Benefits and limitations of genome-wide association studies

V Tam, N Patel, M Turcotte, Y Bossé, G Paré… - Nature Reviews …, 2019 - nature.com
Genome-wide association studies (GWAS) involve testing genetic variants across the
genomes of many individuals to identify genotype–phenotype associations. GWAS have …

Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity

M Pigeyre, FT Yazdi, Y Kaur, D Meyre - Clinical science, 2016 - portlandpress.com
In high-, middle-and low-income countries, the rising prevalence of obesity is the underlying
cause of numerous health complications and increased mortality. Being a complex and …

Genetics of obesity: what have we learned?

H Choquet, D Meyre - Current genomics, 2011 - ingentaconnect.com
Candidate gene and genome-wide association studies have led to the discovery of nine loci
involved in Mendelian forms of obesity and 58 loci contributing to polygenic obesity. These …

Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug–induced weight gain

AK Malhotra, CU Correll, NI Chowdhury… - Archives of general …, 2012 - jamanetwork.com
Context Second-generation antipsychotics (SGAs) are increasingly used in the treatment of
many psychotic and nonpsychotic disorders. Unfortunately, SGAs are often associated with …

Association between Common Polymorphism near the MC4R Gene and Obesity Risk: A Systematic Review and Meta-Analysis

B Xi, GR Chandak, Y Shen, Q Wang, D Zhou - 2012 - journals.plos.org
Background Genome-wide association studies on Europeans have shown that two
polymorphisms (rs17782313, rs12970134) near the melanocortin 4 receptor (MC4R) gene …

Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis

A Hinney, AL Volckmar, N Knoll - Progress in molecular biology and …, 2013 - Elsevier
The melanocortin-4 receptor gene (MC4R) has intensively been analyzed in molecular
genetic obesity research. Decreased MC4R activity leads to obesity. Currently 166 …

New insights regarding genetic aspects of childhood obesity: a minireview

CO Mǎrginean, C Mǎrginean, LE Meliţ - Frontiers in pediatrics, 2018 - frontiersin.org
Introduction: Childhood obesity is occurring at alarming rates in both developed and
developing countries.“Obesogenic” environmental factors must be associated with variants …

Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity

JWM Creemers, H Choquet, P Stijnen, V Vatin… - Diabetes, 2012 - Am Diabetes Assoc
Null mutations in the PCSK1 gene, encoding the proprotein convertase 1/3 (PC1/3), cause
recessive monogenic early onset obesity. Frequent coding variants that modestly impair …

A genome-wide scan study identifies a single nucleotide substitution in ASIP associated with white versus non-white coat-colour variation in sheep (Ovis aries)

MH Li, T Tiirikka, J Kantanen - Heredity, 2014 - nature.com
In sheep, coat colour (and pattern) is one of the important traits of great biological, economic
and social importance. However, the genetics of sheep coat colour has not yet been fully …

Epigenome-wide methylation differences in a group of lean and obese women–A HUNT Study

K Kvaløy, CM Page, TL Holmen - Scientific reports, 2018 - nature.com
Abstract Knowledge of epigenetically regulated biomarkers linked to obesity development is
still scarce. Improving molecular understanding of the involved factors and pathways would …