Three autism candidate genes: a synthesis of human genetic analysis with other disciplines

scientific article published in April 2005

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1016/J.IJDEVNEU.2004.10.004
P698PubMed publication ID15749247
P5875ResearchGate publication ID7985467

P2093author name stringChristopher W Bartlett
James H Millonig
Linda M Brzustowicz
Neda Gharani
P433issue2-3
P921main subjectautismQ38404
P304page(s)221-234
P577publication date2005-04-01
P1433published inInternational Journal of Developmental NeuroscienceQ6051371
P1476titleThree autism candidate genes: a synthesis of human genetic analysis with other disciplines
P478volume23

Reverse relations

cites work (P2860)
Q47575039A candidate circuit approach to investigating autism
Q34285695A genetic survey of fluoxetine action on synaptic transmission in Caenorhabditis elegans
Q28274390A heterogeneity-based genome search meta-analysis for autism-spectrum disorders
Q41879263Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han population
Q38104700Autism spectrum disorders: the quest for genetic syndromes
Q50303536Autism: genetics
Q36772023Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings
Q33892169Bio-collections in autism research
Q38445977Decreased aggression and increased repetitive behavior in Pten haploinsufficient mice
Q23913111Density and function of central serotonin (5-HT) transporters, 5-HT1A and 5-HT2A receptors, and effects of their targeting on BTBR T+tf/J mouse social behavior
Q24627520Genetics of autistic disorders: review and clinical implications
Q28508076Haploinsufficiency for Pten and Serotonin transporter cooperatively influences brain size and social behavior
Q26769948In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders
Q35151007MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders
Q26853035Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders
Q29618652Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains
Q35987563Neonatal serotonin depletion alters behavioral responses to spatial change and novelty
Q53402655Neuroimmunologic and Neurotrophic Interactions in Autism Spectrum Disorders: Relationship to Neuroinflammation.
Q34155796Pharmacogenetics of antidepressant response
Q36462150Review of animal models for autism: implication of thyroid hormone
Q24535886Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus
Q40134586The 5-HTTLPR polymorphism in South African healthy populations: a global comparison
Q34325623The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
Q34542748The developmental neurobiology of autism spectrum disorder.
Q38848403The frontier of RNA metamorphosis and ribosome signature in neocortical development.
Q37469452The mouse Engrailed genes: a window into autism
Q37035245The serotonin transporter gene and effectiveness of SSRIs.
Q28277009The ups and downs of Wnt signaling in prevalent neurological disorders

Search more.