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Stuart Pickering‐Brown

1994–2024 年に発表

別表記
Stuart Pickering-Brown
73
論文数
23,504
被引用数
62
h 指数
71
i10 指数

被引用数

Stuart Pickering‐Brown の年別被引用数1991 年: 被引用 2 件1994 年: 被引用 1 件1995 年: 被引用 7 件1996 年: 被引用 5 件1997 年: 被引用 3 件1998 年: 被引用 23 件1999 年: 被引用 56 件2000 年: 被引用 89 件2001 年: 被引用 90 件2002 年: 被引用 102 件2003 年: 被引用 81 件2004 年: 被引用 131 件2005 年: 被引用 63 件2006 年: 被引用 165 件2007 年: 被引用 305 件2008 年: 被引用 311 件2009 年: 被引用 231 件2010 年: 被引用 234 件2011 年: 被引用 305 件2012 年: 被引用 421 件2013 年: 被引用 389 件2014 年: 被引用 382 件2015 年: 被引用 375 件2016 年: 被引用 391 件2017 年: 被引用 404 件2018 年: 被引用 326 件2019 年: 被引用 883 件2020 年: 被引用 888 件2021 年: 被引用 853 件2022 年: 被引用 581 件2023 年: 被引用 483 件2024 年: 被引用 639 件2025 年: 被引用 298 件2026 年: 被引用 8 件1992〜1993 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,086 件、この内訳の 29.6%イギリス: 引用元論文 1,223 件、この内訳の 11.7%ドイツ: 引用元論文 597 件、この内訳の 5.7%イタリア: 引用元論文 535 件、この内訳の 5.1%カナダ: 引用元論文 514 件、この内訳の 4.9%中国: 引用元論文 411 件、この内訳の 3.9%オランダ: 引用元論文 394 件、この内訳の 3.8%オーストラリア: 引用元論文 368 件、この内訳の 3.5%日本: 引用元論文 357 件、この内訳の 3.4%フランス: 引用元論文 342 件、この内訳の 3.3%ベルギー: 引用元論文 341 件、この内訳の 3.3%スペイン: 引用元論文 301 件、この内訳の 2.9%
0%29.6%その他 18.9%

機関

分野

  • Medicine73.5%
  • Biochemistry, Genetics and Molecular Biology17.5%
  • Neuroscience7.8%
  • Immunology and Microbiology0.5%
  • Agricultural and Biological Sciences0.1%
  • Chemistry0.1%
  • その他0.5%

トピック

  • Amyotrophic Lateral Sclerosis Research14.5%
  • Alzheimer's disease research and treatments13.6%
  • Parkinson's Disease Mechanisms and Treatments7.5%
  • Neurogenetic and Muscular Disorders Research6.2%
  • Neurological diseases and metabolism3.7%
  • Genetic Neurodegenerative Diseases3.5%
  • その他51%

共著者

全論文

検索で開く
  1. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

    著者: Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor - Neuron 2011 被引用: 4,469

  2. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

    著者: Mike Hutton, Corinne Lendon, Patrizia Rizzu, Matt Baker, Susanne Froelich, Henry Houlden, Stuart Pickering‐Brown, Sumi Chakraverty, Adrian M. Isaacs, Andrew Grover, Jennifer Hackett, Jennifer Adamson, Sarah Lincoln, Dennis W. Dickson, Peter J. Davies, Ronald C. Petersen, Martijn Stevens, Esther de Graaff, Erwin Wauters, Jeltje van Baren, Marcel Hillebrand, Marijke Joosse, Jennifer M. Kwon, Petra Nowotny, Lien Kuei, Joanne Norton, John C. Morris, Lee Reed, John Q. Trojanowski, Hans Basun, Lars Lannfelt, Michael Neystat, Stanley Fahn, Francis Dark, Tony Tannenberg, Peter R. Dodd, Nick Hayward, John B. Kwok, Peter R. Schofield, Athena Andreadis, Julie S. Snowden, David Craufurd, David Neary, F. Owen, Ben A. Oostra, John Hardy, Alison Goate, John C. van Swieten, David Mann, Timothy Lynch, Peter Heutink - Nature 1998 被引用: 3,540

  3. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

    著者: Matt Baker, Ian R. Mackenzie, Stuart Pickering‐Brown, Jennifer Gass, Rosa Rademakers, Caroline Lindholm, Julie S. Snowden, Jennifer Adamson, A. Dessa Sadovnick, Sara Rollinson, Ashley Cannon, Emily Dwosh, David Neary, Stacey Melquist, Anna Richardson, Dennis W. Dickson, Zdenek Berger, Jason L. Eriksen, Todd Robinson, Cynthia Zehr, Chad A. Dickey, Richard Crook, Eileen McGowan, David Mann, Bradley F. Boeve, Howard Feldman, Mike Hutton - Nature 2006 被引用: 2,121

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

    著者: Elisa Majounie, Alan E. Renton, Kin Y. Mok, Elise G.P. Dopper, Adrian J. Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simón‐Sánchez, John C. van Swieten, Yevgeniya Abramzon, Janel O. Johnson, Michael Sendtner, Roger Pamphlett, Richard W. Orrell, Simon Mead, Katie Sidle, Henry Houlden, Jonathan D. Rohrer, Karen Morrison, Hardev Pall, Kevin Talbot, Olaf Ansorge, Dena G. Hernandez, Sampath Arepalli, Mario Sabatelli, Gabriele Mora, Massimo Corbo, Fabio Giannini, Andrea Calvo, Elisabet Englund, Giuseppe Borghero, Gianluca Floris, Anne M. Remes, Hannu Laaksovirta, Leo McCluskey, John Q. Trojanowski, Vivianna M. Van Deerlin, Gerard D. Schellenberg, Michael A. Nalls, Vivian E. Drory, Chin‐Song Lu, Tu‐Hsueh Yeh, Hiroyuki Ishiura, Yuji Takahashi, Shoji Tsuji, Isabelle Le Ber, Alexis Brice, Carsten Drepper, Nigel Williams, Janine Kirby, Pamela J. Shaw, John Hardy, Pentti J. Tienari, Peter Heutink, Huw R. Morris, Stuart Pickering‐Brown, Bryan J. Traynor - The Lancet Neurology 2012 被引用: 1,226

  5. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

    著者: Vivianna M. Van Deerlin, Patrick Sleiman, Maria Martinez‐Lage, Alice Chen‐Plotkin, Li-San Wang, Neill R. Graff‐Radford, Dennis W. Dickson, Rosa Rademakers, Bradley F. Boeve, Murray Grossman, Steven E. Arnold, David Mann, Stuart Pickering‐Brown, Harro Seelaar, Peter Heutink, John C. van Swieten, Jill R. Murrell, Bernardino Ghetti, Salvatore Spina, Jordan Grafman, John R. Hodges, Maria Grazia Spillantini, Sid Gilman, Andrew P. Lieberman, Jeffrey Kaye, Randall L. Woltjer, Eileen H. Bigio, Marsel Mesulam, Safa Al‐Sarraj, Claire Troakes, Roger N. Rosenberg, Charles L. White, Isidró Ferrer, Albert Lladó, Manuela Neumann, Hans A. Kretzschmar, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, Bruce L. Miller, Ainhoa Alzualde, Adolfo López de Munain, Ann C. McKee, Marla Gearing, Allan I. Levey, James J. Lah, John Hardy, Jonathan D. Rohrer, Tammaryn Lashley, Ian R. Mackenzie, Howard Feldman, Ronald L. Hamilton, Steven T. DeKosky, Julie van der Zee, Samir Kumar‐Singh, Christine Van Broeckhoven, Richard Mayeux, Jean Paul Vonsattel, Juan C. Troncoso, Jillian J. Kril, John B. Kwok, Glenda M. Halliday, Thomas D. Bird, Paul G. Ince, Pamela J. Shaw, Nigel J. Cairns, John C. Morris, Catriona McLean, Charles DeCarli, William G. Ellis, Stefanie H. Freeman, Matthew P. Frosch, John H. Growdon, Daniel P. Perl, Mary Sano, David A. Bennett, Julie A. Schneider, Thomas G. Beach, Eric M. Reiman, Bryan K. Woodruff, Jeffrey L. Cummings, Harry V. Vinters, Carol A. Miller, Helena C. Chui, Irina Alafuzoff, Päivi Hartikainen, Danielle Seilhean, Douglas Galasko, Eliezer Masliah, Carl W. Cotman, MJ Tuñón, Mònica Martínez, David G. Muñoz, Steven L. Carroll, Daniel Marson, Peter Riederer, Nenad Bogdanović, Gerard D Schellenberg, Håkon Håkonarson, John Q. Trojanowski, Virginia M.‐Y. Lee - Nature Genetics 2010 被引用: 609

  6. C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins

    著者: Sarah Mizielinska, Sebastian Grönke, Teresa Niccoli, Charlotte Ridler, Emma L. Clayton, Anny Devoy, Thomas G. Moens, Frances E. Norona, Ione Woollacott, J. Pietrzyk, Karen Cleverley, Andrew J. Nicoll, Stuart Pickering‐Brown, Jacqueline Dols, Melissa Cabecinha, Oliver Hendrich, Pietro Fratta, Elizabeth Fisher, Linda Partridge, Adrian M. Isaacs - Science 2014 被引用: 776

  7. A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    著者: Michael A. Nalls, Raquel Durán, Grisel Lopez, Marzena Kurzawa‐Akanbi, Ian G. McKeith, Patrick F. Chinnery, Christopher M. Morris, Jessie Theuns, David Crosiers, Patrick Cras, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, David M. A. Mann, Julie S. Snowden, Stuart Pickering‐Brown, Nicola Halliwell, Yvonne S. Davidson, Linda Gibbons, Jenny Harris, Una‐Marie Sheerin, José Brás, John Hardy, Lorraine N. Clark, Karen Marder, Lawrence S. Honig, Daniela Berg, Walter Maetzler, Kathrin Brockmann, Thomas Gasser, Fabiana Novellino, Aldo Quattrone, Grazia Annesi, Elvira Valeria De Marco, Ekaterina Rogaeva, Mario Masellis, Sandra E. Black, Juan M. Bilbao, Tatiana Foroud, Bernardino Ghetti, William C. Nichols, Nathan Pankratz, Glenda M. Halliday, Suzanne Lesage, Stephan Klebe, Alexandra Dürr, Charles Duyckaerts, Alexis Brice, Benoit I. Giasson, John Q. Trojanowski, Howard I. Hurtig, Nahid Tayebi, Claudia Landazabal, Melanie A. Knight, Margaux F. Keller, Andrew Singleton, Tyra G. Wolfsberg, Ellen Sidransky - JAMA Neurology 2013 被引用: 444

  8. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

    著者: Katrina Moore, Jennifer Nicholas, Murray Grossman, Corey T. McMillan, David J. Irwin, Lauren Massimo, Vivianna M Van Deerlin, Jason D. Warren, Nick C. Fox, Martin N. Rossor, Simon Mead, Martina Bocchetta, Bradley F. Boeve, David S. Knopman, Neill R. Graff‐Radford, Leah K. Forsberg, Rosa Rademakers, Zbigniew K. Wszołek, John C. van Swieten, Lize C. Jiskoot, Lieke Meeter, Elise G.P. Dopper, Janne M. Papma, Julie S. Snowden, Jennifer A. Saxon, Matthew Jones, Stuart Pickering‐Brown, Isabelle Le Ber, Agnès Camuzat, Alexis Brice, Paola Caroppo, Roberta Ghidoni, Michela Pievani, Luisa Benussi, Giuliano Binetti, Bradford C. Dickerson, Diane Lucente, Samantha Krivensky, Caroline Graff, Linn Öijerstedt, Marie Fallström, Håkan Thonberg, Nupur Ghoshal, John C. Morris, Barbara Borroni, Alberto Benussi, Alessandro Padovani, Daniela Galimberti, Elio Scarpini, Giorgio Fumagalli, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, Pheth Sengdy, Adam L. Boxer, Howie Rosen, Joanne Taylor, Matthis Synofzik, Carlo Wilke, Patricia Sulzer, John R. Hodges, Glenda M. Halliday, John B. Kwok, Raquel Sánchez‐Valle, Albert Lladó, Sergi Borrego‐Écija, Isabel Santana, Maria Rosário Almeida, Miguel Tábuas‐Pereira, Fermín Moreno, Myriam Barandiarán, Begoña Indakoetxea, Johannes Levin, Adrian Danek, James B. Rowe, Thomas Cope, Markus Otto, Sarah Anderl‐Straub, Alexandre de Mendonça, Carolina Maruta, Mario Masellis, Sandra E. Black, Philippe Couratier, Géraldine Lautrette, Edward D. Huey, Sandro Sorbi, Benedetta Nacmias, Robert Laforce, Marie-Pier L Tremblay, Rik Vandenberghe, Philip Van Damme, Emily Rogalskı, Sandra Weıntraub, Alexander Gerhard, Chiadi U. Onyike, Simon Ducharme, Sokratis G. Papageorgiou, Adeline Su Lyn Ng, Amy Brodtmann, Elizabeth Finger, Rita Guerreiro ほか 71 名 - The Lancet Neurology 2019 被引用: 311

  9. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

    著者: Rita Guerreiro, Owen A. Ross, Célia Kun‐Rodrigues, Dena Hernández, Tatiana Orme, John D. Eicher, Claire E. Shepherd, Laura Parkkinen, Lee Darwent, Michael G. Heckman, Sonja W. Scholz, Juan C. Troncoso, Olga Pletnikova, Olaf Ansorge, Jordi Clarimón, Alberto Lleó, Estrella Morenas‐Rodríguez, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Afina W. Lemstra, Ekaterina Rogaeva, Peter St George‐Hyslop, Elisabet Londos, Henrik Zetterberg, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Janice L. Holton, Yaroslau Compta, Vivianna M. Van Deerlin, Geidy E. Serrano, Thomas G. Beach, Suzanne Lesage, Douglas Galasko, Eliezer Masliah, Isabel Santana, Pau Pástor, Mónica Díez-Fairén, Miquel Aguilar, Pentti J. Tienari, Liisa Myllykangas, Minna Oinas, Tamás Révész, Andrew J. Lees, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Valentina Escott‐Price, Caroline Graff, Nigel J. Cairns, John C. Morris, Stuart Pickering‐Brown, David Mann, Glenda M. Halliday, John Hardy, John Q. Trojanowski, Dennis W. Dickson, Andrew Singleton, David J. Stone, José Brás - The Lancet Neurology 2017 被引用: 289

  10. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

    著者: Jennifer Gass, Ashley Cannon, Ian R. Mackenzie, Bradley F. Boeve, Matt Baker, Jennifer Adamson, Richard Crook, Stacey Melquist, Karen M. Kuntz, Ron Petersen, Keith A. Josephs, Stuart Pickering‐Brown, Neill R. Graff‐Radford, Ryan J. Uitti, Dennis W. Dickson, Zbigniew K. Wszołek, John Gonzalez, Thomas G. Beach, Eileen H. Bigio, Nancy Johnson, Sandra Weıntraub, Marsel Mesulam, Charles L. White, Bryan K. Woodruff, Richard J. Caselli, Ging‐Yuek Robin Hsiung, Howard Feldman, Dave Knopman, Mike Hutton, Rosa Rademakers - Human Molecular Genetics 2006 被引用: 578

  11. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

    著者: José Brás, Rita Guerreiro, Lee Darwent, Laura Parkkinen, Olaf Ansorge, Valentina Escott‐Price, Dena G. Hernandez, Michael A. Nalls, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Wiesje M. van der Flier, Afina W. Lemstra, Philip Scheltens, Ekaterina Rogaeva, Peter St George‐Hyslop, Elisabet Londos, Henrik Zetterberg, Sara Ortega‐Cubero, Pau Pástor, Tanis J. Ferman, Caroline Graff, Owen A. Ross, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Walter Maetzler, Daniela Berg, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Yaroslau Compta, Tamás Révész, Andrew J. Lees, Nigel J. Cairns, Glenda M. Halliday, David Mann, Stuart Pickering‐Brown, Dennis W. Dickson, Andrew Singleton, John Hardy - Human Molecular Genetics 2014 被引用: 240

  12. Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

    著者: Cyril Pottier, Yingxue Ren, Ralph B. Perkerson, Matt Baker, Gregory D. Jenkins, Marka van Blitterswijk, Mariely DeJesus‐Hernandez, Jeroen van Rooij, Melissa E. Murray, Elizabeth Christopher, Shannon K. McDonnell, Zachary C. Fogarty, Anthony Batzler, Shulan Tian, Cristina T. Vicente, Billie J. Matchett, Anna M. Karydas, Ging‐Yuek Robin Hsiung, Harro Seelaar, Merel O. Mol, Elizabeth Finger, Caroline Graff, Linn Öijerstedt, Manuela Neumann, Peter Heutink, Matthis Synofzik, Carlo Wilke, Johannes Prudlo, Patrizia Rizzu, Javier Simón‐Sánchez, Dieter Edbauer, Sigrun Roeber, Janine Diehl‐Schmid, Bret M. Evers, Andrew King, Marsel Mesulam, Sandra Weıntraub, Changiz Geula, Kevin F. Bieniek, Leonard Petrucelli, Geoffrey L. Ahern, Eric M. Reiman, Bryan K. Woodruff, Richard J. Caselli, Edward D. Huey, Martin R. Farlow, Jordan Grafman, Simon Mead, Lea T. Grinberg, Salvatore Spina, Murray Grossman, David J. Irwin, Edward B. Lee, EunRan Suh, Julie S. Snowden, David Mann, Nilüfer Ertekin‐Taner, Ryan J. Uitti, Zbigniew K. Wszołek, Keith A. Josephs, Joseph E. Parisi, David S. Knopman, Ronald C. Petersen, John R. Hodges, Olivier Piguet, Ethan G. Geier, Jennifer S. Yokoyama, Robert A. Rissman, Ekaterina Rogaeva, Julia Keith, Lorne Zinman, Maria Carmela Tartaglia, Nigel J. Cairns, Carlos Cruchaga, Bernardino Ghetti, Julia Kofler, Oscar L. López, Thomas G. Beach, Thomas Arzberger, Jochen Herms, Lawrence S. Honig, Jean Paul Vonsattel, Glenda M. Halliday, John B. Kwok, Charles L. White, Marla Gearing, Jonathan D. Glass, Sara Rollinson, Stuart Pickering‐Brown, Jonathan D. Rohrer, John Q. Trojanowski, Vivianna Van Deerlin, Eileen H. Bigio, Claire Troakes, Safa Al‐Sarraj, Yan W. Asmann, Bruce L. Miller, Neill R. Graff‐Radford, Bradley F. Boeve, William W. Seeley ほか 5 名 - Acta Neuropathologica 2019 被引用: 128

  13. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

    著者: Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin, Bruno A. Benítez, Yefei Cai, Rita Guerreiro, Oscar Harari, Joanne Norton, John Budde, Sarah Bertelsen, Amanda T. Jeng, Breanna Cooper, Tara Skorupa, David Carrell, Denise Levitch, Simon Hsu, Jiyoon Choi, Mina Ryten, John Hardy, Mina Ryten, Daniah Trabzuni, Michael E. Weale, Adaikalavan Ramasamy, Colin Smith, Celeste Sassi, José Brás, J. Raphael Gibbs, Dena G. Hernandez, Michelle K. Lupton, John Powell, Paola Forabosco, Perry G. Ridge, Christopher Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ronald G. Munger, Cameron Schmutz, Maegan Leary, F. Yesim Demirci, Mikhil Bamne, Xingbin Wang, Oscar L. López, Mary Ganguli, Christopher Medway, James Turton, Jenny Lord, Anne Braae, Imelda Barber, Kristelle Brown, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, David Mann, Stuart Pickering‐Brown, Kristelle Brown, Noor Kalsheker, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes, Pau Pástor, Oswaldo Lorenzo‐Betancor, Zoran Brkanac, Erick R. Scott, Eric J. Topol, Kevin Morgan, Ekaterina Rogaeva, Andrew B. Singleton, John Hardy, M. Ilyas Kamboh, Peter St George‐Hyslop, Nigel J. Cairns, John C. Morris, John Kauwe, Alison Goate - Nature 2013 被引用: 476

  14. Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

    著者: Jonathan M. Schott, Sebastian J. Crutch, Minerva M. Carrasquillo, James Uphill, Timothy J. Shakespeare, Natalie S. Ryan, Keir Yong, Manja Lehmann, Nilüfer Ertekin‐Taner, Neill R. Graff‐Radford, Bradley F. Boeve, Melissa E. Murray, Qurat ul Ain Khan, Ronald C. Petersen, Dennis W. Dickson, David S. Knopman, Gil D. Rabinovici, Bruce L. Miller, Aida Suárez González, E Gil-Néciga, Julie S. Snowden, Jenny Harris, Stuart Pickering‐Brown, Eva Louwersheimer, Wiesje M. van der Flier, Philip Scheltens, Yolande A.L. Pijnenburg, Douglas Galasko, Marie Sarazin, Bruno Dubois, Éloi Magnin, Daniela Galimberti, Elio Scarpini, Stefano F. Cappa, John R. Hodges, Glenda M. Halliday, Lauren Bartley, María C. Carrillo, José Brás, John Hardy, Martin N. Rossor, John Collinge, Nick C. Fox, Simon Mead - Alzheimer s & Dementia 2016 被引用: 131

  15. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

    著者: Cyril Pottier, Xiaolai Zhou, Ralph B. Perkerson, Matt Baker, Gregory D. Jenkins, Daniel Serie, Roberta Ghidoni, Luisa Benussi, Giuliano Binetti, Adolfo López de Munain, Miren Zulaica, Fermín Moreno, Isabelle Le Ber, Florence Pasquier, Didier Hannequin, Raquel Sánchez‐Valle, Anna Antonell, Albert Lladó, Tammee M. Parsons, NiCole A. Finch, Elizabeth Finger, Carol F. Lippa, Edward D. Huey, Manuela Neumann, Peter Heutink, Matthis Synofzik, Carlo Wilke, Robert A. Rissman, Jarosław Sławek, Emilia J. Sitek, Peter Johannsen, Jørgen E. Nielsen, Yingxue Ren, Marka van Blitterswijk, Mariely DeJesus‐Hernandez, Elizabeth Christopher, Melissa E. Murray, Kevin F. Bieniek, Bret M. Evers, Camilla Ferrari, Sara Rollinson, Anna Richardson, Elio Scarpini, Giorgio Fumagalli, Alessandro Padovani, John Hardy, Parastoo Momeni, Raffaele Ferrari, Francesca Frangipane, Raffaele Maletta, Maria Anfossi, Maura Gallo, Leonard Petrucelli, EunRan Suh, Oscar L Lopez, Tsz Hang Wong, Jeroen van Rooij, Harro Seelaar, Simon Mead, Richard J. Caselli, Eric M. Reiman, Marwan N. Sabbagh, Mads Kjølby, Anders Nykjær, Anna M. Karydas, Adam L. Boxer, Lea T. Grinberg, Jordan Grafman, Salvatore Spina, Adrian L. Oblak, M-Marsel Mesulam, Sandra Weıntraub, Changiz Geula, John R. Hodges, Olivier Piguet, William S. Brooks, David J. Irwin, John Q. Trojanowski, Edward B. Lee, Keith A. Josephs, Joseph E. Parisi, Nilüfer Ertekin‐Taner, David S. Knopman, Benedetta Nacmias, Irene Piaceri, Silvia Bagnoli, Sandro Sorbi, Marla Gearing, Jonathan D. Glass, Thomas G. Beach, Sandra E. Black, Mario Masellis, Ekaterina Rogaeva, Jean‐Paul Vonsattel, Lawrence S. Honig, Julia Kofler, Amalia C. Bruni, Julie S. Snowden, David Mann, Stuart Pickering‐Brown ほか 33 名 - The Lancet Neurology 2018 被引用: 129

  16. Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups

    著者: Karri Kaivola, Zalak Shah, Ruth Chia, Sandra E. Black, Ziv Gan‐Or, Julia Keith, Mario Masellis, Ekaterina Rogaeva, Alexis Brice, Suzanne Lesage, Georgia Xiromerisiou, Andrea Calvo, Antonio Canosa, Adriano Chiò, Giancarlo Logroscino, Gabriele Mora, Reijko Krüger, Patrick May, Daniel Alcolea, Jordi Clarimón, Juan Fortea, Isabel González Aramburu, Jon Infante, Carmen Lage, Alberto Lleó, Pau Pástor, Pascual Sánchez‐Juan, Francesca Brett, Dag Aarsland, Safa Al‐Sarraj, Johannes Attems, Steve Gentleman, John Hardy, Angela Hodges, Seth Love, Ian G. McKeith, Christopher M. Morris, Huw R. Morris, Laura Palmer, Stuart Pickering‐Brown, Mina Ryten, Alan Thomas, Claire Troakes, Marilyn S. Albert, Matthew J. Barrett, Thomas G. Beach, Lynn M. Bekris, David A. Bennett, Bradley F. Boeve, Clifton L. Dalgard, Ted M. Dawson, Dennis W. Dickson, Kelley Faber, Tanis J. Ferman, Luigi Ferrucci, Margaret E. Flanagan, Tatiana M. Foroud, Bernardino Ghetti, J. Raphael Gibbs, Alison Goate, David S. Goldstein, Caroline Graff, Horacio Kaufmann, Walter A. Kukull, James B. Leverenz, Qinwen Mao, Eliezer Masliah, Edwin S. Monuki, Kathy L. Newell, Jose‐Alberto Palma, Olga Pletnikova, Alan E. Renton, Susan M. Resnick, Liana S. Rosenthal, Owen A. Ross, Clemens R. Scherzer, Geidy E. Serrano, Vikram G. Shakkottai, Ellen Sidransky, Toshiko Tanaka, Eric Topol, Ali Torkamani, Juan C. Troncoso, Randy Woltjer, Zbigniew K. Wszołek, Sonja W. Scholz, Sonja W. Scholz - Brain 2021 被引用: 65

  17. Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

    著者: Wei Wei, Michael J. Keogh, Ian Wilson, Jonathan Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa‐Akanbi, Mauro Santibanez‐Koref, Kevin Talbot, Martin R. Turner, Chris-Anne McKenzie, Claire Troakes, Johannes Attems, Colin Smith, Safa Al Sarraj, Christopher M. Morris, Olaf Ansorge, Stuart Pickering‐Brown, James W. Ironside, Patrick F. Chinnery - Acta Neuropathologica Communications 2017 被引用: 136

  18. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

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  20. C9orf72 dipeptides disrupt the nucleocytoplasmic transport machinery and cause TDP-43 mislocalisation to the cytoplasm

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