proline and Autism

proline has been researched along with Autism in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (66.67)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Sonneville, LM; Hidding, E; Swaab, H; van Engeland, H; Vorstman, JA	1
Cossette, P; Drapeau, P; Fombonne, E; Gauthier, J; Hamdan, FF; Joober, R; Lafrenière, RG; Lapointe, L; Laurent, S; Marineau, C; Mottron, L; Piton, A; Rouleau, GA; Spiegelman, D; St-Onge, J	1
Andres, C; Barthelemy, C; Bendavid, C; Bonnet-Brilhault, F; Briault, S; Campion, D; David, V; Di Rosa, G; Drouin-Garraud, V; Dubourg, C; Faivre, L; Frébourg, T; Germano, E; Goldenberg, A; Guilmatre, A; Henry, C; Impallomeni, C; Joly-Helas, G; Laumonnier, F; Layet, V; Le Vacon, G; Legallic, S; Mosca, AL; Odent, S; Pinoit, JM; Rosier, A; Saugier Veber, P; Tortorella, G	1

Reviews

1 review(s) available for proline and Autism

Article	Year
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. Archives of general psychiatry, 2009, Volume: 66, Issue:9 Topics: Adolescent; Adult; Autistic Disorder; Case-Control Studies; Chromosome Mapping; Comparative Genomic Hybridization; Female; Gene Dosage; Gene Frequency; Genotype; Humans; In Situ Hybridization, Fluorescence; Intellectual Disability; Male; Neurogenesis; Oligonucleotide Array Sequence Analysis; Proline; Psychotic Disorders; Schizophrenia	2009

Article

Year

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

Archives of general psychiatry, 2009, Volume: 66, Issue:9

Topics: Adolescent; Adult; Autistic Disorder; Case-Control Studies; Chromosome Mapping; Comparative Genomic Hybridization; Female; Gene Dosage; Gene Frequency; Genotype; Humans; In Situ Hybridization, Fluorescence; Intellectual Disability; Male; Neurogenesis; Oligonucleotide Array Sequence Analysis; Proline; Psychotic Disorders; Schizophrenia

2009

Other Studies

2 other study(ies) available for proline and Autism

Article	Year
The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome. Clinical genetics, 2016, Volume: 90, Issue:5 Topics: Adolescent; Autistic Disorder; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Epistasis, Genetic; Face; Female; Genotype; Humans; Male; Penetrance; Proline; Sequence Deletion; Social Behavior	2016
Novel de novo SHANK3 mutation in autistic patients. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009, Apr-05, Volume: 150B, Issue:3 Topics: Amino Acid Sequence; Amino Acid Substitution; Autistic Disorder; Carrier Proteins; Case-Control Studies; Cohort Studies; DNA Mutational Analysis; Genetic Markers; Humans; Introns; Male; Microsatellite Repeats; Molecular Sequence Data; Mutation; Mutation, Missense; Nerve Tissue Proteins; Phenotype; Proline; RNA Splice Sites; Sequence Deletion; Sequence Homology, Amino Acid	2009

Article

Year

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.

Clinical genetics, 2016, Volume: 90, Issue:5

Topics: Adolescent; Autistic Disorder; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Epistasis, Genetic; Face; Female; Genotype; Humans; Male; Penetrance; Proline; Sequence Deletion; Social Behavior

2016

Novel de novo SHANK3 mutation in autistic patients.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009, Apr-05, Volume: 150B, Issue:3

Topics: Amino Acid Sequence; Amino Acid Substitution; Autistic Disorder; Carrier Proteins; Case-Control Studies; Cohort Studies; DNA Mutational Analysis; Genetic Markers; Humans; Introns; Male; Microsatellite Repeats; Molecular Sequence Data; Mutation; Mutation, Missense; Nerve Tissue Proteins; Phenotype; Proline; RNA Splice Sites; Sequence Deletion; Sequence Homology, Amino Acid

2009