A. C. Jäger

发表

Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression.

J. Rehfeld, I. Bernstein, F. Nielsen, 1997, American journal of human genetics.

Allelic loss of chromosome 2p21-16.3 is associated with reduced survival in sporadic colorectal cancer.

J. Rehfeld, F. Nielsen, P. Dalgaard, 2001, Scandinavian journal of gastroenterology.

HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLα and hMLH1–hEXO1 complexes

L. Rasmussen, Keshav K. Singh, F. Nielsen, 2001, Oncogene.

Functional characterization of MLH1 missense variants identified in lynch syndrome patients

N. de Wind, L. Rasmussen, I. Bernstein, 2012, Human mutation.

Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.

Jocelyne Bruand, Felix Schlesinger, Paulina Walichiewicz, 2017, Forensic science international. Genetics.

Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA

L. Rasmussen, F. Nielsen, J. Bundgaard, 2004, Oncogene.

Characteristics of the Danish families with multiple endocrine neoplasia type 1

J. Rehfeld, F. Nielsen, T. V. Hansen, 2006, Molecular and Cellular Endocrinology.

Characterization of the human laminin β2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS)

F. Nielsen, T. Khurana, M. Durkin, 1999, Cytogenetic and Genome Research.

Is thyroidectomy necessary in RET mutations carriers of the familial medullary thyroid carcinoma syndrome?

F. Nielsen, C. Godballe, H. S. Hansen, 2000, Cancer.

Hereditary non‐polyposis colorectal cancer (HNPCC): phenotype–genotype correlation between patients with and without identified mutation

I. Bernstein, F. Nielsen, M. Bisgaard, 2002, Human mutation.

Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer.

M. Schwartz, I. Bernstein, F. Nielsen, 2005, Mutation research.

Is thyroidectomy necessary in RET mutations carriers of the familial medullary thyroid carcinoma syndrome?

F. Nielsen, C. Godballe, H. S. Hansen, 2000, Cancer.