Author

N. Matsumoto

CHU Dijon Bourgogne

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Organism:rat· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Kuechler· 1 shared A. Petersen· 1 shared A. Vaknin-Dembinsky· 1 shared A. Waheeb· 1 shared Adam JacksoniD· 1 shared Alexander J.M. DingemansiD· 1 shared Alexander P.A. StegmanniD· 1 shared Alexandre ReymondiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A. Kuechler

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Fetal Kidney Transplantation for In Utero Fetuses

K. Morimoto, S. Yamanaka, K. Matsui, Y. Kinoshita, Y. Inage, S. Yamamoto, N. Koda, N. Matsumoto, Y. Saito, T. Takamura, T. Fujimoto, S. Fukunaga, S. Tajiri, K. Matsumoto, K. Ozawa, , T. Yokoo

This paper describes a novel fetal therapy approach using transplanted fetal kidneys from different species to provide a bridge to dialysis in affected fetuses, demonstrating successful urine production and long-term function without immunosuppressants.

bioRxiv · Apr 15, 2024 · PreprintBioengineering

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin, Alexander J.M. Dingemans, Nicolas Guex, Laurens Wiel, Christoffer Nellåker, Shivarajan Manickavasagam Amudhavalli, Siddarth Banka, Frederique Sloan Bena, Bruria Ben‐Zeev, Vincent Robert Bonagura, Ange‐Line Bruel, Theresa Brunet, Han G. Brunner, , Lisenka E.L.M. Vissers

The paper identifies mutation-specific pathophysiological mechanisms in SATB1 variants causing distinct neurodevelopmental disorders.

The American Journal of Human Genetics · Jan 28, 2021Peer-reviewedGenetics