Benjamin Grenier‐Boley

Active 2010–2025

49
Papers
19,919
Citations
34
h-index
46
i10-index

Citations

Citations per year for Benjamin Grenier‐Boley1972: 1 citations2002: 3 citations2010: 5 citations2011: 7 citations2012: 6 citations2013: 14 citations2014: 91 citations2015: 132 citations2016: 222 citations2017: 234 citations2018: 339 citations2019: 995 citations2020: 1,164 citations2021: 1,210 citations2022: 1,003 citations2023: 894 citations2024: 1,386 citations2025: 705 citations2026: 21 citations1973–2001: no citations, so these years are not shown2003–2009: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,172 citing papers, 24.6% of this breakdownUnited Kingdom: 1,227 citing papers, 9.5% of this breakdownChina: 1,065 citing papers, 8.3% of this breakdownGermany: 690 citing papers, 5.3% of this breakdownNetherlands: 495 citing papers, 3.8% of this breakdownCanada: 475 citing papers, 3.7% of this breakdownAustralia: 466 citing papers, 3.6% of this breakdownFrance: 454 citing papers, 3.5% of this breakdownSweden: 403 citing papers, 3.1% of this breakdownSpain: 389 citing papers, 3% of this breakdownItaly: 306 citing papers, 2.4% of this breakdownNorway: 247 citing papers, 1.9% of this breakdown
0%24.6%Other 27.3%

Fields

  • Medicine38.8%
  • Biochemistry, Genetics and Molecular Biology32.6%
  • Neuroscience18.6%
  • Psychology2.5%
  • Immunology and Microbiology1.8%
  • Computer Science1.3%
  • Other4.4%

Topics

  • Alzheimer's disease research and treatments12.6%
  • Genetic Associations and Epidemiology6.5%
  • Neuroinflammation and Neurodegeneration Mechanisms6.5%
  • Dementia and Cognitive Impairment Research3.9%
  • Bioinformatics and Genomic Networks3.5%
  • Tryptophan and brain disorders2.3%
  • Other64.7%

Coauthors

All papers

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  1. New insights into the genetic etiology of Alzheimer’s disease and related dementias

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ignacio Álvarez, Victoria Álvarez, Nicola J. Armstrong, Anthoula Tsolaki, Carmen Antúnez, Ildebrando Appollonio, Marina Arcaro, Silvana Archetti, Alfonso Arias Pastor, Beatrice Arosio, Lavinia Athanasiu, Henri Bailly, Nerisa Banaj, Miquel Baquero, Sandra Barral, Alexa Beiser, Ana Belén Pastor, Jennifer E. Below, Penelope Benchek, Luisa Benussi, Claudine Berr, Céline Besse, Valentina Bessi, Giuliano Binetti, Alessandra Bizarro, Rafael Blesa, Merçé Boada, Eric Boerwinkle, Barbara Borroni, Silvia Boschi, Paola Bossù, Geir Bråthen, Jan Bressler, Catherine Bresner, Henry Brodaty, Keeley J. Brookes, Luis Ignacio Brusco, Dolores Buiza‐Rueda, Katharina Bürger, Vanessa Burholt, William S. Bush, Miguel Calero, Laura B. Cantwell, Geneviève Chêne, Jaeyoon Chung, Michael L. Cuccaro, Ángel Carracedo, Roberta Cecchetti, Laura Cervera‐Carles, Camille Charbonnier, Hung‐Hsin Chen, Caterina Chillotti, Simona Ciccone, Jurgen A.H.R. Claassen, Christopher Clark, Elisa Conti, Anaïs Corma‐Gómez, Emanuele Maria Costantini, Carlo Custodero, Delphine Daian, Carolina Dalmasso, Antonio Daniele, Efthimios Dardiotis, Jean‐François Dartigues, Peter Paul De Deyn, Kátia de Paiva Lopes, Lot D. de Witte, Stéphanie Debette, Jürgen Deckert, Teodoro del Ser and 1,166 more - Nature Genetics 2022 cited by 2,471

  2. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Merçé Boada, Gary W. Beecham, Jean-Guillaume Garnier, Denise Harold, Annette L. Fitzpatrick, Otto Valladares, Marie-Laure Moutet, Amy Gerrish, Albert V. Smith, Liming Qu, Delphine Bacq, Nicola Denning, Xueqiu Jian, Yi Zhao, Maria Del Zompo, Nick C. Fox, Seung‐Hoan Choi, Ignacio Mateo, Joseph T. Hughes, Hieab H.H. Adams, John Malamon, Florentino Sánchez-García, Yogen Patel, Jennifer A. Brody, Beth A. Dombroski, María Cándida Déniz Naranjo, Makrina Daniilidou, Guðný Eiríksdóttir, Shubhabrata Mukherjee, David Wallon, James Uphill, Thor Aspelund, Laura B. Cantwell, Fabienne Garzia, Daniela Galimberti, Edith Hofer, Mariusz Butkiewicz, Bertrand Fin, Elio Scarpini, Chloé Sarnowski, William S. Bush, Stéphane Meslage, Johannes Kornhuber, Charles C. White, Yuenjoo Song, Robert C. Barber, Sebastiaan Engelborghs, Sabrina Sordon, Dina Voijnovic, Perrie M. Adams, Rik Vandenberghe, Manuel Mayhaus, L. Adrienne Cupples, Marilyn S. Albert, Peter Paul De Deyn, Wei Gu, J.J. Himali, Duane Beekly, Alessio Squassina, Annette M. Hartmann, Adelina Orellana, Deborah Blacker, Eloy Rodríguez‐Rodríguez, Simon Lovestone, Melissa E. Garcia, Rachelle S. Doody, Carmen Munoz-Fernadez, Rebecca Sussams, Honghuang Lin, Thomas Fairchild and 369 more - Nature Genetics 2019 cited by 3,204

  3. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Seung‐Hoan Choi, Christiane Reitz, Florence Pasquier, Paul Hollingworth, Alfredo Ramı́rez, Olivier Hanon, Annette L. Fitzpatrick, Joseph D. Buxbaum, Dominique Campion, Paul K. Crane, Clinton T. Baldwin, Tim Becker, Vilmundur Guðnason, Carlos Cruchaga, David Craig, Najaf Amin, Claudine Berr, Oscar L Lopez, Philip L. De Jager, Vincent Deramecourt, Janet Johnston, Denis A. Evans, Simon Lovestone, Luc Letenneur, Francisco Jesús Morón, David C. Rubinsztein, Gudny Eiriksdottir, Kristel Sleegers, Alison Goate, Nathalie Fiévet, Matthew J. Huentelman, Michael Gill, Kristelle Brown, M. Ilyas Kamboh, Lina Keller, Pascale Barberger‐Gateau, Bernadette McGuinness, Eric B. Larson, Robert C. Green, Amanda Myers, Carole Dufouil, Stephen Todd, David Wallon, Seth Love, Ekaterina Rogaeva, John Gallacher, Peter St George‐Hyslop, Jordi Clarimón, Alberto Lleó, Anthony Bayer, Debby W. Tsuang, Lei Yu, Magda Tsolaki, Paola Bossù, Gianfranco Spalletta, Petroula Proitsi, John Collinge, Sandro Sorbi, Florentino Sánchez-García, Nick C. Fox, John Hardy, María Cándida Déniz Naranjo, Paolo Bosco, Robert Clarke, Carol Brayne, Daniela Galimberti, Michelangelo Mancuso, Fiona E. Matthews, Susanne Moebus, Patrizia Mecocci and 84 more - Nature Genetics 2013 cited by 4,659

  4. Analysis of shared heritability in common disorders of the brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte and 477 more - Science 2018 cited by 2,050

  5. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lindsay A. Farrer, María Victoria Fernández, Nick C. Fox, Daniela Galimberti, Emmanuelle Génin, Johan J. P. Gille, Yann Le Guen, Rita Guerreiro, Jonathan L. Haines, Clive Holmes, M. Arfan Ikram, M. Kamran Ikram, Iris E. Jansen, Robert Kraaij, M Lathrop, Afina W. Lemstra, Alberto Lleó, Lauren Luckcuck, Marcel M. A. M. Mannens, Iain Marshall, Eden R. Martin, Carlo Masullo, Richard Mayeux, Patrizia Mecocci, Alun Meggy, Merel O. Mol, Kevin Morgan, R Myers, Benedetta Nacmias, Adam C. Naj, Valerio Napolioni, Florence Pasquier, Pau Pástor, Margaret A. Pericak‐Vance, Rachel Raybould, Richard Redon, Marcel Reinders, Anne‐Claire Richard, Steffi G. Riedel‐Heller, Fernando Rivadeneira, Stéphane Rousseau, Natalie S. Ryan, Salha Saad, Pascual Sánchez‐Juan, Gerard D. Schellenberg, Philip Scheltens, Jonathan M. Schott, Davide Seripa, Sudha Seshadri, Daoud Sie, Erik A. Sistermans, Sandro Sorbi, Resie van Spaendonk, Gianfranco Spalletta, Niccoló Tesi, Betty M. Tijms, André G. Uitterlinden, Sven J. van der Lee, Pieter Jelle Visser, Michael Wagner, David Wallon, Li-San Wang, Aline Zaréa, Jordi Clarimón, John C. van Swieten, Michael D. Greicius, Jennifer S. Yokoyama, Carlos Cruchaga, John Hardy, Alfredo Ramı́rez and 7 more - Nature Genetics 2022 cited by 219

  6. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Seung-Hoan Choi, Gary W. Beecham, Cécile Dulary, Stefan Herms, Albert V. Smith, Cory C. Funk, Céline Derbois, Andreas J. Forstner, Shahzad Ahmad, Hong‐Dong Li, Delphine Bacq, Denise Harold, Claudia L. Satizábal, Otto Valladares, Alessio Squassina, Rhodri Thomas, Jennifer A. Brody, Liming Qu, Pascual Sánchez‐Juan, Taniesha Morgan, Frank J. Wolters, Yi Zhao, Florentino Sánchez-García, Nicola Denning, Myriam Fornage, John Malamon, María Cándida Déniz Naranjo, Elisa Majounie, Thomas H. Mosley, Beth A. Dombroski, David Wallon, Michelle K. Lupton, Josée Dupuis, Patrice L. Whitehead, Laura Fratiglioni, Christopher Medway, Xueqiu Jian, Shubhabrata Mukherjee, Lina Keller, Kristelle Brown, Honghuang Lin, Laura B. Cantwell, Francesco Panza, Bernadette McGuinness, Sonia Moreno–Grau, Jeremy D. Burgess, Vincenzo Solfrizzi, Petra Proitsi, Hieab H.H. Adams, Mariet Allen, Davide Seripa, Pau Pástor, L. Adrienne Cupples, Nathan D. Price, Didier Hannequin, Ana Frank, Daniel Levy, Paramita Chakrabarty, Paolo Caffarra, Ina Giegling, Alexa Beiser, Vilmantas Giedraitis, Harald Hampel, Melissa E. Garcia, Xue Wang, Lars Lannfelt, Patrizia Mecocci, Gudny Eiriksdottir, Paul K. Crane, Florence Pasquier and 350 more - Nature Genetics 2017 cited by 1,104

  7. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mónica Díez-Fairén, Carmen Lage, Sebastián García‐Madrona, Pablo García‐González, Emilio Alarcón‐Martín, Sergi Valero, Óscar Sotolongo‐Grau, Abbe Ullgren, Adam C. Naj, Afina W. Lemstra, Alba Benaque, Alba Pérez‐Cordón, Alberto Benussi, Alberto Rábano, Alessandro Padovani, Alessio Squassina, Alexandre de Mendonça, Alfonso Arias Pastor, Almar A. L. Kok, Alun Meggy, Ana Belén Pastor, Ana Espinosa, Anaïs Corma‐Gómez, Ángel Martín Montes, Ángela Sanabria, Anita L. DeStefano, Anja Schneider, Annakaisa Haapasalo, Anne Kinhult Ståhlbom, Anne Tybjærg‐Hansen, Annette M. Hartmann, Annika Spottke, Arturo Corbatón Anchuelo, Arvid Rongve, Barbara Borroni, Beatrice Arosio, Benedetta Nacmias, Børge G. Nordestgaard, Brian W. Kunkle, Camille Charbonnier, Carla Abdelnour, Carlo Masullo, Carmen Martínez Rodríguez, Carmen Muñoz-Fernández, Carole Dufouil, Caroline Graff, Catarina B. Ferreira, Caterina Chillotti, Chandra A. Reynolds, Chiara Fenoglio, Christine Van Broeckhoven, Christopher Clark, Claudia Pisanu, Claudia L. Satizábal, Clive Holmes, Dolores Buiza‐Rueda, Dag Aarsland, Dan Rujescu, Daniel Alcolea, Daniela Galimberti, David Wallon, Davide Seripa, Edna Grünblatt, Efthimios Dardiotis, Emrah Düzel, Elio Scarpini, Elisa Conti, Elisa Rubino, Ellen Gelpí, Eloy Rodríguez‐Rodríguez and 472 more - Nature Communications 2021 cited by 338

  8. Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease

    Authors: , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2016 cited by 263

  9. Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raquel Sánchez‐Valle, Victoria Álvarez, Merçé Boada, Pablo García‐González, Raquel Puerta, Pablo Mir, Luís Miguel Real, Gerard Piñol‐Ripoll, José María García‐Alberca, José Luís Royo, Eloy Rodríguez‐Rodríguez, Hilkka Soininen, Teemu Kuulasmaa, Alexandre de Mendonça, Shima Mehrabian, Jakub Hort, Martin Vyhnálek, Sven J. van der Lee, Caroline Graff, Goran Papenberg, Vilmantas Giedraitis, Anne Boland, Delphine Bacq‐Daian, Jean‐François Deleuze, Gaël Nicolas, Carole Dufouil, Florence Pasquier, Olivier Hanon, Stéphanie Debette, Edna Grünblatt, Julius Popp, Luisa Benussi, Daniela Galimberti, Beatrice Arosio, Patrizia Mecocci, Vincenzo Solfrizzi, Lucilla Parnetti, Alessio Squassina, Lucio Tremolizzo, Barbara Borroni, Benedetta Nacmias, Sandro Sorbi, Paolo Caffarra, Davide Seripa, Innocenzo Rainero, Antonio Daniele, Carlo Masullo, Gianfranco Spalletta, Julie Williams, Philippe Amouyel, Frank Jessen, Patrick G. Kehoe, Magda Tsolaki, Giacomina Rossi, Pascual Sánchez‐Juan, Kristel Sleegers, Martin Ingelsson, Ole A. Andreassen, Mikko Hiltunen, Cornelia M. van Duijn, Rebecca Sims, Wiesje M. van der Flier, Agustı́n Ruiz, Alfredo Ramı́rez, Jean‐Charles Lambert, Ruth Frikke‐Schmidt - JAMA Network Open 2023 cited by 93

  10. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Rebecca Sims, Valentina Escott‐Price, Richard Mayeux, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Jean‐Charles Lambert, Cornelia M. van Duijn, Lenore J. Launer, Sudha Seshadri, Julie Williams, Philippe Amouyel, Gerard D. Schellenberg, Bin Zhang, Ingrid B. Borecki, John S.K. Kauwe, Carlos Cruchaga, Ke Hao, Alison Goate - Nature Neuroscience 2017 cited by 471

  11. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Merçé Boada, Anne Boland, Katharina Büerger, Ángel Carracedo, Laura Cervera‐Carles, Geneviève Chêne, Jurgen A.H.R. Claassen, Stéphanie Debette, Jean‐François Deleuze, Peter Paul De Deyn, Janine Diehl‐Schmid, Srdjan Djurovic, Oriol Dols‐Icardo, Carole Dufouil, Emmanuelle Duron, Emrah Düzel, Tormod Fladby, Juan Fortea, Lutz Frölich, Pablo García‐González, María García‐Martínez, Ina Giegling, Oliver Goldhardt, Johan Gobom, Timo Grimmer, Annakaisa Haapasalo, Harald Hampel, Olivier Hanon, Lucrezia Hausner, Stefanie Heilmann‐Heimbach, Seppo Helisalmi, Michael T. Heneka, Isabel Hernández, Sanna‐Kaisa Herukka, Henne Holstege, Jonas Alexander Jarholm, Silke Kern, Anne‐Brita Knapskog, Anne M. Koivisto, Johannes Kornhuber, Teemu Kuulasmaa, Carmen Lage, Christoph Laske, Ville Leinonen, Piotr Lewczuk, Alberto Lleó, Adolfo López de Munain, Sara López‐García, Wolfgang Maier, Marta Marquié, Merel O. Mol, Laura Montrreal, Fermín Moreno, Sonia Moreno–Grau, Gaël Nicolas, Markus M. Nöthen, Adelina Orellana, Lene Pålhaugen, Janne M. Papma, Florence Pasquier, Robert Perneczky, Oliver Peters, Yolande A.L. Pijnenburg, Julius Popp, Daniëlle Posthuma, Ana Pozueta, Josef Priller, Raquel Puerta, Inés Quintela, Inez Ramakers and 47 more - Acta Neuropathologica 2022 cited by 138

  12. Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease

    Authors: , , , - Molecular Psychiatry 2023 cited by 83

  13. Genetics of Alzheimer’s disease: where we are, and where we are going

    Authors: , , - Current Opinion in Neurobiology 2019 cited by 217

  14. Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ruth Frikke‐Schmidt, Julie Williams, Agustı́n Ruiz, Jean‐Charles Lambert, Michael D. Greicius, Members of the EADB, GR@ACE, DEGESCO, DemGene, GERAD, and EADI Groups, Beatrice Arosio, Luisa Benussi, Anne Boland, Barbara Borroni, Paolo Caffarra, Delphine Daian, Antonio Daniele, Stéphanie Debette, Carole Dufouil, Emrah Düzel, Daniela Galimberti, Vilmantas Giedraitis, Timo Grimmer, Caroline Graff, Edna Grünblatt, Olivier Hanon, Lucrezia Hausner, Stefanie Heilmann‐Heimbach, Henne Holstege, Jakub Hort, Jürgen Deckert, Teemu Kuulasmaa, Aad van der Lugt, Carlo Masullo, Patrizia Mecocci, Shima Mehrabian, Alexandre de Mendonça, Susanne Moebus, Benedetta Nacmias, Gaël Nicolas, Robert Olaso, Goran Papenberg, Lucilla Parnetti, Florence Pasquier, Oliver Peters, Yolande A.L. Pijnenburg, Julius Popp, Innocenzo Rainero, Inez Ramakers, Steffi G. Riedel‐Heller, Nikolaos Scarmeas, Philip Scheltens, Norbert Scherbaum, Anja Schneider, Davide Seripa, Hilkka Soininen, Vincenzo Solfrizzi, Gianfranco Spalletta, Alessio Squassina, John C. van Swieten, Thomas Tegos, Lucio Tremolizzo, Frans Verhey, Martin Vyhnálek, Jens Wiltfang, Merçé Boada, Pablo García‐González, Raquel Puerta, Luís Miguel Real, Victoria Álvarez, María J. Bullido, Jordi Clarimón, José María García‐Alberca, Pablo Mir and 10 more - JAMA Neurology 2022 cited by 93

  15. Tau deletion promotes brain insulin resistance

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - The Journal of Experimental Medicine 2017 cited by 202

  16. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jacques Epelbaum, Marc Mercken, Eric Karran, Marcus Bantscheff, Gerard Drewes, Gérard Joberty, Dominique Campion, J-N Octave, Claudine Berr, Mark Lathrop, Patrick Callaerts, David M. A. Mann, Julie Williams, Luc Buée, Ilse Dewachter, Christine Van Broeckhoven, Philippe Amouyel, Dieder Moechars, Bart Dermaut, J-C Lambert - Molecular Psychiatry 2013 cited by 440

  17. A novel Alzheimer disease locus located near the gene encoding tau protein

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tatiana Foroud, S-H Choi, Anne Boland, Tim Becker, Walter A. Kukull, Sven J. van der Lee, Florence Pasquier, Carlos Cruchaga, Duane Beekly, Annette L. Fitzpatrick, Olivier Hanon, Michael Gill, Robert C. Barber, Vilmundur Guðnason, Dominique Campion, Seth Love, David A. Bennett, Najaf Amin, Claudine Berr, Magda Tsolaki, Joseph D. Buxbaum, Oscar L. López, Vincent Deramecourt, Nick C. Fox, Laura B. Cantwell, Lluís Tárraga, Carole Dufouil, John Hardy, Paul K. Crane, Gudny Eiriksdottir, Didier Hannequin, Robert Clarke, Denis A. Evans, Thomas H. Mosley, Luc Letenneur, Carol Brayne, Wolfgang Maier, Philip L. De Jager, Valur Emilsson, Dartigues Jf, Harald Hampel, M. Ilyas Kamboh, Renée F.A.G. de Bruijn, Christophe Tzourio, Pau Pástor, Eric B. Larson, Jerome I. Rotter, Michael O‘Donovan, Thomas J. Montine, Michael A. Nalls, Simon Mead, Eric M. Reiman, Pálmi V. Jónsson, Clive Holmes, Peter St George‐Hyslop, Merçé Boada, Peter Passmore, Jens R. Wendland, R. Schmidt, Kevin Morgan, Ashley R. Winslow, John Powell, M Carasquillo, Steven G. Younkin, Jóhanna Jakobsdóttir, John Kauwe, K C Wilhelmsen, Dan Rujescu, Markus M. Nöthen, Albert Hofman and 329 more - Molecular Psychiatry 2015 cited by 309

  18. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stacey Gabriel, Emmanuelle Génin, Richard A. Gibbs, Alison Goate, Benjamin Grenier‐Boley, Namrata Gupta, Jonathan L. Haines, Aki S. Havulinna, Seppo Helisalmi, Mikko Hiltunen, Daniel P. Howrigan, M. Arfan Ikram, Jaakko Kaprio, Jan Konrad, Amanda Kuzma, Eric S. Lander, Mark Lathrop, Terho Lehtimäki, Honghuang Lin, Kari Mattila, Richard Mayeux, Donna M. Muzny, Waleed Nasser, Benjamin M. Neale, Kwangsik Nho, Gaël Nicolas, Devanshi Patel, Margaret A. Pericak‐Vance, Markus Perola, Bruce M. Psaty, Olivier Quenez, Farid Rajabli, Richard Redon, Christiane Reitz, Anne M. Remes, Veikko Salomaa, Chloé Sarnowski, Helena Schmidt, Michael A. Schmidt, Reinhold Schmidt, Hilkka Soininen, Timothy Thornton, Giuseppe Tosto, Christophe Tzourio, Sven J. van der Lee, Cornelia M. van Duijn, Otto Valladares, Badri N. Vardarajan, Li-San Wang, Weixin Wang, Ellen M. Wijsman, Richard K. Wilson, Daniela Witten, Kim C. Worley, Xiaoling Zhang, Alzheimer’s Disease Sequencing Project, Céline Bellenguez, Jean‐Charles Lambert, Mitja I. Kurki, Aarno Palotie, Mark J. Daly, Eric Boerwinkle, Kathryn L. Lunetta, Anita L. DeStefano, Josée Dupuis, Eden R. Martin, Gerard D. Schellenberg, Sudha Seshadri, Adam C. Naj, Myriam Fornage and 1 more - Molecular Psychiatry 2018 cited by 266

  19. Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jordi Clarimón, Antonio Daniele, D.H. Darling, Stéphanie Debette, Jean‐François Deleuze, Martin Dichgans, Carole Dufouil, Emmanuel During, Emrah Düzel, Daniela Galimberti, Guillermo García‐Ribas, José María García‐Alberca, Pablo García-González, Vilmantas Giedraitis, Oliver Goldhardt, Caroline Graff, Edna Grünblatt, Olivier Hanon, Lucrezia Hausner, Stefanie Heilmann‐Heimbach, Henne Holstege, Jakub Hort, Yoo Jin Jung, Jürgen Deckert, Silke Kern, Teemu Kuulasmaa, Kun Ho Lee, Ling Lin, Carlo Masullo, Patrizia Mecocci, Shima Mehrabian, Alexandre de Mendonça, Merçé Boada, Pablo Mir, Susanne Moebus, Fermín Moreno, Benedetta Nacmias, Gaël Nicolas, Shumpei Niida, Børge G. Nordestgaard, Goran Papenberg, Janne M. Papma, Lucilla Parnetti, Florence Pasquier, Pau Pástor, Oliver Peters, Yolande A.L. Pijnenburg, Gerard Piñol‐Ripoll, Julius Popp, Laura Molina‐Porcel, Raquel Puerta, Jordi Pérez‐Tur, Innocenzo Rainero, Inez H.G.B. Ramakers, Luís Miguel Real, Steffi G. Riedel‐Heller, Eloy Rodríguez‐Rodríguez, Owen A. Ross, José Luís Royo, Dan Rujescu, Nikolaos Scarmeas, Philip Scheltens, Norbert Scherbaum, Anja Schneider, Davide Seripa, Ingmar Skoog, Vincenzo Solfrizzi, Gianfranco Spalletta, Alessio Squassina, John C. van Swieten and 835 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2023 cited by 51

  20. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

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