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Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders : Mental HealthYOUNG SHIN KIM; STATE, Matthew W.International journal of epidemiology. 2014, Vol 43, Num 2, pp 465-475, issn 0300-5771, 11 p.Article

Recent advances in the genetics of autism : Advances in understanding and treating autism spectrum disordersGUPTA, Abha R; STATE, Matthew W.Biological psychiatry (1969). 2007, Vol 61, Num 4, pp 429-437, issn 0006-3223, 9 p.Article

Progress in Cytogenetics: Implications for Child PsychopathologyHOFFMAN, Ellen J; STATE, Matthew W.Journal of the American Academy of Child and Adolescent Psychiatry. 2010, Vol 49, Num 8, pp 736-751, issn 0890-8567, 16 p.Article

L-Histidine Decarboxylase and Tourette's SyndromeERCAN-SENCICEK, A. Gulhan; STILLMAN, Althea A; TISCHFIELD, Jay A et al.The New England journal of medicine. 2010, Vol 362, Num 20, pp 1901-1908, issn 0028-4793, 8 p.Article

Susceptibility loci for intracranial aneurysm in European and Japanese populationsBILGUVAR, Kaya; YASUNO, Katsuhito; GAAL, Emilia et al.Nature genetics. 2008, Vol 40, Num 12, pp 1472-1477, issn 1061-4036, 6 p.Article

De novo mutations revealed by whole-exome sequencing are strongly associated with autismSANDERS, Stephan J; MURTHA, Michael T; WALKER, Michael F et al.Nature (London). 2012, Vol 485, Num 7397, pp 237-241, issn 0028-0836, 5 p.Article

Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with AutismFERNANDEZ, Thomas V; SANDERS, Stephan J; BILGUVAR, Kaya et al.Biological psychiatry (1969). 2012, Vol 71, Num 5, pp 392-402, issn 0006-3223, 11 p.Article

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationTÜYSÜZ, Beyhan; BAYRAKLI, Fatih; OZTURK, Ali K et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 2, pp 119-125, issn 1364-6745, 7 p.Article

Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous TraitCHASTE, Pauline; KLEI, Lambertus; GESCHWIND, Daniel et al.Biological psychiatry (1969). 2013, Vol 74, Num 8, pp 576-584, issn 0006-3223, 9 p.Article

Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with EpilepsyNOVARINO, Gaia; EL-FISHAWY, Paul; GULHAN ERCAN-SENCICEK, A et al.Science (Washington, D.C.). 2012, Vol 338, Num 6105, pp 394-397, issn 0036-8075, 4 p.Article

High levels of histidine decarboxylase in the striatum of mice and ratsKRUSONG, Kuakarun; GULHAN ERCAN-SENCICEK, A; MEIYU XU et al.Neuroscience letters. 2011, Vol 495, Num 2, pp 110-114, issn 0304-3940, 5 p.Article

Molecular Characterization of a Patient With 3p Deletion Syndrome and a Review of the LiteratureFERNANDEZ, Thomas V; GARCIA-GONZALEZ, I. J; GONZALEZ-CRUZ, M et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 21, pp 2746-2752, issn 1552-4825, 7 p.Article

Sequence variants in SLITRK1 are associated with Tourette's syndromeABELSON, Jesse F; KWAN, Kenneth Y; DAVIS, Nicole R et al.Science (Washington, D.C.). 2005, Vol 310, Num 5746, pp 317-320, issn 0036-8075, 4 p.Article

Rare independent mutations in renal salt handling genes contribute to blood pressure variationWEIZHEN JI; JIA NEE FOO; O'ROAK, Brian J et al.Nature genetics. 2008, Vol 40, Num 5, pp 592-599, issn 1061-4036, 8 p.Article

Haplotype Evolution of SLITRK1, a Candidate Gene for Gilles de la Tourette SyndromeSPEED, William C; O'ROAK, Brian J; TARNOK, Zsanett et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 4, pp 463-466, issn 1552-4841, 4 p.Article

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