List of works - Jacob J Michaelson

A complete mass-spectrometric map of the yeast proteome applied to quantitative trait analysis

scientific article

Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment

scientific article

Author Correction: Forecasting risk gene discovery in autism with machine learning and genome-scale data

scientific article published on 26 November 2020

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

scientific article published on 21 October 2020

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

scientific article

Community attitudes on genetic research of gender identity, sexual orientation, and mental health

scientific article published on 08 July 2020

Data-driven assessment of eQTL mapping methods

scientific article

Detection and interpretation of expression quantitative trait loci (eQTL).

scientific article

Differential relationship of DNA replication timing to different forms of human mutation and variation

scientific article

Endoplasmic reticulum chaperone genes encode effectors of long-term memory

scientific article published on 23 March 2022

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

scientific article published on 23 August 2019

Forecasting risk gene discovery in autism with machine learning and genome-scale data

scientific article published on 12 March 2020

Genetic Approaches to Understanding Psychiatric Disease.

scientific article published on 12 June 2017

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

scientific article published on December 2011

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

scientific article published on 19 June 2017

Integrated genetic and epigenetic prediction of coronary heart disease in the Framingham Heart Study

scientific article published on 2 January 2018

Integrative analysis of low- and high-resolution eQTL

scientific article

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

scientific article published on 01 October 2020

Neuronal PAS Domain Proteins 1 and 3 Are Master Regulators of Neuropsychiatric Risk Genes.

scientific article published on 06 April 2017

Novel and ultra-rare damaging variants in neuropeptide signaling are associated with disordered eating behaviors

scientific article published on 28 August 2017

PSSM-Suc: Accurately predicting succinylation using position specific scoring matrix into bigram for feature extraction

scientific article published on 5 May 2017

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

scientific article published on 11 April 2014

SLINGER: large-scale learning for predicting gene expression

scientific article published on 20 December 2016

SucStruct: Prediction of succinylated lysine residues by using structural properties of amino acids.

scientific article published on 28 March 2017

Teamwork: improved eQTL mapping using combinations of machine learning methods

scientific article

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

scientific article published on December 2012

cerebroViz: an R package for anatomical visualization of spatiotemporal brain data.

scientific article

forestSV: structural variant discovery through statistical learning

scientific article

p53-mediated neurodegeneration in the absence of the nuclear protein Akirin2

scientific article published on 25 January 2022

List of works by Jacob J Michaelson

A complete mass-spectrometric map of the yeast proteome applied to quantitative trait analysis

Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment

Author Correction: Forecasting risk gene discovery in autism with machine learning and genome-scale data

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

Community attitudes on genetic research of gender identity, sexual orientation, and mental health

Data-driven assessment of eQTL mapping methods

Detection and interpretation of expression quantitative trait loci (eQTL).

Differential relationship of DNA replication timing to different forms of human mutation and variation

Endoplasmic reticulum chaperone genes encode effectors of long-term memory

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Forecasting risk gene discovery in autism with machine learning and genome-scale data

Genetic Approaches to Understanding Psychiatric Disease.

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Integrated genetic and epigenetic prediction of coronary heart disease in the Framingham Heart Study

Integrative analysis of low- and high-resolution eQTL

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Neuronal PAS Domain Proteins 1 and 3 Are Master Regulators of Neuropsychiatric Risk Genes.

Novel and ultra-rare damaging variants in neuropeptide signaling are associated with disordered eating behaviors

PSSM-Suc: Accurately predicting succinylation using position specific scoring matrix into bigram for feature extraction

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

SLINGER: large-scale learning for predicting gene expression

SucStruct: Prediction of succinylated lysine residues by using structural properties of amino acids.

Teamwork: improved eQTL mapping using combinations of machine learning methods

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

cerebroViz: an R package for anatomical visualization of spatiotemporal brain data.

forestSV: structural variant discovery through statistical learning

p53-mediated neurodegeneration in the absence of the nuclear protein Akirin2