Detalhe da pesquisa
1.
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry.
BMC Genomics
; 25(1): 208, 2024 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408933
2.
Shared genetics and causal relationships between migraine and thyroid function traits.
Cephalalgia
; 43(2): 3331024221139253, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739509
3.
Decreased Immunoglobulin G Core Fucosylation, A Player in Antibody-dependent Cell-mediated Cytotoxicity, is Associated with Autoimmune Thyroid Diseases.
Mol Cell Proteomics
; 19(5): 774-792, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32024769
4.
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
PLoS Genet
; 15(12): e1008517, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31805045
5.
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
PLoS Genet
; 14(12): e1007813, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566500
6.
Functional Analysis of Calcium-Sensing Receptor Variants Identified in Families Provisionally Diagnosed with Familial Hypocalciuric Hypercalcaemia.
Calcif Tissue Int
; 107(3): 230-239, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32638038
7.
Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.
Hum Mol Genet
; 26(14): 2791-2802, 2017 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28472463
8.
How many cases of disease in a pedigree imply familial disease?
Ann Hum Genet
; 82(2): 109-113, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29058319
9.
The longitudinal effects of peritonitis on peritoneal membrane functionâ©.
Clin Nephrol
; 88(12): 311-316, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29139376
10.
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.
BMC Genomics
; 17: 136, 2016 Feb 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26911590
11.
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Hum Mol Genet
; 23(11): 3054-68, 2014 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24430505
12.
HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer.
BMC Med Genet
; 17(1): 60, 2016 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27530615
13.
Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.
Clin Endocrinol (Oxf)
; 84(2): 278-283, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25683181
14.
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
PLoS Genet
; 9(2): e1003266, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23408906
15.
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.
PLoS Genet
; 8(7): e1002745, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22792071
16.
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.
PLoS Genet
; 7(4): e1002025, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21533175
17.
Case Presentation: Functional Assessment of a CASR Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism.
Case Rep Endocrinol
; 2024: 6652801, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38343604
18.
Epigenome-wide Association Study Shows Differential DNA Methylation of MDC1, KLF9, and CUTA in Autoimmune Thyroid Disease.
J Clin Endocrinol Metab
; 109(4): 992-999, 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37962983
19.
Enhanced resolution profiling in twins reveals differential methylation signatures of type 2 diabetes with links to its complications.
EBioMedicine
; 103: 105096, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38574408
20.
A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study.
Am J Hum Genet
; 87(3): 430-5, 2010 Sep 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-20826269