Author

Noriko Miyake

Yokohama City UniversityORCID 0000-0003-0987-310XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Organism:Drosophila· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Naomichi MatsumotoiD· 3 shared A. James BarkovichiD· 1 shared Akira MurakamiiD· 1 shared Alban C. ZiegleriD· 1 shared Alexandra AfenjariD· 1 shared Allan Micheil InnesiD· 1 shared Amy Sarah Kimball· 1 shared Andrea PrunottoiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersGenetics

Naomichi MatsumotoORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

GeneticsNeuronPeer-reviewedMar 4, 2020

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang…·Elliott H. Sherr

This study identifies DDX3X mutations as causing neurodevelopmental disorders by disrupting RNA metabolism and neurogenesis during fetal cortical development.

213 citationstop 1%

humanmouse

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GenomicsNature CommunicationsPeer-reviewedJun 28, 2019

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Konstantinos Nikopoulos, Katarina Vizar Cisarova, Mathieu Quinodoz…·Carlo Rivolta

The paper identifies a common variant in the Japanese population that shows quasi-Mendelian inheritance patterns in rare retinal ciliopathy.

41 citations

humanwhole-exome sequencing

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GeneticsbioRxivPreprintSep 25, 2018

Identification of SMARCD1 as a syndromic intellectual disability gene that is required for memory and context-dependent regulation of neuronal genes in Drosophila

Kevin C.J. Nixon, Justine Rousseau, Max H. Stone…·DDD study

The paper identifies SMARCD1 mutations as a cause of intellectual disability and shows its role in regulating neuronal gene expression during development in Drosophila.

2 citations

Drosophilastatistical model

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