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Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Transl Psychiatry. 2020 Jul 5;10(1):215. doi: 10.1038/s41398-020-00906-2.
Transl Psychiatry. 2020.
PMID: 32624584
Free PMC article.
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Waltes R, Duketis E, Knapp M, Anney RJ, Huguet G, Schlitt S, Jarczok TA, Sachse M, Kämpfer LM, Kleinböck T, Poustka F, Bölte S, Schmötzer G, Voran A, Huy E, Meyer J, Bourgeron T, Klauck SM, Freitag CM, Chiocchetti AG.
Waltes R, et al. Among authors: voran a.
Hum Genet. 2014 Jun;133(6):781-92. doi: 10.1007/s00439-013-1416-y. Epub 2014 Jan 19.
Hum Genet. 2014.
PMID: 24442360
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Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range.
Waltes R, Gfesser J, Haslinger D, Schneider-Momm K, Biscaldi M, Voran A, Freitag CM, Chiocchetti AG.
Waltes R, et al. Among authors: voran a.
J Neural Transm (Vienna). 2014 Sep;121(9):1107-16. doi: 10.1007/s00702-014-1230-2. Epub 2014 May 13.
J Neural Transm (Vienna). 2014.
PMID: 24818597
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Gaming Disorder and Computer-Mediated Communication in Children and Adolescents with Autism Spectrum Disorder.
Paulus FW, Sander CS, Nitze M, Kramatschek-Pfahler AR, Voran A, von Gontard A.
Paulus FW, et al. Among authors: voran a.
Z Kinder Jugendpsychiatr Psychother. 2020;48(2):113-122. doi: 10.1024/1422-4917/a000674. Epub 2019 May 27.
Z Kinder Jugendpsychiatr Psychother. 2020.
PMID: 31132021
Free article.
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Fabrication and Testing of a Bi-2223 Test Coil for High Field NMR Magnets.
Marshall WS, Bird MD, Larbalestier DC, McRae DM, Noyes PD, Voran AJ, Walsh RP.
Marshall WS, et al. Among authors: voran aj.
IEEE Trans Appl Supercond. 2018 Apr;28(3):4301204. doi: 10.1109/TASC.2018.2801296. Epub 2018 Feb 2.
IEEE Trans Appl Supercond. 2018.
PMID: 30122885
Free PMC article.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimäki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK; DDD Study; Homozygosity Mapping Collaborative for Autism; UK10K Consortium; Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD.
De Rubeis S, et al. Among authors: voran a.
Nature. 2014 Nov 13;515(7526):209-15. doi: 10.1038/nature13772. Epub 2014 Oct 29.
Nature. 2014.
PMID: 25363760
Free PMC article.
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Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.
Chiocchetti AG, Kopp M, Waltes R, Haslinger D, Duketis E, Jarczok TA, Poustka F, Voran A, Graab U, Meyer J, Klauck SM, Fulda S, Freitag CM.
Chiocchetti AG, et al. Among authors: voran a.
Mol Psychiatry. 2015 Jul;20(7):839-49. doi: 10.1038/mp.2014.103. Epub 2014 Sep 16.
Mol Psychiatry. 2015.
PMID: 25224256
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[The oral vitamin E tolerance test--an attempt at standardization].
Jost WH, Voran A, Trabert W, König J, Schimrigk K.
Jost WH, et al. Among authors: voran a.
Wien Klin Wochenschr. 1999 Jul 9;111(13):517-22.
Wien Klin Wochenschr. 1999.
PMID: 10444805
German.
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