Naomi L. Bowers

St Mary's Hospital
Manchester, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 32 publications

Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2-related schwannomatosis.

Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2-related schwannomatosis.

Journal: Journal of medical genetics

Published: July 02, 2024

NF2-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study.

NF2-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study.

Journal: Journal of medical genetics

Published: April 23, 2024

Re-evaluation of missense variant classifications in NF2.

Re-evaluation of missense variant classifications in NF2.

Journal: Human mutation

Published: October 15, 2021

Screening of potential novel candidate genes in schwannomatosis patients.

Screening of potential novel candidate genes in schwannomatosis patients.

Journal: Human mutation

Published: September 30, 2021

Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability.

Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability.

Journal: Cancers

Published: July 26, 2021

Implementation of Multigene Germline and Parallel Somatic Genetic Testing in Epithelial Ovarian Cancer: SIGNPOST Study.

Implementation of Multigene Germline and Parallel Somatic Genetic Testing in Epithelial Ovarian Cancer: SIGNPOST Study.

Journal: Cancers

Published: July 08, 2021

Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer.

Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 15, 2021

Extended gene panel testing in lobular breast cancer.

Extended gene panel testing in lobular breast cancer.

Journal: Familial cancer

Published: January 20, 2021

Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers.

Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers.

Journal: Journal of medical genetics

Published: October 25, 2020

High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.

High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.

Journal: Journal of medical genetics

Published: July 17, 2020

Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives.

Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives.

Journal: European journal of human genetics : EJHG

Published: July 17, 2020

Assessment of mismatch repair deficiency in ovarian cancer.

Assessment of mismatch repair deficiency in ovarian cancer.

Journal: Journal of medical genetics

Published: June 15, 2020

Showing 1-12 of 32

Last Updated: 09/26/2026