Ghent University Academic Bibliography

Your filters: cql: author="Dunning, Alison M" or (type any "bookEditor issueEditor" and editor="Dunning, Alison M")

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Large-scale meta–genome-wide association study reveals common genetic factors linked to radiation-induced acute toxicities across cancer types

Elnaz Naderi, Miguel E Aguado-Barrera, Line M H Schack, Leila Dorling, Tim Rattay, Laura Fachal, Holly Summersgill, Laura Martínez-Calvo, Ceilidh Welsh, Tom Dudding, et al.

(2023) JNCI CANCER SPECTRUM. 7(6).
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Gisella Figlioli, Massimo Bogliolo, Irene Catucci, Laura Caleca, Sandra Viz Lasheras, Roser Pujol, Johanna I Kiiski, Taru A Muranen, Daniel R Barnes, Joe Dennis, et al.

(2019) NPJ BREAST CANCER. 5.
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Shared heritability and functional enrichment across six solid cancers

Xia Jiang, Hilary K Finucane, Fredrick R Schumacher, Stephanie L Schmit, Jonathan P Tyrer, Younghun Han, Kyriaki Michailidou, Corina Lesseur, Karoline B Kuchenbaecker, Joe Dennis, et al.

(2019) NATURE COMMUNICATIONS. 10.
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Manuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, Kristiina Aittomaki, Irene L Andrulis, Hoda Anton-Culver, Adalgeir Arason, Volker Arndt, Kristan J Aronson, Banu K Arun, et al.

(2019) NATURE COMMUNICATIONS. 10.
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BRCA2 hypomorphic missense variants confer moderate risks of breast cancer

Hermela Shimelis, Romy LS Mesman, Catharina Von Nicolai, Asa Ehlen, Lucia Guidugli, Charlotte Martin, Fabienne MGR Calléja, Huong Meeks, Emily Hallberg, Jamie Hinton, et al.

(2017) CANCER RESEARCH. 77(11). p.2789-2799
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Roger L Milne, Karoline B Kuchenbaecker, Kyriaki Michailidou, Jonathan Beesley, Siddhartha Kar, Sara Lindström, Shirley Hui, Audrey Lemaçon, Penny Soucy, Joe Dennis, et al.

(2017) NATURE GENETICS. 49(12). p.1767-1778
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Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients

Christian Nicolaj Andreassen, Barry S Rosenstein, Sarah L Kerns, Harry Ostrer, Dirk De Ruysscher, Jamie A Cesaretti, Gillian C Barnett, Alison M Dunning, Leila Dorling, Catharine ML West, et al.

(2016) RADIOTHERAPY AND ONCOLOGY. 121(3). p.431-439
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BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

Huong D Meeks, Honglin Song, Kyriaki Michailidou, Manjeet K Bolla, Joe Dennis, Qin Wang, Daniel Barrowdale, Debra Frost, Lesley McGuffog, Steve Ellis, et al.

(2016) JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE. 108(2).
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Alison M Dunning, Kyriaki Michailidou, Karoline B Kuchenbaecker, Deborah Thompson, Juliet D French, Jonathan Beesley, Catherine S Healey, Siddhartha Kar, Karen A Pooley, Elena Lopez-Knowles, et al.

(2016) NATURE GENETICS. 48(4). p.374-386
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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Melissa Southey, David E Goldgar, Robert Winqvist, Katri Pylkäs, Fergus Couch, Marc Tischkowitz, William D Foulkes, Joe Dennis, Kyriaki Michailidou, Elizabeth J van Rensburg, et al.

(2016) JOURNAL OF MEDICAL GENETICS. 53(12). p.800-811

Academic Bibliography

Large-scale meta–genome-wide association study reveals common genetic factors linked to radiation-induced acute toxicities across cancer types

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Shared heritability and functional enrichment across six solid cancers

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

BRCA2 hypomorphic missense variants confer moderate risks of breast cancer

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients

BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

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