Genome‐wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non‐BRCA1/2 families: Suggestive linkage to 10q23.32‐q25.3

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

2002 • 2,637 citations

PedCheck: A Program for Identification of Genotype Incompatibilities in Linkage Analysis

1998 • 2,089 citations

A high-resolution recombination map of the human genome

2002 • 1,730 citations

Genetic analysis of breast cancer in the cancer and steroid hormone study.

1991 • 915 citations

Polygenic susceptibility to breast cancer and implications for prevention

2002 • 902 citations

Mutations in SUFU predispose to medulloblastoma

2002 • 796 citations

Polygenic inheritance of breast cancer: Implications for design of association studies

2003 • 238 citations

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

2000 • 188 citations

Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

2003 • 185 citations

Molecular classification of familial non- BRCA1/BRCA2 breast cancer

2003 • 183 citations

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.

1997 • 181 citations

Candidate Genes in Breast Cancer Revealed by Microarray-Based Comparative Genomic Hybridization of Archived Tissue

2005 • 136 citations

Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8.

1995 • 132 citations

A genome wide linkage search for breast cancer susceptibility genes

2006 • 131 citations

Polymorphisms in DNA repair gene XRCC1 and increased genetic susceptibility to breast cancer

2005 • 127 citations

Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families

1997 • 121 citations

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.

2003 • 119 citations

After BRCA1 and BRCA2—What Next? Multifactorial Segregation Analyses of Three-Generation, Population-Based Australian Families Affected by Female Breast Cancer

2001 • 112 citations

20q11.1 amplification in giant‐cell tumor of bone: Array CGH, FISH, and association with outcome

2006 • 112 citations

Pooled Analysis of Loss of Heterozygosity in Breast Cancer: a Genome Scan Provides Comparative Evidence for Multiple Tumor Suppressors and Identifies Novel Candidate Regions

2003 • 105 citations

SAFB2, a New Scaffold Attachment Factor Homolog and Estrogen Receptor Corepressor

2003 • 87 citations

Inhibiting mutations in the transforming growth factor beta type 2 receptor in recurrent human breast cancer.

2001 • 76 citations

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

2000 • 75 citations

High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer

2001 • 62 citations

Loss of heterozygosity in familial breast carcinomas.

1993 • 50 citations

Genome-wide scanning for linkage in Finnish breast cancer families

2003 • 39 citations

Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p

2000 • 36 citations

The role of TGF‐β production in growth inhibition of breast‐tumor cells by progestins

1995 • 30 citations

A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques

2005 • 29 citations

First BRCA1 and BRCA2 Gene Testing Implemented in the Health Care System of Stockholm

2001 • 15 citations

A region close to Tp53 shows LOH in familial breast cancer

2002 • 3 citations