Yohei Nitta

Title	Postdoc Fellows and Associates
Institution	Baylor College of Medicine
Department	PostDoc
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Bibliographic

selected publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

Komatsu K, Sugie A, Nitta Y, Osaka J, Mansoor Hussain UH, Kubota M, Shimozawa N, Carter MT, Zwijnenburg PJG, Waisfisz Q, Boschann F, Horn D, Nakashima M, Saitsu H. Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder. Eur J Hum Genet. 2026 Nov; 34(11):1718. PMID: 42728323.

Citations:
Ma M, Lei X, Li J, Zheng Y, Yuan Y, Nitta Y, Mao X, Guo Z, Lu S, Deng M, Pan X, Kanca O, Liu S, Wang H, Xiao B, Schot R, Demirdas S, van Bever Y, van Slegtenhorst M, Barakat TS, Bian S, Bellen HJ, Long L. Bi-allelic variants in the secretory pathway gene SEC16A are associated with a neurodevelopmental disorder. J Clin Invest. 2026 Oct 13. PMID: 42867917.

Citations:
Komatsu K, Sugie A, Nitta Y, Osaka J, Mansoor Hussain UH, Kubota M, Shimozawa N, Carter MT, Zwijnenburg PJG, Waisfisz Q, Boschann F, Horn D, Nakashima M, Saitsu H. Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder. Eur J Hum Genet. 2026 Aug; 34(8):1047-1058. PMID: 42337333; PMCID: PMC13424086.

Citations: 1 Fields:
Gen Genetics
Translation:Humans Animals
Chauvin SD, Ando S, Holley JA, Sugie A, Zhao FR, Poddar S, Kato R, Miner CA, Nitta Y, Krishnamurthy SR, Saito R, Ning Y, Hatano Y, Kitahara S, Koide S, Stinson WA, Fu J, Surve N, Kumble L, Qian W, Polishchuk O, Andhey PS, Chiang C, Liu G, Colombeau L, Rodriguez R, Manel N, Kakita A, Artyomov MN, Schultz DC, Coates PT, Roberson EDO, Belkaid Y, Greenberg RA, Cherry S, Gack MU, Hardy T, Onodera O, Kato T, Miner JJ. Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans. Nat Commun. 2024 06 01; 15(1):4696. PMID: 38824133; PMCID: PMC11144269.

Citations:
Iida T, Igarashi A, Fukunaga K, Aoki T, Hidai T, Yanagi K, Yamamori M, Satou K, Go H, Kosho T, Maki R, Suzuki T, Nitta Y, Sugie A, Asaoka Y, Furutani-Seiki M, Kimura T, Matsubara Y, Kaname T. Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype. Front Genet. 2024; 15:1383176. PMID: 38601074; PMCID: PMC11004488.

Citations:
Yamada M, Nitta Y, Uehara T, Suzuki H, Miya F, Takenouchi T, Tamura M, Ayabe S, Yoshiki A, Maeno A, Saga Y, Furuse T, Yamada I, Okamoto N, Kosaki K, Sugie A. Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences. Eur J Med Genet. 2023 Aug; 66(8):104804. PMID: 37369308.

Citations:
Nitta Y, Kawai H, Maki R, Osaka J, Hakeda-Suzuki S, Nagai Y, Doubkov? K, Uehara T, Watanabe K, Kosaki K, Suzuki T, Tavosanis G, Sugie A. Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA. Hum Mol Genet. 2023 04 20; 32(9):1524-1538. PMID: 36611008.

Citations:
Itai T, Sugie A, Nitta Y, Maki R, Suzuki T, Shinkai Y, Watanabe Y, Nakano Y, Ichikawa K, Okamoto N, Utsuno Y, Koshimizu E, Fujita A, Hamanaka K, Uchiyama Y, Tsuchida N, Miyake N, Misawa K, Mizuguchi T, Miyatake S, Matsumoto N. Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes. Sci Rep. 2023 Mar 09; 13(1):3954. PMID: 36894578; PMCID: PMC9998850.

Citations:
Itai T, Sugie A, Nitta Y, Maki R, Suzuki T, Shinkai Y, Watanabe Y, Nakano Y, Ichikawa K, Okamoto N, Utsuno Y, Koshimizu E, Fujita A, Hamanaka K, Uchiyama Y, Tsuchida N, Miyake N, Misawa K, Mizuguchi T, Miyatake S, Matsumoto N. A novel NONO variant that causes developmental delay and cardiac phenotypes. Sci Rep. 2023 01 18; 13(1):975. PMID: 36653413; PMCID: PMC9849200.

Citations:
Sakamoto M, Sasaki K, Sugie A, Nitta Y, Kimura T, G?rsoy S, Cinleti T, Iai M, Sengoku T, Ogata K, Suzuki A, Okamoto N, Iwama K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Miyatake S, Mizuguchi T, Taguri M, Ito S, Takahashi H, Miyake N, Matsumoto N. De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality. Hum Mol Genet. 2021 12 17; 31(1):69-81. PMID: 34346499.

Citations:

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