C. Moutou

发表

Allele‐specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy

C. Moutou, N. Gardés, C. Rongières, 2001, Prenatal diagnosis.

Birth after pre‐implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2)

C. Moutou, N. Gardés, S. Viville, 2008, Prenatal diagnosis.

Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation Δ F508 by fluorescent polymerase chain reaction

C. Moutou, S. Viville, 1999, Prenatal Diagnosis.

Strategies and outcomes of PGD of familial adenomatous polyposis.

C. Moutou, N. Gardés, S. Viville, 2007, Molecular human reproduction.

The ESHRE PGD Consortium: 10 years of data collection.

J C Harper, C. Moutou, V. Goossens, 2012, Human reproduction update.

Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia.

H. van Bokhoven, C. Moutou, S. Viville, 2007, American journal of human genetics.

ESHRE PGD consortium best practice guidelines for amplification-based PGD.

C. Moutou, M. De Rycke, J. Traeger-Synodinos, 2011, Human reproduction.

ESHRE PGD Consortium 'Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)'.

M. Robinson, C. Moutou, K. Sermon, 2005, Human reproduction.

Cancers in relatives of children with non-Hodgkin's lymphoma.

C. Bonaïti‐pellié, N. Poisson, A. Chompret, 1996, Leukemia research.

ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008.

C. Moutou, V. Goossens, M. De Rycke, 2010, Human reproduction.

ESHRE PGD Consortium data collection V: cycles from January to December 2002 with pregnancy follow-up to October 2003.

N. Muntjewerff, K. Vesela, C. Moutou, 2008, Human reproduction.

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee.

K. Vesela, C. Moutou, V. Goossens, 2010, Human reproduction.

What next for preimplantation genetic screening?

K. Vesela, C. Moutou, K. Sermon, 2008, Human reproduction.

ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006.

C. Moutou, K. Sermon, V. Goossens, 2008, Human reproduction.

Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic.

J. Mandel, C. Moutou, V. Biancalana, 1997, Human molecular genetics.

ARCAD: A method for estimating age‐dependent disease risk associated with mutation carrier status from family data

C. Bonaïti‐pellié, C. Moutou, L. Brugières, 1995, Genetic epidemiology.

Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas

C. Bonaïti‐pellié, N. Poisson, A. Chompret, 1996, Cancer.

Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene

C. Moutou, N. Gardés, S. Viville, 2006, Prenatal diagnosis.

Duplex PCR for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy

C. Moutou, N. Gardés, S. Viville, 2003, Prenatal diagnosis.

ESHRE PGD Consortium data collection IV: May-December 2001.

C. Moutou, S. Viville, K. Sermon, 2005, Human reproduction.

NEW DEBATE What next for preimplantation genetic screening

K. Vesela, C. Moutou, K. Sermon, 2008 .

ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004.

K. Vesela, C. Moutou, S. Viville, 2007, Human reproduction.

ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007.

C. Moutou, V. Goossens, J. Traeger-Synodinos, 2009, Human reproduction.

Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study

S. Dhanjal, C. Moutou, J. Dreesen, 2013, European Journal of Human Genetics.

Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests

C. Moutou, N. Gardés, C. Rongières, 2015, European Journal of Human Genetics.

ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011.

C. Moutou, V. Goossens, M. De Rycke, 2015, Human reproduction.

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010.

C. Moutou, V. Goossens, M. De Rycke, 2014, Human reproduction.

ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005.

C. Moutou, S. Viville, K. Sermon, 2008, Human reproduction.

ESHRE PGT Consortium good practice recommendations for the organisation of PGT†

C. Rubio, C. Moutou, V. Goossens, 2020, Human reproduction open.

ESHRE PGT Consortium data collection XVI–XVIII: cycles from 2013 to 2015†

C. Rubio, C. Rubio, C. Moutou, 2020, Human reproduction open.

ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders

C. Moutou, V. Goossens, J. Dreesen, 2020, Human reproduction open.

ESHRE PGD Consortium data collection XIV–XV: cycles from January 2011 to December 2012 with pregnancy follow-up to October 2013

C. Moutou, V. Goossens, M. De Rycke, 2017, Human reproduction.

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations.

M. Koenig, V. Campuzano, M. Cossée, 1997, Proceedings of the National Academy of Sciences of the United States of America.

High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis

M. Peschanski, J. Tournois, C. Moutou, 2010, In Vitro Cellular & Developmental Biology - Animal.

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

C Junien, C. Junien, C. Bonaïti‐pellié, 1992, Journal of medical genetics.

Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties.

C. Philippe, C. Moutou, N. Gardés, 2003, Human reproduction.

Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis

C. Moutou, N. Gardés, S. Viville, 2002, European Journal of Human Genetics.

ESHRE PGD Consortium data collection XI: cycles from January to December 2008 with pregnancy follow-up to October 2009.

C. Moutou, V. Goossens, M. De Rycke, 2012, Human reproduction.

Identification of novel mutations in the MTM1 gene causing severe and mild forms of X‐linked myotubular myopathy

J. Mandel, C. Moutou, V. Biancalana, 1999, Human mutation.

A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy

D. Ellison, C. Moutou, C. Kennedy, 2000, Neuromuscular Disorders.

ESHRE PGT Consortium data collection XIX–XX: PGT analyses from 2016 to 2017†

C. Rubio, C. Moutou, V. Goossens, 2021, Human reproduction open.

Genetics and epidemiology of Wilms' tumor: the French Wilms' tumor study.

C. Bonaïti‐pellié, J. Hochez, A. Chompret, 1992, Medical and pediatric oncology.

Screening for germ line p53 mutations in children with malignant tumors and a family history of cancer.

C. Bonaïti‐pellié, N. Poisson, A. Chompret, 1993, Cancer research.

New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications

C. Moutou, N. Gardés, S. Viville, 2004, European Journal of Human Genetics.

Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule

P. Calvas, C. Moutou, C. Goizet, 2020, Scientific Reports.

Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule

R. Favre, P. Calvas, C. Moutou, 2020, Scientific Reports.

Le syndrome du retard mental avec X fragile

J. Mandel, C. Moutou, V. Biancalana, 1996 .

Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

C. Moutou, S. Viville, I. Liebaers, 2011, European Journal of Human Genetics.

Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach

C. Moutou, S. Viville, N. Gardès, 2004, Prenatal diagnosis.

The experience of 3 years of external quality assessment of preimplantation genetic diagnosis for cystic fibrosis

Z. Deans, C. Moutou, V. Goossens, 2012, European Journal of Human Genetics.

The French Wilms' tumour study: no clear evidence for cancer prone families.

C. Bonaïti‐pellié, J. Hochez, A. Chompret, 1994, Journal of medical genetics.