Valérie Serre - Concepedia

Author

Valérie Serre

Inserm ORCID

Also Known As

Erik Renström, Laurent Schibler, Serre, Valérie, V Serre, V. Serre, VALERIE SERRE, Valerie Serre, Valérie Serre

Publications

5.6K

Citations

H-Index

104

Concepts

All Affiliations

Inserm Université Paris Cité Hôpital Necker-Enfants Malades Centre National de la Recherche Scientifique Délégation Paris 5

About

Valérie Serre is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	35	3.8K
2	Natural Sciences	6	6	817
3	Health Sciences	3	3	184
4	Engineering	1	1	150
5	Public Health	1	1	59

Valérie Serre

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis Slaheddine Marrakchi, Philippe Guigue, Blair R. Renshaw, New England Journal of Medicine	2011	965
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion Alice Bourdon, Limor Minai, Valérie Serre, Nature Genetics Genome InstabilityMitochondrial FunctionP53-controlled Ribonucleotide ReductaseGeneticsNatural Sciences	2007	517
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Brain Motor Neuron DiseaseGeneticsMitochondrial MyopathyAlzheimer's DiseaseMitochondrial Origin	2014	490
CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures Julie Mollet, Agnès Delahodde, Valérie Serre, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceMendelian DisorderGenetic DisorderGenetics	2008	290
DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III Nathalie Dagoneau, Marie Goulet, David Geneviève, The American Journal of Human Genetics Genetic DisorderGeneticsShort Rib-polydactyly SyndromePathologyDegenerative Disease	2009	255
Twinkle helicase <i>(PEO1)</i> gene mutation causes mitochondrial DNA depletion Emmanuelle Sarzi, Steffi Goffart, Valérie Serre, Annals of Neurology	2007	172
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome Carine Le Goff, Clémentine Mahaut, Avinash Abhyankar, Nature Genetics Mad Homology 2Mendelian DisorderGenetic DisorderGeneticsMolecular Biology	2011	151
Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy Louise Galmiche, Valérie Serre, Marine Beinat, Human Mutation EngineeringMitochondrial BiogenesisMitochondrial FunctionGenetic DisorderExome Sequencing	2011	150
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy Isabelle Perrault, Sylvain Hanein, Xavier Zanlonghi, Nature Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderMedicine	2012	144
Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the<i>APOE</i>p.Leu167del Mutation Marie Marduel, Khadija Ouguerram, Valérie Serre, Human Mutation GeneticsApoe GenePathologyMolecular BiologyHyperlipidemia	2012	126

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