Ute Hehr

7.9k citations

86 papers · 2.6k indexed · h-index 27

Molecular Biology top 5%
Genetics top 2%
Cellular and Molecular Neuroscience top 5%
Genetics top 5%
Cell Biology top 5%

Co-authors: Maximilian Muenke Jürgen Winkler Erich Roessler Gabriele Gillessen‐Kaesbach Claudia Groß Luisa Nanni Deeann Wallis Antônio Richieri‐Costa
Topics: Muscle Physiology and Disorders (15 papers)Cleft Lip and Palate Research (10 papers)Hedgehog Signaling Pathway Studies (10 papers)
Cited by: Genetics Cellular and Molecular Neuroscience
Journals: Nature Communications Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Germany United States Türkiye

In The Last Decade

Ute Hehr

83 papers receiving 2.5k citations

Peers

Countries citing papers authored by Ute Hehr

Since Specialization

Citations

This map shows the geographic impact of Ute Hehr'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 Ute Hehr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ute Hehr more than expected).

Fields of papers citing papers by Ute Hehr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ute Hehr. 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 Ute Hehr. The network helps show where Ute Hehr may publish in the future.

Co-authorship network of co-authors of Ute Hehr

This figure shows the co-authorship network connecting the top 25 collaborators of Ute Hehr. A scholar is included among the top collaborators of Ute Hehr 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 Ute Hehr. Ute Hehr 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	Late‐onset Krabbe disease presenting as spastic paraplegia – implications of GCase and CTSB/D 2024 ·Annals of Clinical and Translational Neurology ·(unknown),(unknown),Ute Hehr,Alexander Weiß,Matthias Kettwig,Lucia Laugwitz,Samuel Groeschel,Manuel Schmidt,Philipp Arnold,Martin Regensburger,Friederike Zunke	0
2	Heterogenous Disease Course and Long-Term Outcome of Children’s Interstitial Lung Disease Related to Filamin A Gene Variants 2022 ·Annals of the American Thoracic Society ·Julia Carlens,(unknown),Andrew Bush,Diane M. Renz,Ute Hehr,Florian Laenger,Claire Hogg,Martin Wetzke,Nicolaus Schwerk,Jonathan H. Rayment	10
3	MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease 2021 ·European Journal of Medical Genetics ·(unknown),Gökhan Yigit,(unknown),Janine Altmüller,Hölger Thiele,Peter Nürnberg,Nursel Elçioğlu,(unknown),Ute Hehr,Anja Stein,Adela Della Marina,Angela Köninger,Christel Depienne,Frank J. Kaiser,Bernd Wollnik,Alma Kuechler	6
4	CARASIL with coronary artery disease and distinct cerebral microhemorrhage: A case report and literature review 2020 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),(unknown),(unknown),Ute Hehr,Jan Liman,Gerd Hasenfuß,Mathias Bähr,Christian Heiner Riedel,Jan Christoph Koch	4
5	The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy 2019 ·Orphanet Journal of Rare Diseases ·(unknown),Ulrike Hüffmeier,Regina Trollmann,Ute Hehr,Steffen Uebe,Arif B. Ekici,Cornelia Kraus,Mandy Krumbiegel,André Reis,Christian T. Thiel,Bernt Popp	42
6	Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction 2015 ·The American Journal of Human Genetics ·K. Nicole Weaver,Kristin E. Noack Watt,Robert B. Hufnagel,Joaquín Navajas Acedo,Luke L. Linscott,Kristen L. Sund,Patricia L. Bender,Rainer König,Charles Marques Lourenço,Ute Hehr,Robert J. Hopkin,Dietmar Lohmann,Paul A. Trainor,Dagmar Wieczorek,Howard M. Saal	54
7	Taking the next step forward – Diagnosing inherited infantile cholestatic disorders with next generation sequencing 2015 ·Molecular and Cellular Probes ·(unknown),(unknown),Carsten Posovszky,Frank Jochum,(unknown),Josef Schroeder,Thomas F.E. Barth,Ute Hehr,Michael Melter,(unknown)	30
8	Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy 2013 ·Neurogenetics ·Tobias Geis,Klaus Marquard,(unknown),(unknown),(unknown),Thekla von Kalle,Antje Bornemann,Ute Hehr,Markus Blankenburg	52
9	Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome 2010 ·Nature Genetics ·Johannes G. Dauwerse,Jill Dixon,Saskia Seland,Claudia Ruivenkamp,Arie van Haeringen,Lies H. Hoefsloot,Dorien J.M. Peters,(unknown),Cornelia Daumer‐Haas,Robert Maiwald,Christiane Zweier,Bronwyn Kerr,Ana María Cobo,Joaquín Fernández Toral,A. Jeannette M. Hoogeboom,Dietmar Lohmann,Ute Hehr,Michael J. Dixon,Martijn H. Breuning,Dagmar Wieczorek	243
10	Polar Body Diagnosis for Monogenic Disorders in Regensburg 2009 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·Andreas Hehr,Burkhardt Seifert,Ute Hehr,M. Bals‐Pratsch	2
11	Andermann Syndrome can be a Phenocopy of Hereditary Motor and Sensory Neuropathy – Report of a Discordant Sibship with a Compound Heterozygous Mutation of theKCC3Gene 2009 ·Neuropediatrics ·Sabine Rudnik‐Schöneborn,Ute Hehr,Thekla von Kalle,A. Bornemann,Jürgen Winkler,Klaus Zerres	16
12	Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and mental retardation—New MCA/MR syndrome in two affected sibs and a mildly affected mother? 2007 ·American Journal of Medical Genetics Part A ·Dagmar Wieczorek,Charles Shaw‐Smith,Jürgen Kohlhase,W Schmitt,Karin Buiting,Alison J. Coffey,Eleanor Howard,Ute Hehr,Gabriele Gillessen‐Kaesbach	12
13	Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K) 2006 ·UCL Discovery (University College London) ·Sebahattin Çirak,G. Uyanık,Ralf Herrmann,Claudia Groß,Ute Hehr,T. Voit	1
14	Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome 2006 ·Neurology ·G. Uyanık,Nursel Elçioğlu,Johannes Penzien,(unknown),(unknown),(unknown),Ercan Demir,(unknown),K. Scheglmann,Beate Winner,Ulrich Bogdahn,Haluk Topaloğlu,Ute Hehr,Jürgen Winkler	51
15	A case of Walker–Warburg syndrome resulting from a homozygous POMT1 mutation 2006 ·European Journal of Paediatric Neurology ·Uluç Yiş,Gökhan Uyanık,Semra Hız Kurul,Eray Dırık,Erdener Özer,Claudia Groß,Ute Hehr	10
16	Empfehlungen zur genetischen Diagnostik bei Aborten 2005 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·Peter Wieacker,(unknown),Ute Hehr,(unknown)	1
17	Stellungnahme der Arbeitsgemeinschaft Reproduktionsgenetik der Deutschen Gesellschaft für Reproduktionsmedizin: Empfehlung zur genetischen Diagnostik bei Kinderwunschpaaren 2004 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·Michael Ludwig,Jörg Gromoll,Ute Hehr,Peter Wieacker	3
18	X-Linked Lissencephaly with Abnormal Genitalia Associated with Renal Phosphate Wasting 2004 ·Neuropediatrics ·Andrew D. Hahn,(unknown),Gökhan Uyanık,Ute Hehr,(unknown),G. Alzen,Bernd A. Neubauer	13
19	Agenesis of the Corpus Callosum, Abnormal Genitalia and Intractable Epilepsy due to a Novel Familial Mutation in the Aristaless-Related Homeobox Gene 2004 ·Neuropediatrics ·Hans Hartmann,G. Uyanık,(unknown),Ute Hehr,Thomas Lücke,Mine Arslan‐Kirchner,(unknown),Anibh M. Das,Jürgen Winkler	23
20	Craniosynostosis Syndromes: From Genes to Premature Fusion of Skull Bones 1999 ·Molecular Genetics and Metabolism ·Ute Hehr,Maximilian Muenke	71

About Ute Hehr

Ute Hehr is a scholar working on Genetics, Cellular and Molecular Neuroscience and Genetics, having authored 86 papers that have together received 2.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (15 papers), Cleft Lip and Palate Research (10 papers) and Hedgehog Signaling Pathway Studies (10 papers). The work is most often cited by research in Genetics (948 citations), Cellular and Molecular Neuroscience (541 citations) and Genetics (307 citations). Ute Hehr has collaborated with scholars based in Germany, United States and Türkiye. Frequent co-authors include Maximilian Muenke, Jürgen Winkler, Erich Roessler, Gabriele Gillessen‐Kaesbach, Claudia Groß, Luisa Nanni, Deeann Wallis, Antônio Richieri‐Costa, Tim Wiltshire and Johanna M. Rommens. Their work appears in journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

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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