Lynn Greenhalgh

Crown Street
Liverpool, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 24 publications

Targeted Prostate Cancer Screening in Carriers of BRCA1 or BRCA2 Pathogenic Germline Variants Detects Clinically Relevant Disease: 5-year Results from the IMPACT Study.

Targeted Prostate Cancer Screening in Carriers of BRCA1 or BRCA2 Pathogenic Germline Variants Detects Clinically Relevant Disease: 5-year Results from the IMPACT Study.

Journal: European urology

Published: October 23, 2025

The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers.

The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers.

Journal: BJU international

Published: June 05, 2024

Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families.

Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families.

Journal: European journal of human genetics : EJHG

Published: February 06, 2023

Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes.

Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes.

Journal: Annals of oncology : official journal of the European Society for Medical Oncology

Published: March 03, 2022

Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome.

Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome.

Journal: AJNR. American journal of neuroradiology

Published: February 24, 2022

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.

Journal: American journal of human genetics

Published: February 22, 2022

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project.

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project.

Journal: Genome medicine

Published: February 02, 2022

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.

Journal: The Lancet. Oncology

Published: July 02, 2021

PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.

PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.

Journal: Neurology. Genetics

Published: November 03, 2020

Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy.

Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy.

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

Published: June 29, 2020

Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.

Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.

Journal: European urology

Published: March 27, 2019

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.

Journal: Human mutation

Published: July 03, 2018

Showing 1-12 of 24

Last Updated: 09/26/2026