Beate Leo‐Kottler

2.1k total citations · 1 hit paper
28 papers, 1.5k citations indexed

About

Beate Leo‐Kottler is a scholar working on Molecular Biology, Ophthalmology and Clinical Biochemistry. According to data from OpenAlex, Beate Leo‐Kottler has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 7 papers in Ophthalmology and 5 papers in Clinical Biochemistry. Recurrent topics in Beate Leo‐Kottler's work include Mitochondrial Function and Pathology (21 papers), ATP Synthase and ATPases Research (14 papers) and Retinal Development and Disorders (6 papers). Beate Leo‐Kottler is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), ATP Synthase and ATPases Research (14 papers) and Retinal Development and Disorders (6 papers). Beate Leo‐Kottler collaborates with scholars based in Germany, United Kingdom and Australia. Beate Leo‐Kottler's co-authors include Bernd Wissinger, Georg Auburger, Ulrich Kellner, Marcela Votruba, Christiane Alexander, Miguel Rodríguez, Dawn L. Thiselton, Anthony T. Moore, Simone Mayer and Dorothea Besch and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and American Journal of Ophthalmology.

In The Last Decade

Beate Leo‐Kottler

27 papers receiving 1.5k 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.

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

2000 1.0k citations Christiane Alexander, Marcela Votruba et al. Nature Genetics profile →

Peers

Countries citing papers authored by Beate Leo‐Kottler

Since Specialization

Citations

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

Fields of papers citing papers by Beate Leo‐Kottler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beate Leo‐Kottler. 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 Beate Leo‐Kottler. The network helps show where Beate Leo‐Kottler may publish in the future.

Co-authorship network of co-authors of Beate Leo‐Kottler

This figure shows the co-authorship network connecting the top 25 collaborators of Beate Leo‐Kottler. A scholar is included among the top collaborators of Beate Leo‐Kottler 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 Beate Leo‐Kottler. Beate Leo‐Kottler 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	Encephalopathic Susac’s Syndrome associated with livedo racemosa in a young woman before the completion of family planning 2013 ·BMC Neurology ·Maik Engeholm, Beate Leo‐Kottler, Hansjörg Rempp, Tobias Lindig, Holger Lerche, Ilka Kleffner, Melanie Henes, Marcel Dihné	16
2	Evaluation of Fixation Pattern and Reading Ability in Patients With Leber Hereditary Optic Neuropathy 2013 ·Journal of Neuro-Ophthalmology ·Elke Altpeter, (unknown), Beate Leo‐Kottler, (unknown), Susanne Trauzettel‐Klosinski	14
3	Lebersche Optikusneuropathie 2011 ·Der Ophthalmologe ·Beate Leo‐Kottler, Bernd Wissinger	3
4	Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy 2010 ·Molecular Neurodegeneration ·Nico Fuhrmann, Simone Schimpf, York Kamenisch, Beate Leo‐Kottler, Christiane Alexander, Georg Auburger, Eberhart Zrenner, Bernd Wissinger, Marcel V. Alavi	15
5	Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy 2009 ·Journal of Medical Genetics ·Nico Fuhrmann, Marcel V. Alavi, Pierre Bitoun, (unknown), Georg Auburger, Beate Leo‐Kottler, Patrick Yu‐Wai‐Man, Patrick F. Chinnery, Bernd Wissinger	42
6	Antiphospholipid-Syndrom: Neurologische Komplikationen und therapeutische Möglichkeiten 2008 ·DMW - Deutsche Medizinische Wochenschrift ·Michael Weller, Beate Leo‐Kottler, (unknown), H. Wiethölter	0
7	Autosomal-dominant erbliche Optikusatrophie vs. Lebersche Optikusneuropathie – Wie kann man sie unterscheiden? 2007 ·Der Ophthalmologe ·Beate Leo‐Kottler, Herbert Jägle, (unknown), Simone Schimpf	3
8	Inner retinal contributions to the multifocal electroretinogram: patients with Leber's hereditary optic neuropathy (LHON) 2004 ·Documenta Ophthalmologica ·Anne Kurtenbach, Beate Leo‐Kottler, Eberhart Zrenner	18
9	Detecting color vision in a malingerer 2003 ·Documenta Ophthalmologica ·Herbert Jägle, Bettina Sadowski, Jan Kremers, Hendrik P. N. Scholl, Beate Leo‐Kottler, Lindsay T. Sharpe	1
10	Leber’s hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery 2002 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Beate Leo‐Kottler, (unknown), Dorothea Besch, (unknown), Sascha Fauser	22
11	A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy 2002 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·(unknown), Beate Leo‐Kottler, Dorothea Besch, Sascha Fauser	13
12	Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy 2002 ·Ophthalmic Genetics ·Sascha Fauser, Beate Leo‐Kottler, Dorothea Besch, (unknown)	22
13	OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 breakdown → 2000 ·Nature Genetics ·Christiane Alexander, Marcela Votruba, (unknown), Dawn L. Thiselton, Simone Mayer, Anthony T. Moore, Miguel Rodríguez, Ulrich Kellner, Beate Leo‐Kottler, Georg Auburger, (unknown), Bernd Wissinger	1033
14	Pupillary light reflexes in patients with Leber's hereditary optic neuropathy 1999 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Holger Lüdtke, (unknown), Beate Leo‐Kottler, Helmut Wilhelm	19
15	Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene 1999 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Dorothea Besch, Beate Leo‐Kottler, Eberhart Zrenner, Bernd Wissinger	26
16	Leber's hereditary optic neuropathy (LHON) in women and children 1999 ·Der Ophthalmologe ·Beate Leo‐Kottler, (unknown)	8
17	Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ ( DAGK3 ): assessment of its role in dominant optic atrophy ( OPA1 ) 1999 ·Human Genetics ·Heidi Stöhr, (unknown), Andrea Gehrig, Michael Köehler, Bernhard Jurklies, Ulrich Kellner, Beate Leo‐Kottler, Michael Schmid, Bernhard H. F. Weber	6
18	Ocular symptoms in association with antiphospholipid antibodies 1998 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Beate Leo‐Kottler, Reinhild Klein, Peter A. Berg, Eberhart Zrenner	25
19	Misdiagnosis of Leber's hereditary optic neuropathy (LHON): role of clinical and molecular genetic examinations 1998 ·Der Ophthalmologe ·Beate Leo‐Kottler, (unknown), Bernd Wissinger, Eberhart Zrenner	2
20	Mutation Analysis of the ND6 Gene in Patients with Lebers Hereditary Optic Neuropathy 1997 ·Biochemical and Biophysical Research Communications ·Bernd Wissinger, Dorothea Besch, Britta Baumann, Sascha Fauser, (unknown), Bernhard Jurklies, Eberhart Zrenner, Beate Leo‐Kottler	48

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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