Sign in
Author
|
Conference
|
Journal
|
Organization
|
Year
|
DOI
Look for results that meet for the following criteria:
since
equal to
before
between
and
Search in all fields of study
Limit my searches in the following fields of study
Agriculture Science
Arts & Humanities
Biology
Chemistry
Computer Science
Economics & Business
Engineering
Environmental Sciences
Geosciences
Material Science
Mathematics
Medicine
Physics
Social Science
Multidisciplinary
Co-authors
(107)
Chris Van Geet
35
Chantal Thys
20
Marc F. Hoylaerts
17
Christine Wittevrongel
16
Jos Vermylen
13
Journals
(25)
HUM MOL GENET
5
J THROMB HAEMOST
4
Blood
3
EUR J PEDIAT
2
J CLIN ENDOCRINOL METAB
2
Keywords
(90)
Embed
Subscribe
Academic
Authors
Kathleen Freson
Kathleen Freson,Catholic University of Leuven,Genetics & Genealogy,Molecular Biology,Cardiology
Edit
Kathleen Freson
Catholic University of Leuven
Publications:
44
|
Citations:
355
Fields:
Genetics & Genealogy
,
Molecular Biology
,
Cardiology
View FAQ about top research areas and Fields of study
Collaborated with
107 co-authors
from 1998 to 2011
|
Cited by
1130 authors
Cumulative
Annual
Sort by:
Publications
(44)
BibTeX
|
RIS
|
RefWorks
Download
An integrated proteomics and genomics analysis to unravel a heterogeneous platelet secretion defect
Michela Di Michele
,
Chantal Thys
,
Etienne Waelkens
,
Lut Overbergh
,
Wannes D'Hertog
,
Chantal Mathieu
,
Rita De Vos
,
Kathelijne Peerlinck
,
Chris Van Geet
,
Kathleen Freson
Journal:
Journal of Proteomics - J PROTEOMICS
, vol. 74, no. 6, pp. 902-913, 2011
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1mutation
(
Citations: 2
)
Kathleen Freson
,
Koen Devriendt
,
Gert Matthijs
,
Achiel Van Hoof
,
Rita De Vos
,
Chantal Thys
,
Kristien Minner
,
Marc F. Hoylaerts
,
Jos Vermylen
,
Chris Van Geet
Published in 2010.
SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles
(
Citations: 3
)
D. Castermans
,
K. Volders
,
A. Crepel
,
L. Backx
,
R. De Vos
,
K. Freson
,
S. Meulemans
,
J. R. Vermeesch
,
C. T. R. M. Schrander-Stumpel
,
P. De Rijk
,
J. Del-Favero
,
C. Van Geet
http://academic.research.microsoft.com/io.ashx?type=5&id=37623874&selfId1=23678019&selfId2=0&maxNumber=12&query=
Journal:
Human Molecular Genetics - HUM MOL GENET
, vol. 19, no. 7, pp. 1368-1378, 2010
Regulators of Platelet cAMP Levels: Clinical and Therapeutic Implications
(
Citations: 1
)
L. Noe
,
K. Peeters
,
B. Izzi
,
C. Van Geet
,
K. Freson
Journal:
Current Medicinal Chemistry - CURR MEDICINAL CHEM
, vol. 17, no. 26, pp. 2897-2905, 2010
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system
Benedetta Izzi
,
Brigitte Decallonne
,
Koen Devriendt
,
Roger Bouillon
,
Dirk Vanderschueren
,
Elena Levtchenko
,
Francis de Zegher
,
Annick Van den Bruel
,
Diether Lambrechts
,
Chris Van Geet
,
Kathleen Freson
Journal:
Clinica Chimica Acta - CLIN CHIM ACTA
, vol. 411, no. 23, pp. 2033-2039, 2010
Sort by:
Citations
(355 times by 259 publications)
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
(
Citations: 4
)
Irina Voineagu
,
Xinchen Wang
,
Patrick Johnston
,
Jennifer K. Lowe
,
Yuan Tian
,
Steve Horvath
,
Jonathan Mill
,
Rita M. Cantor
,
Benjamin J. Blencowe
,
Daniel H. Geschwind
Journal:
Nature
, vol. 474, no. 7351, pp. 380-384, 2011
Platelet receptor signaling in thrombus formation
(
Citations: 1
)
David Stegner
,
Bernhard Nieswandt
Journal:
Journal of Molecular Medicine-jmm
, vol. 89, no. 2, pp. 109-121, 2011
A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
(
Citations: 1
)
Guntram Borck
,
Heidrun Wunram
,
Angela Steiert
,
Alexander E. Volk
,
Friederike Körber
,
Sigrid Roters
,
Peter Herkenrath
,
Bernd Wollnik
,
Deborah J. Morris-Rosendahl
,
Christian Kubisch
Journal:
Human Genetics - HUM GENET
, vol. 129, no. 1, pp. 45-50, 2011
Dendritic spine formation and synaptic function require neurobeachin
(
Citations: 1
)
Katharina Niesmann
,
Dorothee Breuer
,
Johannes Brockhaus
,
Gesche Born
,
Ilka Wolff
,
Carsten Reissner
,
Manfred W. Kilimann
,
Astrid Rohlmann
,
Markus Missler
Journal:
Nature Communications
, vol. 2, 2011
Characterization of the Deleted in Autism 1 Protein Family: Implications for Studying Cognitive Disorders
Azhari Aziz
,
Sean P. Harrop
,
Naomi E. Bishop
,
Jörg Hoheisel
Journal:
PLOS One
, vol. 6, no. 1, 2011
Comments