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Yaser Heshmati, Ph.D.

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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. Atta H, Gheinani AH, Wacker A, Heshmati Y, Bigger-Allen A, Lambrinos G, Gao Y, Bielenberg DR, Adam RM. A Single Cell Dissociation Approach for Molecular Analysis of Urinary Bladder in the Mouse Following Spinal Cord Injury. J Vis Exp. 2020 06 17; (160). PMID: 32628176.
    Citations:    Fields:    Translation:AnimalsCells
  2. Heshmati Y, Kharazi S, Türköz G, Chang D, Kamali Dolatabadi E, Boström J, Krstic A, Boukoura T, Wagner E, Kadri N, Månsson R, Altun M, Qian H, Walfridsson J. The histone chaperone NAP1L3 is required for haematopoietic stem cell maintenance and differentiation. Sci Rep. 2018 07 25; 8(1):11202. PMID: 30046127.
    Citations:    Fields:    Translation:HumansAnimalsCells
  3. Xiao P, Sandhow L, Heshmati Y, Kondo M, Bouderlique T, Dolinska M, Johansson AS, Sigvardsson M, Ekblom M, Walfridsson J, Qian H. Distinct roles of mesenchymal stem and progenitor cells during the development of acute myeloid leukemia in mice. Blood Adv. 2018 06 26; 2(12):1480-1494. PMID: 29945938.
    Citations: 6     Fields:    Translation:AnimalsCells
  4. Heshmati Y, Türköz G, Harisankar A, Kharazi S, Boström J, Dolatabadi EK, Krstic A, Chang D, Månsson R, Altun M, Qian H, Walfridsson J. The chromatin-remodeling factor CHD4 is required for maintenance of childhood acute myeloid leukemia. Haematologica. 2018 07; 103(7):1169-1181. PMID: 29599201.
    Citations: 2     Fields:    Translation:HumansCells
  5. Herold N, Rudd SG, Ljungblad L, Sanjiv K, Myrberg IH, Paulin CB, Heshmati Y, Hagenkort A, Kutzner J, Page BD, Calderón-Montaño JM, Loseva O, Jemth AS, Bulli L, Axelsson H, Tesi B, Valerie NC, Höglund A, Bladh J, Wiita E, Sundin M, Uhlin M, Rassidakis G, Heyman M, Tamm KP, Warpman-Berglund U, Walfridsson J, Lehmann S, Grandér D, Lundbäck T, Kogner P, Henter JI, Helleday T, Schaller T. Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignancies. Nat Med. 2017 Feb; 23(2):256-263. PMID: 28067901.
    Citations: 29     Fields:    Translation:HumansAnimals
  6. Rezazadeh M, Khorrami A, Yeghaneh T, Talebi M, Kiani SJ, Heshmati Y, Gharesouran J. Genetic Factors Affecting Late-Onset Alzheimer's Disease Susceptibility. Neuromolecular Med. 2016 Mar; 18(1):37-49. PMID: 26553058.
    Citations: 7     Fields:    Translation:Humans
  7. Sadeghi B, Heshmati Y, Khoein B, Kaipe H, Uzunel M, Walfridsson J, Ringdén O. Xeno-immunosuppressive properties of human decidual stromal cells in mouse models of alloreactivity in vitro and in vivo. Cytotherapy. 2015 Dec; 17(12):1732-45. PMID: 26481415.
    Citations: 6     Fields:    Translation:HumansAnimalsCells
  8. Rafati M, Seyyedaboutorabi E, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Javadi GR, Dastan J, Mosavi-Jarrahi A, Hoseini A, Purhoseini M, Ghaffari SR. "Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes. Mol Cytogenet. 2012 Jan 29; 5(1):9. PMID: 22283845.
    Citations: 3     
  9. Rafati M, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Dastan J, Hoseini A, Purhoseini M, Ghaffari SR. "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements. Mol Cytogenet. 2012 Jan 19; 5(1):4. PMID: 22260313.
    Citations: 3     
  10. Zarif Yeganeh M, Mirabzadeh A, Khorram Khorshid HR, Kamali K, Heshmati Y, Gozalpour E, Veissy K, Olad Nabi M, Najmabadi H, Ohadi M. Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease. . 2010 Jan 05; 153B(1):347-9. PMID: 19475601.
    Citations: 6     Translation:Humans
  11. Heshmati Y, Mirabzadeh A, Feizzade G, Gilanipour M, Etminan MR, Khoram Khorshid HR, Kamali K, Fakhri M, Moghimi N, Najmabadi H, Ohadi M. A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; extra-short alleles and accumulated allele homozygosity. . 2009 Mar 05; 150B(2):248-53. PMID: 18561140.
    Citations: 5     Translation:HumansCells
  12. Moheb LA, Tzschach A, Garshasbi M, Kahrizi K, Darvish H, Heshmati Y, Kordi A, Najmabadi H, Ropers HH, Kuss AW. Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome. Eur J Hum Genet. 2008 Feb; 16(2):270-3. PMID: 18043714.
    Citations: 28     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.