A. Bardoel

发表

Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.

P. Devilee, R. Cornelis, C. Cornelisse, 1993, Oncogene.

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

C. Wijmenga, R. Houwen, P. Pearson, 2004, Genes and Immunity.

Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction.

P. Devilee, M. Beekman, C. Cornelisse, 1998, Human pathology.

Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma.

A. Cleton-Jansen, P. Hogendoorn, J. Bovée, 2000, The American journal of pathology.

Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL

M. James, G. Fleuren, P. Devilee, 1994, Genes, chromosomes & cancer.

Allelotype of human breast carcinoma: Present status and deletion-mapping on chromosomes 3p, 6, and 18q.

P. Devilee, C. Cornelisse, M. Vliet, 1991 .

PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue.

P. Devilee, C. Cornelisse, R. Frants, 1993, British Journal of Cancer.

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia

R. Ophoff, C. Wijmenga, R. Kahn, 2008, Molecular Psychiatry.

Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families

C. Wijmenga, M. Bitner-Glindzicz, D. Kelsell, 2001, Journal of medical genetics.

Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.

P. Devilee, C. Cornelisse, P. Pearson, 1991, Cancer research.

Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17.

C. Wijmenga, R. Bank, H. Pruijs, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Genes and outcome after aneurysmal subarachnoid haemorrhage

C. Wijmenga, G. Rinkel, C. Frijns, 2005, Journal of Neurology.

Identification of PLOD2 as Telopeptide Lysyl Hydroxylase, an Important Enzyme in Fibrosis*

C. Wijmenga, D. Sillence, T. Huizinga, 2003, Journal of Biological Chemistry.

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

J. Weber, P. Devilee, P. Heutink, 1992, Human molecular genetics.

Confinement of PGL, an Imprinted Gene Causing Hereditary Paragangliomas, to a 2-cM Interval on 11q22–q23 and Exclusion of DRD2 and NCAM as Candidate Genes

J. Weissenbach, P. Devilee, C. Cornelisse, 1996, European journal of human genetics : EJHG.

A major non-HLA locus in celiac disease maps to chromosome 19.

C. Wijmenga, R. Houwen, P. Pearson, 2003, Gastroenterology.

Further Localization of the Gene for Hereditary Paragangliomas and Evidence for Linkage in Unrelated Families

P. Devilee, P. Heutink, B. Oostra, 1994, European journal of human genetics : EJHG.

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

P. Devilee, R. Cornelis, D. Lindhout, 1993, American journal of human genetics.