Detalhe da pesquisa
1.
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.
Am J Hum Genet
; 104(1): 112-138, 2019 01 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30595373
2.
Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report.
BMC Med Genet
; 20(1): 152, 2019 09 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31488071
3.
Genetic Variations in the Human G Protein-coupled Receptor Class C, Group 6, Member A (GPRC6A) Control Cell Surface Expression and Function.
J Biol Chem
; 292(4): 1524-1534, 2017 01 27.
Artigo
Inglês
| MEDLINE | ID: mdl-27986810
4.
Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity.
BMC Med Genet
; 19(1): 199, 2018 11 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30442103
5.
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
Eur Heart J
; 36(37): 2523-9, 2015 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26159999
6.
A glycogene mutation map for discovery of diseases of glycosylation.
Glycobiology
; 25(2): 211-24, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25267602
7.
Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case-control study.
BMC Med Genet
; 16: 105, 2015 Nov 11.
Artigo
Inglês
| MEDLINE | ID: mdl-26558825
8.
Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes.
Genome Biol
; 25(1): 22, 2024 Jan 16.
Artigo
Inglês
| MEDLINE | ID: mdl-38229171
9.
Correction: Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiography.
PLoS One
; 18(10): e0293765, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37883362
10.
Insulin resistance genetic risk score and burden of coronary artery disease in patients referred for coronary angiography.
PLoS One
; 16(6): e0252855, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34143812
11.
Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity.
J Clin Endocrinol Metab
; 106(1): 80-90, 2021 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32944759
12.
Are graph databases ready for bioinformatics?
Bioinformatics
; 29(24): 3107-8, 2013 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24135261
13.
Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants.
PLoS One
; 14(8): e0220805, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31415576
14.
Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes.
PLoS One
; 14(1): e0210114, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30629617
15.
Genetic Determinants of Weight Loss After Bariatric Surgery.
Obes Surg
; 29(8): 2554-2561, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31001758
16.
Association of alcohol consumption with allergic disease and asthma: a multi-centre Mendelian randomization analysis.
Addiction
; 114(2): 216-225, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30209858
17.
Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiography.
PLoS One
; 13(12): e0208645, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-30566436
18.
A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.
PLoS One
; 12(3): e0174204, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28333968
19.
High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus.
J Endocr Soc
; 1(6): 681-690, 2017 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29264522
20.
Association study between CDH2 and Gilles de la Tourette syndrome in a Danish cohort.
Psychiatry Res
; 228(3): 974-5, 2015 Aug 30.
Artigo
Inglês
| MEDLINE | ID: mdl-26032459