Aiko Iwata‐Otsubo

Also affiliated with University of Michigan, Michigan Medicine

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Epigenetic, genetic and maternal effects enable stable centromere inheritance”.

Epigenetic, genetic and maternal effects enable stable centromere inheritance

Nature Cell Biology(2022)10.1038/s41556-022-00897-w

N/A

0.500DataRank · unranked

27 citations

Aiko Iwata‐Otsubo, Aspasia Destouni, Jennine M. Dawicki-McKenna, Katelyn G. Boese, Ben E. Black +2 more

Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing

Journal of Molecular Diagnostics(2020)10.1016/j.jmoldx.2020.10.011

N/A

0DataRank · unranked

9 citations

Pınar Bayrak‐Toydemir, Ty C. Lynnes, Rong Mao, James D. Metcalf, Kasinathan Muralidharan +9 more

Analysis of CACTA transposase genes unveils the mechanism of intron loss and distinct small RNA silencing pathways underlying divergent evolution of Brassica genomes

The Plant Journal(2020)10.1111/tpj.15037

N/A

0DataRank · unranked

10 citations

Aiko Iwata‐Otsubo, Diya Yang, Robert L. Baker, Chun Liang, Scott A. Jackson +4 more

Dominant-negative variants in CBX1 cause a neurodevelopmental disorder

Genetics in Medicine(2023)10.1016/j.gim.2023.100861

N/A

0DataRank · unranked

7 citations

Aiko Iwata‐Otsubo, Kerith‐Rae Dias, Suzanna E.L. Temple, Koji Nagao, Lachlan De Hayr +28 more

Heterozygous loss-of-function SMC3 variants are associated with variable and incompletely penetrant growth and developmental features

medRxiv(2023)10.1101/2023.09.27.23294269

N/A

0DataRank · unranked

1 citations

Kamli N. W. Faour, Akiko Shimamura, Graeme R. Grimes, Emeline M. Kao, Erica R. Denhoff +50 more

Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100273

N/A

0DataRank · unranked

3 citations

Kamli N. W. Faour, Akiko Shimamura, Graeme R. Grimes, Emeline M. Kao, Erica R. Denhoff +51 more

BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.003

N/A

0DataRank · unranked

48 citations

Tahsin Stefan Barakat, Brittany C. Michel, Nazar Mashtalir, Jennifer B. Phillips, Alfredo M. Valencia +48 more

Biallelic variants in GTF3C5, a regulator of RNA polymerase III-mediated transcription, cause a multisystem developmental disorder

Human Genetics(2024)10.1007/s00439-024-02656-3

N/A

0DataRank · unranked

2 citations

Cara Skraban, Atsunori Yoshimura, Toyonori Sakata, Cesar Alves, Sarah K. Fiordaliso +16 more