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Author Details

Dheeraj Malhotra
MS Research Unit
1980
48
27
PMIDPaper TitleJournal TitlePublished Year
36732511Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2023
36732511Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2023
37533636A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid.Cell Rep Methods2023
37533636A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid.Cell Rep Methods2023
35093191Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility.Neuron2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35915177Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders.Nat Neurosci2022
35093191Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility.Neuron2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35915177Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders.Nat Neurosci2022
33758076CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq data.Life Sci Alliance2021
33758076CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq data.Life Sci Alliance2021
33207193Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression.Cell Rep2020
33257685muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics data.Nat Commun2020
33207193Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression.Cell Rep2020
33257685muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics data.Nat Commun2020
30655364A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogs.Life Sci Alliance2019
30655364A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogs.Life Sci Alliance2019
31279534Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.Biol Psychiatry2019
30747918Altered human oligodendrocyte heterogeneity in multiple sclerosis.Nature2019
31279534Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.Biol Psychiatry2019
30747918Altered human oligodendrocyte heterogeneity in multiple sclerosis.Nature2019
29691040Progress in Understanding and Treating SCN2A-Mediated Disorders.Trends Neurosci2018
29696747Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.Hum Mutat2018
29691040Progress in Understanding and Treating SCN2A-Mediated Disorders.Trends Neurosci2018
29696747Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.Hum Mutat2018
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
28216146Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis.Stem Cell Reports2017
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
28216146Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis.Stem Cell Reports2017
27018473Frequency and Complexity of De Novo Structural Mutation in Autism.Am J Hum Genet2016
27018473Frequency and Complexity of De Novo Structural Mutation in Autism.Am J Hum Genet2016
27786187Translating genome-wide association findings into new therapeutics for psychiatry.Nat Neurosci2016
27786187Translating genome-wide association findings into new therapeutics for psychiatry.Nat Neurosci2016
26985448Characterization of molecular and cellular phenotypes associated with a heterozygous <i>CNTNAP2</i> deletion using patient-derived hiPSC neural cells.NPJ Schizophr2015
26985448Characterization of molecular and cellular phenotypes associated with a heterozygous <i>CNTNAP2</i> deletion using patient-derived hiPSC neural cells.NPJ Schizophr2015
26391891The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.J Child Neurol2015
26391891The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.J Child Neurol2015
23871472Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.Biol Psychiatry2014
23871472Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.Biol Psychiatry2014
24722188Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2014
24722188Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2014
23325106Implication of a rare deletion at distal 16p11.2 in schizophrenia.JAMA Psychiatry2013
23325106Implication of a rare deletion at distal 16p11.2 in schizophrenia.JAMA Psychiatry2013
22071774Association of variants in BAT1-LTA-TNF-BTNL2 genes within 6p21.3 region show graded risk to leprosy in unrelated cohorts of Indian population.Hum Genet2012
22424231CNVs: harbingers of a rare variant revolution in psychiatric genetics.Cell2012
22596152Genetics: Fish heads and human disease.Nature2012
23260136Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.Cell2012
22071774Association of variants in BAT1-LTA-TNF-BTNL2 genes within 6p21.3 region show graded risk to leprosy in unrelated cohorts of Indian population.Hum Genet2012
23260136Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.Cell2012
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Collaborators

Jonathan Sebat
University of California San Diego
Co-authored papers 21
Shane McCarthy
Wellcome Sanger Institute
Co-authored papers 10
Michael Gill
Co-authored papers 6
Vladimir Vacic
Stanley Institute for Cognitive Genomics
Co-authored papers 6
Abhishek Bhandari
B.P. Koirala Institute of Health Sciences
Co-authored papers 6
Patrick F Sullivan
University of North Carolina at Chapel Hill
Co-authored papers 6
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers 5
Michael C O'Donovan
Co-authored papers 5
Sven Cichon
University Hospital Basel and University of Basel
Co-authored papers 5
George Kirov
Co-authored papers 5
Michael J Owen
Co-authored papers 5
Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
Co-authored papers 5
Mary-Claire King
University of Washington
Co-authored papers 5
Aiden Corvin
Co-authored papers 5
Pablo V Gejman
Co-authored papers 4
James R Lupski
Baylor College of Medicine
Co-authored papers 4
Vladimir Makarov
Center for Immunotherapy and Precision-Immuno-Oncology, Cleveland Clinic
Co-authored papers 4
Judith L Rapoport
National Institute of Mental Health, National Institutes of Health
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Elliot S Gershon
University of Chicago
Co-authored papers 4
Thomas G Schulze
SUNY Upstate Medical University
Co-authored papers 4
Anil K Malhotra
Co-authored papers 4
Douglas F Levinson
Stanford University School of Medicine
Co-authored papers 4
Tom Walsh
University of Washington
Co-authored papers 4
Pamela Sklar
Co-authored papers 4
Christina M Hultman
Karolinska Institutet
Co-authored papers 4
Mary Kusenda
Clinic for Cattle, University of Veterinary Medicine Hannover
Co-authored papers 4
Derek W Morris
Co-authored papers 4
Alan R Sanders
Center for Psychiatric Genetics, NorthShore University HealthSystem
Co-authored papers 4
John R Kelsoe
University of California
Co-authored papers 4
Seungtai Yoon
Co-authored papers 4
Release 1.2