Andreas Ohlenbusch

1.8k total citations
49 papers, 1.2k citations indexed

About

Andreas Ohlenbusch is a scholar working on Molecular Biology, Genetics and Parasitology. According to data from OpenAlex, Andreas Ohlenbusch has authored 49 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 10 papers in Genetics and 10 papers in Parasitology. Recurrent topics in Andreas Ohlenbusch's work include Vector-borne infectious diseases (10 papers), RNA regulation and disease (8 papers) and DNA Repair Mechanisms (6 papers). Andreas Ohlenbusch is often cited by papers focused on Vector-borne infectious diseases (10 papers), RNA regulation and disease (8 papers) and DNA Repair Mechanisms (6 papers). Andreas Ohlenbusch collaborates with scholars based in Germany, United States and Poland. Andreas Ohlenbusch's co-authors include Jutta Gärtner, Helmut Eiffert, Knut Brockmann, Hendrik Rosewich, Andrew Spielman, H.‐J. Christen, F. Hanefeld, D. Richter, R. Thomssen and Peter Nürnberg and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Neurology.

In The Last Decade

Andreas Ohlenbusch

48 papers receiving 1.2k citations

Peers

Countries citing papers authored by Andreas Ohlenbusch

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Ohlenbusch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Ohlenbusch

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Ohlenbusch. A scholar is included among the top collaborators of Andreas Ohlenbusch 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 Andreas Ohlenbusch. Andreas Ohlenbusch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	A novel remitting leukodystrophy associated with a variant in FBP2 2021 ·Brain Communications ·Agnieszka Gizak, (unknown), Steffi Dreha‐Kulaczewski, Janusz Wiśniewski, Przemysław Duda, Andreas Ohlenbusch, Brenda Huppke, Marco Henneke, Wolfgang Höhne, Janine Altmüller, Holger Thiele, Peter Nürnberg, Dariusz Rakus, Jutta Gärtner, Peter Huppke	2
2	Splice variants of the endonucleases XPF and XPG contain residual DNA repair capabilities and could be a valuable tool for personalized medicine 2017 ·Oncotarget ·Janin Lehmann, Steffen Schubert, Christina Seebode, (unknown), Andreas Ohlenbusch, Steffen Emmert	2
3	A novel ATP1A3 mutation with unique clinical presentation 2014 ·Journal of the Neurological Sciences ·Hendrik Rosewich, Martina Baethmann, Andreas Ohlenbusch, Jutta Gärtner, Knut Brockmann	20
4	Characterization of Three XPG-Defective Patients Identifies Three Missense Mutations that Impair Repair and Transcription 2013 ·Journal of Investigative Dermatology ·(unknown), Steffen Schubert, Alexei Gratchev, Christina Seebode, (unknown), Petra Laspe, Lars Hofmann, Andreas Ohlenbusch, Toshio Mori, Nobuhiko Kobayashi, (unknown), Michael P. Schön, Steffen Emmert	20
5	Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiency 2012 ·Orphanet Journal of Rare Diseases ·Andreas Ohlenbusch, Simon Edvardson, (unknown), (unknown), Ann Saada, Orly Elpeleg, Jutta Gärtner, Knut Brockmann	42
6	Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study 2012 ·The Lancet Neurology ·Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch, Ulrike Maschke, Janine Altmüller, Peter Frommolt, Birgit Zirn, Friedrich Ebinger, H. Siemes, Peter Nürnberg, Knut Brockmann, Jutta Gärtner	173
7	Imaging evidence of early brain tissue degeneration in patients with vanishing white matter disease: A multimodal MR study 2011 ·Journal of Magnetic Resonance Imaging ·Xiaoqi Ding, Annette Bley, Andreas Ohlenbusch, Alfried Kohlschütter, Jens Fiehler, Wenzhen Zhu, Heinrich Lanfermann	6
8	Maternal Segmental Disomy in Leigh Syndrome with Cytochrome c Oxidase Deficiency Caused by Homozygous SURF1 Mutation 2006 ·Neuropediatrics ·(unknown), Hana Antonická, Andreas Ohlenbusch, Eric A. Shoubridge, Ekkehard Wilichowski	13
9	Autoantibodies to Human Manganese Superoxide Dismutase (MnSOD) in Children with Facial Palsy due to Neuroborreliosis 2005 ·Neuropediatrics ·Helmut Eiffert, A. Karsten, Klaus Ritter, Andreas Ohlenbusch, Thilo Schlott, Rainer Laskawi, H.‐J. Christen	3
10	Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2 2005 ·American Journal of Medical Genetics Part A ·Peter Huppke, Andreas Ohlenbusch, Cornelia Brendel, Franco Laccone, Jutta Gärtner	15
11	Identification of ten novel mutations in patients with eIF2B-related disorders 2005 ·Human Mutation ·Andreas Ohlenbusch, Marco Henneke, Knut Brockmann, (unknown), F. Hanefeld, Alfried Kohlschütter, Jutta Gärtner	37
12	Acute Peripheral Facial Palsy in Lyme Disease - A Distal Neuritis at the Infection Site 2004 ·Neuropediatrics ·Helmut Eiffert, A. Karsten, Thilo Schlott, Andreas Ohlenbusch, Rainer Laskawi, Michael Hoppert, H.‐J. Christen	16
13	Chlamydia pneumoniae in children with MS 2003 ·Neurology ·K. Rostásy, Hansotto Reiber, Daniela Pohl, Peter Lange, Andreas Ohlenbusch, Helmut Eiffert, Matthias Maass, F. Hanefeld	27
14	Myelin Oligodendrocyte Gene Polymorphisms and Childhood Multiple Sclerosis 2002 ·Pediatric Research ·Andreas Ohlenbusch, Daniela Pohl, F. Hanefeld	12
15	Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia 2000 ·Human Mutation ·Wilfried Kugler, (unknown), (unknown), Andreas Ohlenbusch, Petra Laspe, (unknown), Hilary Muirhead, W. Schr�ter, M. Lakomek	16
16	Characterization of the Mitochondrial Genome in Childhood Multiple Sclerosis. - I. Optic Neuritis and LHON Mutations 1998 ·Neuropediatrics ·Andreas Ohlenbusch, Ekkehard Wilichowski, F. Hanefeld	17
17	Etiology of the Acrodermatitis Chronica Atrophicans Lesion in Lyme Disease 1996 ·The Journal of Infectious Diseases ·Andreas Ohlenbusch, F.-R. Matuschka, D. Richter, H.‐J. Christen, R. Thomssen, Andrew Spielman, Helmut Eiffert	42
18	Characteristics of Lyme Disease Spirochetes in Archived European Ticks 1996 ·The Journal of Infectious Diseases ·F.-R. Matuschka, Andreas Ohlenbusch, Helmut Eiffert, D. Richter, Andrew Spielman	23
19	Nondifferentiation between Lyme Disease Spirochetes from Vector Ticks and Human Cerebrospinal Fluid 1995 ·The Journal of Infectious Diseases ·Helmut Eiffert, Andreas Ohlenbusch, H.‐J. Christen, R. Thomssen, A Spielman, (unknown)	61
20	Amplifying Role of Edible Dormice in Lyme Disease Transmission in Central Europe 1994 ·The Journal of Infectious Diseases ·(unknown), Helmut Eiffert, Andreas Ohlenbusch, Andrew Spielman	33

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.

Explore authors with similar magnitude of impact