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Nathalie Boddaert

Nathalie Boddaert,Assistance Publique Hôpitaux de Paris,Neuroscience,Pharmacology,Genetics & Genealogy

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Nathalie Boddaert

Assistance Publique Hôpitaux de Paris

Publications: 136 | Citations: 1413

Fields: Neuroscience, Pharmacology, Genetics & Genealogy

Collaborated with 543 co-authors from 2000 to 2011 | Cited by 5012 authors

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Publications (136)

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A FOXG1 mutation in a boy with congenital variant of Rett syndrome (Citations: 2)

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Journal: Neurogenetics , vol. 12, no. 1, pp. 1-8, 2011

Subtypes of Developmental Coordination Disorder: Research on Their Nature and Etiology

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Journal: Developmental Neuropsychology - DEVELOP NEUROPSYCHOL , vol. 36, no. 5, pp. 614-643, 2011

Épilepsie et maladies mitochondriales

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Journal: Archives De Pediatrie - ARCHIVES PEDIATRIE , vol. 18, no. 5, pp. H132-H133, 2011

Atypical teratoid rhabdoid tumor mimicking beta-catenin-positive nodular medulloblastoma

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Journal: Acta Neuropathologica - ACTA NEUROPATHOL , vol. 121, no. 3, pp. 429-430, 2011

Feature selection and classification of imbalanced datasets

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Journal: Neuroimage , vol. 57, no. 3, pp. 1003-1014, 2011

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Citations (1413 times by 1116 publications)

SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates (Citations: 2)

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Journal: Nature Immunology - NAT IMMUNOL , vol. 13, no. 3, pp. 223-228, 2012

Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans

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Journal: PLOS Biology - PLOS BIOL , vol. 10, no. 3, 2012

Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies

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Journal: Journal of Human Genetics - J HUM GENET , vol. 57, no. 1, pp. 70-72, 2012

ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation

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Journal: PLOS One , vol. 7, no. 1, 2012

Who's Missing the Point? A Commentary on Claims that Autistic Persons Have a Specific Deficit in Figurative Language Comprehension

Journal: Metaphor and Symbol - METAPHOR SYMB , vol. 27, no. 1, pp. 93-105, 2012

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Co-authors (543)

Conferences (1)

Journals (58)

Keywords (252)

Nathalie Boddaert,Assistance Publique Hôpitaux de Paris,Neuroscience,Pharmacology,Genetics & Genealogy

Publications (136)

BibTeX | RIS | RefWorks Download

A FOXG1 mutation in a boy with congenital variant of Rett syndrome (Citations: 2)

Subtypes of Developmental Coordination Disorder: Research on Their Nature and Etiology

Épilepsie et maladies mitochondriales

Atypical teratoid rhabdoid tumor mimicking beta-catenin-positive nodular medulloblastoma

Feature selection and classification of imbalanced datasets

Citations (1413 times by 1116 publications)

SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates (Citations: 2)

Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans

Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies

ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation

Who's Missing the Point? A Commentary on Claims that Autistic Persons Have a Specific Deficit in Figurative Language Comprehension


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Nathalie Boddaert,Assistance Publique Hôpitaux de Paris,Neuroscience,Pharmacology,Genetics & Genealogy

Publications (136) BibTeX | RIS | RefWorks Download

A FOXG1 mutation in a boy with congenital variant of Rett syndrome (Citations: 2)

SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates (Citations: 2)

Publications (136)

BibTeX | RIS | RefWorks Download