Detalhe da pesquisa
1.
Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant.
Brain;
2024 May 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38804604
2.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Hum Mol Genet;
27(11): 2025-2038, 2018 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29659830
3.
Modeling prior information of common genetic variants improves gene discovery for neuroticism.
Hum Mol Genet;
26(22): 4530-4539, 2017 11 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28973307
4.
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
Hum Mol Genet;
25(9): 1867-74, 2016 05 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26908601
5.
Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms.
Blood;
128(8): 1121-8, 2016 08 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27365426
6.
Age-induced and photoinduced changes in gene expression profiles in facial skin of Caucasian females across 6 decades of age.
J Am Acad Dermatol;
78(1): 29-39.e7, 2018 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29146147
7.
Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling.
J Allergy Clin Immunol;
139(4): 1148-1157, 2017 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27554816
8.
Shared genetic variants suggest common pathways in allergy and autoimmune diseases.
J Allergy Clin Immunol;
140(3): 771-781, 2017 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28188724
9.
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
Hum Mol Genet;
24(9): 2700-8, 2015 May 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25628336
10.
Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.
PLoS Genet;
9(2): e1003299, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23468642
11.
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
PLoS Genet;
8(5): e1002746, 2012 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22693459
12.
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS Genet;
8(3): e1002548, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22438815
13.
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.
J Allergy Clin Immunol;
133(6): 1564-71, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24388013
14.
Replicability and robustness of genome-wide-association studies for behavioral traits.
Psychol Sci;
25(11): 1975-86, 2014 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25287667
15.
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PLoS Genet;
7(6): e1002141, 2011 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21738487
16.
Web-based, participant-driven studies yield novel genetic associations for common traits.
PLoS Genet;
6(6): e1000993, 2010 Jun 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20585627
17.
Genetic variants associated with breast size also influence breast cancer risk.
BMC Med Genet;
13: 53, 2012 Jun 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22747683
18.
Genome-wide association study of pain sensitivity assessed by questionnaire and the cold pressor test.
Pain;
163(9): 1763-1776, 2022 09 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34924555
19.
Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report.
Chest;
161(2): 373-381, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34656525
20.
Genome-wide association study identifies 48 common genetic variants associated with handedness.
Nat Hum Behav;
5(1): 59-70, 2021 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32989287