Jurgen Del‐Favero

27.5k total citations · 1 hit paper
141 papers, 6.8k citations indexed

About

Jurgen Del‐Favero is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jurgen Del‐Favero has authored 141 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 51 papers in Genetics and 25 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jurgen Del‐Favero's work include Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (18 papers) and Genomics and Rare Diseases (15 papers). Jurgen Del‐Favero is often cited by papers focused on Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (18 papers) and Genomics and Rare Diseases (15 papers). Jurgen Del‐Favero collaborates with scholars based in Belgium, Sweden and United States. Jurgen Del‐Favero's co-authors include Christine Van Broeckhoven, Peter De Jonghe, Lieve Claes, Berten Ceulemans, Lieven Lagae, Peter De Rijk, Stephan Claes, D. Goossens, Cornelia M. van Duijn and Rolf Adolfsson and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Jurgen Del‐Favero

140 papers receiving 6.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

2001 916 citations Lieve Claes, Jurgen Del‐Favero et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jurgen Del‐Favero Belgium	45	2.5k	1.7k	1.5k	1.4k	664	141	6.8k
Andrea Schmitt Germany	48	3.3k 1.3×	1.0k 0.6×	1.8k 1.2×	1.4k 1.0×	1.2k 1.8×	254	8.6k
Robert H. Lipsky United States	44	2.6k 1.0×	806 0.5×	962 0.6×	2.5k 1.7×	743 1.1×	112	8.1k
Sabine Bahn United Kingdom	48	3.5k 1.4×	1.2k 0.7×	1.4k 1.0×	1.9k 1.3×	901 1.4×	176	8.3k
Peter Holmans United Kingdom	55	3.8k 1.5×	4.3k 2.5×	1.9k 1.2×	1.9k 1.3×	548 0.8×	209	9.4k
Allison E. Ashley‐Koch United States	48	2.2k 0.9×	1.8k 1.1×	599 0.4×	1.3k 0.9×	531 0.8×	210	8.3k
Michael Wong United States	47	3.1k 1.2×	1.5k 0.8×	1.4k 0.9×	2.3k 1.6×	2.6k 3.9×	151	7.6k
Steven A. Kushner Netherlands	44	2.0k 0.8×	874 0.5×	642 0.4×	2.0k 1.4×	233 0.4×	137	6.7k
Chiara Maria Mazzanti Italy	38	2.1k 0.8×	1.0k 0.6×	1.3k 0.9×	1.6k 1.1×	356 0.5×	159	6.9k
Tadao Arinami Japan	53	2.6k 1.0×	1.7k 1.0×	1.4k 0.9×	2.6k 1.8×	1.7k 2.6×	211	9.3k
Panos Roussos United States	44	2.4k 1.0×	1.2k 0.7×	696 0.5×	822 0.6×	626 0.9×	140	5.0k

Countries citing papers authored by Jurgen Del‐Favero

Since Specialization

Citations

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

Fields of papers citing papers by Jurgen Del‐Favero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jurgen Del‐Favero. 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 Jurgen Del‐Favero. The network helps show where Jurgen Del‐Favero may publish in the future.

Co-authorship network of co-authors of Jurgen Del‐Favero

This figure shows the co-authorship network connecting the top 25 collaborators of Jurgen Del‐Favero. A scholar is included among the top collaborators of Jurgen Del‐Favero 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 Jurgen Del‐Favero. Jurgen Del‐Favero 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

Szatkiewicz, Jin, James J. Crowley, Annelie Nordin Adolfsson, et al.. (2019). The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. Translational Psychiatry. 9(1). 60–60. 11 indexed citations

Gielis, Els M., Charlie Beirnaert, Amélie Dendooven, et al.. (2018). Plasma donor-derived cell-free DNA kinetics after kidney transplantation using a single tube multiplex PCR assay. PLoS ONE. 13(12). e0208207–e0208207. 58 indexed citations

Zwarts, Liesbeth, et al.. (2016). Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila. Psychopharmacology. 233(9). 1751–1762. 5 indexed citations

Gielis, Els M., Kristien J. Ledeganck, Hans Wils, et al.. (2016). SO002QUANTIFICATION OF PLASMA DONOR-DERIVED CELL-FREE DNA TO MONITOR KIDNEY TRANSPLANT HEALTH: PRELIMINARY RESULTS OF A SINGLE TUBE MULTIPLEX PCR ASSAY. Nephrology Dialysis Transplantation. 31(suppl_1). i1–i1. 4 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

Wikgren, Mikael, Martin Maripuu, Thomas Karlsson, et al.. (2011). Short Telomeres in Depression and the General Population Are Associated with a Hypocortisolemic State. Biological Psychiatry. 71(4). 294–300. 139 indexed citations

Claes, Stephan, Aye-Mu Myint, Katharina Domschke, et al.. (2011). The kynurenine pathway in major depression: Haplotype analysis of three related functional candidate genes. Psychiatry Research. 188(3). 355–360. 53 indexed citations

Castermans, Dries, Karolien Volders, Liesbeth Backx, et al.. (2010). SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles. Human Molecular Genetics. 19(7). 1368–1378. 72 indexed citations

Gijselinck, Ilse, Kristel Sleegers, Sebastiaan Engelborghs, et al.. (2007). Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Ghent University Academic Bibliography (Ghent University). 3 indexed citations

10.

Eede, Filip Van Den, Jurgen Del‐Favero, Karl‐Fredrik Norrback, et al.. (2007). Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in recurrent major depressive disorder. Psychiatry Research. 153(1). 17–25. 13 indexed citations

11.

Goossens, D., Noel N. Williams, Lien Heyrman, et al.. (2007). Gene copy number variation in schizophrenia. Schizophrenia Research. 96(1-3). 93–99. 50 indexed citations

12.

Bogaerts, Veerle, Sebastiaan Engelborghs, Samir Kumar‐Singh, et al.. (2007). A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder. Brain. 130(9). 2277–2291. 34 indexed citations

13.

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

14.

Mendlewicz, Julien, Pierre Oswald, Stephan Claes, et al.. (2005). Patient-control association study of substance P-related genes in unipolar and bipolar affective disorders. The International Journal of Neuropsychopharmacology. 8(4). 505–505. 22 indexed citations

15.

Massat, Isabelle, Daniel Souery, Jurgen Del‐Favero, et al.. (2004). Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study. Molecular Psychiatry. 10(6). 598–605. 126 indexed citations

16.

Claes, Stephan, Sandra Villafuerte, Thomas Forsgren, et al.. (2003). The corticotropin-releasing hormone binding protein is associated with major depression in a population from Northern Sweden. Biological Psychiatry. 54(9). 867–872. 49 indexed citations

17.

Gestel, Sofie Van, Stephan Claes, Jurgen Del‐Favero, et al.. (2002). Heritability and genetics of personality in healthy families and families with affective disorders from Sweden. Behavior Genetics. 487–487. 1 indexed citations

18.

Claes, Lieve, Jurgen Del‐Favero, Berten Ceulemans, et al.. (2001). De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy. The American Journal of Human Genetics. 68(6). 1327–1332. 916 indexed citations breakdown →

19.

Goossens, D., S Villafuerte, Sofie Van Gestel, et al.. (2000). No CAG or CCG repeats within 18Q2133-q23 involved in bipolar disorder. American Journal of Medical Genetics Part A. 96(4). 5657. 1 indexed citations

20.

Villafuerte, Sandra, Geert R. Verheyen, Jurgen Del‐Favero, et al.. (1998). Manic depressive disorder and chromosome 18. American Journal of Medical Genetics Part A. 81(6). 475–476. 4 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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