Mylène Béri‐Dexheimer

Author

Centre Hospitalier Régional et Universitaire de Nancy

Also Known As

Beri-Dexheimer, Mylène, Frdric Huet, M Béri-Dexheimer, M. Béri-Dexheimer, Mylène Beri-Dexheimer, Mylène Beri‐Dexheimer, Mylène Béri-Dexheimer, Mylène Béri‐Dexheimer, Myléne Beri-Dexheimer

Publications

Citations

H-Index

Concepts

All Affiliations

Centre Hospitalier Régional et Universitaire de Nancy Inserm Hôpital Necker-Enfants Malades Université de Lorraine Hospices Civils de Lyon

About

Mylène Béri‐Dexheimer is an author at Centre Hospitalier Régional et Universitaire de Nancy specializing in molecular genetics, medicine, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	648
2	Molecular Genetics	2	2	648
3	Pathology	1	1	94
4	Clinical Genetics	1	1	94
5	Developmental Biology	1	1	554

Mylène Béri‐Dexheimer

Publications

982

Citations

H-Index

Page 1

	Year	Citations
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 Robin Walters, Sébastien Jacquemont, Armand Valsesia, Nature ObesityMetabolic SyndromeChildhood ObesityDevelopmental BiologyMetabolic Disorder	2010	554
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech Céline Bonnet, Joris Andrieux, Mylène Béri‐Dexheimer, Journal of Medical Genetics	2010	107
Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions Mylène Béri‐Dexheimer, Véronique Latger‐Cannard, Christophe Philippe, European Journal of Human Genetics Allelic VariantPoint MutationsGenetic DisorderGeneticsGermline Runx1 Haploinsufficiency	2008	94
Further delineation of the <i>MECP2</i> duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features Marguerite Miguet, Laurence Faivre, Jeanne Amiel, Journal of Medical Genetics	2018	61
Gene–gene interactions of IL13 and IL4RA variants in immediate allergic reactions to betalactam antibiotics Rosa‐Maria Guéant‐Rodriguez, Antonino Romano, Mylène Béri‐Dexheimer, Pharmacogenetics and Genomics	2006	52
Intragenic <i>CAMTA1</i> rearrangements cause non-progressive congenital ataxia with or without intellectual disability Julien Thévenon, Estelle Lopez, Boris Keren, Journal of Medical Genetics	2012	45
Cobalamin Potentiates Vinblastine Cytotoxicity Through Downregulation of mdr-1 Gene Expression in HepG2 Cells Véronique Marguerite, Mylène Béri‐Dexheimer, Sandrine Ortiou, Cellular Physiology and Biochemistry	2007	26
Retracted: Exploring the potential role of disease-causing mutation in a gene desert: Duplication of noncoding elements 5′ of <i>GRIA3</i> is associated with <i>GRIA3</i> silencing and X-linked intellectual disability Céline Bonnet, Alice Masurel‐Paulet, Asma Ali Khan, Human Mutation	2011	15
De novo complex X chromosome rearrangement unmasking maternally inherited <i>CSF2RA</i> deletion in a girl with pulmonary alveolar proteinosis Julie Auger, Céline Bonnet, Mylène Valduga, American Journal of Medical Genetics Part A	2013	15
Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability Claire Bénéteau, Emilie Landais, Martine Doco‐Fenzy, Journal of Medical Genetics	2011	13

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