Heymut Omran

26.4k total citations · 3 hit papers
176 papers, 10.2k citations indexed

About

Heymut Omran is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Heymut Omran has authored 176 papers receiving a total of 10.2k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Genetics, 80 papers in Pulmonary and Respiratory Medicine and 75 papers in Molecular Biology. Recurrent topics in Heymut Omran's work include Genetic and Kidney Cyst Diseases (86 papers), Cystic Fibrosis Research Advances (73 papers) and Neonatal Respiratory Health Research (37 papers). Heymut Omran is often cited by papers focused on Genetic and Kidney Cyst Diseases (86 papers), Cystic Fibrosis Research Advances (73 papers) and Neonatal Respiratory Health Research (37 papers). Heymut Omran collaborates with scholars based in Germany, United States and United Kingdom. Heymut Omran's co-authors include Manfred Fliegauf, Thomas Benzing, Heike Olbrich, Maimoona A. Zariwala, Michael R. Knowles, Niki T. Loges, Jane S. Lucas, Claudius Werner, Andreas Kispert and Kim G. Nielsen and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Heymut Omran

163 papers receiving 10.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

When cilia go bad: cilia defects and ciliopathies

2007 932 citations Manfred Fliegauf, Thomas Benzing et al. profile →
Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma

2011 739 citations Heymut Omran et al. profile →
Motile ciliopathies

2020 204 citations Julia Wallmeier, Kim G. Nielsen et al. profile →

Peers

Countries citing papers authored by Heymut Omran

Since Specialization

Citations

This map shows the geographic impact of Heymut Omran's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Heymut Omran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heymut Omran more than expected).

Fields of papers citing papers by Heymut Omran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heymut Omran. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Heymut Omran. The network helps show where Heymut Omran may publish in the future.

Co-authorship network of co-authors of Heymut Omran

This figure shows the co-authorship network connecting the top 25 collaborators of Heymut Omran. A scholar is included among the top collaborators of Heymut Omran based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Heymut Omran. Heymut Omran is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Primary Ciliary Dyskinesia Associated Disease-Causing Variants in CCDC39 and CCDC40 Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7 2024 ·Cells ·(unknown), Inga M. Höben, Alexander Wolter, Niki T. Loges, Heike Olbrich, Isabella Aprea, Bernd Dworniczak, Johanna Raidt, Heymut Omran	2
2	Long-Term Lung Function and Pseudomonas aeruginosa Infection in Genotyped Primary Ciliary Dyskinesia 2024 ·Annals of the American Thoracic Society ·(unknown), June K. Marthin, Johanna Raidt, Tavs Qvist, Helle Krogh Johansen, Heymut Omran, Kim G. Nielsen	2
3	Primary ciliary dyskinesia 2023 ·La Presse Médicale ·Johanna Raidt, Niki T. Loges, Heike Olbrich, Julia Wallmeier, Petra Pennekamp, Heymut Omran	17
4	Pathogenic variants in CLXN encoding the outer dynein arm docking–associated calcium-binding protein calaxin cause primary ciliary dyskinesia 2023 ·Genetics in Medicine ·Rim Hjeij, Isabella Aprea, Marco Poeta, Tabea Nöthe-Menchen, (unknown), Johanna Raidt, (unknown), Gerard W. Dougherty, Heike Olbrich, Oliver Schwartz, Ulrike Keller, Harald Nüsse, Karin E. M. Diderich, Christian Vogelberg, Francesca Santamaria, Heymut Omran	6
5	Male minipuberty in human and non-human primates: planting the seeds of future fertility 2023 ·Reproduction ·Alexander S. Busch, (unknown), Nina Neuhaus, Joachim Wistuba, Stefan Schlatt, Anders Juul, Heymut Omran	5
6	Amiodarone–sirolimus interaction in a neonate with tuberous sclerosis complex 2022 ·Cardiology in the Young ·Daniel Ebrahimi‐Fakhari, Hans-Gerd Kehl, Heymut Omran	0
7	Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility 2021 ·PLoS Genetics ·Isabella Aprea, Johanna Raidt, Inga M. Höben, Niki T. Loges, Tabea Nöthe-Menchen, Petra Pennekamp, Heike Olbrich, Thomas Kaiser, (unknown), Frank Tüttelmann, Judit Horváth, Maria Schubert, Claudia Krallmann, Sabine Kliesch, Heymut Omran	58
8	A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice 2020 ·Disease Models & Mechanisms ·Zakia Abdelhamed, (unknown), Sandra Cindrić, Heymut Omran, Rolf W. Stottmann	11
9	Registries and collaborative studies for primary ciliary dyskinesia in Europe 2020 ·ERJ Open Research ·Cristina Ardura‐Garcia, Myrofora Goutaki, S.B. Carr, Suzanne Crowley, Florian S. Halbeisen, Kim G. Nielsen, Petra Pennekamp, Johanna Raidt, Guillaume Thouvenin, Panayiotis K. Yiallouros, Heymut Omran, Claudia E. Kuehni	19
10	SPEF2- and HYDIN -Mutant Cilia Lack the Central Pair–associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics 2019 ·American Journal of Respiratory Cell and Molecular Biology ·Sandra Cindrić, Gerard W. Dougherty, Heike Olbrich, Rim Hjeij, Niki T. Loges, Israel Amirav, (unknown), June K. Marthin, Kim G. Nielsen, Sivagurunathan Sutharsan, Johanna Raidt, Claudius Werner, Petra Pennekamp, Bernd Dworniczak, Heymut Omran	49
11	Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis 2019 ·Journal of Clinical Investigation ·Martin D. Burkhalter, Arthi Sridhar, (unknown), (unknown), (unknown), Cornelia Donow, (unknown), Maja Hempel, Paul Walther, Petra Pennekamp, Heymut Omran, Susana S. Lopes, Stephanie M. Ware, Melanie Philipp	42
12	Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect 2017 ·Human Mutation ·Christine Edelbusch, Sandra Cindrić, Gerard W. Dougherty, Niki T. Loges, Heike Olbrich, Joseph Rivlin, Julia Wallmeier, Petra Pennekamp, Israel Amirav, Heymut Omran	49
13	Cyclin O ( Ccno ) functions during deuterosome‐mediated centriole amplification of multiciliated cells 2015 ·The EMBO Journal ·Maja C. Funk, (unknown), Tabea Menchen, Georg Kuales, Kerstin Thriene, Soeren S. Lienkamp, Jörn Dengjel, Heymut Omran, Marcus Frank, Sebastian J. Arnold	67
14	Creating a large multinational dataset of patients with primary ciliary dyskinesia (PCD) 2014 ·European Respiratory Journal ·Elisabeth Maurer, Myrofora Goutaki, Laura Behan, Mieke Boon, Carmen Casaulta, Margaret W. Leigh, Lucy Morgan, Kim G. Nielsen, Heymut Omran, Francesca Santamaria, Nicolaus Schwerk, Panayiotis K. Yiallouros, Claudia E. Kuehni	0
15	Factors influencing age at diagnosis of primary ciliary dyskinesia in European children 2010 ·European Respiratory Journal ·Claudia E. Kuehni, T. Frischer, Marie‐Pierre F. Strippoli, Elisabeth Maurer, Andrew Bush, Kim G. Nielsen, Amparo Escribano, Jane S. Lucas, Panayiotis K. Yiallouros, Heymut Omran, E. Eber, C O’Callaghan, Deborah Snijders, A Barbato	218
16	Immunofluorescence Staining of Ciliated Respiratory Epithelial Cells 2009 ·Methods in cell biology ·Heymut Omran, Niki T. Loges	25
17	Congenital Heart Disease and Other Heterotaxic Defects in a Large Cohort of Patients With Primary Ciliary Dyskinesia 2007 ·Circulation ·Marcus P. Kennedy, Heymut Omran, Margaret W. Leigh, Sharon Dell, Lucy Morgan, Paul L. Molina, B. Robinson, Susan L. Minnix, Heike Olbrich, Thomas Severin, Peter Ahrens, Lars Lange, (unknown), Peadar G. Noone, Maimoona A. Zariwala, Michael R. Knowles	275
18	The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth 2006 ·The Journal of Cell Biology ·Bernhard Schermer, Cristina Ghenoiu, Malte P. Bartram, Roman Ulrich Müller, Fruzsina Kotsis, Martin Höhne, W Kühn, (unknown), Roland Nitschke, Hanswalter Zentgraf, Manfred Fliegauf, Heymut Omran, Gerd Walz, Thomas Benzing	145
19	A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome 2006 ·Human Genetics ·Bartłomiej Budny, Wei Chen, Heymut Omran, Manfred Fliegauf, Andreas Tzschach, Marzena Wiśniewska, Lars Riff Jensen, Martine Raynaud, Sarah A. Shoichet, (unknown), Steffen Lenzner, Anna Latos‐Bieleńska, Hans‐Hilger Ropers	122
20	Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia 2005 ·American Journal of Respiratory and Critical Care Medicine ·Manfred Fliegauf, Heike Olbrich, Judit Horváth, Johannes H. Wildhaber, Maimoona A. Zariwala, Marcus P. Kennedy, Michael R. Knowles, Heymut Omran	199

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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