Sonia De Zutter

484 total citations
12 papers, 326 citations indexed

About

Sonia De Zutter is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Sonia De Zutter has authored 12 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Psychiatry and Mental health. Recurrent topics in Sonia De Zutter's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Sonia De Zutter is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Sonia De Zutter collaborates with scholars based in Belgium, Sweden and United Kingdom. Sonia De Zutter's co-authors include Jurgen Del‐Favero, Karl‐Fredrik Norrback, Rolf Adolfsson, Lien Heyrman, Kristel Sleegers, Ann Van Den Bogaert, An‐Sofie Lenaerts, Christine Van Broeckhoven, Peter De Rijk and D. Goossens and has published in prestigious journals such as PLoS ONE, Virology and Schizophrenia Research.

In The Last Decade

Sonia De Zutter

12 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sonia De Zutter Belgium	10	120	118	85	79	52	12	326
Nagesh Aragam United States	12	214 1.8×	184 1.6×	50 0.6×	73 0.9×	30 0.6×	13	483
Fumiko Sunaga Japan	9	170 1.4×	345 2.9×	67 0.8×	51 0.6×	52 1.0×	11	503
Claudia Hanses Germany	5	287 2.4×	195 1.7×	90 1.1×	59 0.7×	55 1.1×	6	508
Rodrigo R. R. Duarte United Kingdom	14	113 0.9×	168 1.4×	48 0.6×	46 0.6×	48 0.9×	26	465
Alexandros Hatzimanolis Greece	10	62 0.5×	80 0.7×	71 0.8×	47 0.6×	76 1.5×	25	311
An‐a Kazuno Japan	11	139 1.2×	217 1.8×	97 1.1×	77 1.0×	47 0.9×	13	350
Jordan M. Ramsey United Kingdom	10	101 0.8×	89 0.8×	60 0.7×	22 0.3×	99 1.9×	10	332
Ivana Furač Croatia	10	142 1.2×	91 0.8×	60 0.7×	85 1.1×	33 0.6×	20	290
Wenzel Glanz Germany	5	64 0.5×	51 0.4×	38 0.4×	59 0.7×	91 1.8×	10	313
Lalit Kaurani Germany	10	62 0.5×	207 1.8×	55 0.6×	33 0.4×	34 0.7×	16	387

Countries citing papers authored by Sonia De Zutter

Since Specialization

Citations

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

Fields of papers citing papers by Sonia De Zutter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sonia De Zutter. 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 Sonia De Zutter. The network helps show where Sonia De Zutter may publish in the future.

Co-authorship network of co-authors of Sonia De Zutter

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

All Works

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12 of 12 papers shown

Forero, Diego A., Sonia De Zutter, Karl‐Fredrik Norrback, et al.. (2016). A network of synaptic genes associated with schizophrenia and bipolar disorder. Schizophrenia Research. 172(1-3). 68–74. 26 indexed citations

Bossche, Maarten Van Den, Mojca Stražišar, Anthony Liekens, et al.. (2013). Identification of rare copy number variants in high burden schizophrenia families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(3). 273–282. 20 indexed citations

Bossche, Maarten Van Den, Mandy Johnstone, Mojca Stražišar, et al.. (2012). Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(7). 812–822. 26 indexed citations

Bossche, Maarten Van Den, Mojca Stražišar, Chris Bervoets, et al.. (2012). Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(4). 465–475. 22 indexed citations

Zutter, Sonia De, Lien Heyrman, Karl‐Fredrik Norrback, et al.. (2011). Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population. Bipolar Disorders. 13(7-8). 614–623. 17 indexed citations

Moens, Lotte, Peter De Rijk, Joke Reumers, et al.. (2011). Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population. PLoS ONE. 6(8). e23450–e23450. 51 indexed citations

Moens, Lotte, Maaike Alaerts, Maarten Van Den Bossche, et al.. (2010). PCM1 and schizophrenia: A replication study in the Northern Swedish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(6). 1240–1243. 8 indexed citations

Alaerts, Maaike, Diego A. Forero, Lotte Moens, et al.. (2009). Support for NRG1 as a Susceptibility Factor for Schizophrenia in a Northern Swedish Isolated Population. Archives of General Psychiatry. 66(8). 828–828. 29 indexed citations

Alaerts, Maaike, Diego A. Forero, Lotte Moens, et al.. (2008). Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(4). 585–592. 17 indexed citations

10.

Bogaert, Ann Van Den, Kristel Sleegers, Sonia De Zutter, et al.. (2006). Association of Brain-Specific Tryptophan Hydroxylase, TPH2, With Unipolar and Bipolar Disorder in a Northern Swedish, Isolated Population. Archives of General Psychiatry. 63(10). 1103–1103. 88 indexed citations

11.

Bogaert, Ann Van Den, Kristel Sleegers, Sonia De Zutter, et al.. (2006). No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population. Psychiatric Genetics. 16(5). 209–212. 7 indexed citations

12.

Beirnaert, Els, Sonia De Zutter, Wouter Janssens, & Guido van der Groen. (2001). Potent Broad Cross-Neutralizing Sera Inhibit Attachment of Primary HIV-1 Isolates (Groups M and O) to Peripheral Blood Mononuclear Cells. Virology. 281(2). 305–314. 15 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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