| Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report |
15 |
| Colorectal carcinoma in the course of inflammatory bowel diseases |
14 |
| The effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysis |
11 |
| Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes |
7 |
| Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature |
6 |
| The association between non-breast and ovary cancers and BRCA mutation in first- and second-degree relatives of high-risk breast cancer patients: a large-scale study of Koreans |
5 |
| German National Case Collection for familial pancreatic Cancer (FaPaCa) - acceptance and psychological aspects of a pancreatic cancer screening program |
5 |
| Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study |
4 |
| Platinum-based neoadjuvant chemotherapy in BRCA1-positive breast cancer: a retrospective cohort analysis and literature review |
4 |
| Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls |
4 |
| Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia |
4 |
| Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory |
4 |
| A qualitative study of barriers to genetic counseling and potential for mobile technology education among women with ovarian cancer |
3 |
| Single-center study of Lynch syndrome screening in colorectal polyps |
3 |
| Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study |
3 |
| BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway |
3 |
| A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease |
3 |
| Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds |
3 |
| Polyglobulia in patients with hemangioblastomas is related to tumor size but not to serum erythropoietin |
3 |
| High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population |
3 |
| BRCA mutation screening and patterns among high-risk Lebanese subjects |
3 |
| Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews |
3 |
| A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families |
3 |
| Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations |
2 |
| Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS) |
2 |
| Challenges in recruiting African-American women for a breast cancer genetics study |
2 |
| Genetic counselling and personalised risk assessment in the Australian pancreatic cancer screening program |
2 |
| CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome |
2 |
| Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study |
1 |
| Serum selenium level and cancer risk: a nested case-control study |
1 |
| Allelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian population |
1 |
| Prevalence and spectrum of MLH MSH and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients |
1 |
| Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report |
1 |
| Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes |
1 |
| Endometrioid endometrial cancer recurring as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence? |
1 |
| Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomy |
0 |
| Clinical Genetics of Cancer 2017 Szczecin, Poland. 21-22 September 2017 Abstracts |
0 |
| CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis |
0 |
| Meeting abstracts from the Annual Conference Clinical Genetics of Cancer 2018: Szczecin, Poland. 11-12 October 2018 Abstracts |
0 |
| Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome |
0 |
| A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China |
0 |
| BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer |
0 |
| Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service |
0 |
| Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences |
0 |
| Validation of a digital identification tool for individuals at risk for hereditary cancer syndromes |
0 |
| Somatic variants of potential clinical significance in the tumors of BRCA phenocopies |
0 |
| Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland |
0 |
| Selected Abstracts from the 3rd European Hereditary Tumour Group Meeting (EHTG 2018) Abstracts |
0 |
| Germline c.1A > C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case report |
0 |
