Christoph Hübner

6.6k total citations · 1 hit paper
77 papers, 4.1k citations indexed

About

Christoph Hübner is a scholar working on Molecular Biology, Genetics and Biochemistry. According to data from OpenAlex, Christoph Hübner has authored 77 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 15 papers in Genetics and 15 papers in Biochemistry. Recurrent topics in Christoph Hübner's work include Neurogenetic and Muscular Disorders Research (15 papers), Antioxidant Activity and Oxidative Stress (15 papers) and Muscle Physiology and Disorders (10 papers). Christoph Hübner is often cited by papers focused on Neurogenetic and Muscular Disorders Research (15 papers), Antioxidant Activity and Oxidative Stress (15 papers) and Muscle Physiology and Disorders (10 papers). Christoph Hübner collaborates with scholars based in Germany, United States and United Kingdom. Christoph Hübner's co-authors include Markus Schuelke, Alfried Kohlschütter, Thomas Braun, James F. Tobin, Leslie E. Stolz, T Riebel, Kathryn R. Wagner, Se‐Jin Lee, Barbara Finckh and Hans‐Anton Lehr and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Christoph Hübner

76 papers receiving 4.0k 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.

Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child

2004 1.1k citations Markus Schuelke, Christoph Hübner et al. profile →

Peers

Countries citing papers authored by Christoph Hübner

Since Specialization

Citations

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

Fields of papers citing papers by Christoph Hübner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christoph Hübner

This figure shows the co-authorship network connecting the top 25 collaborators of Christoph Hübner. A scholar is included among the top collaborators of Christoph Hübner 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 Christoph Hübner. Christoph Hübner 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	Expanding the clinical and molecular spectrum of ATP6V1A related metabolic cutis laxa 2020 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), Ágnes Herczegfalvi, Heike Kölbel, (unknown), Ulrike Schara, Manuel Holtgrewe, Sabine Krause, Rita Horváth, Markus Schuelke, Christoph Hübner, Stefan Mundlos, Andreas Roos, Hanns Lochmüller, Veronika Karcagi, Uwe Kornak, Björn Fischer‐Zirnsak	10
2	First Recognized Patient with Genetic Vitamin E Deficiency Stable after 36 Years of Controlled Supplement Therapy 2020 ·Neurodegenerative Diseases ·Alfried Kohlschütter, Barbara Finckh, Miriam Nickel, Annette Bley, Christoph Hübner	22
3	Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation 2017 ·PLoS Genetics ·(unknown), Hao Hu, Scott A. Yuzwa, Luis R. Hernández-Miranda, Nadine Kraemer, Olaf Ninnemann, Luciana Musante, Eugen Boltshauser, Detlev Schindler, Angela Hübner, Hans-Christian Reinecker, (unknown), Carmen Birchmeier, Freda D. Miller, Thomas F. Wienker, Christoph Hübner, Angela M. Kaindl	22
4	Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation 2016 ·eLife ·(unknown), Timothy Wai, Hao Hu, Thomas MacVicar, Luciana Musante, Björn Fischer‐Zirnsak, Werner Stenzel, Ralph Gräf, Lambert van den Heuvel, (unknown), (unknown), Christoph Hübner, Thomas Langer, Angela M. Kaindl	96
5	Klüver–Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C) 2016 ·European Journal of Human Genetics ·Hao Hu, Christoph Hübner, Zoltán Lukács, Luciana Musante, Esther Gill, Thomas F. Wienker, Hans‐Hilger Ropers, Ellen Knierim, Markus Schuelke	2
6	HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing 2009 ·European Journal of Human Genetics ·Wenke Seifert, (unknown), Katrin Hoffmann, Tom H. Lindner, C. Bassir, Fuat Aksu, Christoph Hübner, Nienke E. Verbeek, Stefan Mundlos, Denise Horn	22
7	Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 protein levels in five patients with infantile and juvenile disease 2008 ·Journal of Molecular Medicine ·Ulf‐Peter Guenther, Lusy Handoko, Raymonda Varon, Ulrich Stephani, Chang‐Yong Tsao, Jerry R. Mendell, Susanne Lützkendorf, Christoph Hübner, Katja von Au, Sibylle Jablonka, Gunnar Dittmar, Udo Heinemann, A. Schuetz, Markus Schuelke	45
8	Clinical and mutational profile in spinal muscular atrophy with respiratory distress (SMARD): defining novel phenotypes through hierarchical cluster analysis 2007 ·Human Mutation ·Ulf‐Peter Guenther, Raymonda Varon, (unknown), (unknown), Alexander E. Volk, Christoph Hübner, Katja von Au, Markus Schuelke	58
9	Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit 2006 ·The American Journal of Human Genetics ·Katrin Hoffmann, Juliane Müller, Sigmar Stricker, André Mégarbané, Anna Rajab, Tom H. Lindner, Monika Cohen, Éliane Chouery, (unknown), Ismat Ghanem, Valérie Delague, Eugen Boltshauser, Beril Talim, Rita Horváth, Peter N. Robinson, Hanns Lochmüller, Christoph Hübner, Stefan Mundlos	100
10	Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalities 2006 ·Muscle & Nerve ·Claudia Weiß, Sibylle Jakubiczka, Angela Huebner, Eva Klopocki, Wolfram Kreß, Thomas Voït, Christoph Hübner, Markus Schuelke	5
11	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
12	Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis 2005 ·Neuromuscular Disorders ·Maja von der Hagen, (unknown), Angela M. Kaindl, Katrin Koehler, (unknown), Angela Abicht, Ulrike Grieben, Rudolf Korinthenberg, (unknown), Arpad von Moers, Juliane Müller, Ulrike Schara, Matthias Vorgerd, Maggie C. Walter, C. Müller‐Reible, Christoph Hübner, Hanns Lochmüller, Angela Huebner	16
13	Clinical stable systemic mastocytosis with interferon alpha 2b therapy. 1997 ·Journal of Internal Medicine ·Christoph Hübner, Ulrich Wedding, Jörn Sträter, Bernd Limberg, Wolfgang Stremmel	15
14	Muscarinic acetylcholine receptor stimulation of biliary epithelial cells and its effect on bile secretion in the isolated perfused liver 1997 ·Hepatology ·Christoph Elsing, Christoph Hübner, B.A. Fitscher, Astrid Kassner, Wolfgang Stremmel	23
15	How Different Constituents of Low Density Lipoprotein Determine its Oxidizability by Copper: A Correlational Approach 1996 ·Free Radical Research ·Anatol Kontush, Christoph Hübner, Barbara Finckh, (unknown), Ulrike Beisiegel	44
16	Monitoring of Ubiquinol-10, Ubiquinone-10, Carotenoids, and Tocopherols in Neonatal Plasma Microsamples Using High-Performance Liquid Chromatography with Coulometric Electrochemical Detection 1995 ·Analytical Biochemistry ·Barbara Finckh, Anatol Kontush, (unknown), Christoph Hübner, M. Burdelski, Alfried Kohlschütter	89
17	Exposure of HIV-infected cells to phospholipid leads to membrane alterations and selective growth retardation 1992 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·(unknown), Christoph Hübner, (unknown), (unknown)	4
18	Role of leukotrienes in leukocyte adhesion following systemic administration of oxidatively modified human low density lipoprotein in hamsters. 1991 ·Journal of Clinical Investigation ·Hans‐Anton Lehr, Christoph Hübner, Barbara Finckh, Sabine Angermüller, D. Nölte, Ulrike Beisiegel, Alfried Kohlschütter, K. Meßmer	71
19	Membrane fluidity and lipid composition of rat small intestinal brush-border membranes during postnatal maturation 1988 ·Biochimica et Biophysica Acta (BBA) - Biomembranes ·Christoph Hübner, (unknown), (unknown), (unknown), Alfried Kohlschütter	42
20	Decreased membrane fluidity of lymphocytes from patients with juvenile neuronal ceroid-lipofuscinosis 1988 ·American Journal of Medical Genetics ·Alfried Kohlschütter, Christoph Hübner, Jutta Gärtner, James F. Reynolds, Raju K. Pullarkat	11

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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