Author details

Full Name

Ewan Birney

Affiliation

European Bioinformatics Institute

ORCID

Career Start Year

1992

Papers

257

H Index

111

Expertise

CM4AI Collaborator

Emma Lundberg (CM4AI)

PMID	Paper Title	Journal Title	Published Year
37933859	AlphaFold Protein Structure Database in 2024: providing structure coverage for over 214 million protein sequences.	Nucleic Acids Res	2024
37933859	AlphaFold Protein Structure Database in 2024: providing structure coverage for over 214 million protein sequences.	Nucleic Acids Res	2024
36593407	Dynamic, adaptive sampling during nanopore sequencing using Bayesian experimental design.	Nat Biotechnol	2023
37693611	Natural genetic variation quantitatively regulates heart rate and dimension.	bioRxiv	2023
36840709	Using Nanocompore to Identify RNA Modifications from Direct RNA Nanopore Sequencing Data.	Curr Protoc	2023
37460203	A multilayered approach to the analysis of genetic data from individuals with suspected albinism.	J Med Genet	2023
36848389	Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.	PLoS Genet	2023
36593407	Dynamic, adaptive sampling during nanopore sequencing using Bayesian experimental design.	Nat Biotechnol	2023
37693611	Natural genetic variation quantitatively regulates heart rate and dimension.	bioRxiv	2023
37460203	A multilayered approach to the analysis of genetic data from individuals with suspected albinism.	J Med Genet	2023
36848389	Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.	PLoS Genet	2023
36840709	Using Nanocompore to Identify RNA Modifications from Direct RNA Nanopore Sequencing Data.	Curr Protoc	2023
34791371	AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models.	Nucleic Acids Res	2022
35388217	A joint NCBI and EMBL-EBI transcript set for clinical genomics and research.	Nature	2022
35701578	Publisher Correction: Genomic reconstruction of the SARS CoV-2 epidemic in England.	Nature	2022
35507016	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources.	Genet Med	2022
35803923	The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism.	Nat Commun	2022
35486737	Selective clonal persistence of human retroviruses in vivo: Radial chromatin organization, integration site, and host transcription.	Sci Adv	2022
36779085	CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank.	Cell Genom	2022
36691609	Using machine learning to model older adult inpatient trajectories from electronic health records data.	iScience	2022
34791371	AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models.	Nucleic Acids Res	2022
34850134	The European Bioinformatics Institute (EMBL-EBI) in 2021.	Nucleic Acids Res	2022
35244721	Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.	Nucleic Acids Res	2022
34872952	Mendelian Randomization.	Cold Spring Harb Perspect Med	2022
35803923	The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism.	Nat Commun	2022
35507016	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources.	Genet Med	2022
35701578	Publisher Correction: Genomic reconstruction of the SARS CoV-2 epidemic in England.	Nature	2022
35486737	Selective clonal persistence of human retroviruses in vivo: Radial chromatin organization, integration site, and host transcription.	Sci Adv	2022
35388217	A joint NCBI and EMBL-EBI transcript set for clinical genomics and research.	Nature	2022
36691609	Using machine learning to model older adult inpatient trajectories from electronic health records data.	iScience	2022
36779085	CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank.	Cell Genom	2022
35244721	Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.	Nucleic Acids Res	2022
34850134	The European Bioinformatics Institute (EMBL-EBI) in 2021.	Nucleic Acids Res	2022
34872952	Mendelian Randomization.	Cold Spring Harb Perspect Med	2022
33245775	The European Bioinformatics Institute: empowering cooperation in response to a global health crisis.	Nucleic Acids Res	2021
34293799	Highly accurate protein structure prediction for the human proteome.	Nature	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
34264324	The International Human Genome Project.	Hum Mol Genet	2021
34021280	REMBI: Recommended Metadata for Biological Images-enabling reuse of microscopy data in biology.	Nat Methods	2021
33245775	The European Bioinformatics Institute: empowering cooperation in response to a global health crisis.	Nucleic Acids Res	2021
34662343	Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.	PLoS Genet	2021
34893601	RNA modifications detection by comparative Nanopore direct RNA sequencing.	Nat Commun	2021
34489576	Personalized profiles for disease risk must capture all facets of health.	Nature	2021
35128509	International federation of genomic medicine databases using GA4GH standards.	Cell Genom	2021
35072136	GA4GH: International policies and standards for data sharing across genomic research and healthcare.	Cell Genom	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
35128509	International federation of genomic medicine databases using GA4GH standards.	Cell Genom	2021
35072136	GA4GH: International policies and standards for data sharing across genomic research and healthcare.	Cell Genom	2021
34893601	RNA modifications detection by comparative Nanopore direct RNA sequencing.	Nat Commun	2021
34489576	Personalized profiles for disease risk must capture all facets of health.	Nature	2021

1 - 50 of 514

Marta Gut

Universitat de Barcelona (UB)

Career Start Year 2010

Number of shared co-authors 95

Nuno A Fonseca

European Bioinformatics Institute

Career Start Year 2008

Number of shared co-authors 49

Raoul J P Bonnal

National Institute for Molecular Genetics "Romeo ed Enrica Invernizzi"

Career Start Year 2006

Number of shared co-authors 27

Geir Kjetil Sandve

University of Oslo

Career Start Year 2006

Number of shared co-authors 7

Gareth A Palidwor

Ottawa Hospital Research Institute

Career Start Year 2005

Number of shared co-authors 0

Jeffrey A Rosenfeld

Cancer Institute of New Jersey

Career Start Year 2004

Number of shared co-authors 22

Brad A Chapman

Harvard T.H. Chan School of Public Health

Career Start Year 2003

Number of shared co-authors 23

Lachlan J M Coin

The Peter Doherty Institute for Infection and Immunity, The University of Melbourne

Career Start Year 2003

Number of shared co-authors 74

Scott J Emrich

The Pennsylvania State University College of Medicine

Career Start Year 2002

Number of shared co-authors 46

Jun Wang

Zhongnan Hospital of Wuhan University

Career Start Year 2002

Number of shared co-authors 126

Don Gilbert

Indiana University

Career Start Year 2002

Number of shared co-authors 75

Pjotr Prins

Wageningen University & Research

Career Start Year 2001

Number of shared co-authors 35

Martin C Frith

Artificial Intelligence Research Center, University of Tokyo

Career Start Year 2001

Number of shared co-authors 62

Brent S Pedersen

Center for Molecular Medicine, University Medical Center Utrecht

Career Start Year 2001

Number of shared co-authors 9

Jeong-Hyeon Choi

National Marine Biodiversity Institute of Korea

Career Start Year 2000

Number of shared co-authors 32

C Titus Brown

University of California davis

Career Start Year 1999

Number of shared co-authors 67

Vineet Bafna

University of California San Diego

Career Start Year 1998

Number of shared co-authors 89

Frederick P Roth

University of Toronto

Career Start Year 1998

Number of shared co-authors 28

Sarah J Wheelan

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1998

Number of shared co-authors 35

David R Powell

Biomedicine Discovery Institute, Monash University

Career Start Year 1998

Number of shared co-authors 7

Jay Shendure

University of Washington

Career Start Year 1996

Number of shared co-authors 100

Ron Shamir

Tel Aviv University

Career Start Year 1995

Number of shared co-authors 8

Jared C Roach

Institute for Systems Biology

Career Start Year 1995

Number of shared co-authors 23

Elizabeth A Worthey

Heersink School of Medicine, The University of Alabama at Birmingham

Career Start Year 1995

Number of shared co-authors 33

Bonnie Berger

Massachusetts Institute of Technology

Career Start Year 1994

Number of shared co-authors 36

Alejandro A Sch??ffer

National Cancer Institute, National Institutes of Health

Career Start Year 1993

Number of shared co-authors 16

Winston Hide

Harvard Medical School

Career Start Year 1991

Number of shared co-authors 133

Miguel A Andrade-Navarro

Institute of Organismic and Molecular Evolution, Johannes Gutenberg University

Career Start Year 1991

Number of shared co-authors 19

Samuel Levy

Bluestar Genomics Inc.

Career Start Year 1991

Number of shared co-authors 71

Justin T Reese

Lawrence Berkeley National Laboratory

Career Start Year 1985

Number of shared co-authors 111

row(s) 1 - 30 of 30

Paul Flicek

European Bioinformatics Institute

Co-authored papers 38

Richard Durbin

University of Cambridge

Co-authored papers 34

Tim Hubbard

Co-authored papers 32

Fiona Cunningham

European Bioinformatics Institute

Co-authored papers 21

Ian Dunham

European Bioinformatics Institute (EMBL-EBI)

Co-authored papers 21

Stephen M J Searle

Wellcome Trust Sanger Institute

Co-authored papers 20

Michele Clamp

Harvard University

Co-authored papers 19

Damian Keefe

University of Adelaide

Co-authored papers 18

Abel Ureta-Vidal

Co-authored papers 15

Laura Clarke

Co-authored papers 14

Rolf Apweiler

European Bioinformatics Institute (EMBL-EBI)

Co-authored papers 14

Guy Cochrane

European Bioinformatics Institute

Co-authored papers 13

Damian Smedley

William Harvey Research Institute, Queen Mary University of London

Co-authored papers 12

Arek Kasprzyk

European Bioinformatics Institute (EBI)

Co-authored papers 12

Henning Hermjakob

European Bioinformatics Institute (EMBL-EBI)

Co-authored papers 12

Alex Bateman

European Bioinformatics Institute (EMBL-EBI)

Co-authored papers 12

Roderic Guig??

Barcelona Institute of Science and Technology

Co-authored papers 11

Thomas A Down

Co-authored papers 11

Karyn Megy

University of Cambridge

Co-authored papers 10

Gregory E Crawford

Center for Genomic & Computational Biology, Duke University

Co-authored papers 10

Jennifer Harrow

Co-authored papers 10

Eric S Lander

Vanderbilt-Ingram Cancer Center, Vanderbilt University

Co-authored papers 10

Stefan Gr??f

Heart and Lung Research Institute, University of Cambridge

Co-authored papers 10

David Haussler

Genomics Institute, University of California Santa Cruz

Co-authored papers 10

Michael Schuster

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences

Co-authored papers 10

Ross C Hardison

Co-authored papers 9

Kim C Worley

Baylor College of Medicine

Co-authored papers 9

Jane Rogers

The Wellcome Trust Sanger Institute

Co-authored papers 9

Jason D Lieb

The University of Chicago

Co-authored papers 9

Eduardo Eyras

Co-authored papers 9

1 - 30

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