about
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersDe Novo Genome and Transcriptome Assembly of the Canadian Beaver (Castor canadensis)Hypermethylation of RASSF1A in human and rhesus placentas.Human placental-specific epipolymorphism and its association with adverse pregnancy outcomesDNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia.Extensive epigenetic reprogramming in human somatic tissues between fetus and adultGenome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies.Genome-wide DNA methylation identifies trophoblast invasion-related genes: Claudin-4 and Fucosyltransferase IV control mobility via altering matrix metalloproteinase activityPatterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation.Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia.Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum.The Database of Genomic Variants: a curated collection of structural variation in the human genome.Review: A high capacity of the human placenta for genetic and epigenetic variation: implications for assessing pregnancy outcome.PP065. dNK and dNK-CM mediated alterations of DNA methylation in extravillous cytotrophoblasts (EVTS).DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic Variants.Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015.Evaluating DNA methylation and gene expression variability in the human term placenta.Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.IFPA Meeting 2010 Workshop Report I: Immunology; ion transport; epigenetics; vascular reactivity; epitheliochorial placentation; proteomics.Development of a high-resolution Y-chromosome microarray for improved male infertility diagnosis.Are we ready for DNA methylation-based prenatal testing?The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersor human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networksLength of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington DiseaseGlutaminase Deficiency Caused by Short Tandem Repeat Expansion inExpanding the neurodevelopmental phenotypes of individuals with de novo variantsSynaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-ASA large data resource of genomic copy number variation across neurodevelopmental disordersPredictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disordersPathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain sizeA framework for an evidence-based gene list relevant to autism spectrum disorderSegregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Ryan Yuen
@ast
Ryan Yuen
@en
Ryan Yuen
@es
Ryan Yuen
@nl
Ryan Yuen
@sl
type
label
Ryan Yuen
@ast
Ryan Yuen
@en
Ryan Yuen
@es
Ryan Yuen
@nl
Ryan Yuen
@sl
prefLabel
Ryan Yuen
@ast
Ryan Yuen
@en
Ryan Yuen
@es
Ryan Yuen
@nl
Ryan Yuen
@sl
P1053
J-4876-2012
P106
P1153
16302333300
P21
P2798
P31
P3829
P496
0000-0001-7273-4968