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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 30, 2023. (Total: 223474Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Breast Neoplasms and SLX4[original query]
Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.
Breast cancer research and treatment 2011 Dec 130 (3): 1021-8.
Landwehr Rosa, Bogdanova Natalia V, Antonenkova Natalia, Meyer Andreas, Bremer Michael, Park-Simon Tjoung-Won, Hillemanns Peter, Karstens Johann H, Schindler Detlev, Dörk Thi
Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.
Human mutation 2013 Jan 34 (1): 70-3.
Bakker Janine L, van Mil Saskia E, Crossan Gerry, Sabbaghian Nelly, De Leeneer Kim, Poppe Bruce, Adank Muriel, Gille Hans, Verheul Henk, Meijers-Heijboer Hanne, de Winter Johan P, Claes Kathleen, Tischkowitz Marc, Waisfisz Quint
Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families.
BMC cancer 2012 12 (1): 84.
Fernández-Rodríguez Juana, Quiles Francisco, Blanco Ignacio, Teulé Alex, Feliubadaló Lídia, Valle Jesús Del, Salinas Mónica, Izquierdo Angel, Darder Esther, Schindler Detlev, Capellá Gabriel, Brunet Joan, Lázaro Conxi, Pujana Miguel Ang
Assessment of SLX4 Mutations in Hereditary Breast Cancers.
PloS one 2013 8 (6): e66961.
Shah Sohela, Kim Yonghwan, Ostrovnaya Irina, Murali Rajmohan, Schrader Kasmintan A, Lach Francis P, Sarrel Kara, Rau-Murthy Rohini, Hansen Nichole, Zhang Liyng, Kirchhoff Tomas, Stadler Zsofia, Robson Mark, Vijai Joseph, Offit Kenneth, Smogorzewska Aga
Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Jul 32 (19): 2001-9.
Kurian Allison W, Hare Emily E, Mills Meredith A, Kingham Kerry E, McPherson Lisa, Whittemore Alice S, McGuire Valerie, Ladabaum Uri, Kobayashi Yuya, Lincoln Stephen E, Cargill Michele, Ford James
A low-frequency haplotype spanning SLX4/FANCP constitutes a new risk locus for early-onset breast cancer (<60 years) and is associated with reduced DNA repair capacity.
International journal of cancer 2018 02 142 (4): 757-768.
Surowy Harald, Varga Dominic, Burwinkel Barbara, Marmé Frederik, Sohn Christof, Luedeke Manuel, Rinckleb Antje, Maier Christiane, Deissler Helmut, Volcic Meta, Wiesmüller Lisa, Hasenburg Annette, Klar Maximilian, Hoegel Josef, Vogel Walth
Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis.
Breast cancer research and treatment 2020 Jun .
Alter Blanche P, Best Ana
Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil.
Breast cancer research and treatment 2022 3 193 (2): 485-494.
Felix Gabriela E S, Guindalini Rodrigo Santa Cruz, Zheng Yonglan, Walsh Tom, Sveen Elisabeth, Lopes Taisa Manuela Machado, Côrtes Juliana, Zhang Jing, Carôzo Polyanna, Santos Irlânia, Bonfim Thaís Ferreira, Garicochea Bernardo, Toralles Maria Betânia Pereira, Meyer Roberto, Netto Eduardo Martins, Abe-Sandes Kiyoko, King Mary-Claire, de Oliveira Nascimento Ivana Lucia, Olopade Olufunmilayo
The ctDNA-based postoperative molecular residual disease status in different subtypes of early-stage breast cancer.
Gland surgery 2023 1 11 (12): 1924-1935.
Yang Yang, Zhang Jie, Li Jiao-Yang, Xu Lu, Wang Si-Ning, Zhang Jun-Qi, Xun Zhou, Xia Yu, Cao Jian-Bo, Liu Yang, Shi Li-Yan, Li Wei, Shi Yong-Lei, He Yuan-Ge, Gu De-Jian, Yu Zheng-Yuan, Chen Kai, Lan Ji
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