Jessada Thutkawkorapin

Stockholm, AB 17176, Sweden

Last Updated: 09/26/2026

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Found 21 publications

A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives.

A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives.

Journal: Hereditary cancer in clinical practice

Published: June 10, 2024

A Swedish genome-wide haplotype association analysis identifies novel candidate loci associated with endometrial cancer risk.

A Swedish genome-wide haplotype association analysis identifies novel candidate loci associated with endometrial cancer risk.

Journal: PloS one

Published: May 10, 2024

A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31.

A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31.

Journal: International journal of molecular sciences

Published: December 13, 2022

Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk.

Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk.

Journal: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)

Published: September 22, 2022

A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16.

A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16.

Journal: Cancers

Published: December 31, 2021

A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients.

A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients.

Journal: Scientific reports

Published: April 18, 2021

Colorectal cancer risk susceptibility loci in a Swedish population.

Colorectal cancer risk susceptibility loci in a Swedish population.

Journal: Molecular carcinogenesis

Published: April 05, 2021

Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes.

Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes.

Journal: Scientific reports

Published: March 07, 2021

Massive parallel sequencing in a family with rectal cancer.

Massive parallel sequencing in a family with rectal cancer.

Journal: Hereditary cancer in clinical practice

Published: December 02, 2020

Identification of known and novel familial cancer genes in Swedish colorectal cancer families.

Identification of known and novel familial cancer genes in Swedish colorectal cancer families.

Journal: International journal of cancer

Published: November 22, 2020

pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing.

pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing.

Journal: BMC bioinformatics

Published: September 30, 2019

Whole-genome sequencing of synchronous thyroid carcinomas identifies aberrant DNA repair in thyroid cancer dedifferentiation.

Whole-genome sequencing of synchronous thyroid carcinomas identifies aberrant DNA repair in thyroid cancer dedifferentiation.

Journal: The Journal of pathology

Published: May 26, 2019

Showing 1-12 of 21

Last Updated: 09/26/2026