Daniah Beleford, MD, PhD

Title(s)Postdoctoral Scholar, Office of the CEO
SchoolChancellor/EVC/FAS
Address600 16th Street
San Francisco CA 94158
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ORCID ORCID Icon0000-0003-1766-1094 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Francisco, CA2020Diversity, Equity, and Inclusion Champion Training
    University of California, San FranciscoClinical Fellowship2019Genetics and Genomics
    University of California, San FranciscoResidency2018Genetics and Genomics
    Mayo Clinic College of MedicineMD, PhD - Biochemistry and Molecular BiologyMedical Scientist Training Program
    Cornell UniversityBA (Daniah Thompson)Genetics and Development

    Collapse Research 
    Collapse Research Activities and Funding
    Deciphering the role of PTPN14 in BMP9-Smad/Hippo-TAZ signaling and vascular malformations in Hereditary Hemorrhagic Telangiectasia
    University of California UC President's Postdoctoral FellowshipJul 1, 2021 - Jun 30, 2023
    Role: University of California President's Postdoctoral Fellow

    Collapse Bibliographic 
    Collapse Publications
    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. Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders. NPJ Genom Med. 2021 Oct 12; 6(1):88. Shieh JT, Penon-Portmann M, Wong KHY, Levy-Sakin M, Verghese M, Slavotinek A, Gallagher RC, Mendelsohn BA, Tenney J, Beleford D, Perry H, Chow SK, Sharo AG, Brenner SE, Qi Z, Yu J, Klein OD, Martin D, Kwok PY, Boffelli D. PMID: 34642307; PMCID: PMC8511154.
      View in: PubMed   Mentions:
    2. The YAP/TAZ antagonist, PTPN14, stabilizes SMAD4 through direct interactions in endothelial cells: Implications for Hereditary Hemorrhagic Telangiectasia. bioRxiv. 2021. Ons Mamai, Daniah T. Beleford, Mark Taylor, Sugandha Basu, Xinjian Cen, Suprita Trilok, Jiamin Zhang, Allan Balmain, Rosemary J. Akhurst. View Publication.
    3. Application of full-genome analysis to diagnose rare monogenic disorders. NPJ Genom Med. 2021 Sep 23; 6(1):77. Shieh JT, Penon-Portmann M, Wong KHY, Levy-Sakin M, Verghese M, Slavotinek A, Gallagher RC, Mendelsohn BA, Tenney J, Beleford D, Perry H, Chow SK, Sharo AG, Brenner SE, Qi Z, Yu J, Klein OD, Martin D, Kwok PY, Boffelli D. PMID: 34556655; PMCID: PMC8460793.
      View in: PubMed   Mentions: 2  
    4. BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations. medRxiv. 2021. Angela Peron, Felice D’Arco, Kimberly A. Aldinger, Constance Smith-Hicks, Christiane Zweier, Gyri A. Gradek, Kimberley Bradbury, Andrea Accogli, Erica F. Andersen, Ping Yee Billie Au, Roberta Battini, Daniah Beleford, Lynne M. Bird, Arjan Bouman, Ange-Line Bruel, Øyvind Løvold Busk, Philippe M. Campeau, Valeria Capra, Colleen Carlston, Jenny Carmichael, Anna Chassevent, Jill Clayton-Smith, Michael J Bamshad, Dawn L. Earl, Laurence Faivre, Christophe Philippe, Patrick Ferrerira, Luitgard Graul-Neumann, Mary J. Green, Darrah Haffner, Parthiv Haldipur, Suhair Hanna, Gunnar Houge, Jane Hurst, Cornelia Kraus, Birgit Elisabeth Kristiansen, James Lespinasse, Karen J. Low, Sally Ann Lynch, Sofia Maia, Rong Mao, Ruta Marcinkute, Catherine Melver, Kimberly McDonald, Tara Montgomery, Manuela Morleo, Constance Motter, Amanda S. Openshaw, Janice Cox Palumbos, Aditi Shah Parikh, Richard Person, Megha Desai, Juliette Piard, Rolph Pfundt, Marcello Scala, Margaux Serey-Gaut, Anne Slavotinek, Mohnish Suri, Claire Turner, Tatiana Tvrdik, Karin Weiss, Ingrid M. Wentzensen, Marcella Zollino, C4RCD Research Group, Telethon Undiagnosed Disease Program (TUDP), University of Washington Center for Mendelian Genomics (UW-CMG), Bert B.A. de Vries, Francois Guillemot, William B. Dobyns, David Viskochil, Cristina Dias. View Publication.
    5. Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness. Hum Mol Genet. 2020 08 03; 29(13):2218-2239. Slavotinek A, Misceo D, Htun S, Mathisen L, Frengen E, Foreman M, Hurtig JE, Enyenihi L, Sterrett MC, Leung SW, Schneidman-Duhovny D, Estrada-Veras J, Duncan JL, Haaxma CA, Kamsteeg EJ, Xia V, Beleford D, Si Y, Douglas G, Treidene HE, van Hoof A, Fasken MB, Corbett AH. PMID: 32504085; PMCID: PMC7399534.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimals
    6. A missense variant, p.(Ile269Asn), in MC4R as a secondary finding in a child with BCL11A-related intellectual disability. Eur J Med Genet. 2020 Sep; 63(9):103969. Beleford DT, Van Ziffle J, Hodoglugil U, Slavotinek AM. PMID: 32534219.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    7. A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophy. Am J Med Genet A. 2020 03; 182(3):513-520. Mendelsohn BA, Beleford DT, Abu-El-Haija A, Alsaleh NS, Rahbeeni Z, Martin PM, Rego S, Huang A, Capodanno G, Shieh JT, Van Ziffle J, Risch N, Alkuraya FS, Slavotinek AM. PMID: 31880405.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    8. X-linked duplication copy number variation in a familial overgrowth condition. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):644-649. Ha TK, Mardy AH, Beleford D, Spanier A, Wayman BV, Penon-Portmann M, Wiita AP, Shieh JT. PMID: 31762227.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    9. Schimke immunoosseous dysplasia and management considerations for vascular risks. Am J Med Genet A. 2019 07; 179(7):1246-1252. Beleford DT, Diab M, Qubty WF, Malloy MJ, Long RK, Shieh JT. PMID: 31039288.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review. Am J Med Genet A. 2019 06; 179(6):966-977. Kumar A, Zastrow DB, Kravets EJ, Beleford D, Ruzhnikov MRZ, Grove ME, Dries AM, Kohler JN, Waggott DM, Yang Y, Huang Y, Undiagnosed Diseases Network, Mackenzie KM, Eng CM, Fisher PG, Ashley EA, Teng JM, Stevenson DA, Shieh JT, Wheeler MT, Bernstein JA. PMID: 30920161; PMCID: PMC6488410.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    11. Neuro-Oncology. PATH-07. FAMILIAL MELANOMA-ASTROCYTOMA SYNDROME: SYNCHRONOUS DIFFUSE ASTROCYTOMA AND PLEOMORPHIC XANTHOASTROCYTOMA IN A PATIENT WITH GERMLINE CDKN2A/B DELETION AND A SIGNIFICANT FAMILY HISTORY. 2017; 19(suppl_6):vi171–vi172. Winward Choy, Andrew K Chan, Seunggu J Han, Daniah Beleford, Manish K Aghi, Mitchel S Berger, Joseph T Shieh, Andrew W Bollen, Arie Perry, Joanna J Phillips, Nicholas Butowski, David A Solomon. View Publication.
    12. Familial melanoma-astrocytoma syndrome: synchronous diffuse astrocytoma and pleomorphic xanthoastrocytoma in a patient with germline CDKN2A/B deletion and a significant family history. Clin Neuropathol. 2017 Sep/Oct; 36(5):213-221. Chan AK, Han SJ, Choy W, Beleford D, Aghi MK, Berger MS, Shieh JT, Bollen AW, Perry A, Phillips JJ, Butowski N, Solomon DA. PMID: 28699883; PMCID: PMC5628627.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    13. Role of heparan sulfatases in ovarian and breast cancer. Am J Cancer Res. 2013; 3(1):34-45. Khurana A, Beleford D, He X, Chien J, Shridhar V. PMID: 23359864; PMCID: PMC3555198.
      View in: PubMed   Mentions: 23  
    14. Handbook of Proteolytic Enzymes. Chapter 572 - HtrA3 Peptidase. 2012; 3:2584-2590. Daniah Beleford and Viji Shridhar. . View Publication.
    15. Cleavage of PGRP-LC receptor in the Drosophila IMD pathway in response to live bacterial infection in S2 cells. Self Nonself. 2011 Jul; 2(3):125-141. Schmidt RL, Rinaldo FM, Hesse SE, Hamada M, Ortiz Z, Beleford DT, Page-McCaw A, Platt JL, Tang AH. PMID: 22496930; PMCID: PMC3323661.
      View in: PubMed   Mentions: 6  
    16. High temperature requirement A3 (HtrA3) promotes etoposide- and cisplatin-induced cytotoxicity in lung cancer cell lines. J Biol Chem. 2010 Apr 16; 285(16):12011-27. Beleford D, Rattan R, Chien J, Shridhar V. PMID: 20154083; PMCID: PMC2852939.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    17. Methylation induced gene silencing of HtrA3 in smoking-related lung cancer. Clin Cancer Res. 2010 Jan 15; 16(2):398-409. Beleford D, Liu Z, Rattan R, Quagliuolo L, Boccellino M, Baldi A, Maguire J, Staub J, Molina J, Shridhar V. PMID: 20068077.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansAnimalsCells
    18. Cell proliferation and epidermal growth factor signaling in non-small cell lung adenocarcinoma cell lines are dependent on Rin1. J Biol Chem. 2009 Sep 25; 284(39):26331-9. Tomshine JC, Severson SR, Wigle DA, Sun Z, Beleford DA, Shridhar V, Horazdovsky BF. PMID: 19570984; PMCID: PMC2785321.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    19. A role for candidate tumor-suppressor gene TCEAL7 in the regulation of c-Myc activity, cyclin D1 levels and cellular transformation. Oncogene. 2008 Dec 11; 27(58):7223-34. Chien J, Narita K, Rattan R, Giri S, Shridhar R, Staub J, Beleford D, Lai J, Roberts LR, Molina J, Kaufmann SH, Prendergast GC, Shridhar V. PMID: 18806825; PMCID: PMC2754286.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
    20. Identification and characterization of the chromatin-binding domains of the HIV-1 integrase interactor LEDGF/p75. J Mol Biol. 2006 Jul 21; 360(4):760-73. Llano M, Vanegas M, Hutchins N, Thompson D, Delgado S, Poeschla EM. PMID: 16793062.
      View in: PubMed   Mentions: 108     Fields:    Translation:HumansCells
    21. Identification of the LEDGF/p75 HIV-1 integrase-interaction domain and NLS reveals NLS-independent chromatin tethering. J Cell Sci. 2005 Apr 15; 118(Pt 8):1733-43. Vanegas M, Llano M, Delgado S, Thompson D, Peretz M, Poeschla E. PMID: 15797927.
      View in: PubMed   Mentions: 98     Fields:    Translation:HumansAnimalsCells
    22. CCR5 and CXCR4 usage by non-clade B human immunodeficiency virus type 1 primary isolates. J Virol. 2002 Mar; 76(6):3059-64. Thompson DA, Cormier EG, Dragic T. PMID: 11861874; PMCID: PMC135972.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    23. Human immunodeficiency virus type 1 entry inhibitors PRO 542 and T-20 are potently synergistic in blocking virus-cell and cell-cell fusion. J Infect Dis. 2001 Apr 01; 183(7):1121-5. Nagashima KA, Thompson DA, Rosenfield SI, Maddon PJ, Dragic T, Olson WC. PMID: 11237840.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansAnimalsCells
    24. Entry of R5X4 and X4 human immunodeficiency virus type 1 strains is mediated by negatively charged and tyrosine residues in the amino-terminal domain and the second extracellular loop of CXCR4. Virology. 2000 Jun 05; 271(2):240-7. Kajumo F, Thompson DA, Guo Y, Dragic T. PMID: 10860877.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    25. Specific interaction of CCR5 amino-terminal domain peptides containing sulfotyrosines with HIV-1 envelope glycoprotein gp120. Proc Natl Acad Sci U S A. 2000 May 23; 97(11):5762-7. Cormier EG, Persuh M, Thompson DA, Lin SW, Sakmar TP, Olson WC, Dragic T. PMID: 10823934; PMCID: PMC18507.
      View in: PubMed   Mentions: 79     Fields:    Translation:HumansCells
    26. A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5. Proc Natl Acad Sci U S A. 2000 May 09; 97(10):5639-44. Dragic T, Trkola A, Thompson DA, Cormier EG, Kajumo FA, Maxwell E, Lin SW, Ying W, Smith SO, Sakmar TP, Moore JP. PMID: 10779565; PMCID: PMC25881.
      View in: PubMed   Mentions: 152     Fields:    Translation:HumansAnimalsCells
    27. Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5. J Virol. 1999 May; 73(5):4145-55. Olson WC, Rabut GE, Nagashima KA, Tran DN, Anselma DJ, Monard SP, Segal JP, Thompson DA, Kajumo F, Guo Y, Moore JP, Maddon PJ, Dragic T. PMID: 10196311; PMCID: PMC104194.
      View in: PubMed   Mentions: 93     Fields:    Translation:HumansCells
    28. CCR5-Mediated human immunodeficiency virus entry depends on an amino-terminal gp120-binding site and on the conformational integrity of all four extracellular domains. J Virol. 1999 Feb; 73(2):1645-8. Genoud S, Kajumo F, Guo Y, Thompson D, Dragic T. PMID: 9882373; PMCID: PMC103992.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
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