Hans atli dahl - publications

SCN8A: a novel gene for benign infantile seizures and paroxysmal dyskinesia. Møller RS, Heron  S, Larsen LHG, Lim CX, Ricos CM, Bayly MS, Kempen MJAv, Klinkenberg S, Andrews I, Kelley K, Ronen GM, Callen D, McMahon JM, Yendle SC, Carvill GL, Mefford HC, Nabbout R, Poduri A, Striano P, Baglietto MG, Zara F,  Smith NJ, Pridmore C, Gardella E, Nikanorova M, Dahl HA, Gellert P, Scheffer IE, Gunning B, Kragh-Olsen B, Dibbens LM. Mutations in KCNT1 cause different epileptic phenotypes including cardiac abnormalities. Under review in Epilepsia Gardella E, Becker F, Møller RS, Schubert J, Lemke J, Larsen LHG, Eiberg H, Tiele H, Altmüller J, Syrbe S, Merkenschlager A, Bast T, Steinhoff B, Nürnberg P, Mang Y, Møller LB, Gellert P, Heron S, Dibbens L, Weckhuysen S, Dahl HA, Tommerup N, Hjalgrim H, Lerche H, Beniczky S, Weber Y. Submitted for Annals of Neurology 

Clinical phenotype of GNAO1: Case report and Review of literature. Talvik I,  Møller RS, Vaher M, Vaher U, Larsen LHG, Dahl HA, Ilves P, Talvik T. Child Neurology Open, Accepted for publishing February 2015 

Are TMEM genes potential candidate genes for panic disorder? Gregersen NO, Buttenschøn HN, Hedemand A, Dahl HA, Kristensen AS, Clementsen B, Woldbye DPD, Koefoed P, Erhardt A, Kruse TA, Wang AG, Børglum AD, Mors OD., Psychiatr Genet. 2014 Feb;24(1):37-41. 

The role of SLC2A1 in Early Onset and Childhood Absence Epilepsies. Muhle H, Helbig I, Frøslev TG, Suls A, von Spiczak S, Klitten LL, Dahl HA, Brusgaard K, Neubauer B, De Jonghe P, Tommerup N, Stephani U, Hjalgrim H, Møller RS; Epilepsy Res. 2013 Jul;105(1-2):229-33 

A genomewide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene. Gregersen, N, Dahl, HA, Buttenschøn, HN, Nyegaard, M, Hedemand, A, Als, TD , Wang, AG , Joensen, S , Woldbye, DP , Koefoed, P , Kristensen, AS, Kruse, TA, Børglum, A & Mors, O., European Journal of Human Genetics, 2012, vol 20, s. 84-90. 

Genetics of Panic Disorder on the Faroe Islands: A replication study of chromosome 9 and Panic Disorder. Wang, A.G.; Dahl,H.A.; Vang,M.; Ewald,H.; Kruse,T.A.; Mors,O. Psychiatr Genet. 2006 Jun;16(3):99-104.

A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands. M B Lauritsen, T D Als, H A Dahl, T J Flint, A G Wang, M Vang, T A Kruse, H Ewald and O Mors. Molecular Psychiatry (2006) 11, 37–46. 

Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands. Als,T.D.; Dahl,H.A.; Flint,T.J.; Wang,A.G.; Vang, M.; Mors, O.; Kruse,T.A.; Ewald,H. Mol Psychiatry. 2004; 9(1): 93-98. 

Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands. Jorgensen,T.H.; Borglum,A.D.; Mors,O.; Wang,A.G.; Pinaud,M.; Flint,T.J.; Dahl,H.A.; Vang,M.; Kruse,T.A.; Ewald,H.. Am.J.Med.Genet. 114.2 (2002): 245-52.

Search for susceptibility loci on selected chromosomes in patients with mental disorders from the Faroe Islands.
Dahl,H.A. ; Wang,A.G. ; Vang,M. ; Østerø,A.E. ; Degn,B. ; Mors,O.; Ewald,H. ; Joensen,S.; Nyegaard,M. ; Kruse,T.A. Ann. Soc. Sci. Far. 48 (2001): 55-60.