Oliver Bartsch

5.1k citations

153 papers · 2.7k indexed · h-index 29

Molecular Biology top 5%
Genetics top 1%
Surgery top 10%
Pediatrics, Perinatology and Child Health top 5%
Plant Science top 10%

Co-authors: Thomas Haaf Georg Klaus Hinkel E. Schwinger Ulrich Zechner Katrin Õunap E Seemanová Margareta Mikkelsen Vera M. Kalscheuer
Topics: Genomic variations and chromosomal abnormalities (57 papers)Prenatal Screening and Diagnostics (25 papers)Chromosomal and Genetic Variations (21 papers)
Cited by: Developmental Biology Genetics Sensory Systems
Journals: SHILAP Revista de lepidopterologíaThe Journal of Immunology PLoS ONE
Partner nations: Germany United States Estonia

In The Last Decade

Oliver Bartsch

147 papers receiving 2.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	FGFR1 variants contributed to families with tooth agenesis 2023 ·Human Genomics ·(unknown),(unknown),Min Gu,Chengcheng Zhang,Oliver Bartsch,Barbara Vona,Liwen Fan,(unknown),Yongchu Pan	1
2	The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience 2022 ·European Journal of Human Genetics ·Sofia Douzgou,(unknown),(unknown),(unknown),(unknown),(unknown),Sylvia Huisman,Brittany Simpson,(unknown),Donatella Milani,Oliver Bartsch,Didier Lacombe,Sixto García‐Miñáur,Raoul C. M. Hennekam	5
3	A Highly Specific Assay for the Detection of SARS-CoV-2–Reactive CD4+ and CD8+ T Cells in COVID-19 Patients 2020 ·The Journal of Immunology ·Henning Zelba,(unknown),Johannes Harter,Natalia Pieper,(unknown),Simone Kayser,(unknown),Oliver Bartsch,(unknown),Saskia Biskup	13
4	Sema3a plays a role in the pathogenesis of CHARGE syndrome 2018 ·Human Molecular Genetics ·Roser Ufartes,(unknown),(unknown),Christiane Neuhofer,Janika Möller,Peter Wehner,Conny M.A. van Ravenswaaij‐Arts,(unknown),Ina Schanze,Andreas Tzschach,Oliver Bartsch,Annette Borchers,Silke Pauli	20
5	Homozygote und „compound“-heterozygote RYR1-Mutationen: Neue Erkenntnisse zu Prävalenz und Penetranz der malignen Hyperthermie 2014 ·Der Anaesthesist ·(unknown),(unknown),Nicolai Kohlschmidt,(unknown),Oliver Bartsch,Ulrich Zechner,I. Tzanova	0
6	Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics 2013 ·BMJ Open ·(unknown),Birgit Zirn,Luitgard Graul‐Neumann,(unknown),M. Suckfüll,Annegret Buske,Axel Bohring,Christian Kubisch,Stefanie Vogt,Gertrud Strobl‐Wildemann,Marie T. Greally,Oliver Bartsch,Daniela Steinberger	38
7	Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653–5655delTAT, causing harlequin ichthyosis 2013 ·Gene ·(unknown),(unknown),Catharina Whybra,Eva Mildenberger,(unknown),Ulrich Zechner,Oliver Bartsch	8
8	Novel <b><i>VANGL1</i></b> Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects 2012 ·Molecular Syndromology ·Oliver Bartsch,(unknown),A. Thiede,(unknown),(unknown),Ioan Ştefan Florian,Thomas Haaf,Ulrich Zechner,L Sabová,Fabian Horn	24
9	Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism 2011 ·Journal of Applied Genetics ·(unknown),(unknown),Oliver Bartsch	4
10	A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12 2011 ·European Journal of Medical Genetics ·Oliver Bartsch,Detlev Schindler,Vera Beyer,Stefan Gesk,Ruben van’t Slot,(unknown),Arjan Buijs,Nicolaas G.J. Jaspers,Reiner Siebert,Thomas Haaf,Martin Poot	7
11	Girl With Partial Turner Syndrome and Absence Epilepsy 2008 ·Pediatric Neurology ·(unknown),Riina Žordania,(unknown),Oliver Bartsch,Katrin Õunap	10
12	A region on human chromosome 4 (q35.1→qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis 2005 ·Genes Chromosomes and Cancer ·(unknown),Bettina Rudolph,R Kühne-Heid,Vera M. Kalscheuer,Oliver Bartsch,Lars Jansen,Katrin Beer,Birgit Meyer,Achim Schneider,Matthias Dürst	15
13	Failure to detect DUP25 in lymphoblastoid cells derived from patients with panic disorder and control individuals representing European and American populations 2004 ·European Journal of Human Genetics ·Guanshan Zhu,Oliver Bartsch,Cristina Skrypnyk,Alessandro Rotondo,(unknown),Claudia R. Harris,Matti Virkkunen,Giovanni B. Cassano,David Goldman	11
14	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 2004 ·American Journal of Medical Genetics Part A ·Denise Horn,Holger Tönnies,Heidemarie Neitzel,Dagmar Wahl,Georg Klaus Hinkel,Arpad von Moers,Oliver Bartsch	37
15	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 2004 ·American Journal of Medical Genetics Part A ·Sabine Walter,(unknown),Georg Klaus Hinkel,Beate Mitulla,Katrin Õunap,(unknown),(unknown),Barbara Utermann,(unknown),Vera M. Kalscheuer,Oliver Bartsch	26
16	FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy 1999 ·European Journal of Human Genetics ·Oliver Bartsch,(unknown),Georg Klaus Hinkel,(unknown),Markus Stümm,(unknown),(unknown),Sevim Balcı,Frank Majewski	65
17	The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case 1999 ·Cytogenetic and Genome Research ·Oliver Bartsch,Wolfram Kreß,Andrew Wagner,E Seemanová	25
18	A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region 1997 ·Human Genetics ·Oliver Bartsch,Georg Klaus Hinkel,(unknown),(unknown),Merete Bugge,Margareta Mikkelsen,Dimitris Avramopoulos,Michael A. Morris,Stylianos E. Antonarakis	19
19	Fryns syndrome: two further cases without lateral diaphragmatic defects 1995 ·Clinical Dysmorphology ·Oliver Bartsch,Peter Meinecke,(unknown)	13
20	DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor 1995 ·Human Genetics ·Simone Schuffenhauer,Oliver Bartsch,Markus Stümm,Tina Buchholz,Theoni Petropoulou,(unknown),Bernd H. Belohradsky,Georg Klaus Hinkel,Thomas Meitinger,Rolf‐Dieter Wegner	46

About Oliver Bartsch

Oliver Bartsch is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 153 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (57 papers), Prenatal Screening and Diagnostics (25 papers) and Chromosomal and Genetic Variations (21 papers). The work is most often cited by research in Developmental Biology (269 citations), Genetics (1.3k citations) and Sensory Systems (207 citations). Oliver Bartsch has collaborated with scholars based in Germany, United States and Estonia. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

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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