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Author Details

Andrew S McCallion
Johns Hopkins University School of Medicine
1996
73
32
PMIDPaper TitleJournal TitlePublished Year
36824793Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.Res Sq2023
38001699Ring Chromosomes in Hematological Malignancies Are Associated with <i>TP53</i> Gene Mutations and Characteristic Copy Number Variants.Cancers (Basel)2023
37286935Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.BMC Genomics2023
36824793Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.Res Sq2023
36747739Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.bioRxiv2023
38001699Ring Chromosomes in Hematological Malignancies Are Associated with <i>TP53</i> Gene Mutations and Characteristic Copy Number Variants.Cancers (Basel)2023
37286935Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.BMC Genomics2023
36747739Evaluating the mouse neural precursor line, SN4741, as a suitable proxy for midbrain dopaminergic neurons.bioRxiv2023
36076238Neuroinflammation represents a common theme amongst genetic and environmental risk factors for Alzheimer and Parkinson diseases.J Neuroinflammation2022
36076238Neuroinflammation represents a common theme amongst genetic and environmental risk factors for Alzheimer and Parkinson diseases.J Neuroinflammation2022
34378773Development and optimization of an in vivo electrocardiogram recording method and analysis program for adult zebrafish.Dis Model Mech2021
33693707SOX9 modulates cancer biomarker and cilia genes in pancreatic cancer.Hum Mol Genet2021
34378773Development and optimization of an in vivo electrocardiogram recording method and analysis program for adult zebrafish.Dis Model Mech2021
33693707SOX9 modulates cancer biomarker and cilia genes in pancreatic cancer.Hum Mol Genet2021
32303558Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.Genome Res2020
31962144Establishment of an eHAP1 human haploid cell line hybrid reference genome assembled from short and long reads.Genomics2020
32303558Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.Genome Res2020
32829096Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease.Parkinsonism Relat Disord2020
31962144Establishment of an eHAP1 human haploid cell line hybrid reference genome assembled from short and long reads.Genomics2020
32829096Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease.Parkinsonism Relat Disord2020
30455415ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.Nat Genet2019
30455415ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.Nat Genet2019
29760202Survey of Human Chromosome 21 Gene Expression Effects on Early Development in <i>Danio rerio</i>.G3 (Bethesda)2018
30503521Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.Am J Hum Genet2018
29760202Survey of Human Chromosome 21 Gene Expression Effects on Early Development in <i>Danio rerio</i>.G3 (Bethesda)2018
29499164Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection for Sporadic Parkinson Disease.Am J Hum Genet2018
30503521Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.Am J Hum Genet2018
29499164Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection for Sporadic Parkinson Disease.Am J Hum Genet2018
28659821Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
28974934Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
28751573Sox10<sup>+</sup> Cells Contribute to Vascular Development in Multiple Organs-Brief Report.Arterioscler Thromb Vasc Biol2017
28659821Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
28974934Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
28751573Sox10<sup>+</sup> Cells Contribute to Vascular Development in Multiple Organs-Brief Report.Arterioscler Thromb Vasc Biol2017
26749308Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.Am J Hum Genet2016
26749308Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.Am J Hum Genet2016
27276213Functional Characterization of Schizophrenia-Associated Variation in CACNA1C.PLoS One2016
27276213Functional Characterization of Schizophrenia-Associated Variation in CACNA1C.PLoS One2016
25968237Carbamate nerve agent prophylatics exhibit distinct toxicological effects in the zebrafish embryo model.Neurotoxicol Teratol2015
25839327Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability.Am J Hum Genet2015
25915584Targeted inhibition of tumor-specific glutaminase diminishes cell-autonomous tumorigenesis.J Clin Invest2015
25968237Carbamate nerve agent prophylatics exhibit distinct toxicological effects in the zebrafish embryo model.Neurotoxicol Teratol2015
26206884Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.Hum Mol Genet2015
26075791A method to predict the impact of regulatory variants from DNA sequence.Nat Genet2015
26075791A method to predict the impact of regulatory variants from DNA sequence.Nat Genet2015
26206884Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.Hum Mol Genet2015
25839327Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability.Am J Hum Genet2015
25915584Targeted inhibition of tumor-specific glutaminase diminishes cell-autonomous tumorigenesis.J Clin Invest2015
25170925Rbm24a and Rbm24b are required for normal somitogenesis.PLoS One2014
25416705Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling.G3 (Bethesda)2014
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Collaborators

New York University Grossman School of Medicine
Co-authored papers 9
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 8
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 7
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 7
Center for Epigenomics, University of California San Diego
Co-authored papers 6
Perelman School of Medicine University of Pennsylvania
Co-authored papers 6
Johns Hopkins School of Medicine
Co-authored papers 6
The Johns Hopkins University
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
Johns Hopkins Hospital
Co-authored papers 3
Co-authored papers 3
Hospital for Sick Children
Co-authored papers 3
Universite de Montreal
Co-authored papers 3
Northwestern University
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Co-authored papers 2
Mayo Clinic
Co-authored papers 2
Technical University of Denmark
Co-authored papers 2
Johns Hopkins University School of Medicine
Co-authored papers 2
Frazer Institute, The University of Queensland, Dermatology Research Centre
Co-authored papers 1
Co-authored papers 1
University of California San Diego
Co-authored papers 1
Moores Cancer Center, University of California
Co-authored papers 1
Duke University Medical Center
Co-authored papers 1
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Altius Institute for Biomedical Sciences
Co-authored papers 1
Co-authored papers 1
Institut de Genetique Medicale d'Alsace, Hopitaux Universitaires de Strasbourg
Co-authored papers 1
NIH and National Human Genome Research Institute
Co-authored papers 1