Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
2017 · Nature Neuroscience · 910 citations
https://doi.org/10.1038/nn.4524
M
Melissa T. Carter
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
69
Papers
5.3K
Citations
28
h-index
45
i10-index
Melissa T. Carter is an academic researcher from University of Ottawa. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Genetics and Neurodevelopmental Disorders & Genomics and Rare Diseases. The author has an h-index of 28, co-authored 59 publications.
ORCID: 0000-0001-7211-3731Papers by this author
worksDetection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing
2013 · The American Journal of Human Genetics · 491 citations
https://doi.org/10.1016/j.ajhg.2013.06.012
A large data resource of genomic copy number variation across neurodevelopmental disorders
2019 · npj Genomic Medicine · 189 citations
https://doi.org/10.1038/s41525-019-0098-3
Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities
2019 · European Journal of Human Genetics · 30 citations
https://doi.org/10.1038/s41431-019-0487-1
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature
2023 · Journal of Medical Genetics · 13 citations
https://doi.org/10.1136/jmg-2023-109141
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage
2017 · npj Genomic Medicine · 3 citations
https://doi.org/10.1038/s41525-017-0031-6
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat