Publications by authors named "Bugsu Ovunc"

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Pediatric P-ANCA vasculitis following COVID-19.
Yaron Fireizen, Cyrus Shahriary, Maria E Imperial, Inderpal Randhawa, Nastasia Nianiaris, Bugsu Ovunc

Pediatr Pulmonol· October 2021

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Quality metrics in cardiac catheterization for congenital heart disease: utility of 30-day mortality.
Carl H Backes, Lisa Bergersen, Jonathan J Rome, Sarosh P Batlivala, Andrew C Glatz, Bugsu Ovunc

Catheter Cardiovasc Interv· January 2015

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ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.
Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf, Toby W Hurd, Virginia Vega-Warner, Bugsu Ovunc

J Clin Invest· August 2013

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Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.
Bugsu Ovunc, Shazia Ashraf, Virginia Vega-Warner, Detlef Bockenhauer, Neveen A Soliman Elshakhs

Nephron Clin Pract· February 2013

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Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.
Bugsu Ovunc, Edgar A Otto, Virginia Vega-Warner, Pawaree Saisawat, Shazia Ashraf

J Am Soc Nephrol· October 2011

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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
Saskia F Heeringa, Gil Chernin, Moumita Chaki, Weibin Zhou, Alexis J Sloan, Bugsu Ovunc

J Clin Invest· May 2011

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Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
Dominik S Schoeb, Gil Chernin, Saskia F Heeringa, Verena Matejas, Susanne Held, Bugsu Ovunc

Nephrol Dial Transplant· September 2010

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Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Gil Chernin, Virginia Vega-Warner, Dominik S Schoeb, Saskia F Heeringa, Bugsu Ovunc

Clin J Am Soc Nephrol· September 2010

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A systematic approach to mapping recessive disease genes in individuals from outbred populations.
Friedhelm Hildebrandt, Saskia F Heeringa, Franz Rüschendorf, Massimo Attanasio, Gudrun Nürnberg, Bugsu Ovunc

PLoS Genet· January 2009

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