ScholarIQanswers from OpenAlex & ORCID
Dominik S. Schoeb
ResearcherPublications, citations & collaboration network
Dominik S. Schoeb is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Dominik S. Schoeb have?
ScholarIQindexed works
Dominik S. Schoeb has 63 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Dominik S. Schoeb have?
ScholarIQcitation count
Dominik S. Schoeb has 1,719 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Dominik S. Schoeb?
ScholarIQh-index
Dominik S. Schoeb has an h-index of 17 in OpenAlex.
What is the i10-index of Dominik S. Schoeb?
ScholarIQi10-index
Dominik S. Schoeb has an i10-index of 24 in OpenAlex.
What is the ORCID of Dominik S. Schoeb?
ScholarIQorcid
The ORCID for Dominik S. Schoeb is on the source record.
What is the OpenAlex record for Dominik S. Schoeb?
ScholarIQopenalex
The OpenAlex for Dominik S. Schoeb is on the source record.
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
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
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
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
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