Hirotomo Saitsu

Also affiliated with Hamamatsu University, Hamamatsu University School of Medicine

Biochemistry, Genetics and Molecular BiologyMedicine

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 6 papers. Top paper: “Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant”.

Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant

Journal of Human Genetics(2021)10.1038/s10038-021-00948-4

N/A

0.396DataRank · unranked

13 citations

Taihei Tanaka, Yohei Masunaga, Yumiko Ohkubo, Mitsuko Nakashima, Tokiko Fukuda +3 more

Faculty Opinions recommendation of Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature(2020)10.3410/f.737001613.793572920

N/A

0DataRank · unranked

0 citations

Hirotomo Saitsu

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

Human Genetics(2021)10.1007/s00439-021-02283-2

N/A

0DataRank · unranked

36 citations

Daphné Lehalle, Caroline Nava, Erin Torti, Elsa Leitão, Richard Person +40 more

Faculty Opinions recommendation of Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature(2021)10.3410/f.738775288.793582393

N/A

0DataRank · unranked

0 citations

Hirotomo Saitsu

Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome

EMBO Molecular Medicine(2024)10.1038/s44321-024-00178-z

N/A

0DataRank · unranked

1 citations

Peggy Tilly, Stephan C. Collins, José Rivera Alvarez, Meghna Kannan, Lucile Tonneau +26 more

Japanese siblings with neuronal ceroid lipofuscinosis type 7 showing different initial symptoms due to biallelic MFSD8 variants: A case report

Brain and Development Case Reports(2025)10.1016/j.bdcasr.2025.100114

N/A

0DataRank · unranked

0 citations

Noriko Nishikura, Takao Morimune, Hiroki Sobajima, Yoshihiro Maruo, Mitsuko Nakashima +4 more