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Brendan Crawford

TitleAssistant Professor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPeds Pediatrics, College of Medicine
DivisionPeds Nephrology
Address800 Marshall Street
Mail Slot # 512-14
Little Rock AR 72202
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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. Don't see publications published under other names? Login to add alternative names.
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    1. Sanders E, Brown CC, Blaszak RT, Crawford B, Prodhan P. Cardiac Manifestation among Children with Hemolytic Uremic Syndrome. J Pediatr. 2021 Aug; 235:144-148.e4. PMID: 33819463.
      View in: PubMed
    2. Ranabothu S, Blaszak R, Larsen C, Crawford B. Rocky road-an uncommon reason for kidney allograft dysfunction: Questions. Pediatr Nephrol. 2021 Jun; 36(6):1457-1459. PMID: 33025202.
      View in: PubMed
    3. Ranabothu S, Blaszak R, Larsen C, Crawford B. Rocky road-an uncommon reason for kidney allograft dysfunction: Answers. Pediatr Nephrol. 2021 Jun; 36(6):1461-1463. PMID: 33025203.
      View in: PubMed
    4. Robertson CC, Gillies CE, Putler RKB, Ng D, Reidy KJ, Crawford B, Sampson MG. An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts. Nephrol Dial Transplant. 2017 Dec 01; 32(12):2051-2058. PMID: 27638911.
      View in: PubMed
    5. Crawford BD, Gipson DS. Improving the evidence for the management of childhood nephrotic syndrome. Kidney Int. 2017 07; 92(1):21-23. PMID: 28646993.
      View in: PubMed
    6. Crawford BD, Gillies CE, Robertson CC, Kretzler M, Otto EA, Vega-Warner V, Sampson MG. Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability. Pediatr Nephrol. 2017 07; 32(7):1285. PMID: 28349212.
      View in: PubMed
    7. Crawford BD, Gillies CE, Robertson CC, Kretzler M, Otto EA, Vega-Warner V, Sampson MG. Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability. Pediatr Nephrol. 2017 03; 32(3):467-476. PMID: 27766458.
      View in: PubMed
    8. Gillies CE, Otto EA, Vega-Warner V, Robertson CC, Sanna-Cherchi S, Gharavi A, Crawford B, Bhimma R, Winkler C, Kang HM, Sampson MG. tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine. BMC Bioinformatics. 2016 Jun 10; 17(1):233. PMID: 27287006.
      View in: PubMed
    9. Staiman A, Crawford BD, McLain KK, Gattari TB, Mychaliska KP. Evaluating Educational Needs of Parents at Newborn Discharge: A Pilot Study. Hosp Pediatr. 2016 May; 6(5):310-4. PMID: 27094251.
      View in: PubMed
    10. Sampson MG, Gillies CE, Robertson CC, Crawford B, Vega-Warner V, Otto EA, Kretzler M, Kang HM. Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort. J Am Soc Nephrol. 2016 07; 27(7):1970-83. PMID: 26534921.
      View in: PubMed
    11. Oravecz-Wilson KI, Philips ST, Yilmaz OH, Ames HM, Li L, Crawford BD, Gauvin AM, Lucas PC, Sitwala K, Downing JR, Morrison SJ, Ross TS. Persistence of leukemia-initiating cells in a conditional knockin model of an imatinib-responsive myeloproliferative disorder. Cancer Cell. 2009 Aug 04; 16(2):137-48. PMID: 19647224.
      View in: PubMed
    12. Crawford BD, Hess JL. MLL core components give the green light to histone methylation. ACS Chem Biol. 2006 Sep 19; 1(8):495-8. PMID: 17168535.
      View in: PubMed
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