| human | Q5 |
| P106 | occupation | researcher | Q1650915 |
| Q57250674 | A common coding variant in CASP8 is associated with breast cancer risk |
| Q37272982 | A genome wide linkage search for breast cancer susceptibility genes |
| Q28943448 | A genome-wide association study identifies susceptibility loci for Wilms tumor |
| Q33855633 | A genome-wide association study of testicular germ cell tumor |
| Q37272989 | A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers |
| Q57305942 | A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer |
| Q34546389 | ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles |
| Q57903143 | Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22 |
| Q45979098 | Association analysis identifies 65 new breast cancer risk loci. |
| Q24646663 | Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants |
| Q35532898 | Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium |
| Q57056093 | Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis |
| Q38758618 | Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation |
| Q34327945 | Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 |
| Q57305977 | Breast-Cancer Risk in Families With Mutations in PALB2 |
| Q34148873 | Breast-cancer risk in families with mutations in PALB2 |
| Q31082788 | Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
| Q34181322 | Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer |
| Q57278898 | Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
| Q57250672 | Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk |
| Q59041387 | Erratum: Identification of the breast cancer susceptibility gene BRCA2 |
| Q33894527 | Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium |
| Q57266727 | Evaluation ofRAD50 in familial breast cancer predisposition |
| Q34017597 | Gene-gene interactions in breast cancer susceptibility |
| Q34114293 | Genome-wide association study identifies five new breast cancer susceptibility loci |
| Q24645441 | Genome-wide association study identifies novel breast cancer susceptibility loci |
| Q24628710 | Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls |
| Q28245028 | Germline mutations in RAD51D confer susceptibility to ovarian cancer |
| Q57266937 | Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation |
| Q36922317 | Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14 |
| Q46103372 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer |
| Q28215462 | Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations |
| Q28388006 | Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer |
| Q35221378 | Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25 |
| Q36785681 | Mutation and association analysis of GEN1 in breast cancer susceptibility |
| Q24615080 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene |
| Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
| Q37194147 | Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer |
| Q56625730 | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles |
| Q33904964 | Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility |
| Q29417028 | Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer |
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