Detalhe da pesquisa
1.
Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects.
Hum Mol Genet
; 33(10): 894-904, 2024 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38433330
2.
Social and genetic associations with educational performance in a Scandinavian welfare state.
Proc Natl Acad Sci U S A
; 119(25): e2201869119, 2022 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35709318
3.
No association between long-chain n-3 fatty acid intake during pregnancy and risk of type 1 diabetes in offspring in two large Scandinavian pregnancy cohorts.
Diabetologia
; 67(6): 1023-1028, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38502240
4.
Parental genetically predicted liability for coronary heart disease and risk of adverse pregnancy outcomes: a cohort study.
BMC Med
; 22(1): 35, 2024 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38273336
5.
Extending protein interaction networks using proteoforms and small molecules.
Bioinformatics
; 39(10)2023 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37756698
6.
Impaired glucose tolerance and cardiovascular risk factors in relation to infertility: a Mendelian randomization analysis in the Norwegian Mother, Father, and Child Cohort Study.
Hum Reprod
; 39(2): 436-441, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37949105
7.
Smoking during pregnancy and its effect on placental weight: a Mendelian randomization study.
BMC Pregnancy Childbirth
; 24(1): 238, 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38575863
8.
Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes.
Diabetologia
; 66(12): 2226-2237, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37798422
9.
Structural and biophysical characterization of transcription factor HNF-1A as a tool to study MODY3 diabetes variants.
J Biol Chem
; 298(4): 101803, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35257744
10.
Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios.
Hum Mol Genet
; 29(23): 3845-3858, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33291140
11.
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
12.
Associations between health behaviours, fertility and reproductive outcomes: triangulation of evidence in the Norwegian Mother, Father and Child Cohort Study (MoBa).
BMC Med
; 21(1): 125, 2023 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37013617
13.
Developmental milestones in early childhood and genetic liability to neurodevelopmental disorders.
Psychol Med
; 53(5): 1750-1758, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37310338
14.
Bounding the average causal effect in Mendelian randomisation studies with multiple proposed instruments: An application to prenatal alcohol exposure and attention deficit hyperactivity disorder.
Paediatr Perinat Epidemiol
; 37(4): 326-337, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36722651
15.
Congenital hyperinsulinism. / Medfødt hyperinsulinisme.
Tidsskr Nor Laegeforen
; 143(18)2023 12 12.
Artigo
em Inglês, Norueguês
| MEDLINE | ID: mdl-38088279
16.
The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity.
J Biol Chem
; 296: 100661, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33862081
17.
SeeCiTe: a method to assess CNV calls from SNP arrays using trio data.
Bioinformatics
; 37(13): 1876-1883, 2021 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33459766
18.
The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice.
Pancreatology
; 22(8): 1099-1111, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36379850
19.
Early manifestations of genetic risk for neurodevelopmental disorders.
J Child Psychol Psychiatry
; 63(7): 810-819, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34605010
20.
On the importance of parenting in externalizing disorders: an evaluation of indirect genetic effects in families.
J Child Psychol Psychiatry
; 63(10): 1186-1195, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35778910