Anna Rohlin

Parallel sequencing used in detection of mosaic mutations: Comparison with four diagnostic DNA screening techniques

Anna Rohlin, Josephine Wernersson, Yvonne Engwall et al. · Human Mutation · 2009 · 189 citations

Genetic Testing, Genetics, Pathology +18

A mutation in POLE predisposing to a multi-tumour phenotype

Anna Rohlin, Theofanis Zagoras, Staffan Nilsson et al. · International Journal of Oncology · 2014 · 72 citations · Full text

Genetics, Pathology, Molecular Biology +17

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Alisa Olkinuora, Taina T. Nieminen, Emma Mårtensson et al. · Genetics in Medicine · 2018 · 58 citations · Full text

Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis

Anna Rohlin, Yvonne Engwall, Kaisa Fritzell et al. · Oncogene · 2011 · 57 citations · Full text

Adenomatous Polyposis Coli, Partial Gene Silencing, Genetic Disorder +15

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

Anna Rohlin, Eva Rambech, Anders Kvist et al. · Familial Cancer · 2016 · 57 citations · Full text

Genetic Testing, Cancer Pathology, Gene Panel +15