Sonja de Munnik

729 total citations
6 papers, 175 citations indexed

About

Sonja de Munnik is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sonja de Munnik has authored 6 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Sonja de Munnik's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Chromatin Dynamics (1 paper). Sonja de Munnik is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Chromatin Dynamics (1 paper). Sonja de Munnik collaborates with scholars based in Netherlands, United States and Germany. Sonja de Munnik's co-authors include Linda B. Baughn, Jamie M. Kramer, Marjolein H. Willemsen, Margarita Sáenz, Annette Schenck, Margot R.F. Reijnders, Levinus A. Bok, Rolph Pfundt, Alexander P.A. Stegmann and Conny M.A. van Ravenswaaij‐Arts and has published in prestigious journals such as PLoS Genetics, European Journal of Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Sonja de Munnik

5 papers receiving 171 citations

Peers

Countries citing papers authored by Sonja de Munnik

Since Specialization

Citations

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

Fields of papers citing papers by Sonja de Munnik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sonja de Munnik. 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 Sonja de Munnik. The network helps show where Sonja de Munnik may publish in the future.

Co-authorship network of co-authors of Sonja de Munnik

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B 2025 ·American Journal of Medical Genetics Part A ·Servi J.C. Stevens, (unknown), Nicole Y. Souren, Merryn Macville, (unknown), Brigitte H. W. Faas, Bart de Koning, Arthur van den Wijngaard, Sonja de Munnik, Masoud Zamani Esteki	0
2	MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency 2021 ·European Journal of Human Genetics ·Karen Knapp, (unknown), (unknown), Frederike L. Harms, (unknown), Charlotte W. Ockeloen, Sonja de Munnik, Ernie M.H.F. Bongers, Jennie Murray, Nicholas Pachter, Jonas Denecke, Kerstin Kutsche, Louise S. Bicknell	13
3	S847 DISTINCT AND COMMON DEREGULATED PATHWAYS IN RUNX1, GATA1 AND GFI1B ASSOCIATED BLEEDING DISORDERS 2019 ·HemaSphere ·(unknown), Anna E. Marneth, Floris van Alphen, Jeroen W. A. Jansen, (unknown), Saskia E.M. Schols, Sonja de Munnik, A. Simons, Emile van den Akker, Alexander B. Meijer, Bert van der Reijden	1
4	Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene 2018 ·Molecular Genetics & Genomic Medicine ·Vyne van der Schoot, Sonja de Munnik, Hanka Venselaar, Mariet W. Elting, Grazia M.S. Mancini, Conny M.A. van Ravenswaaij‐Arts, Britt‐Marie Anderlid, Han G. Brunner, Servi J.C. Stevens	18
5	Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder 2017 ·PLoS Genetics ·Tom S. Koemans, Tjitske Kleefstra, (unknown), (unknown), Margot R.F. Reijnders, Sonja de Munnik, Marjolein H. Willemsen, Michaela Fencková, Connie T. R. M. Stumpel, Levinus A. Bok, Margarita Sáenz, (unknown), Linda B. Baughn, Alexander P.A. Stegmann, Rolph Pfundt, Huiqing Zhou, Hans van Bokhoven, Annette Schenck, Jamie M. Kramer	100
6	Central 22q11.2 deletions 2014 ·American Journal of Medical Genetics Part A ·Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren‐Bemelmans, Hermine E. Veenstra‐Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, William Reardon, Sonja de Munnik, (unknown), Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema‐Raddatz, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts	43

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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