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Thomas Folkmann Hansen

ResearcherPublications, citations & collaboration network

Thomas Folkmann Hansen is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Thomas Folkmann Hansen have?

ScholarIQindexed works

Thomas Folkmann Hansen has 380 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Thomas Folkmann Hansen have?

ScholarIQcitation count

Thomas Folkmann Hansen has 44,498 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Thomas Folkmann Hansen?

ScholarIQh-index

Thomas Folkmann Hansen has an h-index of 76 in OpenAlex.

What is the i10-index of Thomas Folkmann Hansen?

ScholarIQi10-index

Thomas Folkmann Hansen has an i10-index of 236 in OpenAlex.

What is the ORCID of Thomas Folkmann Hansen?

ScholarIQorcid

The ORCID for Thomas Folkmann Hansen is on the source record.

What is the OpenAlex record for Thomas Folkmann Hansen?

ScholarIQopenalex

The OpenAlex for Thomas Folkmann Hansen is on the source record.

What are the most-cited papers on Thomas Folkmann Hansen?

ScholarIQmost cited works
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke, B M Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, H Huang, Menachem Fromer, Jacqueline I. Goldstein, Mark J. Daly, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberly D. Chambert, Giulio Genovese, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Steven A. McCarroll, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Tune H. Pers, J. N. Hirschhorn, Alkes Price, Eli Stahl, Esko T, Aiden Corvin, Paul Cormican, Gary Donohoe, Derek W. Morris, Michael Gill, James T. R. Walters, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Michael O‘Donovan, David A. Collier, Younes Mokrab, Ingrid Agartz, Erik Söderman, Erik G. Jönsson, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Esben Agerbo, Preben Bo Mortensen, Ditte Demontis, Thomas Folkmann Hansen, Manuel Mattheisen, Ole Mors, Line Olsen, H Kruuse Rasmussen, Anders D. Børglum, Werge Tm, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, S Bacanu, Tim B. Bigdeli, Bradley T. Webb, Brandon K. Wormley, Martin Begemann, Christian Hammer, Sergi Papiol, Hannelore Ehrenreich, Béné Jj, Béla Melegh, Anna K. Kähler, Patrik K. E. Magnusson, Christina M. Hultman, Patrick F. Sullivan, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Joshua L. Roffman, William Byerley, Wiepke Cahn, René S. Kahn, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Buxbaum Jn, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman
Nature. 20148,164 CitationsOPEN ACCESS
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen, Naomi R. Wray, 23andMe, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M. Byrne, Abdel Abdellaoui, Mark J. Adams, Esben Agerbo, Tracy Air, Till F. M. Andlauer, Silviu‐Alin Bacanu, Marie Bækvad‐Hansen, Aartjan T.F. Beekman, Tim B. Bigdeli, Elisabeth B. Binder, Douglas Blackwood, Julien Bryois, Henriette N. Buttenschøn, Jonas Bybjerg‐Grauholm, Na Cai, Enrique Castelao, Jane Christensen, Toni‐Kim Clarke, Jonathan R. I. Coleman, Lucía Colodro‐Conde, Baptiste Couvy‐Duchesne, Nick Craddock, Gregory E. Crawford, Cheynna Crowley, Hassan S. Dashti, Gail Davies, Ian J. Deary, Franziska Degenhardt, Eske M. Derks, Neşe Direk, Conor V. Dolan, Erin C. Dunn, Thalia C. Eley, Nicholas Eriksson, Valentina Escott‐Price, Farnush Hassan Farhadi Kiadeh, Hilary K. Finucane, Andreas J. Forstner, Josef Frank, Héléna A. Gaspar, Michael Gill, Paola Giusti‐Rodríguez, Fernando S. Goes, Scott D. Gordon, Jakob Grove, Lynsey S. Hall, Eilís Hannon, Christine Søholm Hansen, Thomas Folkmann Hansen, Stefan Herms, Ian B. Hickie, Per Hoffmann, Georg Homuth, Carsten Horn, Jouke‐Jan Hottenga, David M. Hougaard, Ming Hu, Craig Hyde, Marcus Ising, Rick Jansen, Fulai Jin, Eric Jorgenson, James A. Knowles, Isaac S. Kohane, Julia Kraft, Warren W. Kretzschmar, Jesper Krogh, Zoltán Kutalik, Jacqueline M. Lane, Yihan Li, Yun Li, Penelope A. Lind, Xiaoxiao Liu, Leina Lu, Donald J. MacIntyre, Dean F. MacKinnon, Robert Maier, Wolfgang Maier, Jonathan Marchini, Hamdi Mbarek, Patrick J. McGrath, Peter McGuffin, Sarah E. Medland, Divya Mehta, Christel M. Middeldorp, Evelin Mihailov, Yuri Milaneschi, Lili Milani, Jonathan Mill, Francis M. Mondimore, Grant W. Montgomery, Sara Mostafavi, Niamh Mullins
Nature Genetics. 20183,337 CitationsOPEN ACCESS
Large recurrent microdeletions associated with schizophrenia
GROUP, Hreinn Stefánsson, Dan Rujescu, Sven Cichon, Olli Pietiläinen, Andrés Ingason, Stacy Steinberg, Ragnheiður Fossdal, Engilbert Sigurðsson, Thordur Sigmundsson, Jacobine E. Buizer‐Voskamp, Thomas Folkmann Hansen, Klaus D. Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M. Matthews, Arnaldur Gylfason, Bjarni V. Halldórsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Björnsson, Sigurborg Mattiasdottir, Thórarinn Blöndal, Magnús Haraldsson, Brynja B. Magnúsdóttir, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson
Nature. 20081,778 CitationsOPEN ACCESS
Common variants conferring risk of schizophrenia
†Genetic Risk and Outcome in Psychosis (GROUP), Hreinn Stefánsson, Roel A. Ophoff, Stacy Steinberg, Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli Pietiläinen, Ole Mors, Preben Bo Mortensen, Engilbert Sigurðsson, Ómar Gústafsson, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Folkmann Hansen, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Anders D. Børglum, Annette M. Hartmann, Anders Fink‐Jensen, Merete Nordentoft, David M. Hougaard, Bent Nørgaard‐Pedersen, Yvonne Böttcher, Jes Olesen, René Breuer, Hans‐Jürgen Möller, 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. 20091,720 CitationsOPEN ACCESS
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
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
Nature Genetics. 20161,158 CitationsOPEN ACCESS

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