Результати пошуку - Sean V. Tavtigian
- Показ 1 - 20 результатів із 73
- На наступну сторінку
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In silico analysis of missense substitutions using sequence-alignment based methods за авторством Sean V. Tavtigian, Marc S. Greenblatt, Fabienne Lesueur, Graham Byrnes
Опубліковано 2008Artigo -
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Fitting a naturally scaled point system to the ACMG/AMP variant classification guidelines за авторством Sean V. Tavtigian, Steven M. Harrison, Kenneth M. Boucher, Leslie G. Biesecker
Опубліковано 2020Artigo -
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Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods за авторством Ewy A. Mathé, Magali Olivier, Shunsuke Kato, Chikashi Ishioka, Pierre Hainaut, Sean V. Tavtigian
Опубліковано 2006Artigo -
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A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data with Application to <i>BRCA1</i> за авторством Edwin S. Iversen, Fergus J. Couch, David E. Goldgar, Sean V. Tavtigian, Álvaro N.A. Monteiro
Опубліковано 2011Artigo -
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Impact of mutant p53 functional properties on<i>TP53</i>mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database за авторством Audrey Petitjean, Ewy A. Mathé, Shunsuke Kato, Chikashi Ishioka, Sean V. Tavtigian, Pierre Hainaut, Magali Olivier
Опубліковано 2007Artigo -
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Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2 за авторством David E. Goldgar, Douglas F. Easton, Amie M. Deffenbaugh, Álvaro N.A. Monteiro, Sean V. Tavtigian, Fergus J. Couch
Опубліковано 2004Artigo -
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Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework за авторством Sean V. Tavtigian, Marc S. Greenblatt, Steven M. Harrison, Robert L. Nussbaum, Snehit Prabhu, Kenneth M. Boucher, Leslie G. Biesecker
Опубліковано 2018Artigo -
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Prostate cancer susceptibility genes: lessons learned and challenges posed. за авторством Jacques Simard, Martine Dumont, Damian Labuda, Daniel Sinnett, Catherine Meloche, Mohamed Elalfy, Louise Berger, Emma Lees, Fernand Labrie, Sean V. Tavtigian
Опубліковано 2003Revisão -
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Molecular characterization of breast cancer in young Brazilian women за авторством Leda Viegas de Carvalho, Emílio M. Pereira, Lucien Frappart, Mathieu Boniol, Wanderley Marques Bernardo, Vicente Tarricone, Sean V. Tavtigian, Melissa C. Southey
Опубліковано 2010Artigo -
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A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS) за авторством Noralane M. Lindor, Lucia Guidugli, Xianshu Wang, Maxime Vallée, Álvaro N.A. Monteiro, Sean V. Tavtigian, David E. Goldgar, Fergus J. Couch
Опубліковано 2011Revisão -
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Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs за авторством Maxime Vallée, Tiana C. Francy, Megan K. Judkins, Davit Babikyan, Fabienne Lesueur, Amanda Gammon, David E. Goldgar, Fergus J. Couch, Sean V. Tavtigian
Опубліковано 2011Artigo -
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Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus за авторством Sonia Garritano, Federica Gemignani, Catherine Voegele, Tú Nguyen‐Dumont, Florence Le Calvez‐Kelm, Deepika de Silva, Fabienne Lesueur, Stefano Landi, Sean V. Tavtigian
Опубліковано 2009Artigo -
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ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classification за авторством Leslie G. Biesecker, Alicia B. Byrne, Steven M Harrison, Tina Pesaran, Alejandro A. Schäffer, Brian H. Shirts, Sean V Tavtigian, Heidi L Rehm
Опубліковано 2023Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Genetics
Gene
Medicine
Mutation
Computational biology
Cancer
Missense mutation
Internal medicine
Bioinformatics
Breast cancer
Computer science
Oncology
Germline mutation
Phenotype
Cancer research
Colorectal cancer
Genetic testing
Germline
Allele
Microbiology
Pathogenicity
Pathology
Population
DNA mismatch repair
Medical genetics
RNA
RNA splicing
Environmental health
Genome