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Genotype-Phenotype Correlation of CTNNB1 Mutations Reveals Different B-Catenin Activation Levels in Hepatocellular Tumors with High Activity Associated with Malignancy

Journal of hepatology, 2016, Vol.64 (2), p.S578-S578

2016

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P0266 : Adeno-Associated Virus 2 (AAV2) induces recurrent insertional mutagenesis in Human Hepatocellular Carcinomas

Journal of hepatology, 2015-04, Vol.62, p.S406-S406

2015

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G05 : Exome sequencing of 243 liver tumors identifies new mutational signatures and potential therapeutic targets

Journal of hepatology, 2015-04, Vol.62, p.S189-S189

2015

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PD-0608: Risk of metastasis and death in rectal cancer is increased with 8p deletion but not with gene expression

Radiotherapy and oncology, 2013-03, Vol.106, p.S235-S235

2013

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Disomie paternelle pangénomique en mosaïque : nouveau mécanisme de tumorigénèse surrénalienne dans le syndrome de Beckwith–Wiedemann ?

Annales d'endocrinologie, 2013-09, Vol.74 (4), p.275-276

2013

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Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumors

Hormone and metabolic research, 2015-06, Vol.47 (7), p.497-503

2015

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Recherche pangénomique des gènes impliqués dans les corticosurrénalomes

Annales d'endocrinologie, 2014-10, Vol.75 (5), p.278-278

2014

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Les mutations d’ARMC5 et KDM1A sont associées à des profils différentiels d’expression de récepteurs illégitimes dans l’hyperplasie macronodulaire bilatérale des surrénales

Annales d'endocrinologie, 2022-10, Vol.83 (5), p.321-322

2022

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FRI-088 - Genotype-Phenotype Correlation of CTNNB1 Mutations Reveals Different B-Catenin Activation Levels in Hepatocellular Tumors with High Activity Associated with Malignancy

Journal of hepatology, 2016, Vol.64 (2), p.S578-S578

2016

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Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study

The lancet oncology, 2022-01, Vol.23 (1), p.161-171

2022

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Recurrent INHBE-GLI1 fusions in hepatocellular adenomas with sonic hedgehog pathway activation

Journal of hepatology, 2017, Vol.66 (1), p.S14-S14

2017

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Prospective Evidence That Hepatocellular Carcinoma Surveillance in Patients with Compensated Viral Cirrhosis Increases the Probability of Curative Treatment and Survival Taking into Account Lead-Time Bias (Anrs Co12 Cirvir Cohort)

Journal of hepatology, 2016, Vol.64 (2), p.S194-S195

2016

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125 PROGNOSTIC VALUE OF CHROMOSOMAL IMBALANCIES AND THE COLON GENE EXPRESSION SIGNATURES IN RECTAL CANCER

Radiotherapy and oncology, 2012-03, Vol.102, p.S53-S53

2012

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170 oral TOWARDS A LYON MOLECULAR PROGNOSTIC SIGNATURE FOR RECTAL CANCER

Radiotherapy and oncology, 2011, Vol.99, p.S66-S66

2011

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1073 INTEGRATED GENOMIC ANALYSIS IN HEPATOCELLULAR ADENOMA

Journal of hepatology, 2013-04, Vol.58, p.S440-S440

2013

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15 LANDSCAPE OF SOMATIC MUTATION IN HEPATOCELLULAR CARCINOMA

Journal of hepatology, 2012-04, Vol.56, p.S8-S8

2012

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L’Epidermal Growth Factor Receptor (EGFR) est une cible thérapeutique pour un sous-groupe de tumeurs de vessie agressives de phénotype de type basal

Progrès en urologie (Paris), 2014-11, Vol.24 (13), p.806-806

2014

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Towards a “Lyon molecular signature” to individualize the treatment of rectal cancer. Prognostic analysis of a prospective cohort of 94 rectal cancers T1-2-3 Nx MO to be the basis of a molecular signature

Cancer radiothérapie, 2012-12, Vol.16 (8), p.688-696

2012

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Génomique intégrée des Hyperplasies Macronodulaires Bilatérales primitives des Surrénales (HMBS)

Annales d'endocrinologie, 2020-09, Vol.81 (4), p.179-179

2020

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PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases: Int J Cancer

International journal of cancer, 2019, Vol.144 (3), p.533-544

2019

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On the privacy-conscientious use of mobile phone data

Scientific data, 2018-12, Vol.5 (1), p.180286-6, Article 180286

2018

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L’étude génomique de l’hyperplasie macronodulaire bilatérale primitive des surrénales (HMBPS) révèle 3 groupes aux caractéristiques clinico-pathologiques distinctes, un lié à ARMC5 et un deuxième à un nouveau gène responsable du syndrome de Cushing dépendant de l’alimentation : LSD1/KDM1A, étendant le spectre des causes génétiques du syndrome de Cushing surrénalien

Annales d'endocrinologie, 2021-10, Vol.82 (5), p.239-239

2021

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Modular α-Helical Mimetics with Antiviral Activity against Respiratory Syncitial Virus

Journal of the American Chemical Society, 2006-10, Vol.128 (40), p.13284-13289

2006

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PS-019 - Recurrent INHBE-GLI1 fusions in hepatocellular adenomas with sonic hedgehog pathway activation

Journal of hepatology, 2017, Vol.66 (1), p.S14-S14

2017

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Genotype-Phenotype Correlation of CTNNB1 Mutations Reveals Different B-Catenin Activation Levels in Hepatocellular Tumors with High Activity Associated with Malignancy

P0266 : Adeno-Associated Virus 2 (AAV2) induces recurrent insertional mutagenesis in Human Hepatocellular Carcinomas

G05 : Exome sequencing of 243 liver tumors identifies new mutational signatures and potential therapeutic targets

PD-0608: Risk of metastasis and death in rectal cancer is increased with 8p deletion but not with gene expression

Disomie paternelle pangénomique en mosaïque : nouveau mécanisme de tumorigénèse surrénalienne dans le syndrome de Beckwith–Wiedemann ?

Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumors

Recherche pangénomique des gènes impliqués dans les corticosurrénalomes

Les mutations d’ARMC5 et KDM1A sont associées à des profils différentiels d’expression de récepteurs illégitimes dans l’hyperplasie macronodulaire bilatérale des surrénales

FRI-088 - Genotype-Phenotype Correlation of CTNNB1 Mutations Reveals Different B-Catenin Activation Levels in Hepatocellular Tumors with High Activity Associated with Malignancy

Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study

Recurrent INHBE-GLI1 fusions in hepatocellular adenomas with sonic hedgehog pathway activation

Prospective Evidence That Hepatocellular Carcinoma Surveillance in Patients with Compensated Viral Cirrhosis Increases the Probability of Curative Treatment and Survival Taking into Account Lead-Time Bias (Anrs Co12 Cirvir Cohort)

125 PROGNOSTIC VALUE OF CHROMOSOMAL IMBALANCIES AND THE COLON GENE EXPRESSION SIGNATURES IN RECTAL CANCER

170 oral TOWARDS A LYON MOLECULAR PROGNOSTIC SIGNATURE FOR RECTAL CANCER

1073 INTEGRATED GENOMIC ANALYSIS IN HEPATOCELLULAR ADENOMA

15 LANDSCAPE OF SOMATIC MUTATION IN HEPATOCELLULAR CARCINOMA

L’Epidermal Growth Factor Receptor (EGFR) est une cible thérapeutique pour un sous-groupe de tumeurs de vessie agressives de phénotype de type basal

Towards a “Lyon molecular signature” to individualize the treatment of rectal cancer. Prognostic analysis of a prospective cohort of 94 rectal cancers T1-2-3 Nx MO to be the basis of a molecular signature

Génomique intégrée des Hyperplasies Macronodulaires Bilatérales primitives des Surrénales (HMBS)

PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases: Int J Cancer

On the privacy-conscientious use of mobile phone data

Modular α-Helical Mimetics with Antiviral Activity against Respiratory Syncitial Virus

PS-019 - Recurrent INHBE-GLI1 fusions in hepatocellular adenomas with sonic hedgehog pathway activation

PS116 - Prospective Evidence That Hepatocellular Carcinoma Surveillance in Patients with Compensated Viral Cirrhosis Increases the Probability of Curative Treatment and Survival Taking into Account Lead-Time Bias (Anrs Co12 Cirvir Cohort)

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