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Author Details

Dalila Pinto
Icahn School of Medicine at Mount Sinai
1997
74
41
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36274170High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.Acta Neuropathol Commun2022
36274170High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.Acta Neuropathol Commun2022
36443832Correction: High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.Acta Neuropathol Commun2022
36443832Correction: High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy.Acta Neuropathol Commun2022
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
34332145Direct reprogramming induces vascular regeneration post muscle ischemic injury.Mol Ther2021
34332145Direct reprogramming induces vascular regeneration post muscle ischemic injury.Mol Ther2021
32522981mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.Nat Commun2020
32640236Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis.Cell Rep2020
32522981mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.Nat Commun2020
32640236Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis.Cell Rep2020
30545856Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.Science2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30545856Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.Science2018
30177761Influenza virus infection causes global RNAPII termination defects.Nat Struct Mol Biol2018
29805045Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.Am J Hum Genet2018
29805045Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.Am J Hum Genet2018
30177761Influenza virus infection causes global RNAPII termination defects.Nat Struct Mol Biol2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
28407363De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.Am J Med Genet A2017
29262854Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Genome Med2017
29213072Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects.Sci Rep2017
28252112Parallel changes in serum proteins and diffusion tensor imaging in methamphetamine-associated psychosis.Sci Rep2017
27927641Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.Ann Rheum Dis2017
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
28252112Parallel changes in serum proteins and diffusion tensor imaging in methamphetamine-associated psychosis.Sci Rep2017
28407363De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.Am J Med Genet A2017
29213072Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects.Sci Rep2017
29262854Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Genome Med2017
27927641Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.Ann Rheum Dis2017
25861698Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder.Biol Psychiatry2016
25861698Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder.Biol Psychiatry2016
26740508Identification of novel genetic causes of Rett syndrome-like phenotypes.J Med Genet2016
27668389Gene expression elucidates functional impact of polygenic risk for schizophrenia.Nat Neurosci2016
27668389Gene expression elucidates functional impact of polygenic risk for schizophrenia.Nat Neurosci2016
26740508Identification of novel genetic causes of Rett syndrome-like phenotypes.J Med Genet2016
25421404The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Mol Psychiatry2015
25421404The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Mol Psychiatry2015
26010655Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.Hum Mutat2015
26605881The PsychENCODE project.Nat Neurosci2015
26598658HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.Proc Natl Acad Sci U S A2015
26342108Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN).J Med Genet2015
26598658HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.Proc Natl Acad Sci U S A2015
26342108Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN).J Med Genet2015
26605881The PsychENCODE project.Nat Neurosci2015
26010655Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.Hum Mutat2015
24343915A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.J Med Genet2014
25392729The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.Mol Autism2014
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Collaborators

The Hospital for Sick Children
Co-authored papers 46
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Hospital for Sick Children, University of Toronto
Co-authored papers 16
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Monash University
Co-authored papers 12
Icahn School of Medicine at Mount Sinai
Co-authored papers 11
Memorial University of Newfoundland
Co-authored papers 11
Co-authored papers 10
University of California los angeles
Co-authored papers 10
NIHR Biomedical Research Centre, University of Oxford
Co-authored papers 10
INSERM U
Co-authored papers 9
Vanderbilt Genetics Institute, Vanderbilt University
Co-authored papers 9
Co-authored papers 9
Oxford Brookes University
Co-authored papers 8
Co-authored papers 8
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 8
Stark Neurosciences Research Institute, Indiana University School of Medicine
Co-authored papers 8
University of North Carolina at Chapel Hill
Co-authored papers 8
Stanford University School of Medicine
Co-authored papers 8
Co-authored papers 8
Co-authored papers 8
The Ohio State University
Co-authored papers 8
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Co-authored papers 8
McMaster University
Co-authored papers 7
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The Hospital for Sick Children
Co-authored papers 7
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