Works matching IS 13899600 AND DT 2022 AND VI 21 AND IP 2

Results: 14

Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 157, doi. 10.1007/s10689-021-00261-1
By:
- Meiser, Bettina;
- Woodward, Paula;
- Gleeson, Margaret;
- Kentwell, Maira;
- Fan, Helen Mar;
- Antill, Yoland;
- Butow, Phyllis N.;
- Boyle, Frances;
- Best, Megan;
- Taylor, Natalie;
- Bell, Katy;
- Tucker, Kathy
Publication type:
Article
Questioning the validity of clinically available breast cancer polygenic risk scores: comparison of two labs reveals discrepancies.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 125, doi. 10.1007/s10689-021-00260-2
By:
- Wynn, Julia;
- Levinson, Elana;
- Koval, Carrie;
- Ernst, Michelle E.;
- Chung, Wendy K.
Publication type:
Article
The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 241, doi. 10.1007/s10689-021-00259-9
By:
- Crook, Ashley;
- Kwa, Rebekah;
- Ephraums, Sarah;
- Wilding, Mathilda;
- Thiyagarajan, Lavvina;
- Fleming, Jane;
- Moore, Katrina;
- Berman, Yemima
Publication type:
Article
CDH1 pathogenic variants and cancer risk in an unselected patient population.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 235, doi. 10.1007/s10689-021-00257-x
By:
- Bar-Mashiah, Ariel;
- Soper, Emily R.;
- Cullina, Sinead;
- Belbin, Gillian M.;
- Kenny, Eimear E.;
- Lucas, Aimee L.;
- Abul-Husn, Noura S.
Publication type:
Article
Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations?
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 121, doi. 10.1007/s10689-021-00255-z
By:
- Ludman, Mark D.;
- Philipsborn, Shira Litz;
- Hartmajer, Shulamit;
- Shwartzman, Nitzan Sharon;
- Reinstein, Eyal
Publication type:
Article
Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 229, doi. 10.1007/s10689-021-00252-2
By:
- Fugaru, Ioana;
- Goudie, Catherine;
- Capolicchio, John-Paul
Publication type:
Article
Extended gene panel testing in lobular breast cancer.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 129, doi. 10.1007/s10689-021-00241-5
By:
- van Veen, Elke M.;
- Evans, D. Gareth;
- Harkness, Elaine F.;
- Byers, Helen J.;
- Ellingford, Jamie M.;
- Woodward, Emma R.;
- Bowers, Naomi L.;
- Wallace, Andrew J.;
- Howell, Sacha J.;
- Howell, Anthony;
- Lalloo, Fiona;
- Newman, William G.;
- Smith, Miriam J.
Publication type:
Article
The clinical features of polymerase proof-reading associated polyposis (PPAP) and recommendations for patient management.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 197, doi. 10.1007/s10689-021-00256-y
By:
- Palles, Claire;
- Martin, Lynn;
- Domingo, Enric;
- Chegwidden, Laura;
- McGuire, Josh;
- Cuthill, Vicky;
- Heitzer, Ellen;
- Kerr, Rachel;
- Kerr, David;
- Kearsey, Stephen;
- Clark, Susan K.;
- Tomlinson, Ian;
- Latchford, Andrew
Publication type:
Article
"I wish that there was more info": characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 143, doi. 10.1007/s10689-021-00251-3
By:
- Reyes, Kathryn G.;
- Clark, Cheyla;
- Gerhart, Meredith;
- Newson, Ainsley J.;
- Ormond, Kelly E.
Publication type:
Article
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse population.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 167, doi. 10.1007/s10689-021-00243-3
By:
- Mittendorf, Kathleen F.;
- Ukaegbu, Chinedu;
- Gilmore, Marian J.;
- Lindberg, Nangel M.;
- Kauffman, Tia L.;
- Eubanks, Donna J.;
- Shuster, Elizabeth;
- Allen, Jake;
- McMullen, Carmit;
- Feigelson, Heather Spencer;
- Anderson, Katherine P.;
- Leo, Michael C.;
- Hunter, Jessica Ezzell;
- Sasaki, Sonia Okuyama;
- Zepp, Jamilyn M.;
- Syngal, Sapna;
- Wilfond, Benjamin S.;
- Goddard, Katrina A. B.
Publication type:
Article
A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 137, doi. 10.1007/s10689-021-00242-4
By:
- Majidzadeh-A, Keivan;
- Zarinfam, Shiva;
- Abdoli, Nasrin;
- Yadegari, Fatemeh;
- Esmaeili, Rezvan;
- Farahmand, Leila;
- Teimourzadeh, Azin;
- Taghizadeh, Mahdieh;
- Salehi, Mansoor;
- Zamani, Mohamad
Publication type:
Article
Malignancy risk in individuals with familial adenomatous polyposis receiving biologics and immunomodulators.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 189, doi. 10.1007/s10689-021-00250-4
By:
- Faisal, Muhammad Salman;
- Burke, Carol A.;
- Achkar, Jean-Paul;
- Click, Benjamin;
- O'Malley, Margaret;
- LaGuardia, Lisa;
- Milicia, Susan;
- Leach, Brandie;
- Liska, David;
- Church, James;
- Kalady, Matthew;
- Mankaney, Gautam
Publication type:
Article
A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancer.
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 181, doi. 10.1007/s10689-021-00249-x
By:
- Kedar, I.;
- Walsh, L.;
- Levi, G. Reznick;
- Lieberman, S.;
- Shtaya, A. Abu;
- Nathan, S. Naftaly;
- Lagovsky, I.;
- Tomashov-Matar, R.;
- Goldenberg, M.;
- Basel-Salmon, L.;
- Katz, L.;
- Aleme, O.;
- Peretz, T. Yablonski;
- Hubert, A.;
- Rothstein, D.;
- Castellvi-Bel, S.;
- Walsh, T.;
- King, M. C.;
- Pritchard, C. C.;
- Levi, Z.
Publication type:
Article
First international workshop of the ATM and cancer risk group (4-5 December 2019).
Published in:
Familial Cancer, 2022, v. 21, n. 2, p. 211, doi. 10.1007/s10689-021-00248-y
By:
- Lesueur, Fabienne;
- Easton, Douglas F.;
- Renault, Anne-Laure;
- Tavtigian, Sean V.;
- Bernstein, Jonine L.;
- Kote-Jarai, Zsofia;
- Eeles, Rosalind A.;
- Plaseska-Karanfia, Dijana;
- Feliubadaló, Lidia;
- Spanish ATM working group;
- Moles-Fernández, Alejandro;
- Santamariña-Pena, Marta;
- Sánchez, Alysson T.;
- López-Novo, Anael;
- Porras, Luz-Marina;
- Blanco, Ana;
- Capellá, Gabriel;
- de la Hoya, Miguel;
- Molina, Ignacio J.;
- Osorio, Ana
Publication type:
Article