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Nature Genetics|November 1, 2011
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancerChristopher A Haiman, Gary K Chen, Celine M Vachon, et al.
Cell Reports. Medicine|May 4, 2024
Genetic variants for head size share genes and pathways with cancerMaria J Knol, Raymond A Poot, Tavia E Evans, et al.
Human Molecular Genetics|November 19, 2013
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 consortiumRoger L Milne, Jesús Herranz, Kyriaki Michailidou, et al.
JAMA Psychiatry|October 31, 2019
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition, Dennis van der Meer, Ida E Sønderby, et al.
Molecular Psychiatry|October 5, 2018
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Molecular Psychiatry|February 2, 2019
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.
Translational Psychiatry|March 23, 2021
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humansIda E Sønderby, Dennis van der Meer, Clara Moreau, et al.
Human Molecular Genetics|June 15, 2014
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor gradeKristen S Purrington, Seth Slettedahl, Manjeet K Bolla, et al.
Nature Genetics|September 21, 2010
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 populationAntonis C Antoniou, Xianshu Wang, Zachary S Fredericksen, et al.
Breast Cancer Research : BCR|June 3, 2014
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control studyNichola Johnson, Frank Dudbridge, Nick Orr, et al.
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