Works matching IS 17312302 AND DT 2019 AND VI 17 AND IP 1

Results: 32

Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0127-3

By:

Dominguez-Valentin, Mev;
Seppälä, Toni T.;
Sampson, Julian R.;
Macrae, Finlay;
Winship, Ingrid;
Evans, D. Gareth;
Scott, Rodney J.;
Burn, John;
Möslein, Gabriela;
Bernstein, Inge;
Pylvänäinen, Kirsi;
Renkonen-Sinisalo, Laura;
Lepistö, Anna;
Lindblom, Annika;
Plazzer, John-Paul;
Tjandra, Douglas;
Thomas, Huw;
Green, Kate;
Lalloo, Fiona;
Crosbie, Emma J.

Publication type:

Article

Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0125-5

By:

Rashid, Muhammad Usman;
Muhammad, Noor;
Naeemi, Humaira;
Khan, Faiz Ali;
Hassan, Mariam;
Faisal, Saima;
Gull, Sidra;
Amin, Asim;
Loya, Asif;
Hamann, Ute

Publication type:

Article

A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0126-4

By:

Li, Wenhui;
Li, Lei;
Wu, Ming

Publication type:

Article

Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0122-8

By:

Pan, Jennifer;
Slattery, Masha;
Shea, Natalie;
Macrae, Finlay

Publication type:

Article

Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0123-7

By:

McGarragle, Kaitlin M.;
Aronson, Melyssa;
Semotiuk, Kara;
Holter, Spring;
Hare, Crystal J.;
Ferguson, Sarah E.;
Cohen, Zane;
Hart, Tae L.

Publication type:

Article

Serum selenium level and cancer risk: a nested case-control study.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0131-7

By:

Narod, Steven A.;
Huzarski, Tomasz;
Jakubowska, Anna;
Gronwald, Jacek;
Cybulski, Cezary;
Oszurek, Oleg;
Dębniak, Tadeusz;
Jaworska-Bieniek, Katarzyna;
Lener, Marcin;
Białkowska, Katarzyna;
Sukiennicki, Grzegorz;
Muszyńska, Magdalena;
Marciniak, Wojciech;
Sun, Ping;
Kotsopoulos, Joanne;
Lubiński, Jan

Publication type:

Article

Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0132-6

By:

Clift, Kristin E.;
Macklin, Sarah K.;
Hines, Stephanie L.

Publication type:

Article

Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0130-8

By:

Mittendorf, Kathleen F.;
Hunter, Jessica Ezzell;
Schneider, Jennifer L.;
Shuster, Elizabeth;
Rope, Alan F.;
Zepp, Jamilyn;
Gilmore, Marian J.;
Muessig, Kristin R.;
Davis, James V.;
Kauffman, Tia L.;
Bergen, Kellene M.;
Wiesner, Georgia L.;
Acheson, Louise S.;
Peterson, Susan K.;
Syngal, Sapna;
Reiss, Jacob A.;
Goddard, Katrina A. B.

Publication type:

Article

Genetic counselling and personalised risk assessment in the Australian pancreatic cancer screening program.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0129-1

By:

Dwarte, Tanya;
McKay, Skye;
Johns, Amber;
Tucker, Katherine;
Spigelman, Allan D.;
Williams, David;
Stoita, Alina

Publication type:

Article

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0128-2

By:

Rashid, Muhammad Usman;
Naeemi, Humaira;
Muhammad, Noor;
Loya, Asif;
Lubiński, Jan;
Jakubowska, Anna;
Yusuf, Muhammed Aasim

Publication type:

Article

Germline c.1A>C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case report.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0124-6

By:

Carrera, Sergio;
Beristain, Elena;
Sancho, Aintzane;
Iruarrizaga, Eluska;
Rivero, Pilar;
Mañe, Juan Manuel;
López Vivanco, Guillermo

Publication type:

Article

A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0121-9

By:

Vanbinst, Anne-Marie;
Brussaard, Carola;
Vergauwen, Evelynn;
Van Velthoven, Vera;
Kuijpers, Robert;
Michel, Olaf;
Foulon, Ina;
Jansen, Anna C.;
Lefevere, Bieke;
Bohler, Susanne;
Keymolen, Kathelijn;
de Mey, Johan;
Michielsen, Dirk;
Andreescu, Corina E.;
Gläsker, Sven

Publication type:

Article

Somatic variants of potential clinical significance in the tumors of BRCA phenocopies.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0117-5

By:

Buckingham, Lela;
Mitchell, Rachel;
Maienschein-Cline, Mark;
Green, Stefan;
Hu, Vincent Hong;
Cobleigh, Melody;
Rotmensch, Jacob;
Burgess, Kelly;
Usha, Lydia

Publication type:

Article

Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0119-3

By:

Arvai, Kevin J.;
Roberts, Maegan E.;
Torene, Rebecca I.;
Susswein, Lisa R.;
Marshall, Megan L.;
Zhang, Zhancheng;
Carter, Natalie J.;
Yackowski, Lauren;
Rinella, Erica S.;
Klein, Rachel T.;
Hruska, Kathleen S.;
Retterer, Kyle

Publication type:

Article

Endometrioid endometrial cancer "recurring" as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0112-x

By:

Jiang, Wei;
Gao, Tong;
Tao, Xiang;
Zhu, Menghan;
Yao, Liangqing;
Feng, Weiwei

Publication type:

Article

Single-center study of Lynch syndrome screening in colorectal polyps.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0108-6

By:

Zhu, FangChao;
Pan, Da;
Zhang, Hui;
Ye, Qiong;
Xu, PeiSong;
Pan, Jie

Publication type:

Article

Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0120-x

By:

Cortés, Carolina;
Rivera, Ana Lucía;
Trochez, David;
Solarte, Melissa;
Gómez, Daniela;
Cifuentes, Laura;
Barreto, Guillermo

Publication type:

Article

Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0113-9

By:

Wangensteen, Teresia;
Felde, Caroline Nangota;
Ahmed, Deeqa;
Mæhle, Lovise;
Ariansen, Sarah Louise

Publication type:

Article

Colorectal carcinoma in the course of inflammatory bowel diseases.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0118-4

By:

Hnatyszyn, Andrzej;
Hryhorowicz, Szymon;
Kaczmarek-Ryś, Marta;
Lis, Emilia;
Słomski, Ryszard;
Scott, Rodney J.;
Pławski, Andrzej

Publication type:

Article

The effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysis.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0111-y

By:

Caramelo, Olga;
Silva, Cristina;
Caramelo, Francisco;
Frutuoso, Cristina;
Almeida-Santos, Teresa

Publication type:

Article

Allelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian population.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0116-6

By:

Hilz, Philip;
Heinrihsone, Reicela;
Pätzold, Lukas Alexander;
Qi, Qi;
Trofimovics, Genadijs;
Gailite, Linda;
Irmejs, Arvids;
Gardovskis, Janis;
Miklasevics, Edvins;
Daneberga, Zanda

Publication type:

Article

Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0114-8

By:

McGarragle, Kaitlin M.;
Hare, Crystal;
Holter, Spring;
Facey, Dorian Anglin;
McShane, Kelly;
Gallinger, Steven;
Hart, Tae L.

Publication type:

Article

Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0110-z

By:

Suarez-Kelly, Lorena P.;
Yu, Lianbo;
Kline, David;
Schneider, Eric B.;
Agnese, Doreen M.;
Carson, William E.

Publication type:

Article

The association between non-breast and ovary cancers and BRCA mutation in first- and second-degree relatives of high-risk breast cancer patients: a large-scale study of Koreans.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0103-3

By:

Kim, Hakyoung;
Choi, Doo Ho;
Park, Won;
Im, Young-Hyuck;
Ahn, Jin Seok;
Park, Yeon Hee;
Nam, Seok Jin;
Kim, Seok Won;
Lee, Jeong Eon;
Yu, Jong Hwan;
Lee, Se Kyung;
Jung, Boo Yeon

Publication type:

Article

Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomy.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0109-5

By:

Menkiszak, Janusz;
Chudecka-Głaz, Anita;
Cymbaluk-Płoska, Aneta;
Celewicz, Aleksander;
Kojs, Zbigniew;
Szajda, Mariusz;
Świniarska, Maria;
Bedner, Ryszard;
Jurczak, Anna;
Celewicz, Marta;
Cieszyńska, Monika;
Lubiński, Jan;
Gronwald, Jacek

Publication type:

Article

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0106-8

By:

Seppälä, Toni T.;
Ahadova, Aysel;
Dominguez-Valentin, Mev;
Macrae, Finlay;
Evans, D. Gareth;
Therkildsen, Christina;
Sampson, Julian;
Scott, Rodney;
Burn, John;
Möslein, Gabriela;
Bernstein, Inge;
Holinski-Feder, Elke;
Pylvänäinen, Kirsi;
Renkonen-Sinisalo, Laura;
Lepistö, Anna;
Lautrup, Charlotte Kvist;
Lindblom, Annika;
Plazzer, John-Paul;
Winship, Ingrid;
Tjandra, Douglas

Publication type:

Article

BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0107-7

By:

Kwiatkowski, Fabrice;
Gay-Bellile, Mathilde;
Dessenne, Pascal;
Laquet, Claire;
Boussion, Véronique;
Béguinot, Marie;
Petit, Marie-Françoise;
Grémeau, Anne-Sophie;
Verlet, Céline;
Chaptal, Charlotte;
Broult, Marilyn;
Jouvency, Sylvie;
Duclos, Martine;
Bignon, Yves-Jean

Publication type:

Article

Meeting abstracts from the Annual Conference Clinical Genetics of Cancer 2018.

Published in:: 2019
Publication type:: Calendar

Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0102-4

By:

Henn, Jonas;
Spier, Isabel;
Adam, Ronja S.;
Holzapfel, Stefanie;
Uhlhaas, Siegfried;
Kayser, Katrin;
Plotz, Guido;
Peters, Sophia;
Aretz, Stefan

Publication type:

Article

BRCA mutation screening and patterns among high-risk Lebanese subjects.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0105-9

By:

Farra, Chantal;
Dagher, Christelle;
Badra, Rebecca;
Hammoud, Miza Salim;
Alameddine, Raafat;
Awwad, Johnny;
Seoud, Muhieddine;
Abbas, Jaber;
Boulos, Fouad;
El Saghir, Nagi;
Mukherji, Deborah

Publication type:

Article

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS).

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0104-x

By:

Ramírez-Calvo, Marta;
García-Casado, Zaida;
Fernández-Serra, Antonio;
de Juan, Inmaculada;
Palanca, Sarai;
Oltra, Silvestre;
Soto, José Luis;
Castillejo, Adela;
Barbera, Víctor M;
Juan-Fita, Ma José;
Segura, Ángel;
Chirivella, Isabel;
Sánchez, Ana Beatriz;
Tena, Isabel;
Chaparro, Carolina;
Salas, Dolores;
López-Guerrero, José Antonio

Publication type:

Article

Validation of a digital identification tool for individuals at risk for hereditary cancer syndromes.

Published in:

Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0099-8

By:

Bucheit, Leslie;
Johansen Taber, Katherine;
Ready, Kaylene

Publication type:

Article