Bugsu Ovunc

Title(s)	Associate Health Sciences Professor, Pediatrics
School	School of Medicine
Address	1001 Health Sciences Road Irvine CA 92697-3950
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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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Pediatric P-ANCA vasculitis following COVID-19. Pediatr Pulmonol. 2021 10; 56(10):3422-3424. Fireizen Y, Shahriary C, Imperial ME, Randhawa I, Nianiaris N, Ovunc B. PMID: 34379888; PMCID: PMC8441809.

View in: PubMed Mentions: 19 Fields:
Ped Pediatrics Pul Pulmonary Medicine
Translation:Humans Cells
Quality metrics in cardiac catheterization for congenital heart disease: utility of 30-day mortality. Catheter Cardiovasc Interv. 2015 Jan 01; 85(1):104-10. Backes CH, Bergersen L, Rome JJ, Batlivala SP, Glatz AC, Ovunc B, David S, Rivera BK, Haque U, Kollins K, Yin H, Holzer RJ. PMID: 25257572.

View in: PubMed Mentions: 10 Fields:
Car Cardiology
Translation:Humans
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling. J Clin Invest. 2013 Aug; 123(8):3243-53. Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, Ovunc B, Frishberg Y, Soliman NA, Fathy HM, Goebel H, Hoefele J, Weber LT, Innis JW, Faul C, Han Z, Washburn J, Antignac C, Levy S, Otto EA, Hildebrandt F. PMID: 23867502; PMCID: PMC3726174.

View in: PubMed Mentions: 123 Fields:
Med Medicine (General)
Translation:Humans Animals Cells
Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients. Nephron Clin Pract. 2012; 120(3):c139-46. Ovunc B, Ashraf S, Vega-Warner V, Bockenhauer D, Elshakhs NA, Joseph M, Hildebrandt F, Gesellschaft für Pädiatrische Nephrologie (GPN) Study Group. PMID: 22584503; PMCID: PMC5593135.

View in: PubMed Mentions: 16 Fields:
Nep Nephrology
Translation:Humans
Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria. J Am Soc Nephrol. 2011 Oct; 22(10):1815-20. Ovunc B, Otto EA, Vega-Warner V, Saisawat P, Ashraf S, Ramaswami G, Fathy HM, Schoeb D, Chernin G, Lyons RH, Yilmaz E, Hildebrandt F. PMID: 21903995; PMCID: PMC3187182.

View in: PubMed Mentions: 63 Fields:
Nep Nephrology
Translation:Humans
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest. 2011 May; 121(5):2013-24. Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, Xie LX, Salviati L, Hurd TW, Vega-Warner V, Killen PD, Raphael Y, Ashraf S, Ovunc B, Schoeb DS, McLaughlin HM, Airik R, Vlangos CN, Gbadegesin R, Hinkes B, Saisawat P, Trevisson E, Doimo M, Casarin A, Pertegato V, Giorgi G, Prokisch H, Rötig A, Nürnberg G, Becker C, Wang S, Ozaltin F, Topaloglu R, Bakkaloglu A, Bakkaloglu SA, Müller D, Beissert A, Mir S, Berdeli A, Varpizen S, Zenker M, Matejas V, Santos-Ocaña C, Navas P, Kusakabe T, Kispert A, Akman S, Soliman NA, Krick S, Mundel P, Reiser J, Nürnberg P, Clarke CF, Wiggins RC, Faul C, Hildebrandt F. PMID: 21540551; PMCID: PMC3083770.

View in: PubMed Mentions: 193 Fields:
Med Medicine (General)
Translation:Humans Animals Cells
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations. Clin J Am Soc Nephrol. 2010 Sep; 5(9):1655-62. Chernin G, Vega-Warner V, Schoeb DS, Heeringa SF, Ovunc B, Saisawat P, Cleper R, Ozaltin F, Hildebrandt F, Members of the GPN Study Group. PMID: 20595692; PMCID: PMC2974408.

View in: PubMed Mentions: 48 Fields:
Nep Nephrology
Translation:Humans
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Nephrol Dial Transplant. 2010 Sep; 25(9):2970-6. Schoeb DS, Chernin G, Heeringa SF, Matejas V, Held S, Vega-Warner V, Bockenhauer D, Vlangos CN, Moorani KN, Neuhaus TJ, Kari JA, MacDonald J, Saisawat P, Ashraf S, Ovunc B, Zenker M, Hildebrandt F, Gesselschaft für Paediatrische Nephrologie (GPN) Study Group. PMID: 20172850; PMCID: PMC2948833.

View in: PubMed Mentions: 34 Fields:
Nep Nephrology Tra Transplantation
Translation:Humans
A systematic approach to mapping recessive disease genes in individuals from outbred populations. PLoS Genet. 2009 Jan; 5(1):e1000353. Hildebrandt F, Heeringa SF, Rüschendorf F, Attanasio M, Nürnberg G, Becker C, Seelow D, Huebner N, Chernin G, Vlangos CN, Zhou W, O'Toole JF, Hoskins BE, Wolf MT, Hinkes BG, Chaib H, Ashraf S, Schoeb DS, Ovunc B, Allen SJ, Vega-Warner V, Wise E, Harville HM, Lyons RH, Washburn J, Macdonald J, Nürnberg P, Otto EA. PMID: 19165332; PMCID: PMC2621355.

View in: PubMed Mentions: 102 Fields:
Gen Genetics
Translation:Humans