Volume 15, Issue 4

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October 2016

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25 articles in this issue

Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis
Renaud Sabatier
Elise Lavit
Patrice Viens
Original Article 01 February 2016 Pages: 497 - 506
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population
Henriette Roed Nielsen
Mef Nilbert
Christina Therkildsen
Original Article 01 February 2016 Pages: 507 - 512
Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk
Jada G. Hamilton
Darren Mays
Kenneth P. Tercyak
Original Article 05 February 2016 Pages: 513 - 522
No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families
Henriette Roed Nielsen
Janne Petersen
Anne-Bine Skytte
Original Article 07 March 2016 Pages: 523 - 528
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer
Aryana S. Jacobs
Marc D. Schwartz
Beth N. Peshkin
Original Article 11 March 2016 Pages: 529 - 539
Angelina and Brad effect
Francois Eisinger
Letter to the Editor 03 May 2016 Pages: 541 - 542
Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer
Olle Sjöström
Lars Lindholm
Beatrice Melin
Original Article Open access 02 March 2016 Pages: 543 - 551
Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies
Masakazu Kohda
Kensuke Kumamoto
Yasushi Okazaki
Original Article 02 February 2016 Pages: 553 - 562
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
Z. Ghorbanoghli
M. H. Nieuwenhuis
J. T. Wijnen
Original Article Open access 15 February 2016 Pages: 563 - 570
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation
Aurélia Nguyen
Gaelle Bougeard
Natacha Entz-Werle
Short Communication 26 March 2016 Pages: 571 - 577
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome
Aysel Ahadova
Magnus von Knebel Doeberitz
Matthias Kloor
Original Article 09 March 2016 Pages: 579 - 586
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency
Maureen E. Mork
Ester Borras
Eduardo Vilar
Short Communication 26 March 2016 Pages: 587 - 591
Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes
Sara E. Dobbins
Peter Broderick
Richard S. Houlston
Original Article Open access 29 June 2016 Pages: 593 - 599
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma
Borum Sagong
Young Joon Seo
In Seok Moon
Original Article 01 February 2016 Pages: 601 - 606
Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma
Roeliene C. Kruizinga
Denise M. S. van Marion
Annemiek M. E. Walenkamp
Original Article Open access 26 February 2016 Pages: 607 - 616
Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India
Manjunath Goroshi
Tushar Bandgar
Nalini S. Shah
Original Article 23 February 2016 Pages: 617 - 624
MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics
Jessica Oliboni Scapineli
Lucieli Ceolin
Ana Luiza Maia
Original Article 26 February 2016 Pages: 625 - 633
Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations
Francesca Ponti
Serena Corsini
Luca Sangiorgi
Original Article 08 March 2016 Pages: 635 - 643
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome
Tiziana Cavalli
Francesco Giudici
Francesco Tonelli
Original Article 12 April 2016 Pages: 645 - 649
Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families
Jazlyn Read
Judith Symmons
Nicholas K. Hayward
Original Article 23 April 2016 Pages: 651 - 663
An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC)
Nina Hallowell
Shirlene Badger
Julia Lawton
Original Article 02 June 2016 Pages: 665 - 676
Occurrence of renal cell carcinoma and hematologic malignancies (predominantly lymphoid) in individuals and in families
Janice P. Dutcher
Peter H. Wiernik
Rangaswamy Chintapatla
Original Article 22 June 2016 Pages: 677 - 687
Evaluation of laboratory perspectives on hereditary cancer panels
Jessica Stoll
Scott M. Weissman
Kristen J. Vogel Postula
Original Article 11 February 2016 Pages: 689 - 696
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study
Mary B. Daly
Susan Montgomery
Karen Ruth
Original Article Open access 20 February 2016 Pages: 697 - 706
A model for patient-direct screening and referral for familial cancer risk
Kristin B. Niendorf
Melissa A. Geller
Robert D. Madoff
Original Article 27 June 2016 Pages: 707 - 716

Volume 15, Issue 4

Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis

BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population

Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk

No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families

Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer

Angelina and Brad effect

Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer

Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation

CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome

Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency

Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes

A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma

Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma

Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India

MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics

Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations

Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC)

Occurrence of renal cell carcinoma and hematologic malignancies (predominantly lymphoid) in individuals and in families

Evaluation of laboratory perspectives on hereditary cancer panels

Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study

A model for patient-direct screening and referral for familial cancer risk

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