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Co-authors
(279)
Ben A. Oostra
32
Peter Heutink
23
Vincenzo Bonifati
18
Alessio Di Fonzo
9
Christan F. Rohe (Christan F. Rohé)
7
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Authors
Guido J. Breedveld
Guido J. Breedveld,Erasmus MC, University Medical Center Rotterdam,Genetics & Genealogy,Neuroscience,Molecular Biology
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Guido J. Breedveld
Erasmus MC, University Medical Center Rotterdam
Publications:
47
|
Citations:
1046
Fields:
Genetics & Genealogy
,
Neuroscience
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
279 co-authors
from 1991 to 2011
|
Cited by
3545 authors
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Annual
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Publications
(47)
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Novel ATP13A2 ( PARK9 ) homozygous mutation in a family with marked phenotype variability
(
Citations: 5
)
Lucio Santoro
,
Guido J. Breedveld
,
Fiore Manganelli
,
Rosa Iodice
,
Chiara Pisciotta
,
Maria Nolano
,
Francesca Punzo
,
Mario Quarantelli
,
Sabina Pappatà
,
Alessio Di Fonzo
,
Ben A. Oostra
,
Vincenzo Bonifati
Journal:
Neurogenetics
, vol. 12, no. 1, pp. 33-39, 2011
Loss of Nuclear Activity of the FBXO7 Protein in Patients with Parkinsonian-Pyramidal Syndrome (PARK15)
Tianna Zhao
,
Esther De Graaff
,
Guido J. Breedveld
,
Agnese Loda
,
Lies-Anne Severijnen
,
Cokkie H. Wouters
,
Frans W. Verheijen
,
Marieke C. J. Dekker
,
Pasquale Montagna
,
Rob Willemsen
,
Ben A. Oostra
,
Vincenzo Bonifati
Journal:
PLOS One
, vol. 6, no. 2, 2011
Tagged mutagenesis by efficient minos-based germ line transposition
(
Citations: 5
)
Wit de T. P. M
,
S. Dekker
,
A. Maas
,
G. J. Breedveld
,
T. A. Knoch
,
A. Langeveld
,
D. Szumska
,
R. Craig
,
S. Bhattacharya
,
F. G. Grosveld
,
D. D. Drabek
Journal:
Molecular and Cellular Biology - MOL CELL BIOL
, vol. 30, no. 1, pp. 68-77, 2010
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred
(
Citations: 2
)
Guido J. Breedveld
,
Giovanni Fabbrini
,
Ben A. Oostra
,
Alfredo Berardelli
,
Vincenzo Bonifati
Journal:
Neurogenetics
, vol. 11, no. 4, pp. 417-423, 2010
No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease
(
Citations: 1
)
Steven J. Collins
,
Maaike Schuur
,
Alison Boyd
,
Victoria Lewis
,
Genevieve M. Klug
,
Amelia McGlade
,
Andrew van Oosterhout
,
Guido Breedveld
,
Ben A. Oostra
,
Colin Masters
,
Cornelia M. Van Duijn
Journal:
Neuroscience Letters - NEUROSCI LETT
, vol. 472, no. 1, pp. 16-18, 2010
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Citations
(1046 times by 816 publications)
Mutations in a P-Type ATPase Gene Cause Axonal Degeneration
Xianjun Zhu
,
Richard T. Libby
,
Wilhelmine N. de Vries
,
Richard S. Smith
,
Dana L. Wright
,
Roderick T. Bronson
,
Kevin L. Seburn
,
Simon W. M. John
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 8, 2012
Common Pathogenic Effects of Missense Mutations in the P-Type ATPase ATP13A2 (PARK9) Associated with Early-Onset Parkinsonism
Agata Podhajska
,
Alessandra Musso
,
Alzbeta Trancikova
,
Klodjan Stafa
,
Roger Moser
,
Sarah Sonnay
,
Liliane Glauser
,
Darren J. Moore
Journal:
PLOS One
, vol. 7, no. 6, 2012
Brain-Lung-Thyroid Disease: Clinical Features of a Kindred With a Novel Thyroid Transcription Factor 1 Mutation
Joseph M. Ferrara
,
Octavian R. Adam
,
Susan M. Kirwin
,
David J. Houghton
,
Casey Shepherd
,
Kathy M. B. Vinette
,
Irene Litvan
Journal:
Journal of Child Neurology - JCN
, vol. 27, no. 1, pp. 68-73, 2012
Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders
Rebekah E McWhirter
,
Ruth McQuillan
,
Elizabeth Visser
,
Carl Counsell
,
James F Wilson
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 2, pp. 198-202, 2012
Developmental Origins of Cerebrovascular Disease II: Considering Gene-Environment Interactions When Developing Neuroprotective Strategies
Mark S. Scher
Journal:
Journal of Child Neurology - JCN
, vol. 27, no. 2, pp. 238-250, 2012
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