Homa Majd, PhD

Title(s)Postdoctoral Scholar, Cellular Molecular Pharmacology
SchoolSchool of Medicine
Address600 16th Street, #S576
San Francisco CA 94158
ORCID ORCID Icon0000-0002-2048-1839 Additional info
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    Collapse Biography 
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    University of CambridgePhD2016Biological Sciences
    University of TehranBSc2012Biotechnology

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Differentiation of Enteric Nervous System Lineages from Human Pluripotent Stem Cells. J Vis Exp. 2024 May 17; (207). Majd H, Richter MN, Samuel RM, Kalantari A, Ramirez JT, Fattahi F. PMID: 38829111.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    2. A call for a unified and multimodal definition of cellular identity in the enteric nervous system. bioRxiv. 2024 Feb 05. Majd H, Cesiulis A, Samuel RM, Richter MN, Elder N, Guyer RA, Hao MM, Stamp LA, Goldstein AM, Fattahi F. PMID: 38293133; PMCID: PMC10827084.
      View in: PubMed   Mentions:
    3. Modeling enteric glia development, physiology and disease using human pluripotent stem cells. Neurosci Lett. 2023 08 10; 811:137334. Scantlen MD, Majd H, Fattahi F. PMID: 37315730.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    4. Deriving Schwann cells from hPSCs enables disease modeling and drug discovery for diabetic peripheral neuropathy. Cell Stem Cell. 2023 05 04; 30(5):632-647.e10. Majd H, Amin S, Ghazizadeh Z, Cesiulis A, Arroyo E, Lankford K, Majd A, Farahvashi S, Chemel AK, Okoye M, Scantlen MD, Tchieu J, Calder EL, Le Rouzic V, Shibata B, Arab A, Goodarzi H, Pasternak G, Kocsis JD, Chen S, Studer L, Fattahi F. PMID: 37146583; PMCID: PMC10249419.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    5. Generation of Schwann cell derived melanocytes from hPSCs identifies pro-metastatic factors in melanoma. bioRxiv. 2023 Mar 07. Samuel RM, Navickas A, Maynard A, Gaylord EA, Garcia K, Bhat S, Majd H, Richter MN, Elder N, Le D, Nguyen P, Shibata B, Llabata ML, Selleri L, Laird DJ, Darmanis S, Goodarzi H, Fattahi F. PMID: 36945537; PMCID: PMC10028814.
      View in: PubMed   Mentions: 1  
    6. Androgens increase excitement in brain organoid research. Cell Stem Cell. 2022 04 07; 29(4):495-497. Samuel RM, Majd H, Richter MN, Fattahi F. PMID: 35395183.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    7. Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men. Cell Stem Cell. 2020 12 03; 27(6):876-889.e12. Samuel RM, Majd H, Richter MN, Ghazizadeh Z, Zekavat SM, Navickas A, Ramirez JT, Asgharian H, Simoneau CR, Bonser LR, Koh KD, Garcia-Knight M, Tassetto M, Sunshine S, Farahvashi S, Kalantari A, Liu W, Andino R, Zhao H, Natarajan P, Erle DJ, Ott M, Goodarzi H, Fattahi F. PMID: 33232663; PMCID: PMC7670929.
      View in: PubMed   Mentions: 148     Fields:    Translation:HumansAnimalsCells
    8. Androgen Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men. bioRxiv. 2020 May 15. Ghazizadeh Z, Majd H, Richter M, Samuel R, Zekavat SM, Asgharian H, Farahvashi S, Kalantari A, Ramirez J, Zhao H, Natarajan P, Goodarzi H, Fattahi F. PMID: 32511360; PMCID: PMC7263488.
      View in: PubMed   Mentions:
    9. BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature. 2019 08; 572(7771):614-619. Yoneshiro T, Wang Q, Tajima K, Matsushita M, Maki H, Igarashi K, Dai Z, White PJ, McGarrah RW, Ilkayeva OR, Deleye Y, Oguri Y, Kuroda M, Ikeda K, Li H, Ueno A, Ohishi M, Ishikawa T, Kim K, Chen Y, Sponton CH, Pradhan RN, Majd H, Greiner VJ, Yoneshiro M, Brown Z, Chondronikola M, Takahashi H, Goto T, Kawada T, Sidossis L, Szoka FC, McManus MT, Saito M, Soga T, Kajimura S. PMID: 31435015; PMCID: PMC6715529.
      View in: PubMed   Mentions: 196     Fields:    Translation:HumansAnimalsCells
    10. Screening of candidate substrates and coupling ions of transporters by thermostability shift assays. Elife. 2018 10 15; 7. Majd H, King MS, Palmer SM, Smith AC, Elbourne LD, Paulsen IT, Sharples D, Henderson PJ, Kunji ER. PMID: 30320551; PMCID: PMC6211832.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansAnimalsCells
    11. Pathogenic mutations of the human mitochondrial citrate carrier SLC25A1 lead to impaired citrate export required for lipid, dolichol, ubiquinone and sterol synthesis. Biochim Biophys Acta Bioenerg. 2018 Jan; 1859(1):1-7. Majd H, King MS, Smith AC, Kunji ERS. PMID: 29031613.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    12. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016 12 01; 99(6):1405. Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL, He L, Lodi T, Jones SA, Fattal-Valevski A, Fraenkel ND, Saada A, Haham A, Isohanni P, Vara R, Barbosa IA, Simpson MA, Deshpande C, Puusepp S, Bonnen PE, Rodenburg RJ, Suomalainen A, Õunap K, Elpeleg O, Ferrero I, McFarland R, Kunji ERS, Taylor RW. PMID: 27912046; PMCID: PMC5142113.
      View in: PubMed   Mentions: 15     Fields:    
    13. Corrigendum to "The transport mechanism of the mitochondrial ADP/ATP carrier" [Biochim. Biophys. Acta 1863/10 (2016) 2379-2393]. Biochim Biophys Acta. 2016 12; 1863(12):3169. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. PMID: 27713079.
      View in: PubMed   Mentions: 1     Fields:    
    14. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016 10 06; 99(4):860-876. Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL, He L, Lodi T, Jones SA, Fattal-Valevski A, Fraenkel ND, Saada A, Haham A, Isohanni P, Vara R, Barbosa IA, Simpson MA, Deshpande C, Puusepp S, Bonnen PE, Rodenburg RJ, Suomalainen A, Õunap K, Elpeleg O, Ferrero I, McFarland R, Kunji ER, Taylor RW. PMID: 27693233; PMCID: PMC5065686.
      View in: PubMed   Mentions: 54     Fields:    Translation:HumansCells
    15. The transport mechanism of the mitochondrial ADP/ATP carrier. Biochim Biophys Acta. 2016 10; 1863(10):2379-93. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. PMID: 27001633.
      View in: PubMed   Mentions: 76     Fields:    Translation:HumansAnimalsCells
    16. The mitochondrial dicarboxylate and 2-oxoglutarate carriers do not transport glutathione. FEBS Lett. 2015 Feb 27; 589(5):621-8. Booty LM, King MS, Thangaratnarajah C, Majd H, James AM, Kunji ER, Murphy MP. PMID: 25637873; PMCID: PMC4332691.
      View in: PubMed   Mentions: 29     Fields:    Translation:Cells
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