Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation
2019 · Stem Cell Reports · 47 citations
https://doi.org/10.1016/j.stemcr.2019.11.003
M
Miriam S. Reuter
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Miriam S. Reuter is an academic researcher from University of Toronto. The author has contributed to research in topics: Genomics and Rare Diseases & Genetics and Neurodevelopmental Disorders & Genomic variations and chromosomal abnormalities. The author has an h-index of 27, co-authored 67 publications.
ORCID: 0000-0001-8662-6685Papers by this author
worksAssessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
2021 · JAMA Network Open · 45 citations
https://doi.org/10.1001/jamanetworkopen.2021.10446
Return of genetic and genomic research findings: experience of a pediatric biorepository
2019 · BMC Medical Genomics · 36 citations
https://doi.org/10.1186/s12920-019-0618-0
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
2022 · Nature Communications · 27 citations
https://doi.org/10.1038/s41467-022-34112-z
Genome sequencing in families with congenital limb malformations
2021 · Human Genetics · 25 citations
https://doi.org/10.1007/s00439-021-02295-y
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder
2021 · npj Genomic Medicine · 22 citations
https://doi.org/10.1038/s41525-021-00254-0
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