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Refinado por: assunto: Science & Technology remover
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Cognitive performances across individuals at high genetic risk for schizophrenia, high genetic risk for bipolar disorder, and low genetic risks: a combined polygenic risk score approach
Cognitive performances across individuals at high genetic risk for schizophrenia, high genetic risk for bipolar disorder, and low genetic risks: a combined polygenic risk score approach
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Cognitive performances across individuals at high genetic risk for schizophrenia, high genetic risk for bipolar disorder, and low genetic risks: a combined polygenic risk score approach

Ohi, Kazutaka ; Nishizawa, Daisuke ; Sugiyama, Shunsuke ; Takai, Kentaro ; Fujikane, Daisuke ; Kuramitsu, Ayumi ; Hasegawa, Junko ; Soda, Midori ; Kitaichi, Kiyoyuki ; Hashimoto, Ryota ; Ikeda, Kazutaka ; Shioiri, Toshiki

Psychological medicine, 2023-07, Vol.53 (10), p.4454-4463 [Periódico revisado por pares]

Cambridge, UK: Cambridge University Press

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12
Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial
Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial
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Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial

Marston, Nicholas A ; Kamanu, Frederick K ; Nordio, Francesco ; Gurmu, Yared ; Roselli, Carolina ; Sever, Peter S ; Pedersen, Terje R ; Keech, Anthony C ; Wang, Huei ; Lira Pineda, Armando ; Giugliano, Robert P ; Lubitz, Steven A ; Ellinor, Patrick T ; Sabatine, Marc S ; Ruff, Christian T

Circulation (New York, N.Y.), 2020-02, Vol.141 (8), p.616-623 [Periódico revisado por pares]

United States: by the American College of Cardiology Foundation and the American Heart Association, Inc

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13
Genetic risk for alzheimer disease is distinct from genetic risk for amyloid deposition
Genetic risk for alzheimer disease is distinct from genetic risk for amyloid deposition
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Genetic risk for alzheimer disease is distinct from genetic risk for amyloid deposition

Leonenko, Ganna ; Shoai, Maryam ; Bellou, Eftychia ; Sims, Rebecca ; Williams, Julie ; Hardy, John ; Escott‐Price, Valentina

Annals of neurology, 2019-09, Vol.86 (3), p.427-435 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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14
Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders : Evidence through univariate and multivariate mega-analysis including 6420 participants from the ENIGMA MDD working group
Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders : Evidence through univariate and multivariate mega-analysis including 6420 participants from the ENIGMA MDD working group
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Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders : Evidence through univariate and multivariate mega-analysis including 6420 participants from the ENIGMA MDD working group

Opel, Nils ; Thalamuthu, Anbupalam ; Milaneschi, Yuri ; Grotegerd, Dominik ; Flint, Claas ; Leenings, Ramona ; Goltermann, Janik ; Richter, Maike ; Hahn, Tim ; Woditsch, Georg ; Berger, Klaus ; Hermesdorf, Marco ; McIntosh, Andrew ; Whalley, Heather C ; Harris, Mathew A ; MacMaster, Frank P ; Walter, Henrik ; Veer, Ilya M ; Frodl, Thomas ; Carballedo, Angela ; Krug, Axel ; Nenadic, Igor ; Kircher, Tilo ; Aleman, Andre ; Groenewold, Nynke A ; Stein, Dan J ; Soares, Jair C ; Zunta-Soares, Giovana B ; Mwangi, Benson ; Wu, Mon-Ju ; Walter, Martin ; Li, Meng ; Harrison, Ben J ; Davey, Christopher G ; Cullen, Kathryn R ; Klimes-Dougan, Bonnie ; Mueller, Bryon A ; Sämann, Philipp G ; Penninx, Brenda ; Nawijn, Laura ; Veltman, Dick J ; Aftanas, Lyubomir ; Brak, Ivan V ; Filimonova, Elena A ; Osipov, Evgeniy A ; Reneman, Liesbeth ; Schrantee, Anouk ; Grabe, Hans J ; Van der Auwera, Sandra ; Wittfeld, Katharina ; Hosten, Norbert ; Völzke, Henry ; Sim, Kang ; Gotlib, Ian H ; Sacchet, Matthew D ; Lagopoulos, Jim ; Hatton, Sean N ; Hickie, Ian ; Pozzi, Elena ; Thompson, Paul M ; Jahanshad, Neda ; Schmaal, Lianne ; Baune, Bernhard T ; Dannlowski, Udo

Molecular psychiatry, 2021-09, Vol.26 (9), p.4839-4852 [Periódico revisado por pares]

England: Nature Publishing Group UK

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15
Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer’s disease
Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer’s disease
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Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer’s disease

Coughlan, Gillian ; Coutrot, Antoine ; Khondoker, Mizanur ; Minihane, Anne-Marie ; Spiers, Hugo ; Hornberger, Michael

Proceedings of the National Academy of Sciences - PNAS, 2019-05, Vol.116 (19), p.9285-9292 [Periódico revisado por pares]

United States: National Academy of Sciences

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16
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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Genome-wide association study reveals genetic risk underlying Parkinson's disease

Singleton, Andrew B ; Gasser, Thomas ; Simón-Sánchez, Javier ; Schulte, Claudia ; Bras, Jose M ; Sharma, Manu ; Gibbs, J Raphael ; Berg, Daniela ; Paisan-Ruiz, Coro ; Lichtner, Peter ; Scholz, Sonja W ; Hernandez, Dena G ; Krüger, Rejko ; Federoff, Monica ; Klein, Christine ; Goate, Alison ; Perlmutter, Joel ; Bonin, Michael ; Nalls, Michael A ; Illig, Thomas ; Gieger, Christian ; Houlden, Henry ; Steffens, Michael ; Okun, Michael S ; Racette, Brad A ; Cookson, Mark R ; Foote, Kelly D ; Fernandez, Hubert H ; Traynor, Bryan J ; Schreiber, Stefan ; Arepalli, Sampath ; Zonozi, Ryan ; Gwinn, Katrina ; van der Brug, Marcel ; Lopez, Grisel ; Chanock, Stephen J ; Schatzkin, Arthur ; Park, Yikyung ; Hollenbeck, Albert ; Gao, Jianjun ; Huang, Xuemei ; Wood, Nick W ; Lorenz, Delia ; Deuschl, Günther ; Chen, Honglei ; Riess, Olaf ; Hardy, John A

Nature genetics, 2009-12, Vol.41 (12), p.1308-1312 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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17
Association Between Low-Density Lipoprotein Cholesterol–Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis
Association Between Low-Density Lipoprotein Cholesterol–Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis
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Association Between Low-Density Lipoprotein Cholesterol–Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis

Lotta, Luca A ; Sharp, Stephen J ; Burgess, Stephen ; Perry, John R. B ; Stewart, Isobel D ; Willems, Sara M ; Luan, Jian’an ; Ardanaz, Eva ; Arriola, Larraitz ; Balkau, Beverley ; Boeing, Heiner ; Deloukas, Panos ; Forouhi, Nita G ; Franks, Paul W ; Grioni, Sara ; Kaaks, Rudolf ; Key, Timothy J ; Navarro, Carmen ; Nilsson, Peter M ; Overvad, Kim ; Palli, Domenico ; Panico, Salvatore ; Quirós, Jose-Ramón ; Riboli, Elio ; Rolandsson, Olov ; Sacerdote, Carlotta ; Salamanca-Fernandez, Elena ; Slimani, Nadia ; Spijkerman, Annemieke M. W ; Tjonneland, Anne ; Tumino, Rosario ; van der A, Daphne L ; van der Schouw, Yvonne T ; McCarthy, Mark I ; Barroso, Inês ; O’Rahilly, Stephen ; Savage, David B ; Sattar, Naveed ; Langenberg, Claudia ; Scott, Robert A ; Wareham, Nicholas J

JAMA : the journal of the American Medical Association, 2016-10, Vol.316 (13), p.1383-1391 [Periódico revisado por pares]

United States: American Medical Association

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18
Genetic and non‐genetic risk factors for pre‐eclampsia: umbrella review of systematic reviews and meta‐analyses of observational studies
Genetic and non‐genetic risk factors for pre‐eclampsia: umbrella review of systematic reviews and meta‐analyses of observational studies
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Genetic and non‐genetic risk factors for pre‐eclampsia: umbrella review of systematic reviews and meta‐analyses of observational studies

Giannakou, K. ; Evangelou, E. ; Papatheodorou, S. I.

Ultrasound in obstetrics & gynecology, 2018-06, Vol.51 (6), p.720-730 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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19
A Common Genetic Variant Risk Score is Associated with Drug-Induced QT Prolongation and Torsade de Pointes Risk: A Pilot Study
A Common Genetic Variant Risk Score is Associated with Drug-Induced QT Prolongation and Torsade de Pointes Risk: A Pilot Study
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A Common Genetic Variant Risk Score is Associated with Drug-Induced QT Prolongation and Torsade de Pointes Risk: A Pilot Study

Strauss, David G ; Vicente, Jose ; Johannesen, Lars ; Blinova, Ksenia ; Mason, Jay W ; Weeke, Peter ; Behr, Elijah R ; Roden, Dan ; Woosley, Raymond ; Kosova, Gulum ; Rosenberg, Michael A ; Newton-Cheh, Christopher

Circulation (New York, N.Y.), 2017-04, Vol.135 (14), p.1300-1310 [Periódico revisado por pares]

United States: by the American College of Cardiology Foundation and the American Heart Association, Inc

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20
Genetic risk of dementia mitigated by cognitive reserve: A cohort study
Genetic risk of dementia mitigated by cognitive reserve: A cohort study
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Genetic risk of dementia mitigated by cognitive reserve: A cohort study

Dekhtyar, Serhiy ; Marseglia, Anna ; Xu, Weili ; Darin‐Mattsson, Alexander ; Wang, Hui‐Xin ; Fratiglioni, Laura

Annals of neurology, 2019-07, Vol.86 (1), p.68-78 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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