Claire Forde

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 15

Top Topics

Breast Cancer Risk

Amyotrophic Lateral Sclerosis

Top Venues

Journal of medical genetics

European journal of human genetics : EJHG

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

Publications

Dafydd Gareth Evans, Sacha J Howell, George Joseph Burghel, Claire Forde, Fiona Lalloo, Miriam Jane Smith, Anthony Howell, Ashu Gandhi, Emma Roisin Woodward
Germline testing for breast cancer patients in England: illogical to prioritise grade 1 breast cancer aged 30-39 over grade 3 aged 40-49 years? Journal of medical genetics (2024)
Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics 61 (4) (2024)
Dafydd Gareth Evans, George Joseph Burghel, Sacha J Howell, Sarah Pugh, Claire Forde, Anthony Howell, Fiona Lalloo, Emma Roisin Woodward
Pathogenic variant detection rate varies considerably in male breast cancer families and sporadic cases: minimal additional contribution beyond BRCA2, BRCA1 and CHEK2 . Journal of medical genetics (2024)
Dafydd Gareth Evans, George Joseph Burghel, Sacha J Howell, Sarah Pugh, Claire Forde, Anthony Howell, Fiona Lalloo, Emma Roisin Woodward
Pathogenic variant detection rate varies considerably in male breast cancer families and sporadic cases: minimal additional contribution beyond BRCA2, BRCA1 and CHEK2 . Journal of medical genetics 61 (9) (2024)
Claire Forde, Miriam Jane Smith, George Joseph Burghel, Naomi Bowers, Nicola Roberts, Tim Lavin, Jane Halliday, Andrew Thomas King, Scott Rutherford, Omar N Pathmanaban, Simon Lloyd, Simon Freeman, Dorothy Halliday, Allyson Parry, Patrick Axon, Juliette J Gair, Shazia Afridi, Rupert Obholzer, Roger Laitt, Owen Thomas, Stavros Michael Stivaros, Grace Vassallo, Dafydd Gareth Evans
NF2 -related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study. Journal of medical genetics (2024)
Claire Forde, Miriam Jane Smith, George Joseph Burghel, Naomi Bowers, Nicola Roberts, Tim Lavin, Jane Halliday, Andrew Thomas King, Scott Rutherford, Omar N Pathmanaban, Simon Lloyd, Simon Freeman, Dorothy Halliday, Allyson Parry, Patrick Axon, Juliette J Gair, Shazia Afridi, Rupert Obholzer, Roger Laitt, Owen Thomas, Stavros Michael Stivaros, Grace Vassallo, Dafydd Gareth Evans
NF2 -related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study. Journal of medical genetics 61 (9) (2024)
Claire Forde, Miriam Jane Smith, George Joseph Burghel, Naomi Bowers, Nicola Roberts, Tim Lavin, Jane Halliday, Andrew Thomas King, Scott Rutherford, Omar N Pathmanaban, Simon Lloyd, Simon Freeman, Dorothy Halliday, Allyson Parry, Patrick Axon, Juliette J Gair, Shazia Afridi, Rupert Obholzer, Roger Laitt, Owen Thomas, Stavros Michael Stivaros, Grace Vassallo, Dafydd Gareth Evans
NF2 -related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study. Journal of medical genetics 61 (9) (2024)
Dafydd Gareth Evans, George Joseph Burghel, Sacha J Howell, Sarah Pugh, Claire Forde, Anthony Howell, Fiona Lalloo, Emma Roisin Woodward
Pathogenic variant detection rate varies considerably in male breast cancer families and sporadic cases: minimal additional contribution beyond BRCA2, BRCA1 and CHEK2 . Journal of medical genetics 61 (9) (2024)
Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics 61 (4) (2024)
Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics (2023)
Dafydd Gareth Evans, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Detection of pathogenic variants in breast cancer susceptibility genes in bilateral breast cancer. Journal of medical genetics (2023)
Dafydd Gareth Evans, Siva Sithambaram, Elke Maria van Veen, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Helen Byers, Jamie M Ellingford, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Differential involvement of germline pathogenic variants in breast cancer genes between DCIS and low-grade invasive cancers. Journal of medical genetics (2022)
Claire Forde, Andrew T King, Scott A Rutherford, Charlotte Hammerbeck-Ward, Simon K Lloyd, Simon R Freeman, Omar N Pathmanaban, Emma Stapleton, Owen M Thomas, Roger D Laitt, Stavros Stivaros, John-Paul Kilday, Grace Vassallo, Catherine McBain, Simon Kerrigan, Miriam J Smith, Martin G McCabe, Elaine F Harkness, D Gareth Evans
Disease course of neurofibromatosis type 2: a 30-year follow-up study of 353 patients seen at a single institution. Neuro-oncology 23 (7) (2021)
Claire Forde, Emma Burkitt-Wright, Peter D Turnpenny, Eric Haan, John Ealing, Shehla Mohammed, Muriel Holder, Nayana Lahiri, Abhijit Dixit, Annie Procter, Laurence Pacot, Dominique Vidaud, Yline Capri, Marion Gerard, Hélène Dollfus, Elise Schaefer, Chloé Quelin, Sabine Sigaudy, Tiffany Busa, Gabriella Vera, Lena Damaj, Ludwine Messiaen, David A Stevenson, Peter Davies, Sheila Palmer-Smith, Alison Callaway, Pierre Wolkenstein, Eric Pasmant, Meena Upadhyaya
Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study. European journal of human genetics : EJHG 30 (3) (2021)
Claire Forde, Kate Brunstrom, Emma Woodward, Naomi Bowers, Marta Pereira, Andrew J Wallace, Fiona Lalloo, Elaine F Harkness, Dafydd Gareth Evans
Uptake of pre-symptomatic testing for BRCA1 and BRCA2 is age, gender, offspring and time-dependent. Journal of medical genetics (2020)