Zerin Hyder

Manchester, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 13 publications

Evaluation of whole-body MRI for cancer early detection in Li-Fraumeni syndrome.

Evaluation of whole-body MRI for cancer early detection in Li-Fraumeni syndrome.

Journal: Journal of medical genetics

Published: February 17, 2025

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

Correction to: Survival from breast cancer in women with a BRCA2 mutation by treatment.

Correction to: Survival from breast cancer in women with a BRCA2 mutation by treatment.

Journal: British journal of cancer

Published: January 13, 2023

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

Journal: The New England journal of medicine

Published: November 10, 2021

Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.

Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.

Journal: Clinical genetics

Published: August 18, 2021

Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis.

Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis.

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

Published: April 12, 2021

ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy.

ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy.

Journal: European journal of human genetics : EJHG

Published: July 28, 2020

Survival from breast cancer in women with a BRCA2 mutation by treatment.

Survival from breast cancer in women with a BRCA2 mutation by treatment.

Journal: British journal of cancer

Published: July 14, 2020

Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals.

Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals.

Journal: Clinical genetics

Published: July 03, 2020

Constitutional de novo deletion CNV encompassing REST predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN).

Constitutional de novo deletion CNV encompassing REST predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN).

Journal: Journal of medical genetics

Published: April 17, 2020

Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in BRCA1, BRCA2, and TP53 Genes in Women with Very Early-Onset (<36 Years) Breast Cancer.

Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in BRCA1, BRCA2, and TP53 Genes in Women with Very Early-Onset (<36 Years) Breast Cancer.

Journal: Cancers

Published: November 08, 2019

Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity.

Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity.

Journal: Clinical dysmorphology

Published: May 03, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026