Detalhe da pesquisa
1.
A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.
Hum Mol Genet
; 27(13): 2383-2391, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29659823
2.
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci.
Hum Genet
; 136(6): 771-800, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391526
3.
Fine Mapping and Identification of BMI Loci in African Americans.
Am J Hum Genet
; 93(4): 661-71, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24094743
4.
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
; 9(1): e1003171, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23341774
5.
A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.
Hum Mol Genet
; 27(13): 2406, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29860498
6.
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
Am J Med Genet A
; 167A(12): 2975-84, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26284702
7.
Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms.
Hum Mol Genet
; 19(7): 1286-301, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20071345
8.
Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells.
Blood
; 115(23): 4923-33, 2010 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-20203263
9.
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
Am J Med Genet A
; 158A(12): 3137-47, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23165927
10.
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
PLoS Genet
; 5(9): e1000649, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19763161
11.
C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene.
J Infect Dis
; 204(11): 1654-62, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22039568
12.
Neuropathy target esterase gene mutations cause motor neuron disease.
Am J Hum Genet
; 82(3): 780-5, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18313024
13.
Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.
J Med Genet
; 47(10): 692-9, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20522424
14.
A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.
PLoS Genet
; 4(7): e1000125, 2008 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18618000
15.
(1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function.
J Proteome Res
; 9(6): 3083-90, 2010 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-20408573
16.
The 5q31 variants associated with psoriasis and Crohn's disease are distinct.
Hum Mol Genet
; 17(19): 2978-85, 2008 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18614543
17.
Identification of distinct plasma biomarker signatures in patients with rapid and slow declining forms of COPD.
COPD
; 7(1): 51-8, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20214463
18.
Linkage analysis of Tourette syndrome in a large Utah pedigree.
Am J Med Genet B Neuropsychiatr Genet
; 153B(2): 656-662, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19777563
19.
Germline mutation rates in young adults predict longevity and reproductive lifespan.
Sci Rep
; 10(1): 10001, 2020 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32561805
20.
High-sensitivity nanoLC-MS/MS analysis of urinary desmosine and isodesmosine.
Anal Chem
; 81(5): 1881-7, 2009 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19178285