Christian Kubisch

22.7k total citations · 3 hit papers
144 papers, 7.3k citations indexed

About

Christian Kubisch is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Christian Kubisch has authored 144 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 33 papers in Genetics and 21 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Christian Kubisch's work include Ion channel regulation and function (18 papers), RNA Research and Splicing (14 papers) and Cardiac electrophysiology and arrhythmias (12 papers). Christian Kubisch is often cited by papers focused on Ion channel regulation and function (18 papers), RNA Research and Splicing (14 papers) and Cardiac electrophysiology and arrhythmias (12 papers). Christian Kubisch collaborates with scholars based in Germany, United States and United Kingdom. Christian Kubisch's co-authors include Thomas J. Jentsch, Björn C. Schroeder, Peter Propping, Alfredo Ramı́rez, Valentin Stein, Samuel F. Berkovic, Ortrud K. Steinlein, Christian Biervert, Thomas Friedrich and Ingrid Goebel and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Christian Kubisch

139 papers receiving 7.1k 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.

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

2006 881 citations Alfredo Ramı́rez, Meliha Karsak et al. Nature Genetics profile →
A Potassium Channel Mutation in Neonatal Human Epilepsy

1998 854 citations Christian Kubisch, Peter Propping et al. profile →
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

1999 682 citations Christian Kubisch, Thomas J. Jentsch et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Christian Kubisch Germany	37	4.6k	2.2k	1.5k	1.1k	971	144	7.3k
Giorgio Casari Italy	55	5.6k 1.2×	2.3k 1.1×	815 0.5×	1.4k 1.3×	1.1k 1.1×	144	10.5k
Lori L. Isom United States	60	8.1k 1.7×	5.9k 2.7×	3.2k 2.1×	367 0.3×	818 0.8×	138	10.6k
Albee Messing United States	65	8.8k 1.9×	4.8k 2.2×	550 0.4×	1.3k 1.2×	1.7k 1.8×	174	14.5k
Joel A. Black United States	61	6.1k 1.3×	5.2k 2.4×	611 0.4×	1.5k 1.4×	389 0.4×	135	11.2k
Stephan Züchner United States	46	3.2k 0.7×	2.4k 1.1×	410 0.3×	1.1k 1.0×	912 0.9×	177	6.6k
Michaela Schweizer Germany	47	4.7k 1.0×	1.9k 0.9×	420 0.3×	251 0.2×	503 0.5×	127	7.5k
Inmaculada Silos‐Santiago United States	38	3.3k 0.7×	3.9k 1.8×	421 0.3×	333 0.3×	404 0.4×	70	7.4k
Andrea L. Meredith United States	36	2.5k 0.5×	1.7k 0.8×	1.1k 0.7×	310 0.3×	273 0.3×	91	4.4k
Nikolaj Klöcker Germany	39	2.9k 0.6×	2.2k 1.0×	429 0.3×	353 0.3×	285 0.3×	81	5.1k
Andreas Bringmann Germany	52	7.1k 1.5×	3.4k 1.5×	190 0.1×	495 0.5×	389 0.4×	223	11.5k

Countries citing papers authored by Christian Kubisch

Since Specialization

Citations

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

Fields of papers citing papers by Christian Kubisch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Kubisch

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Kubisch. A scholar is included among the top collaborators of Christian Kubisch 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 Christian Kubisch. Christian Kubisch 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

Ven, Amelie T. van der, Maja Hempel, Chris G. Kruse, et al.. (2025). Homozygous DBX1 Nonsense Variant in a Case of Atypical Congenital Central Hypoventilation. Neurology Genetics. 11(5). e200302–e200302.

Kakar, Naseebullah, Gandham SriLakshmi Bhavani, Manisha Goyal, et al.. (2024). Multi‐gene panel sequencing in highly consanguineous families and patients with congenital forms of skeletal dysplasias. Clinical Genetics. 106(1). 47–55. 1 indexed citations

Mir, Thomas S., Gerhard Schön, Kerstin Kutsche, et al.. (2024). Late diagnosis of Marfan syndrome is associated with unplanned aortic surgery and cardiovascular death. Journal of Thoracic and Cardiovascular Surgery. 169(4). 1201–1209.e33.

Postma, Alex V., Christina Rapp, Katrin Knoflach, et al.. (2023). Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension. SHILAP Revista de lepidopterología. 1(1). 100811–100811. 1 indexed citations

Reuter, Miriam S., Michael Zech, Maja Hempel, et al.. (2022). Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies. European Journal of Human Genetics. 30(5). 611–618. 3 indexed citations

Schob, Claudia, Maja Hempel, Dana Šafka Brožková, et al.. (2021). Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia. Annals of Neurology. 90(5). 738–750. 6 indexed citations

Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations

Lessel, Davor, et al.. (2021). A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A‐related pathologies. American Journal of Medical Genetics Part A. 188(1). 216–223. 6 indexed citations

Ven, Amelie T. van der, Jessika Johannsen, Fanny Kortüm, et al.. (2021). Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort. Clinical Genetics. 100(6). 766–770. 8 indexed citations

10.

Kloth, Katja, Bernarda Lozić, Mariëtte J.V. Hoffer, et al.. (2021). ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants. Neurogenetics. 22(4). 263–269. 14 indexed citations

11.

Mailer, Reiner K., Marco Heestermans, Michaela Schweizer, et al.. (2020). Xenotropic and polytropic retrovirus receptor 1 regulates procoagulant platelet polyphosphate. Blood. 137(10). 1392–1405. 30 indexed citations

12.

Lüttgen, Sabine, Sigrid Fuchs, Holger Thiele, et al.. (2020). Two novel cases further expand the phenotype of TOR1AIP1-associated nuclear envelopathies. Human Genetics. 139(4). 483–498. 12 indexed citations

13.

Yang, Yuanhao, Huiying Zhao, Dorret I. Boomsma, et al.. (2018). Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics. 26(8). 1202–1216. 54 indexed citations

14.

Lessel, Davor, Ayse Bilge Ozel, Susan Campbell, et al.. (2018). Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations. Human Genetics. 137(11-12). 921–939. 16 indexed citations

15.

Rosenbohm, Angela, Steffen Hirsch, Alexander E. Volk, et al.. (2018). The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy. Journal of Neurology. 265(5). 1026–1036. 26 indexed citations

16.

Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 indexed citations

17.

Zirn, Birgit, Luitgard Graul‐Neumann, M. Suckfüll, et al.. (2013). Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. BMJ Open. 3(3). e001917–e001917. 38 indexed citations

18.

Volk, Alexander E., Peter Herkenrath, Guntram Borck, et al.. (2011). Horizontal gaze palsy with progressive scoliosis: three novel ROBO3 mutations and descriptions of the phenotypes of four patients.. PubMed. 17. 1978–86. 23 indexed citations

19.

Karsak, Meliha, Martine Cohen‐Solal, Jan Freudenberg, et al.. (2005). Cannabinoid receptor type 2 gene is associated with human osteoporosis. Human Molecular Genetics. 14(22). 3389–3396. 161 indexed citations

20.

Betz, Regina C., Benedikt Schoser, K. Ricker, et al.. (2001). Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease. Nature Genetics. 28(3). 218–219. 143 indexed citations

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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