Anna K. Kähler

Active 2008–2024

25
Papers
19,526
Citations
21
h-index
24
i10-index

Citations

Citations per year for Anna K. Kähler1994: 1 citations1995: 1 citations1996: 1 citations1999: 1 citations2002: 1 citations2009: 2 citations2010: 9 citations2011: 24 citations2012: 19 citations2013: 28 citations2014: 172 citations2015: 351 citations2016: 412 citations2017: 472 citations2018: 427 citations2019: 1,104 citations2020: 1,054 citations2021: 1,013 citations2022: 690 citations2023: 427 citations2024: 518 citations2025: 230 citations2026: 7 citations1997–1998: no citations, so these years are not shown2000–2001: no citations, so these years are not shown2003–2008: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,571 citing papers, 25% of this breakdownUnited Kingdom: 1,430 citing papers, 10% of this breakdownGermany: 872 citing papers, 6.1% of this breakdownChina: 700 citing papers, 4.9% of this breakdownNetherlands: 590 citing papers, 4.1% of this breakdownAustralia: 583 citing papers, 4.1% of this breakdownCanada: 561 citing papers, 3.9% of this breakdownItaly: 503 citing papers, 3.5% of this breakdownSweden: 485 citing papers, 3.4% of this breakdownFrance: 437 citing papers, 3.1% of this breakdownSpain: 380 citing papers, 2.7% of this breakdownJapan: 366 citing papers, 2.6% of this breakdown
0%25%Other 26.6%

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

All papers

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  1. Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

    Authors: , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2014 cited by 3,490

  2. Biological insights from 108 schizophrenia-associated genetic loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  3. 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

  4. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  5. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  6. A polygenic burden of rare disruptive mutations in schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven A. McCarroll, Pamela Sklar - Nature 2014 cited by 1,461

  7. Quantifying prion disease penetrance using large population control cohorts

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fang Fang, Unnur Valdimarsdóttir - The Lancet Regional Health - Europe 2023 cited by 44

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  11. The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Communications 2020 cited by 91

  13. Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kāri Stefánsson, Markus Hansson, Unnur Þorsteinsdóttir, Björn Nilsson - Nature Communications 2015 cited by 1,213

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

    Authors: , , , , , , , , , , , , , , , , , , , , , - Journal of Psychiatric Research 2010 cited by 215

  15. Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach

    Authors: , , , , , , , , , , , , , - The Lancet Psychiatry 2016 cited by 136

  16. Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia

    Authors: , , , , , , , , , , , , , , - Neurobiology of Disease 2009 cited by 76

  17. Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene

    Authors: , , , , , , , , , , , , - American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008 cited by 120

  18. Mental health indicators in Sweden over a 12-month period during the COVID-19 pandemic – Baseline data of the Omtanke2020 Study

    Authors: , , , , , , , , , , - Journal of Affective Disorders 2022 cited by 26

  19. Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  20. 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: , , , , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Regional Health - Europe 2023 cited by 15

  21. Sex-dependent association of common variants of microcephaly genes with brain structure

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  22. Inherited DNA Repair Gene Mutations in Men with Lethal Prostate Cancer

    Authors: , , , , , , , , - Genes 2020 cited by 22

  23. Short-term improvement of mental health after a COVID-19 vaccination

    Authors: , , , , , , , - PLoS ONE 2023 cited by 19

  24. A burden of rare copy number variants in obsessive-compulsive disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2024 cited by 14