5 results match your criteria: "Cardiff University S.[Affiliation]"

Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders.

Neuropsychopharmacology

January 2024

Cardiff University's Brain Research Imaging Centre (CUBRIC), School of Psychology, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Although many genetic risk factors for psychiatric and neurodevelopmental disorders have been identified, the neurobiological route from genetic risk to neuropsychiatric outcome remains unclear. 22q11.2 deletion syndrome (22q11.

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The inherited chronic pain patient.

Aust Fam Physician

December 2016

FRACGP, MMed, MBBS, BMedSc, DipPracDerm(Cardiff), is a general practitioner, Romsey Victoria, Honorary Lecturer, Department of General Practice, The University of Melbourne, Victoria and a tutor with Cardiff University's Diploma of Practical Dermatology course.

Background: The 'inherited' patient, where a patient switches to a new doctor, is a common and potentially challenging scenario, especially where drugs of dependence are involved. There are few resources to guide general practitioners (GPs) with an approach that ensures compassion and rational clinical decision-making.

Objective: The aim of this article is to guide GPs in an approach to taking over the care of an inherited patient and focuses on considerations of rational prescribing.

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Measures of Psychosis Proneness and Genetic Risk for Schizophrenia-Reply.

JAMA Psychiatry

June 2016

Centre for Academic Mental Health, School of Social and Community Medicine, University of Bristol, Bristol, England3MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University S.

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Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population.

JAMA Psychiatry

March 2016

Centre for Academic Mental Health, School of Social and Community Medicine, University of Bristol, Bristol, England3MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University S.

Importance: Schizophrenia is a highly heritable, polygenic condition characterized by a relatively diverse phenotype and frequent comorbid conditions, such as anxiety and depression. At present, limited evidence explains how genetic risk for schizophrenia is manifest in the general population.

Objective: To investigate the extent to which genetic risk for schizophrenia is associated with different phenotypes during adolescence in a population-based birth cohort.

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Do the former colonizing powers, like their former colonies, have "postcolonial medicine," and if so, where does it take place, who practices it, and upon whom? How has British medicine in particular responded to the huge cultural shifts represented by the rise of the New Commonwealth and associated postcolonial immigration? I address these questions through a case study of the medical and political responses to vitamin D deficiency among Britain's South Asian communities since the 1960s. My research suggests that in these contexts, diet frequently became a proxy or shorthand for culture (and religion, and race), while disease justified pressure to assimilate.

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