Publications by authors named "Jonathan D Picker"

17Publications

Revising the Psychiatric Phenotype of Homocystinuria.

Genet Med 2019 08 15;21(8):1827-1831. Epub 2019 Jan 15.

Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

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http://www.nature.com/articles/s41436-018-0419-4
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http://dx.doi.org/10.1038/s41436-018-0419-4DOI Listing
August 2019

Expanding the phenotypic spectrum associated with OPHN1 variants.

Eur J Med Genet 2019 Feb 28;62(2):137-143. Epub 2018 Jun 28.

Division of Genetics & Genomics, Department of Medicine, Boston Children's Hospital and Harvard Medical School Boston, MA, 02115, USA; The Manton Center for Orphan Disease Research, Department of Medicine, Boston Children's Hospital and Harvard Medical School Boston, MA, 02115, USA; Division of Newborn Medicine, Department of Medicine, Boston Children's Hospital and Harvard Medical School Boston, MA, 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2018.06.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310103PMC
February 2019

Utility of Genetic Testing in Fetal Alcohol Spectrum Disorder.

J Pediatr 2018 05 3;196:270-274.e1. Epub 2018 Feb 3.

Division of Genetics, Boston Children's Hospital, Harvard Medical School, Boston, MA.

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http://dx.doi.org/10.1016/j.jpeds.2017.12.046DOI Listing
May 2018

Review of Salient Investigational Drugs for the Treatment of Fragile X Syndrome.

J Child Adolesc Psychopharmacol 2017 Dec 5;27(10):850-863. Epub 2017 May 5.

1 Department of Psychiatry, Boston Children's Hospital , Boston, Massachusetts.

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http://dx.doi.org/10.1089/cap.2016.0200DOI Listing
December 2017

A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene.

Eur J Hum Genet 2016 12 22;24(12):1826-1827. Epub 2016 Jun 22.

Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.

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http://www.nature.com/articles/ejhg201674
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http://dx.doi.org/10.1038/ejhg.2016.74DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117927PMC
December 2016

New innovations: therapeutic opportunities for intellectual disabilities.

Ann Neurol 2013 Sep;74(3):382-90

Division of Genetics, Boston Children's Hospital, and Howard Hughes Medical Institute, Boston, MA; Departments of Pediatrics and Neurology,, Harvard Medical School, Boston, MA.

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http://dx.doi.org/10.1002/ana.24002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876407PMC
September 2013

Phenotypic characterization of mice heterozygous for a null mutation of glutamate carboxypeptidase II.

Synapse 2009 Aug;63(8):625-35

Department of Psychiatry, Laboratory of Molecular and Psychiatric Neuroscience, Harvard Medical School and McLean Hospital, Belmont, Massachusetts 02478, USA.

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http://dx.doi.org/10.1002/syn.20649DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749286PMC
August 2009

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

Neuroreport 2006 Apr;17(5):541-4

Department of Genetics, Children's Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1097/01.wnr.0000208995.38695.2fDOI Listing
April 2006

Do maternal folate and homocysteine levels play a role in neurodevelopmental processes that increase risk for schizophrenia?

Harv Rev Psychiatry 2005 Jul-Aug;13(4):197-205

Department of Genetics, Harvard Medical School; McLean Hospital, Belmont, MA, USA.

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http://dx.doi.org/10.1080/10673220500243372DOI Listing
January 2006

Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema.

J Pediatr 2003 Mar;142(3):349-52

Divisions of Genetics and Neuropathology, Children's Hospital Boston, the Department of Neurology, Massachusetts General Hospital, Cambridge, Massachusetts 02115, USA.

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http://dx.doi.org/10.1067/mpd.2003.97DOI Listing
March 2003