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Author Details

David L Nelson
Baylor College of Medicine
1968
247
67
PMIDPaper TitleJournal TitlePublished Year
34871737Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome.Neurobiol Dis2022
35617426Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome.Proc Natl Acad Sci U S A2022
34995503Stephen T. Warren, Ph.D. (1953-2021): A remembrance.Am J Hum Genet2022
34871737Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome.Neurobiol Dis2022
35617426Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome.Proc Natl Acad Sci U S A2022
34995503Stephen T. Warren, Ph.D. (1953-2021): A remembrance.Am J Hum Genet2022
34111553Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.J Mol Diagn2021
33856019Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model.Hum Mol Genet2021
34111553Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.J Mol Diagn2021
34267372Stephen T. Warren 1953-2021.Nat Genet2021
34417305Stephen T. Warren: Human geneticist who advanced understanding of mutational mechanisms and developmental disorders.Proc Natl Acad Sci U S A2021
33856019Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model.Hum Mol Genet2021
34417305Stephen T. Warren: Human geneticist who advanced understanding of mutational mechanisms and developmental disorders.Proc Natl Acad Sci U S A2021
34267372Stephen T. Warren 1953-2021.Nat Genet2021
31364704Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome.Cereb Cortex2020
31364704Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome.Cereb Cortex2020
30476102Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndrome.Hum Mol Genet2019
30476102Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndrome.Hum Mol Genet2019
308493212018 Presidential Address: Who Are We?Am J Hum Genet2019
31206741Intellectual and developmental disabilities research centers: Fifty years of scientific accomplishments.Ann Neurol2019
30770808Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy.Nat Commun2019
31206741Intellectual and developmental disabilities research centers: Fifty years of scientific accomplishments.Ann Neurol2019
30770808Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy.Nat Commun2019
308493212018 Presidential Address: Who Are We?Am J Hum Genet2019
29477468Turning the corner from observation to intervention in human genetics.J Genet Genomics2018
29477468Turning the corner from observation to intervention in human genetics.J Genet Genomics2018
282576842016 William Allan Award Introduction: James Gusella.Am J Hum Genet2017
282576842016 William Allan Award Introduction: James Gusella.Am J Hum Genet2017
27383586Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.J Neurosci2016
27383586Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.J Neurosci2016
25271084MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes.Eur J Hum Genet2015
25552647The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice.Hum Mol Genet2015
25790165The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome.Cell Cycle2015
25271084MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes.Eur J Hum Genet2015
25790165The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome.Cell Cycle2015
25552647The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice.Hum Mol Genet2015
24108107Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome.Hum Mol Genet2014
25456134FXR1P limits long-term memory, long-lasting synaptic potentiation, and de novo GluA2 translation.Cell Rep2014
24108107Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome.Hum Mol Genet2014
24986919CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome.Hum Mol Genet2014
25136376Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome.J Neurodev Disord2014
25456134FXR1P limits long-term memory, long-lasting synaptic potentiation, and de novo GluA2 translation.Cell Rep2014
24986919CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome.Hum Mol Genet2014
25136376Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome.J Neurodev Disord2014
23553836Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration.Proc Natl Acad Sci U S A2013
23473314The unstable repeats--three evolving faces of neurological disease.Neuron2013
23553836Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration.Proc Natl Acad Sci U S A2013
23616559Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome.J Neurosci2013
23616559Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome.J Neurosci2013
23473314The unstable repeats--three evolving faces of neurological disease.Neuron2013
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Collaborators

University of Washington
Co-authored papers 19
Co-authored papers 18
Baylor College of Medicine
Co-authored papers 17
Co-authored papers 12
Baylor College of Medicine
Co-authored papers 8
NIH/National Institute of Ageing
Co-authored papers 7
Baylor College of Medicine
Co-authored papers 6
The Genome Center at Washington University, Washington University School of Medicine
Co-authored papers 6
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Co-authored papers 6
Baylor College of Medicine
Co-authored papers 5
Monash University
Co-authored papers 5
Vanderbilt Genetics Institute, Vanderbilt University
Co-authored papers 5
The Genome Institute at Washington University
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Baylor College of Medicine Human Genome Sequencing Center
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Regeneron Pharmaceuticals Inc.
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Co-authored papers 4