Detalhe da pesquisa
1.
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
PLoS Genet
; 16(10): e1008718, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33045005
2.
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
Hum Mol Genet
; 25(2): 389-403, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604143
3.
Risk of Cardiomyopathy in Younger Persons With a Family History of Death from Cardiomyopathy: A Nationwide Family Study in a Cohort of 3.9 Million Persons.
Circulation
; 132(11): 1013-9, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26276887
4.
Determination of NAT2 acetylation status in the Greenlandic population.
Arch Toxicol
; 90(4): 883-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25794903
5.
Epilepsy, anti-epileptic medication use and risk of cancer.
Int J Cancer
; 134(4): 932-8, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23901034
6.
Continuous Glucose Monitoring-Based Metrics and Hypoglycemia Duration in Insulin-Experienced Individuals With Long-standing Type 2 Diabetes Switched From a Daily Basal Insulin to Once-Weekly Insulin Icodec: Post Hoc Analysis of ONWARDS 2 and ONWARDS 4.
Diabetes Care
; 47(4): 729-738, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38380954
7.
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
JAMA
; 310(7): 714-21, 2013 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23989729
8.
Risk of Congenital Heart Defects in Offspring of Affected Mothers and Fathers.
Circ Genom Precis Med
; 15(4): e003533, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35608601
9.
Multivariate Hawkes process models of the occurrence of regulatory elements.
BMC Bioinformatics
; 11: 456, 2010 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20828413
10.
Association Between Maternal Folic Acid Supplementation and Congenital Heart Defects in Offspring in Birth Cohorts From Denmark and Norway.
J Am Heart Assoc
; 8(6): e011615, 2019 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30857459
11.
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
Eur J Hum Genet
; 26(4): 561-569, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29379196
12.
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.
Nat Genet
; 47(12): 1449-1456, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26482879
13.
Common variants associated with general and MMR vaccine-related febrile seizures.
Nat Genet
; 46(12): 1274-82, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344690
14.
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.
Nat Genet
; 46(9): 957-63, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25108383
15.
Family history of premature death and risk of early onset cardiovascular disease.
J Am Coll Cardiol
; 60(9): 814-21, 2012 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-22917005
16.
Familial aggregation of lone atrial fibrillation in young persons.
J Am Coll Cardiol
; 60(10): 917-21, 2012 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22726627
17.
Time trends in human fecundability in Sweden.
Epidemiology
; 19(2): 191-6, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18223482
18.
Feasibility of the current-duration approach to studying human fecundity.
Epidemiology
; 17(4): 440-9, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16755258