Edward M. Leter

Maastricht, LI, Netherlands

Last Updated: 09/26/2026

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Found 18 publications

Case Report: Epidermal growth factor receptor germline variant associated with epilepsy and rare, distinctive cerebral MRI abnormalities.

Case Report: Epidermal growth factor receptor germline variant associated with epilepsy and rare, distinctive cerebral MRI abnormalities.

Journal: Frontiers in radiology

Published: January 07, 2026

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Journal: BJC reports

Published: February 13, 2025

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

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

Published: August 12, 2024

Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS).

Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS).

Journal: Cancers

Published: January 08, 2024

Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome.

Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome.

Journal: Journal of the National Cancer Institute

Published: April 13, 2022

Evaluation of yield and experiences of age-related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome.

Evaluation of yield and experiences of age-related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome.

Journal: International journal of cancer

Published: February 20, 2020

Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition.

Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition.

Journal: Journal of the National Cancer Institute

Published: January 23, 2019

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

Journal: Familial cancer

Published: January 05, 2019

Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study.

Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study.

Journal: Journal of the American Academy of Dermatology

Published: August 12, 2018

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 08, 2017

New mutations and an updated database for the patched-1 (PTCH1) gene.

New mutations and an updated database for the patched-1 (PTCH1) gene.

Journal: Molecular genetics & genomic medicine

Published: July 13, 2017

Postzygotic mosaicism in basal cell naevus syndrome.

Postzygotic mosaicism in basal cell naevus syndrome.

Journal: The British journal of dermatology

Published: September 15, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026