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International Journal of Molecular Sciences
|
August 1, 2017
Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder
Jessie M Cameron, Valeriy Levandovskiy, Wendy Roberts, et al.
Human Mutation
|
January 15, 2013
HGV2012: leveraging next-generation technology and large datasets to advance disease research
Nina Gonzaludo, Hong-Xiang Zheng, Jiucun Wang, et al.
Human Molecular Genetics
|
November 28, 2022
ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome
Zain Awamleh, Sanaa Choufani, Cheryl Cytrynbaum, et al.
Clinical Case Reports
|
August 28, 2018
An <i>ANKRD26</i> nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
K M Furkan Uddin, Robed Amin, Sabbiha Nadia Majumder, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Seminars in Pediatric Neurology
|
May 18, 2011
The NeuroDevNet Autism Spectrum Disorders Demonstration Project
Lonnie Zwaigenbaum, Stephen Scherer, Peter Szatmari, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
November 8, 2019
Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort
Eduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, et al.
Research Square
|
December 8, 2025
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, et al.
Research Square
|
January 18, 2024
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications
Ruben Gur, Carrie Bearden, Sébastien Jacquemont, et al.
Cancer Research
|
March 17, 2019
Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma
Mary Hoffman, Aaron H Gillmor, Daniel J Kunz, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
International Journal of Molecular Sciences
|
August 1, 2017
Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder
Jessie M Cameron, Valeriy Levandovskiy, Wendy Roberts, et al.
Human Mutation
|
January 15, 2013
HGV2012: leveraging next-generation technology and large datasets to advance disease research
Nina Gonzaludo, Hong-Xiang Zheng, Jiucun Wang, et al.
Human Molecular Genetics
|
November 28, 2022
ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome
Zain Awamleh, Sanaa Choufani, Cheryl Cytrynbaum, et al.
Clinical Case Reports
|
August 28, 2018
An <i>ANKRD26</i> nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
K M Furkan Uddin, Robed Amin, Sabbiha Nadia Majumder, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Seminars in Pediatric Neurology
|
May 18, 2011
The NeuroDevNet Autism Spectrum Disorders Demonstration Project
Lonnie Zwaigenbaum, Stephen Scherer, Peter Szatmari, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
November 8, 2019
Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort
Eduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, et al.
Research Square
|
December 8, 2025
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, et al.
Research Square
|
January 18, 2024
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications
Ruben Gur, Carrie Bearden, Sébastien Jacquemont, et al.
Cancer Research
|
March 17, 2019
Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma
Mary Hoffman, Aaron H Gillmor, Daniel J Kunz, et al.
Page
of 2