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List of important publications in 2015

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  1. Large-scale genomics unveil polygenic architecture of human cortical surface area, Nature Communications

Chi-Hua Chen,Qian Peng,Andrew J. Schork,Min-Tzu Lo,Chun-Chieh Fan,Yunpeng Wang, Rahul S. Desikan,Francesco Bettella,Donald J. Hagler,Pediatric Imaging, Neurocognition and Genetics Study,Alzheimer’s Disease Neuroimaging Initiative,Lars T. Westlye,William S. Kremen,Terry L. Jernigan,Stephanie Le Hellard,Vidar M. Steen,Thomas Espeseth,Matt Huentelman,Asta K. Håberg,Ingrid Agartz,Srdjan Djurovic,Ole A. Andreassen,Nicholas Schork& Anders M. Dale

  1. Common genetic variants influence human subcortical brain structures, Nature 

Derrek P. Hibar,Jason L. Stein,Miguel E. Renteria,Alejandro Arias-Vasquez,Sylvane Desrivières,Neda Jahanshad,Roberto Toro,Katharina Wittfeld,Lucija Abramovic,Micael Andersson,Benjamin S. Aribisala,Nicola J. Armstrong,Manon Bernard,Marc M. Bohlken, Marco P. Boks,Janita Bralten,Andrew A. Brown,M. Mallar Chakravarty,Qiang Chen, Christopher R. K. Ching,Gabriel Cuellar-Partida,Anouk den Braber,Sudheer Giddaluru, Le Hellard S , Steen VM Aaron L. Goldman,Oliver Grimm et al.

 

  1. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Mol Psychiatry.

Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, Postmus I, Smith AV, Smith JA, Thalamuthu A, Thomson R, Vitart V, Wang J, Yu L, Zgaga L, Zhao W, Boxall R, Harris SE, Hill WD, Liewald DC, Luciano M, Adams H, Ames D, Amin N, Amouyel P, Assareh AA, Au R, Becker JT, Beiser A, Berr C, Bertram L, Boerwinkle E, Buckley BM, Campbell H, Corley J, De Jager PL, Dufouil C, Eriksson JG, Espeseth T, Faul JD, Ford I; Generation Scotland, Gottesman RF, Griswold ME, Gudnason V, Harris TB, Heiss G, Hofman A, Holliday EG, Huffman J, Kardia SL, Kochan N, Knopman DS, Kwok JB, Lambert JC, Lee T, Li G, Li SC, Loitfelder M, Lopez OL, Lundervold AJ, Lundqvist A, Mather KA, Mirza SS, Nyberg L, Oostra BA, Palotie A, Papenberg G, Pattie A, Petrovic K, Polasek O, Psaty BM, Redmond P, Reppermund S, Rotter JI, Schmidt H, Schuur M, Schofield PW, Scott RJ, Steen VM, Stott DJ, van Swieten JC, Taylor KD, Trollor J, Trompet S, Uitterlinden AG, Weinstein G, Widen E, Windham BG, Jukema JW, Wright AF, Wright MJ, Yang Q, Amieva H, Attia JR, Bennett DA, Brodaty H, de Craen AJ, Hayward C, Ikram MA, Lindenberger U, Nilsson LG, Porteous DJ, Räikkönen K, Reinvang I, Rudan I, Sachdev PS, Schmidt R, Schofield PR, Srikanth V, Starr JM, Turner ST, Weir DR, Wilson JF, van Duijn C, Launer L, Fitzpatrick AL, Seshadri S, Mosley TH Jr, Deary IJ

 

  1. Antipsychotic-induced metabolic effects in the female rat:Direct comparison between long-acting injections of risperidone and olanzapine. J Psychopharmacol

Ersland KM, Skrede S, Røst TH, Berge RK, Steen VM.

 

  1. Olanzapine depot exposure in male rats:Dose-dependent lipogenic effects without concomitant weight gain. Eur Neuropsychopharmacol

Fernø J, Ersland KM, Duus IH, González-García I, Fossan KO, Berge RK, Steen VM, Skrede S.

 

  1. MicroRNAs enrichment in GWAS of complex human phenotypes. BMC Genomics

Goulart LF, Bettella F, Sønderby IE, Schork AJ, Thompson WK, Mattingsdal M, Steen VM, Zuber V, Wang Y, Dale AM, Andreassen OA, Djurovic S

 

  1. Genetic basis of a cognitive complexity metric. PLoS One.

Hansell NK, Halford GS, Andrews G, Shum DH, Harris SE, Davies G, Franic S, Christoforou A, Zietsch B, Painter J, Medland SE, Ehli EA, Davies GE, Steen VM, Lundervold AJ, Reinvang I, Montgomery GW, Espeseth T, Hulshoff Pol HE, Starr JM, Martin NG, Le Hellard S, Boomsma DI, Deary IJ, Wright MJ

 

  1. B56δ-related protein phosphatase 2A dysfunction identified in patients with intellectual disability. J Clin Invest.

Houge G, Haesen D, Vissers LE, Mehta S, Parker MJ, Wright M, Vogt J, McKee S, Tolmie JL, Cordeiro N, Kleefstra T, Willemsen MH, Reijnders MR, Berland S, Hayman E, Lahat E, Brilstra EH, van Gassen KL, Zonneveld-Huijssoon E, de Bie CI, Hoischen A, Eichler EE, Holdhus R, Steen VM, Døskeland SO, Hurles ME, FitzPatrick DR, Janssens V

 

  1. Genome-wide autozygosity is associated with lower general cognitive ability. Mol Psychiatry

Howrigan DP, Simonson MA, Davies G, Harris SE, Tenesa A, Starr JM, Liewald DC, Deary IJ, McRae A, Wright MJ, Montgomery GW, Hansell N, Martin NG, Payton A, Horan M, Ollier WE, Abdellaoui A, Boomsma DI, DeRosse P, Knowles EE, Glahn DC, Djurovic S, Melle I, Andreassen OA, Christoforou A, Steen VM, Hellard SL, Sundet K, Reinvang I, Espeseth T, Lundervold AJ, Giegling I, Konte B, Hartmann AM, Rujescu D, Roussos P, Giakoumaki S, Burdick KE, Bitsios P, Donohoe G, Corley RP, Visscher PM, Pendleton N, Malhotra AK, Neale BM, Lencz T, Keller MC

 

  1. Common variants in the ARC gene are not associated with cognitive abilities. Brain Behav.

Myrum C, Giddaluru S, Jacobsen K, Espeseth T, Nyberg L, Lundervold AJ, Haavik J, Nilsson LG, Reinvang I, Steen VM, Johansson S, Wibrand K, Le Hellard S, Bramham CR

 

  1. Transcriptional, post-transcriptional and chromatin-associated regulation of pri-miRNAs, pre-miRNAs and moRNAs. Nucleic Acids Res.

Nepal C, Coolen M, Hadzhiev Y, Cussigh D, Mydel P, Steen VM, Carninci P, Andersen JB, Bally-Cuif L, Müller F, Lenhard B

 

  1. Incident users of antipsychotic agents and future use of cholesterol-lowering drugs. An observational, pharmacoepidemiological study. J Clin Psychiatry

Skrede S, Tvete IF, Tanum L, Steen VM, Bramness JG

 

  1. Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment. Am J Med Genet B Neuropsychiatr Genet.

Trampush JW, Lencz T, Knowles E, Davies G, Guha S, Pe'er I, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, DeRosse P, Lundervold A, Steen VM, John M, Espeseth T, Räikkönen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Ikeda M, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Horan M, Scult M, Dickinson D, Straub RE, Donohoe G, Morris D, Corvin A, Gill M, Hariri A, Weinberger DR, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK.

 

  1. Syndromic X-linked intellectual disability segregating with a missense variant in RLIM. Eur J Hum Genet

Tønne E, Holdhus R, Stansberg C, Stray-Pedersen A, Petersen K, Brunner HG, Gilissen C, Hoischen A, Prescott T, Steen VM, Fiskerstrand T.