about
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyMolecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionNeurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhoodfMRI investigation of visual change detection in adults with autism.A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.Investigation of two variants in the DOPA decarboxylase gene in patients with autism.Levels of autistic traits in anorexia nervosa: a comparative psychometric studyCase report: an unexpected link between partial deletion of the SHANK3 gene and Heller's dementia infantilis, a rare subtype of autism spectrum disorder.Y chromosome haplogroups in autistic subjectsHypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disordersClinical, cellular, and neuropathological consequences of AP1S2 mutations: further delineation of a recognizable X-linked mental retardation syndrome.Analysis of ten candidate genes in autism by association and linkage.Effect of genetically caused excess of brain gamma-hydroxybutyric acid and GABA on sleep.Tracking social motivation systems deficits: the affective neuroscience view of autism.Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey.Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders.[Left temporal arachnoid cyst and specific learning disorders associated with Pervasive Developmental Disorders - Not Otherwise Specified (PDD-NOS): contributions of an integrative neuropsychomotor, neuropsychological, psychopathological and neurosuWhole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.Perception of complex sounds in autism: abnormal auditory cortical processing in children.[Towards early screening of autism]Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X-linked intellectual disability with distinctive facial appearance.ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
P50
Q28140978-F4F847BA-E1AB-4D0F-9112-3E3B165E4AF8Q28245038-A5ED316B-A6A7-421C-A55B-DDFACBBBD3C2Q28287112-AD554A15-3467-4F33-A2D3-B0FDC11F5901Q30447897-7C71F94F-C5A7-41AF-90DD-AA3DFBD76ED8Q33892998-C099ADCB-6AE4-4F3C-9A33-2E46F551C0DFQ34126958-ADB761D7-89E0-46A3-9224-B4B0EF672D38Q34981901-08F7784D-F30F-461C-8B72-01E4A073E804Q35816456-1089C1CA-AAC1-46A5-B97A-85D1B40158B8Q35854925-A9E24CFB-2C4D-41FD-84AD-178AE240D38EQ36249309-EEBB4206-16B3-4DE0-88D7-1BA80F54FBAAQ36927121-3AF843F7-0C8C-467C-A151-BB6AE097C113Q43825198-84B63AA8-F746-472F-853B-7E64835E0BEBQ45714524-00438A65-137A-4D82-BE13-F8CB901E653CQ46710484-ACD8B3A4-35AE-494E-866F-4715A503619EQ47636360-B78A1860-C5BA-447D-A76A-9526C743112EQ48102182-BF6CFE46-71CC-46DB-89AA-63A22045C9E9Q48331170-239F4D66-5821-4913-ABF4-DD3511BF8D62Q48822360-11B1FE0A-5325-4131-BF29-5A0AF6A5D547Q50301184-6AACD9C8-2DF1-4811-BE0E-986B4D5377CFQ50301262-9D81C4A3-1922-43C2-BCCE-BADB7A2C5FE5Q50307355-953FFD4E-10C6-46F6-AEB8-93252C9289A7Q50344012-D73793CA-AE0E-4B18-884E-1ED1192B93D8Q51909499-697750D0-C346-4A79-AC94-5D6D0F0C17D2Q54261387-07FAB49C-CABE-412D-9B57-07283372F92CQ55044402-9065C33E-1890-410F-9407-63BB56F20170
P50
description
researcher ORCID ID = 0000-0001-8746-0576
@en
wetenschapper
@nl
name
Anne Philippe
@ast
Anne Philippe
@en
Anne Philippe
@es
Anne Philippe
@nl
type
label
Anne Philippe
@ast
Anne Philippe
@en
Anne Philippe
@es
Anne Philippe
@nl
altLabel
Anne PHILIPPE
@en
prefLabel
Anne Philippe
@ast
Anne Philippe
@en
Anne Philippe
@es
Anne Philippe
@nl
P106
P21
P31
P496
0000-0001-8746-0576