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John E Spiro

Showing results (11-20 of 18) with videos related to

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JAMA Psychiatry|December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletionsAndres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variantRaphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Biological Psychiatry|May 21, 2018
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First StudySandra Martin-Brevet, Borja Rodríguez-Herreros, Jared A Nielsen, et al.
Biological Psychiatry|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Plos Biology|February 29, 2024
Recommendations for accelerating open preprint peer review to improve the culture of scienceMichele Avissar-Whiting, Frédérique Belliard, Stefano M Bertozzi, et al.
JAMA Psychiatry|December 3, 2015
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesDebra D'Angelo, Sébastien Lebon, Qixuan Chen, et al.
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Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
JAMA Psychiatry|December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletionsAndres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variantRaphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Biological Psychiatry|May 21, 2018
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First StudySandra Martin-Brevet, Borja Rodríguez-Herreros, Jared A Nielsen, et al.
Biological Psychiatry|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Plos Biology|February 29, 2024
Recommendations for accelerating open preprint peer review to improve the culture of scienceMichele Avissar-Whiting, Frédérique Belliard, Stefano M Bertozzi, et al.
JAMA Psychiatry|December 3, 2015
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesDebra D'Angelo, Sébastien Lebon, Qixuan Chen, et al.
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