Search details
1.
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms.
Cell
; 170(1): 199-212.e20, 2017 Jun 29.
Article
in English
| MEDLINE | ID: mdl-28666119
2.
Genetic insights into biological mechanisms governing human ovarian ageing.
Nature
; 596(7872): 393-397, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34349265
3.
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Ann Neurol
; 90(1): 76-88, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33938021
4.
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry.
Mol Psychiatry
; 26(11): 6209-6217, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34728798
5.
Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease.
Mol Psychiatry
; 26(8): 4254-4264, 2021 08.
Article
in English
| MEDLINE | ID: mdl-31796895
6.
The genetic architecture of type 2 diabetes.
Nature
; 536(7614): 41-47, 2016 08 04.
Article
in English
| MEDLINE | ID: mdl-27398621
7.
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness.
Hum Mol Genet
; 28(22): 3853-3865, 2019 11 15.
Article
in English
| MEDLINE | ID: mdl-31518406
8.
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Proc Natl Acad Sci U S A
; 115(2): 379-384, 2018 01 09.
Article
in English
| MEDLINE | ID: mdl-29279374
9.
Genome-Wide Association Studies of Impulsive Personality Traits (BIS-11 and UPPS-P) and Drug Experimentation in up to 22,861 Adult Research Participants Identify Loci in the CACNA1I and CADM2 genes.
J Neurosci
; 39(13): 2562-2572, 2019 03 27.
Article
in English
| MEDLINE | ID: mdl-30718321
10.
The Latent Genetic Structure of Impulsivity and Its Relation to Internalizing Psychopathology.
Psychol Sci
; 31(8): 1025-1035, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32716714
11.
Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry.
Addict Biol
; 24(1): 121-131, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29058377
12.
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
Hum Mol Genet
; 25(10): 2070-2081, 2016 05 15.
Article
in English
| MEDLINE | ID: mdl-26911676
13.
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.
PLoS Genet
; 11(1): e1004876, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25625282
14.
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
Hum Mol Genet
; 24(2): 559-71, 2015 Jan 15.
Article
in English
| MEDLINE | ID: mdl-25187575
15.
Age-related clonal hematopoiesis associated with adverse outcomes.
N Engl J Med
; 371(26): 2488-98, 2014 Dec 25.
Article
in English
| MEDLINE | ID: mdl-25426837
16.
Inactivating mutations in NPC1L1 and protection from coronary heart disease.
N Engl J Med
; 371(22): 2072-82, 2014 Nov 27.
Article
in English
| MEDLINE | ID: mdl-25390462
17.
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes.
Proc Natl Acad Sci U S A
; 111(36): 13127-32, 2014 Sep 09.
Article
in English
| MEDLINE | ID: mdl-25157153
18.
Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans.
JAMA
; 312(20): 2115-25, 2014 Nov 26.
Article
in English
| MEDLINE | ID: mdl-25393378
19.
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.
JAMA
; 311(22): 2305-14, 2014 Jun 11.
Article
in English
| MEDLINE | ID: mdl-24915262
20.
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals.
EBioMedicine
; : 105086, 2024 Apr 02.
Article
in English
| MEDLINE | ID: mdl-38580523