Jacques Weill

Lille, France

Last Updated: 09/26/2026

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Found 21 publications

The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism.

The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism.

Journal: Endocrine

Published: October 14, 2022

Barriers to Physical Activity in Children and Adults Living With Type 1 Diabetes: A Complex Link With Real-life Glycemic Excursions.

Barriers to Physical Activity in Children and Adults Living With Type 1 Diabetes: A Complex Link With Real-life Glycemic Excursions.

Journal: Canadian journal of diabetes

Published: June 21, 2022

SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations.

SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations.

Journal: Science translational medicine

Published: August 17, 2020

Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension.

Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension.

Journal: Nature medicine

Published: May 12, 2019

CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.

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

Randomized, double-blind, placebo-controlled dose-finding study of the dipeptidyl peptidase-4 inhibitor linagliptin in pediatric patients with type 2 diabetes.

Randomized, double-blind, placebo-controlled dose-finding study of the dipeptidyl peptidase-4 inhibitor linagliptin in pediatric patients with type 2 diabetes.

Journal: Pediatric diabetes

Published: September 15, 2017

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.

Journal: Molecular and cellular endocrinology

Published: September 06, 2017

Marker of coxsackievirus-B4 infection in saliva of patients with type 1 diabetes.

Marker of coxsackievirus-B4 infection in saliva of patients with type 1 diabetes.

Journal: Diabetes/metabolism research and reviews

Published: March 05, 2017

Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach.

Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach.

Journal: BMC medicine

Published: October 03, 2016

Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths.

Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 03, 2016

Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study.

Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study.

Journal: BMC public health

Published: July 27, 2016

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

Journal: European journal of endocrinology

Published: September 15, 2015

Showing 1-12 of 21

Last Updated: 09/26/2026