W H Raskind
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Explore the profile of W H Raskind including associated specialties, affiliations and a list of published articles.
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56
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1239
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Recent Articles
1.
Doyle T, Hayes M, Chen D, Raskind W, Watts V
Biochem Pharmacol
. 2019 Feb;
163:169-177.
PMID: 30772269
Adenylyl cyclases are key points for the integration of stimulatory and inhibitory G protein-coupled receptor (GPCR) signals. Adenylyl cyclase type 5 (AC5) is highly expressed in striatal medium spiny neurons...
2.
Chapman N, Bernier R, Webb S, Munson J, Blue E, Chen D, et al.
Hum Genet
. 2018 Oct;
137(10):807-815.
PMID: 30276537
Hundreds of genes have been implicated in autism spectrum disorders (ASDs). In genetically heterogeneous conditions, large families with multiple affected individuals provide strong evidence implicating a rare variant, and replication...
3.
Rubinstein M, Patowary A, Stanaway I, McCord E, Nesbitt R, Archer M, et al.
Mol Psychiatry
. 2016 Dec;
23(2):231-239.
PMID: 27956748
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder often accompanied by intellectual disability, language impairment and medical co-morbidities. The heritability of autism is high and multiple genes have been...
4.
Korvatska O, Estes A, Munson J, Dawson G, Bekris L, Kohen R, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2011 Mar;
156B(3):303-11.
PMID: 21438139
Linkage to 7q has been the most robust genetic finding in familial autism. A previous scan of multiplex families with autism spectrum disorders found a linkage signal of genome-wide significance...
5.
Zabetian C, Samii A, Mosley A, Roberts J, Leis B, Yearout D, et al.
Neurology
. 2005 Sep;
65(5):741-4.
PMID: 16157909
Referral-based studies indicate that a mutation (G2019S) in exon 41 of the LRRK2 gene might be a common cause of Parkinson disease (PD). The authors sequenced leucine-rich repeat kinase 2...
6.
Chen D, Cimino P, Ranum L, Zoghbi H, Yabe I, Schut L, et al.
Neurology
. 2005 Apr;
64(7):1258-60.
PMID: 15824357
Spinocerebellar ataxia 14 (SCA14) is associated with missense mutations in the protein kinase C gamma gene (PRKCG), rather than a nucleotide repeat expansion. In this large-scale study of PRKCG in...
7.
Raskind W, Igo R, Chapman N, Berninger V, Thomson J, Matsushita M, et al.
Mol Psychiatry
. 2005 Mar;
10(7):699-711.
PMID: 15753956
Dyslexia is a common and complex developmental disorder manifested by unexpected difficulty in learning to read. Multiple different measures are used for diagnosis, and may reflect different biological pathways related...
8.
Raskind W, Hsu L, Berninger V, Thomson J, Wijsman E
Behav Genet
. 2001 Mar;
30(5):385-96.
PMID: 11235984
There is evidence for genetic contributions to reading disability, but the phenotypic heterogeneity associated with the clinical diagnosis may make identification of the underlying genetic basis difficult. In order to...
9.
Wijsman E, Peterson D, Leutenegger A, Thomson J, Goddard K, Hsu L, et al.
Am J Hum Genet
. 2000 Aug;
67(3):631-46.
PMID: 10924405
Dyslexia is a common and complex disorder with evidence for a genetic component. Multiple loci (i.e., quantitative-trait loci [QTLs]) are likely to be involved, but the number is unknown. Diagnosis...
10.
Raskind W, Niakan K, Wolff J, Matsushita M, Vaughan T, Stamatoyannopoulos G, et al.
Blood
. 2000 Mar;
95(7):2262-8.
PMID: 10733494
X-linked thrombocytopenia with thalassemia (XLTT; Online Mendelian Inheritance in Man [OMIM] accession number 314050) is a rare disorder characterized by thrombocytopenia, platelet dysfunction, splenomegaly, reticulocytosis, and unbalanced hemoglobin chain synthesis....