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Publications by Chan Yang
Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample
Journal of Molecular Neuroscience
Medicine
Molecular Neuroscience
Cellular
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An Autism Spectrum Disorder-Related De Novo Mutation Hotspot Discovered in the GEF1 Domain of Trio
Nature Communications
Astronomy
Genetics
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Biochemistry
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Whole Exome Sequencing in Extended Families With Autism Spectrum Disorder Implicates Four Candidate Genes
Human Genetics
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Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology
Psychiatry Investigation
Psychiatry
Mental Health
Biological Psychiatry
Exome Sequencing to Identify De Novo Mutations in Sporadic ALS Trios
Nature Neuroscience
Neuroscience
A De Novo Heterozygous Frameshift Mutation Identified in BCL11B Causes Neurodevelopmental Disorder by Whole Exome Sequencing
Molecular genetics & genomic medicine
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Using Dried Blood Spot Samples From a Trio for Linked-Read Whole-Exome Sequencing
European Journal of Human Genetics
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Identification of Novel EXT Mutations in Patients With Hereditary Multiple Exostoses Using Whole-Exome Sequencing
Orthopaedic surgery
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Orthopedics
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Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations
PLoS ONE
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Imprinting: The Achilles Heel of Trio-Based Exome Sequencing
Genetics in Medicine
Medicine
Genetics