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Hilde Peeters

Showing results (81-90 of 99) with videos related to

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BMC Neuroscience|September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neuronsSahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Nature Genetics|December 8, 2020
Insights into the genetic architecture of the human faceJulie D White, Karlijne Indencleef, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotypeLeonie A Menke, Martine J van Belzen, Marielle Alders, et al.
Human Molecular Genetics|February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesityNina De Rocker, Sarah Vergult, David Koolen, et al.
Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.
Nature Neuroscience|June 20, 2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsMadeleine R Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Molecular Psychiatry|June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autismBin Yu, Shimeng Zhu, Linhu Xiao, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
BMC Neuroscience|September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neuronsSahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Nature Genetics|December 8, 2020
Insights into the genetic architecture of the human faceJulie D White, Karlijne Indencleef, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotypeLeonie A Menke, Martine J van Belzen, Marielle Alders, et al.
Human Molecular Genetics|February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesityNina De Rocker, Sarah Vergult, David Koolen, et al.
Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.
Nature Neuroscience|June 20, 2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsMadeleine R Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Molecular Psychiatry|June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autismBin Yu, Shimeng Zhu, Linhu Xiao, et al.
Pageof 10