Ohcanbohtosat - Anna K. Kähler

Aiddostahte ozu
  1. 1
    Conformational Stability of Fibrillar Amyloid-Beta Oligomers via Protofilament Pair Formation – A Systematic Computational Study

    Conformational Stability of Fibrillar Amyloid-Beta Oligomers via Protofilament Pair Formation – A Systematic Computational Study Dahkki Anna K. Kähler, Heinrich Sticht, Anselm H. C. Horn

    Almmustuhtton 2013
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  2. 2
    Short-term improvement of mental health after a COVID-19 vaccination

    Short-term improvement of mental health after a COVID-19 vaccination Dahkki Charilaos Chourpiliadis, Anikó Lovik, Anna K. Kähler, Unnur Valdimarsdóttir, Emma M. Frans, Fredrik Nyberg, Patrick F. Sullivan, Fang Fang

    Almmustuhtton 2023
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  3. 3
    Association analysis of schizophrenia on 18 genes involved in neuronal migration: <i>MDGA1</i> as a new susceptibility gene

    Association analysis of schizophrenia on 18 genes involved in neuronal migration: <i>MDGA1</i> as a new susceptibility gene Dahkki Anna K. Kähler, Srdjan Djurovic, Bettina Kulle, Erik G. Jönsson, Ingrid Agartz, Håkan Hall, Stein Opjordsmoen, Klaus D. Jakobsen, Thomas Hansen, Ingrid Melle, Thomas Werge, Vidar M. Steen, Ole A. Andreassen

    Almmustuhtton 2008
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  4. 4
    Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach

    Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach Dahkki Douglas M. Ruderfer, Alexander W. Charney, Ben Readhead, Brian Kidd, Anna K. Kähler, Paul J. Kenny, Michael J. Keiser, Jennifer L. Moran, Christina M. Hultman, Stuart A. Scott, Patrick F. Sullivan, Shaun Purcell, Joel T. Dudley, Pamela Sklar

    Almmustuhtton 2016
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  5. 5
    Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

    Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort Dahkki Lavinia Athanasiu, Morten Mattingsdal, Anna K. Kähler, Andrew Brown, Ómar Gústafsson, Ingrid Agartz, Ina Giegling, Pierandrea Muglia, Sven Cichon, Marcella Rietschel, Olli Pietiläinen, Leena Peltonen, Elvira Bramon, David Collier, David St Clair, Engilbert Sigurðsson, Hannes Pétursson, Dan Rujescu, Ingrid Melle, Vidar M. Steen, Srdjan Djurovic, Ole A. Andreassen

    Almmustuhtton 2010
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  6. 6
    Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

    Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia Dahkki Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti‐Rodríguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur, Anna K. Kähler, NaEshia Ancalade, Martilias S. Farrell, James J. Crowley, Yun Li, Patrik K. E. Magnusson, Ulf Gyllensten, Christina M. Hultman, Patrick F. Sullivan, Jin Szatkiewicz

    Almmustuhtton 2020
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  7. 7
    Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

    Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence Dahkki Giulio Genovese, Anna K. Kähler, Robert E. Handsaker, Johan Lindberg, Samuel A. Rose, Samuel F. Bakhoum, Kimberly Chambert, Eran Mick, Benjamin M. Neale, Menachem Fromer, Shaun Purcell, Oscar Svantesson, Mikael Landén, Martin Höglund, Sören Lehmann, Stacey B. Gabriel, Jennifer L. Moran, Eric S. Lander, Patrick F. Sullivan, Pamela Sklar, Henrik Grönberg, Christina M. Hultman, Steven A. McCarroll

    Almmustuhtton 2014
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  8. 8
    Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma

    Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma Dahkki Bhairavi Swaminathan, Guðmar Þorleifsson, Magnus Jöud, Mina Ali, Ellinor Johnsson, Ram Ajore, Patrick Sulem, Britt-Marie Halvarsson, Guðmundur I. Eyjólfsson, Vilhelmína Haraldsdóttir, Christina M. Hultman, Erik Ingelsson, Sigurður Y. Kristinsson, Anna K. Kähler, Stig Lenhoff, Gísli Másson, Ulf‐Henrik Mellqvist, Robert Månsson, Sven Nelander, Ísleifur Ólafsson, Ólöf Sigurðardóttir, Hlíf Steingrímsdóttir, Annette Juul Vangsted, Ulla Vogel, Anders Waage, Hareth Nahi, Daníel F. Guðbjartsson, Þórunn Rafnar, Ingemar Turesson, Urban Gullberg, Kāri Stefánsson, Markus Hansson, Unnur Þorsteinsdóttir, Björn Nilsson

    Almmustuhtton 2015
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  9. 9
    Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

    Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia Dahkki Jennifer G. Mullé, Ann E. Pulver, John A. McGrath, Paula Wolyniec, Anne Dodd, David J. Cutler, Jonathan Sebat, Dheeraj Malhotra, Gerald Nestadt, Donald F. Conrad, Matthew E. Hurles, C. Barnes, Masashi Ikeda, Nakao Iwata, Douglas F. Levinson, Pablo V. Gejman, Alan R. Sanders, Jubao Duan, Adele A. Mitchell, Inga Peter, Pamela Sklar, Colm Ó'Dúshláine, Detelina Grozeva, Michael O’Donovan, Michael J. Owen, Christina M. Hultman, Anna K. Kähler, Patrick F. Sullivan, George Kirov, Stephen T. Warren

    Almmustuhtton 2013
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  10. 10
    COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and Denmark

    COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and Denmark Dahkki Qing Shen, Emily E. Joyce, Omid V. Ebrahimi, Maria Didriksen, Anikó Lovik, Karen Sól Sævarsdóttir, Ingibjörg Magnúsdóttir, Dorte Helenius Mikkelsen, Anna Bára Unnarsdóttir, Arna Hauksdóttir, Asle Hoffart, Anna K. Kähler, Edda Björk Þórðardóttir, Elías Eyþórsson, Emma M. Frans, Gunnar Tómasson, Helga Ask, Hrönn Harðardóttir, Jóhanna Jakobsdóttir, Kelli Lehto, Li Lu, Ole A. Andreassen, Patrick F. Sullivan, Runólfur Pálsson, Christian Erikstrup, Sisse Rye Ostrowski, Thomas Werge, Thor Aspelund, Ole Birger Pedersen, Sverre Urnes Johnson, Fang Fang, Unnur Valdimarsdóttir

    Almmustuhtton 2023
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  11. 11
    A polygenic burden of rare disruptive mutations in schizophrenia

    A polygenic burden of rare disruptive mutations in schizophrenia Dahkki Shaun Purcell, Jennifer L. Moran, Menachem Fromer, Douglas M. Ruderfer, Nadia Solovieff, Panos Roussos, Colm Ó'Dúshláine, Kimberly Chambert, Sarah E. Bergen, Anna K. Kähler, Laramie E. Duncan, Eli Stahl, Giulio Genovese, Esperanza Fernández, Mark O. Collins, Noboru H. Komiyama, Jyoti S. Choudhary, Patrik K. E. Magnusson, Eric Banks, Khalid Shakir, Kiran Garimella, Tim Fennell, Mark A. DePristo, Seth G. N. Grant, Stephen J. Haggarty, Stacey Gabriel, Edward M. Scolnick, Eric S. Lander, Christina M. Hultman, Patrick F. Sullivan, Steven A. McCarroll, Pamela Sklar

    Almmustuhtton 2014
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  12. 12
    The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

    The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia Dahkki Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen, Christina Bell, Tarjinder Singh, Aditi Trehan, J. L. Sherwood, Danielle K. Manning, Emily Peirent, Rhea Malik, Ellen J. Guss, Derek Hawes, Amanda Beccard, Anne M. Bara, Dane Z. Hazelbaker, Emanuela Zuccaro, Giulio Genovese, Alexander A. Loboda, Anna Neumann, Christina Lilliehöök, Outi Kuismin, Eija Hämäläinen, Mitja Kurki, Christina M. Hultman, Anna K. Kähler, João A. Paulo, Andrea Ganna, Jon M. Madison, Bruce M. Cohen, Donna L. McPhie, Rolf Adolfsson, Roy H. Perlis, Ricardo E. Dolmetsch, Samouil L. Farhi, Steven A. McCarroll, Steven E. Hyman, Ben Neale, Lindy E. Barrett, J. Wade Harper, Aarno Palotie, Mark J. Daly, Kevin Eggan

    Almmustuhtton 2022
    Viečča ollesdeavstta Viečča ollesdeavstta
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  13. 13
    Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations

    Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations Dahkki Anna Bára Unnarsdóttir, Anikó Lovik, Chloe Fawns‐Ritchie, Helga Ask, Kadri Kõiv, Kristen Hagen, Maria Didriksen, Lea Arregui Nordahl Christoffersen, Alexander Berg Garðarsson, Andrew M. McIntosh, Anna K. Kähler, Archie Campbell, Arna Hauksdóttir, Christian Erikstrup, Dorte Helenius Mikkelsen, Drew Altschul, Edda Björk Þórðardóttir, Emma M. Frans, Gerd Kvale, Gunnar Tómasson, Hanna Maria Kariis, Harpa Lind Jónsdóttir, Harpa Rúnarsdóttir, Ingibjörg Magnúsdóttir, Jarle Eid, Jóhanna Jakobsdóttir, Kaspar René Nielsen, Kathrine Agergård Kaspersen, Lili Milani, Lill-Iren Schou Trogstad, Yi Lu, Mie Topholm Bruun, Patrick F. Sullivan, Per Magnus, Qing Shen, Ragnar Nesvåg, Ragnhild Eek Brandlistuen, Reedik Mägi, Sisse Rye Ostrowski, Solveig Løkhammer, Stian Solem, Ted Reichborn‐Kjennerud, Thomas Hansen, Thomas Werge, Thor Aspelund, David J. Porteous, Fang Fang, Kelli Lehto, Ole A. Andreassen, Ole Birger Pedersen, Stéphanie Le Hellard, Unnur Valdimarsdóttir

    Almmustuhtton 2021
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  14. 14
    Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Genome-wide association analysis identifies 13 new risk loci for schizophrenia Dahkki Stephan Ripke, Colm Ó'Dúshláine, Kimberly Chambert, Jennifer L. Moran, Anna K. Kähler, Susanne Akterin, Sarah E. Bergen, Ann L. Collins, James J. Crowley, Menachem Fromer, Yunjung Kim, Sang Lee, Patrik K. E. Magnusson, Nick Sanchez, Eli A. Stahl, Stephanie Williams, Naomi R. Wray, Kai Xia, Francesco Bettella, Anders D. Børglum, Brendan Bulik‐Sullivan, Paul Cormican, Nick Craddock, Christiaan de Leeuw, Naser Durmishi, Michael Gill, В. Е. Голимбет, Marian L. Hamshere, Peter Holmans, David M Hougaard, Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Miloš Milovančević, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O’Donovan, Hreinn Stefánsson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan

    Almmustuhtton 2013
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  15. 15
    Quantifying prion disease penetrance using large population control cohorts

    Quantifying prion disease penetrance using large population control cohorts Dahkki Eric Vallabh Minikel, Sonia M. Vallabh, Monkol Lek, Karol Estrada, Kaitlin E. Samocha, J. Fah Sathirapongsasuti, Cory Y. McLean, Joyce Y. Tung, Linda P. C. Yu, Pierluigi Gambetti, Janis Blevins, Shulin Zhang, Yvonne Cohen, Wei Chen, Masahito Yamada, Tsuyoshi Hamaguchi, Nobuo Sanjo, Hidehiro Mizusawa, Yosikazu Nakamura, Tetsuyuki Kitamoto, Steven Collins, Alison Boyd, Robert Will, Richard Knight, Claudia Ponto, Inga Zerr, Theo F. J. Kraus, Sabina Eigenbrod, Armin Giese, Miguel Calero, Jesús de Pedro‐Cuesta, Stéphane Haı̈k, Jean Laplanche, Elodie Bouaziz‐Amar, J.-P. Brandel, Sabina Capellari, Piero Parchi, Anna Poleggi, Anna Ladogana, Anne O’Donnell‐Luria, Konrad J. Karczewski, Jamie L. Marshall, Michael Boehnke, Markku Laakso, Karen L. Mohlke, Anna K. Kähler, Kimberly Chambert, Steven A. McCarroll, Patrick F. Sullivan, Christina M. Hultman, Shaun Purcell, Pamela Sklar, Sven J. van der Lee, Annemieke J.M. Rozemüller, Casper Jansen, Albert Hofman, Robert Kraaij, Jeroen van Rooij, M. Arfan Ikram, André G. Uitterlinden, Cornelia M. van Duijn, Mark J. Daly, Daniel G. MacArthur

    Almmustuhtton 2016
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  16. 16
    Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study

    Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study Dahkki Ingibjörg Magnúsdóttir, Anikó Lovik, Anna Bára Unnarsdóttir, Daniel L. McCartney, Helga Ask, Kadri Kõiv, Lea Arregui Nordahl Christoffersen, Sverre Urnes Johnson, Arna Hauksdóttir, Chloe Fawns‐Ritchie, Dorte Helenius, Juan González‐Hijón, Li Lu, Omid V. Ebrahimi, Asle Hoffart, David J. Porteous, Fang Fang, Jóhanna Jakobsdóttir, Kelli Lehto, Ole A. Andreassen, Ole Birger Pedersen, Thor Aspelund, Unnur Valdimarsdóttir, Ingibjörg Magnúsdóttir, Anikó Lovik, Anna Bára Unnarsdóttir, Daniel L. McCartney, Helga Ask, Kadri Kõiv, Lea Arregui Nordahl Christoffersen, Sverre Urnes Johnson, Andrew M. McIntosh, Anna K. Kähler, Archie Campbell, Arna Hauksdóttir, Chloe Fawns‐Ritchie, Christian Erikstrup, Dorte Helenius, Drew Altschul, Edda Björk Þórðardóttir, Elías Eyþórsson, Emma M. Frans, Gunnar Tómasson, Harpa Lind Jónsdóttir, Harpa Rúnarsdóttir, Henrik Hjalgrim, Hrönn Harõardóttir, Juan González‐Hijón, Karina Banasik, Khoa Manh Dinh, Li Lu, Lili Milani, Lill Trogstad, Maria Didriksen, Omid V. Ebrahimi, Patrick F. Sullivan, Per Magnus, Qing Shen, Ragnar Nesvåg, Reedik Mägi, Runólfur Pálsson, Sisse Rye Ostrowski, Thomas Werge, Asle Hoffart, David J. Porteous, Fang Fang, Jóhanna Jakobsdóttir, Kelli Lehto, Ole A. Andreassen, Ole Birger Pedersen, Thor Aspelund, Unnur Valdimarsdóttir

    Almmustuhtton 2022
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  17. 17
    Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

    Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss Dahkki Natalia Trpchevska, Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou, Barbara Vona, Charles E. Bishop, Argyro Bizaki-Vallaskangas, Barbara Canlon, Fabio Castellana, Daniel I. Chasman, Stacey S. Cherny, Kaare Christensen, Maria Pina Concas, Adolfo Correa, Ran Elkon, Jonas Mengel‐From, Yan Gao, Anne B.S. Giersch, Giorgia Girotto, Alexander Guðjónsson, Vilmundur Guðnason, Nancy L. Heard‐Costa, Ronna Hertzano, Jacob Hjelmborg, Jens Hjerling‐Leffler, Howard J. Hoffman, Jaakko Kaprio, Johannes Kettunen, Kristi Krebs, Anna K. Kähler, François Lallemend, Lenore J. Launer, I‐Min Lee, Hampton L. Leonard, Chuan-Ming Li, Hubert Löwenheim, Patrik K. E. Magnusson, Joyce B. J. van Meurs, Lili Milani, Cynthia C. Morton, Antti Mäkitie, Mike A. Nalls, Giuseppe Giovanni Nardone, Marianne Nygaard, Teemu Palviainen, Sheila R. Pratt, Nicola Quaranta, Joel Rämö, Elmo Saarentaus, Rodolfo Sardone, Claudia L. Satizábal, John M. Schweinfurth, Sudha Seshadri, Eric J. Shiroma, Eldad D. Shulman, Eleanor M. Simonsick, Christopher Spankovich, Anke Tropitzsch, Volker M. Lauschke, Patrick F. Sullivan, André Goedegebure, Christopher R. Cederroth, Frances M. K. Williams, A. Paul Nagtegaal, Andres Metspalu, Mari Nelis, Reedik Mägi, Tõnu Esko

    Almmustuhtton 2022
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  18. 18
    Sex-dependent association of common variants of microcephaly genes with brain structure

    Sex-dependent association of common variants of microcephaly genes with brain structure Dahkki Lars M. Rimol, Ingrid Agartz, Srdjan Djurovic, Andrew Brown, J. Cooper Roddey, Anna K. Kähler, Morten Mattingsdal, Lavinia Athanasiu, Alexander H. Joyner, Nicholas J. Schork, Eric Halgren, Kjetil Sundet, Ingrid Melle, Anders M. Dale, Ole A. Andreassen, Michael W. Weiner, Leon J. Thal, Ronald Petersen, Clifford R. Jack, William J. Jagust, John Q. Trojanowki, Arthur W. Toga, Laurel Beckett, Robert C. Green, Anthony Gamst, William Z. Potter, Tom Montine, Dale Anders, Matt A. Bernstein, Joel P. Felmlee, Nick C. Fox, Paul M. Thompson, Norbert Schuff, Gene E. Alexander, Dan Bandy, Robert A. Koeppe, Norm Foster, Eric M. Reiman, Kewei Chen, John Q. Trojanowki, Les Shaw, Virginia M.‐Y. Lee, Magdalena Korecka, Arthur W. Toga, Karen Crawford, Scott Neu, Danielle Harvey, Anthony Gamst, John Kornak, Zaven Kachaturian, Richard Frank, Peter J. Snyder, Susan Molchan, Jeffrey Kaye, Remi Vorobik, Joseph Quinn, Lon S. Schneider, Sonia Pawluczyk, Bryan Spann, Adam Fleisher, Helen Vanderswag, Judith L. Heidebrink, Joanne Lord, Kris Johnson, Rachelle S. Doody, Javier Villanueva‐Meyer, Munir Chowdhury, Yaakov Stern, Lawrence S. Honig, Karen L. Bell, John C. Morris, Mark A. Mintun, Stacy Schneider, Daniel Marson, Randall Griffith, Beverly Badger, Hillel Grossman, Cheuk Y. Tang, Jessica Stern, Leyla deToledo‐Morrell, Raj C. Shah, Julie Bach, Ranjan Duara, Richard Isaacson, Silvia Strauman, Marilyn S. Albert, Julia Pedroso, Jaimie Toroney, Henry Rusinek, Mony J. de Leon, Susan M De Santi, P. Murali Doraiswamy, Jeffrey R. Petrella, Marilyn Aiello, Christopher M. Clark, Cassie Pham, Jessica Nuñez, Charles D. Smith, Curtis A. Given, Peter Hardy

    Almmustuhtton 2009
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  19. 19
    New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

    New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis Dahkki Sang Lee, Enda M. Byrne, Christina M. Hultman, Anna K. Kähler, Anna A. E. Vinkhuyzen, Stephan Ripke, Ole A. Andreassen, Thomas Frisell, Alexander Gusev, Xinli Hu, Robert Karlsson, Vasilis X Mantzioris, John J. McGrath, Divya Mehta, Eli A. Stahl, Qiongyi Zhao, Kenneth S. Kendler, Patrick F. Sullivan, Alkes L. Price, Michael O’Donovan, Yukinori Okada, Bryan Mowry, Soumya Raychaudhuri, Naomi R. Wray, William Byerley, Wiepke Cahn, Rita M. Cantor, Sven Cichon, Paul Cormican, David Curtis, Srdjan Djurovic, Valentina Escott‐Price, Pablo V. Gejman, Lyudmila Georgieva, Ina Giegling, Thomas Hansen, Andrés Ingason, Yunjung Kim, Bettina Konte, Sang Hyuck Lee, Andrew M. McIntosh, Andrew McQuillin, Derek W. Morris, Markus M. Nöthen, Colm Ó'Dúshláine, Ann Olincy, Line Olsen, Carlos N. Pato, Michele T. Pato, Ben Pickard, Daniëlle Posthuma, Henrik Berg Rasmussen, Marcella Rietschel, Dan Rujescu, Thomas G. Schulze, Jeremy M. Silverman, Srinivasa Thirumalai, Thomas Werge, Ingrid Agartz, Farooq Amin, Maria Helena Pinto de Azevedo, Nicholas Bass, Donald W. Black, Douglas Blackwood, Richard Bruggeman, Nancy G. Buccola, Khalid Choudhury, Robert Cloninger, Aiden Corvin, Nicholas John Craddock, Mark J. Daly, Susmita Datta, Gary Donohoe, Jubao Duan, Frank Dudbridge, Ayman H. Fanous, Robert Freedman, Nelson B. Freimer, Marion Friedl, Michael Gill, Hugh Gurling, Lieuwe de Haan, Marian L. Hamshere, Annette M. Hartmann, Peter Holmans, René S. Kahn, Matthew C. Keller, Elaine Kenny, George Kirov, Lydia Krabbendam, Robert Krasucki, Jacob Lawrence, Todd Lencz, Douglas F. Levinson, Jeffrey A. Lieberman, D. Y. Lin, Don Linszen, Patrik K. E. Magnusson, Wolfgang Maier, Anil K. Malhotra

    Almmustuhtton 2015
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  20. 20
    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases Dahkki Alexander Gusev, Sang Lee, Gosia Trynka, Hilary K. Finucane, Bjarni J. Vilhjálmsson, Han Xu, Chongzhi Zang, Stephan Ripke, Brendan Bulik‐Sullivan, Eli A. Stahl, Anna K. Kähler, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Mark J. Daly, Bogdan Paşaniuc, Patrick F. Sullivan, Benjamin M. Neale, Naomi R. Wray, Soumya Raychaudhuri, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Anders D. Børglum, 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, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael H. Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, 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

    Almmustuhtton 2014
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