Nelle Lambert

Brussels, BRU 1070, Belgium

Last Updated: 09/26/2026

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Found 8 publications

Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother.

Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother.

Journal: Journal of human genetics
Published: January 12, 2018

Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation.

Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation.

Journal: Cell
Published: November 13, 2017

A familial heterozygous null mutation of MET in autism spectrum disorder.

A familial heterozygous null mutation of MET in autism spectrum disorder.

Journal: Autism research : official journal of the International Society for Autism Research
Published: December 17, 2013

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.

Journal: Journal of medical genetics
Published: July 02, 2013

tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.

tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.

Journal: PLoS genetics
Published: May 14, 2013

Pyramidal neurons derived from human pluripotent stem cells integrate efficiently into mouse brain circuits in vivo.

Pyramidal neurons derived from human pluripotent stem cells integrate efficiently into mouse brain circuits in vivo.

Journal: Neuron
Published: December 03, 2012

Kinetochore KMN network gene CASC5 mutated in primary microcephaly.

Kinetochore KMN network gene CASC5 mutated in primary microcephaly.

Journal: Human molecular genetics
Published: September 18, 2012

Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturation.

Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturation.

Journal: Cell
Published: December 12, 2011
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Last Updated: 09/26/2026