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Author Details
Full Name
Christopher Castaldi
Affiliation
Yale Center for Genome Analysis, Yale School of Medicine
ORCID
Career Start Year
2015
Papers
19
H Index
12
Expertise
CM4AI Collaborator
Wade Schulz (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36791724
Accelerated SARS-CoV-2 intrahost evolution leading to distinct genotypes during chronic infection.
Cell Rep Med
2023
36722941
HERV1-env Induces Unfolded Protein Response Activation in Autoimmune Liver Disease: A Potential Mechanism for Regulatory T Cell Dysfunction.
J Immunol
2023
36879130
Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts.
Nat Med
2023
34623748
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.
Am J Med Genet A
2022
35545661
Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 variants Alpha and Iota.
Commun Biol
2022
35399324
Rapid emergence of SARS-CoV-2 Omicron variant is associated with an infection advantage over Delta in vaccinated persons.
Med
2022
35064122
Single-cell multi-omics reveals dyssynchrony of the innate and adaptive immune system in progressive COVID-19.
Nat Commun
2022
33432185
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Nat Genet
2021
34125151
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease.
JAMA Neurol
2021
34230938
Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 lineages.
medRxiv
2021
33433624
Neuroinvasion of SARS-CoV-2 in human and mouse brain.
J Exp Med
2021
32989326
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Nat Genet
2020
33077954
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.
Nat Med
2020
32935108
Neuroinvasion of SARS-CoV-2 in human and mouse brain.
bioRxiv
2020
30578106
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.
Neuron
2019
29983323
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.
Neuron
2018
28856709
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
Ann Neurol
2017
28991257
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Nat Genet
2017
25516354
Exploring the folding pathway of green fluorescent protein through disulfide engineering.
Protein Sci
2015
1 - 19 of 19
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