ScholarIQanswers from OpenAlex
Uniwersytecki Szpital Dziecięcy
InstitutionResearch output, impact & collaborations
Uniwersytecki Szpital Dziecięcy is a institution indexed in ScholarIQ from OpenAlex.
What is known about Uniwersytecki Szpital Dziecięcy?
ScholarIQrecord summary
Uniwersytecki Szpital Dziecięcy is a research organisation in Krakow, PL. OpenAlex records 3,485 works and 154,231 citations for it. 993 researchers list it as their most recent affiliation.
How many works does Uniwersytecki Szpital Dziecięcy have?
ScholarIQindexed works
Uniwersytecki Szpital Dziecięcy has 3,485 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Uniwersytecki Szpital Dziecięcy have?
ScholarIQcitation count
Uniwersytecki Szpital Dziecięcy has 154,231 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Uniwersytecki Szpital Dziecięcy?
ScholarIQresearcher count
Uniwersytecki Szpital Dziecięcy has 993 researchers in the ScholarIQ index.
What is the average h-index at Uniwersytecki Szpital Dziecięcy?
ScholarIQavg h-index
Uniwersytecki Szpital Dziecięcy has an average h-index of 85.5 in OpenAlex.
What is the ROR of Uniwersytecki Szpital Dziecięcy?
ScholarIQror
The ROR for Uniwersytecki Szpital Dziecięcy is on the source record.
What is the OpenAlex record for Uniwersytecki Szpital Dziecięcy?
ScholarIQopenalex
The OpenAlex for Uniwersytecki Szpital Dziecięcy is on the source record.
Who are the most-cited researchers behind Uniwersytecki Szpital Dziecięcy?
ScholarIQtop researchers by citations
What are the most-cited papers on Uniwersytecki Szpital Dziecięcy?
ScholarIQmost cited works
When cilia go bad: cilia defects and ciliopathies
Manfred Fliegauf, Thomas Benzing, Heymut Omran
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann, Martin Vollmer, Eva-Maria Ruf, Irina Maier-Lutz, Frank Beekmann, Andrea Fekete, Heymut Omran, Delphine Feldmann, David V. Milford, Nicola Jeck, Martin Konrad, Daniel Landau, Nine V.A.M. Knoers, Corinne Antignac, Ralf Sudbrak, Andreas Kispert, Friedhelm Hildebrandt
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
Edgar A. Otto, Bart Loeys, Hemant Khanna, Jan Hellemans, Ralf Sudbrak, Shuling Fan, Ulla Muerb, John F. O’Toole, Juliana Helou, Massimo Attanasio, Boris Utsch, John A. Sayer, Concepción Lillo, David Jimeno, Paul Coucke, Anne De Paepe, Richard Reinhardt, Sven Klages, Motoyuki Tsuda, I. Kawakami, Takehiro Kusakabe, Heymut Omran, Anita Imm, Melissa Tippens, Pamela A. Raymond, JO Hill, Phil Beales, Shirley He, Andreas Kispert, Benjamin Margolis, David S. Williams, Anand Swaroop, Friedhelm Hildebrandt
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Rachel H. Giles, Rui Chen, Gisela G. Slaats, Hui Wang, Toby W. Hurd, Weibin Zhou, Andrew Cluckey, Heon Yung Gee, Gokul Ramaswami, Chen‐Jei Hong, Bruce A. Hamilton, Igor Červenka, Ranjani Sri Ganji, Vı́tězslav Bryja, Heleen H. Arts, Jeroen van Reeuwijk, Machteld M. Oud, Stef J.F. Letteboer, Ronald Roepman, Hervé Husson, Oxana Ibraghimov‐Beskrovnaya, Takayuki Yasunaga, Gerd Walz, Lorraine Eley, John A. Sayer, Bernhard Schermer, Max C. Liebau, Thomas Benzing, Stéphanie Le Corre, Iain A. Drummond, Sabine Janssen, Susan J. Allen, S. Natarajan, John F. O’Toole, Massimo Attanasio, Sophie Saunier, Corinne Antignac, Robert K. Koenekoop, Huanan Ren, Irma López, Ahmet Nayır, Corinne Stoetzel, Hélène Dollfus, Rustin Massoudi, Joseph G. Gleeson, Sharon Andreoli, D Doherty, Anna Lindstrad, Christelle Golzio, Nicholas Katsanis, Lars Pape, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, Heymut Omran, Eva Y.-H.P. Lee, Shaohui Wang, JoAnn Sekiguchi, Rudel A. Saunders, Colin A. Johnson, Elizabeth Garner, Katja Vanselow, Jens Andersen, Joseph Shlomai, Gudrun Nürnberg, Peter Nürnberg, Shawn Levy, Agata Smogorzewska, Edgar A. Otto, Friedhelm Hildebrandt
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
Heike Olbrich, Manfred Fliegauf, Julia Hoefele, Andreas Kispert, Edgar A. Otto, Andreas Volz, Matthias T. F. Wolf, Gürsel Sasmaz, Ute Trauer, Richard Reinhardt, Ralf Sudbrak, Corinne Antignac, Norbert Gretz, Gerd Walz, Bernhard Schermer, Thomas Benzing, Friedhelm Hildebrandt, Heymut Omran
How much of the research on Uniwersytecki Szpital Dziecięcy is open access?
ScholarIQopen access share
60%OPEN ACCESS