Detalhe da pesquisa
1.
The Genetic Basis of Metabolic Disease.
Cell
; 177(1): 146-161, 2019 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30901536
2.
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance.
Cell
; 176(4): 729-742.e18, 2019 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30661757
3.
KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidation.
Cell
; 155(4): 765-77, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24209692
4.
Genomics of disease risk in globally diverse populations.
Nat Rev Genet
; 20(9): 520-535, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31235872
5.
Author Correction: Genomics of disease risk in globally diverse populations.
Nat Rev Genet
; 20(9): 562, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31270439
6.
Obesity-Associated GNAS Mutations and the Melanocortin Pathway.
N Engl J Med
; 385(17): 1581-1592, 2021 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34614324
7.
Predicting novel candidate human obesity genes and their site of action by systematic functional screening in Drosophila.
PLoS Biol
; 19(11): e3001255, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34748544
8.
The impact of population-level HbA1c screening on reducing diabetes diagnostic delay in middle-aged adults: a UK Biobank analysis.
Diabetologia
; 66(2): 300-309, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36411396
9.
The influence of rare variants in circulating metabolic biomarkers.
PLoS Genet
; 16(3): e1008605, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32150548
10.
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
11.
A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development.
Am J Hum Genet
; 104(5): 985-989, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31006513
12.
Genetic architecture of human thinness compared to severe obesity.
PLoS Genet
; 15(1): e1007603, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30677029
13.
Controlled Release of Epigenetically-Enhanced Extracellular Vesicles from a GelMA/Nanoclay Composite Hydrogel to Promote Bone Repair.
Int J Mol Sci
; 23(2)2022 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35055017
14.
The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits.
Diabetologia
; 64(12): 2653-2664, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34595549
15.
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency.
Am J Hum Genet
; 103(6): 1038-1044, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30503519
16.
The UK10K project identifies rare variants in health and disease.
Nature
; 526(7571): 82-90, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26367797
17.
ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls.
PLoS Genet
; 14(10): e1007591, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30325923
18.
Bullying investigations need a code of conduct.
Nature
; 565(7740): 429, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30675047
19.
Genome-wide association study of type 2 diabetes in Africa.
Diabetologia
; 62(7): 1204-1211, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31049640
20.
Genetic aetiology of glycaemic traits: approaches and insights.
Hum Mol Genet
; 26(R2): R172-R184, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28977447