Gunnar Houge

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 15

Top Topics

Top Venues

European journal of human genetics : EJHG

Autism research : official journal of the International Society for Autism Research

American journal of medical genetics. Part A

Clinical case reports

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)
Gunnar Houge, Mirjam Langeveld, Joao-Paulo Oliveira
GLA insufficiency should not be called Fabry disease. European journal of human genetics : EJHG (2024)
Jacob Sampson, null null, Gunnar Houge, Siddharth Banka
Locus conversions are rare in the LRFN5 locus. Autism research : official journal of the International Society for Autism Research (2023)
Ileana Cristea, Hugo Hernán Abarca Barriga, Anne E Christensen Mellgren, Milana Trubnykova, Roya Mehrasa, Dorien J M Peters, Gunnar Houge, Raoul C M Hennekam, Eyvind Rødahl, Ove Bruland, Cecilie Bredrup
A Pellino-2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium-digital keloid dysplasia. FEBS letters (2023)
Helle Lybaek, Michael Robson, Nicole de Leeuw, Jayne Y Hehir-Kwa, Aaron Jeffries, Bjørn Ivar Haukanes, Siren Berland, Diederik de Bruijn, Stefan Mundlos, Malte Spielmann, Gunnar Houge
LRFN5 locus structure is associated with autism and influenced by the sex of the individual and locus conversions. Autism research : official journal of the International Society for Autism Research 15 (3) (2022)
Gunnar Houge, Andreas Laner, Sebahattin Cirak, Nicole de Leeuw, Hans Scheffer, Johan T den Dunnen
Stepwise ABC system for classification of any type of genetic variant. European journal of human genetics : EJHG (2021)
Silvia Martin-Almedina, Kazim Ogmen, Ege Ozkan, Dionysios Grigoriadis, Christina Karapouliou, Noeline Nadarajah, Cathrine Ebbing, Jenny Lord, Rhiannon Mellis, Fanny Kortuem, Mary Beth Dinulos, Cassandra Polun, Sherri Bale, Giles Atton, Alexandra Robinson, Hallvard Reigstad, Gunnar Houge, Axel von der Wense, Wolf-Henning Becker, Steve Jeffery, Peter S Mortimer, Kristiana Gordon, Katherine S Josephs, Sarah Robart, Mark David Kilby, Stephanie Vallee, Jerome L Gorski, Maja Hempel, Siren Berland, Shehla Mohammed, Pia Ostergaard
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes. Genetics in medicine : official journal of the American College of Medical Genetics 23 (7) (2021)
Siren Berland, Jørgen Jareld, Nicholas Hickson, Helene Schlecht, Gunnar Houge, Sofia Douzgou Houge
The blended phenotype of a germline RIT1 and a mosaic PIK3CA variant. Cold Spring Harbor molecular case studies 7 (6) (2021)
Parisa Hemati, Anya Revah-Politi, Haim Bassan, Slavé Petrovski, Colleen G Bilancia, Keri Ramsey, Nicole G Griffin, Louise Bier, Megan T Cho, Monica Rosello, Sally Ann Lynch, Sophie Colombo, Astrid Weber, Marte Haug, Erin L Heinzen, Tristan T Sands, Vinodh Narayanan, Michelle Primiano, Vimla S Aggarwal, Francisca Millan, Shannon G Sattler-Holtrop, Alfonso Caro-Llopis, Nir Pillar, Janice Baker, Rebecca Freedman, Hester Y Kroes, Stephanie Sacharow, Nick Stong, Pablo Lapunzina, Michael C Schneider, Nancy J Mendelsohn, Amanda Singleton, Valerie Loik Ramey, Karen Wou, Alla Kuzminsky, Sandra Monfort, Monica Weiss, Samantha Doyle, Alejandro Iglesias, Francisco Martinez, Fiona Mckenzie, Carmen Orellana, Koen L I van Gassen, Maria Palomares, Lily Bazak, Andy Lee, Ana Bircher, Lina Basel-Vanagaite, Maria Hafström, Gunnar Houge, null null, null null, David B Goldstein, Kwame Anyane-Yeboa
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. American journal of medical genetics. Part A 176 (11) (2018)
Kjersti Eline Stige, Ivar Otto Gjerde, Gunnar Houge, Per Morten Knappskog, Charalampos Tzoulis
Beta-propeller protein-associated neurodegeneration: a case report and review of the literature. Clinical case reports 6 (2) (2018)
Aida Telegrafi, Susanna Balcells, Sarah M Robbins, Carlos E Speck-Martins, David FitzPatrick, Leah R Fleming, Richard Redett, Andreas Dufke, Gunnar Houge, Jeske J T van Harssel, Alain Verloes, Angela Robles, Irini Manoli, Elizabeth C Engle, null null, Ethylin W Jabs, David Valle, John Carey, Julie Elizabeth Hoover-Fong, Nara L M Sobreira
Identification of STAC3 variants in non-Native American families with overlapping features of Carey-Fineman-Ziter syndrome and Moebius syndrome. American journal of medical genetics. Part A 173 (10) (2017)
Marte G Haug, Atle Brendehaug, Gunnar Houge, Masayo Kagami, Tsutomu Ogata
Mosaic upd(14)pat in a patient with mild features of Kagami-Ogata syndrome. Clinical case reports 6 (1) (2017)