Katrina Conard

TitleVolunteer Faculty
InstitutionThomas Jefferson University
DepartmentFaculty Records
Address833 Chestnut Street
Philadelphia PA 19107
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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. Schultz KAP, Nelson A, Harris AK, Finch M, Field A, Jarzembowski JA, Wilhelm M, Mize W, Kreiger P, Conard K, Walter A, Olson T, Mitchell S, Runco DV, Bechtel A, Klawinski D, Bradfield S, Gettinger K, Stewart DR, Messinger Y, Dehner LP, Ashley Hill D. Pleuropulmonary blastoma-like peritoneal sarcoma: a newly described malignancy associated with biallelic DICER1 pathogenic variation. Mod Pathol. 2020 10; 33(10):1922-1929. PMID: 32415267.
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    2. Hurd LM, Thacker MM, Okenfuss E, Duker AL, Lou Y, Harty MP, Conard K, Lian JB, Bober MB. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. Am J Med Genet A. 2017 Dec; 173(12):3205-3210. PMID: 29080333.
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    3. Robbins KM, Stabley DL, Holbrook J, Sahraoui R, Sadreameli A, Conard K, Baker L, Gripp KW, Sol-Church K. Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma. Am J Med Genet A. 2016 12; 170(12):3197-3206. PMID: 27589201.
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    4. Gripp KW, Baker L, Kandula V, Conard K, Scavina M, Napoli JA, Griffin GC, Thacker M, Knox RG, Clark GR, Parker VE, Semple R, Mirzaa G, Keppler-Noreuil KM. Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation. Am J Med Genet A. 2016 10; 170(10):2559-69. PMID: 27191687.
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    5. Lin P, Raikar S, Jimenez J, Conard K, Furuya KN. Novel mutation in a patient with cholesterol ester storage disease. Case Rep Genet. 2015; 2015:347342. PMID: 25722898.
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    6. Fitzgerald KK, Bhat AM, Conard K, Hyland J, Pizarro C. Novel SMAD3 Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm. Case Rep Genet. 2014; 2014:591516. PMID: 24711937.
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    7. Rabinowitz MR, Levi J, Conard K, Shah UK. Castleman disease in the pediatric neck: a literature review. Otolaryngol Head Neck Surg. 2013 Jun; 148(6):1028-36. PMID: 23459702.
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    8. Brennan SO, Davis RL, Conard K, Savo A, Furuya KN. Novel fibrinogen mutation ?314Thr?Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia. Liver Int. 2010 Nov; 30(10):1541-7. PMID: 20666993.
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    9. Tsirikos AI, Mackenzie W, Conard KA, Czulewicz Reese L. Synovial chondromatosis in the pediatric patient. Am J Orthop (Belle Mead NJ). 2005 Mar; 34(3):129-32. PMID: 15828516.
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    10. Taylor KF, Yingsakmongkol W, Conard KA, Stanton RP. Multicentric giant cell tumor of bone: a case report and review of the literature. Clin Orthop Relat Res. 2003 May; (410):267-73. PMID: 12771839.
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