Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sankalp Sonar"'
Autor:
Hala Harony-Nicolas, Maya Kay, Johann du Hoffmann, Matthew E Klein, Ozlem Bozdagi-Gunal, Mohammed Riad, Nikolaos P Daskalakis, Sankalp Sonar, Pablo E Castillo, Patrick R Hof, Matthew L Shapiro, Mark G Baxter, Shlomo Wagner, Joseph D Buxbaum
Publikováno v:
eLife, Vol 6 (2017)
Mutations in the synaptic gene SHANK3 lead to a neurodevelopmental disorder known as Phelan-McDermid syndrome (PMS). PMS is a relatively common monogenic and highly penetrant cause of autism spectrum disorder (ASD) and intellectual disability (ID), a
Externí odkaz:
https://doaj.org/article/15f3de3779bb415499c0098f7ef83e2d
Autor:
Sankalp Sonar, Michael S. Breen, Kristi Niblo, Hala Harony-Nicolas, Silvia De Rubeis, Natalie Burlant, Andrew W. Browne, Mark G. Baxter, Daniele Di Marino, Lacin Koro, Joseph D. Buxbaum, Carla E. M. Golden
Publikováno v:
Cerebral Cortex (New York, NY)
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the FMR1 gene. It is a leading monogenic cause of autism spectrum disorder and inherited intellectual disability and is often comorbid with attention deficits. Most FXS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed54736a53bba72ba7ef418e7ce3f7e3
http://europepmc.org/articles/PMC6458915
http://europepmc.org/articles/PMC6458915
Autor:
Silvia De Rubeis, Carla E. M. Golden, Joseph D. Buxbaum, Hala Harony-Nicolas, Sankalp Sonar, Mark G. Baxter, Michael S. Breen, Lacin Koro, Kristi Niblo, Daniele Di Marino, Andrew W. Browne
Fragile X Syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the FMR1 gene. FXS is a leading monogenic cause of autism spectrum disorder (ASD) and inherited intellectual disability (ID). In most cases, the mutation is an expansion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9d64f576e8ffe9234422296dadc5af9
Autor:
You Jeong Park, Eli A. Stahl, Claudia Feng, Noam D. Beckmann, Eric E. Schadt, Lora Liharska, Sankalp Sonar, Alexander W. Charney
Publikováno v:
European Neuropsychopharmacology. 29:S142-S143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::837f9336da6279a2f056e2d0192779a5
https://doi.org/10.1016/j.euroneuro.2019.08.057
https://doi.org/10.1016/j.euroneuro.2019.08.057
Autor:
Eric E. Schadt, Claudia Feng, Noam D. Beckmann, Laura M. Huckins, Sankalp Sonar, Pamela Sklar, Brian H. Kopell, Alexander W. Charney, You Jeong Park, Lora Liharska
Publikováno v:
European Neuropsychopharmacology. 29:S144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef00a45b173a485e0d1caa73a69c2ea7
https://doi.org/10.1016/j.euroneuro.2019.08.059
https://doi.org/10.1016/j.euroneuro.2019.08.059
Autor:
Maya Kay, Johann du Hoffmann, Sankalp Sonar, Mohammed Riad, Patrick R. Hof, Nikolaos P. Daskalakis, Matthew E. Klein, Matthew L. Shapiro, Mark G. Baxter, Pablo E. Castillo, Hala Harony-Nicolas, Joseph D. Buxbaum, Ozlem Bozdagi-Gunal, Shlomo Wagner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d35e332bd057bd6c1d08d7a7356eb5f
https://doi.org/10.7554/elife.18904.017
https://doi.org/10.7554/elife.18904.017