Sonja A. de Munnik

1.1k total citations
9 papers, 209 citations indexed

About

Sonja A. de Munnik is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Sonja A. de Munnik has authored 9 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Hematology. Recurrent topics in Sonja A. de Munnik's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Platelet Disorders and Treatments (2 papers). Sonja A. de Munnik is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Platelet Disorders and Treatments (2 papers). Sonja A. de Munnik collaborates with scholars based in Netherlands, United States and Belgium. Sonja A. de Munnik's co-authors include Nine Knoers, Ernie M.H.F. Bongers, Jeroen Schoots, Han G. Brunner, Jolt Roukema, Andrew P. Jackson, Joanne Verheij, Frederik G. Dikkers, Nicole de Leeuw and Lies H. Hoefsloot and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and eLife.

In The Last Decade

Sonja A. de Munnik

9 papers receiving 205 citations

Peers

Sonja A. de Munnik

GENET

MB

PPCH

HEMAT

GENET

Jill K. Northup United States

Aline Receveur France

Shu Yau United Kingdom

M. Elizabeth McCready Canada

Emiel Baten Belgium

Neda Zadeh United States

Renqian Du China

Carmelo Laganà Italy

Arjan Bouman Netherlands

Cynthia Lim United States

Jill K. Northup United States

Sonja A. de Munnik

155 ×1.3

GENET

115 ×1.1

MB

26 ×1.1

PPCH

15 ×0.7

HEMAT

27 ×1.4

GENET

Citations per year, relative to Sonja A. de Munnik Sonja A. de Munnik (= 1×) peers Jill K. Northup

Countries citing papers authored by Sonja A. de Munnik

Since Specialization

Citations

This map shows the geographic impact of Sonja A. 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 A. 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 A. de Munnik more than expected).

Fields of papers citing papers by Sonja A. de Munnik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Sonja A. de Munnik. A scholar is included among the top collaborators of Sonja A. 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 A. de Munnik. Sonja A. 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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9 of 9 papers shown

1.

Verdonschot, Job A.J., Vanessa van Empel, Sonja A. de Munnik, et al.. (2024). Clinical Guideline for Preimplantation Genetic Testing in Inherited Cardiac Diseases. Circulation Genomic and Precision Medicine. 17(2). e004416–e004416. 8 indexed citations

2.

Simons, Annet, Janneke Schuurs-Hoeijmakers, Evelien Zonneveld‐Huijssoon, et al.. (2022). Trio-based whole exome sequencing in patients with suspected sporadic inborn errors of immunity: A retrospective cohort study. eLife. 11. 4 indexed citations

3.

Marneth, Anna E., Arie J. Hoogendijk, Floris P. J. van Alphen, et al.. (2021). Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders. Blood. 138(1). 86–90. 10 indexed citations

4.

Geest, Ferdy S. van, Marcel E. Meima, Kyra E. Stuurman, et al.. (2020). Clinical and Functional Consequences of C-Terminal Variants in MCT8: A Case Series. The Journal of Clinical Endocrinology & Metabolism. 106(2). 539–553. 5 indexed citations

5.

Simons, Annet, Sonja A. de Munnik, Marten R. Nijziel, et al.. (2018). Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia. 25(1). 127–135. 19 indexed citations

6.

Munnik, Sonja A. de, Jolt Roukema, Jeroen Schoots, et al.. (2015). Meier-Gorlin syndrome. Orphanet Journal of Rare Diseases. 10(1). 114–114. 58 indexed citations

7.

Beunders, Gea, Sonja A. de Munnik, Nathalie Van der Aa, et al.. (2014). Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. European Journal of Human Genetics. 23(6). 803–807. 22 indexed citations

8.

Munnik, Sonja A. de, Sixto García‐Miñáur, Alexander Hoischen, et al.. (2013). A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome. European Journal of Human Genetics. 22(6). 844–846. 36 indexed citations

9.

Verheij, Joanne, Sonja A. de Munnik, Trijnie Dijkhuizen, et al.. (2009). An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions. European Journal of Medical Genetics. 52(5). 353–357. 47 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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