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Ora Karp Gordon

Title(s)HS Clinical Professor, Pediatrics
SchoolMedicine
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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. Do Patients with DCIS or Invasive Breast Cancer Carry the Same Risk for Genetic Mutation? Ann Surg Oncol. 2025 Sep 04. Orozco JIJ, Valdez BJ, Trasatti ES, Brown SM, Childers K, Gordon OK, Grumley JG. PMID: 40908455.
      View in: PubMed   Mentions:    Fields:    
    2. Geno4ME Study: implementation of whole genome sequencing for population screening in a large healthcare system. NPJ Genom Med. 2025 Jul 01; 10(1):50. Lucas Beckett IA, Emery KR, Wagner JT, Jade K, Cosgrove BA, Welle J, Rinaldi JB, Dickey L, Jones K, Wagner N, Shull EM, Clemens J, Trachana K, Anderson L, Kudla A, Smith B, Verespej H, Yuan LC, Denne E, Ramos E, Lovejoy JC, Olszewski K, Reese MG, Reynolds MJ, Miller MM, Dowdell AK, Beck B, Scanlan JM, Campbell MB, Magis AT, Vartanian K, Piening BD, Bifulco CB, Gordon OK. PMID: 40593689; PMCID: PMC12218075.
      View in: PubMed   Mentions:
    3. Experiences across a genetic screening and testing programme pathway: a qualitative study of mammogram patient perspectives. BMJ Open. 2024 Oct 23; 14(10):e089884. Devine C, Emery KR, Childers KK, Brown S, Gordon O, Roth SE. PMID: 39448212; PMCID: PMC11499760.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors. Genet Med. 2024 Jul; 26(7):101128. Mabey B, Hughes E, Kucera M, Simmons T, Hullinger B, Pederson HJ, Yehia L, Eng C, Garber J, Gary M, Gordon O, Klemp JR, Mukherjee S, Vijai J, Offit K, Olopade OI, Pruthi S, Kurian A, Robson ME, Whitworth PW, Pal T, Ratzel S, Wagner S, Lanchbury JS, Taber KJ, Slavin TP, Gutin A. PMID: 38829299.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    5. The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration. Cancer. 2024 Oct 01; 130(19):3297-3304. Karloski E, Dudley B, Diergaarde B, Blanco A, Everett JN, Levinson E, Rangarajan T, Stanich PP, Childers K, Brown S, Drogan C, Cavestro GM, Gordon K, Singh A, Simeone DM, Reich H, Kastrinos F, Zakalik D, Hampel H, Pearlman R, Gordon OK, Kupfer SS, Puzzono M, Zuppardo RA, Brand RE. PMID: 38809542; PMCID: PMC11371512.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Acupuncture for Chronic Radiation-Induced Xerostomia in Head and Neck Cancer: A Multicenter Randomized Clinical Trial. JAMA Netw Open. 2024 05 01; 7(5):e2410421. Cohen L, Danhauer SC, Garcia MK, Dressler EV, Rosenthal DI, Chambers MS, Cusimano A, Brown WM, Ochoa JM, Yang P, Chiang JS, Gordon O, Crutcher R, Kim JK, Russin MP, Lukenbill J, Porosnicu M, Yost KJ, Weaver KE, Lesser GJ. PMID: 38739392; PMCID: PMC11091764.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansPHPublic Health
    7. Analytical validation of HER2DX genomic test for early-stage HER2-positive breast cancer. ESMO Open. 2024 Mar; 9(3):102903. Marín-Aguilera M, Jares P, Sanfeliu E, Villacampa G, Hernández-Lllán E, Martínez-Puchol AI, Shankar S, González-Farré B, Waks AG, Brasó-Maristany F, Pardo F, Manning DK, Abery JA, Curaba J, Moon L, Gordon O, Galván P, Wachirakantapong P, Castillo O, Nee CM, Blasco P, Senevirathne TH, Sirenko V, Martínez-Sáez O, Aguirre A, Krop IE, Li Z, Spellman P, Metzger Filho O, Polyak K, Michaels P, Puig-Butillé JA, Vivancos A, Matito J, Buckingham W, Perou CM, Villagrasa-González P, Prat A, Parker JS, Paré L. PMID: 38452436; PMCID: PMC10937240.
      View in: PubMed   Mentions: 7  Translation:Humans
    8. Participation in genetic screening: testing different outreach methods across a diverse hospital system based patient population. Front Genet. 2023; 14:1272931. Dickey L, Gronowski B, Jones K, Rinaldi JB, Emery K, Clemens J, Gordon O, Vartanian K. PMID: 37900185; PMCID: PMC10602775.
      View in: PubMed   Mentions: 2  
    9. Can Acupuncture be a Part of the Treatment for Breast Cancer-Related Lymphedema? A Systematic Review of the Safety and Proposed Model for Care. Lymphology. 2023; 56(1):27-39. Kim JK, Loo C, Kim JS, Pranskevich C, Gordon OK. PMID: 38019877.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition. JCO Precis Oncol. 2022 Nov; 6:e2200084. Hughes E, Wagner S, Pruss D, Bernhisel R, Probst B, Abkevich V, Simmons T, Hullinger B, Judkins T, Rosenthal E, Roa B, Domchek SM, Eng C, Garber J, Gary M, Klemp J, Mukherjee S, Offit K, Olopade OI, Vijai J, Weitzel JN, Whitworth P, Yehia L, Gordon O, Pederson H, Kurian A, Slavin TP, Gutin A, Lanchbury JS. PMID: 36331239; PMCID: PMC9666117.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    11. Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study. BMC Med. 2021 Nov 03; 19(1):288. Haverfield EV, Esplin ED, Aguilar SJ, Hatchell KE, Ormond KE, Hanson-Kahn A, Atwal PS, Macklin-Mantia S, Hines S, Sak CW, Tucker S, Bleyl SB, Hulick PJ, Gordon OK, Velsher L, Gu JYJ, Weissman SM, Kruisselbrink T, Abel C, Kettles M, Slavotinek A, Mendelsohn BA, Green RC, Aradhya S, Nussbaum RL. PMID: 34732190; PMCID: PMC8567716.
      View in: PubMed   Mentions: 3     Fields:    
    12. Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study. BMC Med. 2021 08 18; 19(1):199. Haverfield EV, Esplin ED, Aguilar SJ, Hatchell KE, Ormond KE, Hanson-Kahn A, Atwal PS, Macklin-Mantia S, Hines S, Sak CW, Tucker S, Bleyl SB, Hulick PJ, Gordon OK, Velsher L, Gu JYJ, Weissman SM, Kruisselbrink T, Abel C, Kettles M, Slavotinek A, Mendelsohn BA, Green RC, Aradhya S, Nussbaum RL. PMID: 34404389; PMCID: PMC8371767.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    13. Painting a portrait: Analysis of national health survey data for cancer genetic counseling. Cancer Med. 2019 03; 8(3):1306-1314. Stamp MH, Gordon OK, Childers CP, Childers KK. PMID: 30734520; PMCID: PMC6434212.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansPHPublic Health
    14. SNPs and breast cancer risk prediction for African American and Hispanic women. Breast Cancer Res Treat. 2015 Dec; 154(3):583-9. Allman R, Dite GS, Hopper JL, Gordon O, Starlard-Davenport A, Chlebowski R, Kooperberg C. PMID: 26589314; PMCID: PMC4661211.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    15. BRCA-mutated Invasive Breast Carcinomas: Immunohistochemical Analysis of Insulin-like Growth Factor II mRNA-binding Protein (IMP3), Cytokeratin 8/18, and Cytokeratin 14. Breast J. 2015 Nov-Dec; 21(6):596-603. Mohanty SK, Lai JP, Gordon OK, Pradhan D, Bose S, Dadmanesh F. PMID: 26390986.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    16. Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Res. 2015 Mar; 25(3):305-15. Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, Jarvik ER, Itsara A, Turner EH, Herman DS, Schleit J, Burt A, Jamal SM, Abrudan JL, Johnson AD, Conlin LK, Dulik MC, Santani A, Metterville DR, Kelly M, Foreman AK, Lee K, Taylor KD, Guo X, Crooks K, Kiedrowski LA, Raffel LJ, Gordon O, Machini K, Desnick RJ, Biesecker LG, Lubitz SA, Mulchandani S, Cooper GM, Joffe S, Richards CS, Yang Y, Rotter JI, Rich SS, O'Donnell CJ, Berg JS, Spinner NB, Evans JP, Fullerton SM, Leppig KA, Bennett RL, Bird T, Sybert VP, Grady WM, Tabor HK, Kim JH, Bamshad MJ, Wilfond B, Motulsky AG, Scott CR, Pritchard CC, Walsh TD, Burke W, Raskind WH, Byers P, Hisama FM, Rehm H, Nickerson DA, Jarvik GP. PMID: 25637381; PMCID: PMC4352885.
      View in: PubMed   Mentions: 203     Fields:    Translation:Humans
    17. Exome sequencing for the diagnosis of 46,XY disorders of sex development. J Clin Endocrinol Metab. 2015 Feb; 100(2):E333-44. Baxter RM, Arboleda VA, Lee H, Barseghyan H, Adam MP, Fechner PY, Bargman R, Keegan C, Travers S, Schelley S, Hudgins L, Mathew RP, Stalker HJ, Zori R, Gordon OK, Ramos-Platt L, Pawlikowska-Haddal A, Eskin A, Nelson SF, Délot E, Vilain E. PMID: 25383892; PMCID: PMC4318895.
      View in: PubMed   Mentions: 92     Fields:    Translation:Humans
    18. Impact of family history on choosing risk-reducing surgery among BRCA mutation carriers. Am J Obstet Gynecol. 2013 Apr; 208(4):329.e1-6. Singh K, Lester J, Karlan B, Bresee C, Geva T, Gordon O. PMID: 23333547.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    19. Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. JAMA. 2012 Jan 25; 307(4):382-90. Bolton KL, Chenevix-Trench G, Goh C, Sadetzki S, Ramus SJ, Karlan BY, Lambrechts D, Despierre E, Barrowdale D, McGuffog L, Healey S, Easton DF, Sinilnikova O, Benítez J, García MJ, Neuhausen S, Gail MH, Hartge P, Peock S, Frost D, Evans DG, Eeles R, Godwin AK, Daly MB, Kwong A, Ma ES, Lázaro C, Blanco I, Montagna M, D'Andrea E, Nicoletto MO, Johnatty SE, Kjær SK, Jensen A, Høgdall E, Goode EL, Fridley BL, Loud JT, Greene MH, Mai PL, Chetrit A, Lubin F, Hirsh-Yechezkel G, Glendon G, Andrulis IL, Toland AE, Senter L, Gore ME, Gourley C, Michie CO, Song H, Tyrer J, Whittemore AS, McGuire V, Sieh W, Kristoffersson U, Olsson H, Borg Å, Levine DA, Steele L, Beattie MS, Chan S, Nussbaum RL, Moysich KB, Gross J, Cass I, Walsh C, Li AJ, Leuchter R, Gordon O, Garcia-Closas M, Gayther SA, Chanock SJ, Antoniou AC, Pharoah PD, EMBRACE, kConFab Investigators, Cancer Genome Atlas Research Network. PMID: 22274685; PMCID: PMC3727895.
      View in: PubMed   Mentions: 311     Fields:    Translation:Humans
    20. Capturing the power of the family history. Virtual Mentor. 2009 Sep 01; 11(9):690-6. Geva T, Gordon O. PMID: 23199465.
      View in: PubMed   Mentions:    Fields:    
    21. Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension. J Headache Pain. 2008 Apr; 9(2):99-102. Schievink WI, Gordon OK, Hyland JC, Ala-Kokko L. PMID: 18264665; PMCID: PMC3476180.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    22. Connective tissue disorders with spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension: a prospective study. Neurosurgery. 2004 Jan; 54(1):65-70; discussion 70-1. Schievink WI, Gordon OK, Tourje J. PMID: 14683542.
      View in: PubMed   Mentions: 60     Fields:    Translation:Humans
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