Guido J. Breedveld - Concepedia

Author

Guido J. Breedveld

Also Known As

Breedveld, Guido J., Chokri Mhiri, Erik J Simons, G Breedveld, G J Breedveld, G. Breedveld, G. J. Breedveld, G.J. Breedveld, GUIDO BREEDVELD, Guido Breedveld

121

Publications

11.5K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Sapienza University of Rome Radboud University Nijmegen Universidade de São Paulo

About

Guido J. Breedveld is an author at Erasmus MC specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	43	7.3K
2	Social Sciences	5	5	2.9K
3	Public Health	2	2	106
4	Engineering	1	1	14
5	Natural Sciences	1	1	69

Guido J. Breedveld

Publications

11K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Science GeneticsDisease Gene IdentificationSocial SciencesMendelian DisorderDj-1 Protein	2003	2.8K
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Alessio Di Fonzo, Christan F. Rohé, Joaquim J. Ferreira, The Lancet Molecular NeuroscienceMendelian DisorderAutosomal Dominant ParkinsonGenetic DisorderParkinson Disease	2005	529
Mutations in <i>Col4a1</i> Cause Perinatal Cerebral Hemorrhage and Porencephaly Douglas B. Gould, F. Campbell Phalan, Guido J. Breedveld, Science Knockout MouseDevelopmental AnomalyMutant MiceMolecular NeuroscienceDevelopmental Biology	2005	523
Disruption of a long-range cis-acting regulator for <i>Shh</i> causes preaxial polydactyly Laura A. Lettice, T. Horikoshi, Simon J. H. Heaney, Proceedings of the National Academy of Sciences	2002	456
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease Marialuisa Quadri, Antonio Federico, Tianna Zhao, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderParkinson DiseaseGeneticsChronic Liver Disease	2012	411
PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36 Cornelia M. van Duijn, Marieke Dekker, Vincenzo Bonifati, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2001	377
<i>FBXO7</i> mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome Alessio Di Fonzo, Marieke C. J. Dekker, P. Montagna, Neurology	2008	353
Early-onset parkinsonism associated with <i>PINK1</i> mutations Vincenzo Bonifati, Christan F. Rohé, Guido J. Breedveld, Neurology	2005	335
Mutation in the<i>SYNJ1</i>Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism Marialuisa Quadri, Mingyan Fang, Marina Picillo, Human Mutation Neurodegenerative DiseasesEarly-onset ParkinsonismMendelian DisorderGenetic DisorderExome Sequencing	2013	309
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan Alessio Di Fonzo, Yah‐Huei Wu‐Chou, Chin-Song Lu, Neurogenetics Neurodegenerative DiseasesMendelian DisorderDisease RiskGenetic DisorderGenetics	2006	228

Page 1