2008 | 45 | 2008 |
| Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder M Song, CA Mathews, SE Stewart, SV Shmelkov, JG Mezey, ... PLoS One 12 (1), e0169994, 2017 | 40 | 2017 |
Daniel T. O'ConnorUniversity of California at San Diego在 ucsd.edu 的电子邮件经过验证
