Works matching IS 13899600 AND DT 2016 AND VI 15 AND IP 4

Results: 25

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 553, doi. 10.1007/s10689-016-9872-x

By:

Kohda, Masakazu;
Kumamoto, Kensuke;
Eguchi, Hidetaka;
Hirata, Tomoko;
Tada, Yuhki;
Tanakaya, Kohji;
Akagi, Kiwamu;
Takenoshita, Seiichi;
Iwama, Takeo;
Ishida, Hideyuki;
Okazaki, Yasushi

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 497, doi. 10.1007/s10689-016-9873-9

By:

Sabatier, Renaud;
Lavit, Elise;
Moretta, Jessica;
Lambaudie, Eric;
Noguchi, Tetsuro;
Eisinger, François;
Cherau, Elisabeth;
Provansal, Magali;
Livon, Doriane;
Rabayrol, Laetitia;
Popovici, Cornel;
Charaffe-Jauffret, Emmanuelle;
Sobol, Hagay;
Viens, Patrice

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 601, doi. 10.1007/s10689-016-9874-8

By:

Sagong, Borum;
Seo, Young;
Lee, Hyun-Jin;
Kim, Mi;
Kim, Un-Kyung;
Moon, In

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 507, doi. 10.1007/s10689-016-9875-7

By:

Nielsen, Henriette;
Nilbert, Mef;
Petersen, Janne;
Ladelund, Steen;
Thomassen, Mads;
Pedersen, Inge;
Hansen, Thomas;
Skytte, Anne-Bine;
Borg, Åke;
Therkildsen, Christina

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 513, doi. 10.1007/s10689-016-9876-6

By:

Hamilton, Jada;
Mays, Darren;
DeMarco, Tiffani;
Tercyak, Kenneth

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 563, doi. 10.1007/s10689-016-9877-5

By:

Ghorbanoghli, Z.;
Nieuwenhuis, M.;
Houwing-Duistermaat, J.;
Jagmohan-Changur, S.;
Hes, F.;
Tops, C.;
Wagner, A.;
Aalfs, C.;
Verhoef, S.;
Gómez García, E.;
Sijmons, R.;
Menko, F.;
Letteboer, T.;
Hoogerbrugge, N.;
Wezel, T.;
Vasen, H.;
Wijnen, J.

Publication type:

Article

Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma.

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 607, doi. 10.1007/s10689-016-9879-3

By:

Kruizinga, Roeliene;
Marion, Denise;
Dunnen, Wilfred;
Groot, Jan;
Hoving, Eelco;
Oosting, Sjoukje;
Timmer-Bosscha, Hetty;
Derks, Rosalie;
Cornelissen, Chantal;
Luijt, Rob;
Links, Thera;
Vries, Elisabeth;
Walenkamp, Annemiek

Publication type:

Article

Evaluation of laboratory perspectives on hereditary cancer panels.

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 689, doi. 10.1007/s10689-016-9880-x

By:

Stoll, Jessica;
Weissman, Scott;
Hook, Nicole;
Selkirk, Christina;
Johnson, Amy;
Newlin, Anna;
Vogel Postula, Kristen

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 697, doi. 10.1007/s10689-016-9889-1

By:

Daly, Mary;
Montgomery, Susan;
Bingler, Ruth;
Ruth, Karen

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 617, doi. 10.1007/s10689-016-9891-7

By:

Goroshi, Manjunath;
Bandgar, Tushar;
Lila, Anurag;
Jadhav, Swati;
Khare, Shruti;
Shrikhande, Shailesh;
Uchino, Shinya;
Dalvi, Abhay;
Shah, Nalini

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 625, doi. 10.1007/s10689-016-9892-6

By:

Scapineli, Jessica;
Ceolin, Lucieli;
Puñales, Márcia;
Dora, José;
Maia, Ana

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 571, doi. 10.1007/s10689-016-9894-4

By:

Nguyen, Aurélia;
Bougeard, Gaelle;
Koob, Meriam;
Chenard, Marie;
Schneider, Anne;
Maugard, Christine;
Entz-Werle, Natacha

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 635, doi. 10.1007/s10689-016-9895-3

By:

Ponti, Francesca;
Corsini, Serena;
Gnoli, Maria;
Pedrini, Elena;
Mordenti, Marina;
Sangiorgi, Luca

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 523, doi. 10.1007/s10689-016-9898-0

By:

Nielsen, Henriette;
Petersen, Janne;
Krogh, Lotte;
Nilbert, Mef;
Skytte, Anne-Bine

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 665, doi. 10.1007/s10689-016-9910-8

By:

Hallowell, Nina;
Badger, Shirlene;
Richardson, Sue;
Caldas, Carlos;
Hardwick, Richard;
Fitzgerald, Rebecca;
Lawton, Julia

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 579, doi. 10.1007/s10689-016-9899-z

By:

Ahadova, Aysel;
von Knebel Doeberitz, Magnus;
Bläker, Hendrik;
Kloor, Matthias

Publication type:

Article

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.

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 587, doi. 10.1007/s10689-016-9902-8

By:

Mork, Maureen;
Borras, Ester;
Taggart, Melissa;
Cuddy, Amanda;
Bannon, Sarah;
You, Y.;
Lynch, Patrick;
Ramirez, Pedro;
Rodriguez-Bigas, Miguel;
Vilar, Eduardo

Publication type:

Article

Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome.

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 645, doi. 10.1007/s10689-016-9906-4

By:

Cavalli, Tiziana;
Giudici, Francesco;
Santi, Raffaella;
Nesi, Gabriella;
Brandi, Maria;
Tonelli, Francesco

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 651, doi. 10.1007/s10689-016-9907-3

By:

Read, Jazlyn;
Symmons, Judith;
Palmer, Jane;
Montgomery, Grant;
Martin, Nicholas;
Hayward, Nicholas

Publication type:

Article

Angelina and Brad effect.

Published in:

2016

By:

Eisinger, Francois

Publication type:

Letter

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 529, doi. 10.1007/s10689-016-9900-x

By:

Jacobs, Aryana;
Schwartz, Marc;
Valdimarsdottir, Heiddis;
Nusbaum, Rachel;
Hooker, Gillian;
DeMarco, Tiffani;
Heinzmann, Jessica;
McKinnon, Wendy;
McCormick, Shelley;
Davis, Claire;
Forman, Andrea;
Lebensohn, Alexandra;
Dalton, Emily;
Tully, Diana;
Graves, Kristi;
Similuk, Morgan;
Kelly, Scott;
Peshkin, Beth

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 677, doi. 10.1007/s10689-016-9911-7

By:

Dutcher, Janice;
Wiernik, Peter;
Varella, Leticia;
Chintapatla, Rangaswamy

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 707, doi. 10.1007/s10689-016-9912-6

By:

Niendorf, Kristin;
Geller, Melissa;
Vogel, Rachel;
Church, Timothy;
Leininger, Anna;
Bakke, Angela;
Madoff, Robert

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 593, doi. 10.1007/s10689-016-9914-4

By:

Dobbins, Sara;
Broderick, Peter;
Chubb, Daniel;
Kinnersley, Ben;
Sherborne, Amy L.;
Houlston, Richard

Publication type:

Article

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

Published in:

Familial Cancer, 2016, v. 15, n. 4, p. 543, doi. 10.1007/s10689-016-9867-7

By:

Sjöström, Olle;
Lindholm, Lars;
Tavelin, Björn;
Melin, Beatrice

Publication type:

Article