Harvard Catalyst Profiles

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Ayumi Nishiyama, Ph.D., M.D.


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.
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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.
  1. Suzuki N, Nishiyama A, Warita H, Aoki M. Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy. J Hum Genet. 2022 Jun 13. PMID: 35691950.
    Citations: 3     Fields:    
  2. Ueda S, Aoki H, Yasuda Y, Nishiyama A, Hayashi Y, Honaga K, Tanuma A, Takakura T, Kurosu A, Hatori K, Hayashi A, Fujiwara T. The MMT of Elbow Flexion and the AFE Predict Impairment and Disability at 3 Weeks in Patients With Acute Stroke. Front Neurol. 2022; 13:831800. PMID: 35432154; PMCID: PMC9005853.
  3. Mitsuzawa S, Suzuki N, Akiyama T, Ishikawa M, Sone T, Kawada J, Funayama R, Shirota M, Mitsuhashi H, Morimoto S, Ikeda K, Shijo T, Ohno A, Nakamura N, Ono H, Ono R, Osana S, Nakagawa T, Nishiyama A, Izumi R, Kaneda S, Ikeuchi Y, Nakayama K, Fujii T, Warita H, Okano H, Aoki M. Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations. Stem Cell Reports. 2021 06 08; 16(6):1527-1541. PMID: 34048688; PMCID: PMC8190591.
    Citations:    Fields:    Translation:HumansAnimalsCells
  4. Hisahara S, Nishiyama A, Tsuda E, Suzuki S, Matsumura A, Ishikawa A, Sakurai A, Motoike IN, Aoki M, Aoki Y, Shimohama S. Possible Somatic Mosaicism of Novel FUS Variant in Familial Amyotrophic Lateral Sclerosis. Neurol Genet. 2021 Feb; 7(1):e552. PMID: 33987464; PMCID: PMC8112850.
    Citations: 2     
  5. Shibuya K, Sawai S, Sugiyama A, Koide M, Nishiyama A, Aoki M, Kuwabara S. Facial onset amyotrophic lateral sclerosis with K3E variant in the Cu/Zn superoxide dismutase gene. Amyotroph Lateral Scler Frontotemporal Degener. 2021 02; 22(1-2):144-146. PMID: 32729725.
    Citations:    Fields:    Translation:Humans
  6. Leventoux N, Morimoto S, Hara K, Nakamura S, Ozawa F, Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Warita H, Aoki M, Okano H. Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation. Stem Cell Res. 2020 Jun 28; 47:101896. PMID: 32659732.
    Citations: 1     Fields:    
  7. Suzuki N, Nishiyama A, Kato M, Warita H, Aoki M. [Familial Amyotrophic Lateral Sclerosis]. Brain Nerve. 2019 Nov; 71(11):1169-1181. PMID: 31722303.
    Citations: 3     Fields:    Translation:HumansAnimalsCells
  8. Akiyama T, Suzuki N, Ishikawa M, Fujimori K, Sone T, Kawada J, Funayama R, Fujishima F, Mitsuzawa S, Ikeda K, Ono H, Shijo T, Osana S, Shirota M, Nakagawa T, Kitajima Y, Nishiyama A, Izumi R, Morimoto S, Okada Y, Kamei T, Nishida M, Nogami M, Kaneda S, Ikeuchi Y, Mitsuhashi H, Nakayama K, Fujii T, Warita H, Okano H, Aoki M. Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons. EBioMedicine. 2019 Jul; 45:362-378. PMID: 31262712; PMCID: PMC6642224.
    Citations: 21     Fields:    Translation:HumansAnimalsCells
  9. Takeda T, Iijima M, Shimizu Y, Yoshizawa H, Miyashiro M, Onizuka H, Yamamoto T, Nishiyama A, Suzuki N, Aoki M, Shibata N, Kitagawa K. p.N345K mutation in TARDBP in a patient with familial amyotrophic lateral sclerosis: An autopsy case. Neuropathology. 2019 Aug; 39(4):286-293. PMID: 31124595.
    Citations: 1     Fields:    Translation:HumansCells
  10. Shijo T, Warita H, Suzuki N, Ikeda K, Mitsuzawa S, Akiyama T, Ono H, Nishiyama A, Izumi R, Kitajima Y, Aoki M. Antagonizing bone morphogenetic protein 4 attenuates disease progression in a rat model of amyotrophic lateral sclerosis. Exp Neurol. 2018 09; 307:164-179. PMID: 29932880.
    Citations: 7     Fields:    Translation:HumansAnimals
  11. Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Kato M, Warita H, Izumi R, Osana S, Koyama S, Kato T, Suzuki Y, Aoki M. TARDBP p.G376D mutation, found in rapid progressive familial ALS, induces mislocalization of TDP-43. eNeurologicalSci. 2018 Jun; 11:20-22. PMID: 29928714; PMCID: PMC6006914.
    Citations: 5     
  12. Shijo T, Warita H, Suzuki N, Kitajima Y, Ikeda K, Akiyama T, Ono H, Mitsuzawa S, Nishiyama A, Izumi R, Aoki M. Aberrant astrocytic expression of chondroitin sulfate proteoglycan receptors in a rat model of amyotrophic lateral sclerosis. J Neurosci Res. 2018 02; 96(2):222-233. PMID: 28752900.
    Citations: 6     Fields:    Translation:HumansAnimalsCells
  13. Nishiyama A, Niihori T, Warita H, Izumi R, Akiyama T, Kato M, Suzuki N, Aoki Y, Aoki M. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. Neurobiol Aging. 2017 05; 53:194.e1-194.e8. PMID: 28160950.
    Citations: 21     Fields:    Translation:Humans
  14. Nishiyama A, Warita H, Takahashi T, Suzuki N, Nishiyama S, Tano O, Akiyama T, Watanabe Y, Takahashi K, Kuroda H, Kato M, Tateyama M, Niihori T, Aoki Y, Aoki M. Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutation. Clin Neurol Neurosurg. 2016 Nov; 150:194-196. PMID: 27543311.
    Citations: 2     Fields:    Translation:Humans
  15. Akiyama T, Warita H, Kato M, Nishiyama A, Izumi R, Ikeda C, Kamada M, Suzuki N, Aoki M. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan. Muscle Nerve. 2016 09; 54(3):398-404. PMID: 26823199.
    Citations: 9     Fields:    Translation:Humans
  16. Izumi R, Warita H, Niihori T, Takahashi T, Tateyama M, Suzuki N, Nishiyama A, Shirota M, Funayama R, Nakayama K, Mitsuhashi S, Nishino I, Aoki Y, Aoki M. Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutation. Neurol Genet. 2015 Oct; 1(3):e23. PMID: 27066560; PMCID: PMC4809462.
    Citations: 11     
  17. Izumi R, Niihori T, Suzuki N, Sasahara Y, Rikiishi T, Nishiyama A, Nishiyama S, Endo K, Kato M, Warita H, Konno H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Nakayama K, Kure S, Matsubara Y, Aoki Y, Aoki M. GNE myopathy associated with congenital thrombocytopenia: a report of two siblings. Neuromuscul Disord. 2014 Dec; 24(12):1068-72. PMID: 25257349.
    Citations: 25     Fields:    Translation:HumansCells
  18. Yoshida S, Kikuchi A, Tateyama M, Tano O, Nishiyama A, Akaishi T, Kato M, Aoki M. A case of steroid-responsive MADSAM with late appearance of a partial conduction block in the forearm. J Neurol. 2014 Apr; 261(4):825-7. PMID: 24570277.
    Citations:    Fields:    Translation:Humans
  19. Nishiyama A, Sugeno N, Tateyama M, Nishiyama S, Kato M, Aoki M. Postural leg tremor in X-linked spinal and bulbar muscular atrophy. J Clin Neurosci. 2014 May; 21(5):799-802. PMID: 24256885.
    Citations: 6     Fields:    Translation:Humans
  20. Tsuboi H, Sugeno N, Nishiyama A, Tateyama M, Aoki M. [Radial nerve palsy as a presenting feature of neuralgic amyotrophy]. Rinsho Shinkeigaku. 2013; 53(4):312-5. PMID: 23603548.
    Citations:    Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.