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Co-authors
(73)
Philippe Jonveaux
4
Christophe Philippe
3
Celine Bonnet (Céline Bonnet)
3
Damien Sanlaville
2
Cedric Le Caignec (Cédric Le Caignec)
2
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(5)
AM J MED GENET PART A
2
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1
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Authors
Mylene Beri
Mylene Beri (Mylène Beri),Genetics & Genealogy,Immunology,Ophthalmology
Edit
Mylene Beri (Mylène Beri)
Publications:
6
|
Citations:
22
Fields:
Genetics & Genealogy
,
Immunology
,
Ophthalmology
View FAQ about top research areas and Fields of study
Collaborated with
73 co-authors
from 2008 to 2011
|
Cited by
188 authors
Cumulative
Annual
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Publications
(6)
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Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation
(
Citations: 1
)
Christèle Dubourg
,
Damien Sanlaville
,
Martine Doco-Fenzy
,
Cédric Le Caignec
,
Chantal Missirian
,
Sylvie Jaillard
,
Caroline Schluth-Bolard
,
Emilie Landais
,
Odile Boute
,
Nicole Philip
,
Annick Toutain
,
Albert David
Mylène Beri
http://academic.research.microsoft.com/io.ashx?type=5&id=49660636&selfId1=25353674&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Medical Genetics - EUR J MED GENET
, vol. 54, no. 2, pp. 144-151, 2011
Delineation of 15q13.3 microdeletions
(
Citations: 9
)
A Masurel-Paulet
,
J Andrieux
,
P Callier
,
JM Cuisset
,
C Le Caignec
,
M Holder
,
C Thauvin-Robinet
,
B Doray
,
E Flori
,
MP Alex-Cordier
,
M Beri
,
O Boute
http://academic.research.microsoft.com/io.ashx?type=5&id=30353682&selfId1=25353674&selfId2=0&maxNumber=12&query=
Journal:
Clinical Genetics - CLIN GENET
, vol. 78, no. 2, pp. 149-161, 2010
A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations
(
Citations: 6
)
M. Valduga
,
C. Philippe
,
P. Bach Segura
,
O. Thiebaugeorges
,
A. Miton
,
M. Beri
,
C. Bonnet
,
C. Nemos
,
B. Foliguet
,
P. Jonveaux
Journal:
Prenatal Diagnosis - PRENATAL DIAG
, 2010
Clinical and molecular characterization of a large family with an interstitial 15q11q13 duplication
(
Citations: 1
)
Juliette Piard
,
Christophe Philippe
,
Marie Marvier
,
Claire Beneteau
,
Virginie Roth
,
Mylène Valduga
,
Mylène Béri
,
Céline Bonnet
,
Marie-José Grégoire
,
Philippe Jonveaux
,
Bruno Leheup
Journal:
American Journal of Medical Genetics Part A - AM J MED GENET PART A
, vol. 152A, no. 8, pp. 1933-1941, 2010
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardation
(
Citations: 2
)
C. Bonnet
,
B. Leheup
,
M. Béri
,
C. Philippe
,
M.-J. Grégoire
,
P. Jonveaux
Journal:
American Journal of Medical Genetics Part A - AM J MED GENET PART A
, vol. 149A, no. 6, pp. 1280-1289, 2009
Sort by:
Citations
(22 times by 22 publications)
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond
,
Jutta Heinrich
,
Richard Delorme
,
Christian Proepper
,
Catalina Betancur
,
Guillaume Huguet
,
Marina Konyukh
,
Pauline Chaste
,
Elodie Ey
,
Maria Rastam
,
Henrik Anckarsäter
,
Gudrun Nygren
http://academic.research.microsoft.com/io.ashx?type=5&id=57409742&selfId1=25353674&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 2, 2012
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes
Jill A Rosenfeld
,
Lindsey E Stephens
,
Justine Coppinger
,
Blake C Ballif
,
Joe J Hoo
,
Beatrice N French
,
Valerie C Banks
,
Wendy E Smith
,
David Manchester
,
Anne Chun-Hui Tsai
,
Katrina Merrion
,
Roberto Mendoza-Londono
http://academic.research.microsoft.com/io.ashx?type=5&id=56548354&selfId1=25353674&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 5, pp. 547-554, 2011
Germline deletion of the miR17∼92 cluster causes skeletal and growth defects in humans
Loïc de Pontual
,
Evelyn Yao
,
Patrick Callier
,
Laurence Faivre
,
Valérie Drouin
,
Sandra Cariou
,
Arie Van Haeringen
,
David Geneviève
,
Alice Goldenberg
,
Myriam Oufadem
,
Sylvie Manouvrier
,
Arnold Munnich
http://academic.research.microsoft.com/io.ashx?type=5&id=56593813&selfId1=25353674&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 10, pp. 1026-1030, 2011
9q22 Deletion - First Familial Case
Linda Siggberg
,
Maarit Peippo
,
Marjatta Sipponen
,
Taina Miikkulainen
,
Keiko Shimojima
,
Toshiyuki Yamamoto
,
Jaakko Ignatius
,
Sakari Knuutila
Journal:
Orphanet Journal of Rare Diseases - ORPHANET J RARE DIS
, vol. 6, no. 1, pp. 1-14, 2011
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow
Malgorzata Srebniak
,
Marjan Boter
,
Grétel Oudesluijs
,
Marieke Joosten
,
Lutgarde Govaerts
,
Diane Van Opstal
,
Robert-Jan H Galjaard
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 12, pp. 1230-1237, 2011
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