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Showing results (491-500 of 536) with videos related to

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Nature Communications|April 17, 2019
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancerManuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, et al.
Nature Genetics|June 20, 2018
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancerLang Wu, Wei Shi, Jirong Long, et al.
Nature Communications|September 24, 2014
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulationMaya Ghoussaini, Stacey L Edwards, Kyriaki Michailidou, et al.
Nature Genetics|April 25, 2017
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer riskFelix R Day, Deborah J Thompson, Hannes Helgason, et al.
American Journal of Human Genetics|December 23, 2014
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1Dylan M Glubb, Mel J Maranian, Kyriaki Michailidou, et al.
Human Molecular Genetics|February 6, 2015
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2Nick Orr, Frank Dudbridge, Nicola Dryden, et al.
Nature Genetics|July 9, 2024
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.
Nature Communications|February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
Breast Cancer Research : BCR|July 28, 2016
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locusChenjie Zeng, Xingyi Guo, Jirong Long, et al.
Nature Communications|May 15, 2021
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
Pageof 54

Showing results (491-500 of 536) with videos related to

Sort By:
Pageof 54
Nature Communications|April 17, 2019
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancerManuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, et al.
Nature Genetics|June 20, 2018
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancerLang Wu, Wei Shi, Jirong Long, et al.
Nature Communications|September 24, 2014
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulationMaya Ghoussaini, Stacey L Edwards, Kyriaki Michailidou, et al.
Nature Genetics|April 25, 2017
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer riskFelix R Day, Deborah J Thompson, Hannes Helgason, et al.
American Journal of Human Genetics|December 23, 2014
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1Dylan M Glubb, Mel J Maranian, Kyriaki Michailidou, et al.
Human Molecular Genetics|February 6, 2015
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2Nick Orr, Frank Dudbridge, Nicola Dryden, et al.
Nature Genetics|July 9, 2024
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.
Nature Communications|February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
Breast Cancer Research : BCR|July 28, 2016
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locusChenjie Zeng, Xingyi Guo, Jirong Long, et al.
Nature Communications|May 15, 2021
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
Pageof 54