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Cited by in F6Publishing
For: Watanabe K, Nakashima M, Kumada S, Mashimo H, Enokizono M, Yamada K, Kato M, Saitsu H. Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review. J Hum Genet 2021. [PMID: 34211110 DOI: 10.1038/s10038-021-00956-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Shah YB, Lin P, Chen S, Zheng A, Alcaraz W, Towne MC, Gabriel C, Bhoj EJ, Lambert MP, Olson TS, Frank DM, Ellis CA, Babushok DV. Inherited bone marrow failure with macrothrombocytopenia due to germline tubulin beta class I (TUBB) variant. Br J Haematol 2023;200:222-8. [PMID: 36207145 DOI: 10.1111/bjh.18491] [Reference Citation Analysis]
2 Hiraide T, Akita T, Uematsu K, Miyamoto S, Nakashima M, Sasaki M, Fukuda A, Kato M, Saitsu H. A novel de novo KCNB1 variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome. J Hum Genet 2023;68:25-31. [PMID: 36257979 DOI: 10.1038/s10038-022-01090-5] [Reference Citation Analysis]
3 Nakashima M, Argilli E, Nakano S, Sherr EH, Kato M, Saitsu H. De novo CLCN3 variants affecting Gly327 cause severe neurodevelopmental syndrome with brain structural abnormalities. J Hum Genet 2022. [PMID: 36536096 DOI: 10.1038/s10038-022-01106-0] [Reference Citation Analysis]
4 Miyamoto S, Nakashima M, Fukumura S, Kumada S, Saitsu H. An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulation. Neurogenetics 2022;23:129-35. [PMID: 35147852 DOI: 10.1007/s10048-022-00686-5] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]