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51

Genotype–phenotype correlations in hereditary familial retinoblastoma

Melissa Taylor, Catherine Dehainault, Laurence Desjardins, François Doz, Christine Levy, Xavier Sastre, Jérôme Couturier, Dominique Stoppa-Lyonnet, Claude Houdayer, Marion Gauthier-Villars

Journal:

Year:

2007

Language:

english

File:

PDF, 260 KB

english, 2007

52

The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Amandine I. Garcia, David G. Cox, Laure Barjhoux, Carole Verny-Pierre, Daniel Barnes, Gemo Study Collaborators, Antonis C. Antoniou, Dominique Stoppa-Lyonnet, Olga M. Sinilnikova, Sylvie Mazoyer

Journal:

Year:

2011

Language:

english

File:

PDF, 122 KB

english, 2011

53

Heterostructures of La0.67Sr0.33MnO3/SrTiO3/La0.67Sr0.33MnO3 grown by pulsed laser deposition on (001) SrTiO3

R. Lyonnet, J.-L. Maurice, M.J. Hÿtch, D. Michel, J.-P. Contour

Journal:

Applied Surface Science

Year:

2000

Language:

english

File:

PDF, 577 KB

english, 2000

54

Mortality Associated with Neurofibromatosis 1: A Cohort Study of 1895 Patients in 1980-2006 in France

Tu Anh Duong, Emilie Sbidian, Laurence Valeyrie-Allanore, Cédric Vialette, Salah Ferkal, Smaïl Hadj-Rabia, Christophe Glorion, Stanislas Lyonnet, Michel Zerah, Isabelle Kemlin, Diana Rodriguez, Sylvie

Journal:

Orphanet Journal of Rare Diseases

Year:

2011

Language:

english

File:

PDF, 316 KB

english, 2011

55

Radiofrequency Ablation of Renal Tumors with an Expandable Multitined Electrode: Results, Complications, and Pilot Evaluation of Cooled Pyeloperfusion for Collecting System Protection

Olivier Rouvière, Lionel Badet, François Joseph Murat, Jean Marie Maréchal, Marc Colombel, Xavier Martin, Denis Lyonnet, Albert Gelet

Journal:

CardioVascular and Interventional Radiology

Year:

2008

Language:

english

File:

PDF, 344 KB

english, 2008

56

Germline mutations inBRCA1andBRCA2genes in ethnically diverse high risk families in Israel

Yael Laitman, Roni Tsipora Borsthein, Dominique Stoppa-Lyonnet, Efrat Dagan, Laurent Castera, Maud Goislard, Ruth Gershoni-Baruch, Hadassah Goldberg, Bella Kaufman, Noa Ben-Baruch, Jamal Zidan, Taisee

Journal:

Breast Cancer Research and Treatment

Year:

2011

Language:

english

File:

PDF, 197 KB

english, 2011

57

Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study

Caux-Moncoutier, Virginie, Pagès-Berhouet, Sabine, Michaux, Dorothée, Asselain, Bernard, Castéra, Laurent, De Pauw, Antoine, Buecher, Bruno, Gauthier-Villars, Marion, Stoppa-Lyonnet, Dominique, Houday

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 181 KB

english, 2009

58

Genetics of limb anomalies in humans

Sylvie Manouvrier-Hanu, Muriel Holder-Espinasse, Stanislas Lyonnet

Journal:

Trends in Genetics

Year:

1999

Language:

english

File:

PDF, 263 KB

english, 1999

59

On-Line Reliability Prediction via Dynamic Failure Rate Model

Toscano, R., Lyonnet, P.

Journal:

IEEE Transactions on Reliability

Year:

2008

Language:

english

File:

PDF, 187 KB

english, 2008

60

CL004 - Expression de marqueurs de pluripotence dans des cellules de tératome sacro-coccygien

A. Arnaud, C. Crétolle, C. Babarit, L. Galmiche, A. Munnich, S. Lyonnet, M. Vekemans, H. Etchevers, S. Sarnacki

Journal:

Archives de Pédiatrie

Year:

2010

Language:

french

File:

PDF, 56 KB

french, 2010

61

L’ataxie-télangiectasie : évolution à long terme et risque néoplasique Étude du registre du centre de référence des déficits immunitaires héréditaires (CEREDIH)

F. Suarez, R. Micol, N. Mahlaoui, C. Andriamanga, O. Hermine, D. Stoppa-Lyonnet, A. Fischer

Journal:

Archives de Pédiatrie

Year:

2011

Language:

french

File:

PDF, 1.52 MB

french, 2011

62

PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome

Delphine Trochet, Louise M. O'Brien, David Gozal, Ha Trang, Agneta Nordenskjöld, Béatrice Laudier, Pär-Johan Svensson, Sabine Uhrig, Trevor Cole, Arnold Munnich, Claude Gaultier, Stanislas Lyonnet, Je

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 597 KB

english, 2005

63

A Kalman Optimization Approach for Solving Some Industrial Electronics Problems

Toscano, R., Lyonnet, P.

Journal:

IEEE Transactions on Industrial Electronics

Year:

2012

Language:

english

File:

PDF, 307 KB

english, 2012

64

Rétinoblastome

J.-M. Zucker, L. Desjardins, D. Stoppa-Lyonnet, F. Doz

Journal:

EMC - Pédiatrie

Year:

2005

Language:

french

File:

PDF, 591 KB

french, 2005

65

Pathways systematically associated to Hirschsprung’s disease

Fernández, Raquel M, Bleda, Marta, Luzón-Toro, Berta, García-Alonso, Luz, Arnold, Stacey, Sribudiani, Yunia, Besmond, Claude, Lantieri, Francesca, Doan, Betty, Ceccherini, Isabella, Lyonnet, Stanislas

Journal:

Orphanet Journal of Rare Diseases

Year:

2013

Language:

english

File:

PDF, 632 KB

english, 2013

66

OA52 Douleurs de l’arriere-pied chez le sujet sportif : etiologies et conduite a tenir en imagerie

Mouly, J., Mougenot, V., Bordet, B., Ltaief, A., Lyonnet, D.

Journal:

Journal de Radiologie

Year:

2006

Language:

french

File:

PDF, 1.28 MB

french, 2006

67

Les Anges et leur mission d'après les Pères de l'Église. (Collection « Irenikon », N. S. 5)by J. Daniélou

Review by: S. Lyonnet

Journal:

Year:

1957

File:

PDF, 266 KB

1957

68

CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study

Del Giudice, Ennio, Macca, Marina, Imperati, Floriana, D’Amico, Alessandra, Parent, Philippe, Pasquier, Laurent, Layet, Valerie, Lyonnet, Stanislas, Stamboul-Darmency, Veronique, Thauvin-Robinet, Chri

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 480 KB

english, 2014

69

Polykarp von Smyrna und die Pastoralbriefeby Hans von Campenhausen

Review by: S. Lyonnet

Journal:

Year:

1954

File:

PDF, 269 KB

1954

70

Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009

Santoro, Claudia, Malan, Valérie, Bertoli, Marta, Boddaert, Nathalie, Vidaud, Dominique, Lyonnet, Stanislas

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 205 KB

english, 2013

71

The C20orf133 gene is disrupted in a patient with Kabuki syndrome

Maas, N. M C, Van de Putte, T., Melotte, C., Francis, A., Schrander-Stumpel, C. T R M, Sanlaville, D., Genevieve, D., Lyonnet, S., Dimitrov, B., Devriendt, K., Fryns, J.-P., Vermeesch, J. R

Journal:

Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 2.14 MB

english, 2007

72

Le syndrome Kabuki : mise au point et revue de la littérature

Arnaud, M., Barat-Houari, M., Gatinois, V., Sanchez, E., Lyonnet, S., Touitou, I., Geneviève, D.

Journal:

Archives de Pédiatrie

Year:

2015

File:

PDF, 921 KB

2015

73

Identifying Essential Components of Lean Approach

Lyonnet, Barbara, Pillet, Maurice, Pralus, Magali

Journal:

Advanced Materials Research

Year:

2012

Language:

english

File:

PDF, 328 KB

english, 2012

74

Hommage à Henri de Contenson || Tall Knediğ. Die Ergebnisse der Ausgrabungen des Vorderasiatischen Museums Berlin in Nordost-Syrien von 1993 bis 1998by Evelyn Klengel-Brandt; Sabina Kulemann-Ossen; Lutz Martin

Review by: Bertille Lyonnet

Journal:

Year:

2006

Language:

french

File:

PDF, 813 KB

french, 2006

75

Lean manufacturing in the screw cutting sector: assessment of maturity level

Lyonnet, Barbara, Pillet, Maurice, Pralus, Magali

Journal:

International Journal of Rapid Manufacturing

Year:

2010

Language:

english

File:

PDF, 456 KB

english, 2010

76

Il primo pensiero cristiano III. Il pensiero di S. Paolo. Seconda edizione accresciutaby L. Tondelli;L'Eucaristia vista da un esegeta (Biblica, Serie II)by L. Tondelli

Review by: S. Lyonnet

Journal:

Year:

1954

File:

PDF, 277 KB

1954

77

Théologie de l'Agapè

Review by: Stanislas Lyonnet

Journal:

Year:

1963

Language:

french

File:

PDF, 416 KB

french, 1963

78

Le culte dans l'Église primitive, 2eéd. (Cahiers théologiques de l'actualité protestante n° 8)by O. Cullmann;Les Sacrements dans l'Évangile johannique. La vie de Jésus et le culte dans l'Église primitive (Études d'histoire et de philosophie religieuses publiées par la fucalté de théologie protestante de l'Université de Strasbourg n° 42)by O. Cullmann

Review by: S. Lyonnet

Journal:

Year:

1955

Language:

french

File:

PDF, 563 KB

french, 1955

79

Studies in Ephesiansby F. L. Cross

Review by: S. Lyonnet

Journal:

Year:

1959

File:

PDF, 194 KB

1959

80

Tacrolimus/Mycophenolate Mofetil Improved Natural Killer Lymphocyte Reconstitution One Year After Kidney Transplant by Reference to Cyclosporine/Azathioprine

Vacher-Coponat, Henri, Brunet, Corinne, Moal, Val??rie, Loundou, Andersen, Bonnet, Elodie, Lyonnet, Luc, Ravet, Sophie, Sampol-Manos, Emmanuelle, Sampol, Jos??, Berland, Yvon, George, Fran??oise Digna

Journal:

Transplantation Journal

Year:

2006

Language:

english

File:

PDF, 545 KB

english, 2006

81

Prediction of the aerodynamic effect of model deformation during transonic wind tunnel tests

Mouton, Sylvain, Sant, Yves Le, Lyonnet, Marianne

Journal:

International Journal of Engineering Systems Modelling and Simulation

Year:

2013

Language:

english

File:

PDF, 957 KB

english, 2013

82

Current perspectives on recommendations for BRCA genetic testing in ovarian cancer patients

Vergote, Ignace, Banerjee, Susana, Gerdes, Anne-Marie, van Asperen, Christi, Marth, Christian, Vaz, Fatima, Ray-Coquard, Isabelle, Stoppa-Lyonnet, Dominique, Gonzalez-Martin, Antonio, Sehouli, Jalid,

Journal:

European Journal of Cancer

Year:

2016

Language:

english

File:

PDF, 514 KB

english, 2016

83

Functional Assessment of Disease-Associated Regulatory Variants In Vivo Using a Versatile Dual Colour Transgenesis Strategy in Zebrafish

Bhatia, Shipra, Gordon, Christopher T., Foster, Robert G., Melin, Lucie, Abadie, Véronique, Baujat, Geneviève, Vazquez, Marie-Paule, Amiel, Jeanne, Lyonnet, Stanislas, van Heyningen, Veronica, Kleinja

Journal:

Year:

2015

Language:

english

File:

PDF, 15.36 MB

english, 2015

84

Anatomical and functional abnormalities on MRI in kabuki syndrome

Boisgontier, Jennifer, Tacchella, Jean Marc, Lemaître, Hervé, Lehman, Natacha, Saitovitch, Ana, Gatinois, Vincent, Boursier, Guilaine, Sanchez, Elodie, Rechtman, Elza, Fillon, Ludovic, Lyonnet, Stanis

Journal:

NeuroImage: Clinical

Year:

2018

Language:

english

File:

PDF, 717 KB

english, 2018

85

“Decoding hereditary breast cancer” Benefits and questions from multigene panel testing

Colas, Chrystelle, Golmard, Lisa, de Pauw, Antoine, Caputo, Sandrine M., Stoppa-Lyonnet, Dominique

Journal:

Year:

2019

Language:

english

File:

PDF, 369 KB

english, 2019

86

Diagnosis support systems for rare diseases: a scoping review

Faviez, Carole, Chen, Xiaoyi, Garcelon, Nicolas, Neuraz, Antoine, Knebelmann, Bertrand, Salomon, RÃ©mi, Lyonnet, Stanislas, Saunier, Sophie, Burgun, Anita

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 945 KB

2020

87

Should autism spectrum disorder be considered part of CHARGE syndrome? A cross-sectional study of 46 patients

Abadie, VÃ©ronique, Hamiaux, Priscilla, Ragot, StÃ©phanie, Legendre, Marine, Malecot, Gaelle, Burtin, Alexia, Attie-Bitach, Tania, Lyonnet, Stanislas, Bilan, FrÃ©dÃ©ric, Gilbert-Dussardier, Brigitte,

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 1.23 MB

2020

88

Comment prendre en compte le risque gÃ©nÃ©tique de cancer du sein ? GÃ¨nes impliquÃ©s et risques tumoraux associÃ©s

Stoppa-Lyonnet, Dominique, Buecher, Bruno, Gauthier-Villars, Marion, Houdayer, Claude, de Pauw, Antoine, de la Rochefordiere, Anne, This, Pascale, Asselain, Bernard, Andrieu, Nadine

Year:

2009

File:

PDF, 173 KB

2009

89

Development and Validation of a Fully GMP-Compliant Process for Manufacturing Stromal Vascular Fraction: A Cost-Effective Alternative to Automated Methods

FranÃ§ois, Pauline, Giraudo, Laurent, Veran, Julie, Bertrand, Baptiste, Dumoulin, ChloÃ©, Aboudou, Houssein, Grimaud, Fanny, Vogtensperger, Marie, Velier, MÃ©lanie, Arnaud, Laurent, Lyonnet, Luc, Simo

Journal:

Year:

2020

File:

PDF, 4.13 MB

2020

90

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association

Bahuau, Michel, Flintoff, Wayne, Assouline, Brigitte, Lyonnet, Stanislas, Le Merrer, Martine, Prieur, Marguerite, Guilloud-Bataille, Michel, Feingold, Nicole, Munnich, Arnold, Vidaud, Michel, Vidaud,

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 807 KB

english, 1996

91

Microsatellite DNA markers detects 95% of chromosome 22q11 deletions

Bonnet, Damien, Cormier-Daire, Valérie, Kachaner, Jean, Szezepanski, Isabelle, Souillard, Patrick, Sidi, Daniel, Munnich, Arnold, Lyonnet, Stanislas

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 97 KB

english, 1997

92

Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome

Cormier-Daire, Valérie, Le Merrer, Martine, Gigarel, Nadine, Morichon, Nicole, Prieur, Marguerite, Lyonnet, Stanislas, Vekemans, Michel, Munnich, Arnold

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 151 KB

english, 1997

93

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome

Bahuau, Michel, Houdayer, Claude, Assouline, Brigitte, Blanchet-Bardon, Claudine, Le Merrer, Martine, Lyonnet, Stanislas, Giraud, Sophie, R�can, Dominique, Lakhdar, Hakima, Vidaud, Michel, Vidaud, Dom

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 265 KB

english, 1998

94

Clinical homogeneity of the St�ve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2

Cormier-Daire, V., Superti-Furga, A., Munnich, A., Lyonnet, S., Rustin, P., Delezoide, A.L., De Lonlay, P., Giedion, A., Maroteaux, P., Le Merrer, M.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 217 KB

english, 1998

95

Ebstein anomaly associated with rearrangements of chromosomal region 11q

de Lonlay-Debeney, Pascale, de Blois, Marie-Christine, Bonnet, Damien, Amiel, Jeanne, Abadie, V�ronique, Picq, Monique, Lyonnet, Stanislas, Sidi, Daniel, Munnich, Arnold, Vekemans, Michel, Cormier-Dai

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 172 KB

english, 1998

96

Expression of theRET proto-oncogene in human Embryos

Atti�-Bitach, Tania, Abitbol, Marc, G�rard, Marion, Delezoide, Anne-Lise, Aug�, Joelle, Pelet, Anna, Amiel, Jeanne, Pachnis, Vassilis, Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 731 KB

english, 1998

97

No evidence for germline PTEN mutations in families with breast and brain tumours

Anthony Laugé, Céline Lefebvre, Pierre Laurent-Puig, Virginie Caux, Sophie Gad, Charis Eng, Michel Longy, Dominique Stoppa-Lyonnet

Journal:

International Journal of Cancer

Year:

1999

Language:

english

File:

PDF, 117 KB

english, 1999

98

Germline brca2 sequence variants in patients with ocular melanoma

Olga M. Sinilnikova, Kathleen M. Egan, Jennifer L. Quinn, Laetitia Boutrand, Gilbert M. Lenoir, Dominique Stoppa-Lyonnet, Laurence Desjardins, Christine Levy, David Goldgar, Evangelos S. Gragoudas

Journal:

International Journal of Cancer

Year:

1999

Language:

english

File:

PDF, 75 KB

english, 1999

99

Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case report

L. Lohmann, N. Chelloug, B. Rosales, C. Guérin, S. Lyonnet, P. Jonveaux, B. Simon-Bouy

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 85 KB

english, 2000

100

Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysis

Pascale Saugier-Veber, Cosette Martin, Nathalie Le Meur, Stanislas Lyonnet, Arnold Munnich, Albert David, Alain Hénocq, Delphine Héron, Philippe Jonveaux, Sylvie Odent, Sylvie Manouvrier, Anne Moncla,

Journal:

Year:

1998

Language:

english

File:

PDF, 314 KB

english, 1998

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