Gilad D Evrony

Gilad D Evrony

UNVERIFIED PROFILE

Are you Gilad D Evrony?   Register this Author

Register author
Gilad D Evrony

Gilad D Evrony

Publications by authors named "Gilad D Evrony"

Are you Gilad D Evrony?   Register this Author

18Publications

574Reads

18Profile Views

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.

Eur J Hum Genet 2019 Apr 12. Epub 2019 Apr 12.

Department of Genetics, Microbiology and Statistics, Faculty of Biology, University of Barcelona, IBUB, IRSJD, CIBERER, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41431-019-0394-5DOI Listing
April 2019

DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.

Eur J Hum Genet 2019 Mar 15. Epub 2019 Mar 15.

Department of Genetics, Microbiology and Statistics, Faculty of Biology, University of Barcelona, IBUB, IRSJD, CIBERER, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41431-019-0374-9DOI Listing
March 2019

One brain, many genomes.

Authors:
Gilad D Evrony

Science 2016 11;354(6312):557-558

Harvard Medical School, Boston, MA 02115, USA, and Mount Sinai Hospital, New York, NY 10029, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.aak9761DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141038PMC
November 2016

A PIECE OF MY MIND. A Wild Rotation.

Authors:
Gilad D Evrony

JAMA 2016 Aug;316(7):713-4

Harvard Medical School, Boston, Massachusetts, and Mount Sinai Hospital, New York, New York.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jama.2016.4994DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179038PMC
August 2016

Resolving rates of mutation in the brain using single-neuron genomics.

Elife 2016 Feb 22;5. Epub 2016 Feb 22.

Division of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children's Hospital, Boston, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.7554/eLife.12966DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805530PMC
February 2016

Somatic mutation in single human neurons tracks developmental and transcriptional history.

Science 2015 Oct;350(6256):94-98

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.aab1785DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664477PMC
October 2015

Loss of PCLO function underlies pontocerebellar hypoplasia type III.

Neurology 2015 Apr 1;84(17):1745-50. Epub 2015 Apr 1.

From Monogenic Molecular Genetics (M.Y.A., B.A.C., E.L.B., A.H.C.), University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Exeter; Centre for Human Genetics (M.Y.A., B.A.C., E.L.B., M.A.P., A.H.C.), St. George's, University of London, UK; National Genetic Center (A.R.), Ministry of Health, Muscat, Sultanate of Oman; Division of Genetics and Genomics, Department of Medicine (K.S.-A., J.N.P., R.S.H., G.D.E., S.S., K.M., C.A.W., G.H.M.), Manton Center for Orphan Disease Research (K.S.-A., J.N.P., R.S.H., G.D.E., S.S., K.M., C.A.W., G.H.M.), and Howard Hughes Medical Institute (J.N.P., R.S.H., G.D.E., S.S., C.A.W.), Boston Children's Hospital; Departments of Pediatrics (K.S.-A., K.M., C.A.W., G.H.M.) and Neurology (C.A.W.), and Program in Biological and Biomedical Sciences (G.D.E.), Harvard Medical School, Boston; Program in Medical and Population Genetics (K.S.-A., K.M., C.A.W.), Broad Institute of MIT and Harvard University, Cambridge, MA; Department of Biology (A.A.-K.), College of Science, Sultan Qaboos University, Sultanate of Oman; Wellcome Trust Sanger Institute (S.A.-T., M.E.H.), Wellcome Trust Genome Campus, Hinxton, Cambridge, UK; Department of Neurology (A.Y.A.-M.), Atkinson Morley Wing, St. George's Hospital, London, UK; and Pediatric Neurology Unit (G.H.M.), Department of Neurology, Massachusetts General Hospital, Boston, MA.

View Article

Download full-text PDF

Source
http://www.walshlab.org/uploads/publications/266/2015neurolo
Web Search
http://www.neurology.org/content/84/17/1745.full.pdf
Web Search
http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000152
Publisher Site
http://dx.doi.org/10.1212/WNL.0000000000001523DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424132PMC
April 2015

Cell lineage analysis in human brain using endogenous retroelements.

Neuron 2015 Jan;85(1):49-59

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neuron.2014.12.028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299461PMC
January 2015

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.

Cell Rep 2014 Sep 21;8(5):1280-9. Epub 2014 Aug 21.

Division of Genetics and Genomics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02138, USA; Program of Biological and Biomedical Sciences, Harvard Medical School, Boston, MA 02115, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.celrep.2014.07.043DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272008PMC
September 2014

METTL23, a transcriptional partner of GABPA, is essential for human cognition.

Hum Mol Genet 2014 Jul 5;23(13):3456-66. Epub 2014 Feb 5.

Division of Genetics and Genomics, Department of Medicine Manton Center for Orphan Disease Research and Department of Pediatrics Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddu054DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049305PMC
July 2014

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning.

Science 2014 Feb;343(6172):764-8

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.1244392DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480613PMC
February 2014

Somatic mutation, genomic variation, and neurological disease.

Science 2013 Jul;341(6141):1237758

Department of Neurology, Boston Children's Hospital, Boston, MA 02115, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.1237758DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909954PMC
July 2013

Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons.

Biomaterials 2007 Dec 14;28(34):5176-84. Epub 2007 Sep 14.

Department of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.biomaterials.2007.08.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435502PMC
December 2007