Author details

Full Name

StÃ©phane Cauchi

Affiliation

ORCID

Career Start Year

1992

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33509692	Live attenuated Bordetella pertussis vaccine candidate BPZE1 transiently protects against lethal pneumococcal disease in mice.	Vaccine	2022
35739108	Live attenuated pertussis vaccine for prevention and treatment of allergic airway inflammation in mice.	npj Vaccines	2022
35719839	Association of DNA methylation and genetic variations of the gene with the risk of diabetic dyslipidemia.	Biomedical Reports	2022
31293826	Estrogen receptor 1 gene polymorphisms (PvuII and XbaI) are associated with type 2 diabetes in Palestinian women.	PeerJ	2019
29728363	Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes.		2018
30170548	Common FTO rs9939609 variant and risk of type 2 diabetes in Palestine.	BMC Medical Genetics	2018
30581436	Non-specific Effects of Live Attenuated Pertussis Vaccine Against Heterologous Infectious and Inflammatory Diseases.	Frontiers in Immunology	2018
28566273	An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.	Diabetes	2017
27911795	KLB is associated with alcohol drinking, and its gene product Î²-Klotho is necessary for FGF21 regulation of alcohol preference.	Proc Natl Acad Sci U S A	2016
25182131	Fine-scale human genetic structure in Western France.	European Journal of Human Genetics	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25882144	A rare case of a scuba diver's death due to propeller injuries of a desalination pump.		2015
25673413	Genetic studies of body mass index yield new insights for obesity biology.	Nature	2015
26095709	Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study.	Lancet Diabetes Endocrinol	2015
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
25224167	Weight loss independent association of TCF7 L2 gene polymorphism with fasting blood glucose after Roux-en-Y gastric bypass in type 2 diabetic patients.		2014
25282103	Defining the role of common variation in the genomic and biological architecture of adult human height.	Nat Genet	2014
24318358	Coffee and tea consumption, genotype-based CYP1A2 and NAT2 activity and colorectal cancer risk-results from the EPIC cohort study.	Int J Cancer	2014
24296717	Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity.	Diabetes	2014
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
23160641	Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.	Diabetologia	2013
24040077	Meal frequencies modify the effect of common genetic variants on body mass index in adolescents of the northern Finland birth cohort 1986.	PLoS ONE	2013
23942764	Parental history of type 2 diabetes, TCF7L2 variant and lower insulin secretion are associated with incident hypertension. Data from the DESIR and RISC cohorts.	Diabetologia	2013
23852171	Association between large detectable clonal mosaicism and type 2 diabetes with vascular complications.	Nature Genetics	2013
23508304	Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels.	Diabetologia	2013
22210315	Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk.	Diabetes	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22693455	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.	PLoS Genet	2012
22923658	Response to comment on: Marquez et al. Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes 2012;61:524-530.		2012
22885922	Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.	Nat Genet	2012
22685556	The interplay of variants near LEKR and CCNL1 and social stress in relation to birth size.	PLoS ONE	2012
22463974	European genetic variants associated with type 2 diabetes in North African Arabs.		2012
22238593	A genome-wide association search for type 2 diabetes genes in African Americans.	PLoS One	2012
21760635	Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesity.		2012
22069379	Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.	PLoS Med	2011
21798992	Characterization of the human SLC30A8 promoter and intronic enhancer.	Journal of Molecular Endocrinology	2011
21911746	Effects of genetic susceptibility for type 2 diabetes on the evolution of glucose homeostasis traits before and after diabetes diagnosis: data from the D.E.S.I.R. Study.		2011
20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Nat Genet	2010
19286335	TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia.		2010
20818381	A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.	Nat Genet	2010
20138556	Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets.	Molecular Genetics and Metabolism	2010
20032493	TCF7L2 rs7903146-macronutrient interaction in obese individuals' responses to a 10-wk randomized hypoenergetic diet.	Am J Clin Nutr	2010
19885641	Association of a common variant in TCF7L2 gene with type 2 diabetes mellitus in the Palestinian population.	Acta Diabetologica	2010
20030815	PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women.	BMC Medical Genetics	2009
19368707	Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study.	BMC Medical Genetics	2009
19734900	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.	Nat Genet	2009
19255736	Combined effects of MC4R and FTO common genetic variants on obesity in European general populations.	Journal of Molecular Medicine	2009
19153581	Common genetic variation near MC4R is associated with eating behaviour patterns in European populations.	International Journal of Obesity	2009
19377085	The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects.	Hum Mol Genet	2009
19060909	A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.	Nature Genetics	2009