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| Personal omics profiling reveals dynamic molecular and medical phenotypes R Chen, GI Mias, J Li-Pook-Than, L Jiang, HYK Lam, R Chen, E Miriami, ... Cell 148 (6), 1293-1307, 2012 | 1373 | 2012 |
| Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011 | 712 | 2011 |
| The 1000 Genomes Project: data management and community access L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ... Nature methods 9 (5), 459-462, 2012 | 342 | 2012 |
| The functional spectrum of low-frequency coding variation GT Marth, F Yu, AR Indap, K Garimella, S Gravel, WF Leong, ... Genome biology 12, 1-17, 2011 | 242 | 2011 |
| Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway GM Enns, V Shashi, M Bainbridge, MJ Gambello, FR Zahir, T Bast, ... Genetics in Medicine 16 (10), 751-758, 2014 | 229 | 2014 |
| Impacts of variation in the human genome on gene regulation RR Haraksingh, MP Snyder Journal of molecular biology 425 (21), 3970-3977, 2013 | 195 | 2013 |
| Detecting and annotating genetic variations using the HugeSeq pipeline HYK Lam, C Pan, MJ Clark, P Lacroute, R Chen, R Haraksingh, ... Nature biotechnology 30 (3), 226-229, 2012 | 143 | 2012 |
| Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562 B Zhou, SS Ho, SU Greer, X Zhu, JM Bell, JG Arthur, N Spies, X Zhang, ... Genome research 29 (3), 472-484, 2019 | 103 | 2019 |
| Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis B Zhou, SS Ho, X Zhang, R Pattni, RR Haraksingh, AE Urban Journal of medical genetics 55 (11), 735-743, 2018 | 100 | 2018 |
| Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms RR Haraksingh, A Abyzov, M Gerstein, AE Urban, M Snyder PloS one 6 (11), e27859, 2011 | 86 | 2011 |
| Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans RR Haraksingh, A Abyzov, AE Urban BMC genomics 18, 1-14, 2017 | 83 | 2017 |
| Computational and bioinformatics frameworks for next‐generation whole exome and genome sequencing MP Dolled-Filhart, M Lee Jr, C Ou-Yang, RR Haraksingh, JCH Lin The Scientific World Journal 2013 (1), 730210, 2013 | 74 | 2013 |
| Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss RR Haraksingh, F Jahanbani, J Rodriguez-Paris, J Gelernter, KC Nadeau, ... BMC genomics 15, 1-19, 2014 | 37 | 2014 |
| Child development and structural variation in the human genome Y Zhang, R Haraksingh, F Grubert, A Abyzov, M Gerstein, S Weissman, ... Child development 84 (1), 34-48, 2013 | 29 | 2013 |
| Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease MP Dolled-Filhart, A Lordemann, W Dahl, RR Haraksingh, CW Ou-Yang, ... Personalized medicine 9 (8), 805-819, 2012 | 10 | 2012 |
| Implementation of genomic surveillance of SARS-Cov-2 in the caribbean: lessons learned for sustainability in resource-limited settings NSD Sahadeo, S Nicholls, FRR Moreira, Á O’Toole, V Ramkissoon, ... PLOS global public health 3 (2), e0001455, 2023 | 6 | 2023 |
| A situational analysis of breast cancer early detection services in Trinidad and Tobago K Badal, F Rampersad, WA Warner, AT Toriola, H Mohammed, ... Cancer Causes & Control 29, 33-42, 2018 | 6 | 2018 |
| Factors associated with breast cancer recurrence and survival at Sangre Grande Hospital, Trinidad K Badal, R Ali, WA Warner, A Maniam, A Carrington, JE Foster, ... Cancer Causes & Control 32, 763-772, 2021 | 5 | 2021 |
| Prevalence of CYP2C19*2 and CYP2C19*3 Allelic Variants and Clopidogrel Use in Patients with Cardiovascular Disease in Trinidad & Tobago D Jones, S Persad-Ramdeensingh, SC Abrahim, N Seecheran, ... Cardiology and Therapy 13 (1), 191-203, 2024 | 1 | 2024 |
Alexander Eckehart UrbanAssociate Professor of Psychiatry and Behavioral Sciences, and of Genetics, Stanford University在 stanford.edu 的电子邮件经过验证
