Kết quả tìm kiếm - Jacqueline MacArthur
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1
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants Bằng Jacqueline MacArthur, Joannella Morales, Ray Tully, Alex Astashyn, Laurent Gil, Elspeth A. Bruford, Pontus Larsson, Paul Flicek, Raymond Dalgleish, Donna Maglott, Fiona Cunningham
Được phát hành 2013Artigo -
2
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations Bằng Danielle Welter, Jacqueline MacArthur, Joannella Morales, Tony Burdett, Peggy Hall, Heather Junkins, Alan Klemm, Paul Flicek, Teri A. Manolio, Lucia A. Hindorff, Helen Parkinson
Được phát hành 2013Artigo -
3
Scaling up data curation using deep learning: An application to literature triage in genomic variation resources Bằng Kyubum Lee, Maria Livia Famiglietti, Aoife McMahon, Chih-Hsuan Wei, Jacqueline MacArthur, Sylvain Poux, Lionel Breuza, Alan Bridge, Fiona Cunningham, Ioannis Xénarios, Zhiyong Lu
Được phát hành 2018Artigo -
4
The Polygenic Score Catalog: an open database for reproducibility and systematic evaluation Bằng Samuel A. Lambert, Laurent Gil, Simon Jupp, Scott C. Ritchie, Yu Xu, Annalisa Buniello, Gad Abraham, Michael Chapman, Helen Parkinson, John Danesh, Jacqueline MacArthur, Michael Inouye
Được phát hành 2020Pré-impressão -
5
The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation Bằng Samuel A. Lambert, Laurent Gil, Simon Jupp, Scott C. Ritchie, Yu Xu, Annalisa Buniello, Aoife McMahon, Gad Abraham, Michael Chapman, Helen Parkinson, John Danesh, Jacqueline MacArthur, Michael Inouye
Được phát hành 2021Artigo -
6
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog) Bằng Jacqueline MacArthur, Emily Bowler-Barnett, María Cerezo, Laurent Gil, Peggy Hall, Emma Hastings, Heather Junkins, Aoife McMahon, Annalisa Milano, Joannella Morales, Zoë May Pendlington, Danielle Welter, Tony Burdett, Lucia A. Hindorff, Paul Flicek, Fiona Cunningham, Helen Parkinson
Được phát hành 2016Artigo -
7
A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog Bằng Joannella Morales, Danielle Welter, Emily Bowler-Barnett, María Cerezo, Laura W. Harris, Aoife McMahon, Peggy Hall, Heather Junkins, Annalisa Milano, Emma Hastings, Claudio Malangone, Annalisa Buniello, Tony Burdett, Paul Flicek, Helen Parkinson, Fiona Cunningham, Lucia A. Hindorff, Jacqueline MacArthur
Được phát hành 2018Carta -
8
The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 Bằng Annalisa Buniello, Jacqueline MacArthur, María Cerezo, Laura W. Harris, James Hayhurst, Claudio Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis, Dániel Süveges, Olga Vrousgou, Patricia L. Whetzel, Ridwan Amode, José Ángel Guillén, Harpreet Singh Riat, Stephen J. Trevanion, Peggy Hall, Heather Junkins, Paul Flicek, Tony Burdett, Lucia A. Hindorff, Fiona Cunningham, Helen Parkinson
Được phát hành 2018Artigo -
9
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource Bằng Elliot Sollis, Abayomi Mosaku, Ala Abid, Annalisa Buniello, María Cerezo, Laurent Gil, Tudor Groza, Osman Güneş, Peggy Hall, James Hayhurst, Arwa Ibrahim, Yue Ji, Sajo John, Elizabeth Lewis, Jacqueline MacArthur, Aoife McMahon, David Osumi-Sutherland, Kalliope Panoutsopoulou, Zoë May Pendlington, Santhi Ramachandran, Ray Stefancsik, Jonathan Stewart, Patricia L. Whetzel, Robert Wilson, Lucia A. Hindorff, Fiona Cunningham, Samuel A. Lambert, Michael Inouye, Helen Parkinson, Laura W. Harris
Được phát hành 2022Artigo -
10
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics Bằng Maya Ghoussaini, Edward Mountjoy, Miguel Carmona, Gareth Peat, Ellen M. Schmidt, Andrew Hercules, Luca Fumis, Alfredo Miranda, Denise Carvalho‐Silva, Annalisa Buniello, Tony Burdett, James Hayhurst, Jarrod Baker, Javier Ferrer, Asier Gonzalez‐Uriarte, Simon Jupp, Mohd Anisul Karim, Gautier Koscielny, Sandra Machlitt‐Northen, Claudio Malangone, Zoë May Pendlington, Paola Roncaglia, Dániel Süveges, Daniel J. Wright, Olga Vrousgou, Eliseo Papa, Helen Parkinson, Jacqueline MacArthur, John A. Todd, Jeffrey C. Barrett, Jeremy Schwartzentruber, David G. Hulcoop, David Ochoa, Ellen M. McDonagh, Ian Dunham
Được phát hành 2020Artigo -
11
Improving reporting standards for polygenic scores in risk prediction studies Bằng Hannah Wand, Samuel A. Lambert, Cecelia P. Tamburro, Michael A. Iacocca, Jack W. O’Sullivan, Catherine H. Sillari, Iftikhar J. Kullo, Robb Rowley, Jacqueline S. Dron, Deanna Brockman, Eric Venner, Mark I. McCarthy, Antonis C. Antoniou, Douglas F. Easton, Robert A. Hegele, Amit V. Khera, Nilanjan Chatterjee, Charles Kooperberg, Karen L. Edwards, Katherine Vlessis, Kim Kinnear, John Danesh, Helen Parkinson, Erin M. Ramos, Megan C. Roberts, Kelly E. Ormond, Muin J. Khoury, A. Cecile J.W. Janssens, Katrina A.B. Goddard, Peter Kraft, Jacqueline MacArthur, Michael Inouye, Genevieve L. Wojcik
Được phát hành 2021Revisão -
12
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease Bằng Angharad M. Roberts, James S. Ware, Daniel S. Herman, Sebastian Schäfer, John Baksi, Alexander G. Bick, Rachel Buchan, Roddy Walsh, Shibu John, Stephen Wilkinson, Francesco Mazzarotto, Leanne E. Felkin, Sungsam Gong, Jacqueline MacArthur, Fiona Cunningham, Jason Flannick, Stacey Gabriel, David Altshuler, Peter S. Macdonald, Matthias Heinig, Anne Keogh, Christopher S. Hayward, Nicholas R. Banner, Dudley J. Pennell, Declan P. O’Regan, Ru San Tan, Antonio de Marvao, Timothy J. W. Dawes, Ankur Gulati, Emma J. Birks, Magdi H. Yacoub, Michaël Radkë, Michael Gotthardt, James Wilson, Christopher J. O’Donnell, Sanjay Prasad, Paul J.R. Barton, Diane Fatkin, Norbert Hübner, Jonathan G. Seidman, Christine E. Seidman, Stuart A. Cook
Được phát hành 2015Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Computational biology
Computer science
Gene
Genetics
Data science
World Wide Web
Genome-wide association study
Genotype
Information retrieval
Single-nucleotide polymorphism
Bioinformatics
Biochemistry
Genome
Genomics
Medicine
Metadata
Computer network
Environmental health
Exome
Exome sequencing
Exon
Gibbs isotherm
Human genetics
Interface (matter)
Mathematics
Mutation
Operating system
Population
Pulmonary surfactant