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Author Details

James H Millonig
Rutgers Robert Wood Johnson Medical School, The State University of New Jersey
1989
36
20
PMIDPaper TitleJournal TitlePublished Year
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
33852756Engrailed-2 is a cell autonomous regulator of neurogenesis in cultured hippocampal neural stem cells.Dev Neurobiol2021
32578145Using iPSC-Based Models to Understand the Signaling and Cellular Phenotypes in Idiopathic Autism and 16p11.2 Derived Neurons.Adv Neurobiol2020
32578146Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders.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
24507165Engrailed2 modulates cerebellar granule neuron precursor proliferation, differentiation and insulin-like growth factor 1 signaling during postnatal development.Mol Autism2014
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
22848008Medium chain acyl-CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screening.Am J Med Genet A2012
21752929Specific and integrated roles of Lmx1a, Lmx1b and Phox2a in ventral midbrain development.Development2011
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
16935268En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder.Brain Res2006
15749247Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.Int J Dev Neurosci2005
16252243Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.Am J Hum Genet2005
15024396Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.Mol Psychiatry2004
15183721Roof plate and dorsal spinal cord dl1 interneuron development in the dreher mutant mouse.Dev Biol2004
10693804The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS.Nature2000
10488902Neurogenetics of the cerebellar system.J Child Neurol1999
8630252Functional analysis of the weaver mutant GIRK2 K+ channel and rescue of weaver granule cells.Neuron1996
9009075A high-density molecular genetic map around the weaver locusMamm Genome1996
8678987A high-density molecular genetic map around the weaver locus.Mamm Genome1996
7540720Molecular analysis of the distal enhancer of the mouse alpha-fetoprotein gene.Mol Cell Biol1995
2503677Mutations that alter the helix-turn-helix region of the spollAC protein: a Bacillus subtilis sporulation-specific sigma factor.Mol Microbiol1989
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Collaborators

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Co-authored papers 1
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Co-authored papers 1
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Co-authored papers 1
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Co-authored papers 1
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Co-authored papers 1
Harry Perkins Institute of Medical Research, University of Western Australia
Co-authored papers 1
Co-authored papers 1
College of Medicine, The Ohio State University
Co-authored papers 1