Detalhe da pesquisa
1.
Personal omics profiling reveals dynamic molecular and medical phenotypes.
Cell
; 148(6): 1293-307, 2012 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22424236
2.
Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562.
Genome Res
; 29(3): 472-484, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30737237
3.
Factors associated with breast cancer recurrence and survival at Sangre Grande Hospital, Trinidad.
Cancer Causes Control
; 32(7): 763-772, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33835281
4.
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis.
J Med Genet
; 55(11): 735-743, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30061371
5.
A situational analysis of breast cancer early detection services in Trinidad and Tobago.
Cancer Causes Control
; 29(1): 33-42, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28801763
6.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
BMC Genomics
; 18(1): 321, 2017 04 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28438122
7.
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.
BMC Genomics
; 15: 1155, 2014 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25528277
8.
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.
Genet Med
; 16(10): 751-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24651605
9.
Prevalence of CYP2C19*2 and CYP2C19*3 Allelic Variants and Clopidogrel Use in Patients with Cardiovascular Disease in Trinidad & Tobago.
Cardiol Ther
; 13(1): 191-203, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38285330
10.
Child development and structural variation in the human genome.
Child Dev
; 84(1): 34-48, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23311762
11.
Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing.
ScientificWorldJournal
; 2013: 730210, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23365548
12.
Implementation of genomic surveillance of SARS-CoV-2 in the Caribbean: Lessons learned for sustainability in resource-limited settings.
PLOS Glob Public Health
; 3(2): e0001455, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36963002
13.
Correction: Implementation of Genomic Surveillance of SARS-CoV-2 in the Caribbean: Lessons learned for sustainability in resource-limited settings.
PLOS Glob Public Health
; 3(9): e0002393, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37695757
14.
Impacts of variation in the human genome on gene regulation.
J Mol Biol
; 425(21): 3970-7, 2013 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23871684
15.
Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease.
Per Med
; 9(8): 805-819, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29776237
16.
Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
PLoS One
; 6(11): e27859, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22140474
17.
Detecting and annotating genetic variations using the HugeSeq pipeline.
Nat Biotechnol
; 30(3): 226-9, 2012 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22398614