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How has Dominik S. Schoeb's publication output changed over time?
ScholarIQpublication output · 2009–2021
Output grew100% over the shown period — from 1 works in 2009 to 2 in 2021.
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20092010201120132018201920202021
What are the most-cited papers on Dominik S. Schoeb?
ScholarIQmost cited works
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
Saskia F. Heeringa, Gil Chernin, Moumita Chaki, Weibin Zhou, Alexis Sloan, Ziming Ji, Letian Xie, Leonardo Salviati, Toby W. Hurd, Virginia Vega-Warner, Paul D. Killen, Yehoash Raphael, Shazia Ashraf, Buğsu Övünç, Dominik S. Schoeb, Heather M. McLaughlin, Rannar Airik, Christopher N. Vlangos, Rasheed Gbadegesin, Bernward Hinkes, Pawaree Saisawat, Eva Trevisson, Mara Doimo, Alberto Casarin, Vanessa Pertegato, Gianpietro Giorgi, Holger Prokisch, Agnès Rötig, Gudrun Nürnberg, Christian Becker, Su Wang, Fatih Özaltın, Rezan Topaloğlu, Ayşı̇n Bakkaloğlu, Sevcan A. Bakkaloğlu, Dominik N. Müller, Antje Beissert, Sevgı Mır, Afig Berdelı, Seza πzen, Martin Zenker, Verena Matejas, Carlos Santos‐Ocaña, Plácido Navas, Takehiro Kusakabe, Andreas Kispert, Sema Akman, Neveen A. Soliman, Stefanie Krick, Peter Mündel, Jochen Reiser, Peter Nürnberg, Catherine F. Clarke, Roger C. Wiggins, Christian Faul, Friedhelm Hildebrandt
S114430552. 2011404 CitationsOPEN ACCESS
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf, Toby W. Hurd, Virginia Vega-Warner, Humphrey Fang, Bodo B. Beck, Olivier Gribouval, Weibin Zhou, Katrina A. Diaz, S. Natarajan, Roger C. Wiggins, Svjetlana Lovric, Gil Chernin, Dominik S. Schoeb, Buğsu Övünç, Yaacov Frishberg, Neveen A. Soliman, Hanan Fathy, Heike Goebel, Julia Hoefele, Lutz T. Weber, Jeffrey W. Innis, Christian Faul, Zhe Han, Joseph Washburn, Corinne Antignac, Shawn Levy, Edgar A. Otto, Friedhelm Hildebrandt
S114430552. 2013241 CitationsOPEN ACCESS
A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations
Friedhelm Hildebrandt, Saskia F. Heeringa, Franz Rüschendorf, Massimo Attanasio, Gudrun Nürnberg, Christian Becker, Dominik Seelow, Norbert Huebner, Gil Chernin, Christopher N. Vlangos, Weibin Zhou, John F. O’Toole, Bethan E. Hoskins, Matthias T. F. Wolf, Bernward Hinkes, Hassan Chaı̈b, Shazia Ashraf, Dominik S. Schoeb, Buğsu Övünç, Susan J. Allen, Virginia Vega-Warner, Eric L. Wise, Heather M. Harville, Robert H. Lyons, Joseph Washburn, James W. MacDonald, Peter Nürnberg, Edgar A. Otto
S103870658. 2009166 CitationsOPEN ACCESS
Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
Gil Chernin, Virginia Vega-Warner, Dominik S. Schoeb, Saskia F. Heeringa, Buğsu Övünç, Pawaree Saisawat, Roxana Cleper, Fatih Özaltın, Friedhelm Hildebrandt
Clinical Journal of the American Society of Nephrology. 2010123 CitationsOPEN ACCESS
Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria
Buğsu Övünç, Edgar A. Otto, Virginia Vega-Warner, Pawaree Saisawat, Shazia Ashraf, Gokul Ramaswami, Hanan Fathy, Dominik S. Schoeb, Gil Chernin, Robert H. Lyons, Engin Yılmaz, Friedhelm Hildebrandt
Journal of the American Society of Nephrology. 2011113 CitationsOPEN ACCESS
Related on ScholarIQ
University of Freiburg
Institution
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
Paper
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
Paper
A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations
Paper
Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
Paper
Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria
Paper