Kristian Tveten

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 15

Top Topics

Intellectual Disability

Dna Methylation

Dna Damage Response

Top Venues

Science advances

European journal of human genetics : EJHG

Journal of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nicola de Prisco, Caitlin Ford, Nathan D Elrod, Winston Lee, Lauren C Tang, Kai-Lieh Huang, Ai Lin, Ping Ji, Venkata S Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica Hsiung Wojcik, Jill Anne Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin-To Fong, Jaya K George-Abraham, Catherine A Buchanan, Andrea Hanson-Kahn, Jonathan A Bernstein, Aikaterini A Nella, Wendy K Chung, Vicky L Brandt, Marko Jovanovic, Kimara L Targoff, Hari Krishna Yalamanchili, Eric J Wagner, Vincenzo A Gennarino
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Science advances 9 (7) (2023)
Nadra Samra, Shir Toubiana, Hilde Yttervik, Aya Tzur-Gilat, Ilham Morani, Chen Itzkovich, Liran Giladi, Kamal Abu Jabal, John Z Cao, Lucy A Godley, Adi Mory, Hagit Baris Feldman, Kristian Tveten, Sara Selig, Karin Weiss
RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function. Journal of human genetics 66 (11) (2021)
Elin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero, Ulrikke Straume Wiig, Mari Ann Kulseth, Magnus Dehli Vigeland, Ying Sheng, Charlotte von der Lippe, Kristian Tveten, Torstein Ragnar Meling, Eirik Helseth, Ketil Riddervold Heimdal
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis. European journal of human genetics : EJHG 29 (6) (2020)
David A Dyment, Paulien A Terhal, Cecilie F Rustad, Kristian Tveten, Christopher Griffith, Parul Jayakar, Marwan S Shinawi, Sara Ellingwood, Rosemarie Smith, Koen van Gassen, Kirsty McWalter, A Micheil Innes, Matthew A Lines
De novo substitutions of TRPM3 cause intellectual disability and epilepsy. European journal of human genetics : EJHG 27 (10) (2019)
Sandra Jansen, Ilse M van der Werf, A Micheil Innes, Alexandra Afenjar, Pankaj B Agrawal, Ilse J Anderson, Paldeep S Atwal, Ellen van Binsbergen, Marie-José van den Boogaard, Lucia Castiglia, Zeynep H Coban-Akdemir, Anke van Dijck, Diane Doummar, Albertien M van Eerde, Anthonie J van Essen, Koen L van Gassen, Maria J Guillen Sacoto, Mieke M van Haelst, Ivan Iossifov, Jessica L Jackson, Elizabeth Judd, Charu Kaiwar, Boris Keren, Eric W Klee, Jolien S Klein Wassink-Ruiter, Marije E Meuwissen, Kristin G Monaghan, Sonja A de Munnik, Caroline Nava, Charlotte W Ockeloen, Rosa Pettinato, Hilary Racher, Tuula Rinne, Corrado Romano, Victoria R Sanders, Rhonda E Schnur, Eric J Smeets, Alexander P A Stegmann, Asbjørg Stray-Pedersen, David A Sweetser, Paulien A Terhal, Kristian Tveten, Grace E VanNoy, Petra F de Vries, Jessica L Waxler, Marcia Willing, Rolph Pfundt, Joris A Veltman, R Frank Kooy, Lisenka E L M Vissers, Bert B A de Vries
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms. European journal of human genetics : EJHG 27 (5) (2019)