Gunnar Schmidt

1.1k total citations
29 papers, 184 citations indexed

About

Gunnar Schmidt is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Gunnar Schmidt has authored 29 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Gunnar Schmidt's work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and DNA Repair Mechanisms (3 papers). Gunnar Schmidt is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and DNA Repair Mechanisms (3 papers). Gunnar Schmidt collaborates with scholars based in Germany, France and Sweden. Gunnar Schmidt's co-authors include Bernd Auber, Brigitte Schlegelberger, Sandra von Hardenberg, Doris Steinemann, Winfried Hofmann, Reinhold Schmidt, Faranaz Atschekzei, Georgios Sogkas, Colin Davenport and Stephanie Schubert and has published in prestigious journals such as Journal of Clinical Oncology, International Journal of Molecular Sciences and International Journal of Cancer.

In The Last Decade

Gunnar Schmidt

28 papers receiving 181 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gunnar Schmidt Germany 8 81 66 38 32 27 29 184
Loreall Pooler United States 8 87 1.1× 80 1.2× 39 1.0× 15 0.5× 41 1.5× 13 207
Vera Riehmer Germany 7 142 1.8× 54 0.8× 46 1.2× 18 0.6× 33 1.2× 11 229
Ninad Oak United States 8 131 1.6× 126 1.9× 69 1.8× 17 0.5× 20 0.7× 14 260
Thomas R. W. Oliver United Kingdom 5 119 1.5× 70 1.1× 90 2.4× 29 0.9× 20 0.7× 9 252
Virginie Saillour Canada 7 116 1.4× 65 1.0× 46 1.2× 20 0.6× 18 0.7× 10 191
Moonjung Jung United States 8 89 1.1× 37 0.6× 25 0.7× 30 0.9× 13 0.5× 17 181
Lenka Stolařová Czechia 4 65 0.8× 72 1.1× 38 1.0× 7 0.2× 39 1.4× 6 156
Marcus Danielsson Sweden 5 93 1.1× 55 0.8× 20 0.5× 47 1.5× 13 0.5× 5 168
Matthew Pun United States 6 140 1.7× 50 0.8× 54 1.4× 24 0.8× 60 2.2× 9 235
Marion Bähr Germany 5 155 1.9× 20 0.3× 40 1.1× 15 0.5× 25 0.9× 5 198

Countries citing papers authored by Gunnar Schmidt

Since Specialization
Citations

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

Fields of papers citing papers by Gunnar Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gunnar Schmidt

This figure shows the co-authorship network connecting the top 25 collaborators of Gunnar Schmidt. A scholar is included among the top collaborators of Gunnar Schmidt 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 Gunnar Schmidt. Gunnar Schmidt 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.
Sogkas, Georgios, Nadezhda Camacho-Ordóñez, Gunnar Schmidt, et al.. (2024). Novel hypermorphic variants in IRF2BP2 identified in patients with common variable immunodeficiency and autoimmunity. Clinical Immunology. 266. 110326–110326. 1 indexed citations
2.
Junk, Stefanie V., Gunnar Schmidt, Martin Zimmermann, et al.. (2024). Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia—a case-control study. Leukemia. 38(4). 887–892. 2 indexed citations
3.
Jahn, Kirsten, Gunnar Schmidt, Lutz Wiehlmann, et al.. (2023). Comparison of methylation estimates obtained via MinION nanopore sequencing and sanger bisulfite sequencing in the TRPA1 promoter region. BMC Medical Genomics. 16(1). 257–257. 9 indexed citations
4.
Schmidt, Axel, Nicolaus Schwerk, Diane M. Renz, et al.. (2023). Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children. Pediatric Pulmonology. 58(11). 3095–3105. 7 indexed citations
5.
Hardenberg, Sandra von, et al.. (2023). A holistic approach to maximise diagnostic output in trio exome sequencing. Frontiers in Pediatrics. 11. 1183891–1183891. 5 indexed citations
6.
Auber, Bernd, et al.. (2023). Diagnostic genomic sequencing in critically ill children. Medizinische Genetik. 35(2). 105–112.
7.
Schmidt, Gunnar, Anke K. Bergmann, Oliver Brandau, et al.. (2023). Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders. American Journal of Medical Genetics Part A. 191(7). 1849–1857. 1 indexed citations
8.
Schmidt, Gunnar, et al.. (2022). GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss. PLoS Computational Biology. 18(9). e1009785–e1009785. 3 indexed citations
9.
Osmanovic, Alma, Helge Martens, Kathrin Müller, et al.. (2021). Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients. Genes. 13(1). 84–84. 7 indexed citations
10.
Hauke, Jan, Barbara Wappenschmidt, Ulrike Faust, et al.. (2021). Aktualisierte Kriterien des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zur Klassifizierung von Keimbahn-Sequenzvarianten in Risikogenen für familiären Brust- und Eierstockkrebs. Senologie - Zeitschrift für Mammadiagnostik und -therapie. 18(2). 136–162. 3 indexed citations
11.
Morlot, Susanne, Gunnar Schmidt, Bernd Auber, et al.. (2020). De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia. Clinical Genetics. 98(4). 374–378. 5 indexed citations
12.
Wappenschmidt, Barbara, Jan Hauke, Ulrike Faust, et al.. (2020). Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants in Risk Genes for Hereditary Breast and Ovarian Cancer. Geburtshilfe und Frauenheilkunde. 80(4). 410–429. 14 indexed citations
13.
Golas, Monika M., Bernd Auber, Tim Ripperger, et al.. (2019). Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. American Journal of Medical Genetics Part A. 179(7). 1383–1389. 9 indexed citations
14.
Sogkas, Georgios, Felix C. Ringshausen, Ulrich Baumann, et al.. (2019). A novel NFKBIA variant substituting serine 36 of IκBα causes immunodeficiency with warts, bronchiectasis and juvenile rheumatoid arthritis in the absence of ectodermal dysplasia. Clinical Immunology. 210. 108269–108269. 17 indexed citations
15.
Schubert, Stephanie, Gunnar Schmidt, Winfried Hofmann, et al.. (2019). From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high‐throughput sequencing. Molecular Genetics & Genomic Medicine. 8(9). e1045–e1045. 3 indexed citations
16.
Behrens, Yvonne Lisa, Kathrin Thomay, Gunnar Schmidt, et al.. (2019). Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?. Genes Chromosomes and Cancer. 58(3). 139–148. 4 indexed citations
17.
Penkert, Judith, Gunnar Schmidt, Winfried Hofmann, et al.. (2018). Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast Cancer Research. 20(1). 87–87. 6 indexed citations
18.
Margalit, Avishai, et al.. (2012). Politik der Würde : über Achtung und Verachtung. Suhrkamp eBooks. 7 indexed citations
19.
Schmidt, Gunnar. (2003). Das Gesicht : eine Mediengeschichte. Bayerische Staatsbibliothek. 1 indexed citations
20.
Schmidt, Gunnar, et al.. (2003). Mikrologien. transcript Verlag eBooks. 1 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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