Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Neurological disorders[original query] |
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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2012 Nov 11 (11): 951-62. Traylor Matthew, Farrall Martin, Holliday Elizabeth G, Sudlow Cathie, Hopewell Jemma C, Cheng Yu-Ching, Fornage Myriam, Ikram M Arfan, Malik Rainer, Bevan Steve, Thorsteinsdottir Unnur, Nalls Mike A, Longstreth Wt, Wiggins Kerri L, Yadav Sunaina, Parati Eugenio A, Destefano Anita L, Worrall Bradford B, Kittner Steven J, Khan Muhammad Saleem, Reiner Alex P, Helgadottir Anna, Achterberg Sefanja, Fernandez-Cadenas Israel, Abboud Sherine, Schmidt Reinhold, Walters Matthew, Chen Wei-Min, Ringelstein E Bernd, O'Donnell Martin, Ho Weang Kee, Pera Joanna, Lemmens Robin, Norrving Bo, Higgins Peter, Benn Marianne, Sale Michele, Kuhlenbäumer Gregor, Doney Alexander S F, Vicente Astrid M, Delavaran Hossein, Algra Ale, Davies Gail, Oliveira Sofia A, Palmer Colin N A, Deary Ian, Schmidt Helena, Pandolfo Massimo, Montaner Joan, Carty Cara, de Bakker Paul I W, Kostulas Konstantinos, Ferro Jose M, van Zuydam Natalie R, Valdimarsson Einar, Nordestgaard Børge G, Lindgren Arne, Thijs Vincent, Slowik Agnieszka, Saleheen Danish, Paré Guillaume, Berger Klaus, Thorleifsson Gudmar, , Hofman Albert, Mosley Thomas H, Mitchell Braxton D, Furie Karen, Clarke Robert, Levi Christopher, Seshadri Sudha, Gschwendtner Andreas, Boncoraglio Giorgio B, Sharma Pankaj, Bis Joshua C, Gretarsdottir Solveig, Psaty Bruce M, Rothwell Peter M, Rosand Jonathan, Meschia James F, Stefansson Kari, Dichgans Martin, Markus Hugh S, |
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
Neuron 2013 Apr 78 (2): 256-68. Cruchaga Carlos, Kauwe John S K, Harari Oscar, Jin Sheng Chih, Cai Yefei, Karch Celeste M, Benitez Bruno A, Jeng Amanda T, Skorupa Tara, Carrell David, Bertelsen Sarah, Bailey Matthew, McKean David, Shulman Joshua M, De Jager Philip L, Chibnik Lori, Bennett David A, Arnold Steve E, Harold Denise, Sims Rebecca, Gerrish Amy, Williams Julie, Van Deerlin Vivianna M, Lee Virginia M-Y, Shaw Leslie M, Trojanowski John Q, Haines Jonathan L, Mayeux Richard, Pericak-Vance Margaret A, Farrer Lindsay A, Schellenberg Gerard D, Peskind Elaine R, Galasko Douglas, Fagan Anne M, Holtzman David M, Morris John C, , , , Goate Alison |
Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.
Neurobiology of aging 2013 Jan . Martinelli-Boneschi F, Giacalone G, Magnani G, Biella G, Coppi E, Santangelo R, Brambilla P, Esposito F, Lupoli S, Clerici F, Benussi L, Ghidoni R, Galimberti D, Squitti R, Confaloni A, Bruno G, Pichler S, Mayhaus M, Riemenschneider M, Mariani C, Comi G, Scarpini E, Binetti G, Forloni G, Franceschi M, Albani D |
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2014 Sep 13 (9): 893-903. Authors are not available |
Frontotemporal dementia and its subtypes: a genome-wide association study.
The Lancet. Neurology 2014 Jul 13 (7): 686-99. Ferrari Raffaele, Hernandez Dena G, Nalls Michael A, Rohrer Jonathan D, Ramasamy Adaikalavan, Kwok John B J, Dobson-Stone Carol, Brooks William S, Schofield Peter R, Halliday Glenda M, Hodges John R, Piguet Olivier, Bartley Lauren, Thompson Elizabeth, Haan Eric, Hernández Isabel, Ruiz Agustín, Boada Mercè, Borroni Barbara, Padovani Alessandro, Cruchaga Carlos, Cairns Nigel J, Benussi Luisa, Binetti Giuliano, Ghidoni Roberta, Forloni Gianluigi, Galimberti Daniela, Fenoglio Chiara, Serpente Maria, Scarpini Elio, Clarimón Jordi, Lleó Alberto, Blesa Rafael, Waldö Maria Landqvist, Nilsson Karin, Nilsson Christer, Mackenzie Ian R A, Hsiung Ging-Yuek R, Mann David M A, Grafman Jordan, Morris Christopher M, Attems Johannes, Griffiths Timothy D, McKeith Ian G, Thomas Alan J, Pietrini P, Huey Edward D, Wassermann Eric M, Baborie Atik, Jaros Evelyn, Tierney Michael C, Pastor Pau, Razquin Cristina, Ortega-Cubero Sara, Alonso Elena, Perneczky Robert, Diehl-Schmid Janine, Alexopoulos Panagiotis, Kurz Alexander, Rainero Innocenzo, Rubino Elisa, Pinessi Lorenzo, Rogaeva Ekaterina, St George-Hyslop Peter, Rossi Giacomina, Tagliavini Fabrizio, Giaccone Giorgio, Rowe James B, Schlachetzki Johannes C M, Uphill James, Collinge John, Mead Simon, Danek Adrian, Van Deerlin Vivianna M, Grossman Murray, Trojanowski John Q, van der Zee Julie, Deschamps William, Van Langenhove Tim, Cruts Marc, Van Broeckhoven Christine, Cappa Stefano F, Le Ber Isabelle, Hannequin Didier, Golfier Véronique, Vercelletto Martine, Brice Alexis, Nacmias Benedetta, Sorbi Sandro, Bagnoli Silvia, Piaceri Irene, Nielsen Jørgen E, Hjermind Lena E, Riemenschneider Matthias, Mayhaus Manuel, Ibach Bernd, Gasparoni Gilles, Pichler Sabrina, Gu Wei, Rossor Martin N, Fox Nick C, Warren Jason D, Spillantini Maria Grazia, Morris Huw R, Rizzu Patrizia, Heutink Peter, Snowden Julie S, Rollinson Sara, Richardson Anna, Gerhard Alexander, Bruni Amalia C, Maletta Raffaele, Frangipane Francesca, Cupidi Chiara, Bernardi Livia, Anfossi Maria, Gallo Maura, Conidi Maria Elena, Smirne Nicoletta, Rademakers Rosa, Baker Matt, Dickson Dennis W, Graff-Radford Neill R, Petersen Ronald C, Knopman David, Josephs Keith A, Boeve Bradley F, Parisi Joseph E, Seeley William W, Miller Bruce L, Karydas Anna M, Rosen Howard, van Swieten John C, Dopper Elise G P, Seelaar Harro, Pijnenburg Yolande A L, Scheltens Philip, Logroscino Giancarlo, Capozzo Rosa, Novelli Valeria, Puca Annibale A, Franceschi Massimo, Postiglione Alfredo, Milan Graziella, Sorrentino Paolo, Kristiansen Mark, Chiang Huei-Hsin, Graff Caroline, Pasquier Florence, Rollin Adeline, Deramecourt Vincent, Lebert Florence, Kapogiannis Dimitrios, Ferrucci Luigi, Pickering-Brown Stuart, Singleton Andrew B, Hardy John, Momeni Parast |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
Genome-Wide Association Study of Dietary Pattern Scores.
Nutrients 2017 Jun 9 (7): . Guénard Frédéric, Bouchard-Mercier Annie, Rudkowska Iwona, Lemieux Simone, Couture Patrick, Vohl Marie-Clau |
Heritability and genome-wide associations studies of cerebral blood flow in the general population.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2017 06 271678X17715861. Ikram M Arfan, Zonneveld Hazel I, Roshchupkin Gennady, Smith Albert V, Franco Oscar H, Sigurdsson Sigurdur, van Duijn Cornelia, Uitterlinden André G, Launer Lenore J, Vernooij Meike W, Gudnason Vilmundur, Adams Hieab |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Stroke 2018 Jul . Jian Xueqiu, Satizabal Claudia L, Smith Albert V, Wittfeld Katharina, Bis Joshua C, Smith Jennifer A, Hsu Fang-Chi, Nho Kwangsik, Hofer Edith, Hagenaars Saskia P, Nyquist Paul A, Mishra Aniket, Adams Hieab H H, Li Shuo, Teumer Alexander, Zhao Wei, Freedman Barry I, Saba Yasaman, Yanek Lisa R, Chauhan Ganesh, van Buchem Mark A, Cushman Mary, Royle Natalie A, Bryan R Nick, Niessen Wiro J, Windham Beverly G, DeStefano Anita L, Habes Mohamad, Heckbert Susan R, Palmer Nicholette D, Lewis Cora E, Eiriksdottir Gudny, Maillard Pauline, Mathias Rasika A, Homuth Georg, Valdés-Hernández Maria Del C, Divers Jasmin, Beiser Alexa S, Langner Sönke, Rice Kenneth M, Bastin Mark E, Yang Qiong, Maldjian Joseph A, Starr John M, Sidney Stephen, Risacher Shannon L, Uitterlinden André G, Gudnason Vilmundur G, Nauck Matthias, Rotter Jerome I, Schreiner Pamela J, Boerwinkle Eric, van Duijn Cornelia M, Mazoyer Bernard, von Sarnowski Bettina, Gottesman Rebecca F, Levy Daniel, Sigurdsson Sigurdur, Vernooij Meike W, Turner Stephen T, Schmidt Reinhold, Wardlaw Joanna M, Psaty Bruce M, Mosley Thomas H, DeCarli Charles S, Saykin Andrew J, Bowden Donald W, Becker Diane M, Deary Ian J, Schmidt Helena, Kardia Sharon L R, Ikram M Arfan, Debette Stéphanie, Grabe Hans J, Longstreth W T, Seshadri Sudha, Launer Lenore J, Fornage Myriam, |
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
The Lancet. Neurology 2018 Jun 17 (6): 548-558. Pottier Cyril, Zhou Xiaolai, Perkerson Ralph B, Baker Matt, Jenkins Gregory D, Serie Daniel J, Ghidoni Roberta, Benussi Luisa, Binetti Giuliano, López de Munain Adolfo, Zulaica Miren, Moreno Fermin, Le Ber Isabelle, Pasquier Florence, Hannequin Didier, Sánchez-Valle Raquel, Antonell Anna, Lladó Albert, Parsons Tammee M, Finch NiCole A, Finger Elizabeth C, Lippa Carol F, Huey Edward D, Neumann Manuela, Heutink Peter, Synofzik Matthis, Wilke Carlo, Rissman Robert A, Slawek Jaroslaw, Sitek Emilia, Johannsen Peter, Nielsen Jørgen E, Ren Yingxue, van Blitterswijk Marka, DeJesus-Hernandez Mariely, Christopher Elizabeth, Murray Melissa E, Bieniek Kevin F, Evers Bret M, Ferrari Camilla, Rollinson Sara, Richardson Anna, Scarpini Elio, Fumagalli Giorgio G, Padovani Alessandro, Hardy John, Momeni Parastoo, Ferrari Raffaele, Frangipane Francesca, Maletta Raffaele, Anfossi Maria, Gallo Maura, Petrucelli Leonard, Suh EunRan, Lopez Oscar L, Wong Tsz H, van Rooij Jeroen G J, Seelaar Harro, Mead Simon, Caselli Richard J, Reiman Eric M, Noel Sabbagh Marwan, Kjolby Mads, Nykjaer Anders, Karydas Anna M, Boxer Adam L, Grinberg Lea T, Grafman Jordan, Spina Salvatore, Oblak Adrian, Mesulam M-Marsel, Weintraub Sandra, Geula Changiz, Hodges John R, Piguet Olivier, Brooks William S, Irwin David J, Trojanowski John Q, Lee Edward B, Josephs Keith A, Parisi Joseph E, Ertekin-Taner Nilüfer, Knopman David S, Nacmias Benedetta, Piaceri Irene, Bagnoli Silvia, Sorbi Sandro, Gearing Marla, Glass Jonathan, Beach Thomas G, Black Sandra E, Masellis Mario, Rogaeva Ekaterina, Vonsattel Jean-Paul, Honig Lawrence S, Kofler Julia, Bruni Amalia C, Snowden Julie, Mann David, Pickering-Brown Stuart, Diehl-Schmid Janine, Winkelmann Juliane, Galimberti Daniela, Graff Caroline, Öijerstedt Linn, Troakes Claire, Al-Sarraj Safa, Cruchaga Carlos, Cairns Nigel J, Rohrer Jonathan D, Halliday Glenda M, Kwok John B, van Swieten John C, White Charles L, Ghetti Bernardino, Murell Jill R, Mackenzie Ian R A, Hsiung Ging-Yuek R, Borroni Barbara, Rossi Giacomina, Tagliavini Fabrizio, Wszolek Zbigniew K, Petersen Ronald C, Bigio Eileen H, Grossman Murray, Van Deerlin Vivianna M, Seeley William W, Miller Bruce L, Graff-Radford Neill R, Boeve Bradley F, Dickson Dennis W, Biernacka Joanna M, Rademakers Ro |
Genetic architecture of subcortical brain structures in 38,851 individuals.
Nature genetics 2019 (11): 1624-1636. Satizabal Claudia L, Adams Hieab H H, Hibar Derrek P, White Charles C, Knol Maria J, Stein Jason L, Scholz Markus, Sargurupremraj Muralidharan, Jahanshad Neda, Roshchupkin Gennady V, Smith Albert V, Bis Joshua C, Jian Xueqiu, Luciano Michelle, Hofer Edith, Teumer Alexander, van der Lee Sven J, Yang Jingyun, Yanek Lisa R, Lee Tom V, Li Shuo, Hu Yanhui, Koh Jia Yu, Eicher John D, Desrivières Sylvane, Arias-Vasquez Alejandro, Chauhan Ganesh, Athanasiu Lavinia, Rentería Miguel E, Kim Sungeun, Hoehn David, Armstrong Nicola J, Chen Qiang, Holmes Avram J, den Braber Anouk, Kloszewska Iwona, Andersson Micael, Espeseth Thomas, Grimm Oliver, Abramovic Lucija, Alhusaini Saud, Milaneschi Yuri, Papmeyer Martina, Axelsson Tomas, Ehrlich Stefan, Roiz-Santiañez Roberto, Kraemer Bernd, Håberg Asta K, Jones Hannah J, Pike G Bruce, Stein Dan J, Stevens Allison, Bralten Janita, Vernooij Meike W, Harris Tamara B, Filippi Irina, Witte A Veronica, Guadalupe Tulio, Wittfeld Katharina, Mosley Thomas H, Becker James T, Doan Nhat Trung, Hagenaars Saskia P, Saba Yasaman, Cuellar-Partida Gabriel, Amin Najaf, Hilal Saima, Nho Kwangsik, Mirza-Schreiber Nazanin, Arfanakis Konstantinos, Becker Diane M, Ames David, Goldman Aaron L, Lee Phil H, Boomsma Dorret I, Lovestone Simon, Giddaluru Sudheer, Le Hellard Stephanie, Mattheisen Manuel, Bohlken Marc M, Kasperaviciute Dalia, Schmaal Lianne, Lawrie Stephen M, Agartz Ingrid, Walton Esther, Tordesillas-Gutierrez Diana, Davies Gareth E, Shin Jean, Ipser Jonathan C, Vinke Louis N, Hoogman Martine, Jia Tianye, Burkhardt Ralph, Klein Marieke, Crivello Fabrice, Janowitz Deborah, Carmichael Owen, Haukvik Unn K, Aribisala Benjamin S, Schmidt Helena, Strike Lachlan T, Cheng Ching-Yu, Risacher Shannon L, Pütz Benno, Fleischman Debra A, Assareh Amelia A, Mattay Venkata S, Buckner Randy L, Mecocci Patrizia, Dale Anders M, Cichon Sven, Boks Marco P, Matarin Mar, Penninx Brenda W J H, Calhoun Vince D, Chakravarty M Mallar, Marquand Andre F, Macare Christine, Kharabian Masouleh Shahrzad, Oosterlaan Jaap, Amouyel Philippe, Hegenscheid Katrin, Rotter Jerome I, Schork Andrew J, Liewald David C M, de Zubicaray Greig I, Wong Tien Yin, Shen Li, Sämann Philipp G, Brodaty Henry, Roffman Joshua L, de Geus Eco J C, Tsolaki Magda, Erk Susanne, van Eijk Kristel R, Cavalleri Gianpiero L, van der Wee Nic J A, McIntosh Andrew M, Gollub Randy L, Bulayeva Kazima B, Bernard Manon, Richards Jennifer S, Himali Jayandra J, Loeffler Markus, Rommelse Nanda, Hoffmann Wolfgang, Westlye Lars T, Valdés Hernández Maria C, Hansell Narelle K, van Erp Theo G M, Wolf Christiane, Kwok John B J, Vellas Bruno, Heinz Andreas, Olde Loohuis Loes M, Delanty Norman, Ho Beng-Choon, Ching Christopher R K, Shumskaya Elena, Singh Baljeet, Hofman Albert, van der Meer Dennis, Homuth Georg, Psaty Bruce M, Bastin Mark E, Montgomery Grant W, Foroud Tatiana M, Reppermund Simone, Hottenga Jouke-Jan, Simmons Andrew, Meyer-Lindenberg Andreas, Cahn Wiepke, Whelan Christopher D, van Donkelaar Marjolein M J, Yang Qiong, Hosten Norbert, Green Robert C, Thalamuthu Anbupalam, Mohnke Sebastian, Hulshoff Pol Hilleke E, Lin Honghuang, Jack Clifford R, Schofield Peter R, Mühleisen Thomas W, Maillard Pauline, Potkin Steven G, Wen Wei, Fletcher Evan, Toga Arthur W, Gruber Oliver, Huentelman Matthew, Davey Smith George, Launer Lenore J, Nyberg Lars, Jönsson Erik G, Crespo-Facorro Benedicto, Koen Nastassja, Greve Douglas N, Uitterlinden André G, Weinberger Daniel R, Steen Vidar M, Fedko Iryna O, Groenewold Nynke A, Niessen Wiro J, Toro Roberto, Tzourio Christophe, Longstreth William T, Ikram M Kamran, Smoller Jordan W, van Tol Marie-Jose, Sussmann Jessika E, Paus Tomas, Lemaître Hervé, Schroeter Matthias L, Mazoyer Bernard, Andreassen Ole A, Holsboer Florian, Depondt Chantal, Veltman Dick J, Turner Jessica A, Pausova Zdenka, Schumann Gunter, van Rooij Daan, Djurovic Srdjan, Deary Ian J, McMahon Katie L, Müller-Myhsok Bertram, Brouwer Rachel M, Soininen Hilkka, Pandolfo Massimo, Wassink Thomas H, Cheung Joshua W, Wolfers Thomas, Martinot Jean-Luc, Zwiers Marcel P, Nauck Matthias, Melle Ingrid, Martin Nicholas G, Kanai Ryota, Westman Eric, Kahn René S, Sisodiya Sanjay M, White Tonya, Saremi Arvin, van Bokhoven Hans, Brunner Han G, Völzke Henry, Wright Margaret J, van 't Ent Dennis, Nöthen Markus M, Ophoff Roel A, Buitelaar Jan K, Fernández Guillén, Sachdev Perminder S, Rietschel Marcella, van Haren Neeltje E M, Fisher Simon E, Beiser Alexa S, Francks Clyde, Saykin Andrew J, Mather Karen A, Romanczuk-Seiferth Nina, Hartman Catharina A, DeStefano Anita L, Heslenfeld Dirk J, Weiner Michael W, Walter Henrik, Hoekstra Pieter J, Nyquist Paul A, Franke Barbara, Bennett David A, Grabe Hans J, Johnson Andrew D, Chen Christopher, van Duijn Cornelia M, Lopez Oscar L, Fornage Myriam, Wardlaw Joanna M, Schmidt Reinhold, DeCarli Charles, De Jager Philip L, Villringer Arno, Debette Stéphanie, Gudnason Vilmundur, Medland Sarah E, Shulman Joshua M, Thompson Paul M, Seshadri Sudha, Ikram M Arf |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
PLoS genetics 2020 10 16 (10): e1009089. Li Xinyue, Zhao Hong |
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
Nature communications 2021 05 12 (1): 2909. Elvsåshagen Torbjørn, Shadrin Alexey, Frei Oleksandr, van der Meer Dennis, Bahrami Shahram, Kumar Vinod Jangir, Smeland Olav, Westlye Lars T, Andreassen Ole A, Kaufmann Tobi |
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.
Communications biology 2022 4 5 (1): 336. Sarnowski Chloé, Ghanbari Mohsen, Bis Joshua C, Logue Mark, Fornage Myriam, Mishra Aniket, Ahmad Shahzad, Beiser Alexa S, Boerwinkle Eric, Bouteloup Vincent, Chouraki Vincent, Cupples L Adrienne, Damotte Vincent, DeCarli Charles S, DeStefano Anita L, Djoussé Luc, Fohner Alison E, Franz Carol E, Kautz Tiffany F, Lambert Jean-Charles, Lyons Michael J, Mosley Thomas H, Mukamal Kenneth J, Pase Matthew P, Portilla Fernandez Eliana C, Rissman Robert A, Satizabal Claudia L, Vasan Ramachandran S, Yaqub Amber, Debette Stephanie, Dufouil Carole, Launer Lenore J, Kremen William S, Longstreth William T, Ikram M Arfan, Seshadri Sud |
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