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A Genome-wide Association Study of Myasthenia Gravis
A Genome-wide Association Study of Myasthenia Gravis
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A Genome-wide Association Study of Myasthenia Gravis

Renton, Alan E ; Pliner, Hannah A ; Provenzano, Carlo ; Evoli, Amelia ; Ricciardi, Roberta ; Nalls, Michael A ; Marangi, Giuseppe ; Abramzon, Yevgeniya ; Arepalli, Sampath ; Chong, Sean ; Hernandez, Dena G ; Johnson, Janel O ; Bartoccioni, Emanuela ; Scuderi, Flavia ; Maestri, Michelangelo ; Gibbs, J. Raphael ; Errichiello, Edoardo ; Chiò, Adriano ; Restagno, Gabriella ; Sabatelli, Mario ; Macek, Mark ; Scholz, Sonja W ; Corse, Andrea ; Chaudhry, Vinay ; Benatar, Michael ; Barohn, Richard J ; McVey, April ; Pasnoor, Mamatha ; Dimachkie, Mazen M ; Rowin, Julie ; Kissel, John ; Freimer, Miriam ; Kaminski, Henry J ; Sanders, Donald B ; Lipscomb, Bernadette ; Massey, Janice M ; Chopra, Manisha ; Howard, James F ; Koopman, Wilma J ; Nicolle, Michael W ; Pascuzzi, Robert M ; Pestronk, Alan ; Wulf, Charlie ; Florence, Julaine ; Blackmore, Derrick ; Soloway, Aimee ; Siddiqi, Zaeem ; Muppidi, Srikanth ; Wolfe, Gil ; Richman, David ; Mezei, Michelle M ; Jiwa, Theresa ; Oger, Joel ; Drachman, Daniel B ; Traynor, Bryan J

JAMA neurology, 2015-04, Vol.72 (4), p.396-404 [Periódico revisado por pares]

United States: American Medical Association

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2
A Genome-Wide Association Study of Myasthenia Gravis
A Genome-Wide Association Study of Myasthenia Gravis
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Artigo 		Adicionar ao Meu Espaço

A Genome-Wide Association Study of Myasthenia Gravis

Renton, Alan E ; Pliner, Hannah A ; Provenzano, Carlo ; Evoli, Amelia ; Ricciardi, Roberta ; Nalls, Michael A ; Marangi, Giuseppe ; Abramzon, Yevgeniya ; Arepalli, Sampath ; Chong, Sean ; Hernandez, Dena G ; Johnson, Janel O ; Bartoccioni, Emanuela ; Scuderi, Flavia ; Maestri, Michelangelo ; Gibbs, J Raphael ; Errichiello, Edoardo ; Chiò, Adriano ; Restagno, Gabriella ; Sabatelli, Mario ; Macek, Mark ; Scholz, Sonja W ; Corse, Andrea ; Chaudhry, Vinay ; Benatar, Michael ; Barohn, Richard J ; McVey, April ; Pasnoor, Mamatha ; Dimachkie, Mazen M ; Rowin, Julie ; Kissel, John ; Freimer, Miriam ; Kaminski, Henry J ; Sanders, Donald B ; Lipscomb, Bernadette ; Massey, Janice M ; Chopra, Manisha ; Howard, James F ; Koopman, Wilma J ; Nicolle, Michael W ; Pascuzzi, Robert M ; Pestronk, Alan ; Wulf, Charlie ; Florence, Julaine ; Blackmore, Derrick ; Soloway, Aimee ; Siddiqi, Zaeem ; Muppidi, Srikanth ; Wolfe, Gil ; Richman, David ; Mezei, Michelle M ; Jiwa, Theresa ; Oger, Joel ; Drachman, Daniel B ; Traynor, Bryan J

JAMA Neurology, 2015-04, Vol.72 (4), p.396-404

eScholarship, University of California

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3
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
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Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamad ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J. Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O’Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

JAMA neurology, 2013-10, Vol.70 (10), p.1268-1276 [Periódico revisado por pares]

United States: American Medical Association

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4
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

FOX, Ervin R ; HUNTER YOUNG, J ; RAMACHANDRAN, VasanS ; POLAK, JosefF ; FABSITZ, Richard R ; DRIES, Daniel L ; FARLOW, Deborah N ; REDLINE, Susan ; ADEYEMO, Adebowale ; HIRSCHORN, Joel N ; SUN, Yan V ; WYATT, Sharon B ; YALI LI ; PENMAN, Alan D ; PALMAS, Walter ; ROTTER, Jerome I ; TOWNSEND, Raymond R ; DOUMATEY, Ayo P ; TAYO, Bamidele O ; MOSLEY, Thomas H ; LYON, Helen N ; KANG, Sun J ; ROTIMI, Charles N ; DREISBACH, Albert W ; COOPER, Richard S ; FRANCESCHINI, Nora ; CURB, J. David ; MARTIN, Lisa W ; EATON, Charles B ; KARDIA, Sharon L. R ; TAYLOR, Herman A ; CAULFIELD, Mark J ; EHRET, Georg B ; JOHNSON, Toby ; KEATING, Brendan J ; CHAKRAVARTI, Aravinda ; XIAOFENG ZHU ; LEVY, Daniel ; MUSANI, Solomon K ; KIANG LIU ; MORRISON, Alanna C ; GANESH, Santhi ; KUTLAR, Abdullah

Human molecular genetics, 2011-06, Vol.20 (11), p.2273-2284 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
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Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage

ANDERSON, Christopher D ; BIFFI, Alessandro ; VISWANATHAN, Anand ; WORRALL, Bradford B ; BROTT, Thomas G ; GOLDSTEIN, Joshua N ; BROWN, Devin ; BRODERICK, Joseph P ; NORRVING, Bo ; GREENBERG, Steven M ; SILLIMAN, Scott L ; HANSEN, Björn M ; NALLS, Michael A ; TIRSCHWELL, David L ; LINDGREN, Arne ; SLOWIK, Agnieszka ; SCHMIDT, Reinhold ; SELIM, Magdy ; ROQUER, Jaume ; MONTANER, Joan ; SINGLETON, Andrew B ; KIDWELL, Chelsea S ; WOO, Daniel ; DEVAN, William J ; FURIE, Karen L ; MESCHIA, James F ; ROSAND, Jonathan ; SCHWAB, Kristin ; AYRES, Alison M ; VALANT, Valerie ; ROSS, Owen A ; ROST, Natalia S ; SAXENA, Richa

Stroke (1970), 2013-03, Vol.44 (3), p.612-619 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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6
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

Jensen, Majken K ; Jensen, Richard A ; Mukamal, Kenneth J ; Guo, Xiuqing ; Yao, Jie ; Sun, Qi ; Cornelis, Marilyn ; Liu, Yongmei ; Chen, Ming-Huei ; Kizer, Jorge R ; Djoussé, Luc ; Siscovick, David S ; Psaty, Bruce M ; Zmuda, Joseph M ; Rotter, Jerome I ; Garcia, Melissa ; Harris, Tamara ; Chen, Ida ; Goodarzi, Mark O ; Nalls, Michael A ; Keller, Margaux ; Arnold, Alice M ; Newman, Anne B ; Hoogeveen, Ron C ; Rexrode, Kathryn M ; Rimm, Eric B ; Hu, Frank B ; Ramachandran, Vasan S ; Katz, Ronit ; Pankow, James S ; Ix, Joachim H

Human Molecular Genetics, 2017-06, Vol.26 (11), p.2156-2163

eScholarship, University of California

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7
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

Jensen, Majken K ; Jensen, Richard A ; Mukamal, Kenneth J ; Guo, Xiuqing ; Yao, Jie ; Sun, Qi ; Cornelis, Marilyn ; Liu, Yongmei ; Chen, Ming-Huei ; Kizer, Jorge R ; Djoussé, Luc ; Siscovick, David S ; Psaty, Bruce M ; Zmuda, Joseph M ; Rotter, Jerome I ; Garcia, Melissa ; Harris, Tamara ; Chen, Ida ; Goodarzi, Mark O ; Nalls, Michael A ; Keller, Margaux ; Arnold, Alice M ; Newman, Anne B ; Hoogeveen, Ron C ; Rexrode, Kathryn M ; Rimm, Eric B ; Hu, Frank B ; Ramachandran, Vasan S ; Katz, Ronit ; Pankow, James S ; Ix, Joachim H

Human molecular genetics, 2017-06, Vol.26 (11), p.2156-2163 [Periódico revisado por pares]

England: Oxford University Press

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8
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Majounie, Elisa, PhD ; Renton, Alan E, PhD ; Mok, Kin, MSc ; Dopper, Elise GP ; Waite, Adrian, PhD ; Rollinson, Sara, PhD ; Chiò, Adriano, MD ; Restagno, Gabriella, MD ; Nicolaou, Nayia, MSc ; Simon-Sanchez, Javier, PhD ; van Swieten, John C, Prof ; Abramzon, Yevgeniya ; Johnson, Janel O, PhD ; Sendtner, Michael, Prof ; Pamphlett, Roger, MD ; Orrell, Richard W, MD ; Mead, Simon, MD ; Sidle, Katie C, MD ; Houlden, Henry, Prof ; Rohrer, Jonathan D, MD ; Morrison, Karen E, Prof ; Pall, Hardev, MD ; Talbot, Kevin, Prof ; Ansorge, Olaf, MD ; Hernandez, Dena G, MSc ; Arepalli, Sampath, MS ; Sabatelli, Mario, MD ; Mora, Gabriele, MD ; Corbo, Massimo, MD ; Giannini, Fabio, MD ; Calvo, Andrea, MD ; Englund, Elisabet, MD ; Borghero, Giuseppe, MD ; Floris, Gian Luca, MD ; Remes, Anne M, Prof ; Laaksovirta, Hannu, MD ; McCluskey, Leo, MD ; Trojanowski, John Q, Prof ; Van Deerlin, Vivianna M, MD ; Schellenberg, Gerard D, Prof ; Nalls, Michael A, PhD ; Drory, Vivian E, MD ; Lu, Chin-Song, Prof ; Yeh, Tu-Hsueh, MD ; Ishiura, Hiroyuki, MD ; Takahashi, Yuji, MD ; Tsuji, Shoji, Prof ; Le Ber, Isabelle, MD ; Brice, Alexis, Prof ; Drepper, Carsten, PhD ; Williams, Nigel, PhD ; Kirby, Janine, PhD ; Shaw, Pamela, Prof ; Hardy, John, Prof ; Tienari, Pentti J, MD ; Heutink, Peter, Prof ; Morris, Huw R, MD ; Pickering-Brown, Stuart, Prof ; Traynor, Bryan J, Dr

Lancet neurology, 2012-04, Vol.11 (4), p.323-330 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Frontotemporal dementia and its subtypes: a genome-wide association study
Frontotemporal dementia and its subtypes: a genome-wide association study
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Frontotemporal dementia and its subtypes: a genome-wide association study

Hernandez, Dena G, MSc ; Nalls, Michael A, PhD ; Kwok, John B J, PhD ; Dobson-Stone, Carol, PhD ; Brooks, William S, MBBS ; Schofield, Peter R, Prof ; Halliday, Glenda M, Prof ; Hodges, John R, Prof ; Piguet, Olivier, PhD ; Bartley, Lauren, MSc ; Thompson, Elizabeth, MD ; Haan, Eric, Prof ; Ruiz, Agustín, MD ; Boada, Mercè, MD ; Borroni, Barbara, MD ; Cruchaga, Carlos, PhD ; Benussi, Luisa, PhD ; Galimberti, Daniela, PhD ; Fenoglio, Chiara, PhD ; Serpente, Maria, PhD ; Scarpini, Elio, MD ; Lleó, Alberto, MD ; Waldö, Maria Landqvist, MD ; Nilsson, Karin, PhD ; Hsiung, Ging-Yuek R, MD ; Mann, David M A, Prof ; Morris, Christopher M, PhD ; Attems, Johannes, Prof ; Griffiths, Timothy D, Prof ; McKeith, Ian G, Prof ; Thomas, Alan J, Prof ; Huey, Edward D, MD ; Jaros, Evelyn, PhD ; Pastor, Pau, MD ; Razquin, Cristina, PhD ; Ortega-Cubero, Sara, MD ; Alonso, Elena, BSc ; Perneczky, Robert, MD ; Alexopoulos, Panagiotis, MD ; Kurz, Alexander, MD ; Rubino, Elisa, MD ; Pinessi, Lorenzo, Prof ; St George-Hyslop, Peter, MD ; Rowe, James B, PhD ; Schlachetzki, Johannes C M, MD ; Uphill, James, BSc ; Mead, Simon, Prof ; Danek, Adrian, MD ; Van Deerlin, Vivianna M, PhD ; van der Zee, Julie, PhD ; Deschamps, William, MSc ; Van Broeckhoven, Christine, Prof ; Cappa, Stefano F, Prof ; Le Ber, Isabelle, MD ; Vercelletto, Martine, MD ; Brice, Alexis, MD ; Nacmias, Benedetta, PhD ; Piaceri, Irene, PhD ; Nielsen, Jørgen E, MD ; Hjermind, Lena E, MD ; Riemenschneider, Matthias, Prof ; Gasparoni, Gilles, PhD ; Gu, Wei, PhD ; Rossor, Martin N, Prof ; Fox, Nick C, Prof ; Morris, Huw R, Prof ; Rizzu, Patrizia, PhD ; Heutink, Peter, Prof ; Snowden, Julie S, Prof ; Rollinson, Sara, PhD ; Richardson, Anna, MB ; Bruni, Amalia C, MD ; Maletta, Raffaele, MD ; Frangipane, Francesca, MD ; Bernardi, Livia, PhD ; Anfossi, Maria, PhD ; Gallo, Maura, PhD ; Conidi, Maria Elena, PhD ; Smirne, Nicoletta, BSc ; Baker, Matt, BSc ; Dickson, Dennis W, Prof ; Petersen, Ronald C, Prof ; Boeve, Bradley F, Prof ; Seeley, William W, MD ; Miller, Bruce L, Prof ; Karydas, Anna M, BA ; Rosen, Howard, Prof ; van Swieten, John C, Prof ; Scheltens, Philip, Prof ; Capozzo, Rosa, MD ; Franceschi, Massimo, MD ; Postiglione, Alfredo, Prof ; Chiang, Huei-Hsin, PhD ; Graff, Caroline, Prof ; Rollin, Adeline, MD ; Deramecourt, Vincent, MD ; Lebert, Florence, MD ; Kapogiannis, Dimitrios, MD ; Pickering-Brown, Stuart, Prof ; Hardy, John, Prof

Lancet neurology, 2014-07, Vol.13 (7), p.686-699 [Periódico revisado por pares]

England: Elsevier Ltd

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10
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians
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GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians

Crea, Peter Wild ; Noyce, Alastair J. ; Kauffman, Marcelo ; Tavadyan, Zaruhi ; Hunter, Julie ; Rentería, Miguel E. ; Koks, Sulev ; Rieder, Carlos ; Awad, Paula Saffie ; Fon, Ted ; Olguin, Patricio ; Chan, Piu ; Luo, Wei ; Arboleda, Gonzalo ; Hernandez, Alvaro ; Salama, Mohamed ; Westenberger, Ana ; Illarionova, Anastasia ; Hopfner, Franziska ; Madoev, Harutyun ; Junker, Johanna ; Fang, Zih‐Hua ; Xiromerisiou, Georgia ; Dagklis, Ioannis ; Stefanis, Leonidas ; Medina, Alex ; Divya, KP ; Rajan, Roopa ; Borgohain, Rupam ; Salari, Mehri ; Quattrone, Andrea ; Hattori, Nobutaka ; Shiraishi, Tomotaka ; Krüger, Rejko ; Ahmad‐Annuar, Azlina ; Norlinah, Mohamed Ibrahim ; Azmin, Shahrul ; Lim, Shen‐Yang ; Ojha, Rajeev ; Okubadejo, Njideka ; Cornejo‐Olivas, Mario ; Rosales, Raymond ; Iakovenko, Elena ; Bardien, Soraya ; Jeon, Beomseok ; Cubo, Esther ; Beyer, Katrin ; Zweier, Christiane ; Tinkhauser, Gerd ; Lin, Chin‐Hsien ; Amouri, Rim ; Başak, A. Nazlı ; Genc, Gencer ; Çakmak, Özgür Öztop ; Ertan, Sibel ; Grosset, Donald ; Morris, Huw R ; Williams, Nigel ; Lewis, Patrick Alfryn ; Weil, Rimona ; Stott, Simon ; Jasaityte, Simona ; Obese, Vida ; Espay, Alberto ; O'Grady, Alyssa ; Fiske, Brian ; Jonas, Cabell ; Cruchaga, Carlos ; Pantazis, Caroline B. ; Blauwendraat, Cornelis ; Vitale, Dan ; Mata, Ignacio F. ; Sarmiento, Ignacio Juan Keller ; Kim, Jonggeol Jeff ; Jankovic, Joseph ; Murphy, Kaileigh ; Kieburtz, Karl ; Andersh, Kate ; Markopoulou, Katerina ; Levine, Kristin S. ; Ibanez, Laura ; Marsili, Luca ; Makarious, Mary B ; Nalls, Mike A. ; Mencacci, Niccolò Emanuele ; Albin, Roger ; Chowdhury, Sohini ; Foroud, Tatiana ; Njideka, Okubadejo ; Sani, Abubakar ; Uchechi, Agulanna ; Rufus, Akinyemi ; Abiodun, Bello ; Daniel, Ezuduemoih ; Evewero, Ikwenu ; Morenikeji, Komolafe ; Paul, Nwani ; Franscisca, Nwaokorie ; Godwin, Osaigbovo ; Simon, Ozomma

Movement disorders, 2024-04, Vol.39 (4), p.728-733 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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  1. Genotype
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