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Author Details

Paul G Matteson
Center for Advanced Biotechnology and Medicine, Rutgers University
1995
25
15
PMIDPaper TitleJournal TitlePublished Year
37758766Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.Nat Commun2023
35623351Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.Stem Cell Reports2022
35830838Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.Stem Cell Reports2022
33565183Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects.Hum Mutat2021
32578145Using iPSC-Based Models to Understand the Signaling and Cellular Phenotypes in Idiopathic Autism and 16p11.2 Derived Neurons.Adv Neurobiol2020
29553565Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells (NPCs).J Vis Exp2018
28345005Chronic Enzyme Replacement to the Brain of a Late Infantile Neuronal Ceroid Lipofuscinosis Mouse Has Differential Effects on Phenotypes of Disease.Mol Ther Methods Clin Dev2017
28135291Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.PLoS One2017
27684594Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay.J Vis Exp2016
25753732The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation.Dev Biol2015
26220976Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior.Hum Mol Genet2015
24730055Chronic desipramine treatment rescues depression-related, social and cognitive deficits in Engrailed-2 knockout mice.Genes Brain Behav2014
24520327Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum.PLoS One2014
22180456Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function.Hum Mol Genet2012
22829897Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice.PLoS One2012
20605702NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia.Schizophr Res2010
19255043Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.Am J Psychiatry2009
19615670Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.Biol Psychiatry2009
18250320The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.Proc Natl Acad Sci U S A2008
18796533Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects.Physiol Genomics2008
11862458Genomic imprinting of a placental lactogen gene in Peromyscus.Dev Genes Evol2001
10802670Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus.Nat Genet2000
10950864The Dlk1 and Gtl2 genes are linked and reciprocally imprinted.Genes Dev2000
7719019A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.Mamm Genome1995
8647401Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome.Genetics1995
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Collaborators

Rutgers Robert Wood Johnson Medical School, The State University of New Jersey
Co-authored papers 19
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Co-authored papers 1
Co-authored papers 1
Harry Perkins Institute of Medical Research, University of Western Australia
Co-authored papers 1
Invitae Corporation
Co-authored papers 1
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