Joanne E Morgan
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Explore the profile of Joanne E Morgan including associated specialties, affiliations and a list of published articles.
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20
Citations
830
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Recent Articles
1.
Zahova S, Humby T, Davies J, Morgan J, Isles A
Transl Psychiatry
. 2021 Aug;
11(1):433.
PMID: 34417445
Prader-Willi Syndrome (PWS) is a neurodevelopmental disorder caused by mutations affecting paternal chromosome 15q11-q13, and characterized by hypotonia, hyperphagia, impaired cognition, and behavioural problems. Psychotic illness is a challenging problem...
2.
Morgan J, Channon S, Penny H, Waters C
Eur Child Adolesc Psychiatry
. 2019 Dec;
30(1):5-40.
PMID: 31792693
Maternal depression is associated with adverse child outcomes including antisocial behaviour (ASB). Prospective longitudinal studies have focused on the timing and cumulative exposure to maternal depression to further delineate the...
3.
OBrien H, Hannon E, Hill M, Toste C, Robertson M, Morgan J, et al.
Genome Biol
. 2018 Nov;
19(1):194.
PMID: 30419947
Background: Genetic influences on gene expression in the human fetal brain plausibly impact upon a variety of postnatal brain-related traits, including susceptibility to neuropsychiatric disorders. However, to date, there have...
4.
Watson C, El-Asrag M, Parry D, Morgan J, Logan C, Carr I, et al.
PLoS One
. 2014 Aug;
9(8):e104281.
PMID: 25133751
Purpose: Retinal dystrophies are genetically heterogeneous, resulting from mutations in over 200 genes. Prior to the development of massively parallel sequencing, comprehensive genetic screening was unobtainable for most patients. Identifying...
5.
Bowen K, Morgan J, Moore S, van Goozen S
J Psychopathol Behav Assess
. 2014 Mar;
36(1):60-73.
PMID: 24610972
Antisocial individuals have problems recognizing negative emotions (e.g. Marsh & Blair in Neuroscience and Biobehavioral Reviews 32:454-465, 2009); however, due to issues with sampling and different methods used, previous findings...
6.
Logan C, Szabadkai G, Sharpe J, Parry D, Torelli S, Childs A, et al.
Nat Genet
. 2013 Dec;
46(2):188-93.
PMID: 24336167
Mitochondrial Ca(2+) uptake has key roles in cell life and death. Physiological Ca(2+) signaling regulates aerobic metabolism, whereas pathological Ca(2+) overload triggers cell death. Mitochondrial Ca(2+) uptake is mediated by...
7.
Watson C, Crinnion L, Morgan J, Harrison S, Diggle C, Adlard J, et al.
Hum Mutat
. 2013 Dec;
35(4):434-41.
PMID: 24307375
Targeted hybridization enrichment prior to next-generation sequencing is a widespread method for characterizing sequence variation in a research setting, and is being adopted by diagnostic laboratories. However, the number of...
8.
Chambers P, Stead L, Morgan J, Carr I, Sutton K, Watson C, et al.
Hum Mutat
. 2012 Aug;
34(1):248-54.
PMID: 22915446
We describe a sensitive technique for mutation detection using clonal sequencing. We analyzed DNA extracted from 13 cancer cell lines and 35 tumor samples and applied a novel approach to...
9.
Parry D, Brookes S, Logan C, Poulter J, El-Sayed W, Al-Bahlani S, et al.
Am J Hum Genet
. 2012 Aug;
91(3):565-71.
PMID: 22901946
Autozygosity mapping and clonal sequencing of an Omani family identified mutations in the uncharacterized gene, C4orf26, as a cause of recessive hypomineralized amelogenesis imperfecta (AI), a disease in which the...
10.
Diggle C, Parry D, Logan C, Laissue P, Rivera C, Restrepo C, et al.
Hum Mutat
. 2012 May;
33(8):1175-81.
PMID: 22553128
Pachydermoperiostosis, or primary hypertrophic osteoarthropathy (PHO), is an inherited multisystem disorder, whose features closely mimic the reactive osteoarthropathy that commonly accompanies neoplastic and inflammatory pathologies. We previously described deficiency of...