Department of Medical Biology
In NorwegianFagerheim, Toril
Rettsgenetisk senter
Phone
(+47) 776 46062
E-mail
Office/visiting address
Medisin og Helsefag
MH L6.233E
Mobile private
41686436
Publications in CRIStin
- Østern, Rune André Helland; Fagerheim, Toril; Ørstavik, Kristin; Holmøy, Trygve; Heiberg, Arvid; Lund-Petersen, Inger; Strom, Tim M.; Nilssen, Øivind; Dahl, Arve. Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 gene. Neuromuscular Disorders 2012; Volum 22 (6). ISSN 0960-8966.s 511 - 521.s doi: 10.1016/j.nmd.2012.01.011.
- Alhamidi, Maisoon; Kjeldsen, Elisabeth; Fagerheim, Toril; Brox, Vigdis; Lindal, Sigurd; Van Ghelue, Marijke; Nilssen, Øivind. Fukutin-Related Protein Resides in the Golgi Cisternae of Skeletal Muscle Fibres and Forms Disulfide-Linked Homodimers via an N-Terminal Interaction. PLoS ONE 2011; Volum 6 (8). ISSN 1932-6203.s doi: 10.1371/journal.pone.0022968.
- Rendtorff, Nanna D.; Lodahl, Marianne; Boulahbel, Houda; Johansen, Ida R.; Pandya, Arti; Welch, Katherine O.; Norris, Virginia W.; Arnos, Kathleen S.; Bitner-Glindzicz, Maria; Emery, Sarah B.; Mets, Marilyn B.; Fagerheim, Toril; Eriksson, Kristina; Hansen, Lars; Bruhn, Helene; Möller, Claes; Lindholm, Sture; Ensgaard, Stefan; Lesperance, Marci M.; Tranebjaerg, Lisbeth. Identification of p.A684V Missense Mutation in the WFS1 Gene as a Frequent Cause of Autosomal Dominant Optic Atrophy and Hearing Impairment. American Journal of Medical Genetics 2011; Volum 155A (6). ISSN 0148-7299.s 1298 - 1313.s doi: 10.1002/ajmg.a.33970.
- Siem, Geir; Fagerheim, Toril; Jonsrud, Christoffer; Laurent, Claude H. Claesson; Teig, Erik; Harris, Sten; Leren, Trond Paul; Fruh, Andreas; Heimdal, Ketil Riddervold. Causes of hearing impairment in the Norwegian paediatric cochlear implant program. International Journal of Audiology 2010; Volum 49 (8). ISSN 1499-2027.s 596 - 605.s doi: 10.3109/14992021003743269.
- Biong, Stine Margarethe; Gram, Inger Torhild; Brill, I; Johansen, Fredrik Ekeberg; Solvang, Hiroko Kato; Grenaker, Grethe Irene; Fagerheim, Toril; Bremnes, Yngve; Chanock, Stephen; Burdett, L; Yeager, M; Ursin, Giske; Kristensen, Vessela N.. Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density. BMC Medical Genomics 2010; Volum 3. ISSN 1755-8794.s doi: 10.1186/1755-8794-3-9.
- Müller, Kay; Ingebrigtsen, Tor; Wilsgaard, Tom; Wikran, Gry; Fagerheim, Toril; Romner, Bertil; Waterloo, Knut. PREDICTION OF TIME TRENDS IN RECOVERY OF COGNITIVE FUNCTION AFTER MILD HEAD INJURY. Neurosurgery 2009; Volum 64 (4). ISSN 0148-396X.s 698 - 704.s doi: 10.1227/01.NEU.0000340978.42892.78.
- Fagerheim, Toril; Raeymaekers, Peter; Tønnessen, Finn Egil; Pedersen, Marit; Tranebjærg, Lisbeth; Lubs, Herbert A. A new gene (DYX3) for dyslexia is located on chromosome 2. Journal of Medical Genetics 1999; Volum 36 (9). ISSN 1468-6244.s 664 - 669.
- Tønnessen, Finn Egil; Fagerheim, Toril; Raeymaekers, Peter; Pedersen, Marit; Tranebjærg, Lisbeth; Lubs, Herbert. A new gene (DYX3) for dyslexia is located on chromosome 2. Journal of Medical Genetics 1999; Volum 36. ISSN 0022-2593.
- Tønnessen, Finn Egil; Fagerheim, Toril; Raeymaekers, Peter; Lubs, Herbert; Lundberg, Ingvar; Tønnessen, Finn Egil; Austad, Ingolv. Exclusion of linkage to 1p, 6p and Chromosome 15 in a large Norwegian family with dyslexia. 1999.s 151 - 156.
- Alhamidi, Maisoon; Kjeldsen, Elisabeth; Fagerheim, Toril; Brox, Vigdis; Lindal, Sigurd; Van Ghelue, Marijke; Nilssen, Øivind. Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction interface. Neuromuscular Disorders 2011; Volum 21 (9-10). ISSN 0960-8966.s 665 - 666.s doi: 10.1016/j.nmd.2011.06.840.
- Fagerheim, Toril; McAuley, Erica; Tønnessen, Finn-Egil; Smith, Shelley D.; Olson, Richard K.; Pennington, Bruce F.; DeFries, John C.; Monaco, Anthony P.. Association and linkage analysis of the dyslexia susceptibility locus (DYX3) on chr 2p15-p16. American Society of Human Genetics Annual Meeting 2004-10-26 - 2004-10-30 2004.
- Fagerheim, Toril. Genetiske årsaker til dysleksi. Regional Forskningskonferanse 2004-11-03 - 2004-11-04 2004.
- Fagerheim, Toril. Fra gener til psyke: Genetiske årsaker til dysleksi. Norsk Psykologikongress 2004-08-26 - 2004-08-27 2004.
- Fagerheim, Toril; Raeymaekers, Peter; Tønnessen, Finn Egil; Sandkuijl, Lodewijk; Lubs, Herbert; Tranebjærg, Lisbeth. A genome-wide search for dyslexia loci in a large Norwegian family. American Society of Human Genetics 2000.