Heymut Omran

Overview

Best Publications

• When cilia go bad: cilia defects and ciliopathies

  Manfred Fliegauf;Thomas Benzing;Heymut Omran

  1444
  Citations

• Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma

  Genevieve Schindler;David Capper;David Capper;Jochen Meyer;Wibke Janzarik

  1296
  Citations

• Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry

  Heike Olbrich;Karsten Häffner;Andreas Kispert;Alexander Völkel

  633
  Citations

• European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.

  Jane S. Lucas;Angelo Barbato;Samuel A. Collins;Samuel A. Collins;Myrofora Goutaki;Myrofora Goutaki

  623
  Citations

• Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children.

  A. Barbato;T. Frischer;C. E. Kuehni;D. Snijders

  611
  Citations

• BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas

  Stefan Pfister;Wibke G. Janzarik;Marc Remke;Aurélie Ernst

  565
  Citations

• Mutations in antiquitin in individuals with pyridoxine-dependent seizures

  Philippa B Mills;Eduard Struys;Cornelis Jakobs;Barbara Plecko

  563
  Citations

• Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

  Ralf Birkenhäger;Edgar Otto;Maria J. Schürmann;Martin Vollmer

  559
  Citations

• SARS-CoV-2 targets neurons of 3D human brain organoids.

  Anand Ramani;Lisa Müller;Philipp Niklas Ostermann;Elke Gabriel

  508
  Citations

• Congenital Heart Disease and Other Heterotaxic Defects in a Large Cohort of Patients With Primary Ciliary Dyskinesia

  Marcus P. Kennedy;Heymut Omran;Margaret W. Leigh;Sharon Dell

  494
  Citations

• 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

  464
  Citations

• 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

  431
  Citations

• Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

  Heike Olbrich;Manfred Fliegauf;Julia Hoefele;Andreas Kispert

  428
  Citations

• Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins

  Heymut Omran;Daisuke Kobayashi;Daisuke Kobayashi;Heike Olbrich;Tatsuya Tsukahara

  419
  Citations

• To beat or not to beat: roles of cilia in development and disease

  Inés Ibañez-Tallon;Nathaniel Heintz;Heymut Omran

  410
  Citations

• Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

  Inés Ibañez-Tallon;Axel Pagenstecher;Manfred Fliegauf;Heike Olbrich

  406
  Citations

• Genetic Defects in Ciliary Structure and Function

  Maimoona A. Zariwala;Michael R. Knowles;Heymut Omran

  402
  Citations

• Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

  Carsten Bergmann;Manfred Fliegauf;Nadina Ortiz Brüchle;Valeska Frank

  379
  Citations

• DNAH5 Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects

  Nada Hornef;Heike Olbrich;Judit Horvath;Maimoona B Zariwala

  378
  Citations

• Erratum: When cilia go bad: cilia defects and ciliopathies

  Manfred Fliegauf;Thomas Benzing;Heymut Omran

  3
  Citations