Works matching IS 13899600 AND DT 2021 AND VI 20 AND IP 3

Results: 11

In memoriam Professor Thierry Frébourg.

Published in:

2021

By:

Bougeard, Gaëlle

Publication type:

Editorial

Hereditary medullary thyroid carcinoma syndromes: experience from western India.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 241, doi. 10.1007/s10689-020-00219-9

By:

Diwaker, Chakra;
Sarathi, Vijaya;
Jaiswal, Sanjeet Kumar;
Shah, Ravikumar;
Deshmukh, Anuja;
Thomas, Anand Ebin;
Prakash, Gagan;
Malhotra, Gaurav;
Patil, Virendra;
Lila, Anurag;
Shah, Nalini;
Bandgar, Tushar

Publication type:

Article

Efficacy of paired tumor and germline testing in evaluation of patients with Lynch-like syndrome in a large integrated healthcare setting.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 223, doi. 10.1007/s10689-020-00218-w

By:

Carwana, Holly;
Hoodfar, Elizabeth;
Bergoffen, JoAnn;
Li, Dan

Publication type:

Article

Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genes.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 195, doi. 10.1007/s10689-020-00217-x

By:

Gensini, Francesca;
Sestini, Roberta;
De Luca, Alessandro;
Pinna, Valentina;
Daniele, Paola;
Orzalesi, Lorenzo;
Petrella, Maria Cristina;
Porfirio, Berardino;
Papi, Laura

Publication type:

Article

Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 189, doi. 10.1007/s10689-020-00216-y

By:

Laitman, Yael;
Michaelson-Cohen, Rachel;
Chen-Shtoyerman, Rakefet;
Goldberg, Yael;
Reish, Orit;
Bernstein-Molho, Rinat;
Levy-Lahad, Ephrat;
Baruch, Noa Ephrat Ben;
Kedar, Inbal;
Evans, D. Gareth;
Haim, Sara;
Paluch-Shimon, Shani;
Friedman, Eitan

Publication type:

Article

A novel germline variant in RET gene resulting in an additional cysteine in a family with familial medullary thyroid carcinoma.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 253, doi. 10.1007/s10689-020-00214-0

By:

Oriola, Josep;
Sanchez, Aurora;
Paniello, Blanca;
de la Bellacasa, Jordi Puig;
Biarnés, Josefina

Publication type:

Article

Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 181, doi. 10.1007/s10689-020-00213-1

By:

Lovejoy, Leann A.;
Rummel, Seth K.;
Turner, Clesson E.;
Shriver, Craig D.;
Ellsworth, Rachel E.

Publication type:

Article

Discordant DNA mismatch repair protein status between synchronous or metachronous gastrointestinal carcinomas: frequency, patterns, and molecular etiologies.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 201, doi. 10.1007/s10689-020-00210-4

By:

Vyas, Monika;
Firat, Canan;
Hechtman, Jaclyn F.;
Weiser, Martin R.;
Yaeger, Rona;
Vanderbilt, Chad;
Benhamida, Jamal K.;
Keshinro, Ajaratu;
Zhang, Liying;
Ntiamoah, Peter;
Gonzalez, Marco;
Andrade, Rebecca;
El Dika, Imane;
Markowitz, Arnold J.;
Smith, J. Joshua;
Garcia-Aguilar, Julio;
Vakiani, Efsevia;
Klimstra, David S.;
Stadler, Zsofia K.;
Shia, Jinru

Publication type:

Article

FRAMe: Familial Risk Assessment of Melanoma—a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanoma.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 231, doi. 10.1007/s10689-020-00209-x

By:

Holland, Elizabeth A.;
Lo, Serigne;
Kelly, Blake;
Schmid, Helen;
Cust, Anne E.;
Palmer, Jane M.;
Drummond, Martin;
Hayward, Nicholas K.;
Pritchard, Antonia L.;
Mann, Graham J.

Publication type:

Article

The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 173, doi. 10.1007/s10689-020-00212-2

By:

Escudeiro, Carla;
Pinto, Carla;
Vieira, Joana;
Peixoto, Ana;
Pinto, Pedro;
Pinheiro, Manuela;
Santos, Catarina;
Guerra, Joana;
Lisboa, Susana;
Santos, Rui;
Silva, João;
Leal, Conceição;
Coimbra, Nuno;
Lopes, Paula;
Ferreira, Marco;
Sousa, Ana B.;
Teixeira, Manuel R.

Publication type:

Article

Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.

Published in:

Familial Cancer, 2021, v. 20, n. 3, p. 215, doi. 10.1007/s10689-020-00211-3

By:

Sina, Mohammad;
Ghorbanoghli, Zeinab;
Abedrabbo, Amal;
Al-Mulla, Fahd;
Sghaier, Rihab Ben;
Buisine, Marie-Pierre;
Cortas, George;
Goshayeshi, Ladan;
Hadjisavvas, Andreas;
Hammoudeh, Wail;
Hamoudi, Waseem;
Jabari, Carol;
Loizidou, Maria A.;
Majidzadeh-A, Keivan;
Marafie, Makia J.;
Muslumov, Gurbankhan;
Rifai, Laila;
Seir, Rania Abu;
Talaat, Suzan M.;
Tunca, Berrin

Publication type:

Article