Markus M. Nöthen

1993–2026 年に発表

別表記
Markus M Nöthen
345
論文数
65,673
被引用数
132
h 指数
334
i10 指数

被引用数

Markus M. Nöthen の年別被引用数1939 年: 被引用 1 件1971 年: 被引用 1 件1972 年: 被引用 1 件1986 年: 被引用 1 件1990 年: 被引用 1 件1991 年: 被引用 2 件1992 年: 被引用 1 件1993 年: 被引用 1 件1994 年: 被引用 1 件1995 年: 被引用 1 件1996 年: 被引用 15 件1997 年: 被引用 19 件1998 年: 被引用 33 件1999 年: 被引用 64 件2000 年: 被引用 98 件2001 年: 被引用 97 件2002 年: 被引用 107 件2003 年: 被引用 130 件2004 年: 被引用 161 件2005 年: 被引用 167 件2006 年: 被引用 215 件2007 年: 被引用 204 件2008 年: 被引用 266 件2009 年: 被引用 435 件2010 年: 被引用 660 件2011 年: 被引用 821 件2012 年: 被引用 907 件2013 年: 被引用 868 件2014 年: 被引用 821 件2015 年: 被引用 798 件2016 年: 被引用 730 件2017 年: 被引用 727 件2018 年: 被引用 836 件2019 年: 被引用 2,181 件2020 年: 被引用 2,321 件2021 年: 被引用 2,239 件2022 年: 被引用 1,619 件2023 年: 被引用 1,193 件2024 年: 被引用 1,830 件2025 年: 被引用 880 件2026 年: 被引用 37 件1940〜1970 年は被引用が無いため表示していません1973〜1985 年は被引用が無いため表示していません1987〜1989 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 8,448 件、この内訳の 22.6%イギリス: 引用元論文 3,556 件、この内訳の 9.5%ドイツ: 引用元論文 2,871 件、この内訳の 7.7%中国: 引用元論文 2,062 件、この内訳の 5.5%オランダ: 引用元論文 1,611 件、この内訳の 4.3%カナダ: 引用元論文 1,562 件、この内訳の 4.2%オーストラリア: 引用元論文 1,399 件、この内訳の 3.7%イタリア: 引用元論文 1,331 件、この内訳の 3.6%フランス: 引用元論文 1,161 件、この内訳の 3.1%スウェーデン: 引用元論文 1,159 件、この内訳の 3.1%スペイン: 引用元論文 952 件、この内訳の 2.6%デンマーク: 引用元論文 795 件、この内訳の 2.1%
0%22.6%その他 28%

分野

  • Medicine39.6%
  • Biochemistry, Genetics and Molecular Biology34.6%
  • Neuroscience15%
  • Psychology4.3%
  • Immunology and Microbiology2.8%
  • Computer Science0.6%
  • その他3.1%

トピック

  • Genetic Associations and Epidemiology6%
  • Alzheimer's disease research and treatments3.2%
  • Genetics and Neurodevelopmental Disorders2.5%
  • Neuroinflammation and Neurodegeneration Mechanisms2%
  • Tryptophan and brain disorders2%
  • Genomic variations and chromosomal abnormalities1.8%
  • その他82.5%

共著者

全論文

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  1. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Gavin R. Schnitzler, Damian Smedley, Guðmar Þorleifsson, Moritz von Scheidt, Jacob C. Ulirsch, Biobank Japan, EPIC-CVD, John Danesh, Davíð O. Arnar, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Rajat M. Gupta, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth, Paul S. de Vries, Moritz von Scheidt - Nature Genetics 2022 被引用: 706

  2. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Reinhard Heun, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John S.K. 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, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter Holmans, Michael O‘Donovan, Michael J. Owen, Julie Williams - Nature Genetics 2009 被引用: 3,398

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 477 名 - Science 2018 被引用: 2,050

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 73 名 - Nature Genetics 2011 被引用: 2,083

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 350 名 - Nature Genetics 2017 被引用: 1,104

  6. Genetic Associations with Valvular Calcification and Aortic Stenosis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jerome I. Rotter, Sigurður Sigurðsson, Quenna Wong, Raimund Erbel, Sekar Kathiresan, Olle Melander, Vilmundur Guðnason, Christopher J. O’Donnell, Wendy S. Post - New England Journal of Medicine 2013 被引用: 975

  7. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christel Depienne, Yulia Worbe, Andreas Hartmann, Cathy L. Budman, Renata Rizzo, Gholson J. Lyon, William M. McMahon, James R. Batterson, Daniëlle C. Cath, Irene A. Malaty, Michael S. Okun, Cheston M. Berlin, Douglas W. Woods, Paul C. Lee, Joseph Jankovic, Mary M. Robertson, Donald L. Gilbert, Lawrence W. Brown, Barbara Coffey, Andrea Dietrich, Pieter J. Hoekstra, Samuel Kuperman, Samuel H. Zinner, Pétur Lúðvígsson, Evald Sæmundsen, Ólafur Thorarensen, Gil Atzmon, Nir Barzilai, Michael Wagner, Rainald Moessner, Roel A. Ophoff, Carlos N. Pato, Michele T. Pato, James A. Knowles, Joshua L. Roffman, Jordan W. Smoller, Randy L. Buckner, A. Jeremy Willsey, Jay A. Tischfield, Gary A. Heiman, Hreinn Stefánsson, Kāri Stefánsson, Daniëlle Posthuma, Nancy J. Cox, David L. Pauls, Nelson B. Freimer, Benjamin M. Neale, Lea K. Davis, Peristera Paschou, Giovanni Coppola, Carol A. Mathews, Jeremiah M. Scharf - American Journal of Psychiatry 2019 被引用: 443

  8. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary Susan Burnett, Ian Buysschaert, John F. Carlquist, Li Chen, Sven Cichon, Veryan Codd, R. W. Davies, George Dedoussis, Abbas Dehghan, Serkalem Demissie, Joseph M. Devaney, Patrick Diemert, Ron Do, Angela Doering, Sandra Eifert, Nour Eddine El Mokhtari, Stephen G. Ellis, Roberto Elosúa, James C. Engert, Stephen E. Epstein, Ulf dé Fairé, Marcus Fischer, Aaron R. Folsom, Jennifer Freyer, Bruna Gigante, Domenico Girelli, Sólveig Grétarsdóttir, Vilmundur Guðnason, Jeffrey R. Gulcher, Eran Halperin, Naomi Hammond, Stanley L. Hazen, Albert Hofman, Benjamin D. Horne, Thomas Illig, Carlos Iribarren, Gregory T. Jones, J. Wouter Jukema, Michael Kaiser, Lee M. Kaplan, John J.P. Kastelein, Kay‐Tee Khaw, Joshua W. Knowles, Genovefa Kolovou, Augustine Kong, Reijo Laaksonen, Diether Lambrechts, Karin Leander, Guillaume Lettre, Mingyao Li, Wolfgang Lieb, Christina Loley, Andrew Lotery, Pier Mannuccio Mannucci, Seraya Maouche, Nicola Martinelli, Pascal McKeown, Christa Meisinger, Thomas Meitinger, Olle Melander, Pier Angelica Merlini, Vincent Mooser, Thomas M. Morgan, Thomas W Mühleisen, Joseph B. Muhlestein, Thomas Münzel, Kiran Musunuru, Janja Nahrstaedt, Christopher P. Nelson, Markus M. Nöthen ほか 67 名 - Nature Genetics 2011 被引用: 1,951

  9. A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pierre Deltenre, Henry Völzke, Markus M. Lerch, Julia Mayerle, Florian Eyer, Clemens Schafmayer, Sven Cichon, Markus M. Nöthen, Michael Nothnagel, David Ellinghaus, Klaus Huse, André Franke, Steffen Zopf, Claus Hellerbrand, Christophe Moreno, Denis Franchimont, Marsha Y. Morgan, Jochen Hampe - Nature Genetics 2015 被引用: 559

  10. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christian Fuchsberger, Phoenix Kwan, Tanya M. Teslovich, Pritam Chanda, Man Li, Yingchang Lu, Christian Dina, Dorothée Thuillier, Loïc Yengo, Longda Jiang, Thomas Sparsø, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Mattias Frånberg, Rona J. Strawbridge, Rafn Benediktsson, Ástráður B. Hreiðarsson, Augustine Kong, Gunnar Sigurðsson, Nicola D. Kerrison, Jian’an Luan, Liming Liang, Thomas Meitinger, Michael Roden, Barbara Thorand, Tõnu Esko, Evelin Mihailov, Caroline S. Fox, Ching‐Ti Liu, Denis Rybin, Bo Isomaa, Valeriya Lyssenko, Tiinamaija Tuomi, David Couper, James S. Pankow, Niels Grarup, Christian T. Have, Marit E. Jørgensen, Torben Jørgensen, Allan Linneberg, Marilyn C. Cornelis, Rob M. van Dam, Sarah Hunt, Peter Kraft, Qi Sun, Sarah Edkins, Katharine R. Owen, John R. B. Perry, Andrew R. Wood, Eleftheria Zeggini, Juan Tajes-Fernandes, Gonçalo R. Abecasis, Lori L. Bonnycastle, Peter S. Chines, Heather M. Stringham, Heikki A. Koistinen, Leena Kinnunen, Bengt Sennblad, Thomas W. Mühleisen, Markus M. Nöthen, Sonali Pechlivanis, Damiano Baldassarre, Karl Gertow, Steve E. Humphries, Elena Tremoli, Norman Klopp, Julia Meyer, Gerald Steinbach ほか 75 名 - Diabetes 2017 被引用: 816

  11. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada ほか 81 名 - Nature Genetics 2016 被引用: 628

  12. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kirsten Cremer, Claudia Perne, Regina C. Betz, Tim Bender, Kathrin Grundmann‐Hauser, Tobias B. Haack, Matias Wagner, Theresa Brunet, Heidi Beate Bentzen, Luisa Averdunk, Kimberly Christine Coetzer, Gholson J. Lyon, Malte Spielmann, Christian P. Schaaf, Stefan Mundlos, Markus M. Nöthen, Peter Krawitz - Nature Genetics 2022 被引用: 208

  13. Quantifying Deviations of Brain Structure and Function in Major Depressive Disorder Across Neuroimaging Modalities

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tim Hahn - JAMA Psychiatry 2022 被引用: 190

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 96 名 - Nature Genetics 2011 被引用: 1,954

  15. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chantal Depondt, Orrin Devinsky, Dennis Dlugos, Colin P. Doherty, Christian E. Elger, Johan G. Eriksson, Thomas N. Ferraro, Martha Feucht, Ben Francis, André Franke, Jacqueline A. French, Saskia Freytag, Verena Gaus, Eric B. Geller, Christian Gieger, Tracy A. Glauser, Simon Glynn, David B. Goldstein, Hongsheng Gui, Youling Guo, Kevin F. Haas, Håkon Håkonarson, Kerstin Hallmann, Sheryl R. Haut, Erin L. Heinzen, Ingo Helbig, Christian Hengsbach, Helle Hjalgrim, Michele Iacomino, Andrés Ingason, Jennifer Jamnadas-Khoda, Michael R. Johnson, Reetta Kälviäinen, Anne-Mari Kantanen, Dalia Kasperavičiūtė, Dorothée Kasteleijn‐Nolst Trenité, Heidi E. Kirsch, Robert C. Knowlton, Bobby P.C. Koeleman, Roland Krause, Martin Krenn, Wolfram S. Kunz, Ruben Kuzniecky, Patrick Kwan, Dennis Lal, YL Lau, Anna‐Elina Lehesjoki, Holger Lerche, Costin Leu, Wolfgang Lieb, Dick Lindhout, Warren Lo, Íscia Lopes‐Cendes, Daniel H. Lowenstein, Alberto Malovini, Anthony G Marson, Thomas Mayer, Mark McCormack, James L. Mills, Nasir Mirza, Martina Moerzinger, Rikke S. Møller, Anne M. Molloy, Hiltrud Muhle, Mark R. Newton, Ping-Wing Ng, Markus M. Nöthen, Peter Nürnberg, Terence J. O’Brien, Karen Oliver ほか 58 名 - Nature Communications 2018 被引用: 513

  16. Effects of urban living environments on mental health in adults

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Heike Tost, Nathalie Holz, Emanuel Schwarz, Argyris Stringaris, Maja Neidhart, Frauke Nees, Sebastian Siehl, Ole A. Andreassen, Lars T. Westlye, Dennis van der Meer, Sara Fernández, Rikka Kjelkenes, Helga Ask, Michael A. Rapp, Mira Tschorn, Sarah Jane Böttger, Gaia Novarino, Lena Marr, Mel Slater, Guillem Feixas Viapiana, Francisco José Eiroá‐Orosa, Jaime Gallego, Álvaro Pastor, Andreas J. Forstner, Per Hoffmann, Markus M. Nöthen, Andreas J. Forstner, Isabelle Claus, Abbi Miller, Stefanie Heilmann‐Heimbach, Peter Sommer, Mona Boye, Johannes Wilbertz, Karen M. Schmitt, Viktor Jirsa, Spase Petkoski, Séverine Pitel, Lisa Otten, Anastasios-Polykarpos Athanasiadis, Charlie Pearmund, Bernhard Spanlang, Elena Álvarez, Mavi Sanchez, A. Giner, Sören Hese, Paul Renner, Tianye Jia, Yanting Gong, Yunman Xia, Xiao Chang, Vince D. Calhoun, Jingyu Liu, Paul M. Thompson, Nicholas Clinton, Sylvane Desrivières, Allan H. Young, Bernd Carsten Stahl, George Ogoh - Nature Medicine 2023 被引用: 209

  17. A Systematic Evaluation of Machine Learning–Based Biomarkers for Major Depressive Disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Julia‐Katharina Pfarr, Lea Teutenberg, Paula Usemann, Florian Thomas‐Odenthal, Adrian Wroblewski, Katharina Brosch, Frederike Stein, Andreas Jansen, Hamidreza Jamalabadi, Nina Alexander, Benjamin Straube, Igor Nenadić, Tilo Kircher, Udo Dannlowski, Tim Hahn - JAMA Psychiatry 2024 被引用: 116

  18. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

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

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  20. HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

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  21. Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

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