J. Pevsner

发表

The case for open science: rare diseases.

Peter N. Robinson, E. van Enckevort, C. Nellåker, 2020, JAMIA open.

Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart

Ingo Ruczinski, Jonathan Pevsner, Edward L Spitznagel, 2005, Genome Biology.

DNA methylation signatures within the human brain.

Jonathan Pevsner, Andrew P Feinberg, Sarven Sabunciyan, 2007, American journal of human genetics.

Long-read single-molecule maps of the functional methylome

Jeffrey G. Reifenberger, A. Hastie, H. Cao, 2019, Genome research.

High throughput analysis of gene expression in the human brain

J. Pevsner, C. Colantuoni, A. E. Purcell, 2000, Journal of Neuroscience Research.

Isolation and characterization of an olfactory receptor protein for odorant pyrazines.

S. Snyder, S. Strittmatter, J. Pevsner, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Somatic Mosaicism in the Human Genome

Jonathan Pevsner, Donald N Freed, J. Pevsner, 2014, Genes.

Odorant-binding protein. Characterization of ligand binding.

S. Snyder, A. Snowman, J. Pevsner, 1990, The Journal of biological chemistry.

Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene

Elizabeth T. Cirulli, Jonathan Pevsner, David B. Goldstein, 2010, PLoS genetics.

A novel variant in GABRB2 associated with intellectual disability and epilepsy

A. Fatemi, S. Aradhya, S. Srivastava, 2014, American journal of medical genetics. Part A.

Efficient Array-Based Identification of Novel Cardiac Genes through Differentiation of Mouse ESCs

A. McCallion, J. Gearhart, J. Pevsner, 2008, PloS one.

Reduced representation optical methylation mapping (R2OM2)

Jeffrey G. Reifenberger, A. Hastie, H. Cao, 2017, bioRxiv.

Reduced representation optical methylation mapping (R2OM2)

Jonathan Pevsner, Jeffrey G. Reifenberger, Han Cao, 2017 .

The three-dimensional structure of bovine odorant binding protein and its mechanism of odor recognition

Jonathan Pevsner, L. Mario Amzel, Solomon H. Snyder, 1996, Nature Structural Biology.

Altered Patterns of Cellular Gene Expression in Dermal Microvascular Endothelial Cells Infected with Kaposi's Sarcoma-Associated Herpesvirus

G. Hayward, J. Pevsner, P. Kim, 2002, Journal of Virology.

Leonardo da Vinci's contributions to neuroscience

J. Pevsner, 2002, Trends in Neurosciences.

Leonardo da Vinci's studies of the brain

J. Pevsner, 2019, The Lancet.

Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays.

Ingo Ruczinski, Jonathan Pevsner, Giovanni Parmigiani, 2008, The annals of applied statistics.

Microarray analysis of differential gene expression in lead-exposed astrocytes.

J. Pevsner, J. Laterra, L. Frelin, 2001, Toxicology and applied pharmacology.

Gene expression alterations over large chromosomal regions in cancers include multiple genes unrelated to malignant progression.

Jonathan Pevsner, Nicole Benoit, David Sidransky, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Gene expression in Autism

J. Pevsner, 2005 .

Increased Fibronectin Expression in Sturge-Weber Syndrome Fibroblasts and Brain Tissue

K. Becker, M. Vawter, J. Pevsner, 2003, Pediatric Research.

The transcriptome landscape associated with Disrupted-in-Schizophrenia-1 locus impairment in early development and adulthood

A. Sawa, J. Pevsner, T. Tomoda, 2019, Schizophrenia Research.

Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models

Wenyi Wang, Jonathan Pevsner, Rafael A. Irizarry, 2008, J. Comput. Biol..

Bioinformatics and Functional Genomics 3rd Edition

Jonathan Pevsner, J. Pevsner, 2015 .

Emerging technologies for large-scale screening of human tissues and fluids in the study of severe psychiatric disease.

J. J. Breen, R. Yolken, E. Torrey, 2001, The international journal of neuropsychopharmacology.

The Contribution of Mosaic Variants to Autism Spectrum Disorder

Donald N Freed, J. Pevsner, Donald Freed, 2016, PLoS genetics.

Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia.

C. Ross, C. Tamminga, R. Sweet, 2019, The American journal of psychiatry.

F168. Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia

C. Tamminga, A. Sawa, R. Margolis, 2019, Biological Psychiatry.

Haplotype counting by next-generation sequencing for ultrasensitive human DNA detection.

Brian S. Iglehart, Lisa M Haley, J. Eshleman, 2014, The Journal of molecular diagnostics : JMD.

Review The case for open science: rare diseases

Esther van Enckevort, C. Nellåker, N. Harris, 2020 .

Wireless control of cellular function by activation of a novel protein responsive to electromagnetic fields

P. Celnik, G. Pelled, G. Fridman, 2018, Scientific Reports.

Dragon and Dragon View: Methods for the Annotation, Analysis, and Visualization of Large-Scale Gene Expression Data

J. Pevsner, C. Colantuoni, C. Bouton, 2003 .

Mosaicism in Human Health and Disease.

R. Tupler, J. Pevsner, Jeremy Thorpe, 2020, Annual review of genetics.

The expanding beta 4-galactosyltransferase gene family: messages from the databanks.

J. Pevsner, N. Shaper, J. H. Shaper, 1998, Glycobiology.

Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method

Matthew D. Shirley, Joseph D. Baugher, J. Pevsner, 2013, BMC Genomics.

Adolescent Δ9-THC exposure and astrocyte-specific genetic vulnerability converge on NF-κB-COX-2 signaling to impair memory in adulthood

M. Pletnikov, J. Pevsner, Yuto Hasegawa, 2019 .

Analysis of genomic DNA with the UCSC genome browser.

J. Pevsner, 2009, Methods in molecular biology.

A synaptic vesicle specific GTP-binding protein from ray electric organ.

R. Scheller, J. Pevsner, L. Elferink, 1991, Brain research. Molecular brain research.

The role of Sec1p‐related proteins in vesicle trafficking in the nerve terminal

J. Pevsner, 1996, Journal of neuroscience research.

Human syntaxin 7: a Pep12p/Vps6p homologue implicated in vesicle trafficking to lysosomes.

J. Pevsner, L. Frelin, H. Wang, 1997, Gene.

Mammalian homologues of yeast vacuolar protein sorting (vps) genes implicated in Golgi-to-lysosome trafficking.

R. Scheller, J. Pevsner, S. Hsu, 1996, Gene.

HIF-dependent Anti-tumorigenic Effect of Anti-oxidants In Vivo

G. Semenza, C. Dang, D. Felsher, 2007 .

Unique pharmacological actions of atypical neuroleptic quetiapine: possible role in cell cycle/fate control

A. Sawa, S. Seshadri, J. Pevsner, 2013, Translational Psychiatry.

Molecular mechanisms of neurotransmitter and neuropeptide release

J. Pevsner, 1996 .

Unexpected Relationships and Inbreeding in HapMap Phase III Populations

Matthew D. Shirley, Joseph D. Baugher, J. Pevsner, 2012, PloS one.

Chapter 81 – Sturge–Weber Syndrome

J. Pevsner, D. Marchuk, A. Comi, 2015 .

5'-nucleotidase from the electric ray electric lobe. Primary structure and relation to mammalian and procaryotic enzymes.

J. Pevsner, Y. Misumi, Y. Ikehara, 1991, European journal of biochemistry.

Fetal methylazoxymethanol acetate-induced lesions cause reductions in dopamine receptor-mediated catalepsy and stereotypy

J. Coyle, J. Pevsner, P. Sanberg, 1985, Neuropharmacology.

n-Sec1: a neural-specific syntaxin-binding protein.

R. Scheller, J. Pevsner, S. Hsu, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Control of fusion pore dynamics during exocytosis by Munc18.

R. J. Fisher, J. Pevsner, R. Burgoyne, 2001, Science.

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Matthew D. Shirley, Joseph D. Baugher, B. Cohen, 2013, The New England journal of medicine.

Multicenter Research Data of Epilepsy Management in Patients With Sturge-Weber Syndrome.

M. Lawton, M. Moses, J. Pevsner, 2021, Pediatric neurology.

Identification of a mosaic activating mutation in GNA11 in atypical Sturge-Weber Syndrome.

B. Cohen, J. Pevsner, L. Frelin, 2020, The Journal of investigative dermatology.

Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome.

C. McCulloch, M. Lawton, M. Moses, 2019, Pediatric neurology.

A needle in a haystack: Sturge-Weber syndrome gene discovery.

J. Pevsner, D. Marchuk, A. Comi, 2013, Pediatric Neurology.

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

Ryan E. Mills, J. V. Moran, Jennifer A. Erwin, 2017, Science.

Correction to “Modulation of oncogenic potential by alternative gene use in human prostate cancer”

J. Pevsner, G. Pasternack, J. Brody, 1999, Nature Network Boston.

Dysfunction of mitochondria and GABAergic interneurons in the anterior cingulate cortex of individuals with schizophrenia

A. Sawa, A. Jaffe, J. Pevsner, 2022, Neuroscience Research.

Induction of vascular endothelial growth factor in human astrocytes by lead. Involvement of a protein kinase C/activator protein-1 complex-dependent and hypoxia-inducible factor 1-independent signaling pathway.

J. Pevsner, J. Laterra, C. Bouton, 2000, The Journal of biological chemistry.

mVps24p functions in EGF receptor sorting/trafficking from the early endosome.

J. Pevsner, L. Frelin, P. Hunt, 2005, Experimental cell research.

Molecular Phylogeny and Evolution

J. Pevsner, 2009 .

Leonardo da Vinci's contributions to neuroscience

J. Pevsner, 2002, Trends in Neurosciences.

Nitric Oxide Regulates Exocytosis by S-Nitrosylation of N-ethylmaleimide-Sensitive Factor

M. Yamakuchi, C. Lowenstein, D. Wagner, 2003, Cell.

Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genomes⃞s⃞ The online version of this article (available at http://www.jlr.org) contains supplementary data in the form of 3 Tables. Published, JLR Papers in Press, August 30, 2007.

D. Maiguel, J. Pevsner, P. Watkins, 2007, Journal of Lipid Research.

HIF-dependent antitumorigenic effect of antioxidants in vivo.

Jonathan Pevsner, Linzhao Cheng, Venu Raman, 2007, Cancer cell.

FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.

Jonathan Pevsner, M. Frerking, S. Ojeda, 2007, Human molecular genetics.

FXYD 1 is an MeCP 2 target gene overexpressed in the brains of Rett syndrome patients and Mecp 2-null mice

M. Frerking, S. Ojeda, J. Pevsner, 2007 .

Detection of endogenous biotin in various tissues: novel functions in the hippocampus and implications for its use in avidin-biotin technology

J. Pevsner, H. Wang, Hui Wang, 1999, Cell and Tissue Research.

Basic Local Alignment Search Tool (BLAST)

Jonathan Pevsner, J. Pevsner, 2005 .

X-Linked Adrenoleukodystrophy: Genes, Mutations, and Phenotypes

J. Pevsner, P. Watkins, L. Braiterman, 2004, Neurochemical Research.

The expanding β4-galactosyltransferase gene family: messages from the databanks

J. Pevsner, N. Shaper, J. H. Shaper, 1998 .

Postmortem brain abnormalities of the glutamate neurotransmitter system in autism

J. Pevsner, M. Blue, A. Zimmerman, 2001, Neurology.

Odorant-binding protein: odorant transport function in the vertebrate nasal epithelium

S. Snyder, J. Pevsner, S. Snyder, 1990 .

Molecular cloning of odorant-binding protein: member of a ligand carrier family.

S. Snyder, J. Pevsner, P. Feinstein, 1988, Science.

Regulation of Munc-18/Syntaxin 1A Interaction by Cyclin-dependent Kinase 5 in Nerve Endings*

J. Pevsner, E. Stuenkel, R. Shuang, 1998, The Journal of Biological Chemistry.

Mosaicism in rare disease

J. Pevsner, I. Osei-Owusu, B. Avigdor, 2021, Genomics of Rare Diseases.

Viral Bcl-2 homologs and their role in virus replication and associated diseases.

J. Pevsner, J. Hardwick, B. Polster, 2004, Biochimica et biophysica acta.

Development of human protein reference database as an initial platform for approaching systems biology in humans.

Hanno Steen, Jonathan Pevsner, Minal Menezes, 2003, Genome research.

Human very long-chain acyl-CoA synthetase and two human homologs: initial characterization and relationship to fatty acid transport protein.

J. Pevsner, P. Watkins, S. Steinberg, 1999, Prostaglandins, Leukotrienes and Essential Fatty Acids.

Endothelial GNAQ p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels

D. Zurakowski, M. Sahin, J. Pevsner, 2021, Arteriosclerosis, thrombosis, and vascular biology.

MANF: a new mesencephalic, astrocyte-derived neurotrophic factor with selectivity for dopaminergic neurons.

David I. Smith, J. Pevsner, J. Kelly, 2003, Journal of molecular neuroscience : MN.

Consanguinity in Centre d’Étude du Polymorphisme Humain (CEPH) pedigrees

Joseph D. Baugher, Elisha D O Roberson, T. Downey, 2012, European Journal of Human Genetics.

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2021, Nature Neuroscience.

Copy Number Variants Associated with 14 Cases of Self-Injurious Behavior

L. Hagopian, W. Silverman, J. Pevsner, 2016, PloS one.

The use of genomic microarrays to study chromosomal abnormalities in mental retardation.

Rong Mao, J. Pevsner, 2005, Mental retardation and developmental disabilities research reviews.

Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

G. Ronnett, J. Pevsner, V. Matarazzo, 2003, Molecular and Cellular Neuroscience.

Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

J. V. Moran, Michael E. Coulter, Laurel L. Ball, 2019, bioRxiv.

Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State

Jonathan Pevsner, Joseph D. Baugher, Thomas J. Downey, 2011, PLoS genetics.

Cancer Cell Antitumorigenic Effect of Antioxidants in patients with head and neck or lung cancer

G. Semenza, C. Dang, D. Felsher, 2022 .

Regulation of rat magnocellular neurosecretory system by D-aspartate: evidence for biological role(s) of a naturally occurring free D-amino acid in mammals.

S. Snyder, D. Selkoe, J. Pevsner, 2000, The Journal of endocrinology.

The biology of the mammalian Krüppel-like family of transcription factors.

D. Dang, V. Yang, J. Pevsner, 2000, The international journal of biochemistry & cell biology.

Mitochondrial fission proteins regulate programmed cell death in yeast.

J. Pevsner, J. McCaffery, J. Hardwick, 2004, Genes & development.

Performance assessment of copy number microarray platforms using a spike-in experiment

Ingo Ruczinski, Jonathan Pevsner, Rafael A. Irizarry, 2011, Bioinform..

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission

Mahshid S. Azamian, J. Rosenfeld, J. Gécz, 2019, Science Advances.

Characterization of an unbalanced translocation causing 3q28qter duplication and 10q26.2qter deletion in a patient with global developmental delay and self-injury

Jonathan D. Schmidt, L. Hagopian, J. Pevsner, 2020, Cold Spring Harbor molecular case studies.

Visualization of Shared Genomic Regions and Meiotic Recombination in High-Density SNP Data

Elisha D O Roberson, J. Pevsner, 2009, PloS one.

Adolescent Δ9-Tetrahydrocannabinol Exposure and Astrocyte-Specific Genetic Vulnerability Converge on Nuclear Factor-κB–Cyclooxygenase-2 Signaling to Impair Memory in Adulthood

M. Pletnikov, J. Pevsner, Yuto Hasegawa, 2019, Biological Psychiatry.

A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome

N. Matsumoto, J. Pevsner, Roar Fjær, 2021, Human molecular genetics.

Comprehensive identification of somatic nucleotide variants in human brain tissue

Peter J. Park, Jonathan Pevsner, Eduardo Soriano, 2020, bioRxiv.

Local mean normalization of microarray element signal intensities across an array surface: quality control and correction of spatially systematic artifacts.

Jonathan Pevsner, Carlo Colantuoni, Scott Zeger, 2002, BioTechniques.

The Abnormal Regulation of Gene Expression in Autistic Brain Tissue

J. Pevsner, A. Purcell, O.-H. Jeon, 2001, Journal of autism and developmental disorders.

Microarray-Based Phospho-Proteomic Profiling of Complex Biological Systems12

C. Bettegowda, A. Olivi, Heng Zhu, 2016, Translational oncology.

Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function

Nathaniel D. Miller, J. Pevsner, J. Hoover-Fong, 2009, American journal of medical genetics. Part A.

Odorant-binding protein and its mRNA are localized to lateral nasal gland implying a carrier function.

S H Snyder, S. Snyder, J. Pevsner, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Odorant-binding protein: localization to nasal glands and secretions.

S. Snyder, J. Pevsner, P. Sklar, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain.

Jonathan Pevsner, H Ronald Zielke, Rong Mao, 2003, Genomics.

Molecular mechanisms of olfaction

Jonathan Pevsner, Solomon H. Snyder, S. Snyder, 1988, Trends in Neurosciences.

Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms

D. Benos, K. Kirk, J. Pevsner, 1997, Nature.

Genomic analysis of partial 21q monosomies with variable phenotypes

Elisha D O Roberson, A. Hamosh, J. Pevsner, 2011, European Journal of Human Genetics.

Progress in the use of microarray technology to study the neurobiology of disease

Jonathan Pevsner, Károly Mirnics, J. Pevsner, 2004, Nature Neuroscience.

DRAGON: Database Referencing of Array Genes Online

Jonathan Pevsner, Christopher M. L. S. Bouton, J. Pevsner, 2000, Bioinform..

Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy

A. Fatemi, J. Pevsner, D. Shinde, 2017, American journal of medical genetics. Part A.

Gene Expression Profiling in Postmortem Rett Syndrome Brain: Differential Gene Expression and Patient Classification

Eric P. Hoffman, Jonathan Pevsner, Alex Chenchik, 2001, Neurobiology of Disease.

Clinical Variability in Rett Syndrome

E. Hoffman, M. Johnston, J. Pevsner, 2003, Journal of child neurology.

Bioinformatics and functional genomics

Jonathan Pevsner, J. Pevsner, 2003 .

Modulation of oncogenic potential by alternative gene use in human prostate cancer

J. Pevsner, G. Pasternack, J. Brody, 1999, Nature Medicine.

Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium

A. Sawa, N. Cascella, J. Pevsner, 2016, Translational psychiatry.

Plunc, a Member of the Secretory Gland Protein Family, Is Up-regulated in Nasal Respiratory Epithelium after Olfactory Bulbectomy*

G. Ronnett, C. Moon, J. Pevsner, 2002, The Journal of Biological Chemistry.

Specificity and regulation of a synaptic vesicle docking complex

Jonathan Pevsner, Mark K. Bennett, Richard H. Scheller, 1994, Neuron.

Molecular mechanisms of olfaction.

S. Snyder, J. Pevsner, P. Sklar, 1988, The Journal of biological chemistry.

Olfactory cells via nasal biopsy reflect the developing brain in gene expression profiles: Utility and limitation of the surrogate tissues in research for brain disorders

H. Okano, A. Sawa, A. Jaffe, 2013, Neuroscience Research.

Effects of lead on gene expression.

J. Pevsner, C. Bouton, J Pevsner, 2000, Neurotoxicology.

Two rat homologs of clathrin-associated adaptor proteins.

R. Scheller, J. Pevsner, W. Volknandt, 1994, Gene.

Sturge-Weber Syndrome Patient Registry: Delayed Diagnosis and Poor Seizure Control.

J. Loeb, J. Pevsner, K. Ball, 2019, Jornal de Pediatria.

Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method

Joseph D. Baugher, J. Pevsner, M. Shirley, 2013, BMC Genomics.

Mechanisms of vesicle docking and fusion: insights from the nervous system.

R. Scheller, J. Pevsner, R H Scheller, 1994, Current opinion in cell biology.

Synaptotagmin I is a molecular target for lead

J. Pevsner, L. Frelin, C. Bouton, 2001, Journal of neurochemistry.

Locations and patterns of meiotic recombination in two-generation pedigrees

Elisha D O Roberson, J. Pevsner, Jason C. Ting, 2009, BMC Medical Genetics.

A transcriptional progression model for head and neck cancer.

J. Califano, D. Sidransky, M. Zahurak, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

Syntaxin 7 and VAMP-7 are soluble N-ethylmaleimide-sensitive factor attachment protein receptors required for late endosome-lysosome and homotypic lysosome fusion in alveolar macrophages.

J. Pevsner, J. Kaplan, D. Ward, 2000, Molecular biology of the cell.

Discovering novel phenotype-selective neurotrophic factors to treat neurodegenerative diseases.

David I. Smith, J. Pevsner, J. Kelly, 2004, Progress in brain research.

Bioinformatics and Functional Genomics: Pevsner/Bioinformatics

Jonathan Pevsner, J. Pevsner, 2004 .

Comprehensive identification of somatic nucleotide variants in human brain tissue

J. V. Moran, Lovelace J. Luquette, Laurel L. Ball, 2021, Genome Biology.

Pairwise Sequence Alignment

Jonathan Pevsner, J. Pevsner, 2005 .

DRAGON View: information visualization for annotated microarray data

Jonathan Pevsner, Christopher M. L. S. Bouton, J. Pevsner, 2002, Bioinform..

Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio

Ingo Ruczinski, Jonathan Pevsner, Elisha D O Roberson, 2007, Human mutation.

Neurobiology of Rett syndrome: a genetic disorder of synapse development

M. Johnston, S. Naidu, J. Pevsner, 2001, Brain and Development.

Chromosomal variation in lymphoblastoid cell lines

Jonathan Pevsner, Joseph D. Baugher, Joseph D Baugher, 2012, Human mutation.

Analysis of differential gene expression mediated by clozapine in human postmortem brains

C. Ross, L. Marchionni, A. Sawa, 2017, Schizophrenia Research.

Assessment of Neural Cell Adhesion Molecule (NCAM) in Autistic Serum and Postmortem Brain

J. Pevsner, A. Zimmerman, K. Hyder, 2001, Journal of autism and developmental disorders.

SNOMAD (Standardization and NOrmalization of MicroArray Data): web-accessible gene expression data analysis

Jonathan Pevsner, Carlo Colantuoni, Scott Zeger, 2002, Bioinform..

Parametric influences on catalepsy

J. Coyle, J. Pevsner, P. Sanberg, 2004, Psychopharmacology.

MANF

David I. Smith, J. Pevsner, J. Kelly, 2007, Journal of Molecular Neuroscience.

Genetic and genomic stability across lymphoblastoid cell line expansions

N. Gerry, D. Berlin, J. Pevsner, 2018, BMC Research Notes.

RegulationofCFTRchloride channelsbysyntaxinand Munc 18 isoforms

D. Benos, K. Kirk, J. Pevsner, 1997 .

Snomad: Biologist-Friendly Web Tools for the Standardization and NOrmalization of Microarray Data

Scott L. Zeger, Carlo Colantuoni, George Henry, 2003 .

Estimating Genome-Wide Copy Number Using Allele Specific Mixture Models

Wenyi Wang, Jonathan Pevsner, Rafael A. Irizarry, 2007, RECOMB.

Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2021, Nature Neuroscience.

Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan

Jason C. Ting, Ying Ye, George H. Thomas, 2006, BMC Bioinformatics.

Olfactory Receptor Mechanisms

J. Pevsner, P. Sklar, S. Snyder, 1988 .

Naturally occurring free D-aspartate is a nuclear component of cells in the mammalian hypothalamo-neurohypophyseal system

D. Selkoe, J. Pevsner, J. Morris, 2002, Neuroscience.

Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain.

Rong Mao, J. Pevsner, C. Zielke, 2003, Genomics.

The Molecular Basis of Olfaction

J. Pevsner, 2001, CHIMIA.

UvA-DARE ( Digital Academic Repository ) Molecular biology and pharmacogenetics of x-linked adrenoleukodystrophy

J. Pevsner, P. Watkins, L. Braiterman, 2012 .

Characterization of antipsychotic medications, amino acid signatures, and platelet-activating factor in first-episode psychosis

A. Sawa, J. Pevsner, Ben Orsburn, 2021, Biomarkers in Neuropsychiatry.

Basic Local Alignment Search Tool (BLAST)

J. Pevsner, 2005 .

X-Linked Adrenoleukodystrophy: Genes, Mutations, and Phenotypes

J. Pevsner, P. Watkins, L. Braiterman, 2004, Neurochemical Research.