Alex D Shaw
Overview
Explore the profile of Alex D Shaw including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
166
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Recent Articles
1.
Toma C, Shaw A, Heath A, Pierce K, Mitchell P, Schofield P, et al.
J Psychiatry Neurosci
. 2021 Mar;
46(2):E247-E257.
PMID: 33729739
Background: Bipolar disorder is a highly heritable psychiatric condition for which specific genetic factors remain largely unknown. In the present study, we used combined whole-exome sequencing and linkage analysis to...
2.
Toma C, Shaw A, Overs B, Mitchell P, Schofield P, Cooper A, et al.
JAMA Netw Open
. 2020 May;
3(5):e203382.
PMID: 32383744
No abstract available.
3.
Dobson-Stone C, Hallupp M, Shahheydari H, Ragagnin A, Chatterton Z, Carew-Jones F, et al.
Brain
. 2020 Mar;
143(3):783-799.
PMID: 32185393
Frontotemporal dementia and amyotrophic lateral sclerosis are clinically and pathologically overlapping disorders with shared genetic causes. We previously identified a disease locus on chromosome 16p12.1-q12.2 with genome-wide significant linkage in...
4.
Torrico B, Shaw A, Mosca R, Vivo-Luque N, Hervas A, Fernandez-Castillo N, et al.
J Psychiatry Neurosci
. 2019 May;
44(5):350-359.
PMID: 31094488
Background: Previous research has implicated de novo and inherited truncating mutations in autism-spectrum disorder. We aim to investigate whether the load of inherited truncating mutations contributes similarly to high-functioning autism,...
5.
Toma C, Pierce K, Shaw A, Heath A, Mitchell P, Schofield P, et al.
PLoS Genet
. 2018 Dec;
14(12):e1007535.
PMID: 30586385
The contactin-associated protein-like 2 (CNTNAP2) gene is a member of the neurexin superfamily. CNTNAP2 was first implicated in the cortical dysplasia-focal epilepsy (CDFE) syndrome, a recessive disease characterized by intellectual...
6.
Toma C, Shaw A, Allcock R, Heath A, Pierce K, Mitchell P, et al.
Transl Psychiatry
. 2018 Mar;
8(1):65.
PMID: 29531218
Bipolar disorder (BD) is a complex psychiatric condition with high heritability, the genetic architecture of which likely comprises both common variants of small effect and rare variants of higher penetrance,...
7.
Fullerton J, Klauser P, Lenroot R, Shaw A, Overs B, Heath A, et al.
Transl Psychiatry
. 2018 Jan;
8(1):21.
PMID: 29353880
Brain white matter abnormalities are evident in individuals with schizophrenia, and also their first-degree relatives, suggesting that some alterations may relate to underlying genetic risk. The ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2...
8.
Wilcox H, Fullerton J, Glowinski A, Benke K, Kamali M, Hulvershorn L, et al.
J Am Acad Child Adolesc Psychiatry
. 2017 Nov;
56(12):1073-1080.
PMID: 29173741
Objective: Bipolar disorder (BD) is one of the most heritable psychiatric conditions and is associated with high suicide risk. To explore the reasons for this link, this study examined the...
9.
Aas M, Blokland G, Chawner S, Choi S, Estrada J, Forsingdal A, et al.
Psychiatr Genet
. 2015 Nov;
26(1):1-47.
PMID: 26565519
The XXII World Congress of Psychiatric Genetics, sponsored by the International Society of Psychiatric Genetics, took place in Copenhagen, Denmark, on 12-16 October 2014. A total of 883 participants gathered...
10.
Dobson-Stone C, Shaw A, Hallupp M, Bartley L, McCann H, Brooks W, et al.
Brain
. 2015 May;
138(Pt 10):e385.
PMID: 25953780
No abstract available.