Heymut Omran

Also affiliated with University Hospital Münster, Children's Clinical University Hospital

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 19 papers. Top paper: “An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes”.

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201

N/A

0.831DataRank · unranked

253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

American Journal of Respiratory and Critical Care Medicine(2024)10.1164/rccm.202308-1370oc

N/A

0.775DataRank · unranked

15 citations

Lawrence E. Ostrowski, Tabea Nöthe-Menchen, Johanna Raidt, Andre Schramm, Heike Olbrich +36 more

Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.03.045

N/A

0.672DataRank · unranked

87 citations

Janet Chou, Laura Faletti, Veronika Haunerdinger, Lennart Opitz, Pascal Joset +55 more

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

Disease Models & Mechanisms(2020)10.1242/dmm.045344

N/A

0DataRank · unranked

17 citations

Marshall Lukacs, Sandra Cindrić, Heymut Omran, Rolf W. Stottmann, Zakia Abdelhamed

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

MPG.PuRe (Max Planck Society)(2020)10.17615/9tbv-k579

N/A

0DataRank · unranked

18 citations

Stylianos E. Antonarakis, Nada Hornef, Ralf Sudbrak, Johannes H. Wildhaber, Marcus P. Kennedy +15 more

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia

UNC Libraries(2020)10.17615/mt0m-xq59

N/A

0DataRank · unranked

2 citations

Bernhard Rindlisbacher, David Rigau, Heymut Omran, Kim G. Nielsen, Daan Caudri +27 more

Mutations of DNAI1 in Primary Ciliary Dyskinesia: Evidence of Founder Effect in a Common Mutation

UNC Libraries(2020)10.17615/evkw-v287

N/A

0DataRank · unranked

0 citations

Heike Olbrich, Anne-Marie Bridoux, Franck Ceppa, Lucy C. Morgan, Michael R. Knowles +20 more

Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia

UNC Libraries(2020)10.17615/4v2s-3a32

N/A

0DataRank · unranked

0 citations

Heike Olbrich, Manfred Fliegauf, Heymut Omran, Marcus P. Kennedy, Michael R. Knowles +3 more

DYX1C1 is required for axonemal dynein assembly and ciliary motility

UNC Libraries(2020)10.17615/z79a-w507

N/A

0DataRank · unranked

0 citations

Cecilia Lo, Hannah M. Mitchison, Michael R. Knowles, Maimoona A. Zariwala, Ronald Roepman +6 more

High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

UNC Libraries(2020)10.17615/k10x-s565

N/A

0DataRank · unranked

0 citations

Heymut Omran, Patricia S. Connelly, Nadav Kravitz, Mathew P. Daniels, Iman Sami +23 more

Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

UNC Libraries(2020)10.17615/3853-0b14

N/A

0DataRank · unranked

0 citations

Niki T. Loges, Margaret W. Leigh, Angelina Heer, Hanswalter Zentgraf, Richard Reinhardt +12 more

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

UNC Libraries(2021)10.17615/tf25-rz86

N/A

0DataRank · unranked

18 citations

Johnny L. Carson, Niki T. Loges, Thomas W. Ferkol, Margaret Rosenfeld, Maimoona A. Zariwala +16 more

Consensus nomenclature for dyneins and associated assembly factors

The Journal of Cell Biology(2022)10.1083/jcb.202109014

N/A

0DataRank · unranked

66 citations

Heymut Omran, George B. Witman, Gregory J. Pazour, K. Kevin Pfister, Elspeth A. Bruford +2 more

Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities

Genetics in Medicine(2022)10.1016/j.gim.2022.07.019

N/A

0DataRank · unranked

12 citations

Rim Hjeij, Asaf Vivante, Elizabeth A. Bearce, Laura A. Dyer, Jiaolong Wang +24 more

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

Science(2024)10.1126/science.adf5489

N/A

0DataRank · unranked

48 citations

Sabrina Méchaussier, Patricia L. Yeyati, Fraser McPhie, Jacob R. Anderson, Chen Jing Khoo +75 more

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module

Nature Communications(2020)10.1038/s41467-020-19113-0

N/A

0DataRank · unranked

99 citations

Katsutoshi Mizuno, Tabea Nöthe-Menchen, Yayoi Ikawa, Karsten Boldt, Asaf Ta‐Shma +46 more

Primary Ciliary Dyskinesia

Airway Diseases(2023)10.1007/978-3-031-22483-6_105-1

N/A

0DataRank · unranked

0 citations

Yasemin Gökdemir, Heymut Omran, Emine Atağ

A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance

Nature Medicine(2020)10.1038/s41591-019-0730-x

N/A

0DataRank · unranked

75 citations

Daniel T. Montoro, Hui Min Leung, Jason Yang, Hanan E. Shamseldin, Martin S. Taylor +16 more

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Human Mutation(2020)10.1002/humu.24127

N/A

0DataRank · unranked

21 citations

Lokuliyange D. S. Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma Mujezinović Larsen +25 more