Ulrike Orth

2.5k total citations · 1 hit paper
38 papers, 1.7k citations indexed

About

Ulrike Orth is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ulrike Orth has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 12 papers in Genetics and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ulrike Orth's work include Retinal Development and Disorders (8 papers), Neurological diseases and metabolism (5 papers) and Hereditary Neurological Disorders (5 papers). Ulrike Orth is often cited by papers focused on Retinal Development and Disorders (8 papers), Neurological diseases and metabolism (5 papers) and Hereditary Neurological Disorders (5 papers). Ulrike Orth collaborates with scholars based in Germany, United States and Netherlands. Ulrike Orth's co-authors include Andreas Gal, Eckart Apfelstedt-Sylla, Yun Li, Debra A. Thompson, Samuel G. Jacobson, Douglas Vollrath, E. Schwinger, Kerstin Kutsche, Thomas Rosenberg and Wolfgang Baehr and has published in prestigious journals such as Nature Genetics, Neuroscience and The American Journal of Human Genetics.

In The Last Decade

Ulrike Orth

38 papers receiving 1.7k 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.

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

2000 539 citations Andreas Gal, Yun Li et al. Nature Genetics profile →

Peers

Countries citing papers authored by Ulrike Orth

Since Specialization

Citations

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

Fields of papers citing papers by Ulrike Orth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Orth

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrike Orth. A scholar is included among the top collaborators of Ulrike Orth 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 Ulrike Orth. Ulrike Orth 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	Mutations inTOPORS: A Rare Cause of Autosomal Dominant Retinitis Pigmentosa in Continental Europe? 2009 ·Ophthalmic Genetics ·Claudia Schob, Ulrike Orth, Andreas Gal, Stefan Kindler, Christina Chakarova, Shomi S. Bhattacharya, Klaus Rüther	7
2	Mother and daughter with a terminal Xp deletion: Implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome 2007 ·European Journal of Medical Genetics ·Isabella Wimplinger, Anita Rauch, Ulrike Orth, (unknown), Udo Trautmann, Kerstin Kutsche	29
3	Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome 2006 ·The American Journal of Human Genetics ·Isabella Wimplinger, Manuela Morleo, Georg Rosenberger, Daniela Iaconis, Ulrike Orth, Peter Meinecke, Israela Lerer, Andrea Ballabio, Andreas Gal, Brunella Franco, Kerstin Kutsche	81
4	Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNA 2005 ·Neuroscience ·Christoph Hübner, (unknown), Ulrike Orth, Klaus Zerres, Horst Urbach, Andreas Gal, Sabine Rudnik‐Schöneborn	10
5	Analysis of the frizzled–4 gene in patients with autosomal dominant exudative vitreoretinopathy (FEVR) suggests a mutation hot spot and a high penetrance of the mutated allele. 2004 ·Investigative Ophthalmology & Visual Science ·A. Gal, Ulrike Orth, (unknown), H. Gerding, H. Laqua, C. E. van Nouhuys	1
6	Familiäre Foveahypoplasie - Klinische Einordnung 2003 ·Klinische Monatsblätter für Augenheilkunde ·(unknown), Ulrike Orth, (unknown), Andreas Gal	8
7	Sudden death due to cerebrotendinous xanthomatosis confirmed by mutation analysis 2000 ·International Journal of Legal Medicine ·Jan Sperhake, Jakob Matschke, Ulrike Orth, Andreas Gal, Klaus Püschel	7
8	Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa breakdown → 2000 ·Nature Genetics ·Andreas Gal, Yun Li, Debra A. Thompson, (unknown), Ulrike Orth, Samuel G. Jacobson, Eckart Apfelstedt-Sylla, Douglas Vollrath	539
9	Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation 2000 ·Nature Genetics ·Kerstin Kutsche, Helger G. Yntema, Alexander Brandt, (unknown), Hans Gerd Nothwang, Ulrike Orth, Maria Guida Boavida, D. David, Jamel Chelly, Jean‐Pierre Fryns, Claude Moraine, Hans‐Hilger Ropers, Ben C.J. Hamel, Hans van Bokhoven, Andreas Gal	289
10	Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affected 1997 ·Journal of Neurology Neurosurgery & Psychiatry ·Eva M. Wicklein, Ulrike Orth, Andreas Gal, Klaus Kunze	13
11	Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis 1997 ·Human Genetics ·Esther van de Vosse, Brunella Franco, (unknown), Eugenio Montini, Ulrike Orth, André Hanauer, Nel Tijmes, G.J.B. van Ommen, Andrea Ballabio, Johan T. den Dunnen, Arthur A. Bergen	3
12	Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait 1997 ·American Journal of Medical Genetics ·(unknown), Ulrike Orth, (unknown), Jutta Schröder, Andreas Gal	18
13	A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome 1996 ·Human Mutation ·D. David, Ulrike Orth, H. Heilbronner, Andreas Gal	3
14	New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3 1996 ·American Journal of Medical Genetics ·B Wittwer, Renate Kircheisen, (unknown), Ulrike Orth, Andreas Gal	7
15	Mapping of the Autosomal Dominant Exudative Vitreoretinopathy Locus (EVR1) by Multipoint Linkage Analysis in Four Families 1994 ·Genomics ·(unknown), Ulrike Orth, C. E. van Nouhuys, (unknown), (unknown), E. Schwinger, H. Laqua, Andreas Gal	18
16	X-linked dominant Charcot — Marie — Tooth neuropathy: valine-38-methionine substitution of connexin32 1994 ·Human Molecular Genetics ·Ulrike Orth, (unknown), (unknown), E. Schwinger, Andreas Gal	34
17	Multipoint linkage analysis in X‐linked juvenile retinosclusis 1993 ·Clinical Genetics ·Arthur A. Bergen, Mary J. van Schooneveld, Ulrike Orth, E. M. Bleeker‐Wagemakers, A. Gal	7
18	Posthumous diagnosis of X-linked retinoschisis using DNA analysis 1990 ·Ophthalmic Paediatrics and Genetics ·Mary J. van Schooneveld, Elisabeth M. Bleeker‐Wagemakers, Ulrike Orth, M. Neugebauer, (unknown), Andreas Gal	1
19	Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp 1989 ·Human Genetics ·Andreas Gal, A. Schinzel, Ulrike Orth, Neil Fraser, (unknown), Ian Craig, Torben A. Kruse, Marco Mächler, M. Neugebauer, Liesbeth M. Bleeker-Wagemakers	35
20	Human monoamine oxidase A and B genes map to xp11.23 and are deleted in a patient with norrie disease 1989 ·Genomics ·Nancy C. Lan, Camilla Heinzmann, Andreas Gal, Ivana Klisak, Ulrike Orth, Eric Lai, Joseph Grimsby, Robert S. Sparkes, T. Mohandas, Jean C. Shih	167

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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