proline has been researched along with Autism in 3 studies
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 | 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 |
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.
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 |
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.
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.
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 |