Iandry Rabearivelo
Lille, France
Last Updated: 09/26/2026
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Found 8 publications
CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.
Journal: Molecular metabolism
Published: April 25, 2018
Cdkn2a deficiency promotes adipose tissue browning.
Journal: Molecular metabolism
Published: November 14, 2017
High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 02, 2017
Loss-of-function mutations in ADCY3 cause monogenic severe obesity.
Journal: Nature genetics
Published: April 30, 2017
Expression and functional assessment of candidate type 2 diabetes susceptibility genes identify four new genes contributing to human insulin secretion.
Journal: Molecular metabolism
Published: February 18, 2017
Highly sensitive diagnosis of 43 monogenic forms of diabetes or obesity through one-step PCR-based enrichment in combination with next-generation sequencing.
Journal: Diabetes care
Published: September 18, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026