Samuel Medhin-Gebre

Lund, M 22185, Sweden

Last Updated: 09/26/2026

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Found 13 publications

Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynch syndrome.

Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynch syndrome.

Journal: Scientific reports

Published: September 14, 2023

Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort.

Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort.

Journal: Genes, chromosomes & cancer

Published: February 03, 2022

A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families.

A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families.

Journal: Hereditary cancer in clinical practice

Published: July 27, 2018

Pancreatic cancer occurrence in Ferguson-Smith syndrome.

Pancreatic cancer occurrence in Ferguson-Smith syndrome.

Journal: JAAD case reports

Published: July 13, 2018

Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome.

Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome.

Journal: Journal of community genetics

Published: December 19, 2017

Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort.

Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 20, 2017

Genetic anticipation in Swedish Lynch syndrome families.

Genetic anticipation in Swedish Lynch syndrome families.

Journal: PLoS genetics

Published: March 17, 2017

Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.

Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.

Journal: Familial cancer

Published: October 04, 2016

Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations.

Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations.

Journal: American journal of medical genetics. Part A

Published: May 19, 2016

L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.

L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.

Journal: Clinical genetics

Published: October 06, 2015

Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors.

Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors.

Journal: The American journal of pathology

Published: March 29, 2012

Food intake and meal pattern in IAPP knockout mice with and without infusion of exogenous IAPP.

Food intake and meal pattern in IAPP knockout mice with and without infusion of exogenous IAPP.

Journal: Scandinavian journal of gastroenterology

Published: January 11, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026