| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Addressing uncertainty in hereditary colorectal cancer: the role of a regional expert multidisciplinary team meeting
|
Varde, Avani
|
|
|
24 |
1 |
|
article
|
| 2 |
A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic
|
Haider, Rida
|
|
|
24 |
1 |
|
article
|
| 3 |
A novel likely pathogenic germline variant in CDKN1B in a patient with MEN4 and medullary thyroid cancer
|
Mercè, Fernández
|
|
|
24 |
1 |
|
article
|
| 4 |
Bilateral familial retinoblastoma diagnosed via optical coherence tomography following a normal funduscopic exam
|
Allphin, Mitchell T.
|
|
|
24 |
1 |
|
article
|
| 5 |
BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants
|
Vatsyayan, Aastha
|
|
|
24 |
1 |
|
article
|
| 6 |
Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework
|
Varesco, Liliana
|
|
|
24 |
1 |
|
article
|
| 7 |
Case review of perivascular epithelioid cell tumor occurring in patients with Li-Fraumeni syndrome
|
Abe, Natsuno
|
|
|
24 |
1 |
|
article
|
| 8 |
CHEK2-related breast cancer: real-world challenges
|
Weis, Luiza N.
|
|
|
24 |
1 |
|
article
|
| 9 |
Correction: Benign tumors and non-melanoma skin cancers in patients with fanconi anemia
|
Enache, Aura
|
|
|
24 |
1 |
|
article
|
| 10 |
Correction: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations
|
Sanoba, Shenin A.
|
|
|
24 |
1 |
|
article
|
| 11 |
Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome
|
Brinch, Heidi Hesselø
|
|
|
24 |
1 |
|
article
|
| 12 |
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort
|
Sheth, Harsh
|
|
|
24 |
1 |
|
article
|
| 13 |
Healthcare provider-mediated cascade testing of Lynch syndrome to at-risk family members: an interview study
|
Ong, Serene
|
|
|
24 |
1 |
|
article
|
| 14 |
Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service
|
Fiorentino, Francesca
|
|
|
24 |
1 |
|
article
|
| 15 |
Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing
|
Boedec, Morgane
|
|
|
24 |
1 |
|
article
|
| 16 |
Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland
|
Loughrey, Mechelle
|
|
|
24 |
1 |
|
article
|
| 17 |
Myelodysplastic syndrome with dual germline RUNX1 and DDX41 variants: a rare genetic predisposition case
|
Bove, Virginia
|
|
|
24 |
1 |
|
article
|
| 18 |
New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients
|
Amiot, Julie
|
|
|
24 |
1 |
|
article
|
| 19 |
Optimizing MRI sequences and apparent diffusion coefficient parameters for small pancreatic ductal adenocarcinoma detection
|
Mori, Naoko
|
|
|
24 |
1 |
|
article
|
| 20 |
Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature
|
Gonzalez, Maria Laura
|
|
|
24 |
1 |
|
article
|
| 21 |
Prevalence of cardiometabolic outcomes in women who underwent salpingo-oophorectomy to prevent hereditary breast and ovarian cancer: a meta-analysis
|
Moraes, Francisco Cezar Aquino de
|
|
|
24 |
1 |
|
article
|
| 22 |
Progress report on multiple endocrine neoplasia type 1
|
Halperin, Reut
|
|
|
24 |
1 |
|
article
|
| 23 |
Recurrent paraneoplastic nephrotic syndrome; insights from a Lynch syndrome patient with multiple malignancies
|
de Jong, Myrthe A.
|
|
|
24 |
1 |
|
article
|
| 24 |
Sarcomas arising in MEN1 patients: demonstrating LOH of the MEN1 locus and loss of menin expression
|
van Leeuwaarde, Rachel S.
|
|
|
24 |
1 |
|
article
|
| 25 |
The challenge of preventing gastric cancer in patients under surveillance for familial adenomatous polyposis
|
Bouchiba, Hicham
|
|
|
24 |
1 |
|
article
|
| 26 |
The genetic landscape of Lynch syndrome in the Israeli population
|
Abu Shtaya, Aasem
|
|
|
24 |
1 |
|
article
|
| 27 |
Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis
|
Cleret de Langavant, Boris
|
|
|
24 |
1 |
|
article
|
Journal description