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Christelle Perez
Christelle Perez
French Institute of Health and Medical Research
Mutation
Medicine
Endocrinology
Genetics
Internal medicine
4
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153
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Functional Characterisation of a POU1F1 Mutation Unexpectedly Associated with Isolated Growth Hormone Deficiency (IGHD): A Novel Aetiology of IGHD
2015
Marie-Laure Sobrier
Yu-Cheng Tsai
Christelle Perez
Bruno Leheup
Tahar Bouceba
Philippe Duquesnoy
Daria Sizova
Stephen A. Liebhaber
Nancy E. Cooke
Serge Amselem
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Symptomatic Heterozygotes and Prenatal Diagnoses in a Nonconsanguineous Family with Syndromic Combined Pituitary Hormone Deficiency Resulting from Two Novel LHX3 Mutations
2012
The Journal of Clinical Endocrinology and Metabolism
Marie-Laure Sobrier
Cécile Brachet
Marie-Pierre Vié-Luton
Christelle Perez
Bruno Copin
M. Legendre
Claudine Heinrichs
Serge Amselem
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Citations (22)
Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities.
2012
European Journal of Endocrinology
Christelle Perez
Florence Dastot-Le-Moal
Nathalie Collot
M. Legendre
Isabelle Abadie
Anne-Marie Bertrand
Serge Amselem
Marie-Laure Sobrier
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Citations (6)
Activating mutations in human acute megakaryoblastic leukemia
2008
Blood
Sébastien Malinge
Christine Ragu
Véronique Della Valle
Didier F. Pisani
Stefan N. Constantinescu
Christelle Perez
Jean-Luc Villeval
Dirk Reinhardt
Judith Landman-Parker
Lucienne Michaux
Nicole Dastugue
André Baruchel
William Vainchenker
Jean-Pierre Bourquin
Virginie Penard-Lacronique
Olivier Bernard
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Citations (125)
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