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1 . Dissertation/ Thesis
Identification of low-penetrance alleles, genetic modifiers and mutation analysis in familial breast cancer cases
저자
by
Catucci, Irene
.
소스
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3 . Academic Journal
Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction.
저자
by
Caleca, Laura
;
Catucci, Irene
;
Figlioli, Gisella
;
De Cecco, Loris
;
Pesaran, Tina
, et al.
소스
Frontiers in Oncology; 10/25/2018, pN.PAG-N.PAG, 8p
Web of Science
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7 . Academic Journal
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
저자
by
Southey, Melissa C.
;
Goldgar, David E.
;
Winqvist, Robert
;
Pylkäs, Katri
;
Couch, Fergus
, et al.
소스
Journal of Medical Genetics; Dec2016, Vol. 53 Issue 12, p800-811, 12p, 4 Charts
Full Text (BMJ Journals)
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7 . Academic Journal
Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2.
저자
by
Catucci, Irene
;
Casadei, Silvia
;
Ding, Yuan
;
Volorio, Sara
;
Ficarazzi, Filomena
, et al.
소스
Breast Cancer Research & Treatment; Nov2016, Vol. 160 Issue 1, p121-129, 9p
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7 . Periodical
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
저자
by
Catucci, Irene
;
Osorio, Ana
;
Arver, Brita
;
Neidhardt, Guido
;
Bogliolo, Massimo
, et al.
소스
Genetics in Medicine; April 2018, Vol. 20 Issue: 4 p452-457, 6p
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7 .
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
저자
by
Laura Benedetta Amato
;
Daniela Turchetti
;
Michele Vidone
;
Elena Bonora
;
Irene Catucci
, et al.
소스
International Journal of Molecular Sciences
Volume 22
Issue 11
International Journal of Molecular Sciences, Vol 22, Iss 5832, p 5832 (2021)
Open Access (OpenAIRE)
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7 . Academic Journal
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
저자
by
Peterlongo, Paolo
;
Catucci, Irene
;
Colombo, Mara
;
Caleca, Laura
;
Mucaki, Eliseos
, et al.
소스
Human Molecular Genetics
. Sep 15, 2015 24(18):5345-5355
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7 . Academic Journal
Contribution of MUTYH Variants to Male Breast Cancer Risk: Results From a Multicenter Study in Italy
저자
by
Rizzolo, Piera
;
Silvestri, Valentina
;
Bucalo, Agostino
;
Zelli, Veronica
;
Valentini, Virginia
, et al.
소스
FRONTIERS IN ONCOLOGY
; DEC 4 2018, 8 p583 8p.
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7 . Academic Journal
Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles.
저자
by
Gracia-Aznarez, Francisco Javier
;
Fernandez, Victoria
;
Pita, Guillermo
;
Peterlongo, Paolo
;
Dominguez, Orlando
, et al.
소스
PLoS ONE
. Feb2013, Vol. 8 Issue 2, p1-9. 9p.
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7 . Academic Journal
The SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians
저자
by
Catucci, Irene
;
Verderio, Paolo
;
Pizzamiglio, Sara
;
Bernard, Loris
;
Dallʼolio, Valentina
, et al.
소스
Breast Cancer Research and Treatment
. Jun 01, 2012 133(2):805-807
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