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Statistical Applications in Genetics and Molecular Biology
|
May 1, 2018
Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios
Nele Cosemans, Peter Claes, Nathalie Brison, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
November 3, 2016
Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?
Lien Van Eylen, Bart Boets, Nele Cosemans, et al.
Neurogenetics
|
March 8, 2021
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder
Nele Cosemans, Jarymke Maljaars, Annick Vogels, et al.
European Journal of Medical Genetics
|
February 11, 2018
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder
Nele Cosemans, Laura Vandenhove, Jarymke Maljaars, et al.
Prenatal Diagnosis
|
July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing
Molka Kammoun, Erika Souche, Paul Brady, et al.
Journal of Medical Genetics
|
January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletions
Nele Cosemans, Laura Vandenhove, Annick Vogels, et al.
Molecular Autism
|
January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cells
Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
Nature Genetics
|
February 14, 2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A F Stessman, Bo Xiong, Bradley P Coe, et al.
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Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Statistical Applications in Genetics and Molecular Biology
|
May 1, 2018
Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios
Nele Cosemans, Peter Claes, Nathalie Brison, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
November 3, 2016
Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?
Lien Van Eylen, Bart Boets, Nele Cosemans, et al.
Neurogenetics
|
March 8, 2021
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder
Nele Cosemans, Jarymke Maljaars, Annick Vogels, et al.
European Journal of Medical Genetics
|
February 11, 2018
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder
Nele Cosemans, Laura Vandenhove, Jarymke Maljaars, et al.
Prenatal Diagnosis
|
July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing
Molka Kammoun, Erika Souche, Paul Brady, et al.
Journal of Medical Genetics
|
January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletions
Nele Cosemans, Laura Vandenhove, Annick Vogels, et al.
Molecular Autism
|
January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cells
Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
Nature Genetics
|
February 14, 2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A F Stessman, Bo Xiong, Bradley P Coe, et al.
Page
of 1