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Co-authors
(53)
R. Frank Kooy
5
Edwin Reyniers
3
Nathalie Van der Aa
3
Liesbeth Rooms
2
Bregje W. M. van Bon
2
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Authors
Geert Vandeweyer
Geert Vandeweyer,University of Antwerp,Genetics & Genealogy,Medicine,Bioinformatics & Computational Biology
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Geert Vandeweyer
University of Antwerp
Publications:
5
|
Citations:
29
Fields:
Genetics & Genealogy
,
Medicine
,
Bioinformatics & Computational Biology
View FAQ about top research areas and Fields of study
Collaborated with
53 co-authors
from 2009 to 2011
|
Cited by
196 authors
Cumulative
Annual
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Publications
(5)
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RefWorks
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CNV-WebStore: Online CNV Analysis, Storage and Interpretation
Geert Vandeweyer
,
Edwin Reyniers
,
Wim Wuyts
,
Liesbeth Rooms
,
R. Frank Kooy
Journal:
BMC Bioinformatics
, vol. 12, no. 1, pp. 4-8, 2011
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes
(
Citations: 11
)
Damien L Bruno
,
Britt-Marie Anderlid
,
Anna Lindstrand
,
Conny van Ravenswaaij-Arts
,
Devika Ganesamoorthy
,
Johanna Lundin
,
Christa Lese Martin
,
Jessica Douglas
,
Catherine Nowak
,
Margaret P Adam
,
R Frank Kooy
,
Nathalie Van der Aa
Geert Vandeweyer
http://academic.research.microsoft.com/io.ashx?type=5&id=30639895&selfId1=4795539&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 47, no. 5, pp. 299-311, 2010
A boy with mental retardation, obesity and hypertrichosis caused by a microdeletion of 19p13.12
(
Citations: 1
)
Nathalie Van der Aa
,
Geert Vandeweyer
,
R. Frank Kooy
Journal:
European Journal of Medical Genetics - EUR J MED GENET
, vol. 53, no. 5, pp. 291-293, 2010
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
(
Citations: 15
)
Nathalie Van der Aa
,
Liesbeth Rooms
,
Geert Vandeweyer
,
Jenneke van den Ende
,
Edwin Reyniers
,
Marco Fichera
,
Corrado Romano
,
Barbara Delle Chiaie
,
Geert Mortier
,
Björn Menten
,
Anne Destrée
,
Isabelle Maystadt
http://academic.research.microsoft.com/io.ashx?type=5&id=5616825&selfId1=4795539&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Medical Genetics - EUR J MED GENET
, vol. 52, no. 2, pp. 94-100, 2009
Balanced translocations in mental retardation
(
Citations: 2
)
Geert Vandeweyer
,
R. Frank Kooy
Journal:
Human Genetics - HUM GENET
, vol. 126, no. 1, pp. 133-147, 2009
Sort by:
Citations
(29 times by 28 publications)
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G Kirov
,
A J Pocklington
,
P Holmans
,
D Ivanov
,
M Ikeda
,
D Ruderfer
,
J Moran
,
K Chambert
,
D Toncheva
,
L Georgieva
,
D Grozeva
,
M Fjodorova
http://academic.research.microsoft.com/io.ashx?type=5&id=56564762&selfId1=4795539&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 2, pp. 142-153, 2012
Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency
P-S Cheah
,
H S Ramshaw
,
P Q Thomas
,
K Toyo-oka
,
X Xu
,
S Martin
,
P Coyle
,
M A Guthridge
,
F Stomski
,
M van den Buuse
,
A Wynshaw-Boris
,
A F Lopez
http://academic.research.microsoft.com/io.ashx?type=5&id=56564764&selfId1=4795539&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 4, pp. 451-466, 2012
LIS1 Duplication: Expanding the Phenotype
Jason P. Lockrow
,
Kenton R. Holden
,
Alka Dwivedi
,
Maria G. Matheus
,
Michael J. Lyons
Journal:
Journal of Child Neurology - JCN
, vol. 27, no. 6, pp. 791-795, 2012
A theoretical molecular network for dyslexia: integrating available genetic findings
(
Citations: 2
)
G. J. V. Poelmans
,
J. K. Buitelaar
,
D. L. Pauls
,
B. Franke
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 16, no. 4, pp. 365-382, 2011
Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly
(
Citations: 1
)
Gaëlle Friocourt
,
Pascale Marcorelles
,
Pascale Saugier-Veber
,
Marie-Lise Quille
,
Stephane Marret
,
Annie Laquerrière
Journal:
Acta Neuropathologica - ACTA NEUROPATHOL
, vol. 121, no. 2, pp. 149-170, 2011
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