38 research outputs found
Improving Genetic Prediction by Leveraging Genetic Correlations Among Human Diseases and Traits
- Author
- Adolfsson A.N.
- Agartz I.
- Agerbo E.
- Akil H.
- Albani D.
- Allardyce J.
- Alliey-Rodriguez N.
- Als T.D.
- Amin F.
- Anjorin A.
- Awasthi S.
- Azevedo M.H.
- Badner J.A.
- Barchas J.D.
- Bass N.
- Bauer M.
- Bellivier F.
- Bergen S.E.
- Black D.W.
- Blackwood D.H.R.
- Boks M.
- Boocock J.
- Bruggeman R.
- Buccola N.G.
- Budde M.
- Bunney W.
- Burmeister M.
- Bybjerg-Grauholm J.
- Byerley W.
- Bækvad-Hansen M.
- Børglum A.D.
- Casas M.
- Cervantes P.
- Charney A.W.
- Choudhury K.
- Clarke T.K.
- Cloninger C.R.
- Coleman J.R.I.
- Corvin A.
- Coryell W.
- Craddock N.
- Craig D.
- Cruceanu C.
- Curtis D.
- Czerski P.M.
- Dale A.M.
- Daly M.J.
- Datta S.
- De Haan L.
- de Leeuw C.A.
- Degenhardt F.
- Del-Favero J.
- Djurovic S.
- Dobbyn A.L.
- Donohoe G.J.
- Duan J.
- Dudbridge F.
- Elvsåshagen T.
- Escott-Price V.
- Etain B.
- Fan C.C.
- Fanous A.
- Fischer S.B.
- Flickinger M.
- Foroud T.M.
- Forstner A.J.
- Forty L.
- Frank J.
- Fraser C.
- Freedman R.
- Freimer N.B.
- Friedl M.
- Gade K.
- Garnham J.
- Gaspar H.A.
- Giambartolomei C.
- Gill M.
- Gordon S.D.
- Gordon-Smith Katherine
- Green E.K.
- Green M.J.
- Greenwood T.A.
- Grigoroiu-Serbanescu M.
- Grove J.
- Guan W.
- Gurling H.
- Hamshere M.L.
- Hansen C.S.
- Hartmann A.M.
- Hauser J.
- Hautzinger M.
- Heilbronner U.
- Herms S.
- Hipolito M.
- Hoffmann P.
- Holmans P.A.
- Huckins L.
- Jamain S.
- Juréus A.
- Kahn R.S.
- Kandaswamy R.
- Karlsson R.
- Keller M.C.
- Kennedy J.L.
- Kenny E.
- Kirov G.K.
- Kittel-Schneider S.
- Knott Sarah
- Knowles J.A.
- Kogevinas M.
- Koller A.C.
- Krabbendam L.
- Krasucki R.
- Kupka R.
- Lawrence J.
- Lawson W.B.
- Leber M.
- Leboyer M.
- Lee P.H.
- Lee S.H.
- Lencz T.
- Levinson D.F.
- Levy S.E.
- Li J.Z.
- Lieberman J.A.
- Lin D.-Y.
- Linszen D.H.
- Lissowska J.
- Liu C.
- Lucae S.
- Maaser A.
- MacIntyre D.J.
- Magnusson P.K.E.
- Mahon P.B.
- Maier R.M.
- Maier W.
- Malhotra A.K.
- Mattheisen M.
- Mattingsdal M.
- Mayoral F.
- McCarroll S.A.
- McGuffin P.
- McInnis M.G.
- McKay J.D.
- McQuillin A.
- Medeiros H.
- Medland S.E.
- Melle I.
- Meng F.
- Milani L.
- Milanova V.
- Montgomery G.W.
- Morris D.W.
- Mors O.
- Mortensen P.B.
- Mullins N.
- Myin-Germeys I.
- Mühleisen T.W.
- Neale B.M.
- Nievergelt C.M.
- Nwulia E.A.
- O'Donovan C.
- Olde Loohuis L.M.
- Ophoff R.A.
- Ori A.P.S.
- Oruc L.
- Owen M.J.
- Parra J.G.
- Pedersen C.B.
- Pedersen M.G.
- Perlis R.H.
- Perry Amy
- Pers T.H.
- Pfennig A.
- Pimm J.
- Potash J.B.
- Purcell S.M.
- Puri V.
- Quested D.J.
- Ramos-Quiroga J.A.
- Raymond Depaulo J.
- Regeer E.J.
- Reif A.
- Reinbold C.S.
- Rice J.P.
- Ripke S.
- Rivas F.
- Rivera M.
- Robinson M.R.
- Rossin L.
- Roussos P.
- Ruderfer D.M.
- Sanders A.R.
- Schatzberg A.F.
- Scheftner W.A.
- Schork N.J.
- Shehktman T.
- Shi J.
- Shilling P.D.
- Sigurdsson E.
- Sklar P.
- Slaney C.
- Smeland O.B.
- Sobell J.L.
- Spijker A.T.
- St Clair D.
- Stahl E.A.
- Steffens M.
- Steinberg S.
- Strauss J.S.
- Streit F.
- Strohmaier J.
- Stroup T.S.
- Szelinger S.
- Sánchez-Mora C.
- Thompson R.C.
- Thorgeirsson T.E.
- Treutlein J.
- Trubetskoy V.
- Trzaskowski M.
- Van Os J.
- Vedder H.
- Visscher P.M.
- Wang W.
- Wang Y.
- Watson S.J.
- Weickert C.S.
- Weickert T.W.
- Whitehead Pavlides J.M.
- Wiersma D.
- Witt S.H.
- Wray N.R.
- Xi S.
- Xu W.
- Yang J.
- Young A.H.
- Zammit S.
- Zandi P.
- Zhang P.
- Zhu Z.
- Zollner S.
- Publication venue
- Nature Publishing Group
- Publication date
- 07/03/2018
- Field of study
Genomic prediction has the potential to contribute to precision medicine. However, to date, the utility of such predictors is limited due to low accuracy for most traits. Here theory and simulation study are used to demonstrate that widespread pleiotropy among phenotypes can be utilised to improve genomic risk prediction. We show how a genetic predictor can be created as a weighted index that combines published genome-wide association study (GWAS) summary statistics across many different traits. We apply this framework to predict risk of schizophrenia and bipolar disorder in the Psychiatric Genomics consortium data, finding substantial heterogeneity in prediction accuracy increases across cohorts. For six additional phenotypes in the UK Biobank data, we find increases in prediction accuracy ranging from 0.7 for height to 47 for type 2 diabetes, when using a multi-trait predictor that combines published summary statistics from multiple traits, as compared to a predictor based only on one trait. © 2018 The Author(s)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder
- Author
- Abbott L.
- Adolfsson A.N.
- Adolfsson R.
- Agartz I.
- Agerbo E.
- Akil H.
- Albani D.
- Alda M.
- Alliey-Rodriguez N.
- Als T.D.
- Andreassen O.A.
- Anjorin A.
- Antilla V.
- Awasthi S.
- Backlund L.
- Badner J.A.
- Barchas J.D.
- Bass N.
- Bauer M.
- Baune B.T.
- Belliveau R.
- Bellivier F.
- Bergen S.E.
- Berrettini W.H.
- Biernacka J.M.
- BIOS Consortium
- Blackwood D.H.R.
- Boehnke M.
- Boks M.
- Boocock J.
- Breen G.
- Budde M.
- Bunney W.
- Burmeister M.
- Bybjerg-Grauholm J.
- Byerley W.
- Byrne E.M.
- Bækvad-Hansen M.
- Bøen E.
- Børglum A.D.
- Casas M.
- Cerrato F.
- Cervantes P.
- Chambert K.
- Charney A.W.
- Chen D.
- Churchhouse C.
- Cichon S.
- Clarke T.K.
- Coleman J.R.I.
- Corvin A.
- Coryell W.
- Craddock N.
- Craig D.W.
- Cruceanu C.
- Curtis D.
- Czerski P.M.
- Dale A.M.
- Daly M.J.
- Dannlowski U.
- de Jong S.
- de Leeuw C.A.
- Degenhardt F.
- Del-Favero J.
- DePaulo J.R.
- Di Florio A.
- Djurovic S.
- Dobbyn A.L.
- Dumont A.
- Edenberg H.J.
- Elvsåshagen T.
- eQTLGen Consortium
- Escott-Price V.
- Esko T.
- Etain B.
- Fan C.C.
- Fischer S.B.
- Flickinger M.
- Foroud T.M.
- Forstner A.J.
- Forty L.
- Frank J.
- Fraser C.
- Freimer N.B.
- Frisén L.
- Frye M.
- Fullerton J.M.
- Gade K.
- Gage D.
- Garnham J.
- Gaspar H.A.
- Gershon E.S.
- Giambartolomei C.
- Gill M.
- Goes F.
- Goldstein J.
- Gordon S.D.
- Gordon-Smith Katherine
- Green E.K.
- Green M.J.
- Greenwood T.A.
- Grigoroiu-Serbanescu M.
- Grove J.
- Guan W.
- Guzman-Parra J.
- Hamshere M.L.
- Hauser J.
- Hautzinger M.
- Heilbronner U.
- Herms S.
- Hipolito M.
- Hoffmann P.
- Holland D.
- Holmans P.A.
- Hougaard D.M.
- Huckins L.
- Hultman C.M.
- Jamain S.
- Johnson J.S.
- Jones I.
- Jones Lisa
- Juréus A.
- Kahn R.S.
- Kandaswamy R.
- Karlsson R.
- Kelsoe J.
- Kennedy J.L.
- Kirov G.
- Kittel-Schneider S.
- Knowles J.A.
- Kogevinas M.
- Koller A.C.
- Kupka R.
- Landén M.
- Lavebratt C.
- Lawrence J.
- Lawson W.B.
- Leber M.
- Leboyer M.
- Lee P.H.
- Levy S.E.
- Lewis C.M.
- Li J.Z.
- Li Q.S.
- Lissowska J.
- Liu C.
- Loohuis L.M.O.
- Lucae S.
- Maaser A.
- MacIntyre D.J.
- Mahon P.B.
- Maier W.
- Martin N.G.
- Martinsson L.
- Mattheisen M.
- Mayoral F.
- McCarroll S.
- McElroy S.L.
- McGuffin P.
- McInnis M.G.
- McIntosh A.M.
- McKay J.D.
- McMahon F.J.
- McQuillin A.
- Medeiros H.
- Medland S.E.
- Melle I.
- Meng F.
- Metspalu A.
- Milani L.
- Mitchell P.B.
- Montgomery G.W.
- Morken G.
- Morris D.W.
- Mors O.
- Mortensen P.B.
- Mullins N.
- Myers R.M.
- Mühleisen T.W.
- Müller-Myhsok B.
- Neale B.M.
- Nguyen H.
- Nievergelt C.M.
- Nimgaonkar V.
- Nordentoft M.
- Nurnberger J.I.
- Nwulia E.A.
- Nöthen M.M.
- O'Donovan C.
- O'Donovan M.C.
- Oedegaard K.J.
- Ophoff R.A.
- Ori A.P.S.
- Oruc L.
- Owen M.J.
- Paciga S.A.
- Pato C.
- Pato M.T.
- Pedersen C.B.
- Pedersen M.G.
- Perlis R.H.
- Perry Amy
- Pers T.H.
- Pfennig A.
- Posthuma D.
- Potash J.B.
- Purcell S.M.
- Ramos-Quiroga J.A.
- Regeer E.J.
- Reif A.
- Reinbold C.S.
- Ribasés M.
- Rice J.P.
- Richards A.L.
- Rietschel M.
- Ripke S.
- Rivas F.
- Rivera M.
- Rouleau G.A.
- Roussos P.
- Ruderfer D.M.
- Ryu E.
- Schalling M.
- Schatzberg A.F.
- Scheftner W.A.
- Schofield P.R.
- Schork N.J.
- Schulze T.G.
- Scott L.J.
- Serretti A.
- Shannon Weickert C.
- Shehktman T.
- Shilling P.D.
- Sigurdsson E.
- Sklar P.
- Slaney C.
- Smeland O.B.
- Smoller J.W.
- Sobell J.L.
- Spijker A.T.
- St Clair D.
- Stahl E.A.
- Stefansson H.
- Stefansson K.
- Steffens M.
- Steinberg S.
- Stordal E.
- Strauss J.S.
- Streit F.
- Strohmaier J.
- Sullivan P.F.
- Szelinger S.
- Sánchez-Mora C.
- Søholm Hansen C.
- the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium
- Thompson R.C.
- Thorgeirsson T.E.
- Treutlein J.
- Trubetskoy V.
- Trzaskowski M.
- Turecki G.
- Vaaler A.E.
- Vedder H.
- Vieta E.
- Vincent J.B.
- Wang W.
- Wang Y.
- Watson S.J.
- Weickert T.W.
- Werge T.
- Whitehead Pavlides J.M.
- Witt S.H.
- Wray N.R.
- Xi S.
- Xu W.
- Young A.H.
- Zandi P.
- Zhang P.
- Zöllner S.
- Ösby U.
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2019
- Field of study
This paper is dedicated to the memory of Psychiatric Genomics Consortium (PGC) founding member and Bipolar disorder working group co-chair Pamela Sklar. We thank the participants who donated their time, experiences and DNA to this research, and to the clinical and scientific teams that worked with them. We are deeply indebted to the investigators who comprise the PGC. The views expressed are those of the authors and not necessarily those of any funding or regulatory body. Analyses were carried out on the NL Genetic Cluster Computer (http://www.geneticcluster.org ) hosted by SURFsara, and the Mount Sinai high performance computing cluster (http://hpc.mssm.edu).Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide association study including 20,352 cases and 31,358 controls of European descent, with follow-up analysis of 822 variants with P<1x10-4 in an additional 9,412 cases and 137,760 controls. Eight of the 19 variants that were genome-wide significant (GWS, p < 5x10-8) in the discovery GWAS were not GWS in the combined analysis, consistent with small effect sizes and limited power but also with genetic heterogeneity. In the combined analysis 30 loci were GWS including 20 novel loci. The significant loci contain genes encoding ion channels, neurotransmitter transporters and synaptic components. Pathway analysis revealed nine significantly enriched gene-sets including regulation of insulin secretion and endocannabinoid signaling. BDI is strongly genetically correlated with schizophrenia, driven by psychosis, whereas BDII is more strongly correlated with major depressive disorder. These findings address key clinical questions and provide potential new biological mechanisms for BD.This work was funded in part by the Brain and Behavior Research Foundation, Stanley Medical Research Institute, University of Michigan, Pritzker Neuropsychiatric Disorders Research Fund L.L.C., Marriot Foundation and the Mayo Clinic Center for Individualized Medicine, the NIMH Intramural Research Program; Canadian Institutes of Health Research; the UK Maudsley NHS Foundation Trust, NIHR, NRS, MRC, Wellcome Trust; European Research Council; German Ministry for Education and Research, German Research Foundation IZKF of Münster, Deutsche Forschungsgemeinschaft, ImmunoSensation, the Dr. Lisa-Oehler Foundation, University of Bonn; the Swiss National Science Foundation; French Foundation FondaMental and ANR; Spanish Ministerio de Economía, CIBERSAM, Industria y Competitividad, European Regional Development Fund (ERDF), Generalitat de Catalunya, EU Horizon 2020 Research and Innovation Programme; BBMRI-NL; South-East Norway Regional Health Authority and Mrs. Throne-Holst; Swedish Research Council, Stockholm County Council, Söderström Foundation; Lundbeck Foundation, Aarhus University; Australia NHMRC, NSW Ministry of Health, Janette M O'Neil and Betty C Lynch
Long-range Angular Correlations On The Near And Away Side In P-pb Collisions At √snn=5.02 Tev
- Author
- Abelev B.
- Adam J.
- Adamova D.
- Adare A.M.
- Aggarwal M.
- Aglieri Rinella G.
- Agnello M.
- Agocs A.G.
- Agostinelli A.
- Ahammed Z.
- Ahmad A.
- Ahmad Khan S.
- Ahmad N.
- Ahn S.-A.
- Ahn S.U.
- Ajaz M.
- Akindinov A.
- Alaniz E.C.
- Alarcon do Passo Suaide A.
- Albino R.C.
- Aleksandrov D.
- Alessandro B.
- Alici A.
- Alkin A.
- Almaraz Avina E.J.
- Alme J.
- Alt T.
- Altini V.
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- Altsybeev I.
- Andrei C.
- Andronic A.
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- Anson C.D.
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- Antonioli P.
- Aparecida Moreira De Godoy D.
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- Appelshauser H.
- Arbor N.
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- Armesto N.
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- Augustinus A.
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- Publication venue
- 'Elsevier BV'
- Publication date
- 26/11/2015
- Field of study
7191/Mar294
Mapping local patterns of childhood overweight and wasting in low- and middle-income countries between 2000 and 2017
- Author
- Abbasalizad-Farhangi M.
- Abbasi M.
- Abbastabar H.
- Abdelalim A.
- Abdoli A.
- Abdollahi M.
- Abdollahpour I.
- Abdulkader R.S.
- Abebe N.D.
- Abebo T.A.
- Abegaz K.H.
- Abolhassani H.
- Abreu L.G.
- Abrigo M.R.M.
- Abushouk A.I.
- Accrombessi M.M.K.
- Acharya D.
- Adabi M.
- Adebiyi A.O.
- Adedeji I.A.
- Adekanmbi V.
- Adema B.D.
- Adeoye A.M.
- Adetokunboh O.O.
- Adham D.
- Aduroja P.E.
- Advani S.M.
- Afarideh M.
- Afshin A.
- Aghaali M.
- Agrawal A.
- Ahmad T.
- Ahmadi K.
- Ahmadi S.
- Ahmed M.B.
- Ahmed R.
- Ajumobi O.
- Akal C.G.
- Akalu T.Y.
- Akinyemiju T.
- Akombi B.
- Al-Aly Z.
- Al-Mekhlafi H.M.
- Al-Raddadi R.M.
- Alam S.
- Alamene G.M.
- Alanzi T.M.
- Alema N.M.
- Ali B.A.
- Ali M.
- Alijanzadeh M.
- Alinia C.
- Alipour V.
- Alizade H.
- Aljunid S.M.
- Almasi A.
- Almasi-Hashiani A.
- Altirkawi K.
- Alvis-Guzman N.
- Alvis-Zakzuk N.J.
- Amare A.T.
- Amegah A.K.
- Amini S.
- Amiri F.
- Amit A.M.L.
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- Andrei C.L.
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- Ghashghaee A.
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- Gholamian A.
- Gilani S.A.
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- �rnlöv J.
- Publication venue
- Publication date
- 01/01/2020
- Field of study
A double burden of malnutrition occurs when individuals, household members or communities experience both undernutrition and overweight. Here, we show geospatial estimates of overweight and wasting prevalence among children under 5 years of age in 105 low- and middle-income countries (LMICs) from 2000 to 2017 and aggregate these to policy-relevant administrative units. Wasting decreased overall across LMICs between 2000 and 2017, from 8.4 (62.3 (55.1�70.8) million) to 6.4 (58.3 (47.6�70.7) million), but is predicted to remain above the World Health Organization�s Global Nutrition Target of <5 in over half of LMICs by 2025. Prevalence of overweight increased from 5.2 (30 (22.8�38.5) million) in 2000 to 6.0 (55.5 (44.8�67.9) million) children aged under 5 years in 2017. Areas most affected by double burden of malnutrition were located in Indonesia, Thailand, southeastern China, Botswana, Cameroon and central Nigeria. Our estimates provide a new perspective to researchers, policy makers and public health agencies in their efforts to address this global childhood syndemic. © 2020, The Author(s)
Author Correction: Mapping local patterns of childhood overweight and wasting in low- and middle-income countries between 2000 and 2017 (Nature Medicine, (2020), 26, 5, (750-759), 10.1038/s41591-020-0807-6)
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An amendment to this paper has been published and can be accessed via a link at the top of the paper. © 2020, The Author(s)
Author Correction: Mapping local patterns of childhood overweight and wasting in low- and middle-income countries between 2000 and 2017 (Nature Medicine, (2020), 26, 5, (750-759), 10.1038/s41591-020-0807-6)
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An amendment to this paper has been published and can be accessed via a link at the top of the paper. © 2020, The Author(s)
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