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Co-authors
(95)
Benoit Arveiler (Benoît Arveiler)
11
Didier Lacombe
11
Cyril Goizet
8
Ingrid Burgelin
5
Caroline Rooryck
4
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(13)
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2
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Authors
Isabelle Coupry
Isabelle Coupry,Victor Segalen Bordeaux 2 University,Genetics & Genealogy,Neuroscience,Molecular Biology
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Isabelle Coupry
Victor Segalen Bordeaux 2 University
Publications:
17
|
Citations:
136
Fields:
Genetics & Genealogy
,
Neuroscience
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
95 co-authors
from 1994 to 2011
|
Cited by
536 authors
Cumulative
Annual
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Publications
(17)
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Lung disease associated with periventricular nodular heterotopia and an FLNA mutation
(
Citations: 1
)
Alice Masurel-Paulet
,
Eric Haan
,
Elizabeth M. Thompson
,
Cyril Goizet
,
Christel Thauvin-Robinet
,
Andrew Tai
,
Declan Kennedy
,
Greg Smith
,
Teck Yee Khong
,
Guilhem Solé
,
Elodie Guerineau
,
Isabelle Coupry
http://academic.research.microsoft.com/io.ashx?type=5&id=49660614&selfId1=25149749&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Medical Genetics - EUR J MED GENET
, vol. 54, no. 1, pp. 25-28, 2011
A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia
(
Citations: 5
)
D. Simon
,
B. Laloo
,
M. Barillot
,
T. Barnetche
,
C. Blanchard
,
C. Rooryck
,
M. Marche
,
I. Burgelin
,
I. Coupry
,
N. Chassaing
,
B. Gilbert-Dussardier
,
D. Lacombe
http://academic.research.microsoft.com/io.ashx?type=5&id=37623941&selfId1=25149749&selfId2=0&maxNumber=12&query=
Journal:
Human Molecular Genetics - HUM MOL GENET
, vol. 19, no. 17, pp. 3489-3490, 2010
Ophthalmological Features Associated With COL4A1 Mutations
(
Citations: 1
)
I. Coupry
,
I. Sibon
,
B. Mortemousque
,
F. Rouanet
,
M. Mine
,
C. Goizet
Journal:
Archives of Ophthalmology - ARCH OPHTHALMOL
, vol. 128, no. 4, pp. 483-489, 2010
A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia
(
Citations: 1
)
D. Simon
,
B. Laloo
,
M. Barillot
,
T. Barnetche
,
C. Blanchard
,
C. Rooryck
,
M. Marche
,
I. Burgelin
,
I. Coupry
,
N. Chassaing
,
B. Gilbert-Dussardier
,
D. Lacombe
http://academic.research.microsoft.com/io.ashx?type=5&id=37623964&selfId1=25149749&selfId2=0&maxNumber=12&query=
Journal:
Human Molecular Genetics - HUM MOL GENET
, vol. 19, no. 10, pp. 2015-2027, 2010
Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations
(
Citations: 3
)
G Solé
,
I Coupry
,
C Rooryck
,
E Guérineau
,
F Martins
,
S Devés
,
C Hubert
,
N Souakri
,
O Boute
,
C Marchal
,
L Faivre
,
E Landré
http://academic.research.microsoft.com/io.ashx?type=5&id=38333641&selfId1=25149749&selfId2=0&maxNumber=12&query=
Journal:
Journal of Neurology Neurosurgery and Psychiatry - J NEUROL NEUROSURG PSYCHIAT
, vol. 80, no. 12, pp. 1394-1398, 2009
Sort by:
Citations
(136 times by 116 publications)
Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
(
Citations: 4
)
Sabina Capellari
,
Rosaria Strammiello
,
Daniela Saverioni
,
Hans Kretzschmar
,
Piero Parchi
Journal:
Acta Neuropathologica - ACTA NEUROPATHOL
, vol. 121, no. 1, pp. 21-37, 2011
RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects
Cécile Jeanpierre
,
Guillaume Macé
,
Mélanie Parisot
,
Vincent Morinière
,
Audrey Pawtowsky
,
Marion Benabou
,
Jelena Martinovic
,
Jeanne Amiel
,
Tania Attié-Bitach
,
Anne-Lise Delezoide
,
Philippe Loget
,
Patricia Blanchet
http://academic.research.microsoft.com/io.ashx?type=5&id=59318660&selfId1=25149749&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 48, no. 7, pp. 497-504, 2011
Assessing urban recycling in low- and middle-income countries: Building on modernised mixtures
Anne Scheinberg
,
Sandra Spies
,
Michael H. Simpson
,
Arthur P. J. Mol
Journal:
Habitat International - HABITAT INT
, vol. 35, no. 2, pp. 188-198, 2011
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH
Anne Chun-Hui Tsai
,
Cherilyn J Dossett
,
Carol S Walton
,
Andrea E Cramer
,
Patti A Eng
,
Beata A Nowakowska
,
Amber N Pursley
,
Pawel Stankiewicz
,
Joanna Wiszniewska
,
Sau Wai Cheung
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 1, pp. 43-49, 2011
Body composition changes during the first two years of university
Sareen S. Gropper
,
Anna Newton
,
Paul Harrington
,
Karla P. Simmons
,
Lenda Jo Connell
,
Pamela Ulrich
Journal:
Preventive Medicine - PREV MED
, vol. 52, no. 1, pp. 20-22, 2011
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