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Showing results (481-490 of 511) with videos related to

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Plos Genetics|April 5, 2014
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriersAna Osorio, Roger L Milne, Karoline Kuchenbaecker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 16, 2020
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variantsDaniel R Barnes, Matti A Rookus, Lesley McGuffog, et al.
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 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.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.
Nature Genetics|July 1, 2024
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, 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 52

Showing results (481-490 of 511) with videos related to

Sort By:
Pageof 52
Plos Genetics|April 5, 2014
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriersAna Osorio, Roger L Milne, Karoline Kuchenbaecker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 16, 2020
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variantsDaniel R Barnes, Matti A Rookus, Lesley McGuffog, et al.
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 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.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.
Nature Genetics|July 1, 2024
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, 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 52