Amélie Piton - Concepedia

Author

Amélie Piton

Also Known As

A Piton, A. Piton, Ame'lie Piton, Amelie M. Piton, Amelie Piton, Amlie Piton, Amélie Piton, Bénédicte Gerard, Carlos Marino, Christophe Philippe

162

Publications

Citations

H-Index

105

Concepts

All Affiliations

Inserm Hôpitaux Universitaires de Strasbourg Centre National de la Recherche Scientifique Institut de génétique et de biologie moléculaire et cellulaire Université de Strasbourg

About

Amélie Piton is an author at Inserm specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	49	4.2K
2	Social Sciences	14	14	1.3K
3	Engineering	3	3	296
4	Public Health	3	3	235
5	Natural Sciences	2	2	139

Amélie Piton

Publications

Citations

H-Index

Page 1

	Year	Citations
EXPRESSION OF CYTOCHROMES P450, CONJUGATING ENZYMES AND NUCLEAR RECEPTORS IN HUMAN HEPATOMA HepaRG CELLS Caroline Aninat, Amélie Piton, Denise Glaise, Drug Metabolism and Disposition	2005	669
AnnotSV: an integrated tool for structural variations annotation Véronique Geoffroy, Yvan Herenger, Arnaud Kress, Bioinformatics	2018	475
Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability Fadi F. Hamdan, Julie Gauthier, Yoichi Araki, The American Journal of Human Genetics Genes AssociatedGenetic DisorderGeneticsPsychiatric GeneticsNonsyndromic Intellectual Disability	2011	348
Novel de novo SHANK3 mutation in autistic patients Julie Gauthier, Dan Spiegelman, Amélie Piton, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2008	320
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia Amélie Piton, J Gauthier, Fadi F. Hamdan, Molecular Psychiatry Systematic ResequencingX-chromosome Synaptic GenesGenetic DisorderGeneticsPsychiatric Genetics	2010	315
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing Claire Redin, Bénédicte Gérard, Julia Lauer, Journal of Medical Genetics	2014	270
XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing Amélie Piton, Claire Redin, Jean‐Louis Mandel The American Journal of Human Genetics EngineeringMedicineGeneticsNext-generation SequencingXlid-causing Mutations	2013	251
Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts Philip Awadalla, Julie Gauthier, Rachel A. Myers, The American Journal of Human Genetics PsychiatrySyndromic AutismGeneticsPsychiatric GeneticsGenetic Epidemiology	2010	248
De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, The American Journal of Human Genetics Neurodevelopmental DisordersGenetic DisorderGeneticsFragile X SpectrumLanguage Impairment	2010	233
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function Anna Fassio, Lysanne Patry, Sonia Congia, Human Molecular Genetics	2011	233

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