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Co-authors
(32)
Alain Fautrel
1
Anna-Elina Lehesjoki
1
Jill Clayton-Smith
1
Forbes D. C. Manson
1
Frederic Ezan (Frédéric Ezan)
1
Journals
(3)
PLOS One
1
VIROL J
1
AMER J HUM GENET
1
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Authors
Jabbar Khan
Jabbar Khan,University of Rennes 1,Genetics & Genealogy,Microbiology
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Jabbar Khan
University of Rennes 1
Publications:
3
|
Citations:
22
Fields:
Genetics & Genealogy
,
Microbiology
View FAQ about top research areas and Fields of study
Collaborated with
32 co-authors
from 2004 to 2011
|
Cited by
195 authors
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Annual
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Publications
(3)
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Overexpression of Active Aurora-C Kinase Results in Cell Transformation and Tumour Formation
Jabbar Khan
,
Frédéric Ezan
,
Jean-Yves Crémet
,
Alain Fautrel
,
David Gilot
,
Marine Lambert
,
Christelle Benaud
,
Marie-Bérengère Troadec
,
Claude Prigent
Journal:
PLOS One
, vol. 6, no. 10, 2011
Response to combination therapy of HCV 3a infected Pakistani patients and the role of NS5A protein
Ijaz Ali
,
Sanaullah Khan
,
Sobia Attaullah
,
Shahid Niaz Khan
,
Jabbar Khan
,
Sami Siraj
,
Aqib Iqbal
,
Zahoor A Swati
,
Muhammad Idrees
Journal:
Virology Journal - VIROL J
, vol. 8, no. 1, pp. 1-5, 2011
Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen
(
Citations: 22
)
Juha Kolehmainen
,
Robert Wilkinson
,
Anna-Elina Lehesjoki
,
Kate Chandler
,
Satu Kivitie-Kallio
,
Jill Clayton-Smith
,
Ann-Liz Träskelin
,
Laura Waris
,
Anne Saarinen
,
Jabbar Khan
,
Varda Gross-Tsur
,
Elias I. Traboulsi
http://academic.research.microsoft.com/io.ashx?type=5&id=36195340&selfId1=47529184&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 75, no. 1, pp. 122-127, 2004
Sort by:
Citations
(22 times by 22 publications)
A canine model of Cohen syndrome: Trapped Neutrophil Syndrome
Jeremy R Shearman
,
Alan N Wilton
Journal:
BMC Genomics
, vol. 12, no. 1, pp. 1-8, 2011
High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome
(
Citations: 1
)
Veronica Parri
,
Eleni Katzaki
,
Vera Uliana
,
Francesca Scionti
,
Rossella Tita
,
Rosangela Artuso
,
Ilaria Longo
,
Renske Boschloo
,
Raymon Vijzelaar
,
Angelo Selicorni
,
Francesco Brancati
,
Bruno Dallapiccola
http://academic.research.microsoft.com/io.ashx?type=5&id=37082369&selfId1=47529184&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 18, no. 10, pp. 1133-1140, 2010
Search for the best indicators for the presence of a VPS13B gene mutation and confirmation of diagnostic criteria in a series of 34 patients genotyped for suspected Cohen syndrome
(
Citations: 1
)
Salima El Chehadeh
,
Bernard Aral
,
Nadège Gigot
,
Christel Thauvin-Robinet
,
Anne Donzel
,
Marie-Ange Delrue
,
Didier Lacombe
,
Albert David
,
Lydie Burglen
,
Nicole Philip
,
Anne Moncla
,
Valérie Cormier-Daire
http://academic.research.microsoft.com/io.ashx?type=5&id=30641275&selfId1=47529184&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 47, no. 8, pp. 549-553, 2010
Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians
(
Citations: 3
)
F.-Y. Deng
,
L.-J. Zhao
,
Y.-F. Pei
,
B.-Y. Sha
,
X.-G. Liu
,
H. Yan
,
L. Wang
,
T.-L. Yang
,
R. R. Recker
,
C. J. Papasian
,
H.-W. Deng
Journal:
Osteoporosis International - OSTEOPOROSIS INT
, vol. 21, no. 4, pp. 579-587, 2010
Cohen syndrome diagnosis using whole genome arrays
Nuria Rivera-Brugués
,
Beate Albrecht
,
Dagmar Wieczorek
,
Heinrich Schmidt
,
Thomas Keller
,
Ina Göhring
,
Arif B Ekici
,
Andreas Tzschach
,
Masoud Garshasbi
,
Kathlen Franke
,
Norman Klopp
,
H-Erich Wichmann
http://academic.research.microsoft.com/io.ashx?type=5&id=59318609&selfId1=47529184&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 48, no. 2, pp. 136-140, 2010
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