A. Rolfs

4.8k total citations
51 papers, 1.5k citations indexed

About

A. Rolfs is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Rolfs has authored 51 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Physiology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Rolfs's work include Lysosomal Storage Disorders Research (15 papers), Cellular transport and secretion (8 papers) and Carbohydrate Chemistry and Synthesis (6 papers). A. Rolfs is often cited by papers focused on Lysosomal Storage Disorders Research (15 papers), Cellular transport and secretion (8 papers) and Carbohydrate Chemistry and Synthesis (6 papers). A. Rolfs collaborates with scholars based in Germany, Italy and United Kingdom. A. Rolfs's co-authors include Ulrich Finckh, Eckart Fleck, Vera Regitz‐Zagrosek, Michael Beck, Atul Mehta, H. Lode, Anders Erikson, Bruno Bembi, H. Mauch and Roland Hetzer and has published in prestigious journals such as Circulation, Neurology and Clinical Infectious Diseases.

In The Last Decade

A. Rolfs

49 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Rolfs Germany	20	618	448	403	246	219	51	1.5k
Elena Germinario Italy	24	295 0.5×	766 1.7×	232 0.6×	194 0.8×	19 0.1×	53	1.4k
Mireia Martín‐Satué Spain	23	220 0.4×	565 1.3×	85 0.2×	71 0.3×	50 0.2×	48	1.4k
Hong Dang United States	28	395 0.6×	1.1k 2.4×	210 0.5×	76 0.3×	40 0.2×	77	2.4k
M. N. Hart United States	18	393 0.6×	365 0.8×	185 0.5×	55 0.2×	25 0.1×	33	1.5k
N. Matsuoka Japan	29	269 0.4×	566 1.3×	247 0.6×	69 0.3×	25 0.1×	63	2.6k
Hao Pang China	24	282 0.5×	947 2.1×	138 0.3×	149 0.6×	26 0.1×	112	2.0k
France Piétri‐Rouxel France	20	509 0.8×	936 2.1×	273 0.7×	166 0.7×	17 0.1×	47	1.5k
Heather L. Wilson United Kingdom	25	163 0.3×	1.1k 2.5×	174 0.4×	186 0.8×	25 0.1×	41	2.3k
Cynthia Koziol‐White United States	23	615 1.0×	448 1.0×	151 0.4×	71 0.3×	30 0.1×	66	1.6k
Julie K. Olson United States	23	373 0.6×	625 1.4×	327 0.8×	59 0.2×	11 0.1×	37	3.0k

Countries citing papers authored by A. Rolfs

Since Specialization

Citations

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

Fields of papers citing papers by A. Rolfs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Rolfs

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

Arkadir, David, Tama Dinur, Shoshana Revel‐Vilk, et al.. (2019). Prodromal substantia nigra sonography undermines suggested association between substrate accumulation and the risk for GBA‐related Parkinson's disease. European Journal of Neurology. 26(7). 1013–1018. 12 indexed citations

Sankian, Mojtaba, et al.. (2015). Molecular, biochemical, and structural analysis of a novel mutation in patients with methylmalonyl-CoA mutase deficiency. Gene. 576(1). 208–213. 7 indexed citations

Hovakimyan, Marine, Jana Müller, Andreas Wree, et al.. (2012). Survival of transplanted human neural stem cell line (ReNcell VM) into the rat brain with and without immunosuppression. Annals of Anatomy - Anatomischer Anzeiger. 194(5). 429–435. 24 indexed citations

Kumar, Kishore R., Alfredo Ramı́rez, Nikola Kresojević, et al.. (2012). Glucocerebrosidase mutations in a Serbian Parkinson's disease population. European Journal of Neurology. 20(2). 402–405. 44 indexed citations

Brüggemann, Norbert, J. Hagenah, Peter Bauer, et al.. (2011). Autosomal dominant Parkinson’s disease in a large German pedigree. Acta Neurologica Scandinavica. 126(2). 129–137. 2 indexed citations

Tanislav, Christian, Manfred Kaps, A. Rolfs, et al.. (2010). Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study. European Journal of Neurology. 18(4). 631–636. 33 indexed citations

Griese, Matthias, Frank Brasch, Elina Ikonen, et al.. (2009). Respiratory disease in Niemann‐Pick type C2 is caused by pulmonary alveolar proteinosis. Clinical Genetics. 77(2). 119–130. 63 indexed citations

Rolfs, A., et al.. (2009). Guillain-Barré syndrome in pregnancy: reflections on immunopathogenesis. Acta Neurologica Scandinavica. 89(5). 400–402. 5 indexed citations

Hoffmann, B., et al.. (2008). Morbus Fabry – Komplexe Klinik, einfache Diagnostik, kausale Therapie. DMW - Deutsche Medizinische Wochenschrift. 133(39). 1965–1972.

10.

Cybulla, Markus, Walter K.K. Ho, H. Neumann, et al.. (2007). Morbus Fabry: Demografische Übersicht seit Einführung der Enzymersatztherapie. DMW - Deutsche Medizinische Wochenschrift. 132(28/29). 1505–1509. 8 indexed citations

11.

Usunoff, Kamen G., Dimitar E. Itzev, A. Rolfs, Oliver Schmitt, & Andreas Wree. (2006). Nitric oxide synthase-containing neurons in the amygdaloid nuclear complex of the rat. Anatomy and Embryology. 211(6). 721–737. 9 indexed citations

12.

Steiner, M., et al.. (2004). Antithrombin gene mutation 5356?5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin ?-helix D molecular pathology. Annals of Hematology. 84(1). 56–58. 2 indexed citations

13.

Dettling, Michael, Christoph Sachse, B. Müller‐Oerlinghausen, et al.. (2000). Clozapine-induced Agranulocytosis and Hereditary Polymorphisms of Clozapine Metabolizing Enzymes: No Association with Myeloperoxidase and Cytochrome P4502D6. Pharmacopsychiatry. 33(6). 218–220. 31 indexed citations

14.

Steinhoff, D., H. Lode, G. Ruckdeschel, et al.. (1996). Chlamydia pneumoniae as a Cause of Community-Acquired Pneumonia in Hospitalized Patients in Berlin. Clinical Infectious Diseases. 22(6). 958–964. 63 indexed citations

15.

Rolfs, A., et al.. (1995). Clinical and Immunologic Follow-up Study of Patients with Neurocysticercosis After Treatment with Praziquantel. Neurology. 45(3). 532–538. 18 indexed citations

16.

Wissel, Jörg, et al.. (1995). Guillain-Barr� syndrome in pregnancy ?two case reports and a discussion on management. Archives of Gynecology and Obstetrics. 256(4). 199–203. 6 indexed citations

17.

Sander, T., Helmut Harms, Jan Podschus, et al.. (1995). Dopamine D1, D2 and D3 receptor genes in alcohol dependence. Psychiatric Genetics. 5(4). 171–176. 82 indexed citations

18.

Wissel, Jörg, et al.. (1994). Guillain-Barré syndrome in pregnancy – an indication for caesarian section?. Journal of Perinatal Medicine. 22(5). 393–398. 13 indexed citations

19.

Rolfs, A., et al.. (1994). Mnll polymorphism for the AGTR1 gene. Human Molecular Genetics. 3(1). 213–213. 6 indexed citations

20.

Rolfs, A., et al.. (1994). Genetic Polymorphisms of the Angiotensin II type 1 (AT1) Receptor Gene. European Heart Journal. 15(suppl D). 108–112. 24 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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