Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 1

Results: 22

Association of genetic variations in RTN4 3′-UTR with risk for clear cell renal cell carcinoma.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 129, doi. 10.1007/s10689-017-0005-y

By:

Pu, Yan;
Chen, Peng;
Zhou, Bin;
Zhang, Peng;
Wang, Yanyun;
Song, Yaping;
Zhang, Lin

Publication type:

Article

A single visit multidisciplinary model for managing patients with mutations in moderate and high-risk genes in a community practice setting.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 175, doi. 10.1007/s10689-017-0010-1

By:

O’Leary, Michael P.;
Goldner, Bryan S.;
Abboy, Sridevi;
Mercado, Philip D.;
Plurad, Hong Yoon

Publication type:

Article

Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 141, doi. 10.1007/s10689-017-0011-0

By:

Dominguez-Valentin, Mev;
Nakken, Sigve;
Tubeuf, Hélène;
Vodak, Daniel;
Ekstrøm, Per Olaf;
Nissen, Anke M.;
Morak, Monika;
Holinski-Feder, Elke;
Martins, Alexandra;
Møller, Pål;
Hovig, Eivind

Publication type:

Article

Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testing.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 87, doi. 10.1007/s10689-017-0012-z

By:

Silva-Smith, Rachel;
Sussman, Daniel A.

Publication type:

Article

Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 31, doi. 10.1007/s10689-017-0014-x

By:

Brédart, Anne;
Kop, Jean-Luc;
Antoniou, Antonis C.;
Cunningham, Alex P.;
De Pauw, Antoine;
Tischkowitz, Marc;
Ehrencrona, Hans;
Dolbeault, Sylvie;
Robieux, Léonore;
Rhiem, Kerstin;
Easton, Douglas F.;
Devilee, Peter;
Stoppa-Lyonnet, Dominique;
Schmutlzer, Rita

Publication type:

Article

Next generation sequencing is informing phenotype: a TP53 example.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 123, doi. 10.1007/s10689-017-0002-1

By:

O’Shea, R.;
Clarke, R.;
Berkley, E.;
Giffney, C.;
Farrell, M.;
O’Donovan, E.;
Gallagher, D. J.

Publication type:

Article

RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 63, doi. 10.1007/s10689-017-0003-0

By:

Fennell, Lochlan J.;
Clendenning, Mark;
McKeone, Diane M.;
Jamieson, Saara H.;
Balachandran, Samanthy;
Borowsky, Jennifer;
Liu, John;
Kawamata, Futoshi;
Bond, Catherine E.;
Rosty, Christophe;
Burge, Matthew E.;
Buchanan, Daniel D.;
Leggett, Barbara A.;
Whitehall, Vicki L. J.

Publication type:

Article

A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 23, doi. 10.1007/s10689-017-0004-z

By:

Cock-Rada, A. M.;
Ossa, C. A.;
Garcia, H. I.;
Gomez, L. R.

Publication type:

Article

Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 91, doi. 10.1007/s10689-017-0013-y

By:

Clendenning, Mark;
Huang, Alvin;
Jayasekara, Harindra;
Lorans, Marie;
Preston, Susan;
O’Callaghan, Neil;
Pope, Bernard J.;
Macrae, Finlay A.;
Winship, Ingrid M.;
Milne, Roger L.;
Giles, Graham G.;
English, Dallas R.;
Hopper, John L.;
Win, Aung K.;
Jenkins, Mark A.;
Southey, Melissa C.;
Rosty, Christophe;
Buchanan, Daniel D.;
On behalf of investigators from the Melbourne Collaborative Cohort Study and the Australasian Colorectal Cancer Family Registry Cohort

Publication type:

Article

Development of a high risk pancreatic screening clinic using 3.0 T MRI.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 101, doi. 10.1007/s10689-017-0057-z

By:

Barnes, Chad A.;
Krzywda, Elizabeth;
Lahiff, Shannon;
McDowell, Dena;
Christians, Kathleen K.;
Knechtges, Paul;
Tolat, Parag;
Hohenwalter, Mark;
Dua, Kulwinder;
Khan, Abdul H.;
Evans, Douglas B.;
Geurts, Jennifer;
Tsai, Susan

Publication type:

Article

Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 71, doi. 10.1007/s10689-017-0006-x

By:

Salo-Mullen, Erin E.;
Lynn, Patricio B.;
Wang, Lu;
Walsh, Michael;
Gopalan, Anuradha;
Shia, Jinru;
Tran, Christina;
Man, Fung Ying;
McBride, Sean;
Schattner, Mark;
Zhang, Liying;
Weiser, Martin R.;
Stadler, Zsofia K.

Publication type:

Article

TP53 germline and somatic mutations in a patient with fibrolamellar hepatocellular carcinoma.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 119, doi. 10.1007/s10689-017-9998-5

By:

Andrade, Raissa C.;
de Lima, Maria A. F. D.;
de Faria, Paulo A. S.;
Vargas, Fernando R.

Publication type:

Article

Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriers.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 53, doi. 10.1007/s10689-017-9997-6

By:

Etchegary, Holly;
Dicks, Elizabeth;
Tamutis, Laura;
Dawson, Lesa

Publication type:

Article

The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer.

Published in:

2018

By:

Vasen, Hans F. A.

Publication type:

Editorial

The role of screening MRI in the era of next generation sequencing and moderate-risk genetic mutations.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 167, doi. 10.1007/s10689-017-0007-9

By:

Macklin, Sarah;
Gass, Jennifer;
Mitri, Ghada;
Atwal, Paldeep S.;
Hines, Stephanie

Publication type:

Article

Early onset renal cell carcinoma in an adolescent girl with germline FLCN exon 5 deletion.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 135, doi. 10.1007/s10689-017-0008-8

By:

Schneider, Meike;
Dinkelborg, Katja;
Xiao, Xiuli;
Chan-Smutko, Gayun;
Hruska, Kathleen;
Huang, Dongli;
Sagar, Pallavi;
Harisinghani, Mukesh;
Iliopoulos, Othon

Publication type:

Article

Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 79, doi. 10.1007/s10689-017-0009-7

By:

Abu Freha, Naim;
Leibovici Weissman, Yaara;
Fich, Alexander;
Barnes Kedar, Inbal;
Halpern, Marisa;
Sztarkier, Ignacio;
Behar, Doron M.;
Arbib Sneh, Orly;
Vilkin, Alex;
Baris, Hagit N.;
Gingold, Rachel;
Lejbkowicz, Flavio;
Niv, Yaron;
Goldberg, Yael;
Levi, Zohar

Publication type:

Article

How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 155, doi. 10.1007/s10689-017-9994-9

By:

Dheensa, Sandi;
Crawford, Gillian;
Salter, Claire;
Parker, Michael;
Fenwick, Angela;
Lucassen, Anneke

Publication type:

Article

The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 43, doi. 10.1007/s10689-017-9995-8

By:

Donald, Neil;
Malik, Salim;
McGuire, Joshua L.;
Monahan, Kevin J.

Publication type:

Article

Gestational choriocarcinoma associated with a germline TP53 mutation.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 113, doi. 10.1007/s10689-017-9996-7

By:

Brehin, Anne-Claire;
Patrier-Sallebert, Sophie;
Bougeard, Gaëlle;
Side-Pfennig, Gwendoline;
Llamas Gutierrez, Francisco;
Lamy, Aude;
Colasse, Elodie;
Kandel-Aznar, Christine;
Delnatte, Capucine;
Vuillemin, Eric;
Sadot-Lebouvier, Sophie;
Odent, Sylvie;
Sabourin, Jean-Christophe;
Golfier, François;
Frebourg, Thierry

Publication type:

Article

Is there a genetic anticipation in breast and/or ovarian cancer families with the germline c.3481_3491del11 mutation?

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 5, doi. 10.1007/s10689-017-9999-4

By:

El Tannouri, R.;
Albuisson, E.;
Jonveaux, P.;
Luporsi, E.

Publication type:

Article

Heightened perception of breast cancer risk in young women at risk of familial breast cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 1, p. 15, doi. 10.1007/s10689-017-0001-2

By:

Glassey, Rachael;
O’Connor, Moira;
Ives, Angela;
Saunders, Christobel;
kConFab Investigators;
O’Sullivan, Sarah;
Hardcastle, Sarah J.

Publication type:

Article