K
Ketil Heimdal
Researcher at Oslo University Hospital
Publications - 65
Citations - 2448
Ketil Heimdal is an academic researcher from Oslo University Hospital. The author has contributed to research in topics: Population & Cancer. The author has an hindex of 25, co-authored 65 publications receiving 2024 citations. Previous affiliations of Ketil Heimdal include Rikshospitalet–Radiumhospitalet.
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Journal ArticleDOI
Pathogenesis of the syndrome of hemolysis, elevated liver enzymes, and low platelet count (HELLP): a review.
Ulrich Abildgaard,Ketil Heimdal +1 more
TL;DR: The pathogenetic mechanisms of HELLP syndrome are reviewed with an emphasis on differences between HELLP and early onset PE.
Journal ArticleDOI
The Y deletion gr/gr and susceptibility to testicular germ cell tumor
Katherine L. Nathanson,Peter A. Kanetsky,Rachel Hawes,David J. Vaughn,Richard Letrero,Katherine M. Tucker,Michael Friedlander,Kelly-Anne Phillips,David W. Hogg,Michael A.S. Jewett,Radka Lohynska,Gedske Daugaard,Stéphane Richard,Agnès Chompret,Catherine Bonaïti-Pellié,Axel Heidenreich,Edith Olah,Lajos Géczi,István Bodrogi,Wilma Ormiston,Peter A. Daly,J. Wolter Oosterhuis,Ad J. M. Gillis,Leendert H. J. Looijenga,Parry Guilford,Sophie D. Fosså,Ketil Heimdal,Sergei Tjulandin,Ludmila Liubchenko,Hans Stoll,Walter P. Weber,Matthew Rudd,Robert Huddart,Gillian P. Crockford,David Forman,D. Timothy Oliver,Lawrence H. Einhorn,Barbara L. Weber,Joan Kramer,Mary L. McMaster,Mark H. Greene,Malcolm C. Pike,Victoria K. Cortessis,Chu Chen,Stephen M. Schwartz,D. Timothy Bishop,Douglas F. Easton,Michael R. Stratton,Elizabeth A. Rapley +48 more
TL;DR: Data indicate that the Y microdeletion gr/gr is a rare, low-penetrance allele that confers susceptibility to TGCT.
Journal ArticleDOI
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Asbjørg Stray-Pedersen,Hanne Sørmo Sorte,Pubudu S. Samarakoon,Tomasz Gambin,Tomasz Gambin,Ivan K. Chinn,Zeynep Coban Akdemir,Hans Christian Erichsen,Lisa R. Forbes,Shen Gu,Bo Yuan,Shalini N. Jhangiani,Donna M. Muzny,Olaug K. Rødningen,Ying Sheng,Sarah K. Nicholas,Lenora M. Noroski,Filiz O. Seeborg,Carla M. Davis,Debra Canter,Emily M. Mace,Timothy J. Vece,Carl E. Allen,Harshal Abhyankar,Philip M. Boone,Christine R. Beck,Wojciech Wiszniewski,Børre Fevang,Pål Aukrust,Geir E. Tjønnfjord,Tobias Gedde-Dahl,Henrik Hjorth-Hansen,Ingunn Dybedal,Ingvild Nordøy,Silje F. Jørgensen,Tore G. Abrahamsen,Torstein Øverland,Anne Grete Bechensteen,Vegard Skogen,Liv T. N. Osnes,Mari Ann Kulseth,Trine Prescott,Cecilie F. Rustad,Ketil Heimdal,John W. Belmont,Nicholas L. Rider,Javier Chinen,Tram N. Cao,Eric A. Smith,María Soledad Caldirola,Liliana Bezrodnik,Saul Oswaldo Lugo Reyes,Francisco Javier Espinosa Rosales,Nina Denisse Guerrero-Cursaru,Luis A. Pedroza,Cecilia Poli,Cecilia Poli,José Luis Franco,Claudia Milena Trujillo Vargas,Juan Carlos Aldave Becerra,Nicola A.M. Wright,Thomas B. Issekutz,Andrew C. Issekutz,Jordan K. Abbott,Jason W. Caldwell,Diana K. Bayer,Alice Y. Chan,Alessandro Aiuti,Caterina Cancrini,Eva Holmberg,Christina E. West,Magnus K. O. Burstedt,Ender Karaca,Gozde Yesil,Gozde Yesil,Hasibe Artac,Yavuz Bayram,Mehmed M. Atik,Mohammad K. Eldomery,Mohammad S. Ehlayel,Stephen Jolles,Berit Flatø,Alison A. Bertuch,I. Celine Hanson,Victor Wei Zhang,Lee-Jun C. Wong,Jianhong Hu,Magdalena Walkiewicz,Yaping Yang,Christine M. Eng,Eric Boerwinkle,Eric Boerwinkle,Richard A. Gibbs,William T. Shearer,Robert Lyle,Jordan S. Orange,James R. Lupski +96 more
TL;DR: This high‐throughput genomic approach enabled detection of disease‐related variants in unexpected genes; permitted detection of low‐grade constitutional, somatic, and revertant mosaicism; and provided evidence of a mutational burden in mixed PIDD immunophenotypes.
Journal ArticleDOI
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
Marie E. Faughnan,Johannes J. Mager,Steven W. Hetts,Valerie A. Palda,Kelly Lang-Robertson,Elisabetta Buscarini,Erik Deslandres,Raj S. Kasthuri,Andrea Lausman,David M. Poetker,Felix Ratjen,Mark S. Chesnutt,Marianne S. Clancy,Kevin J. Whitehead,Hanny Al-Samkari,Murali M. Chakinala,Miles Conrad,Daniel Cortes,Claudia Crocione,Jama M. Darling,Els de Gussem,Carol Derksen,Sophie Dupuis-Girod,Patrick Foy,Urban W. Geisthoff,James R. Gossage,Adrienne M. Hammill,Ketil Heimdal,Katharine J. Henderson,Vivek N. Iyer,Anette Drøhse Kjeldsen,Masaki Komiyama,Kevin Korenblatt,Jamie McDonald,Jack McMahon,Justin P. McWilliams,Mary E. Meek,Meir Mei-Zahav,Scott E. Olitsky,Sara Palmer,Rose Pantalone,Jay F. Piccirillo,Beth Plahn,Mary Porteous,Marco C. Post,Ivan Radovanovic,Paul J. Rochon,Josanna Rodriguez-Lopez,Carlo Sabbà,Marcelo M. Serra,Claire L. Shovlin,Dennis L. Sprecher,Andrew J. White,Ingrid Winship,Roberto Zarrabeitia +54 more
TL;DR: The expert panel generated and approved 6 new recommendations that highlight new evidence in existing topics from the first International HHT Guidelines and provide guidance in 3 new areas: anemia, pediatrics, and pregnancy and delivery.
Journal ArticleDOI
Genome-wide linkage screen for testicular germ cell tumour susceptibility loci
Gillian P. Crockford,Rachel Linger,Sarah Hockley,Darshna Dudakia,Lola Johnson,Robert Huddart,Katherine M. Tucker,Michael Friedlander,Kelly-Anne Phillips,David W. Hogg,Michael A.S. Jewett,Radka Lohynska,Gedske Daugaard,Stéphane Richard,Agnès Chompret,Catherine Bonaïti-Pellié,Axel Heidenreich,Peter Albers,Edith Olah,Lajos Géczi,István Bodrogi,Wilma Ormiston,Peter A. Daly,Parry Guilford,Sophie D. Fosså,Ketil Heimdal,Sergei Tjulandin,Ludmila Liubchenko,Hans Stoll,Walter P. Weber,David Forman,T. Oliver,Lawrence H. Einhorn,Mary L. McMaster,Joan Kramer,Mark H. Greene,Barbara L. Weber,Katherine L. Nathanson,Victoria K. Cortessis,Douglas F. Easton,D. Timothy Bishop,Michael R. Stratton,Elizabeth A. Rapley +42 more
TL;DR: The results indicate that no single major locus can account for the majority of the familial aggregation of TGCT, and suggests that multiple susceptibility loci with weak effects contribute to the disease.