Oliver Bartsch

5.1k total citations
153 papers, 2.7k citations indexed

About

Oliver Bartsch is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Oliver Bartsch has authored 153 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Genetics, 81 papers in Molecular Biology and 28 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Oliver Bartsch's work include Genomic variations and chromosomal abnormalities (57 papers), Prenatal Screening and Diagnostics (25 papers) and Chromosomal and Genetic Variations (21 papers). Oliver Bartsch is often cited by papers focused on Genomic variations and chromosomal abnormalities (57 papers), Prenatal Screening and Diagnostics (25 papers) and Chromosomal and Genetic Variations (21 papers). Oliver Bartsch collaborates with scholars based in Germany, United States and Estonia. Oliver Bartsch's co-authors include Thomas Haaf, Georg Klaus Hinkel, E. Schwinger, Ulrich Zechner, Katrin Õunap, E Seemanová, Margareta Mikkelsen, Vera M. Kalscheuer, Jürgen Kohlhase and Martin Hagemann and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Oliver Bartsch

147 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oliver Bartsch Germany 29 1.3k 1.3k 421 387 284 153 2.7k
Carlos A. Bacino United States 38 2.4k 1.8× 3.1k 2.4× 405 1.0× 934 2.4× 521 1.8× 134 5.0k
Margherita Silengo Italy 29 2.0k 1.5× 1.7k 1.3× 489 1.2× 617 1.6× 124 0.4× 114 3.3k
Andreas Winterpacht Germany 33 2.5k 1.8× 1.4k 1.1× 232 0.6× 275 0.7× 115 0.4× 85 3.7k
E Seemanová Czechia 30 2.4k 1.8× 1.1k 0.8× 162 0.4× 202 0.5× 345 1.2× 92 3.4k
Annick Toutain France 36 2.5k 1.8× 1.5k 1.1× 455 1.1× 367 0.9× 131 0.5× 138 4.0k
Keiko Wakui Japan 28 1.3k 1.0× 1.4k 1.0× 192 0.5× 283 0.7× 353 1.2× 89 2.3k
Alan Shanske United States 26 976 0.7× 931 0.7× 240 0.6× 310 0.8× 193 0.7× 84 1.9k
Sylvie Odent France 36 2.7k 2.0× 1.5k 1.2× 333 0.8× 562 1.5× 73 0.3× 152 3.8k
Muriel Holder‐Espinasse France 26 1.1k 0.8× 1.0k 0.8× 358 0.9× 176 0.5× 62 0.2× 74 2.0k
Donatella Milani Italy 24 1.3k 0.9× 994 0.8× 233 0.6× 180 0.5× 124 0.4× 118 2.1k

Countries citing papers authored by Oliver Bartsch

Since Specialization
Citations

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

Fields of papers citing papers by Oliver Bartsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oliver Bartsch

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver Bartsch. A scholar is included among the top collaborators of Oliver Bartsch 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 Oliver Bartsch. Oliver Bartsch 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.
Gu, Min, Chengcheng Zhang, Oliver Bartsch, et al.. (2023). FGFR1 variants contributed to families with tooth agenesis. Human Genomics. 17(1). 93–93. 1 indexed citations
2.
Douzgou, Sofia, Sylvia Huisman, Brittany Simpson, et al.. (2022). The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience. European Journal of Human Genetics. 30(7). 841–847. 5 indexed citations
3.
Zelba, Henning, Johannes Harter, Natalia Pieper, et al.. (2020). A Highly Specific Assay for the Detection of SARS-CoV-2–Reactive CD4+ and CD8+ T Cells in COVID-19 Patients. The Journal of Immunology. 206(3). 580–587. 13 indexed citations
4.
Ufartes, Roser, Christiane Neuhofer, Janika Möller, et al.. (2018). Sema3a plays a role in the pathogenesis of CHARGE syndrome. Human Molecular Genetics. 27(8). 1343–1352. 20 indexed citations
5.
Kohlschmidt, Nicolai, et al.. (2014). Homozygote und „compound“-heterozygote RYR1-Mutationen: Neue Erkenntnisse zu Prävalenz und Penetranz der malignen Hyperthermie. Der Anaesthesist. 63. 643–650.
6.
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
7.
Whybra, Catharina, et al.. (2013). Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653–5655delTAT, causing harlequin ichthyosis. Gene. 531(2). 510–513. 8 indexed citations
8.
Bartsch, Oliver, A. Thiede, Ioan Ştefan Florian, et al.. (2012). Novel <b><i>VANGL1</i></b> Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects. Molecular Syndromology. 3(2). 76–81. 24 indexed citations
9.
Bartsch, Oliver, et al.. (2011). Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism. Journal of Applied Genetics. 52(3). 331–334. 4 indexed citations
10.
Bartsch, Oliver, Detlev Schindler, Vera Beyer, et al.. (2011). A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12. European Journal of Medical Genetics. 55(1). 49–55. 7 indexed citations
11.
Žordania, Riina, et al.. (2008). Girl With Partial Turner Syndrome and Absence Epilepsy. Pediatric Neurology. 38(4). 289–292. 10 indexed citations
12.
Rudolph, Bettina, R Kühne-Heid, Vera M. Kalscheuer, et al.. (2005). A region on human chromosome 4 (q35.1→qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis. Genes Chromosomes and Cancer. 43(3). 260–272. 15 indexed citations
13.
Zhu, Guanshan, Oliver Bartsch, Cristina Skrypnyk, et al.. (2004). Failure to detect DUP25 in lymphoblastoid cells derived from patients with panic disorder and control individuals representing European and American populations. European Journal of Human Genetics. 12(6). 505–508. 11 indexed citations
14.
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
15.
Walter, Sabine, Georg Klaus Hinkel, Beate Mitulla, et al.. (2004). Subtelomere FISH in 50 children with mental retardation and minor anomalies, identified by a checklist, detects 10 rearrangements including a de novo balanced translocation of chromosomes 17p13.3 and 20q13.33. American Journal of Medical Genetics Part A. 128A(4). 364–373. 26 indexed citations
16.
Bartsch, Oliver, et al.. (1999). FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. European Journal of Human Genetics. 7(7). 748–756. 65 indexed citations
17.
Bartsch, Oliver, Wolfram Kreß, Andrew Wagner, & E Seemanová. (1999). The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case. Cytogenetic and Genome Research. 85(3-4). 310–314. 25 indexed citations
18.
Bartsch, Oliver, Georg Klaus Hinkel, Merete Bugge, et al.. (1997). A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region. Human Genetics. 100(5-6). 669–675. 19 indexed citations
19.
Bartsch, Oliver, et al.. (1995). Fryns syndrome: two further cases without lateral diaphragmatic defects. Clinical Dysmorphology. 4(4). 352–358. 13 indexed citations
20.
Schuffenhauer, Simone, Oliver Bartsch, Markus Stümm, et al.. (1995). DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor. Human Genetics. 96(5). 562–571. 46 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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