Greinar um føroyskar ílegur

2016-

Claire S Leblond, Freddy Cliquet, Coralie Carton, Guillaume Huguet, Alexandre Mathieu, Thomas Kergrohen, Julien Buratti, Nathalie Lemière, Laurence Cuisset, Thierry Bienvenu, Anne Boland, Jean-François Deleuze, Tormodur Stora, Rannva Biskupstoe, Jónrit Halling, Guðrið Andorsdóttir, Eva Billstedt, Christopher Gillberg, Thomas Bourgeron.
Both rare and common genetic variants contribute to autism in the Faroe Islands. 12/2019; 4(1)., DOI:10.1038/s41525-018-0075-2

Anna Pelet, Vaclava Skopova, Ulrike Steuerwald, Veronika Baresova, Mohammed Zarhrate, Jean-Marc Plaza, Ales Hnizda, Matyas Krijt, Olga Souckova, Flemming Wibrand, Guðrið Andorsdóttir, Fróði Joensen, David Sedlak, Anthony J Bleyer, Stanislav Kmoch, Stanislas Lyonnet, Marie Zikanova.
PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome. Human Molecular Genetics 10/2019; 28(22)., DOI:10.1093/hmg/ddz237

E.W. Jacobsen, O.B.V. Pedersen, G. Andorsdóttir, G.B.E. Jemec, L.E. Bryld.
Family recurrence risk of alopecia areata in the Faroe Islands. Clinical and Experimental Dermatology 03/2019; 44(7)., DOI:10.1111/ced.13974
Viggo Jønsson, Haneef Awan, Neil D. Jones, Tom B. Johannesen, Bjarni á Steig, Gudrid Andosdottir, Geir E. Tjønnfjord: Inheritance of Susceptibility to Malignant Blood Disorders. Scientific Reports 02/2019; 9(1):2444., DOI:10.1038/s41598-019-38879-y

Ólavur Mortensen, Leivur Nattestad Lydersen, Katrin Didriksen Apol, Guðrið Andorsdóttir, Bjarni á Steig, Noomi Oddmarsdóttir Gregersen.
Using dried blood spot samples from a trio for linked-read whole-exome sequencing. European Journal of Human Genetics 02/2019; 27(6):1., DOI:10.1038/s41431-019-0343-3

A Vang, K R Nielsen, J Midjord, M á F Berbisa, Ó Mortensen, G Andorsdóttir, N O Gregersen, J Burisch.
P823 Study launch: Investigating genetic and environmental factors in the faroese IBD cohort—the INCEPTION study. Journal of Crohn s and Colitis 01/2019; 13(Supplement_1):S534-S535., DOI:10.1093/ecco-jcc/jjy222.947

Guðrið Andorsdóttir.
Both rare and common genetic variants contribute to autism in the Faroe Islands https://rdcu.be/bh8io.

August Gabriel Wang, Noomi Odmarsdóttir Gregersen, Ólavur Mortensen, Marjun Biskopstø, Julia Zachariasen, Tórmódur Stórá, Guðrið Andorsdóttir, Ditte Demontis, Anders Børglum.
SU3DESCRIBING THE GENETIC ARCHITECTURE OF ADHD USING LINKED-READ SEQUENCING: A CASE-CONTROL STUDY FROM THE ISOLATED POPULATION OF THE FAROE ISLANDS. European Neuropsychopharmacology 01/2019; 29:S1269-S1270., DOI:10.1016/j.euroneuro.2018.08.367

F Lescai, T D Als, Q Li, M Nyegaard, G Andorsdottir, M Biskopstø, A Hedemand, A Fiorentino, N O’Brien, A Jarram, J Liang, J Grove, J Pallesen, E Eickhardt, M Mattheisen, L Bolund, D Demontis, AG Wang, A McQuillin, O Mors, J Wang, AD Børglum.
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. Translational Psychiatry 02/2017; 7(2):e1034., DOI:10.1038/tp.2017.3

2014-15

P. Patursson, Guðrið Andorsdóttir, G. A. Rogvi Joensen, Ingun Gaardbo, K. Rubek Nielsen, S. Nielsen, Shahin Gaini.
MON-PP288: Improving Patient Satisfaction and Self Reported Food Intake Using Protein Enriched Food and Additional Servings: A Cross-Sectional Follow-Up Study in Faroe Islands. Clinical Nutrition 09/2015; 34(1):S234., DOI:10.1016/S0261-5614(15)30720-2

P. Patursson, Guðrið Andorsdóttir, Ingun Gaardbo, G. A. Rogvi Joensen, S. Nielsen, K. Rubek Nielsen, Shahin Gaini.
PP270-MON: Self Reported Food Intake and Patient Satisfaction with Food: A Cross-Sectional Study in Faroe Islands. Clinical Nutrition 09/2014; 33:S229., DOI:10.1016/S0261-5614(14)50604-8

Eva Kočovská, Guðrið Andorsdóttir, Pál Weihe, Jónrit Halling, Elisabeth Fernell, Tormóður Stóra, Rannvá Biskupstø, I Carina Gillberg, Robyn Shea, Eva Billstedt, Thomas Bourgeron, Helen Minnis, Christopher Gillberg.
Vitamin D in the General Population of Young Adults with Autism in the Faroe Islands. Journal of Autism and Developmental Disorders 06/2014; 44(12)., DOI:10.1007/s10803-014-2155-1

Thomsen J.A., Lund A.M., Olesen J.H., Mohr M, Rasmussen J.
Is L-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?
JIMD Rep. 2015 Mar 3. [Epub ahead of print]

Rasmussen J, Nielsen OW, Janzen N, Duno M, Gislason H, Køber L, Steuerwald U, Lund AM.
Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands. J Inherit Metab Dis. 2014 Mar;37(2):215-22. doi: 10.1007/s10545-013-9606-2. Epub 2013 May 8.

Rasmussen J, Thomsen JA, Olesen JH, Lund TM, Mohr M, Clementsen J, Nielsen OW, Lund AM.
Carnitine Levels in Skeletal Muscle, Blood, and Urine in Patients with Primary Carnitine Deficiency During Intermission of l-Carnitine Supplementation. JIMD Rep. 2015;20:103-11. doi: 10.1007/8904_2014_398. Epub 2015 Feb 10.

Jan Rasmussen, Allan M. Lund, Lotte Risom, Flemming Wibrand, Hannes Gislason, Olav W. Nielsen, Lars Køber, Morten Duno.
Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency. Molecular Genetics and Metabolism Reports, Volume 1, 2014, Pages 241–248

Maria Skaalum Petersen, Ilaria Guella, Sara Bech, Emil Gustavsson, Matthew J. Farrer.
Parkinson’s disease, genetic variability and the Faroe Islands. Parkinsonism & Related Disorder, Volume 21, Issue 1, January 2015, Pages 75–78. doi:10.1016/j.parkreldis.2014.10.027

Joensen, P.
The Faroe Islands. Pract Neurol. 2015 Feb 3. pii: practneurol-2015-001085. doi: 10.1136/practneurol-2015-001085. [Epub ahead of print]

Joensen, P.
Myasthenia gravis incidence in a general North Atlantic isolated population.
Acta Neurol Scand. 2014 Oct;130(4):222-8. doi: 10.1111/ane.12270. Epub 2014 Jul 1.

Gregersen, N.,  Buttenschøn, H.N., Hedemand, A., Dahl, H.A.,  Kristensen, A.S., Clementsen B., Woldbye D.P., Koefoed P.,  Erhardt A., Kruse, T.A.,  Wang A.G., Børglum, A.D., Mors O.
Are TMEM genes potential candidate genes for panic disorder? Psychiatric Genetics: February 2014 – Volume 24 – Issue 1 – p 37–41. doi: 10.1097/YPG.0000000000000022

Binzer S, Imrell K, Binzer M, Kyvik KO, Hillert J, Stenager E.
High inbreeding in the Faroe Islands does not appear to constitute a risk factor for multiple sclerosis. Mult Scler. 2014 Nov 12. pii: 1352458514557305. [Epub ahead of print]

Als, Thomas Damm; Lescai, Francesco; Dahl, Hans Atli; Grove, Jakob; Demontis, Ditte; Wang, August G.; Andorsdottir, Gudrid; Biskopstø, Marjun; Johansen, Oddbjørg; Nyegaard, Mette; Bolund, Lars; Mors, Ole; Wang, Jun; Børglum, Anders.
Population Structure & Cryptic Relatedness of the isolated Population of the Faroe Islands. 2014. Poster session presented at XXII World Congress of Psychiatric Genetics, København, Danmark.

2011-13
Eva Kočovská, Eva Billstedt, Asa Ellefsen, Hanna Kampmann, I Carina Gillberg, Rannvá Biskupstø, Guðrið Andorsdóttir, Tormóður Stórá, Helen Minnis, Christopher Gillberg.
Autism in the Faroe Islands: Diagnostic Stability from Childhood to Early Adult Life. The Scientific World Journal 02/2013; 2013(2):592371., DOI:10.1155/2013/592371
 

Gronskov K, Dooley C. M, Ostergaard E., Kelsh R. N., Hansen L., Levesque M. P, Vilhelmsen, K Møllgård K, Stemple D.L, Rosenberg T.
Mutations in C10orf11, encoding a melanocyte differentiation gene, cause autosomal recessive Albinism. Am J Hum Genet. 2013 Mar 7;92(3):415-21. doi: 10.1016/j.ajhg.2013.01.006. Epub 2013 Feb 7.

Gal A, Rau I, El ML, et al.
Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease. Am J Hum Genet 2011;88:382-90.

Ostergaard E, Duno M, Batbayli M, et al.
A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases. Mol Vis 2011;17:1485-92.

Joensen, P.
Incidence of amyotrophic lateral sclerosis in the Faroe Islands. Acta Neurol Scand. 2012 Jul;126(1):62-6. doi: 10.1111/j.1600-0404.2011.01611.x. Epub 2011 Oct 29.

Joensen P.
Multiple sclerosis: variation of incidence of onset over time in the Faroe Islands.
Mult Scler. 2011 Aug 26. No abstract available. PMID:21873517

Joensen P.
Multiple sclerosis: variation of incidence of onset over time in the Faroe Islands. Mult Scler. 2011

2000-2010
Pedersen RS, Brasch-Andersen C, Sim SC, Bergmann TK, Halling J, Petersen MS, Weihe P, Edvardsen H, Kristensen VN, Brøsen K, Ingelman-Sundberg M. Linkage disequilibrium between the CYP2C19*17 allele and wildtype CYP2C8 and CYP2C9 alleles: identification of CYP2C haplotypes in healthy Nordic populations. Eur J Clin Pharmacol. 2010 Dec;66(12):1199-205.

Ostergaard E, Batbayli M, Duno M, et al.
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy. J Med Genet 2010;47:665-9.

Joensen P.
Multiple sclerosis incidence in the Faroe Islands 1986-2007. Acta Neurol Scand. 2010 May;121(5):348-53. Epub 2009 Dec 15. PMID: 20015109

Hjortshoj TD, Gronskov K, Brondum-Nielsen K, Rosenberg T.
A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe Islands. Br J Ophthalmol 2009;93:409-13.

Morava E, Steuerwald U, Carrozzo R, Kluijtmans LA, Joensen F, Santer R, Dionisi-Vici C, Wevers RA.
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children. Mitochondrion. 2009 Nov;9(6):438-42. Epub 2009 Aug 8.[http://www.ncbi.nlm.nih.gov/pubmed/19666145]

Wermuth L, Bech S, Petersen MS, Joensen P, Weihe P, Grandjean P.
Prevalence and incidence of Parkinson’s disease in The Faroe Islands. Acta Neurol Scand. 2008 Aug;118(2):126-31. Epub 2008 Feb 19. PMID: 18294341

Halling J, Weihe P, Brosen K.
CYP2D6 polymorphism in relation to tramadol metabolism: a study of faroese patients. Ther Drug Monit. 2008 Jun;30(3):271-5.

Halling J, Petersen MS, Grandjean P, Weihe P, Brosen K.
Genetic predisposition to Parkinson’s disease: CYP2D6 and HFE in the Faroe Islands. Pharmacogenet Genomics. 2008 Mar;18(3):209-12.

Halling J, Weihe P, Brosen K.
The CYP2D6 polymorphism in relation to the metabolism of amitriptyline and nortriptyline in the Faroese population. Br J Clin Pharmacol. 2008 Jan;65(1):134-8. Epub 2007 Aug 31.

Lund AM, Joensen F, Hougaard DM, Jensen LK, Christensen E, Christensen M et al.
Carnitine transporter and holocarboxylase synthetase deficiencies in The Faroe Islands. J Inherit Metab Dis. 2007.

Greinar eldri enn 2000

Ewald H, Wang AG, Vang M, Mors O, Nyegaard M, Kruse TA.
A haplotype-based study of lithium responding patients with bipolar affective disorder on the Faroe Islands. Psychiatr Genet. 1999;9:23-34.

Jantz RL.
Variation among European populations in summary finger ridge-count variables. Ann Hum Biol. 1997;24:97-106.

Joensen P.
ANNALES SOCIETATIS SCIENTIARUM FÆROENSIS SUPPLEMENTUM
No. XWII. 1992, Parts of Faroese Neuroepidemiology. FØROYA Fróðskaparfelag, Torshavn

Fledelius HC, Rosenberg T.
Extreme hypermetropia and posterior microphthalmos in three siblings. An oculometric study. In: Ossoinig KC, ed. Ophthalmic Echography. Dordrecht: Martinus Nijhoff/Junk; 1987: 87-91.

Joensen P.
Prevalence, incidence, and classification of epilepsy in the Faroes. Acta Neurol Scand. 1986 Aug;74(2):150-5. PMID: 3776461

Joensen P.
Subarachnoid hemorrhage in an isolated population. Incidence on the Faroes during the period 1962-1975. Stroke. 1984 May-Jun;15(3):438-40. PMID: 6729871 Free Article

Harvey RG, Suter D.
Digital dermatoglyphics of the Faroe Islanders. Am J Phys Anthropol. 1983;61:337-45.

Joensen P.
Stroke in an isolated population. Incidence on the Faroes during 1962-1975. Acta Med Scand. 1982;212(5):309-11. PMID: 7180581

Joensen P.
Incidence of primary intracranial neoplasms in an isolated population (the Faroes) during the period 1962-1975. Acta Neurol Scand. 1981 Jul;64(1):74-8. PMID: 7324874

Joensen HD, Hansen HE, Henningsen K, Svejgaard A, Andersen I.
A study of the linkage relations of epidermolysis bullosa dystrophica. Hum Hered. 1979;29:221-25.

Cohn J, Wang P, Hauge M, Henningsen K, Jensen B, Svejgaard A.
Amylo-1,60glucosidase deficiency (glycogenosis type III) in the Faroe Islands. Hum Hered. 1975;25:115-26.

Joensen HD.
Epidermolysis bullosa dystrophica dominans in two families in the Faroe Islands. A clinico-genetic study of 56 living individuals. Acta Derm Venereol. 1973;53:53-60.

Fog M.
The Shetland-Orkney-Faroe Project. Acta Neurol Scand. 1966;42:Suppl-8.

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