Concepedia

Author

Marion Marchand

Centre National de la Recherche Scientifique

Also Known As

M Marchand, M. Marchand, M.-S. Marchand, Marion Marchand, T Zenone

14

Publications

1.2K

Citations

9

H-Index

27

Concepts

All Affiliations

Centre National de la Recherche ScientifiqueInsermImperial College LondonInstitut Pasteur de LilleUniversité Paris Cité
MM

About

Marion Marchand is an author at Centre National de la Recherche Scientifique specializing in medicine, genetics, and metabolic syndrome.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

697

2

Diabetes

2

2

679

3

Natural Sciences

1

1

72

4

Cell Biology

1

1

72

5

Cellular Physiology

1

1

72

Marion Marchand

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7

Publications

1.1K

Citations

7

H-Index

YearCitations

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

Nabila Bouatia‐Naji, Amélie Bonnefond, Christine Cavalcanti-Proença,

Nature Genetics

2008

607

A Polymorphism Within the <i>G6PC2</i> Gene Is Associated with Fasting Plasma Glucose Levels

Nabila Bouatia‐Naji, Ghislain Rocheleau, Leentje Van Lommel,

Science

2008

241

G-allele of Intronic rs10830963 in<i>MTNR1B</i>Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release

Thomas Sparsø, Amélie Bonnefond, Ehm A. Andersson,

Diabetes

2009

142

TCF7L2 splice variants have distinct effects on β-cell turnover and function

Olivier Le Bacquer, Luan Shu, Marion Marchand,

Human Molecular Genetics

2011

72

Genetic and Functional Assessment of the Role of the rs13431652-A and rs573225-A Alleles in the <i>G6PC2</i> Promoter That Are Strongly Associated With Elevated Fasting Glucose Levels

Nabila Bouatia‐Naji, Amélie Bonnefond, Devin A. Baerenwald,

Diabetes

2010

38

Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delay

Meena Balasubramanian, Julian Hamilton‐Shield, Carlo L. Acerini,

American Journal of Medical Genetics Part A

2010

22

Loss‐of‐Function Mutations in MC4R Are Very Rare in the Greek Severely Obese Adult Population

Konstantinos Rouskas, Fanny Stutzmann, Konstantinos Paletas,

Obesity

2012

18

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