Cargando…

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders

BACKGROUND: The search for genetic factors underlying autism spectrum disorders (ASD) has led to the identification of hundreds of genes containing thousands of variants that differ in mode of inheritance, effect size, frequency, and function. A major challenge involves assessing the collective evid...

Descripción completa

Detalles Bibliográficos
Autores principales:	Larsen, Eric, Menashe, Idan, Ziats, Mark N., Pereanu, Wayne, Packer, Alan, Banerjee-Basu, Sharmila
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075177/ https://www.ncbi.nlm.nih.gov/pubmed/27790361 http://dx.doi.org/10.1186/s13229-016-0103-y

Ejemplares similares

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB–An Integrative Multi-Study Genetic Database
por: Menashe, Idan, et al.
Publicado: (2013)

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
por: Abrahams, Brett S, et al.
Publicado: (2013)

Co-expression Profiling of Autism Genes in the Mouse Brain
por: Menashe, Idan, et al.
Publicado: (2013)

AutDB: a platform to decode the genetic architecture of autism
por: Pereanu, Wayne, et al.
Publicado: (2018)

The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder
por: Ziats, Mark N., et al.
Publicado: (2016)

A Brain Region-Specific Predictive Gene Map for Autism Derived by Profiling a Reference Gene Set
por: Kumar, Ajay, et al.
Publicado: (2011)

Association between ultrasonography foetal anomalies and autism spectrum disorder
por: Regev, Ohad, et al.
Publicado: (2022)

A Non-inflammatory Role for Microglia in Autism Spectrum Disorders
por: Edmonson, Catherine A., et al.
Publicado: (2016)

Comorbidity and health services' usage in children with autism spectrum disorder: a nested case–control study
por: Dizitzer, Yotam, et al.
Publicado: (2020)

Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
por: Ziats, Mark N, et al.
Publicado: (2013)

Functional genomics of human brain development and implications for autism spectrum disorders
por: Ziats, M N, et al.
Publicado: (2015)

Atypical Social Rank Recognition in Autism Spectrum Disorder
por: Ogawa, Shino, et al.
Publicado: (2019)

Association Between Antenatal Antimicrobial Therapy and Autism Spectrum Disorder—A Nested Case-Control Study
por: Abelson, Nitzan, et al.
Publicado: (2021)

Adherence to treatment and parents’ perspective about effectiveness of melatonin in children with autism spectrum disorder and sleep disturbances
por: Sadeh, Hadar, et al.
Publicado: (2023)

Sleep Disturbances and Sensory Sensitivities Co-Vary in a Longitudinal Manner in Pre-School Children with Autism Spectrum Disorders
por: Manelis-Baram, Liora, et al.
Publicado: (2021)

A Low Rank Model for Phenotype Imputation in Autism Spectrum Disorder
por: Paskov, Kelley M., et al.
Publicado: (2018)

Exploring the familial role of social responsiveness differences between savant and non-savant children with autism
por: Daniel, Edan, et al.
Publicado: (2020)

Cell-type-specific neuroanatomy of cliques of autism-related genes in the mouse brain
por: Grange, Pascal, et al.
Publicado: (2015)

Association of clock gene variants with Autism Spectrum Disorder in South Indian population
por: Alex, Ann Mary, et al.
Publicado: (2014)

The Contribution of Mosaic Variants to Autism Spectrum Disorder
por: Freed, Donald, et al.
Publicado: (2016)

Association between abnormal fetal head growth and autism spectrum disorder
por: Regev, O., et al.
Publicado: (2021)

Genetic Elucidation of Ultrasonography Fetal Anomalies in Children with Autism Spectrum Disorder
por: Regev, O., et al.
Publicado: (2023)

Ranking Biomedical Annotations with Annotator's Semantic Relevancy
por: Wu, Aihua
Publicado: (2014)

Multiple rare variants in the etiology of autism spectrum disorders
por: Buxbaum, Joseph D.
Publicado: (2009)

AutDB: a gene reference resource for autism research
por: Basu, Saumyendra N., et al.
Publicado: (2009)

Building a protein interaction (PIN) database for autism candidate genes
por: Swanwick, Catherine Croft, et al.
Publicado: (2011)

A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder
por: Loureiro, Livia O., et al.
Publicado: (2021)

An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
por: Veatch, Olivia J., et al.
Publicado: (2020)

A multifaceted approach for analyzing complex phenotypic data in rodent models of autism
por: Das, Ishita, et al.
Publicado: (2019)

Autism spectrum disorders
por: Faras, Hadeel, et al.
Publicado: (2010)

Autism Spectrum Disorders
por: Fitzgerald, Kara, et al.
Publicado: (2012)

Birth related parameters are important contributors in autism spectrum disorders
por: Banerjee, Nilanjana, et al.
Publicado: (2022)

Association testing of copy number variants in schizophrenia and autism spectrum disorders
por: Crespi, Bernard J, et al.
Publicado: (2012)

WWP1 germline variants are associated with normocephalic autism spectrum disorder
por: Novelli, Giuseppe, et al.
Publicado: (2020)

Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility
por: Viggiano, Marta, et al.
Publicado: (2022)

Common microRNAs Target Established ASD Genes
por: Banerjee-Basu, Sharmila, et al.
Publicado: (2014)

Similarity hypothesis: understanding of others with autism spectrum disorders by individuals with autism spectrum disorders
por: Komeda, Hidetsugu
Publicado: (2015)

Autism Spectrum Disorder Versus Autism Spectrum Disorders: Terminology, Concepts, and Clinical Practice
por: Oberman, Lindsay M., et al.
Publicado: (2020)

In Search of Biomarkers for Autism Spectrum Disorder
por: Del Valle Rubido, Marta, et al.
Publicado: (2018)

Genomics of autism spectrum disorder: approach to therapy
por: Ayhan, Fatma, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_dl2vkrs3p53as7997kn4ls0iit