Matthias Begemann

3.9k total citations
81 papers, 1.8k citations indexed

About

Matthias Begemann is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Matthias Begemann has authored 81 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 56 papers in Molecular Biology and 41 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Matthias Begemann's work include Genetic Syndromes and Imprinting (55 papers), Epigenetics and DNA Methylation (43 papers) and Prenatal Screening and Diagnostics (41 papers). Matthias Begemann is often cited by papers focused on Genetic Syndromes and Imprinting (55 papers), Epigenetics and DNA Methylation (43 papers) and Prenatal Screening and Diagnostics (41 papers). Matthias Begemann collaborates with scholars based in Germany, United Kingdom and Spain. Matthias Begemann's co-authors include Thomas Eggermann, Lukas Soellner, Miriam Elbracht, Gerhard Binder, Sabrina Spengler, Marcel H. Schulz, Ivan G. Costa, Zhijian Li, Thomas Look and Martin Zenke and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and Blood.

In The Last Decade

Matthias Begemann

80 papers receiving 1.7k citations

Peers

Countries citing papers authored by Matthias Begemann

Since Specialization

Citations

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

Fields of papers citing papers by Matthias Begemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthias Begemann

This figure shows the co-authorship network connecting the top 25 collaborators of Matthias Begemann. A scholar is included among the top collaborators of Matthias Begemann 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 Matthias Begemann. Matthias Begemann 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	Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver–Russell phenotype 2025 ·Clinical Epigenetics ·Matthias Begemann, Anna Lengyel, (unknown), Árpád Ferenc Kovács, György Fekete, (unknown), Jeremias Krause, Miriam Elbracht, Florian Kraft, Thomas Eggermann	0
2	Quality assurance within the context of genome diagnostics (a german perspective) 2023 ·Medizinische Genetik ·Florian Kraft, Anna Benet‐Pagès, Daniel Berner, Anna Teubert, Sebastian Eck, Norbert Arnold, Peter Bauer, Matthias Begemann, Marc Sturm, Stephanie Kleinle, Tobias B. Haack, Thomas Eggermann	1
3	Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability 2021 ·European Journal of Human Genetics ·Natja Haag, Ene‐Choo Tan, Matthias Begemann, (unknown), Florian Kraft, (unknown), Angeline Lai, Maggie Brett, Ganeshwaran H. Mochida, Stephanie DiTroia, Lynn Pais, Jennifer E. Neil, Muna Al‐Saffar, Lailá Bastaki, Christopher A. Walsh, Ingo Kurth, Cordula Knopp	6
4	DNA methylation changes during long-term in vitro cell culture are caused by epigenetic drift 2021 ·Communications Biology ·Julia Franzen, Theodoros Georgomanolis, Anton Selich, Chao‐Chung Kuo, Reinhard Stöger, Lilija Brant, (unknown), Eduardo Fernández‐Rebollo, (unknown), Alina Ostrowska, Matthias Begemann, Miloš Nikolić, Björn Rath, Anthony D. Ho, Michael Rothe, Axel Schambach, Argyris Papantonis, Wolfgang Wagner	39
5	Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same family 2020 ·European Journal of Human Genetics ·Thomas Eggermann, (unknown), Matthias Begemann, Miriam Elbracht	25
6	Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome 2020 ·Clinical Epigenetics ·(unknown), Stephanie Karch, Ute Moog, György Fekete, Anna Lengyel, (unknown), Thomas Eggermann, Matthias Begemann	9
7	DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans 2019 ·Journal of Clinical Investigation ·Gergely Karsai, Florian Kraft, Natja Haag, GC Korenke, (unknown), Alaa Othman, Saranya Suriyanarayanan, R. Steiner, Cordula Knopp, Michael Mull, Markus Bergmann, J. M. Schröder, Joachim Weis, Miriam Elbracht, Matthias Begemann, Thorsten Hornemann, Ingo Kurth	71
8	A novel homozygous splice-site mutation in the SPTBN4 gene causes axonal neuropathy without intellectual disability 2019 ·European Journal of Medical Genetics ·Martin Häusler, Matthias Begemann, Hart G.W. Lidov, Ingo Kurth, Basil T. Darras, Miriam Elbracht	7
9	Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndrome 2019 ·Molecular and Cellular Probes ·(unknown), Robert Meyer, Matthias Begemann, Miriam Elbracht, Thomas Eggermann	8
10	Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations 2019 ·European Journal of Medical Genetics ·Thomas Eggermann, Matthias Begemann, Ingo Kurth, Miriam Elbracht	6
11	Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers 2018 ·European Journal of Human Genetics ·Lukas Soellner, Florian Kraft, (unknown), Matthias Begemann, Ingo Kurth, Miriam Elbracht, Thomas Eggermann	10
12	Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction 2017 ·Molecular Cytogenetics ·Sandra Chantot‐Bastaraud, (unknown), Frédéric Brioude, Matthias Begemann, Miriam Elbracht, Luitgard Graul‐Neumann, Madeleine D. Harbison, Irène Netchine, Thomas Eggermann	20
13	Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management 2017 ·The Journal of Pediatrics ·Robert Meyer, Lukas Soellner, Matthias Begemann, (unknown), György Fekete, Nils Rahner, Klaus Zerres, Miriam Elbracht, Thomas Eggermann	19
14	Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring 2017 ·European Journal of Human Genetics ·Lukas Soellner, Matthias Begemann, Franziska Degenhardt, Annegret Geipel, Thomas Eggermann, Elisabeth Mangold	33
15	Microdeletions of the 7q32.2 imprinted region are associated with Silver–Russell syndrome features 2015 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Matthias Begemann, Lukas Soellner, Thomas Eggermann	27
16	Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing 2015 ·Molecular and Cellular Probes ·Cordula Knopp, Sabine Rudnik‐Schöneborn, Thomas Eggermann, Carsten Bergmann, Matthias Begemann, Katharina Schoner, Klaus Zerres, Nadina Ortiz Brüchle	21
17	Haploinsufficiency of <b><i>ANKRD11</i></b> (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell Syndrome 2013 ·Molecular Syndromology ·Sabrina Spengler, Barbara Oehl‐Jaschkowitz, Matthias Begemann, (unknown), Klaus Zerres, Thomas Eggermann	10
18	Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10 2012 ·American Journal of Medical Genetics Part A ·Thomas Eggermann, Matthias Begemann, (unknown), María Palomares‐Bralo, Elena Vallespín, Luís Fernández, (unknown), Sabrina Spengler, Sixto García‐Miñaúr	7
19	Molecular Karyotyping as a Relevant Diagnostic Tool in Children with Growth Retardation with Silver-Russell Features 2012 ·The Journal of Pediatrics ·Sabrina Spengler, Matthias Begemann, Nadina Ortiz Brüchle, Michael Baudis, Bernd Denecke, (unknown), Barbara Oehl‐Jaschkowitz, Bernd Schulze, (unknown), Christiane Spaich, Peter Blümel, Anna Jauch, Ute Moog, Klaus Zerres, Thomas Eggermann	23
20	Testing of Buccal Swab DNA Does Not Increase the Detection Rate for Imprinting Control Region 1 Hypomethylation in Silver-Russell Syndrome 2011 ·Genetic Testing and Molecular Biomarkers ·Sabrina Spengler, Matthias Begemann, Gerhard Binder, Thomas Eggermann	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.

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