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Journal of Inherited Metabolic Disease
|
January 1, 1996
Clinical presentation of mitochondrial disorders in childhood
A Munnich, A Rötig, D Chretien, et al.
Molecular Psychiatry
|
March 29, 2002
Linkage and association of the glutamate receptor 6 gene with autism
S Jamain, C Betancur, H Quach, et al.
Nature Genetics
|
October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
T Bourgeron, P Rustin, D Chretien, et al.
Translational Psychiatry
|
August 22, 2013
Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening
C Boissart, A Poulet, P Georges, et al.
The Journal of Clinical Investigation
|
June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency
T Bourgeron, D Chretien, J Poggi-Bach, et al.
Translational Psychiatry
|
November 27, 2025
The influence of CHRNA5 and D398N missense variation on social and emotional behaviors in rodents and humans
F de Chaumont, R Icick, P Gorwood, et al.
Genomics
|
April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene
E Seboun, S Barbaux, T Bourgeron, et al.
Molecular Psychiatry
|
February 13, 2002
Y chromosome haplogroups in autistic subjects
S Jamain, H Quach, L Quintana-Murci, et al.
Genes, Brain, and Behavior
|
September 20, 2012
Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4
E Ey, M Yang, A M Katz, et al.
Translational Psychiatry
|
November 12, 2014
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders
C Pagan, R Delorme, J Callebert, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Journal of Inherited Metabolic Disease
|
January 1, 1996
Clinical presentation of mitochondrial disorders in childhood
A Munnich, A Rötig, D Chretien, et al.
Molecular Psychiatry
|
March 29, 2002
Linkage and association of the glutamate receptor 6 gene with autism
S Jamain, C Betancur, H Quach, et al.
Nature Genetics
|
October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
T Bourgeron, P Rustin, D Chretien, et al.
Translational Psychiatry
|
August 22, 2013
Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening
C Boissart, A Poulet, P Georges, et al.
The Journal of Clinical Investigation
|
June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency
T Bourgeron, D Chretien, J Poggi-Bach, et al.
Translational Psychiatry
|
November 27, 2025
The influence of CHRNA5 and D398N missense variation on social and emotional behaviors in rodents and humans
F de Chaumont, R Icick, P Gorwood, et al.
Genomics
|
April 15, 1997
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene
E Seboun, S Barbaux, T Bourgeron, et al.
Molecular Psychiatry
|
February 13, 2002
Y chromosome haplogroups in autistic subjects
S Jamain, H Quach, L Quintana-Murci, et al.
Genes, Brain, and Behavior
|
September 20, 2012
Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4
E Ey, M Yang, A M Katz, et al.
Translational Psychiatry
|
November 12, 2014
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders
C Pagan, R Delorme, J Callebert, et al.
Page
of 5