A. Hout

发表

Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia

H. Brunner, A. Essen, P. Rump, 2008, European Journal of Human Genetics.

Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

D. Altshuler, P. Fasching, P. Hall, 2013, PLoS genetics.

Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

W. Chung, P. Hall, V. Pankratz, 2013, PLoS Genetics.

Region with a Marked Instability in Yeast Artificial Chromosomes

K. Kok, E. Schoenmakers, C. Buys, 1994 .

Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma.

K. Kok, C. Buys, A. H. van der Hout, 1988, Cancer genetics and cytogenetics.

Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy

R. Hofstra, J. T. Dunnen, A. Essen, 2003, American journal of medical genetics. Part A.

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

J. Osinga, K. Kok, P. Postmus, 1987, Nature.

University of Groningen Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk Couch,

F. Couch, B. Bonanni, O. Olopade, 2013 .

A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting

H. Meijers-Heijboer, S. Verhoef, R. Hofstra, 2006, Human mutation.

Title Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA 1 and BRCA 2 mutation carriers

R. Nussbaum, D. Steinemann, V. Pankratz, 2015 .

University of Groningen DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Osorio,

Rensburg, A. Whittemore, D. Steinemann, 2014 .

BRCA1 and BRCA2 heterozygosity and repair of X-ray-induced DNA damage

H. Kampinga, C. Streffer, A. Hout, 2002, International journal of radiation biology.

Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion

J. Aten, C. Buys, A. Hout, 1988, Human Genetics.

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation

M. King, W. Foulkes, C. Lázaro, 2011, Breast Cancer Research and Treatment.

A deletion at the short arm of chromosome 3 is common to all major types of lung cancer

J. Osinga, K. Kok, P. Postmus, 1988 .

SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS

L. H. van den Berg, J. Veldink, H. Scheffer, 2005, Neurology.

A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

A. Wilde, M. P. van den Berg, C. Bezzina, 1999, Circulation research.

TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

H. Meijers-Heijboer, C. Asperen, S. Verhoef, 2010, Journal of Medical Genetics.

University of Groningen Identification of a BRCA 2-Specific Modifier Locus at 6 p 24 Related to Breast Cancer

D. Altshuler, V. Pankratz, F. Couch, 2017 .

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

Mads Thomassen, Nina Ditsch, Muhammad Usman Rashid, 2015, JAMA.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

A. Whittemore, F. Couch, B. Bonanni, 2015 .