Guido J. Breedveld

11.6k total citations · 1 hit paper
77 papers, 6.9k citations indexed

About

Guido J. Breedveld is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Guido J. Breedveld has authored 77 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Neurology, 27 papers in Molecular Biology and 24 papers in Neurology. Recurrent topics in Guido J. Breedveld's work include Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological diseases and metabolism (23 papers) and Genetic Neurodegenerative Diseases (9 papers). Guido J. Breedveld is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (25 papers), Neurological diseases and metabolism (23 papers) and Genetic Neurodegenerative Diseases (9 papers). Guido J. Breedveld collaborates with scholars based in Netherlands, Italy and United States. Guido J. Breedveld's co-authors include Ben A. Oostra, Vincenzo Bonifati, Peter Heutink, Nicola Vanacore, John C. van Swieten, G. Meco, Cornelia M. van Duijn, Marieke Dekker, Marijke J. van Baren and Patrizia Rizzu and has published in prestigious journals such as Science, The Lancet and Nucleic Acids Research.

In The Last Decade

Guido J. Breedveld

75 papers receiving 6.8k citations

Hit Papers

align trajectories

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.

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

2003 2.2k citations Vincenzo Bonifati, Patrizia Rizzu et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Guido J. Breedveld Netherlands	38	3.6k	2.4k	1.9k	1.4k	1.2k	77	6.9k
Aglaia Athanassiadou Greece	21	5.3k 1.4×	2.1k 0.9×	3.0k 1.6×	1.3k 1.0×	1.9k 1.6×	52	7.4k
Ekaterina Rogaeva Canada	53	3.4k 0.9×	3.6k 1.5×	1.6k 0.9×	1.4k 1.0×	3.4k 2.8×	188	8.3k
Patrick A. Dion Canada	42	3.9k 1.1×	3.0k 1.3×	1.5k 0.8×	1.0k 0.7×	803 0.7×	180	6.9k
Saskia Biskup Germany	36	3.0k 0.8×	2.6k 1.1×	1.3k 0.7×	1.2k 0.9×	1.3k 1.0×	158	6.0k
Amalia Dutra United States	23	5.3k 1.4×	3.9k 1.6×	3.0k 1.6×	1.3k 1.0×	2.2k 1.8×	43	9.3k
Giuseppe Di Iorio Italy	19	6.1k 1.7×	2.1k 0.9×	3.5k 1.9×	1.7k 1.2×	2.1k 1.7×	68	8.2k
Giuseppe De Michele Italy	43	3.2k 0.9×	3.0k 1.3×	3.9k 2.1×	1.2k 0.9×	515 0.4×	208	6.8k
Susan Ide United States	13	5.6k 1.5×	2.3k 0.9×	3.2k 1.7×	1.5k 1.1×	1.9k 1.6×	23	7.6k
Vladimir L. Buchman United Kingdom	44	3.9k 1.1×	3.1k 1.3×	3.1k 1.6×	785 0.6×	1.8k 1.5×	142	8.1k
Kevin St. P. McNaught United States	31	3.0k 0.8×	2.4k 1.0×	2.3k 1.2×	795 0.6×	1.1k 0.9×	41	5.6k

Countries citing papers authored by Guido J. Breedveld

Since Specialization

Citations

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

Fields of papers citing papers by Guido J. Breedveld

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guido J. Breedveld. 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 Guido J. Breedveld. The network helps show where Guido J. Breedveld may publish in the future.

Co-authorship network of co-authors of Guido J. Breedveld

This figure shows the co-authorship network connecting the top 25 collaborators of Guido J. Breedveld. A scholar is included among the top collaborators of Guido J. Breedveld 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 Guido J. Breedveld. Guido J. Breedveld 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

Dopper, Elise G.P., Marina Arcaro, Daniela Galimberti, et al.. (2024). Two novel variants in GRN: the relevance of CNV analysis and genetic screening in FTLD patients with a negative family history. Journal of Neurology. 272(1). 64–64. 1 indexed citations

Breedveld, Guido J., et al.. (2023). deCLUTTER2+ – a pipeline to analyze calcium traces in a stem cell model for ventral midbrain patterned astrocytes. Disease Models & Mechanisms. 16(6). 1 indexed citations

Park, Yangshin, Ebba Lohmann, Anneke J.A. Kievit, et al.. (2021). A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease. Parkinsonism & Related Disorders. 89. 63–72. 20 indexed citations

Breedveld, Guido J., Hanneke Geut, Wiggert A. van Cappellen, et al.. (2021). LRP10 interacts with SORL1 in the intracellular vesicle trafficking pathway in non-neuronal brain cells and localises to Lewy bodies in Parkinson’s disease and dementia with Lewy bodies. Acta Neuropathologica. 142(1). 117–137. 14 indexed citations

Vergouw, Leonie J.M., Shamiram Melhem, Laura Donker Kaat, et al.. (2020). LRP10 variants in progressive supranuclear palsy. Neurobiology of Aging. 94. 311.e5–311.e10. 5 indexed citations

Bouwkamp, Christian G., Zaid Afawi, Aviva Fattal‐Valevski, et al.. (2018). ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia. Neurology Genetics. 4(2). e223–e223. 22 indexed citations

Verkerk, Annemieke J.M.H., Guido J. Breedveld, Herma van der Linde, et al.. (2018). CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability. European Journal of Human Genetics. 26(4). 552–560. 10 indexed citations

Moors, Tim E., Silvia Paciotti, Angela Ingrassia, et al.. (2018). Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson’s Disease and Dementia with Lewy Bodies. Molecular Neurobiology. 56(2). 1344–1355. 108 indexed citations

Quadri, Marialuisa, Suvasini Sharma, Simone Olgiati, et al.. (2015). Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes. Movement Disorders. 30(7). 996–1001. 49 indexed citations

10.

Olgiati, Simone, Anna De Rosa, Marialuisa Quadri, et al.. (2014). PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family. Neurogenetics. 15(3). 183–188. 87 indexed citations

11.

Yonova‐Doing, Ekaterina, Masharip Atadzhanov, Marialuisa Quadri, et al.. (2012). Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease. Parkinsonism & Related Disorders. 18(5). 567–571. 40 indexed citations

12.

Santoro, Lucio, Guido J. Breedveld, Fiore Manganelli, et al.. (2010). Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. Neurogenetics. 12(1). 33–39. 78 indexed citations

13.

Verkerk, Annemieke J.M.H., Daniëlle C. Cath, Herma C. van der Linde, et al.. (2006). Genetic and clinical analysis of a large Dutch Gilles de la Tourette family. Molecular Psychiatry. 11(10). 954–964. 45 indexed citations

14.

Gould, Douglas B., Guido J. Breedveld, Saskia E. van Mil, et al.. (2005). Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly. Science. 308(5725). 1167–1171. 366 indexed citations

15.

Brooks, Alice S., Aida M. Bertoli‐Avella, Grzegorz Burzynski, et al.. (2005). Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems. The American Journal of Human Genetics. 77(1). 120–126. 106 indexed citations

16.

Bonifati, Vincenzo, Guido J. Breedveld, Ferdinando Squitieri, et al.. (2002). Localization of autosomal recessive early‐onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset. Annals of Neurology. 51(2). 253–256. 57 indexed citations

17.

Baren, Marijke J. van, Guido J. Breedveld, Marijke Joosse, et al.. (2001). Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction. Mammalian Genome. 12(1). 77–79. 8 indexed citations

18.

Hing, Anne, Marijke J. van Baren, Marijke Joosse, et al.. (1999). A Physical and Transcriptional Map of the Preaxial Polydactyly Locus on Chromosome 7q36. Genomics. 57(3). 342–351. 60 indexed citations

19.

Pakstis, A.J., Peter Heutink, David L. Pauls, et al.. (1991). Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome. PubMed Central. 21 indexed citations

20.

Heutink, Peter, et al.. (1991). Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome.. The American Journal of Human Genetics. 48(2). 281–94. 60 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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