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Author Details

Christopher Castaldi
Yale Center for Genome Analysis, Yale School of Medicine
2015
19
12
Wade Schulz (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36791724Accelerated SARS-CoV-2 intrahost evolution leading to distinct genotypes during chronic infection.Cell Rep Med2023
36722941HERV1-env Induces Unfolded Protein Response Activation in Autoimmune Liver Disease: A Potential Mechanism for Regulatory T Cell Dysfunction.J Immunol2023
36879130Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts.Nat Med2023
34623748D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.Am J Med Genet A2022
35545661Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 variants Alpha and Iota.Commun Biol2022
35399324Rapid emergence of SARS-CoV-2 Omicron variant is associated with an infection advantage over Delta in vaccinated persons.Med2022
35064122Single-cell multi-omics reveals dyssynchrony of the innate and adaptive immune system in progressive COVID-19.Nat Commun2022
33432185Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.Nat Genet2021
34125151DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease.JAMA Neurol2021
34230938Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 lineages.medRxiv2021
33433624Neuroinvasion of SARS-CoV-2 in human and mouse brain.J Exp Med2021
32989326Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.Nat Genet2020
33077954Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.Nat Med2020
32935108Neuroinvasion of SARS-CoV-2 in human and mouse brain.bioRxiv2020
30578106Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.Neuron2019
29983323De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.Neuron2018
28856709GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.Ann Neurol2017
28991257Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.Nat Genet2017
25516354Exploring the folding pathway of green fluorescent protein through disulfide engineering.Protein Sci2015
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Yale School of Medicine, USA Instituto Todos pela Saude
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