Ina Giegling

Active 2001–2025

111
Papers
32,799
Citations
85
h-index
108
i10-index

Citations

Citations per year for Ina Giegling1939: 1 citations1992: 1 citations1994: 1 citations1996: 4 citations2002: 3 citations2003: 2 citations2004: 22 citations2005: 18 citations2006: 24 citations2007: 32 citations2008: 83 citations2009: 260 citations2010: 349 citations2011: 441 citations2012: 511 citations2013: 531 citations2014: 409 citations2015: 414 citations2016: 346 citations2017: 325 citations2018: 430 citations2019: 1,230 citations2020: 1,237 citations2021: 1,231 citations2022: 1,012 citations2023: 679 citations2024: 1,002 citations2025: 459 citations2026: 15 citations1940–1991: no citations, so these years are not shown1993: no citations, so this year is not shown1995: no citations, so this year is not shown1997–2001: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,658 citing papers, 24.7% of this breakdownUnited Kingdom: 1,902 citing papers, 10.1% of this breakdownGermany: 1,213 citing papers, 6.4% of this breakdownChina: 1,047 citing papers, 5.5% of this breakdownNetherlands: 829 citing papers, 4.4% of this breakdownCanada: 800 citing papers, 4.2% of this breakdownAustralia: 738 citing papers, 3.9% of this breakdownSweden: 622 citing papers, 3.3% of this breakdownItaly: 615 citing papers, 3.3% of this breakdownFrance: 566 citing papers, 3% of this breakdownSpain: 492 citing papers, 2.6% of this breakdownSwitzerland: 396 citing papers, 2.1% of this breakdown
0%24.7%Other 26.5%

Fields

  • Biochemistry, Genetics and Molecular Biology36.8%
  • Neuroscience26.5%
  • Medicine25.1%
  • Psychology7%
  • Immunology and Microbiology1.8%
  • Computer Science0.7%
  • Other2.1%

Topics

  • Genetic Associations and Epidemiology7.2%
  • Neuroinflammation and Neurodegeneration Mechanisms5.6%
  • Alzheimer's disease research and treatments5.4%
  • Tryptophan and brain disorders3.8%
  • Genetics and Neurodevelopmental Disorders3.1%
  • Genomic variations and chromosomal abnormalities2.9%
  • Other72%

Coauthors

All papers

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  1. Variant of TREM2 Associated with the Risk of Alzheimer's Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2012 cited by 2,620

  2. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Håkon Håkonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Lars Klareskog, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via, Stéphanie Le Hellard and 111 more - Nature Genetics 2019 cited by 1,181

  3. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bradley T. Webb, Tonya White, Dan E. Arking, Dimitrios Avramopoulos, Robert M. Bilder, Panos Bitsios, Katherine E. Burdick, Tyrone D. Cannon, Ornit Chiba‐Falek, Andrea Christoforou, Elizabeth T. Cirulli, Eliza Congdon, Aiden Corvin, Gail Davies, Ian J. Deary, Pamela DeRosse, Dwight Dickinson, Srdjan Djurovic, Gary Donohoe, Emily Drabant Conley, Johan G. Eriksson, Thomas Espeseth, Nelson B. Freimer, Stella G. Giakoumaki, Ina Giegling, Michael Gill, David C. Glahn, Ahmad R. Hariri, Alex Hatzimanolis, Matthew C. Keller, Emma Knowles, Deborah K. Attix, Bettina Konte, Jari Lahti, Stéphanie Le Hellard, Todd Lencz, David C. Liewald, Edythe London, Astri J. Lundervold, Anil K. Malhotra, Ingrid Melle, Derek W. Morris, Anna C. Need, William Ollier, Aarno Palotie, Antony Payton, Neil Pendleton, Russell A. Poldrack, Katri Räikkönen, Ivar Reinvang, Panos Roussos, Dan Rujescu, Fred W. Sabb, Matthew A. Scult, Olav B. Smeland, Nikolaos Smyrnis, John M. Starr, Vidar M. Steen, Nikos C. Stefanis, Richard E. Straub, Kjetil Sundet, Henning Tiemeier, Aristotle N. Voineskos, Daniel R. Weinberger, Elisabeth Widén, Jin Yu, Gonçalo R. Abecasis, Ole A. Andreassen, Gerome Breen, Lene Christiansen and 17 more - Nature Genetics 2018 cited by 1,418

  4. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Helen Beaumont, Donald Warden, Gordon Wilcock, Seth Love, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Eckart Rüther, Britta Schürmann, Reiner Heun, Heike Kölsch, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, John Gallacher, Michael Hüll, Dan Rujescu, Ina Giegling, Alison Goate, John Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H‐Erich Wichmann, V. Shane Pankratz, Sigrid Botne Sando, Jan Aasly, Maria Barcikowska, Zbigniew K. Wszołek, Dennis W. Dickson, Neill R. Graff‐Radford and 73 more - Nature Genetics 2011 cited by 2,083

  5. 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

  6. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nancy G. Buccola, Randy L. Buckner, Brendan Bulik‐Sullivan, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Wei Cheng, C. Robert Cloninger, David Cohen, Paul Cormican, Nick Craddock, Benedicto Crespo‐Facorro, James J Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Kai-How Farh, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Joseph I. Friedman, Andreas J. Forstner, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Elliot S. Gershon, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Jacob Gratten, Lieuwe de Haan, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Hailiang Huang, Masashi Ikeda, Inge Joa, Anna K. Kähler and 163 more - Nature Genetics 2016 cited by 1,142

  7. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo Martínez, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, C. Franklin, Steven Gallinger, Héléna A. Gaspar, Ina Giegling, Johanna Giuranna, Paola Giusti-Rodríquez, Fragiskos Gonidakis, Scott D. Gordon, Philip Gorwood, Monica Gratacos Mayora, Jakob Grove, Sébastien Guillaume, Yiran Guo, Håkon Håkonarson, Katherine A. Halmi, Ken B. Hanscombe, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Anjali K. Henders, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Anke Hinney, L. John Horwood, Christopher Hübel, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Antonio Julià, Anders Juréus, Gursharan Kalsi, Deborah Kaminská, Allan S. Kaplan, Jaakko Kaprio and 220 more - Nature Genetics 2020 cited by 387

  8. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Per Hoffmann, Jouke‐Jan Hottenga, Martin A. Kennedy, Mervi Alanne-Kinnunen, Bettina Konte, Jari Lahti, Marius Lahti‐Pulkkinen, Dongbing Lai, Lannie Ligthart, Anu Loukola, Brion S. Maher, Hamdi Mbarek, Andrew M. McIntosh, Matthew B. McQueen, Jacquelyn L. Meyers, Yuri Milaneschi, Teemu Palviainen, John F. Pearson, Roseann E. Peterson, Samuli Ripatti, Euijung Ryu, Nancy L. Saccone, Jessica E. Salvatore, Sandra Sanchez‐Roige, Melanie L. Schwandt, Richard Sherva, Fabian Streit, Jana Strohmaier, Nathaniel Thomas, Jen‐Chyong Wang, Bradley T. Webb, Robbee Wedow, Leah Wetherill, Amanda G. Wills, Jason D. Boardman, Danfeng Chen, Doo‐Sup Choi, William Copeland, Robert Culverhouse, Norbert Dahmen, Louisa Degenhardt, Benjamin W. Domingue, Sarah L. Elson, Mark A. Frye, Wolfgang Gäbel, Caroline Hayward, Marcus Ising, Margaret A. Keyes, Falk Kiefer, John R. Kramer, Samuel Kuperman, Susanne Lucae, Michael T. Lynskey, Wolfgang Maier, Karl Mann, Satu Männistö, Bertram Müller‐Myhsok, Alison D. Murray, John I. Nürnberger, Aarno Palotie, Ulrich W. Preuss, Katri Räikkönen, Maureen Reynolds, Monika Ridinger, Norbert Scherbaum, Marc A. Schuckit, Michael Soyka, Jens Treutlein, Stephanie H. Witt, Norbert Wodarz and 67 more - Nature Neuroscience 2018 cited by 711

  9. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Markus Leber, Shuo Li, Karen A. Mather, Ingrid Melle, Derek W. Morris, Christopher Oldmeadow, Teemu Palviainen, Antony Payton, Raha Pazoki, Katja Petrovic, Chandra A. Reynolds, Muralidharan Sargurupremraj, Markus Scholz, Jennifer A. Smith, Albert V. Smith, Natalie Terzikhan, Anbupalam Thalamuthu, Stella Trompet, Sven J. van der Lee, Erin B. Ware, B. Gwen Windham, Margaret J. Wright, Jingyun Yang, Jin Yu, David Ames, Najaf Amin, Philippe Amouyel, Ole A. Andreassen, Nicola J. Armstrong, Amelia A. Assareh, John Attia, Deborah K. Attix, Dimitrios Avramopoulos, David A. Bennett, Anne C. Böhmer, Patricia A. Boyle, Henry Brodaty, Harry Campbell, Tyrone D. Cannon, Elizabeth T. Cirulli, Eliza Congdon, Emily Drabant Conley, Janie Corley, Simon R. Cox, Anders M. Dale, Abbas Dehghan, Danielle M. Dick, Dwight Dickinson, Johan G. Eriksson, Εvangelos Εvangelou, Jessica D. Faul, Ian Ford, Nelson B. Freimer, He Gao, Ina Giegling, Nathan A. Gillespie, Scott D. Gordon, Rebecca F. Gottesman, Michael Griswold, Vilmundur Guðnason, Tamara B. Harris, Annette M. Hartmann, Alex Hatzimanolis, Gerardo Heiss, Elizabeth G. Holliday, Peter K. Joshi, Mika Kähönen, Sharon L. R. Kardia, Ida Karlsson, Luca Kleineidam and 122 more - Nature Communications 2018 cited by 765

  10. Genome-wide association study identifies five new schizophrenia loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stan Zammit, Michael C O'Donovan, Dan-Yu Lin, Roel A Ophoff, Eric Strengman, Rita M Cantor, Nelson B Freimer, Ole A Andreassen, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Edward Scolnick, Shaun Purcell, Benjamin M Neale, Sven Cichon, Manuel Mattheisen, Markus M Nöthen, David St. Clair, Aiden Corvin, Paul Cormican, Gary Donohoe, Michael Gill, Elaine Kenny, Derek W Morris, Colm T O'Dushlaine, Emma M Quinn, Hugh Gurling, Nicholas Bass, Khalid Choudhury, Susmita Datta, Robert Krasucki, Jacob Lawrence, Andrew McQuillin, Jonathan Pimm, Vinay Puri, Thomas Werge, Linh Duong, Thomas Hansen, Andrés Ingason, Klaus D Jakobsen, Line Olsen, Henrik B Rasmussen, Johan H Thygesen, Dan Rujescu, Marion Friedl, Ina Giegling, Annette M Hartmann, Heike Konnerth, Bettina Konte, Douglas H R Blackwood, Alan W Maclean, Pat Malloy, Kevin A McGhee, Andrew McIntosh, Carlos N Pato, Michele T Pato, Anil K Malhotra, Todd Lencz, Frank Dudbridge, Peter M Visscher, Danielle Posthuma, Richard L Amdur, Hreinn Stefansson, Stacy Steinberg, Kari Stefansson, Bryan J Mowry, John J McGrath, Deborah A Nertney, Vera Golimbet and 96 more - Nature Genetics 2011 cited by 1,954

  11. Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Li‐Shiun Chen, Doo‐Sup Choi, S. Patricia Chou, Sven Cichon, William Copeland, Robin P. Corley, Franziska Degenhardt, Marta Di Forti, Nancy Diazgranados, Danielle M. Dick, Benjamin W. Domingue, Johan G. Eriksson, Lindsay A. Farrer, Jerome C. Foo, Tatiana Foroud, Louis Fox, Josef Frank, Mark A. Frye, Wolfgang Gäebel, Raul R. Gainetdinov, Ina Giegling, Nathan A. Gillespie, Alison Goate, David Goldman, Scott D. Gordon, Laura M. Hack, Dana B. Hancock, Kathleen Mullan Harris, Annette M. Hartmann, Andrew C. Heath, Stefanie Heilmann‐Heimbach, Stefan Herms, Victor Hesselbrock, John K. Hewitt, Ian B. Hickie, Colin A. Hodgkinson, Per Hoffmann, Christian J. Hopfer, L. John Horwood, Jouke Jan Hottenga, Daniel P. Howrigan, William G. Iacono, Marcus Ising, Eric O. Johnson, Jaakko Kaprio, Victor M. Karpyak, Kenneth S. Kendler, Martin A. Kennedy, Margaret A. Keyes, А.О. Кибитов, Falk Kiefer, Bettina Konte, John R. Kramer, Kenneth Krauter, Evgeny Krupitsky, Samuel Kuperman, Jari Lahti, Marius Lahti‐Pulkkinen, Dongbing Lai, Аnastasia Levchenko, Lannie Ligthart, Penelope A. Lind, Susanne Lucae, Michael T. Lynskey, Pamela A. F. Madden, Hermine H. Maes, Patrik K. E. Magnusson, Brion S. Maher, Karl Mann, Satu Männistö and 74 more - Nature Mental Health 2023 cited by 227

  12. Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vladimír Bencko, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Laura Carlberg, Matteo Cassina, Carolyn E. Cesta, Sven Cichon, Maurizio Clementi, Sarah Cohen‐Woods, Joni Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, Jim Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Bo Ding, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Thomas Espeseth, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, James Floyd, Manuel Föcker, Lenka Foretová, Monica Forzan, Caroline S. Fox, C. Franklin, Valérie Gaborieau, Steven Gallinger, Giovanni Gambaro, Ina Giegling, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Rebecca Harrison, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard and 136 more - American Journal of Psychiatry 2017 cited by 600

  13. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Raymond C. K. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian and 391 more - Biological Psychiatry 2021 cited by 207

  14. 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

  15. Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pálmi V. Jónsson, Sigurbjörn Björnsson, Jón Snædal, Kari Stefansson - Nature Genetics 2015 cited by 332

  16. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Shaun Purcell, Sven Cichon, Markus M. Nöthen, H‐Erich Wichmann, Stefan Schreiber, Sita H. Vermeulen, Lambertus A. Kiemeney, John H. J. Wokke, Simon Cronin, Russell L. McLaughlin, Orla Hardiman, Katsumi Fumoto, R. Jeroen Pasterkamp, Vincent Meininger, Judith Melki, P. Nigel Leigh, Christopher E. Shaw, John E. Landers, Ammar Al‐Chalabi, Robert H. Brown, Wim Robberecht, Peter M. Andersen, Roel A. Ophoff, Leonard H. van den Berg - Nature Genetics 2009 cited by 404

  17. Common variants conferring risk of schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, István Bitter, János Réthelyi, Brynja B. Magnúsdóttir, Thordur Sigmundsson, Pall I. Olason, Gísli Másson, Jeffrey R. Gulcher, Magnús Haraldsson, Ragnheiður Fossdal, Thorgeir E. Thorgeirsson, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Julio Sanjuán, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Ángel Carracedo, Celso Arango, Javier Costas, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kāri Stefánsson, David Collier - Nature 2009 cited by 1,720

  18. Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , A. Nazli Basak, Matthis Synofzik, on behalf of the RFC1 Study Group, Banu Özen Barut, Başar Bılgıç, Cavit Boz, Cécile Cauquil, Natalie Deininger, Claudia Dufke, Bülent Elibol, Furkan Erbas, Sibel Ertan, Fatma Genç, Ina Giegling, Yeşim Parman, Salvatore Rossi, Celal Salcin, Meli̇ha Tan, Hilal Taştekin, Christine Tranchant, Günes Uygun, Özge Yağcıoğlu Yassa - Neurology 2021 cited by 164

  19. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

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