Detalhe da pesquisa
1.
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.
Cell
; 185(18): 3426-3440.e19, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055201
2.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
; 110(10): 1704-1717, 2023 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37802043
3.
Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.
Am J Respir Crit Care Med
; 203(4): 424-436, 2021 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32966749
4.
Whole-genome bisulfite sequencing with improved accuracy and cost.
Genome Res
; 28(9): 1364-1371, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30093547
5.
Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth.
Am J Respir Crit Care Med
; 202(7): 962-972, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32459537
6.
YES1 amplification is a mechanism of acquired resistance to EGFR inhibitors identified by transposon mutagenesis and clinical genomics.
Proc Natl Acad Sci U S A
; 115(26): E6030-E6038, 2018 06 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875142
7.
Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma.
Am J Respir Crit Care Med
; 197(12): 1552-1564, 2018 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29509491
8.
Differential burden of rare protein truncating variants in Alzheimer's disease patients compared to centenarians.
Hum Mol Genet
; 25(14): 3096-3105, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27260402
9.
Effect of IL28B genotype on early viral kinetics during interferon-free treatment of patients with chronic hepatitis C.
Gastroenterology
; 142(4): 790-5, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22248659
10.
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
bioRxiv
; 2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36778406
11.
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Genetics
; 224(4)2023 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37348055
12.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
medRxiv
; 2023 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37425772
13.
Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.
Pharmacogenet Genomics
; 22(8): 577-89, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22569225
14.
Genomic Epidemiology and Serology Associated with a SARS-CoV-2 R.1 Variant Outbreak in New Jersey.
mBio
; 13(5): e0214122, 2022 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35997285
15.
Accounting for population structure in genetic studies of cystic fibrosis.
HGG Adv
; 3(3): 100117, 2022 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35647563
16.
Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.
Nat Commun
; 13(1): 1632, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35347136
17.
System-wide transcriptome damage and tissue identity loss in COVID-19 patients.
Cell Rep Med
; 3(2): 100522, 2022 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35233546
18.
Genetic variation in UGT1A1 typical of Gilbert syndrome is associated with unconjugated hyperbilirubinemia in patients receiving tocilizumab.
Pharmacogenet Genomics
; 21(7): 365-74, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21412181
19.
Postvaccination SARS-COV-2 among Health Care Workers in New Jersey: A Genomic Epidemiological Study.
Microbiol Spectr
; 9(3): e0188221, 2021 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34787439
20.
Emergence of Multiple SARS-CoV-2 Antibody Escape Variants in an Immunocompromised Host Undergoing Convalescent Plasma Treatment.
mSphere
; 6(4): e0048021, 2021 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34431691