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Expression of RUNX1 correlates with poor patient prognosis in triple negative breast cancer

PloS one, 2014-06, Vol.9 (6), p.e100759-e100759

2014

Volltextzugriff (PDF)

Association between insulin resistance and breast carcinoma: a systematic review and meta-analysis

PloS one, 2014-06, Vol.9 (6), p.e99317-e99317

2014

Volltextzugriff (PDF)

Differential methylation of TCF7L2 promoter in peripheral blood DNA in newly diagnosed, drug-naïve patients with type 2 diabetes

PloS one, 2014-06, Vol.9 (6), p.e99310-e99310

2014

Volltextzugriff (PDF)

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

British journal of cancer, 2012-08, Vol.107 (5), p.800-807

2012

Volltextzugriff (PDF)

β-Amyloid deposition in brains of subjects with diabetes

Neuropathology and applied neurobiology, 2009-02, Vol.35 (1), p.60-68

2009

Volltextzugriff (PDF)

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Clinical genetics, 2015-07, Vol.88 (1), p.68-73

2015

Volltextzugriff (PDF)

Combined risk effects of IDE and NEP gene variants on Alzheimer disease

Journal of neurology, neurosurgery and psychiatry, 2009-11, Vol.80 (11), p.1268-1270

2009

Volltextzugriff (PDF)

Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease

Neurology, 2004-04, Vol.62 (7), p.1170

2004

Volltextzugriff (PDF)

Breast-Cancer Risk in Families with Mutations in PALB2

The New England journal of medicine, 2014-08, Vol.371 (6), p.497-506

2014

Volltextzugriff (PDF)

Midlife income, occupation, APOE status, and dementia: a population-based study

Neurology, 2002-09, Vol.59 (6), p.887

2002

Volltextzugriff (PDF)

Seladin-1 transcription is linked to neuronal degeneration in Alzheimer’s disease

Neuroscience, 2002-01, Vol.113 (2), p.301-310

2002

Volltextzugriff (PDF)

Association of CYP46 intron 2 polymorphism in Finnish Alzheimer’s disease samples and a global scale summary

Journal of neurology, neurosurgery and psychiatry, 2006-03, Vol.77 (3), p.421-422

2006

Volltextzugriff (PDF)

Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families

Clinical genetics, 2007-10, Vol.72 (4), p.311-320

2007

Volltextzugriff (PDF)

Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease: relation to apolipoprotein E polymorphism

Neurology, 1996-02, Vol.46 (2), p.413

1996

Volltextzugriff (PDF)

A recurrent mutation in PALB2 in Finnish cancer families

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

2007

Volltextzugriff (PDF)

Incidence and risk factors for mild cognitive impairment: a population-based three-year follow-up study of cognitively healthy elderly subjects

Dementia and geriatric cognitive disorders, 2004-01, Vol.17 (3), p.196

2004

Volltextzugriff (PDF)

Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes

Neuroscience, 1995-07, Vol.67 (1), p.65-72

1995

Volltextzugriff (PDF)

Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis

Cancer research (Chicago, Ill.), 1995-06, Vol.55 (12), p.2660-2664

1995

Volltextzugriff (PDF)

Apolipoprotein E alleles in women with pre-eclampsia

Journal of clinical pathology, 2001-08, Vol.54 (8), p.652-654

2001

Volltextzugriff (PDF)

Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population

Neurology, 2004-07, Vol.63 (1), p.173

2004

Volltextzugriff (PDF)

Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions

Science translational medicine, 2012-02, Vol.4 (122), p.122ra23

2012

Volltextzugriff (PDF)

FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome

International journal of cancer, 2016-12, Vol.139 (12), p.2760-2770

2016

Volltextzugriff (PDF)

Longitudinal SPECT study in Alzheimer’s disease: relation to apolipoprotein E polymorphism

Journal of neurology, neurosurgery and psychiatry, 1998-06, Vol.64 (6), p.742-746

1998

Volltextzugriff (PDF)

CHEK21100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies

American journal of human genetics, 2004-06, Vol.74 (6), p.1175-1182

2004

Volltextzugriff (PDF)

Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility

Breast cancer research and treatment, 2011-12, Vol.130 (3), p.1003-1010

2011

Volltextzugriff (PDF)

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Expression of RUNX1 correlates with poor patient prognosis in triple negative breast cancer

Association between insulin resistance and breast carcinoma: a systematic review and meta-analysis

Differential methylation of TCF7L2 promoter in peripheral blood DNA in newly diagnosed, drug-naïve patients with type 2 diabetes

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

β-Amyloid deposition in brains of subjects with diabetes

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Combined risk effects of IDE and NEP gene variants on Alzheimer disease

Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease

Breast-Cancer Risk in Families with Mutations in PALB2

Midlife income, occupation, APOE status, and dementia: a population-based study

Seladin-1 transcription is linked to neuronal degeneration in Alzheimer’s disease

Association of CYP46 intron 2 polymorphism in Finnish Alzheimer’s disease samples and a global scale summary

Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families

Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease: relation to apolipoprotein E polymorphism

A recurrent mutation in PALB2 in Finnish cancer families

Incidence and risk factors for mild cognitive impairment: a population-based three-year follow-up study of cognitively healthy elderly subjects

Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes

Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis

Apolipoprotein E alleles in women with pre-eclampsia

Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population

Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions

FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome

Longitudinal SPECT study in Alzheimer’s disease: relation to apolipoprotein E polymorphism

CHEK21100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies

Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility

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