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Publications by Nissen, Anke M.

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Number of items: 5.

Journal article

Morak, Monika; Ibisler, Ayseguel; Keller, Gisela; Jessen, Ellen; Laner, Andreas; Gonzales-Fassrainer, Daniela; Locher, Melanie; Massdorf, Trisari; Nissen, Anke M.; Benet-Pages, Anna; Holinski-Feder, Elke (2018): Comprehensive analysis of the MLH1 promoter region in 480 patients with colorectal cancer and 1150 controls reveals new variants including one with a heritable constitutional MLH1 epimutation. In: Journal of Medical Genetics, Vol. 55, No. 4: pp. 240-248

Dominguez-Valentin, Mev; Evans, D. Gareth R.; Nakken, Sigve; Tubeuf, HLsne; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds. In: Hereditary Cancer in Clinical Practice 16:4 [PDF, 1MB]

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Identification of genetic variants for clinical management of familial colorectal tumors. In: BMC Medical Genetics 19:26 [PDF, 652kB]

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal; Hovig, Eivind (2018): Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families. In: Familial Cancer, Vol. 17, No. 1: pp. 141-153

Morak, Monika; Käsbauer, Sarah; Kerscher, Martina; Massdorf, Trisari; Holinski-Feder, Elke; Laner, Andreas; Nissen, Anke M.; Benet-Pages, Anna; Schackert, Hans K.; Keller, Gisela (2017): Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6. In: Familial Cancer, Vol. 16, No. 4: pp. 491-500

This list was generated on Fri Apr 23 01:45:49 2021 CEST.