Ralph Oehlmann

930 total citations
10 papers, 583 citations indexed

About

Ralph Oehlmann is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ralph Oehlmann has authored 10 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ralph Oehlmann's work include Retinal Development and Disorders (2 papers), RNA regulation and disease (2 papers) and Cell Adhesion Molecules Research (2 papers). Ralph Oehlmann is often cited by papers focused on Retinal Development and Disorders (2 papers), RNA regulation and disease (2 papers) and Cell Adhesion Molecules Research (2 papers). Ralph Oehlmann collaborates with scholars based in United States, Germany and New Zealand. Ralph Oehlmann's co-authors include Bertram Müller‐Myhsok, Donald B. Calne, Rolf D. Horstmann, Thomas Gasser, Vincenzo Bonifati, Benjámin Bereznai, Edito Fabrizio, P. Vieregge, Zbigniew K. Wszołek and Andreas Gal and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Ralph Oehlmann

10 papers receiving 569 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ralph Oehlmann United States	8	311	237	215	163	107	10	583
Gavin Charlesworth United Kingdom	14	472 1.5×	356 1.5×	176 0.8×	93 0.6×	88 0.8×	18	658
Inge A. Meijer Canada	14	129 0.4×	362 1.5×	369 1.7×	169 1.0×	150 1.4×	22	811
Michèle Aguera France	8	245 0.8×	496 2.1×	246 1.1×	41 0.3×	76 0.7×	11	762
S. A. Klyushnikov Russia	10	103 0.3×	238 1.0×	299 1.4×	43 0.3×	47 0.4×	38	441
Ming Sum Ruby Chiang United States	11	99 0.3×	156 0.7×	379 1.8×	228 1.4×	66 0.6×	11	703
Antonio Berretta United Kingdom	11	154 0.5×	158 0.7×	156 0.7×	122 0.7×	68 0.6×	15	486
K. Tanaka Japan	7	59 0.2×	241 1.0×	313 1.5×	98 0.6×	22 0.2×	12	555
Benjamin Ettle Germany	16	448 1.4×	295 1.2×	184 0.9×	276 1.7×	14 0.1×	25	800
Huailian Guo China	12	50 0.2×	119 0.5×	207 1.0×	81 0.5×	58 0.5×	23	461
Sabrina Zechel Germany	14	68 0.2×	147 0.6×	180 0.8×	62 0.4×	15 0.1×	26	472

Countries citing papers authored by Ralph Oehlmann

Since Specialization

Citations

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

Fields of papers citing papers by Ralph Oehlmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Oehlmann

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

All Works

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10 of 10 papers shown

Wakula, Paulina, Egbert Bisping, Jens Kockskämper, et al.. (2010). CMV promoter is inadequate for expression of mutant human RyR2 in transgenic rabbits. Journal of Pharmacological and Toxicological Methods. 63(2). 180–185. 6 indexed citations

Luther, Claudia, et al.. (2004). Alternatively spliced transcripts of the thymus-specific protease PRSS16 are differentially expressed in human thymus. Genes and Immunity. 6(1). 1–7. 10 indexed citations

Gasser, Thomas, Bertram Müller‐Myhsok, Zbigniew K. Wszołek, et al.. (1998). A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nature Genetics. 18(3). 262–265. 350 indexed citations

Veske, Andres, Ralph Oehlmann, Aisha Mohyuddin, et al.. (1996). Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan. Human Molecular Genetics. 5(1). 165–168. 103 indexed citations

Oehlmann, Ralph, L. Ingeborgh van den Born, James L. Weber, et al.. (1995). Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan. Clinical Genetics. 47(3). 122–124. 18 indexed citations

Maw, Marion A., Sheila John, Sibylle Jablonka, et al.. (1995). Oguchi disease: suggestion of linkage to markers on chromosome 2q.. Journal of Medical Genetics. 32(5). 396–398. 21 indexed citations

Oehlmann, Ralph, et al.. (1994). Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19.. PubMed. 54(1). 3–10. 39 indexed citations

Weaver, Eric J., George L. Yeh, Ralph Oehlmann, et al.. (1993). Exclusion of type II and type VI procollagen gene mutations in a five‐generation family with multiple epiphyseal dysplasia. American Journal of Medical Genetics. 45(3). 345–352. 13 indexed citations

Oehlmann, Ralph, Joël Zlotogora, David A. Wenger, & Robert G. Knowlton. (1993). Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis.. PubMed. 53(6). 1250–5. 21 indexed citations

10.

Schwab, M., et al.. (1989). Amplified DNA in cells of genetic melanoma of Xiphophorus.. PubMed. 4(2). 139–44. 2 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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