Detalhe da pesquisa
1.
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.
Am J Hum Genet
; 108(3): 431-445, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33600772
2.
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Genet Epidemiol
; 43(1): 37-49, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30246882
3.
Common and Rare Variants Genetic Association Analysis of Cigarettes per Day Among Ever-Smokers in Chronic Obstructive Pulmonary Disease Cases and Controls.
Nicotine Tob Res
; 21(6): 714-722, 2019 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29767774
4.
Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.
Genet Epidemiol
; 41(3): 244-250, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28019042
5.
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.
Am J Hum Genet
; 96(3): 397-411, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25704602
6.
Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.
Gastroenterology
; 152(1): 206-217.e2, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27693347
7.
Regionally Smoothed Meta-Analysis Methods for GWAS Datasets.
Genet Epidemiol
; 40(2): 154-60, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26707090
8.
Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort.
Genet Epidemiol
; 40(1): 81-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26643968
9.
Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.
Hum Mol Genet
; 23(2): 408-17, 2014 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24014426
10.
Comprehensive literature review and statistical considerations for GWAS meta-analysis.
Nucleic Acids Res
; 40(9): 3777-84, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22241776
11.
Inflammatory Bowel Diseases Before and After 1990.
Gastro Hep Adv
; 2(1): 22-32, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36686985
12.
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
Hum Genet
; 131(7): 1039-46, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22160426
13.
No observed association for mitochondrial SNPs with preterm delivery and related outcomes.
Pediatr Res
; 72(5): 539-44, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22902432
14.
Genome-wide association scan of dental caries in the permanent dentition.
BMC Oral Health
; 12: 57, 2012 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23259602
15.
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families.
Mol Genet Genomic Med
; 5(5): 570-579, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28944239
16.
Genome-Wide Association Study of Meiotic Recombination Phenotypes.
G3 (Bethesda)
; 6(12): 3995-4007, 2016 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27733454
17.
Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study.
PLoS One
; 11(10): e0164134, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27711239
18.
An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.
PLoS One
; 9(6): e99560, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24926858