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Common genetic variants influence human subcortical brain structures.
Nature. 2015 Apr 9;520(7546):224-9. doi: 10.1038/nature14101. Epub 2015 Jan 21.
Nature. 2015.
PMID: 25607358
Free PMC article.
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.
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Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.
Carrion-Castillo A, Maassen B, Franke B, Heister A, Naber M, van der Leij A, Francks C, Fisher SE.
Carrion-Castillo A, et al.
Eur J Hum Genet. 2017 Apr;25(4):452-460. doi: 10.1038/ejhg.2016.194. Epub 2017 Jan 11.
Eur J Hum Genet. 2017.
PMID: 28074887
Free PMC article.
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Nitric oxide synthase genotype modulation of impulsivity and ventral striatal activity in adult ADHD patients and healthy comparison subjects.
Hoogman M, Aarts E, Zwiers M, Slaats-Willemse D, Naber M, Onnink M, Cools R, Kan C, Buitelaar J, Franke B.
Hoogman M, et al.
Am J Psychiatry. 2011 Oct;168(10):1099-106. doi: 10.1176/appi.ajp.2011.10101446. Epub 2011 Jul 1.
Am J Psychiatry. 2011.
PMID: 21724667
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Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.
Franke B, Hoogman M, Arias Vasquez A, Heister JG, Savelkoul PJ, Naber M, Scheffer H, Kiemeney LA, Kan CC, Kooij JJ, Buitelaar JK.
Franke B, et al.
Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1576-9. doi: 10.1002/ajmg.b.30861.
Am J Med Genet B Neuropsychiatr Genet. 2008.
PMID: 18802924
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The 22G>A polymorphism in the adenosine deaminase gene impairs catalytic function but does not affect reactive hyperaemia in humans in vivo.
Riksen NP, Franke B, van den Broek P, Naber M, Smits P, Rongen GA.
Riksen NP, et al.
Pharmacogenet Genomics. 2008 Oct;18(10):843-6. doi: 10.1097/FPC.0b013e328305e630.
Pharmacogenet Genomics. 2008.
PMID: 18794722
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