Xavier Llor

ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 5

Top Venues

Journal of medical genetics

Cancer prevention research (Philadelphia, Pa.)

Familial cancer

This page only lists publications with an associated author ORCID identifier.

Publications

Vinit Singh, Catherine Mezzacappa, Peter Gershkovich, Jessica Di Giovanna, Amanda Ganzak, Joanna Gibson, John Sinard, Rosa M Xicola, Xavier Llor
Systems approach to enhance Lynch syndrome diagnosis through tumour testing. Journal of medical genetics (2022)
Benjamin A Lerner, Rosa M Xicola, Nicolette J Rodriguez, Rachid Karam, Xavier Llor
Simplified and more sensitive criteria for identifying individuals with pathogenic CDH1 variants. Journal of medical genetics (2022)
Suzanne P MacFarland, Jessica E Ebrahimzadeh, Kristin Zelley, Lubna Begum, Lee M Bass, Randall E Brand, Beth Dudley, Douglas S Fishman, Amanda Ganzak, Eve Karloski, Alicia J Latham, Xavier Llor, Sharon Plon, Mary K Riordan, Sarah R Scollon, Zsofia K Stadler, Sapna Syngal, Chinedu Ukaegbu, Jennifer M Weiss, Matthew B Yurgelun, Garrett M Brodeur, Petar Mamula, Bryson W Katona
Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing SMAD4/BMPR1A Variant. Cancer prevention research (Philadelphia, Pa.) 14 (2) (2020)
Rosa M Xicola, Shuwei Li, Nicolette Rodriguez, Patrick Reinecke, Rachid Karam, Virginia Speare, Mary Helen Black, Holly LaDuca, Xavier Llor
Clinical features and cancer risk in families with pathogenic CDH1 variants irrespective of clinical criteria. Journal of medical genetics 56 (12) (2019)
Rosa M Xicola, Julia R Clark, Timothy Carroll, Jurgis Alvikas, Priti Marwaha, Maureen R Regan, Francesc Lopez-Giraldez, Jungmin Choi, Rajyasree Emmadi, Victoria Alagiozian-Angelova, Sonia S Kupfer, Nathan A Ellis, Xavier Llor
Implication of DNA repair genes in Lynch-like syndrome. Familial cancer 18 (3) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Xavier Llor