Harvard Catalyst Profiles

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Kazumi Ida


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. Enomoto Y, Tsurusaki Y, Yokoi T, Abe-Hatano C, Ida K, Naruto T, Mitsui J, Tsuji S, Morishita S, Kurosawa K. CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability. Eur J Med Genet. 2020 Jan; 63(1):103610. PMID: 30602132.
    Citations:    Fields:    Translation:Humans
  2. Kuroda Y, Ohashi I, Naruto T, Ida K, Enomoto Y, Saito T, Nagai JI, Yanagi S, Ueda H, Kurosawa K. Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion. J Hum Genet. 2018 Nov; 63(11):1185-1188. PMID: 30108319.
    Citations: 2     Fields:    Translation:HumansCells
  3. Kuroda Y, Ohashi I, Naruto T, Ida K, Enomoto Y, Saito T, Nagai JI, Kurosawa K. Evaluation of a patient with classical Ehlers-Danlos syndrome due to a 9q34 duplication affecting COL5A1. Congenit Anom (Kyoto). 2018 Nov; 58(6):191-193. PMID: 29520887.
    Citations:    Fields:    Translation:HumansCells
  4. Shimbo H, Yokoi T, Aida N, Mizuno S, Suzumura H, Nagai J, Ida K, Enomoto Y, Hatano C, Kurosawa K. Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome. Mol Genet Genomic Med. 2017 Jul; 5(4):429-437. PMID: 28717667.
    Citations: 4     Fields:    
  5. Kuroda Y, Ohashi I, Naruto T, Ida K, Enomoto Y, Saito T, Nagai J, Wada T, Kurosawa K. Delineation of the KIAA2022 mutation phenotype: two patients with X-linked intellectual disability and distinctive features. Am J Med Genet A. 2015 Jun; 167(6):1349-53. PMID: 25900396.
    Citations: 11     Fields:    Translation:Humans
  6. Kuroda Y, Saito T, Nagai J, Ida K, Naruto T, Masuno M, Kurosawa K. Microdeletion of 19p13.3 in a girl with Peutz-Jeghers syndrome, intellectual disability, hypotonia, and distinctive features. . 2015 Feb; 167A(2):389-93. PMID: 25487640.
    Citations: 5     Translation:HumansCells
  7. Kuroda Y, Ohashi I, Saito T, Nagai J, Ida K, Naruto T, Wada T, Kurosawa K. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2. . 2014 Nov; 164A(11):2873-8. PMID: 25099823.
    Citations: 3     Translation:HumansCells
  8. Kuroda Y, Ohashi I, Saito T, Nagai J, Ida K, Naruto T, Iai M, Kurosawa K. Refinement of the deletion in 8q22.2-q22.3: the minimum deletion size at 8q22.3 related to intellectual disability and epilepsy. . 2014 Aug; 164A(8):2104-8. PMID: 24801133.
    Citations: 4     Translation:HumansCells
  9. Kuroda Y, Ohashi I, Tominaga M, Saito T, Nagai J, Ida K, Naruto T, Masuno M, Kurosawa K. De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesity. . 2014 Jun; 164A(6):1550-4. PMID: 24668897.
    Citations: 7     Translation:HumansCells
  10. Kang HW, Ida K, Yamamoto Y, Muramatsu H. Monitoring of morphology and physical properties of cultured cells using a micro camera and a quartz crystal with transparent indium tin oxide electrodes after injections of glutaraldehyde and trypsin. Anal Chim Acta. 2008 Aug 22; 624(1):154-61. PMID: 18706321.
    Citations: 1     Fields:    Translation:HumansCells
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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.