基本信息
views: 109
Career Trajectory
Bio
Projects
1. 2012 - ---> Identification of STUB1 as a cause of cerebellar ataxia in an inbred family using homozygosity mapping and Next gen Seq. Joint project MEDGEN, Haukeland University Hospital.
2. 2012 - ---> Establishing a genotype-phenotype database for our patients with pathologic findings on array CGH. Joint with Lab.
3. 2003 - ---> Leader, Rikshospitalet’s team for Osler disease .
4. 2003-2010: Co-supervisor, PhD project on genetic causes of hereditary deafness in Norway
Research Interests
Papers共 157 篇Author StatisticsCo-AuthorSimilar Experts
By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
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期刊级别
合作者
合作机构
Synne S. Kennelly, Vegard Hovland, Iren Lindbak Matthews,Finn P. Reinholt,Håvard Skjerven,Ketil Heimdal,Suzanne Crowley
Pediatric Pulmonology (2024)
Daniel O. Dodd,Sabrina Mechaussier,Patricia L. Yeyati,Fraser McPhie,Jacob R. Anderson, Chen Jing Khoo,Amelia Shoemark,Deepesh K. Gupta,Thomas Attard,Maimoona A. Zariwala,Marie Legendre,Diana Bracht,Julia Wallmeier,Miao Gui,Mahmoud R. Fassad,David A. Parry,Peter A. Tennant,Alison Meynert,Gabrielle Wheway,Lucas Fares-Taie,Holly A. Black,Rana Mitri-Frangieh,Catherine Faucon,Josseline Kaplan,Mitali Patel,Lisa McKie,Roly Megaw,Christos Gatsogiannis,Mai A. Mohamed,Stuart Aitken,Philippe Gautier,Finn R. Reinholt,Robert A. Hirst,Chris O'Callaghan,Ketil Heimdal,Mathieu Bottier,Estelle Escudier,Suzanne Crowley,Maria Descartes,Ethylin W. Jabs,Priti Kenia,Jeanne Amiel,Giacomo Maria Bacci,Claudia Calogero,Viviana Palazzo,Lucia Tiberi,Ulrike Bluemlein,Andrew Rogers,Jennifer A. Wambach,Daniel J. Wegner,Anne B. Fulton,Margaret Kenna,Margaret Rosenfeld,Ingrid A. Holm,Alan Quigley,Emma A. Hall,Laura C. Murphy,Diane M. Cassidy,Alex von Kriegsheim,Jean-Francois Papon,Laurent Pasquier,Marlene S. Murris,James D. Chalmers,Claire Hogg,Kenneth A. Macleod,Don S. Urquhart,Stefan Unger,Timothy J. Aitman,Serge Amselem,Margaret W. Leigh,Michael R. Knowles,Heymut Omran,Hannah M. Mitchison,Alan Brown,Joseph A. Marsh,Julie P. I. Welburn,Shih-Chieh Ti,Amjad Horani,Jean-Michel Rozet,Isabelle Perrault,Pleasantine Mill
Mina Susanne Weedon-Fekjær,Hege K. Pihlstrøm, Harald Weedon-Fekjær, Birgitte Berentsen,Jan Gunnar Hatlebakk, Birgitte Bjerkely, Olga Karin Solberg,Ketil Riddervold Heimdal, Kristin Ørstavik, Trond G. Jenssen, Solrun Sigurdardottir
crossref(2024)
Stijn Van de Sompele,Caroline Van Cauwenbergh,Marjolein Carron,Alfredo Duenas Rey,Frauke Coppieters,Toon Rosseel,Hong Tran,Robrecht Cannoodt,Thalia Van Laethem,Brecht Guillemyn,Dimitri Roels, Helena Flipts,Erik Fransen,Marleen Praet,Thomas Langmann,Katharina Dannhausen, Robinato Elisa,Lan Yu, Frances High,Karin Dahan,Madeleine Fanemel,Ketil Heimdal,Flavio Faletra,Wendy Chung,Kris Vleminckx,Andrew Webster,Bart Leroy,Elfride De Baere
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 71-71
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ORPHANET JOURNAL OF RARE DISEASESno. 1 (2023)
Laryngoscope investigative otolaryngologyno. 1 (2023): e1196-e1196
Sigurdardottir Solrun, Bjerkely Birgitte, University of Oslo,Mathisen Per,von der Lippe Charlotte,Ørstavik Kristin,Heimdal Ketil,Dahle Dag Olav,Weedon-Fekjær Mina Susanne,Solberg Olga,Pihlstrøm Hege K.
Ine Cockerell,Jakob Christensen,Christina Hoi-Hansen, Lotte Holst, Mikkel Frederiksen,Caroline Lund,Cecilie Johannessen Landmark,Ketil Heimdal,Ragnar Solhoff,Terje Naerland
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Author Statistics
#Papers: 156
#Citation: 6731
H-Index: 41
G-Index: 80
Sociability: 7
Diversity: 4
Activity: 20
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