Olaf Rittinger

1.5k total citations
40 papers, 785 citations indexed

About

Olaf Rittinger is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Olaf Rittinger has authored 40 papers receiving a total of 785 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 22 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Olaf Rittinger's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Chromosomal and Genetic Variations (6 papers). Olaf Rittinger is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Chromosomal and Genetic Variations (6 papers). Olaf Rittinger collaborates with scholars based in Austria, Germany and United States. Olaf Rittinger's co-authors include Andreas Janecke, Elisabeth M. Messmer, Anselm Kampik, Kenneth R. Kenyon, Gerd Utermann, Dieter Kotzot, Barbara Günther, Josef Smolle, Trevor Cole and Hans Christian Hennies and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Ophthalmology.

In The Last Decade

Olaf Rittinger

40 papers receiving 747 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olaf Rittinger Austria 17 433 384 81 74 66 40 785
Luitgard Graul‐Neumann Germany 19 539 1.2× 457 1.2× 57 0.7× 128 1.7× 97 1.5× 46 884
Yves Lacassie United States 18 475 1.1× 425 1.1× 92 1.1× 77 1.0× 174 2.6× 70 952
Rossella Capolino Italy 18 449 1.0× 369 1.0× 53 0.7× 50 0.7× 92 1.4× 56 825
Greg B. Peters Australia 14 382 0.9× 385 1.0× 101 1.2× 54 0.7× 49 0.7× 22 785
Lakshmi Mehta United States 16 403 0.9× 348 0.9× 86 1.1× 67 0.9× 96 1.5× 46 754
Satoru Sakazume Japan 17 314 0.7× 436 1.1× 151 1.9× 85 1.1× 90 1.4× 34 725
Pagon Ra United States 6 450 1.0× 260 0.7× 49 0.6× 70 0.9× 55 0.8× 291 791
Ghislaine Plessis France 18 431 1.0× 341 0.9× 55 0.7× 129 1.7× 103 1.6× 31 810
Meena Balasubramanian United Kingdom 18 310 0.7× 555 1.4× 72 0.9× 55 0.7× 79 1.2× 74 802
Gülen Eda Ütine Türkiye 14 367 0.8× 373 1.0× 77 1.0× 40 0.5× 66 1.0× 114 715

Countries citing papers authored by Olaf Rittinger

Since Specialization
Citations

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

Fields of papers citing papers by Olaf Rittinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olaf Rittinger

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

All Works

20 of 20 papers shown
1.
Hung, Christina, James D. Baker, Johann Bauer, et al.. (2017). A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure. PLoS ONE. 12(12). e0189324–e0189324. 9 indexed citations
2.
Morscher, Raphael J., Christian Rauscher, Wolfgang Sperl, & Olaf Rittinger. (2017). Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion. Seizure. 50. 118–120. 5 indexed citations
3.
Tatton‐Brown, Katrina, Chey Loveday, Shawn Yost, et al.. (2017). Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. The American Journal of Human Genetics. 100(5). 725–736. 128 indexed citations
4.
Bader, Ingrid, Eva L. Decker, Johannes A. Mayr, et al.. (2016). MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum. European Journal of Medical Genetics. 59(8). 386–391. 13 indexed citations
5.
Rittinger, Olaf, et al.. (2015). Clinical, cytogenetic, and molecular findings in a patient with a 46,XX,del(18)(q22)/46,XX,idic(18)(q22) karyotype. European Journal of Medical Genetics. 58(11). 603–607. 15 indexed citations
6.
Zweier, Christiane, Olaf Rittinger, Ingrid Bader, et al.. (2014). Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 290–301. 20 indexed citations
7.
Höckner, Martina, Andreas Tzschach, Andreas Dufke, et al.. (2012). Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations. Cytogenetic and Genome Research. 136(4). 242–245. 19 indexed citations
8.
Diggle, Christine P., Ian Carr, Emanuel Zitt, et al.. (2010). Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy. Lara D. Veeken. 49(6). 1056–1062. 40 indexed citations
9.
Kopic, Sascha, Katharina Eirich, Beatrice Schuster, et al.. (2010). Hepatoblastoma in a 4‐year‐old girl with Fanconi anaemia. Acta Paediatrica. 100(5). 780–783. 20 indexed citations
10.
Furthner, Dieter, Ariane Biebl, Klaus Schmitt, et al.. (2009). Osteopetrosis due to Homozygous Chloride Channel ClCN7 Mutation Mimicking Metabolic Disease with Haematological and Neurological Impairment. Klinische Pädiatrie. 222(3). 180–183. 5 indexed citations
11.
Rittinger, Olaf, et al.. (2008). The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: Follow up in a 14-year-old girl. European Journal of Medical Genetics. 51(6). 573–579. 17 indexed citations
12.
Messmer, Eli sa beth M., Kenneth R. Kenyon, Olaf Rittinger, Andreas Janecke, & Anselm Kampik. (2005). Ocular manifestations of keratitis– ichthyosis–deafness (KID) syndrome. Ophthalmology. 112(2). e1–e6. 55 indexed citations
13.
Rittinger, Olaf, et al.. (2005). Quantitative Heterozygotentestung und das therapeutische Dilemma bei Menkes-Syndrom. Klinische Pädiatrie. 217(5). 286–290. 1 indexed citations
14.
Falco, Francesca De, Silvia Cainarca, Grazia Andolfi, et al.. (2003). X‐linked Opitz syndrome: Novel mutations in the MID1 gene and redefinition of the clinical spectrum. American Journal of Medical Genetics Part A. 120A(2). 222–228. 72 indexed citations
15.
Rittinger, Olaf. (2001). Klinik und Genetik des Prader-Willi-Syndroms. Klinische Pädiatrie. 213(3). 91–98. 5 indexed citations
16.
Holinski‐Feder, Elke, Olaf Rittinger, Kerry Baldwin Jedele, et al.. (1999). Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region. American Journal of Medical Genetics. 86(2). 102–106. 9 indexed citations
17.
Plöchl, E, et al.. (1999). Clinical, Cytogenetic and Molecular Analysis of Three 46,XX Males. Journal of Pediatric Endocrinology and Metabolism. 12(3). 389–95. 4 indexed citations
18.
Plöchl, E, et al.. (1997). A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism. Klinische Pädiatrie. 209(3). 133–136. 15 indexed citations
19.
Holinski‐Feder, Elke, Astrid Golla, Imma Rost, et al.. (1996). Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). American Journal of Medical Genetics. 64(1). 125–130. 18 indexed citations
20.
Frick, J., et al.. (1994). Mediastinal Tumor andKlinefelter's Syndrome. European Urology. 26(4). 344–346. 4 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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