Catherine Boileau

发表

Software and database for the analysis of mutations in the human LDL receptor gene

Christophe Béroud, Mathilde Varret, Jean-Pierre Rabès, 1997, Nucleic Acids Res..

Marfan Database (third edition): new mutations and new routines for the software

Hanns-Georg Klein, Christophe Béroud, Gwenaëlle Collod-Béroud, 1998, Nucleic Acids Res..

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis

Manfred Stuhrmann, Hartmut Schmidt, Christophe Béroud, 1998, Nucleic Acids Res..

A Comparative Study of Android Malware Behavior in Different Contexts

François Gagnon, Mohamed Mejri, Simon Frenette, 2016, DCNET.

AndroSSL: A Platform to Test Android Applications Connection Security

François Gagnon, Catherine Boileau, Marc-Antoine Ferland, 2015, FPS.

Towards Understanding the Role of Execution Context for Observing Malicious Behavior in Android Malware

François Gagnon, Mohamed Mejri, Simon Frenette, 2016, ICETE.

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene

Thierry Soussi, Christophe Béroud, Gwenaëlle Collod-Béroud, 1997, Nucleic Acids Res..

Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis

Erika Salvi, Mohamad Saad, Eric Hachulla, 2011, PLoS genetics.

UMD‐predictor, a new prediction tool for nucleotide substitution pathogenicity—application to four genes: FBN1, FBN2, TGFBR1, and TGFBR2

Christophe Béroud, Catherine Boileau, Mireille Claustres, 2009, Human mutation.

TGFB2 loss of function mutations cause familial thoracic aortic aneurysms and acute aortic dissections associated with mild systemic features of the Marfan syndrome

Jay Shendure, Mathilde Varret, Catherine Boileau, 2012, Nature Genetics.

Diagnosis and management of aortic dissection.

Raimund Erbel, Fernando Alfonso, Catherine Boileau, 2001, European heart journal.

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease

Catherine Boileau, Päivi Pajukanta, Anne Tybjærg-Hansen, 2013, European heart journal.

Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene

Catherine Boileau, Beat Steinmann, Gábor Mátyás, 2002, Human mutation.

Cohort profile of the CARTaGENE study: Quebec's population-based biobank for public health and personalized genomics.

Catherine Boileau, Bartha Knoppers, Philip Awadalla, 2013, International journal of epidemiology.

Update of the UMD‐FBN1 mutation database and creation of an FBN1 polymorphism database

Gabor Matyas, Christophe Béroud, Claudine Junien, 2003, Human mutation.

Heterozygous TGFBR2 mutations in Marfan syndrome

Yusuke Nakamura, Naomichi Matsumoto, Mathilde Varret, 2004, Nature Genetics.

The UMD‐LDLR database: additions to the software and 490 new entries to the database

Christophe Béroud, Mathilde Varret, Jean-Pierre Rabès, 2002, Human mutation.

Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p.Leu167del Mutation

Mathilde Varret, Jean-Pierre Rabès, Catherine Boileau, 2013, Human mutation.

Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease)

Mathilde Varret, Catherine Boileau, E. Bruckert, 2011, Orphanet journal of rare diseases.

Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis.

Olivier Meyer, Eric Hachulla, Catherine Boileau, 2011, Clinical and experimental rheumatology.

UMD (Universal Mutation Database): 2005 update

Thierry Soussi, Christophe Béroud, Catherine Boileau, 2005, Human mutation.