Cristina Perez-Becerril

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Inflammatory Response

Signaling Pathway

Top Venues

Journal of medical genetics

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

Publications

Cristina Perez-Becerril, George Joseph Burghel, Claire Hartley, Charles F Rowlands, Dafydd Gareth Evans, Miriam Jane Smith
Improved sensitivity for detection of pathogenic variants in familial NF2 -related schwannomatosis. Journal of medical genetics 61 (5) (2024)
Cristina Perez-Becerril, George Joseph Burghel, Claire Hartley, Charles F Rowlands, Dafydd Gareth Evans, Miriam Jane Smith
Improved sensitivity for detection of pathogenic variants in familial NF2 -related schwannomatosis. Journal of medical genetics (2024)
Miriam Jane Smith, Cristina Perez-Becerril, Mwee van der Meer, George Joseph Burghel, Sarah J Waller, Megan Carney, Sancha Bunstone, Katherine Fryer, Naomi L Bowers, Claire L Hartley, Philip T Smith, Scott A Rutherford, Simon R Freeman, Simon K W Lloyd, Omar N Pathmanaban, Andrew Thomas King, Dorothy Halliday, Chris Duff, D Gareth Evans
Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2 -related schwannomatosis. Journal of medical genetics (2024)
Cristina Perez-Becerril, George Joseph Burghel, Claire Hartley, Charles F Rowlands, Dafydd Gareth Evans, Miriam Jane Smith
Improved sensitivity for detection of pathogenic variants in familial NF2 -related schwannomatosis. Journal of medical genetics 61 (5) (2024)
Cristina Perez-Becerril, Andrew J Wallace, Helene Schlecht, Naomi L Bowers, Philip T Smith, Carolyn Gokhale, Helen Eaton, Chris Charlton, Rachel Robinson, Ruth S Charlton, D Gareth Evans, Miriam Jane Smith
Screening of potential novel candidate genes in schwannomatosis patients. Human mutation 43 (10) (2022)
Cristina Perez-Becerril, Dafydd Gareth Evans, Miriam Jane Smith
Pathogenic noncoding variants in the neurofibromatosis and schwannomatosis predisposition genes. Human mutation 42 (10) (2021)