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Targeting collagen XVIII improves the efficiency of ErbB inhibitors in breast cancer models

The Journal of clinical investigation, 2023-09, Vol.133 (18), p.1-19

2023

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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Clinical cancer research, 2006-02, Vol.12 (4), p.1157-1167

2006

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Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility

PLoS genetics, 2023-08, Vol.19 (8), p.e1010889-e1010889

2023

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ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients

Cell death & disease, 2023-05, Vol.14 (5), p.328-328, Article 328

2023

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Heterozygous mutations in PALB2 cause DNA replication and damage response defects

Nature communications, 2013-10, Vol.4 (1), p.2578-2578, Article 2578

2013

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Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility

PLoS genetics, 2016-01, Vol.12 (1), p.e1005816-e1005816

2016

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A recurrent mutation in PALB2 in Finnish cancer families

Nature, 2007-03, Vol.446 (7133), p.316-319

2007

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Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network

PLoS genetics, 2012-06, Vol.8 (6), p.e1002734-e1002734

2012

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Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility

Scientific reports, 2017-04, Vol.7 (1), p.681-681, Article 681

2017

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Penetrance Analysis of the PALB2 c.1592delT Founder Mutation

Clinical cancer research, 2008-07, Vol.14 (14), p.4667-4671

2008

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Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice

Human molecular genetics, 2010-08, Vol.19 (15), p.3021-3029

2010

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Assessment of targeted and non-targeted responses in cells deficient in ATM function following exposure to low and high dose X-rays

PloS one, 2014-03, Vol.9 (3), p.e93211-e93211

2014

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Evaluating the role of NTHL1 p.Q90 allele in inherited breast cancer predisposition

Molecular genetics & genomic medicine, 2020-11, Vol.8 (11), p.e1493-n/a

2020

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Mutation screening of the RNF8, UBC13 and MMS2 genes in Northern Finnish breast cancer families

BMC medical genetics, 2011-07, Vol.12 (1), p.98-98, Article 98

2011

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Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families

BMC cancer, 2008-05, Vol.8 (1), p.146-146, Article 146

2008

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Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families

Familial cancer, 2010-12, Vol.9 (4), p.537-540

2010

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Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Journal of clinical oncology, 2020-03, Vol.38 (7), p.674-685

2020

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Somatic mutation analysis of MYH11 in breast and prostate cancer

BMC cancer, 2008-09, Vol.8 (1), p.263-263

2008

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Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer

European journal of cancer (1990), 2021-01, Vol.143, p.46-51

2021

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Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families

Journal of human genetics, 2010-12, Vol.55 (12), p.842-843

2010

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Using mouse models to investigate the biological and physiological consequences of defects in the Fanconi anaemia/breast cancer DNA repair signalling pathway

The Journal of pathology, 2011-07, Vol.224 (3), p.301-305

2011

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Mutation analysis of the AATF gene in breast cancer families

BMC cancer, 2009-12, Vol.9 (1), p.457-457, Article 457

2009

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Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation

Genes chromosomes & cancer, 2002-08, Vol.34 (4), p.384-389

2002

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PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFβ signaling

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1), p.173-173, Article 173

2024

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Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls

Scientific reports, 2018-09, Vol.8 (1), p.13149-13, Article 13149

2018

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Targeting collagen XVIII improves the efficiency of ErbB inhibitors in breast cancer models

The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility

ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients

Heterozygous mutations in PALB2 cause DNA replication and damage response defects

Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility

A recurrent mutation in PALB2 in Finnish cancer families

Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network

Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility

Penetrance Analysis of the PALB2 c.1592delT Founder Mutation

Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice

Assessment of targeted and non-targeted responses in cells deficient in ATM function following exposure to low and high dose X-rays

Evaluating the role of NTHL1 p.Q90 allele in inherited breast cancer predisposition

Mutation screening of the RNF8, UBC13 and MMS2 genes in Northern Finnish breast cancer families

Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families

Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Somatic mutation analysis of MYH11 in breast and prostate cancer

Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer

Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families

Using mouse models to investigate the biological and physiological consequences of defects in the Fanconi anaemia/breast cancer DNA repair signalling pathway

Mutation analysis of the AATF gene in breast cancer families

Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation

PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFβ signaling

Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls

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