Christopher LaCoursiere

Christopher LaCoursiere

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Christopher LaCoursiere

Christopher LaCoursiere

Publications by authors named "Christopher LaCoursiere"

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An Open-Source Husbandry Repository.

Zebrafish 2018 12 5;15(6):656-658. Epub 2018 Sep 5.

1 Epilepsy Genetics Program, Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital , Boston, Massachusetts.

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https://www.liebertpub.com/doi/10.1089/zeb.2018.1583
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http://dx.doi.org/10.1089/zeb.2018.1583DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426270PMC
December 2018

Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias.

Cell Rep 2017 12;21(13):3754-3766

Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2017.11.106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752134PMC
December 2017

Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish.

PLoS One 2016 9;11(6):e0156498. Epub 2016 Jun 9.

Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0156498PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900632PMC
July 2017

Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.

Am J Med Genet A 2015 Sep 25;167A(9):2017-25. Epub 2015 Apr 25.

Epilepsy Genetics Program, Division of Epilepsy & Clinical Neurophysiology, Boston Children's Hospital, Boston, Massachusetts.

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http://dx.doi.org/10.1002/ajmg.a.37132DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722031PMC
September 2015

Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.

Am J Hum Genet 2015 May 9;96(5):709-19. Epub 2015 Apr 9.

Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, USA; Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.03.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570282PMC
May 2015

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.

Ann Neurol 2015 Apr 26;77(4):720-5. Epub 2015 Feb 26.

Division of Genetics and Genomics, Department of Medicine, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA; Program in Medical and Population Genetics, Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, MA.

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http://dx.doi.org/10.1002/ana.24357DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471336PMC
April 2015