Anna K. Kähler
Active 2008–2024
- 25
- Papers
- 19,526
- Citations
- 21
- h-index
- 24
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology47.2%
- Medicine29.3%
- Neuroscience15%
- Psychology2.4%
- Immunology and Microbiology1.8%
- Computer Science0.7%
- Other3.6%
Topics
- Genetic Associations and Epidemiology8.2%
- Acute Myeloid Leukemia Research4.8%
- Epigenetics and DNA Methylation3.3%
- Tryptophan and brain disorders3.1%
- Schizophrenia research and treatment3.1%
- Genetics and Neurodevelopmental Disorders3%
- Other74.5%
Coauthors
- Patrick F. Sullivan10
- Christina M. Hultman8
- Ole A. Andreassen8
- Anikó Lovik7
- Emma M. Frans6
- Ingrid Agartz6
- Arna Hauksdóttir5
- Edda Björk Þórðardóttir5
- Helga Ask5
- Ingibjörg Magnúsdóttir5
- Jennifer L. Moran5
- Jóhanna Jakobsdóttir5
- Anna Bára Unnarsdóttir4
- Archie Campbell4
- Asle Hoffart4
- Fang Fang4
- Giulio Genovese4
- Ingrid Melle4
- Menachem Fromer4
- Patrik K. E. Magnusson4
- Sarah E. Bergen4
- Shaun Purcell4
- Srdjan Djurovic4
- Stephan Ripke4
All papers
- Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
Authors: 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 - New England Journal of Medicine 2014 cited by 3,490
- Biological insights from 108 schizophrenia-associated genetic loci
Authors: Jacqueline I. Goldstein, Benjamin M. Neale, Stephan Ripke, Hailiang Huang, Kai-How Farh, Hailiang Huang, Menachem Fromer, Brendan Bulik‐Sullivan, Mark J. Daly, Kimberly D. Chambert, Giulio Genovese, Jordan W. Smoller, Phil Lee, Edward M. Scolnick, Stephan Ripke, Elizabeth Bevilacqua, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Richard A. Belliveau, Steven A. McCarroll, Sarah E. Bergen, Joel N. Hirschhorn, Alkes Price, Eli A. Stahl, Tõnu Esko, Aiden Corvin, Paul Cormican, Jacqueline I. Goldstein, Derek W. Morris, Benjamin M. Neale, James T. R. Walters, Hailiang Huang, Noa Carrera, Alkes L. Price, Mark J. Daly, Lyudmila Georgieva, Marian L. Hamshere, Benjamin M. Neale, Jordan W. Smoller, Andrew J. Pocklington, Paul Cormican, Aiden Corvin, Michael Gill, Gary Donohoe, Michael J. Owen, Alexander Richards, David A. Collier, Michael J. Owen, Noa Carrera, Marian L. Hamshere, Nick Craddock, David Kavanagh, Morten Mattingsdal, Peter Holmans, George Kirov, Sophie E. Legge, Valentina Escott‐Price, Nigel Williams, Andrew Pocklington, Lyudmila Georgieva, James Walters, Nick Craddock, Henrik B. Rasmussen, Michael J. Owen, Peter Holmans, David Collier, Younes Mokrab, David Collier, Tune H. Pers, Farooq Amin, Silviu A. Bacanu, Tim B. Bigdeli, Erik Söderman, Brandon K. Wormley, Martin Begemann, Christian Hammer, Srdjan Djurovic, Morten Mattingsdal, Judit Bene, Ole A. Andreassen, Anna K. Kähler, Ingrid Melle, Esben Agerbo, Preben Bo Mortensen, Esben Agerbo, Preben Bo Mortensen, Preben Bo Mortensen, Randy L. Buckner, Henrik B. Rasmussen, Ditte Demontis, Esben Agerbo, Line Olsen, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Thomas Folkmann Hansen, Margot Albus, Madeline Alexander, Claudine Laurent and 197 more - Nature 2014 cited by 8,166
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Authors: Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Peter Holmans, Dalila Pinto, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Zhouzhi Wang, Karin V. Fuentes Fajarado, Michelle S. Maile, Stephan Ripke, Ingrid Agartz, Margot Albus, Madeline Alexander, Farooq Amin, Joshua Atkins, Silviu‐Alin Bacanu, Richard A. Belliveau, Sarah E. Bergen, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, 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
- Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Authors: 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 and 245 more - The American Journal of Human Genetics 2014 cited by 654
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Authors: 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, Milica Pejovic Milovancevic, 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, Kari Stefansson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan - Nature Genetics 2013 cited by 1,565
- A polygenic burden of rare disruptive mutations in schizophrenia
Authors: 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 - Nature 2014 cited by 1,461
- Quantifying prion disease penetrance using large population control cohorts
Authors: 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, Élodie 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 - Science Translational Medicine 2016 cited by 469
- Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Authors: 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, Andres Metspalu, Mari Nelis, Reedik Mägi, Tōnu Esko, 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 - The American Journal of Human Genetics 2022 cited by 75
- COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and Denmark
Authors: 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 - The Lancet Regional Health - Europe 2023 cited by 44
- Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study
Authors: 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 - The Lancet Public Health 2022 cited by 168
- The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Authors: 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 - Nature Communications 2022 cited by 61
- Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
Authors: 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 - Nature Communications 2020 cited by 91
- Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Authors: 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 - Nature Communications 2015 cited by 1,213
- Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
Authors: 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 - Journal of Psychiatric Research 2010 cited by 215
- Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach
Authors: 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 - The Lancet Psychiatry 2016 cited by 136
- Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia
Authors: Mona K. Otnæss, Srdjan Djurovic, Lars M. Rimol, Bettina Kulle, Anna K. Kähler, Erik G. Jönsson, Ingrid Agartz, Kjetil Sundet, Håkan Hall, Sally Timm, Thomas Folkmann Hansen, Joseph H. Callicott, Ingrid Melle, Thomas Werge, Ole A. Andreassen - Neurobiology of Disease 2009 cited by 76
- Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene
Authors: Anna K. Kähler, Srdjan Djurovic, Bettina Kulle, Erik G. Jönsson, Ingrid Agartz, Håkan Hall, Stein Opjordsmoen, Klaus D. Jakobsen, Thomas Folkmann Hansen, Ingrid Melle, Thomas Werge, Vidar M. Steen, Ole A. Andreassen - American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008 cited by 120
- Mental health indicators in Sweden over a 12-month period during the COVID-19 pandemic – Baseline data of the Omtanke2020 Study
Authors: Anikó Lovik, Juan González‐Hijón, Anna K. Kähler, Unnur Valdimarsdóttir, Emma M. Frans, Patrik K. E. Magnusson, Nancy L. Pedersen, Per Hall, Kamila Czene, Patrick F. Sullivan, Fang Fang - Journal of Affective Disorders 2022 cited by 26
- Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations
Authors: 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 Folkmann Hansen, Thomas Werge, Thor Aspelund, David J. Porteous, Fang Fang, Kelli Lehto, Ole A. Andreassen, Ole Birger Pedersen, Stéphanie Le Hellard, Unnur Valdimarsdóttir - International Journal of Epidemiology 2021 cited by 164
- Elevated symptoms of depression and anxiety among family members and friends of critically ill COVID-19 patients – an observational study of five cohorts across four countries
Authors: Anikó Lovik, Juan González‐Hijón, Asle Hoffart, Chloe Fawns‐Ritchie, Ingibjörg Magnúsdóttir, Li Lu, Anna Bára Unnarsdóttir, Anna K. Kähler, Archie Campbell, Arna Hauksdóttir, Charilaos Chourpiliadis, Daniel L. McCartney, Edda Björk Þórðardóttir, Emily E. Joyce, Emma M. Frans, Jóhanna Jakobsdóttir, Lill Trogstad, Ole A. Andreassen, Per Magnus, Sverre Urnes Johnson, Patrick F. Sullivan, Thor Aspelund, David J. Porteous, Helga Ask, Omid V. Ebrahimi, Unnur Valdimarsdóttir, Fang Fang - The Lancet Regional Health - Europe 2023 cited by 15
- Sex-dependent association of common variants of microcephaly genes with brain structure
Authors: 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 and 109 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2009 cited by 114
- Inherited DNA Repair Gene Mutations in Men with Lethal Prostate Cancer
Authors: Tommi Rantapero, Tiina Wahlfors, Anna K. Kähler, Christina M. Hultman, Johan Lindberg, Teuvo L.J. Tammela, Matti Nykter, Johanna Schleutker, Fredrik Wiklund - Genes 2020 cited by 22
- Short-term improvement of mental health after a COVID-19 vaccination
Authors: Charilaos Chourpiliadis, Anikó Lovik, Anna K. Kähler, Unnur Valdimarsdóttir, Emma M. Frans, Fredrik Nyberg, Patrick F. Sullivan, Fang Fang - PLoS ONE 2023 cited by 19
- A burden of rare copy number variants in obsessive-compulsive disorder
Authors: Matthew Halvorsen, Elles de Schipper, Julia Bäckman, Nora I. Strom, Kristen Hagen, Long Long Chen, Diana R. Djurfeldt, Kira D. Höffler, Anna K. Kähler, Paul Lichtenstein, Kathleen M. Morrill, Hyun Ji Noh, Thorstein Olsen Eide, Tetyana Zayats, Kerstin Lindblad‐Toh, Elinor K. Karlsson, Nancy L. Pedersen, John Wallert, Cynthia M. Bulik, Bengt T. Fundín, Mikael Landén, Gerd Kvale, Bjarne Hansen, Jan Haavik, Manuel Mattheisen, Christian Rück, David Mataix‐Cols, James J. Crowley - Molecular Psychiatry 2024 cited by 14
