Arpad von Moers

4.3k total citations · 1 hit paper
58 papers, 2.3k citations indexed

About

Arpad von Moers is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Arpad von Moers has authored 58 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Genetics. Recurrent topics in Arpad von Moers's work include Muscle Physiology and Disorders (16 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Arpad von Moers is often cited by papers focused on Muscle Physiology and Disorders (16 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Arpad von Moers collaborates with scholars based in Germany, United States and United Kingdom. Arpad von Moers's co-authors include Heike Biebermann, Heiko Krude, Annette Grueters, Frank K.H. van Landeghem, Holger Tönnies, Dagmar Weise, George G. J. M. Kuiper, Sahila Balkassmi, Timothy Barrett and Edith C. H. Friesema and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Arpad von Moers

56 papers receiving 2.2k citations

Hit Papers

align trajectories sort by overperformance

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.

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

2004 512 citations Edith C. H. Friesema, Annette Grueters et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arpad von Moers Germany	22	1.1k	742	533	292	280	58	2.3k
Markus Bettendorf Germany	27	944 0.8×	1.3k 1.7×	657 1.2×	298 1.0×	127 0.5×	117	2.4k
Graziella Pinto France	26	1.0k 0.9×	873 1.2×	717 1.3×	324 1.1×	258 0.9×	65	2.1k
N. Sörensen Germany	20	397 0.4×	556 0.7×	237 0.4×	297 1.0×	306 1.1×	62	1.5k
Katsuhiko Tachibana Japan	26	910 0.8×	856 1.2×	638 1.2×	283 1.0×	113 0.4×	78	2.3k
Laurie E. Cohen United States	31	739 0.7×	1.5k 2.0×	629 1.2×	360 1.2×	344 1.2×	78	2.9k
Claudine Heinrichs Belgium	30	1.1k 1.0×	1.1k 1.5×	907 1.7×	269 0.9×	70 0.3×	88	2.6k
Thomas Moshang United States	33	622 0.6×	1.3k 1.7×	396 0.7×	474 1.6×	598 2.1×	83	2.9k
M. Thorén Sweden	28	465 0.4×	1.1k 1.5×	261 0.5×	290 1.0×	126 0.5×	58	2.0k
Yael Segev Israel	24	448 0.4×	745 1.0×	309 0.6×	260 0.9×	152 0.5×	73	2.0k
Natascia Di Iorgi Italy	28	519 0.5×	950 1.3×	389 0.7×	291 1.0×	122 0.4×	86	2.0k

Countries citing papers authored by Arpad von Moers

Since Specialization

Citations

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

Fields of papers citing papers by Arpad von Moers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arpad von Moers. 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 Arpad von Moers. The network helps show where Arpad von Moers may publish in the future.

Co-authorship network of co-authors of Arpad von Moers

This figure shows the co-authorship network connecting the top 25 collaborators of Arpad von Moers. A scholar is included among the top collaborators of Arpad von Moers 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 Arpad von Moers. Arpad von Moers 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

Moers, Arpad von, Petra Bittigau, Gabriel Stölting, et al.. (2024). A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and Hypotonia. Neurology Genetics. 10(5). e200186–e200186. 3 indexed citations

Kleefeld, Felix, Andreas Hentschel, Arpad von Moers, et al.. (2023). Beyond vacuolar pathology: Multiomic profiling of Danon disease reveals dysfunctional mitochondrial homeostasis. Neuropathology and Applied Neurobiology. 49(4). e12920–e12920. 3 indexed citations

Santibanez, Sabine, Rainer Rossi, Hermann Girschick, et al.. (2022). Specifically Increased Rate of Infections in Children Post Measles in a High Resource Setting. Frontiers in Pediatrics. 10. 896086–896086. 3 indexed citations

Kölbel, Heike, Corinna Preuße, Arpad von Moers, et al.. (2021). Inflammation, fibrosis and skeletal muscle regeneration in LGMDR9 are orchestrated by macrophages. Neuropathology and Applied Neurobiology. 47(6). 856–866. 9 indexed citations

Aster, Michael von, et al.. (2021). Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study. Frontiers in Psychology. 12. 697881–697881. 5 indexed citations

Fegert, Jörg M., et al.. (2019). Kinderschutz: verschiedene Professionen, ähnliche Probleme. Lernen und Lernstörungen. 8(2). 73–75. 1 indexed citations

Frericks, Bernd, et al.. (2018). Abuse as a Cause of Childhood Fractures. Deutsches Ärzteblatt international. 115(46). 769–775. 24 indexed citations

Radke, Josefine, Mona Dreesmann, Michaël Radkë, et al.. (2017). The Curse of Apneic Spells. Seminars in Pediatric Neurology. 26. 56–58. 2 indexed citations

Mackenroth, Luisa, Björn Fischer‐Zirnsak, Johannes Egerer, et al.. (2016). An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A. 170(4). 1080–1085. 15 indexed citations

10.

Preuße, Corinna, Yves Allenbach, Olaf Hoffmann, et al.. (2016). Differential roles of hypoxia and innate immunity in juvenile and adult dermatomyositis. Acta Neuropathologica Communications. 4(1). 45–45. 46 indexed citations

11.

Jaite, Charlotte, Christian Bachmann, Marc Dewey, et al.. (2013). Magnetresonanztomographie (MRT) bei Kindern und Jugendlichen. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 41(6). 447–451. 1 indexed citations

12.

Jochum, Frank, Barbara Schmidt, K. Schunk, et al.. (2008). Quality of care of VLBW neonates: relationship between unit volume and outcome is different between metropolitan and rural regions. Acta Paediatrica. 97(10). 1470–1474. 3 indexed citations

13.

Biebermann, Heike, Petra Ambrugger, Patrick Tarnow, et al.. (2005). Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8. European Journal of Endocrinology. 153(3). 359–366. 85 indexed citations

14.

Moers, Arpad von, Gisela Stoltenburg‐Didinger, Yoon S. Shin, et al.. (2005). Delayed or late-onset type II glycogenosis with globular inclusions. Acta Neuropathologica. 110(2). 151–157. 19 indexed citations

15.

Uhlenberg, Birgit, Verena Varnholt, Frank K.H. van Landeghem, et al.. (2005). Atypical manifestation of childhood primary cerebral lymphoma restricted to the leptomeninges. European Journal of Pediatrics. 164(10). 653–654. 3 indexed citations

16.

Horn, Denise, Holger Tönnies, Heidemarie Neitzel, et al.. (2004). Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3. American Journal of Medical Genetics Part A. 128A(1). 85–92. 37 indexed citations

17.

Friesema, Edith C. H., Annette Grueters, Heike Biebermann, et al.. (2004). Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. The Lancet. 364(9443). 1435–1437. 512 indexed citations breakdown →

18.

Gussoni, Emanuela, Richard Rodney Bennett, Kristina R. Muskiewicz, et al.. (2002). Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation. Journal of Clinical Investigation. 110(6). 807–814. 116 indexed citations

19.

Mennerich, Detlev, Markus Schuelke, Gisela Stoltenburg‐Didinger, et al.. (2000). Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy. Neuromuscular Disorders. 10(8). 572–577. 40 indexed citations

20.

Brockmeier, Konrad, et al.. (1998). X-Chromosomal (p21) Muscular Dystrophy and Left Ventricular Diastolic and Systolic Function. Pediatric Cardiology. 19(2). 139–144. 16 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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