MSI Test to Distinguish between HNPCC and Other Predisposing Syndromes – of Value in Tailored Surveillance

por Liljegren, Annelie, Olsson, Louise, Lindblom, Annika
Publicado 2004

Exome sequencing in 51 early onset non‐familial CRC cases

por Thutkawkorapin, Jessada, Lindblom, Annika, Tham, Emma
Publicado 2019

Unravelling genetic variants of a swedish family with high risk of prostate cancer

por Barilla, Serena, Lindblom, Annika, Helgadottir, Hafdis T.
Publicado 2022

Linkage Analysis in Familial Non-Lynch Syndrome Colorectal Cancer Families from Sweden

por Kontham, Vinaykumar, von Holst, Susanna, Lindblom, Annika
Publicado 2013

A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer

por Zhou, Xiao-Lei, Werelius, Barbro, Lindblom, Annika
Publicado 2004

Differential expression of Aquaporin 8 in human colonic epithelial cells and colorectal tumors

por Fischer, Heléne, Stenling, Roger, Rubio, Carlos, Lindblom, Annika
Publicado 2001

Clinicopathological analysis of colorectal cancer: a comparison between emergency and elective surgical cases

por Ghazi, Sam, Berg, Elisabeth, Lindblom, Annika, Lindforss, Ulrik
Publicado 2013

CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer

por Margolin, Sara, Eiberg, Hans, Lindblom, Annika, Bisgaard, Marie Luise
Publicado 2007

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

por Helgadottir, Hafdis T., Thutkawkorapin, Jessada, Lagerstedt-Robinson, Kristina, Lindblom, Annika
Publicado 2021

Screening for germline phosphatase and tensin homolog-mutations in suspected Cowden syndrome and Cowden syndrome-like families among uterine cancer patients

por TZORTZATOS, GERASIMOS, ARAVIDIS, CHRISTOS, LINDBLOM, ANNIKA, MINTS, MIRIAM, THAM, EMMA
Publicado 2015

Cancer risk susceptibility loci in a Swedish population

por Liu, Wen, Jiao, Xiang, Thutkawkorapin, Jessada, Mahdessian, Hovsep, Lindblom, Annika
Publicado 2017

Variants of the PPARD Gene and Their Clinicopathological Significance in Colorectal Cancer

por Ticha, Ivana, Gnosa, Sebastian, Lindblom, Annika, Liu, Tao, Sun, Xiao-Feng
Publicado 2013

Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden

por Wendt, Camilla, Lindblom, Annika, Arver, Brita, von Wachenfeldt, Anna, Margolin, Sara
Publicado 2015

Massive parallel sequencing in a family with rectal cancer

por Wallander, Karin, Thutkawkorapin, Jessada, Sahlin, Ellika, Lindblom, Annika, Lagerstedt-Robinson, Kristina
Publicado 2021

The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees’ outcome

por Platten, Ulla, Rantala, Johanna, Lindblom, Annika, Brandberg, Yvonne, Lindgren, Gunilla, Arver, Brita
Publicado 2012

Exome sequencing in one family with gastric- and rectal cancer

por Thutkawkorapin, Jessada, Picelli, Simone, Kontham, Vinaykumar, Liu, Tao, Nilsson, Daniel, Lindblom, Annika
Publicado 2016

Familial cancer among consecutive uterine cancer patients in Sweden

por Tzortzatos, Gerasimos, Wersäll, Ofra, Danielsson, Kristina Gemzell, Lindblom, Annika, Tham, Emma, Mints, Miriam
Publicado 2014

Immunohistochemical Loss of the DNA Mismatch Repair Proteins MSH2 and MSH6 in Malignant Fibrous Histiocytomas

por Ericson, Kajsa, Engellau, Jacob, Persson, Annette, Lindblom, Annika, Domanski, Henryk, Åkerman, Måns, Nilbert, Mef
Publicado 2004

Risk perception after genetic counseling in patients with increased risk of cancer

por Rantala, Johanna, Platten, Ulla, Lindgren, Gunilla, Nilsson, Bo, Arver, Brita, Lindblom, Annika, Brandberg, Yvonne
Publicado 2009

A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families

por von Wachenfeldt, Anna, Lindblom, Annika, Grönberg, Henrik, Einbeigi, Zakaria, Rosenquist, Richard, Gardman, Camilla, Iselius, Lennart
Publicado 2007