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Medrxiv : the Preprint Server for Health Sciences
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March 18, 2024
Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, et al.
NPJ Genomic Medicine
|
November 20, 2025
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, et al.
The New England Journal of Medicine
|
November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
, Damian Smedley, Katherine R Smith, 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 variants
Daniel R Barnes, Matti A Rookus, Lesley McGuffog, et al.
Nature Communications
|
May 23, 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ioanna Ntalla, Lu-Chen Weng, James H Cartwright, et al.
Nature Communications
|
April 17, 2019
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Manuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, et al.
Nature Genetics
|
September 13, 2016
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Praveen Surendran, Fotios Drenos, Robin Young, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 26, 2017
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Louise V Wain, Ahmad Vaez, Rick Jansen, 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 carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Nature Communications
|
February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Page
of 96
Search research articles
Search
Showing results (931-940 of 952) with videos related to
Sort By:
Page
of 96
Medrxiv : the Preprint Server for Health Sciences
|
March 18, 2024
Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, et al.
NPJ Genomic Medicine
|
November 20, 2025
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, et al.
The New England Journal of Medicine
|
November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
, Damian Smedley, Katherine R Smith, 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 variants
Daniel R Barnes, Matti A Rookus, Lesley McGuffog, et al.
Nature Communications
|
May 23, 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ioanna Ntalla, Lu-Chen Weng, James H Cartwright, et al.
Nature Communications
|
April 17, 2019
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Manuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, et al.
Nature Genetics
|
September 13, 2016
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Praveen Surendran, Fotios Drenos, Robin Young, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 26, 2017
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Louise V Wain, Ahmad Vaez, Rick Jansen, 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 carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Nature Communications
|
February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Page
of 96