Detalhe da pesquisa
1.
Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation.
Am J Hum Genet
; 107(4): 670-682, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32910913
2.
Genome-wide associations for birth weight and correlations with adult disease.
Nature
; 538(7624): 248-252, 2016 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27680694
3.
Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors.
PLoS Genet
; 11(12): e1005694, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26624892
4.
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.
PLoS Genet
; 11(7): e1005230, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26132169
5.
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
; 464(7289): 713-20, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20360734
6.
Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development.
PLoS Genet
; 7(2): e1001307, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21379325
7.
Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966.
PLoS Genet
; 5(3): e1000409, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19266077
8.
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.
PLoS Genet
; 5(6): e1000508, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557161
9.
Life-course analysis of a fat mass and obesity-associated (FTO) gene variant and body mass index in the Northern Finland Birth Cohort 1966 using structural equation modeling.
Am J Epidemiol
; 172(6): 653-65, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20702506
10.
Homozygous Hypomorphic HNF1A Alleles Are a Novel Cause of Young-Onset Diabetes and Result in Sulfonylurea-Sensitive Diabetes.
Diabetes Care
; 43(4): 909-912, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32001615
11.
Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes.
Diabetes Care
; 42(1): 17-26, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30455330
12.
Maturity onset diabetes of the young due to HNF1A variants in Croatia.
Biochem Med (Zagreb)
; 28(2): 020703, 2018 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29666556
13.
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci.
Elife
; 72018 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29412141
14.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Nat Genet
; 50(11): 1505-1513, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30297969
15.
Detailed analysis of variation at and around mitochondrial position 16189 in a large Finnish cohort reveals no significant associations with early growth or metabolic phenotypes at age 31 years.
J Clin Endocrinol Metab
; 92(8): 3219-23, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17535991
16.
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels.
Eur J Hum Genet
; 15(6): 679-84, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17342155
17.
Genes Associated with Pancreas Development and Function Maintain Open Chromatin in iPSCs Generated from Human Pancreatic Beta Cells.
Stem Cell Reports
; 9(5): 1395-1405, 2017 11 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29107594
18.
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin.
Nat Genet
; 48(9): 1055-1059, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27500523
19.
Variation at the insulin gene VNTR (variable number tandem repeat) polymorphism and early growth: studies in a large Finnish birth cohort.
Diabetes
; 53(8): 2126-31, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15277396
20.
Response to Comment on Misra et al. Homozygous Hypomorphic HNF1A Alleles Are a Novel Cause of Young-Onset Diabetes and Result in Sulfonylurea-Sensitive Diabetes. Diabetes Care 2020;43:909-912.
Diabetes Care
; 43(10): e155-e156, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32958621