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Results: 1 to 20 of 98

1.

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios.

Besenbacher S, Liu S, Izarzugaza JM, Grove J, Belling K, Bork-Jensen J, Huang S, Als TD, Li S, Yadav R, Rubio-García A, Lescai F, Demontis D, Rao J, Ye W, Mailund T, Friborg RM, Pedersen CN, Xu R, Sun J, Liu H, Wang O, Cheng X, Flores D, Rydza E, Rapacki K, Damm Sørensen J, Chmura P, Westergaard D, Dworzynski P, Sørensen TI, Lund O, Hansen T, Xu X, Li N, Bolund L, Pedersen O, Eiberg H, Krogh A, Børglum AD, Brunak S, Kristiansen K, Schierup MH, Wang J, Gupta R, Villesen P, Rasmussen S.

Nat Commun. 2015 Jan 19;6:5969. doi: 10.1038/ncomms6969.

PMID:
25597990
[PubMed - in process]
2.

No association of polymorphisms in the serotonin transporter gene with thermal pain sensation in healthy individuals.

Schaldemose EL, Horjales-Araujo E, Demontis D, Børglum AD, Svensson P, Finnerup NB.

Mol Pain. 2014 Dec 4;10(1):76. doi: 10.1186/1744-8069-10-76.

PMID:
25472558
[PubMed - in process]
Free Article
3.

[Genomics of mental disorders.]

Mors O, Børglum AD.

Ugeskr Laeger. 2014 Nov 10;176(46). pii: V08140434. Danish.

PMID:
25394932
[PubMed - as supplied by publisher]
4.

Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers.

Marcheco-Teruel B, Parra EJ, Fuentes-Smith E, Salas A, Buttenschøn HN, Demontis D, Torres-Español M, Marín-Padrón LC, Gómez-Cabezas EJ, Alvarez-Iglesias V, Mosquera-Miguel A, Martínez-Fuentes A, Carracedo A, Børglum AD, Mors O.

PLoS Genet. 2014 Jul 24;10(7):e1004488. doi: 10.1371/journal.pgen.1004488. eCollection 2014 Jul.

PMID:
25058410
[PubMed - in process]
Free PMC Article
5.

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder.

Rajkumar AP, Christensen JH, Mattheisen M, Jacobsen I, Bache I, Pallesen J, Grove J, Qvist P, McQuillin A, Gurling HM, Tümer Z, Mors O, Børglum AD.

Bipolar Disord. 2014 Jul 23. doi: 10.1111/bdi.12239. [Epub ahead of print]

PMID:
25053281
[PubMed - as supplied by publisher]
6.

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.

Forstner AJ, Basmanav FB, Mattheisen M, Böhmer AC, Hollegaard MV, Janson E, Strengman E, Priebe L, Degenhardt F, Hoffmann P, Herms S, Maier W, Mössner R, Rujescu D, Ophoff RA, Moebus S, Mortensen PB, Børglum AD, Hougaard DM, Frank J, Witt SH, Rietschel M, Zimmer A, Nöthen MM, Miró X, Cichon S.

J Psychiatry Neurosci. 2014 Nov;39(6):386-96.

PMID:
24936775
[PubMed - in process]
Free PMC Article
7.

Depression and BMI influences the serum vascular endothelial growth factor level.

Elfving B, Buttenschøn HN, Foldager L, Poulsen PH, Grynderup MB, Hansen ÅM, Kolstad HA, Kaerlev L, Mikkelsen S, Børglum AD, Wegener G, Mors O.

Int J Neuropsychopharmacol. 2014 Sep;17(9):1409-17. doi: 10.1017/S1461145714000273. Epub 2014 Mar 17.

PMID:
24636631
[PubMed - in process]
8.

Are TMEM genes potential candidate genes for panic disorder?

Gregersen NO, Buttenschøn HN, Hedemand A, Dahl HA, Kristensen AS, Clementsen B, Woldbye DP, Koefoed P, Erhardt A, Kruse TA, Wang AG, Børglum AD, Mors O.

Psychiatr Genet. 2014 Feb;24(1):37-41. doi: 10.1097/YPG.0000000000000022.

PMID:
24362369
[PubMed - indexed for MEDLINE]
9.

Polymorphism in serotonin receptor 3B is associated with pain catastrophizing.

Horjales-Araujo E, Demontis D, Lund EK, Finnerup NB, Børglum AD, Jensen TS, Svensson P, Vase L.

PLoS One. 2013 Nov 11;8(11):e78889. doi: 10.1371/journal.pone.0078889. eCollection 2013.

PMID:
24244382
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genome wide assessment of mRNA in astrocyte protrusions by direct RNA sequencing reveals mRNA localization for the intermediate filament protein nestin.

Thomsen R, Pallesen J, Daugaard TF, Børglum AD, Nielsen AL.

Glia. 2013 Nov;61(11):1922-37. doi: 10.1002/glia.22569. Epub 2013 Sep 5.

PMID:
24009167
[PubMed - indexed for MEDLINE]
Free Article
11.

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.

Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT; Multicenter Genetic Studies of Schizophrenia Consortium, Levinson DF, Gejman PV, Kendler KS, Laurent C, Mowry BJ, O'Donovan MC, Owen MJ, Pulver AE, Riley BP, Schwab SG, Wildenauer DB, Dudbridge F, Holmans P, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, O'Neill FA, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B; Psychosis Endophenotypes International Consortium, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Lin K, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Powell J, Rujescu D, Van Os J, Walshe M, Weisbrod M, Wiersma D; Wellcome Trust Case Control Consortium 2, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Donnelly P, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, Barroso I, Deloukas P, Mathew CG, Blackwell JM, Brown MA, Corvin AP, McCarthy MI, Spencer CC, Bramon E, Corvin AP, O'Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF.

Nat Genet. 2013 Oct;45(10):1150-9. doi: 10.1038/ng.2742. Epub 2013 Aug 25.

PMID:
23974872
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

An association study between the norepinephrine transporter gene and depression.

Buttenschøn HN, Jacobsen IS, Grynderup MB, Hansen AM, Kolstad HA, Kaerlev L, Thomsen JF, Nordentoft M, Silahtaroglu A, Tommerup N, Tümer Z, Krogh J, Børglum AD, Mors O.

Psychiatr Genet. 2013 Oct;23(5):217-21. doi: 10.1097/YPG.0000000000000003.

PMID:
23969988
[PubMed - indexed for MEDLINE]
13.

Emotional modulation of muscle pain is associated with polymorphisms in the serotonin transporter gene.

Horjales-Araujo E, Demontis D, Lund EK, Vase L, Finnerup NB, Børglum AD, Jensen TS, Svensson P.

Pain. 2013 Aug;154(8):1469-76. doi: 10.1016/j.pain.2013.05.011. Epub 2013 May 14.

PMID:
23707290
[PubMed - indexed for MEDLINE]
14.

Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians.

Harsløf T, Frost M, Nielsen TL, Husted LB, Nyegaard M, Brixen K, Børglum AD, Mosekilde L, Andersen M, Rejnmark L, Langdahl BL.

Calcif Tissue Int. 2013 May;92(5):467-76. doi: 10.1007/s00223-013-9702-1. Epub 2013 Feb 1.

PMID:
23370486
[PubMed - indexed for MEDLINE]
15.

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.

Børglum AD, Demontis D, Grove J, Pallesen J, Hollegaard MV, Pedersen CB, Hedemand A, Mattheisen M; GROUP investigators10, Uitterlinden A, Nyegaard M, Ørntoft T, Wiuf C, Didriksen M, Nordentoft M, Nöthen MM, Rietschel M, Ophoff RA, Cichon S, Yolken RH, Hougaard DM, Mortensen PB, Mors O.

Mol Psychiatry. 2014 Mar;19(3):325-33. doi: 10.1038/mp.2013.2. Epub 2013 Jan 29.

PMID:
23358160
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

An association study of suicide and candidate genes in the serotonergic system.

Buttenschøn HN, Flint TJ, Foldager L, Qin P, Christoffersen S, Hansen NF, Kristensen IB, Mortensen PB, Børglum AD, Mors O.

J Affect Disord. 2013 Jun;148(2-3):291-8. doi: 10.1016/j.jad.2012.12.011. Epub 2013 Jan 11.

PMID:
23313272
[PubMed - indexed for MEDLINE]
17.

Common variant at 16p11.2 conferring risk of psychosis.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E; GROUP, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B; Wellcome Trust Case Control Consortium 2, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K.

Mol Psychiatry. 2014 Jan;19(1):108-14. doi: 10.1038/mp.2012.157. Epub 2012 Nov 20.

PMID:
23164818
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population.

Saetre P, Grove J, Børglum AD, Mors O, Werge T, Andreassen OA, Vares M, Agartz I, Terenius L, Jönsson EG.

Am J Med Genet B Neuropsychiatr Genet. 2012 Dec;159B(8):981-6. doi: 10.1002/ajmg.b.32104. Epub 2012 Oct 17.

PMID:
23076983
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.

Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL, Lund J, Hedley PL, Camm AJ, Wettrell G, Fosdal I, Christiansen M, Børglum AD.

Am J Hum Genet. 2012 Oct 5;91(4):703-12. doi: 10.1016/j.ajhg.2012.08.015.

PMID:
23040497
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Effect of specific ADRB1/ADRB2/AGT genotype combinations on the association between survival and carvedilol treatment in chronic heart failure: a substudy of the ECHOS trial.

Petersen M, Andersen JT, Jimenez-Solem E, Broedbaek K, Afzal S, Nyegaard M, Børglum AD, Stender S, Torp-Pedersen C, Køber L, Poulsen HE.

Pharmacogenet Genomics. 2012 Oct;22(10):709-15. doi: 10.1097/FPC.0b013e3283540286.

PMID:
22760495
[PubMed - indexed for MEDLINE]
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