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Year Number of Results
2013 1
2014 2
2015 4
2016 2
2017 1
2019 2
2020 1
2021 2
2022 3
2024 0

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14 results

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Page 1
Common genetic variants influence human subcortical brain structures.
Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, Bralten J, Brown AA, Chakravarty MM, Chen Q, Ching CR, Cuellar-Partida G, den Braber A, Giddaluru S, Goldman AL, Grimm O, Guadalupe T, Hass J, Woldehawariat G, Holmes AJ, Hoogman M, Janowitz D, Jia T, Kim S, Klein M, Kraemer B, Lee PH, Olde Loohuis LM, Luciano M, Macare C, Mather KA, Mattheisen M, Milaneschi Y, Nho K, Papmeyer M, Ramasamy A, Risacher SL, Roiz-Santiañez R, Rose EJ, Salami A, Sämann PG, Schmaal L, Schork AJ, Shin J, Strike LT, Teumer A, van Donkelaar MM, van Eijk KR, Walters RK, Westlye LT, Whelan CD, Winkler AM, Zwiers MP, Alhusaini S, Athanasiu L, Ehrlich S, Hakobjan MM, Hartberg CB, Haukvik UK, Heister AJ, Hoehn D, Kasperaviciute D, Liewald DC, Lopez LM, Makkinje RR, Matarin M, Naber MA, McKay DR, Needham M, Nugent AC, Pütz B, Royle NA, Shen L, Sprooten E, Trabzuni D, van der Marel SS, van Hulzen KJ, Walton E, Wolf C, Almasy L, Ames D, Arepalli S, Assareh AA, Bastin ME, Brodaty H, Bulayeva KB, Carless MA, Cichon S, Corvin A, Curran JE, Czisch M, de Zubicaray GI, Dillman A, Du… See abstract for full author list ➔ Hibar DP, et al. Among authors: hakobjan mm. Nature. 2015 Apr 9;520(7546):224-9. doi: 10.1038/nature14101. Epub 2015 Jan 21. Nature. 2015. PMID: 25607358 Free PMC article.
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis.
Horjus J, van Mourik-Banda T, Heerings MAP, Hakobjan M, De Witte W, Heersema DJ, Jansen AJ, Strijbis EMM, de Jong BA, Slettenaar AEJ, Zeinstra EMPE, Hoogervorst ELJ, Franke B, Kruijer W, Jongen PJ, Visser LJ, Poelmans G. Horjus J, et al. Among authors: hakobjan m. Int J Mol Sci. 2022 Sep 28;23(19):11461. doi: 10.3390/ijms231911461. Int J Mol Sci. 2022. PMID: 36232761 Free PMC article.
DNA methylation associated with persistent ADHD suggests TARBP1 as novel candidate.
Weiß AL, Meijer M, Budeus B, Pauper M, Hakobjan M, Groothuismink J, Shi Y, Neveling K, Buitelaar JK, Hoogman M, Franke B, Klein M. Weiß AL, et al. Among authors: hakobjan m. Neuropharmacology. 2021 Feb 15;184:108370. doi: 10.1016/j.neuropharm.2020.108370. Epub 2020 Oct 31. Neuropharmacology. 2021. PMID: 33137342 Free article.
Contribution of common and rare genetic variants in CEP72 on vincristine-induced peripheral neuropathy in brain tumour patients.
Klumpers MJ, Brand ACAM, Hakobjan M, Gattuso G, Schiavello E, Terenziani M, Massimino M, Gidding CEM, Guchelaar HJ, Te Loo DMWM, Coenen MJH. Klumpers MJ, et al. Among authors: hakobjan m. Br J Clin Pharmacol. 2022 Jul;88(7):3463-3473. doi: 10.1111/bcp.15267. Epub 2022 Mar 24. Br J Clin Pharmacol. 2022. PMID: 35150001 Free PMC article.
Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons.
van Rhijn JR, Shi Y, Bormann M, Mossink B, Frega M, Recaioglu H, Hakobjan M, Klein Gunnewiek T, Schoenmaker C, Palmer E, Faivre L, Kittel-Schneider S, Schubert D, Brunner H, Franke B, Nadif Kasri N. van Rhijn JR, et al. Among authors: hakobjan m. Neurobiol Dis. 2022 Feb;163:105587. doi: 10.1016/j.nbd.2021.105587. Epub 2021 Dec 16. Neurobiol Dis. 2022. PMID: 34923109 Free article.
MAOA-VNTR genotype affects structural and functional connectivity in distributed brain networks.
Harneit A, Braun U, Geiger LS, Zang Z, Hakobjan M, van Donkelaar MMJ, Schweiger JI, Schwarz K, Gan G, Erk S, Heinz A, Romanczuk-Seiferth N, Witt S, Rietschel M, Walter H, Franke B, Meyer-Lindenberg A, Tost H. Harneit A, et al. Among authors: hakobjan m. Hum Brain Mapp. 2019 Dec 15;40(18):5202-5212. doi: 10.1002/hbm.24766. Epub 2019 Aug 23. Hum Brain Mapp. 2019. PMID: 31441562 Free PMC article.
Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias.
van de Putte R, Wijers CH, de Blaauw I, Feitz WF, Marcelis CL, Hakobjan M, Sloots CE, van Bever Y, Brunner HG, Roeleveld N, van Rooij IA, van der Zanden LF. van de Putte R, et al. Among authors: hakobjan m. Eur J Pediatr. 2015 May;174(5):583-7. doi: 10.1007/s00431-014-2436-x. Epub 2014 Oct 17. Eur J Pediatr. 2015. PMID: 25319845
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept.
Franke B, Stein JL, Ripke S, Anttila V, Hibar DP, van Hulzen KJE, Arias-Vasquez A, Smoller JW, Nichols TE, Neale MC, McIntosh AM, Lee P, McMahon FJ, Meyer-Lindenberg A, Mattheisen M, Andreassen OA, Gruber O, Sachdev PS, Roiz-Santiañez R, Saykin AJ, Ehrlich S, Mather KA, Turner JA, Schwarz E, Thalamuthu A, Shugart YY, Ho YY, Martin NG, Wright MJ; Schizophrenia Working Group of the Psychiatric Genomics Consortium; ENIGMA Consortium; O'Donovan MC, Thompson PM, Neale BM, Medland SE, Sullivan PF. Franke B, et al. Nat Neurosci. 2016 Mar;19(3):420-431. doi: 10.1038/nn.4228. Epub 2016 Feb 1. Nat Neurosci. 2016. PMID: 26854805 Free PMC article.
BDNF polymorphism associates with decline in set shifting in Parkinson's disease.
van der Kolk NM, Speelman AD, van Nimwegen M, Kessels RP, IntHout J, Hakobjan M, Munneke M, Bloem BR, van de Warrenburg BP. van der Kolk NM, et al. Among authors: hakobjan m. Neurobiol Aging. 2015 Mar;36(3):1605.e1-6. doi: 10.1016/j.neurobiolaging.2014.08.023. Epub 2014 Aug 27. Neurobiol Aging. 2015. PMID: 25444596
14 results