Research graph
References from Optical genome mapping reveals novel structural variations in an autism spectrum disorder cohort. Local targets link to admitted publications; unresolved targets remain external evidence.
Autism spectrum disorder
10.1038/s41572-019-0138-4 · 2020 · External reference
Autism and Asperger syndrome: coexistence with other clinical disorders
10.1034/j.1600-0447.2000.102005321.x · 2000 · External reference
Unresolved reference
External reference
Global prevalence of autism: a systematic review update
10.1002/aur.2696 · 2022 · External reference
Unresolved reference
External reference
Autism spectrum disorder: a review
10.1001/jama.2022.23661 · 2023 · External reference
Epidemiological study of autism spectrum disorder in China
10.1177/0883073807308702 · 2008 · External reference
Unresolved reference
External reference
10.1016/j.cca.2019.12.009
10.1016/j.cca.2019.12.009 · External reference
10.1016/s0140-6736(18)31129-2
10.1016/s0140-6736(18)31129-2 · External reference
Where is the evidence? A narrative literature review of the treatment modalities for autism spectrum disorders
2019 · External reference
10.1542/peds.2010-2825
10.1542/peds.2010-2825 · External reference
Heritability of autism spectrum disorders: a meta-analysis of twin studies
10.1111/jcpp.12499 · 2016 · External reference
10.1016/s1474-4422(15)00044-7
10.1016/s1474-4422(15)00044-7 · External reference
Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses
10.1038/s41398-022-02009-6 · 2022 · External reference
10.1038/ng.3303
10.1038/ng.3303 · External reference
10.1016/j.ajhg.2016.02.018
10.1016/j.ajhg.2016.02.018 · External reference
A global reference for human genetic variation
10.1038/nature15393 · 2015 · External reference
10.1038/nature15394
10.1038/nature15394 · External reference
10.1038/ng.3834
10.1038/ng.3834 · External reference
10.1016/j.tig.2008.03.001
10.1016/j.tig.2008.03.001 · External reference
10.1038/s41586-020-2287-8
10.1038/s41586-020-2287-8 · External reference
10.3390/ijms241713248
10.3390/ijms241713248 · External reference
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan
10.1038/s41598-017-12081-4 · 2017 · External reference
10.1016/j.neuron.2015.09.016
10.1016/j.neuron.2015.09.016 · External reference
Structural variations identified in patients with autism spectrum disorder (ASD) in the Chinese population: a systematic review of case-control studies
10.3390/genes15081082 · 2024 · External reference
10.1038/s41576-018-0007-0
10.1038/s41576-018-0007-0 · External reference
Interpreting the impact of noncoding structural variation in neurodevelopmental disorders
10.1038/s41436-020-00974-1 · 2021 · External reference
10.1126/science.aan2261
10.1126/science.aan2261 · External reference
10.1038/ng.3039
10.1038/ng.3039 · External reference
10.1038/nrg2958
10.1038/nrg2958 · External reference
10.1152/physiolgenomics.00082.2012
10.1152/physiolgenomics.00082.2012 · External reference
A cytogeneticist’s perspective on genomic microarrays
10.1093/humupd/dmh022 · 2004 · External reference
Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing
10.1186/s13059-019-1720-5 · 2019 · External reference
A practical guide for structural variation detection in the human genome
10.1002/cphg.103 · 2020 · External reference
Optical genome mapping in routine human genetic diagnostics-its advantages and limitations
10.3390/genes12121958 · 2021 · External reference
10.1016/j.ajhg.2021.05.012
10.1016/j.ajhg.2021.05.012 · External reference
10.1038/nrg.2016.49
10.1038/nrg.2016.49 · External reference
10.1016/j.csbj.2020.07.018 · Admitted local publication
Tools and pipelines for BioNano data: molecule assembly pipeline and FASTA super scaffolding tool
10.1186/s12864-015-1911-8 · 2015 · External reference
10.1093/bioinformatics/btab359
10.1093/bioinformatics/btab359 · External reference
10.1126/science.abf7117
10.1126/science.abf7117 · External reference
Unresolved reference
External reference
10.1093/bioinformatics/bty191
10.1093/bioinformatics/bty191 · External reference
10.1093/bioinformatics/btp352
10.1093/bioinformatics/btp352 · External reference
10.1093/bib/bbs017
10.1093/bib/bbs017 · External reference
10.1016/j.celrep.2020.107647
10.1016/j.celrep.2020.107647 · External reference
10.1016/j.semcdb.2018.08.004
10.1016/j.semcdb.2018.08.004 · External reference
10.1016/j.anpedi.2024.03.002
10.1016/j.anpedi.2024.03.002 · External reference
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
10.1016/j.ejmg.2022.104669 · 2023 · External reference
10.1016/j.ajhg.2024.01.013
10.1016/j.ajhg.2024.01.013 · External reference
C2H2-type zinc finger proteins in brain development, neurodevelopmental, and other neuropsychiatric disorders: systematic literature-based analysis
10.3389/fneur.2020.00032 · 2020 · External reference
10.1136/jmg-2023-109725
10.1136/jmg-2023-109725 · External reference
Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder
10.1038/jhg.2015.141 · 2016 · External reference
Exome sequencing of two siblings with sporadic autism spectrum disorder and severe speech sound disorder suggests pleiotropic and complex effects
10.1007/s10519-019-09957-8 · 2019 · External reference
10.1016/j.reprotox.2021.10.010
10.1016/j.reprotox.2021.10.010 · External reference
