| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?
|
Johannesma, Paul C.
|
|
2015
|
15 |
2 |
p. 297-300
|
article
|
| 2 |
Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1
|
Porcelli, Bree
|
|
2015
|
15 |
2 |
p. 301-308
|
article
|
| 3 |
CDH1 germline mutations and hereditary lobular breast cancer
|
Corso, Giovanni
|
|
2016
|
15 |
2 |
p. 215-219
|
article
|
| 4 |
Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome
|
Kidambi, Trilokesh D.
|
|
2016
|
15 |
2 |
p. 275-280
|
article
|
| 5 |
Correlation between the germline methylation status in ERβ promoter and the risk in prostate cancer: a prospective study
|
Wang, Lihui
|
|
2015
|
15 |
2 |
p. 309-315
|
article
|
| 6 |
CYP1A1 and GSTP1 gene variations in breast cancer: a systematic review and case–control study
|
Akhtar, Sumaira
|
|
2015
|
15 |
2 |
p. 201-214
|
article
|
| 7 |
Determining the familial risk distribution of colorectal cancer: a data mining approach
|
Chau, Rowena
|
|
2015
|
15 |
2 |
p. 241-251
|
article
|
| 8 |
Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours
|
Jones, G. E.
|
|
2016
|
15 |
2 |
p. 351-355
|
article
|
| 9 |
Development of a novel PTT assay for mutation detection in PALB2 large exons and PALB2 screening in medullary breast cancer
|
Poumpouridou, Nikoleta
|
|
2015
|
15 |
2 |
p. 183-191
|
article
|
| 10 |
Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis
|
Lan, Zhu
|
|
2015
|
15 |
2 |
p. 221-230
|
article
|
| 11 |
Erratum to: Methylation of the miR-126 gene associated with glioma progression
|
Cui, Hongwei
|
|
2015
|
15 |
2 |
p. 325
|
article
|
| 12 |
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis
|
Spier, Isabel
|
|
2016
|
15 |
2 |
p. 281-288
|
article
|
| 13 |
Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer
|
Douma, Kirsten F. L.
|
|
2015
|
15 |
2 |
p. 231-240
|
article
|
| 14 |
Germline BAP1 mutations misreported as somatic based on tumor-only testing
|
Abdel-Rahman, Mohamed H.
|
|
2016
|
15 |
2 |
p. 327-330
|
article
|
| 15 |
Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment
|
Baumgart, Leigh A.
|
|
2015
|
15 |
2 |
p. 331-339
|
article
|
| 16 |
Methylation of the miR-126 gene associated with glioma progression
|
Cui, Hongwei
|
|
2015
|
15 |
2 |
p. 317-324
|
article
|
| 17 |
Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study
|
Baars, J. E.
|
|
2016
|
15 |
2 |
p. 163-171
|
article
|
| 18 |
Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis
|
Haraldsdottir, Sigurdis
|
|
2015
|
15 |
2 |
p. 253-260
|
article
|
| 19 |
Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients
|
Taki, Keiko
|
|
2015
|
15 |
2 |
p. 261-265
|
article
|
| 20 |
Non-genetic health professionals’ attitude towards, knowledge of and skills in discussing and ordering genetic testing for hereditary cancer
|
Douma, Kirsten F. L.
|
|
2015
|
15 |
2 |
p. 341-350
|
article
|
| 21 |
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect
|
Vogelaar, Ingrid P.
|
|
2015
|
15 |
2 |
p. 289-296
|
article
|
| 22 |
Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer
|
Murria Estal, Rosa
|
|
2015
|
15 |
2 |
p. 193-200
|
article
|
| 23 |
Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis
|
Casellas-Cabrera, Nicolás
|
|
2015
|
15 |
2 |
p. 267-274
|
article
|
| 24 |
Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis
|
Oliveira, Eneida Santos de
|
|
2015
|
15 |
2 |
p. 173-181
|
article
|
| 25 |
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety
|
Sermijn, Erica
|
|
2016
|
15 |
2 |
p. 155-162
|
article
|
Journal description