Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Andrea Byrnes
Affiliation
ORCID
Career Start Year
2009
Papers
15
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
31857710
Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.
Nat Neurosci
2020
31171447
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse.
Neuron
2019
31768050
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.
Nat Neurosci
2019
29632380
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
Nat Genet
2018
29861106
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Am J Hum Genet
2018
29517003
Corrigendum: Landscape of X chromosome inactivation across human tissues.
Nature
2018
29022598
Landscape of X chromosome inactivation across human tissues.
Nature
2017
28756411
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.
J Med Genet
2017
27681292
Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Nat Genet
2016
27322543
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Nat Genet
2016
27694993
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.
Nat Neurosci
2016
25979475
Likelihood-based complex trait association testing for arbitrary depth sequencing data.
Bioinformatics
2015
23836599
The value of statistical or bioinformatics annotation for rare variant association with quantitative trait.
Genet Epidemiol
2013
21055717
To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests.
Am J Hum Genet
2010
19503787
Gene expression in peripheral blood leukocytes in monozygotic twins discordant for chronic fatigue: no evidence of a biomarker.
PLoS One
2009
1 - 15 of 15
Column Actions
Search
Recommended Authors
Collaborators
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers
8
Mark J Daly
Massachusetts General Hospital
Co-authored papers
6
Daniel P Howrigan
Co-authored papers
5
Veikko Salomaa
Co-authored papers
4
Mitja I Kurki
Co-authored papers
4
Aarno Palotie
Co-authored papers
4
Eija Hämäläinen
Co-authored papers
3
Yun Li
University of British Columbia
Co-authored papers
3
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers
3
Thomas Werge
Co-authored papers
3
Patrick F Sullivan
University of North Carolina at Chapel Hill
Co-authored papers
3
Andres Metspalu
Co-authored papers
3
Tõnu Esko
Co-authored papers
3
Manuel A Rivas
Stanford University School of Medicine
Co-authored papers
3
Konrad J Karczewski
Broad Institute of MIT and Harvard
Co-authored papers
3
Andrea Ganna
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
Co-authored papers
3
Claire Churchhouse
Co-authored papers
3
Reedik Mägi
Co-authored papers
3
Arn M J M van den Maagdenberg
Leiden University Medical Center
Co-authored papers
2
Hailiang Huang
Massachusetts General Hospital
Co-authored papers
2
Stephane E Castel
Co-authored papers
2
Andrew Kirby
Co-authored papers
2
Mingyao Li
Co-authored papers
2
David A Hinds
23andMe Inc.
Co-authored papers
2
Taru Tukiainen
Co-authored papers
2
Lude Franke
Co-authored papers
2
Dale R Nyholt
Co-authored papers
2
François Aguet
Co-authored papers
2
Paul M Ridker
Co-authored papers
2
Dorret I Boomsma
Co-authored papers
2
1 - 30