Andrew E Jaffe

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Andrew E



Publications in SciGraph latest 50 shown

  • 2019-01-11 Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19) in MOLECULAR PSYCHIATRY
  • 2018-12 Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia in NPJ SCHIZOPHRENIA
  • 2018-11-26 Identification and prioritization of gene sets associated with schizophrenia risk by co-expression network analysis in human brain in MOLECULAR PSYCHIATRY
  • 2018-08-21 Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome in MOLECULAR PSYCHIATRY
  • 2018-08 Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis in NATURE NEUROSCIENCE
  • 2018-06 GAD1 alternative transcripts and DNA methylation in human prefrontal cortex and hippocampus in brain development, schizophrenia in MOLECULAR PSYCHIATRY
  • 2018-06 Convergence of placenta biology and genetic risk for schizophrenia in NATURE MEDICINE
  • 2018-05 Investigating the neuroimmunogenic architecture of schizophrenia in MOLECULAR PSYCHIATRY
  • 2018-05 Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder in MOLECULAR PSYCHIATRY
  • 2018-02 The schizophrenia- and autism-associated gene, transcription factor 4 regulates the columnar distribution of layer 2/3 prefrontal pyramidal neurons in an activity-dependent manner in MOLECULAR PSYCHIATRY
  • 2017-05-09 Altered expression of histamine signaling genes in autism spectrum disorder in TRANSLATIONAL PSYCHIATRY
  • 2017-04 Reproducible RNA-seq analysis using recount2 in NATURE BIOTECHNOLOGY
  • 2017-03 Correcting for cell-type heterogeneity in epigenome-wide association studies: revisiting previous analyses in NATURE METHODS
  • 2016-12 Genetic and epigenetic analysis of schizophrenia in blood—a no-brainer? in GENOME MEDICINE
  • 2016-12 Erratum to: Practical impacts of genomic data “cleaning” on biological discovery using surrogate variable analysis in BMC BIOINFORMATICS
  • 2016-12 Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive in GENOME BIOLOGY
  • 2016-06 A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus in NATURE MEDICINE
  • 2016-04 Schizophrenia-Associated hERG channel Kv11.1-3.1 Exhibits a Unique Trafficking Deficit that is Rescued Through Proteasome Inhibition for High Throughput Screening in SCIENTIFIC REPORTS
  • 2016-01 Mapping DNA methylation across development, genotype and schizophrenia in the human frontal cortex in NATURE NEUROSCIENCE
  • 2015-12 The PsychENCODE project in NATURE NEUROSCIENCE
  • 2015-12 DNA methylation age of blood predicts all-cause mortality in later life in GENOME BIOLOGY
  • 2015-12 Practical impacts of genomic data “cleaning” on biological discovery using surrogate variable analysis in BMC BIOINFORMATICS
  • 2015-03 Ballgown bridges the gap between transcriptome assembly and expression analysis in NATURE BIOTECHNOLOGY
  • 2015-01 Developmental regulation of human cortex transcription and its clinical relevance at single base resolution in NATURE NEUROSCIENCE
  • 2014-09 Genetic neuropathology of obsessive psychiatric syndromes in TRANSLATIONAL PSYCHIATRY
  • 2014-03 Paternal age, de novo mutations and schizophrenia in MOLECULAR PSYCHIATRY
  • 2014-02 Accounting for cellular heterogeneity is critical in epigenome-wide association studies in GENOME BIOLOGY
  • 2014 Measurement, Summary, and Methodological Variation in RNA-sequencing in STATISTICAL ANALYSIS OF NEXT GENERATION SEQUENCING DATA
  • 2014 Pattern Identification in Time-Course Gene Expression Data with the CoGAPS Matrix Factorization in GENE FUNCTION ANALYSIS
  • 2013-12 Gene set bagging for estimating the probability a statistically significant result will replicate in BMC BIOINFORMATICS
  • 2013-12 TE-array—a high throughput tool to study transposon transcription in BMC GENOMICS
  • 2011-12 Identification of functional genetic variation in exome sequence analysis in BMC PROCEEDINGS
  • 2009-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium in NATURE GENETICS
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