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Author Details

Andrew B Stergachis
University of Washington School of Medicine
2011
32
17
Nathan Sheffield (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36798371Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A.bioRxiv2023
37808736Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition.bioRxiv2023
37560121Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A.Neurol Genet2023
37194416Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.Ann Clin Transl Neurol2023
36788024Evaluation of <i>N</i> <sup>6</sup>-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes.Genome Res2023
34478631Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions.Neuron2021
33763331Clinical utility of brain MRS imaging of patients with adult-onset non-cirrhotic hyperammonemia.Mol Genet Metab Rep2021
34605044Single cell biology-a Keystone Symposia report.Ann N Y Acad Sci2021
32541961Biobanks could identify medically actionable findings relevant for COVID-19 clinical care.Nat Med2020
32101728Highly Parallel Quantification and Compartment Localization of Transcription Factors and Nuclear Proteins.Cell Rep2020
33390987Identification of an Identical <i>de Novo</i> SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay.Front Pharmacol2020
32713002A retrospective study of adult patients with noncirrhotic hyperammonemia.J Inherit Metab Dis2020
30335480Integrative Genomics Analysis Identifies ACVR1B as a Candidate Causal Gene of Emphysema Distribution.Am J Respir Cell Mol Biol2019
31658831Identification of Racial Inequities in Access to Specialized Inpatient Heart Failure Care at an Academic Medical Center.Circ Heart Fail2019
31347272Noncirrhotic hyperammonemia after deceased donor kidney transplantation: A case report.Am J Transplant2019
30937933Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism.Ann Neurol2019
28526559A single nucleotide polymorphism of cyclin-dependent kinase inhibitor 1B (p27<sup>Kip1</sup>) associated with human vein graft failure affects growth of human venous adventitial cells but not smooth muscle cells.J Vasc Surg2018
26867746Selecting Optimal Peptides for Targeted Proteomic Experiments in Human Plasma Using In Vitro Synthesized Proteins as Analytical Standards.Methods Mol Biol2016
26100116Using Data Independent Acquisition (DIA) to Model High-responding Peptides for Targeted Proteomics Experiments.Mol Cell Proteomics2015
25102069Panorama: a targeted proteomics knowledge base.J Proteome Res2014
25409825Conservation of trans-acting circuitry during mammalian regulatory evolution.Nature2014
25220462Mapping and dynamics of regulatory DNA and transcription factor networks in A. thaliana.Cell Rep2014
23793028DNase I-hypersensitive exons colocalize with promoters and distal regulatory elements.Nat Genet2013
24337295Exonic transcription factor binding directs codon choice and affects protein evolution.Science2013
23953118Developmental fate and cellular maturity encoded in human regulatory DNA landscapes.Cell2013
22974441SRC Homology 2 Domain Binding Sites in Insulin, IGF-1 and FGF receptor mediated signaling networks reveal an extensive potential interactome.Cell Commun Signal2012
22959076Circuitry and dynamics of human transcription factor regulatory networks.Cell2012
22955981Personal and population genomics of human regulatory variation.Genome Res2012
22955618An expansive human regulatory lexicon encoded in transcription factor footprints.Nature2012
22955617The accessible chromatin landscape of the human genome.Nature2012
22155787The SH2 domain-containing proteins in 21 species establish the provenance and scope of phosphotyrosine signaling in eukaryotes.Sci Signal2011
22056677Rapid empirical discovery of optimal peptides for targeted proteomics.Nat Methods2011
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Collaborators

Altius Institute for Biomedical Sciences
Co-authored papers 12
Altius Institute for Biomedical Sciences
Co-authored papers 8
Altius Institute for Biomedical Sciences
Co-authored papers 7
Altius Institute for Biomedical Sciences
Co-authored papers 7
University of Washington
Co-authored papers 6
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Co-authored papers 6
Max Planck Institute for Evolutionary Anthropology
Co-authored papers 6
University of Washington
Co-authored papers 6
Princeton University
Co-authored papers 5
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Co-authored papers 4
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Co-authored papers 4
Altius Institute for Biomedical Sciences
Co-authored papers 4
Brigham and Women's Hospital
Co-authored papers 4
University of Washington School of Medicine
Co-authored papers 4
Altius Institute for Biomedical Sciences
Co-authored papers 4
University of Washington
Co-authored papers 4
University of Washington
Co-authored papers 4
University of Washington Medical Center
Co-authored papers 4
University of Washington Medical Center
Co-authored papers 4
Altius Institute for Biomedical Sciences
Co-authored papers 4
Altius Institute for Biomedical Sciences
Co-authored papers 4
Kaiser Permanente Washington
Co-authored papers 4
University of Washington
Co-authored papers 3
Altius Institute for Biomedical Sciences
Co-authored papers 3
Institute for Systems Genetics, NYU School of Medicine
Co-authored papers 3
University of Kentucky
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University of Washington
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Altius Institute for Biomedical Sciences
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Altius Institute for Biomedical Sciences
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Seattle Children's Hospital.
Co-authored papers 3