Anorexia Nervosa Research Paper

Anorexia Nervosa Research Paper-20
ANGI (Australia and New Zealand): We thank the Australia & and New Zealand Academy for Eating Disorders for assistance with recruitment and publicity. Communications for their efforts in promoting the study and the Butterfly Foundation for their ongoing support of anorexia nervosa research in Australia and EDANZ in New Zealand. PGC: We are deeply indebted to the investigators who comprise the PGC and to the hundreds of thousands of individuals who have shared their life experiences with PGC investigators and the contributing studies. We thank the QSkin Sun and Health Study for controls. We are grateful to the Children’s Hospital of Philadelphia (CHOP), the Price Foundation Collaborative Group (PFCG), Genetic Consortium for Anorexia Nervosa (GCAN), Wellcome Trust Case-Control Consortium-3 (WTCCC-3), the UK Biobank and all PGC-ED members for their support in providing individual samples used in this study. This study also represents independent research partly funded by the English National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London and the NIHR Bio Resource. You are using a browser version with limited support for CSS.

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Genome-wide summary statistics for the meta-analysis are freely downloadable from the website of the PGC ( was the lead principal investigator of ANGI, and P.

Individual-level data are deposited in db Ga P ( for ANGI-ANZ/SE/US (accession number phs001541.v1.p1) and CHOP/PFCG (accession number phs000679.v1.p1).

Anorexia Nervosa (AN) is a complex and clinically challenging syndrome.

Intended for specialist audiences, this narrative review aims to summarise the available literature related to assessment in the adult patient context, synthesising both research evidence and clinical consensus guidelines.

We thank all study volunteers, study coordinators and research staff who enabled this study.

Anorexia Nervosa Research Paper Sample Argument Essay Topics

ANGI: The Anorexia Nervosa Genetics Initiative is an initiative of the Klarman Family Foundation.

collected and managed the ANGI samples at sites and assisted with site-specific study co-ordination.

PGC-ED members and other individuals contributed to sample acquisition and made individual data from subjects available: R.

We thank SURFsara ( for support in using the Lisa Compute Cluster. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the English Department of Health and Social Care.

High performance computing facilities were funded with capital equipment grants from the GSTT Charity (TR130505) and Maudsley Charity (980).

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