User profiles for "author:Zeinab Ghorbanoghli"

Zeinab Ghorbanoghli

Leiden University Medical Center
Verified email at lumc.nl
Cited by 343

Duodenal adenomas and cancer in MUTYH-associated polyposis: an international cohort study

LE Thomas, JJ Hurley, AA Sanchez… - …, 2021 - gastrojournal.org
1Institute of Medical Genetics, Division of Cancer and Genetics, Cardiff University, School of
Medicine, Cardiff, UK; 2Department of Gastroenterology, Prince Charles Hospital, Merthyr …

Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis

Z Ghorbanoghli, BAJ Bastiaansen… - Journal of medical …, 2018 - jmg.bmj.com
Background Screening of patients with familial adenomatous polyposis (FAP) have led to a
substantial reduction in mortality due to colorectal cancer (CRC). Recent guidelines suggest …

[HTML][HTML] A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families

Z Ghorbanoghli, C Jabari, W Sweidan, W Hammoudeh… - Familial cancer, 2018 - Springer
Colorectal cancer (CRC) has a very high incidence in the western world. Data from registries
in the Middle East showed that the incidence of CRC is relatively low in these countries …

[HTML][HTML] Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries

M Sina, Z Ghorbanoghli, A Abedrabbo, F Al-Mulla… - Familial cancer, 2021 - Springer
Background Lynch syndrome (LS), the most common inherited form of colorectal cancer
(CRC), is responsible for 3% of all cases of CRC. LS is caused by a mismatch repair gene …

[HTML][HTML] Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

Z Ghorbanoghli, MH Nieuwenhuis… - Familial Cancer, 2016 - Springer
Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by
germline mutations in the APC gene and characterized by the development of multiple …

Optimizing the timing of colorectal surgery in patients with familial adenomatous polyposis in clinical practice

HFA Vasen, Z Ghorbanoghli, B de Ruijter… - Scandinavian Journal …, 2019 - Taylor & Francis
Background: Familial adenomatous polyposis (FAP) is characterized by the development of
hundreds of colorectal adenomas in the second decade of life, and prophylactic colectomy is …

Identification of familial colorectal cancer and hereditary colorectal cancer syndromes through the Dutch population-screening program: results ofa pilot study

SJH van Erp, LW Leicher, SD Hennink… - Scandinavian Journal …, 2016 - Taylor & Francis
Abstract Objectives: In 2014, a population-screening program using immuno-faecal occult
blood testing (I-FOBT) has started in the Netherlands. The aims of this study were to …

High yield of surveillance in patients diagnosed with constitutional mismatch repair deficiency

Z Ghorbanoghli, M van Kouwen, B Versluys… - Journal of Medical …, 2023 - jmg.bmj.com
Background Constitutional mismatch repair deficiency (CMMRD) is a rare autosomal
recessively inherited syndrome that is caused by biallelic pathogenic variants of the …

[HTML][HTML] Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP)

CG Daans, Z Ghorbanoghli, ME Velthuizen… - Familial Cancer, 2020 - Springer
Barrett's oesophagus (BE) has been associated with an increased risk of both colorectal
adenomas and colorectal cancer. A recent investigation reported a high frequency of BE in …

Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families

Z Ghorbanoghli, C Jabari, W Sweidan… - Familial …, 2018 - ncbi.nlm.nih.gov
Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern
Mediterranean countries to improve care for high-risk families - PMC Back to Top Skip to main …