ScholarIQanswers from OpenAlex & ORCID
Heymut Omran
ResearcherPublications, citations & collaboration network
Heymut Omran is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Heymut Omran have?
ScholarIQindexed works
Heymut Omran has 434 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Heymut Omran have?
ScholarIQcitation count
Heymut Omran has 27,066 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Heymut Omran?
ScholarIQh-index
Heymut Omran has an h-index of 89 in OpenAlex.
What is the i10-index of Heymut Omran?
ScholarIQi10-index
Heymut Omran has an i10-index of 200 in OpenAlex.
What is the ORCID of Heymut Omran?
ScholarIQorcid
The ORCID for Heymut Omran is on the source record.
What is the OpenAlex record for Heymut Omran?
ScholarIQopenalex
The OpenAlex for Heymut Omran is on the source record.
What are the most-cited papers on Heymut Omran?
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