Hakon Hakonarson

Orcid: 0000-0003-2814-7461

According to our database1, Hakon Hakonarson authored at least 22 papers between 2009 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
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Article 
PhD thesis 
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Links

On csauthors.net:

Bibliography

2023
Clinical decision support with a comprehensive in-EHR patient tracking system improves genetic testing follow up.
J. Am. Medical Informatics Assoc., June, 2023

Characterizing variability of electronic health record-driven phenotype definitions.
J. Am. Medical Informatics Assoc., February, 2023

2022
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Medical Informatics Decis. Mak., 2022

2021
Genomic considerations for FHIR®; eMERGE implementation lessons.
J. Biomed. Informatics, 2021

Performance of model-based multifactor dimensionality reduction methods for epistasis detection by controlling population structure.
BioData Min., 2021

DeepCNV: a deep learning approach for authenticating copy number variations.
Briefings Bioinform., 2021

2020
Elucidation of DNA methylation on N6-adenine with deep learning.
Nat. Mach. Intell., 2020

2019
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J. Biomed. Informatics, 2019

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

2018
DeepPolyA: A Convolutional Neural Network Approach for Polyadenylation Site Prediction.
IEEE Access, 2018

2016
The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth.
NeuroImage, 2016

The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort.
NeuroImage, 2016

Biofilter as a Functional Annotation Pipeline for Common and Rare Copy Number Burden.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
BioData Min., 2015

2014
Neuroimaging of the Philadelphia Neurodevelopmental Cohort.
NeuroImage, 2014

2013
Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth.
NeuroImage, 2013

An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data.
NeuroImage, 2013

2012
Impact of in-scanner head motion on multiple measures of functional connectivity: Relevance for studies of neurodevelopment in youth.
NeuroImage, 2012

Being right is its own reward: Load and performance related ventral striatum activation to correct responses during a working memory task in youth.
NeuroImage, 2012

2011
Mitochondrial Genome Sequence Analysis: A custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy.
BMC Bioinform., 2011

2009
Multiple testing in genome-wide association studies via hidden Markov models.
Bioinform., 2009

ATOM: a powerful gene-based association test by combining optimally weighted markers.
Bioinform., 2009


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