Asta Försti

发表

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

Jane E. Carpenter, Kyriaki Michailidou, France Labrèche, 2014, Human molecular genetics.

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.

Julian Peto, Sergi Castellví-Bel, Jean-Baptiste Cazier, 2008, Human molecular genetics.

Chromosome 7p11.2 (EGFR) variation influences glioma risk.

Melissa Bondy, Andre Franke, Anthony Swerdlow, 2011, Human molecular genetics.

Survival in breast cancer is familial

Asta Försti, Jan Sundquist, Kari Hemminki, 2008, Breast Cancer Research and Treatment.

The CCND1 870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

Asta Försti, Lewin Eisele, Hartmut Goldschmidt, 2013, Nature Genetics.

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

Clement Adebamowo, Olufunmilayo I. Olopade, Robert Johansson, 2010, PLoS genetics.

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

Michael Krawczak, Henry Völzke, Barbara Burwinkel, 2010, Carcinogenesis.

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 2010, Nature Genetics.

Association of NCOA3 Polymorphisms with Breast Cancer Risk

Barbara Burwinkel, Peter Bugert, Asta Försti, 2005, Clinical Cancer Research.

Genome-wide association study on differentiated thyroid cancer.

Barbara Jarzab, Asta Försti, Per Hoffmann, 2013, The Journal of clinical endocrinology and metabolism.

Single nucleotide polymorphisms in chromosomal instability genes and risk and clinical outcome of breast cancer: a Swedish prospective case-control study.

Robert Johansson, Asta Försti, Göran Hallmans, 2009, European journal of cancer.

Functional TLR5 genetic variants affect human colorectal cancer survival.

Jochen Hampe, Asta Försti, Dominik Hartl, 2013, Cancer research.

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

Julian Peto, Henry Völzke, Sergi Castellví-Bel, 2008, Nature Genetics.

Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker.

Robert Johansson, Asta Försti, Kari Hemminki, 2008, Carcinogenesis.

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium.

Julian Peto, Kyriaki Michailidou, Thomas Brüning, 2014, Human molecular genetics.

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

Michael Krawczak, Barbara Burwinkel, Rongxi Yang, 2014, Carcinogenesis.

Opinion: The balance between heritable and environmental aetiology of human disease

Asta Försti, Justo Lorenzo Bermejo, Kari Hemminki, 2006, Nature Reviews Genetics.

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Patrick Neven, Chiun-Sheng Huang, Julian Peto, 2014, Breast Cancer Research.

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer

Jane E. Carpenter, Peter Kraft, Gary K. Chen, 2011, Nature Genetics.

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Ian J. Deary, Archie Campbell, Sergi Castellví-Bel, 2015, Scientific Reports.

Breast cancer genomics based on biobanks.

Asta Försti, Kari Hemminki, K. Hemminki, 2011, Methods in molecular biology.

Survival in familial and non-familial breast cancer by age and stage at diagnosis.

Asta Försti, Kari Hemminki, Kristina Sundquist, 2016, European journal of cancer.

Genetic variation in adipokine genes and risk of colorectal cancer.

Pavel Vodicka, Asta Försti, Justo Lorenzo Bermejo, 2009, European journal of endocrinology.

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

Wei Lu, Nina Ditsch, Julian Peto, 2013, American journal of human genetics.

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

Karl-Heinz Jöckel, Julian Peto, K. D. Sørensen, 2017, Nature Communications.

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s Lymphoma

Karl-Heinz Jöckel, Asta Försti, Lewin Eisele, 2013, Nature Communications.