Tobias Bartolomaeus

489 total citations
6 papers, 49 citations indexed

About

Tobias Bartolomaeus is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Tobias Bartolomaeus has authored 6 papers receiving a total of 49 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Immunology. Recurrent topics in Tobias Bartolomaeus's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Tobias Bartolomaeus is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Tobias Bartolomaeus collaborates with scholars based in Germany, Austria and Costa Rica. Tobias Bartolomaeus's co-authors include Julia Hentschel, Rami Abou Jamra, Bernt Popp, Pia Zacher, Konrad Platzer, Diana Le Duc, Ilona Krey, Johannes R. Lemke, Anja Heinze and Johannes Rebstock and has published in prestigious journals such as Scientific Reports, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Tobias Bartolomaeus

6 papers receiving 49 citations

Peers

Countries citing papers authored by Tobias Bartolomaeus

Since Specialization

Citations

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

Fields of papers citing papers by Tobias Bartolomaeus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tobias Bartolomaeus

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

#	Work	Indexed citations
1	Re-evaluation and re-analysis of 152 research exomes five years after the initial report reveals clinically relevant changes in 18% 2023 ·European Journal of Human Genetics ·Tobias Bartolomaeus, Julia Hentschel, Rami Abou Jamra, Bernt Popp	6
2	The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome 2022 ·Clinical Genetics ·Bernt Popp, Melanie Brügger, (unknown), Tobias Bartolomaeus, (unknown), Julia Hentschel, Nataliya Di Donato, Andreas Rump, Janina Gburek‐Augustat, Elisabeth Graf, Matias Wagner, Ina Sorge, Johannes R. Lemke, Thomas Meitinger, Rami Abou Jamra, Vincent Strehlow, Theresa Brunet	2
3	Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion 2022 ·Scientific Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), Pia Zacher, Tobias Bartolomaeus, (unknown), (unknown), Nicole Scholz, Konrad Platzer, (unknown), Julia Hentschel, Tobias Langenhan, Johannes R. Lemke, Antje Garten, Rami Abou Jamra, Diana Le Duc	2
4	Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental Disorders 2022 ·Genes ·(unknown), Tobias Bartolomaeus, Bernt Popp, (unknown), (unknown), Julia Hentschel, Denny Popp, Rami Abou Jamra	6
5	The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals 2021 ·Genetics in Medicine ·Pia Zacher, (unknown), (unknown), Tobias Bartolomaeus, Diana Le Duc, (unknown), Anja Heinze, Susanne Horn, (unknown), (unknown), Julia Hentschel, (unknown), Ilona Krey, (unknown), Konrad Platzer, Johannes Rebstock, Bernt Popp, Mathias Stiller, (unknown), Rami Abou Jamra, Johannes R. Lemke	31
6	Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain 2021 ·European Journal of Human Genetics ·(unknown), Ilona Krey, (unknown), Rami Abou Jamra, Tobias Bartolomaeus, (unknown), Steffen Syrbe, (unknown), (unknown), Christian Roth, Helga Rehder, (unknown), Diana Le Duc, Susanna Schubert, (unknown), Alejandro Leal, Katharina Schoner, Bernt Popp	2

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.

Explore authors with similar magnitude of impact