Oliver Bartsch

Johannes Gutenberg University Mainz — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

40h-index5.1kcitations372works13.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(69), Prenatal Screening and Diagnostics(29), Chromosomal and Genetic Variations(27), Congenital heart defects research(25), Congenital limb and hand anomalies(21)

Publications367 total

Further Evidence That Chondrocalcinosis 1 ( <scp>CCAL1</scp> ) is a Confirmed Mendelian Phenotype With a Known Molecular Basis
American Journal of Medical Genetics Part A·2025Open Access
In-depth characterization of vaccine-induced neoantigen-specific T cells in patients with IDH1-mutant glioma undergoing personalized peptide vaccination
Journal for ImmunoTherapy of Cancer·2025· 3 citedOpen Access
CTIM-12. A RETROLECTIVE ANALYSIS ON THE SAFETY, EFFICACY AND IMMUNOGENICITY OF 203 GLIOBLASTOMA PATIENTS TREATED WITH PERSONALIZED THERAPEUTIC CANCER VACCINES (PTCV)
Neuro-Oncology·2024Open Access
A real-world observation of patients with glioblastoma treated with a personalized peptide vaccine
Nature Communications·2024· 40 citedOpen Access
<i>De novo</i> and inherited monoallelic variants in <i>TUBA4A</i> cause ataxia and spasticity
Brain·2024· 10 citedOpen Access
Expanding the spectrum of phenotypes for <i>MPDZ</i>: Report of four unrelated families and review of the literature
Clinical Genetics·2024· 3 citedOpen Access
Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement
Journal of Medical Genetics·2024· 35 citedOpen Access
Case Report: Targeting of individual somatic tumor mutations by multipeptide vaccination tailored for HLA class I and II presentation induces strong CD4 and CD8 T-cell responses in a patient with metastatic castration sensitive prostate cancer
Frontiers in Immunology·2023· 7 citedOpen Access
FGFR1 variants contributed to families with tooth agenesis
Human Genomics·2023· 7 citedOpen Access
Additional file 2 of FGFR1 variants contributed to families with tooth agenesis
Figshare·2023Open Access
Adjuvant Treatment for Breast Cancer Patients Using Individualized Neoantigen Peptide Vaccination—A Retrospective Observation
Vaccines·2022· 12 citedOpen Access
Acral lamellar ichthyosis with amino acid substitution in the C‐terminus of keratin 2
Journal of the European Academy of Dermatology and Venereology·2022Open Access
Further characterization of <scp>Borjeson‐Forssman‐Lehmann</scp> syndrome in females due to de novo variants in <scp><i>PHF6</i></scp>
Clinical Genetics·2022· 13 citedOpen Access
The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience
European Journal of Human Genetics·2022· 13 citedOpen Access
Correction to: First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
BMC Ophthalmology·2021Open Access
First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
BMC Ophthalmology·2021· 20 citedOpen Access
Use of plasma ctDNA as a potential biomarker for longitudinal monitoring of a patient with metastatic high-risk upper tract urothelial carcinoma receiving pembrolizumab and personalized neoepitope-derived multipeptide vaccinations: a case report
Journal for ImmunoTherapy of Cancer·2021· 17 citedOpen Access
Additional file 4 of First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
Figshare·2021Open Access
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·2020· 17 citedOpen Access
The phenotypic spectrum of Chitayat syndrome: Six additional affected individuals
University of Southern Denmark Research Portal (University of Southern Denmark)·2020
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Frequent Co-authors

Thomas Haaf(9), Ulrich Zechner(7), Georg Klaus Hinkel(5), E. Schwinger(5), Katrin Õunap(4), Vera M. Kalscheuer(4), E Seemanová(3), Michael B. Petersen(3), Margareta Mikkelsen(3), Stanislav Lechno(3), Nicolai Kohlschmidt(3), Vera Beyer(3), Annette Grüters(2), Patricia Fergelot(2), Julien Van‐Gils(2), Sixto García‐Miñáur(2), Lidia Larizza(2), Didier Lacombe(2), Raoul C. M. Hennekam(2), Siobhan O. Burns(2)