Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly
2018 · Human Genome Variation · 51 citations
https://doi.org/10.1038/s41439-018-0005-y
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Noriko Aida
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Noriko Aida is an academic researcher from Kanagawa Children's Medical Center. The author has contributed to research in topics: Advanced MRI Techniques and Applications & Fetal and Pediatric Neurological Disorders & RNA regulation and disease. The author has an h-index of 32, co-authored 165 publications.
ORCID: 0000-0002-2776-2115Papers by this author
worksA novel UBE2A mutation causes X-linked intellectual disability type Nascimento
2017 · Human Genome Variation · 30 citations
https://doi.org/10.1038/hgv.2017.19
White matter microstructural changes in tuberous sclerosis: Evaluation by neurite orientation dispersion and density imaging (NODDI) and diffusion tensor images
2020 · Scientific Reports · 24 citations
https://doi.org/10.1038/s41598-019-57306-w
Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8
2013 · Brain and Development · 16 citations
https://doi.org/10.1016/j.braindev.2013.08.004
Treatment outcomes and late toxicities in patients with embryonal central nervous system tumors
2014 · Radiation Oncology · 13 citations
https://doi.org/10.1186/1748-717x-9-201
Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates
2021 · Pediatric Research · 9 citations
https://doi.org/10.1038/s41390-021-01398-6
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