Sally I Sharp
Overview
Explore the profile of Sally I Sharp including associated specialties, affiliations and a list of published articles.
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20
Citations
804
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Recent Articles
1.
OBrien N, Quadri G, Lightley I, Sharp S, Guerrini I, Smith I, et al.
Alcohol Alcohol
. 2022 Aug;
57(5):581-588.
PMID: 35952336
Aims: Wernicke-Korsakoff syndrome (WKS) is commonly associated with chronic alcohol misuse, a condition known to have multiple detrimental effects on thiamine metabolism. This study was conducted to identify genetic variants...
2.
Singh T, Poterba T, Curtis D, Akil H, Eissa M, Barchas J, et al.
Nature
. 2022 Apr;
604(7906):509-516.
PMID: 35396579
Rare coding variation has historically provided the most direct connections between gene function and disease pathogenesis. By meta-analysing the whole exomes of 24,248 schizophrenia cases and 97,322 controls, we implicate...
3.
Al Eissa M, Sharp S, OBrien N, Fiorentino A, Bass N, Curtis D, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2019 Mar;
180(4):258-265.
PMID: 30859703
A rare microcephalin 1 gene (MCPH1) variant rs61749465A>G (p.Asp61Gly) with prior evidence for association with schizophrenia (p = 3.78 × 10 ) was tested for association in 2,300 bipolar disorder...
4.
Al Eissa M, Fiorentino A, Sharp S, OBrien N, Wolfe K, Giaroli G, et al.
Ann Hum Genet
. 2017 Nov;
82(2):88-92.
PMID: 29148569
Schizophrenia (SCZ) is a severe, highly heritable psychiatric disorder. Elucidation of the genetic architecture of the disorder will facilitate greater understanding of the altered underlying neurobiological mechanisms. The aim of...
5.
Leonenko G, Richards A, Walters J, Pocklington A, Chambert K, Al Eissa M, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2017 Jul;
174(7):724-731.
PMID: 28719003
Risk of schizophrenia is conferred by alleles occurring across the full spectrum of frequencies from common SNPs of weak effect through to ultra rare alleles, some of which may be...
6.
Fiorentino A, Sharp S, Kandaswamy R, Gurling H, Bass N, McQuillin A
Psychiatr Genet
. 2016 Feb;
26(2):99-100.
PMID: 26901794
No abstract available.
7.
Fiorentino A, Sharp S, McQuillin A
Eur J Hum Genet
. 2014 Nov;
23(9):1200-6.
PMID: 25406999
The SLC1A2 gene encodes the excitatory amino acid transporter 2 (EAAT2). Glutamate is the major mediator of excitatory neurotransmission and EAAT2 is responsible for clearing the neurotransmitter from the synaptic...
8.
OBrien N, Way M, Kandaswamy R, Fiorentino A, Sharp S, Quadri G, et al.
Psychiatr Genet
. 2014 Jul;
24(6):277-8.
PMID: 25046171
No abstract available.
9.
Sharp S, McQuillin A, Marks M, Hunt S, Stanford S, Lydall G, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2014 May;
165B(4):373-80.
PMID: 24817687
Single nucleotide polymorphisms (SNPs) in the tachykinin receptor 1 gene (TACR1) are nominally associated with bipolar affective disorder (BPAD) in a genome-wide association study and in several case-control samples of...
10.
Sharp S, Hu Y, Weymer J, Rizig M, McQuillin A, Hunt S, et al.
Psychiatr Genet
. 2013 Jul;
23(4):153-62.
PMID: 23811784
Objectives: Clathrin-mediated endocytosis (CME) is an intracellular trafficking mechanism for packaging cargo, including G protein-coupled receptors (GPCRs), into clathrin-coated vesicles (CCVs). The antipsychotic chlorpromazine inhibits CCV assembly of adaptor protein...