Area of research
Pathology and Forensic Medicine · Genetics
Research interest
Research interests include Genetic factors in colorectal cancer, Inflammatory Bowel Disease, Colorectal Cancer Screening and Detection, and Cancer, Hypoxia, and Metabolism.
Lynch Syndrome: Similarities and Differences of Recommendations in Published Guidelines
Sleeve gastrectomy reveals the plasticity of the human gastric epithelium
A review of APC somatic mosaicism and specific APC variants - I1307K and promotor variants
Raising the Age for Starting Colonoscopy to 35 Years for Individuals With path_MSH6 Carriers May Lead to Missed Opportunities for Detecting Advanced Neoplasia in a Notable Percentage of Carriers
Senescent cancer-associated fibroblasts in pancreatic adenocarcinoma restrict CD8+ T cell activation and limit responsiveness to immunotherapy in mice
Oral bacteria accelerate pancreatic cancer development in mice
A computer-aided polyp detection system in screening and surveillance colonoscopy: an international, multicentre, randomised, tandem trial
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes
The genetic landscape of Lynch syndrome in the Israeli population
Low ALT Is Associated with IBD and Disease Activity: Results from a Nationwide Study
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
Integrated clinical and genomic analysis identifies driver events and molecular evolution of colitis-associated cancers
Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on <i>APC</i> I1307K and cancer risk
The benefit of pancreatic cancer surveillance in carriers of germline <i>BRCA1/2</i> pathogenic variants
Patients with low ALT levels are at increased risk for severe COVID-19
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Ashkenazi Jewish and Other White APC I1307K Carriers Are at Higher Risk for Multiple Cancers
The Association Between Proton Pump Inhibitors and COVID-19 is Confounded by Hyperglycemia in a Population-Based Study
Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic background
The possible association of proton pump inhibitor use with acute cholangitis in patients with choledocholithiasis: a multi-center study
The Association between Serum Vitamin D Levels and Helicobacter pylori Presence and Eradication
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications
Height in adolescence as a risk factor for glioma subtypes: a nationwide retrospective cohort study of 2.2 million subjects
The Possible Association of Non-Alcoholic Fatty Liver Disease with Acute Cholangitis: A Retrospective Multicenter Cohort Study
Fecal microbiota transplant promotes response in immunotherapy-refractory melanoma patients
Heat Shock Factor 1-dependent extracellular matrix remodeling mediates the transition from chronic intestinal inflammation to colon cancer
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database