Inga Hinrichsen

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

R. Adam, Isabel Spier, Bixiao Zhao et al. · The American Journal of Human Genetics · 2016 · 242 citations · Full text

Somatic Variant, Recessive Subtype, Medicine +10

Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair

Jan Kosiński, Inga Hinrichsen, Janusz M. Bujnicki et al. · Human Mutation · 2010 · 66 citations · Full text

Genome Instability, Engineering, Somatic Variant +14

Refining the role of <i>pms2</i> in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants

Ester Borràs, Marta Pineda, Juan Cadiñanos et al. · Journal of Medical Genetics · 2013 · 65 citations

Comprehensive functional assessment of<i>MLH1</i>variants of unknown significance

Ester Borràs, Marta Pineda, Angela Brieger et al. · Human Mutation · 2012 · 38 citations

Promoter Methylation of MLH1, PMS2, MSH2 and p16 Is a Phenomenon of Advanced-Stage HCCs

Inga Hinrichsen, Matthias Kemp, Jan Peveling‐Oberhag et al. · PLoS ONE · 2014 · 37 citations · Full text

Epigenetic Change, Dna Methylation, Molecular Biology +19