Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: AUTISM, . Treffer: 49

2019

Bölte, S; Girdler, S; Marschik, PB The contribution of environmental exposure to the etiology of autism spectrum disorder.
Cell Mol Life Sci. 2019; 76(7):1275-1297 [OPEN ACCESS]
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Boterberg, S; Charman, T; Marschik, PB; Bölte, S; Roeyers, H Regression in Autism Spectrum Disorder: A Critical Overview of Retrospective Findings and Recommendations for Future Research: Invited Contribution to the Special Issue of Neuroscience and Biobehavioral Reviews on "Regression in Developmental Disorders".
Neurosci Biobehav Rev. 2019;
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Zweier, M; Begemann, A; McWalter, K; Cho, MT; Abela, L; Banka, S; Behring, B; Berger, A; Brown, CW; Carneiro, M; Chen, J; Cooper, GM; Deciphering Developmental Disorders (DDD) Study; Finnila, CR; Guillen Sacoto, MJ; Henderson, A; Hüffmeier, U; Joset, P; Kerr, B; Lesca, G; Leszinski, GS; McDermott, JH; Meltzer, MR; Monaghan, KG; Mostafavi, R; Õunap, K; Plecko, B; Powis, Z; Purcarin, G; Reimand, T; Riedhammer, KM; Schreiber, JM; Sirsi, D; Wierenga, KJ; Wojcik, MH; Papuc, SM; Steindl, K; Sticht, H; Rauch, A Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures.
Eur J Hum Genet. 2019;
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2018

Berggren, S; Fletcher-Watson, S; Milenkovic, N; Marschik, PB; Bölte, S; Jonsson, U Emotion recognition training in autism spectrum disorder: A systematic review of challenges related to generalizability.
Dev Neurorehabil. 2018; 21(3):141-154
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Marschik, PB; Lemcke, S; Einspieler, C; Zhang, D; Bölte, S; Townend, GS; Lauritsen, MB Early development in Rett syndrome - the benefits and difficulties of a birth cohort approach.
Dev Neurorehabil. 2018; 21(1):68-72 [OPEN ACCESS]
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Pilz, S; Zittermann, A; Obeid, R; Hahn, A; Pludowski, P; Trummer, C; Lerchbaum, E; Pérez-López, FR; Karras, SN; März, W The Role of Vitamin D in Fertility and during Pregnancy and Lactation: A Review of Clinical Data.
Int J Environ Res Public Health. 2018; 15(10): 2241 [OPEN ACCESS]
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Roche, L; Zhang, D; Bartl-Pokorny, KD; Pokorny, FB; Schuller, BW; Esposito, G; Bölte, S; Roeyers, H; Poustka, L; Gugatschka, M; Waddington, H; Vollmann, R; Einspieler, C; Marschik, PB Early Vocal Development in Autism Spectrum Disorder, Rett Syndrome, and Fragile X Syndrome: Insights from Studies using Retrospective Video Analysis.
Adv Neurodev Disord. 2018; 2(1): 49-61. [OPEN ACCESS]
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Sigafoos, J; Roche, L; Stevens, M; Waddington, H; Carnett, A; van der Meer, L; O'Reilly, MF; Lancioni, GE; Schlosser, RW; Marschik, PB Teaching two children with autism spectrum disorder to use a speech-generating device
RES PRACT INTELLECT. 2018; 5(1): 75-86.
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Zhang, D; Roche, L; Bartl-Pokorny, KD; Krieber, M; McLay, L; Bölte, S; Poustka, L; Sigafoos, J; Gugatschka, M; Einspieler, C; Marschik, PB Response to name and its value for the early detection of developmental disorders: Insights from autism spectrum disorder, Rett syndrome, and fragile X syndrome. A perspectives paper.
Res Dev Disabil. 2018; 82(6):95-108 [OPEN ACCESS]
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2017

Jonsson, U; Alaie, I; Löfgren Wilteus, A; Zander, E; Marschik, PB; Coghill, D; Bölte, S Annual Research Review: Quality of life and childhood mental and behavioural disorders - a critical review of the research.
J Child Psychol Psychiatry. 2017; 58(4):439-469
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Kapfhammer, HP [The concept of schizoidia in psychiatry : From schizoidia to schizotypy and cluster A personality disorders].
Neuropsychiatr. 2017; 31(4):155-171 [OPEN ACCESS]
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McLay, L; Schafer, MCM; van der Meer, L; Couper, L; McKenzie, E; O'Reilly, MF; Lancioni, GE; Marschik, PB; Sigafoos, J; Sutherland, D; Acquisition, Preference and Follow-up Comparison Across Three AAC Modalities Taught to Two Children with Autism Spectrum Disorder.
INT J DISABIL DEV EDUC. 2017; 64(2): 117-130.
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Muscogiuri, G; Altieri, B; Annweiler, C; Balercia, G; Pal, HB; Boucher, BJ; Cannell, JJ; Foresta, C; Grübler, MR; Kotsa, K; Mascitelli, L; März, W; Orio, F; Pilz, S; Tirabassi, G; Colao, A Vitamin D and chronic diseases: the current state of the art.
Arch Toxicol. 2017; 91(1):97-107
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Setoh, P; Marschik, PB; Einspieler, C; Esposito, G Autism spectrum disorder and early motor abnormalities: Connected or coincidental companions?
Res Dev Disabil. 2017; 60(1):13-15
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2016

Bölte, S; Bartl-Pokorny, KD; Jonsson, U; Berggren, S; Zhang, D; Kostrzewa, E; Falck-Ytter, T; Einspieler, C; Pokorny, FB; Jones, EJ; Roeyers, H; Charman, T; Marschik, PB How can clinicians detect and treat autism early? Methodological trends of technology use in research.
Acta Paediatr. 2016; 105(2):137-144 [OPEN ACCESS]
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D'Angelo, D; Lebon, S; Chen, Q; Martin-Brevet, S; Snyder, LG; Hippolyte, L; Hanson, E; Maillard, AM; Faucett, WA; Macé, A; Pain, A; Bernier, R; Chawner, SJ; David, A; Andrieux, J; Aylward, E; Baujat, G; Caldeira, I; Conus, P; Ferrari, C; Forzano, F; Gérard, M; Goin-Kochel, RP; Grant, E; Hunter, JV; Isidor, B; Jacquette, A; Jønch, AE; Keren, B; Lacombe, D; Le Caignec, C; Martin, CL; Männik, K; Metspalu, A; Mignot, C; Mukherjee, P; Owen, MJ; Passeggeri, M; Rooryck-Thambo, C; Rosenfeld, JA; Spence, SJ; Steinman, KJ; Tjernagel, J; Van Haelst, M; Shen, Y; Draganski, B; Sherr, EH; Ledbetter, DH; van den Bree, MB; Beckmann, JS; Spiro, JE; Reymond, A; Jacquemont, S; Chung, WK; Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study; 16p11.2 European Consortium; Simons Variation in Individuals Project (VIP) Consortium Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
JAMA Psychiatry. 2016; 73(1): 20-30. [OPEN ACCESS]
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Einspieler, C; Peharz, R; Marschik, PB Fidgety movements - tiny in appearance, but huge in impact.
J Pediatr (Rio J). 2016; 92(3 Suppl 1):S64-S70 [OPEN ACCESS]
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Salomone, E; Beranová, Š; Bonnet-Brilhault, F; Briciet Lauritsen, M; Budisteanu, M; Buitelaar, J; Canal-Bedia, R; Felhosi, G; Fletcher-Watson, S; Freitag, C; Fuentes, J; Gallagher, L; Garcia Primo, P; Gliga, F; Gomot, M; Green, J; Heimann, M; Jónsdóttir, SL; Kaale, A; Kawa, R; Kylliainen, A; Lemcke, S; Markovska-Simoska, S; Marschik, PB; McConachie, H; Moilanen, I; Muratori, F; Narzisi, A; Noterdaeme, M; Oliveira, G; Oosterling, I; Pijl, M; Pop-Jordanova, N; Poustka, L; Roeyers, H; Rogé, B; Sinzig, J; Vicente, A; Warreyn, P; Charman, T Use of early intervention for young children with autism spectrum disorder across Europe.
Autism. 2016; 20(2):233-249 [OPEN ACCESS]
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2015

Addis, L; Ahn, JW; Dobson, R; Dixit, A; Ogilvie, CM; Pinto, D; Vaags, AK; Coon, H; Chaste, P; Wilson, S; Parr, JR; Andrieux, J; Lenne, B; Tumer, Z; Leuzzi, V; Aubell, K; Koillinen, H; Curran, S; Marshall, CR; Scherer, SW; Strug, LJ; Collier, DA; Pal, DK Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Hum Mutat. 2015; 36(9):842-850
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McLay, L; van der Meer, L; Schafer, MCM; Couper, L; McKenzie, E; O'Reilly, MF; Lancioni, GE; Marschik, PB; Green, VA; Sigafoos, J; Sutherland, D Comparing Acquisition, Generalization, Maintenance, and Preference Across Three AAC Options in Four Children with Autism Spectrum Disorder
J DEV PHYS DISABIL. 2015; 27(3): 323-339.
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van der Meer, L; Achmadi, D; Cooijmans, M; Didden, R; Lancioni, GE; O'Reilly, MF; Roche, L; Stevens, M; Carnett, A; Hodis, F; Green, VA; Sutherland, D; Lang, R; Rispoli, M; Marschik, PB; Sigafoos, J An iPad-Based Intervention for Teaching Picture and Word Matching to a Student with ASD and Severe Communication Impairment
J DEV PHYS DISABIL. 2015; 27(1): 67-78.
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Zappella, M; Einspieler, C; Bartl-Pokorny, KD; Krieber, M; Coleman, M; Bölte, S; Marschik, PB What do home videos tell us about early motor and socio-communicative behaviours in children with autistic features during the second year of life--An exploratory study.
Early Hum Dev. 2015; 91(10):569-575 [OPEN ACCESS]
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2014

Asadollahi, R; Oneda, B; Joset, P; Azzarello-Burri, S; Bartholdi, D; Steindl, K; Vincent, M; Cobilanschi, J; Sticht, H; Baldinger, R; Reissmann, R; Sudholt, I; Thiel, CT; Ekici, AB; Reis, A; Bijlsma, EK; Andrieux, J; Dieux, A; FitzPatrick, D; Ritter, S; Baumer, A; Latal, B; Plecko, B; Jenni, OG; Rauch, A The clinical significance of small copy number variants in neurodevelopmental disorders.
J Med Genet. 2014; 51(10): 677-688. [OPEN ACCESS]
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Couper, L; van der Meer, L; Schäfer, MC; McKenzie, E; McLay, L; O'Reilly, MF; Lancioni, GE; Marschik, PB; Sigafoos, J; Sutherland, D Comparing acquisition of and preference for manual signs, picture exchange, and speech-generating devices in nine children with autism spectrum disorder.
Dev Neurorehabil. 2014; 17(2):99-109
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Egger, G; Roetzer, KM; Noor, A; Lionel, AC; Mahmood, H; Schwarzbraun, T; Boright, O; Mikhailov, A; Marshall, CR; Windpassinger, C; Petek, E; Scherer, SW; Kaschnitz, W; Vincent, JB Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.
Neurogenetics. 2014; 15(2):117-127
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Einspieler, C; Sigafoos, J; Bartl-Pokorny, KD; Landa, R; Marschik, PB; Bolte, S; Highlighting the first 5 months of life: General movements in infants later diagnosed with autism spectrum disorder or Rett syndrome.
RES AUTISM SPECTR DISORD. 2014; 8(3): 286-291.
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Roche, L; Sigafoos, J; Lancioni, GE; O'Reilly, MF; van der Meer, L; Achmadi, D; Green, VA; Kagohara, D; Sutherland, D; Rayner, C; Marschik, PB Comparing Tangible Symbols, Picture Exchange, and a Direct Selection Response for Enabling Two Boys with Developmental Disabilities to Access Preferred Stimuli
J DEV PHYS DISABIL. 2014; 26(3): 249-261.
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van der Meer, L; Sigafoos, J; Sutherland, D; McLay, L; Lang, R; Lancioni, GE; O'Reilly, MF; Marschik, PB Preference-Enhanced Communication Intervention and Development of Social Communicative Functions in a Child With Autism Spectrum Disorder
CLIN CASE STUD. 2014; 13(3): 282-295.
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Waddington, H; Sigafoos, J; Lancioni, GE; O'Reilly, MF; van der Meer, L; Carnett, A; Stevens, M; Roche, L; Hodis, F; Green, VA; Sutherland, D; Lang, R; Marschik, PB Three children with autism spectrum disorder learn to perform a three-step communication sequence using an iPad®-based speech-generating device.
Int J Dev Neurosci. 2014; 39(9):59-67 (- Case Report)
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2013

Bartl-Pokorny, KD; Pokorny, F; Bolte, S; Langmann, A; Falck-Ytter, T; Wolin, T; Einspieler, C; Sigafoos, J; Marschik, PB Eye Tracking in Basic Research and Clinical Practice
KLIN NEUROPHYSIOL. 2013; 44(3): 193-198.
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Bölte, S; Marschik, PB; Falck-Ytter, T; Charman, T; Roeyers, H; Elsabbagh, M Infants at risk for autism: a European perspective on current status, challenges and opportunities.
Eur Child Adolesc Psychiatry. 2013; 22(6):341-348 [OPEN ACCESS]
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Hinton, R; Budimirovic, DB; Marschik, PB; Talisa, VB; Einspieler, C; Gipson, T; Johnston, MV Parental reports on early language and motor milestones in fragile X syndrome with and without autism spectrum disorders.
Dev Neurorehabil. 2013; 16(1):58-66
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Kagohara, DM; Achmadi, D; van der Meer, L; Lancioni, GE; O'Reilly, MF; Lang, R; Marschik, PB; Sutherland, D; Ramdoss, S; Green, VA; Sigafoos, J Teaching Two Students with Asperger Syndrome to Greet Adults Using Social Stories((TM)) and Video Modeling
J DEV PHYS DISABIL. 2013; 25(2): 241-251.
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Kagohara, DM; van der Meer, L; Ramdoss, S; O'Reilly, MF; Lancioni, GE; Davis, TN; Rispoli, M; Lang, R; Marschik, PB; Sutherland, D; Green, VA; Sigafoos, J Using iPods(®) and iPads(®) in teaching programs for individuals with developmental disabilities: a systematic review.
Res Dev Disabil. 2013; 34(1):147-156
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Lionel, AC; Vaags, AK; Sato, D; Gazzellone, MJ; Mitchell, EB; Chen, HY; Costain, G; Walker, S; Egger, G; Thiruvahindrapuram, B; Merico, D; Prasad, A; Anagnostou, E; Fombonne, E; Zwaigenbaum, L; Roberts, W; Szatmari, P; Fernandez, BA; Georgieva, L; Brzustowicz, LM; Roetzer, K; Kaschnitz, W; Vincent, JB; Windpassinger, C; Marshall, CR; Trifiletti, RR; Kirmani, S; Kirov, G; Petek, E; Hodge, JC; Bassett, AS; Scherer, SW Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
Hum Mol Genet. 2013; 22(10):2055-2066 [OPEN ACCESS]
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Sigafoos, J; Lancioni, GE; O'Reilly, MF; Achmadi, D; Stevens, M; Roche, L; Kagohara, DM; van der Meer, L; Sutherland, D; Lang, R; Marschik, PB; McLay, L; Hodis, F; Green, VA; Teaching two boys with autism spectrum disorders to request the continuation of toy play using an iPad (R)-based speech-generating device.
RES AUTISM SPECTR DISORD. 2013; 7(8): 923-930.
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van der Meer, L; Kagohara, D; Roche, L; Sutherland, D; Balandin, S; Green, VA; O'Reilly, MF; Lancioni, GE; Marschik, PB; Sigafoos, J Teaching multi-step requesting and social communication to two children with autism spectrum disorders with three AAC options.
Augment Altern Commun. 2013; 29(3):222-234
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2012

Achmadi, D; Kagohara, DM; van der Meer, L; O'Reilly, MF; Lancioni, GE; Sutherland, D; Lang, R; Marschik, PB; Green, VA; Sigafoos, J Teaching advanced operation of an iPod-based speech-generating device to two students with autism spectrum disorders.
Research in Autism Spectrum Disorders. 2012; 6(4): 1258-1264.
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Kagohara, DM; van der Meer, L; Achmadi, D; Green, VA; O'Reilly, MF; Lancioni, GE; Sutherland, D; Lang, R; Marschik, PB; Sigafoos, J Teaching picture naming to two adolescents with autism spectrum disorders using systematic instruction and speech-generating devices
RES AUTISM SPECT DIS. 2012; 6(3): 1224-1233.
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Meyer, WK; Arbeithuber, B; Ober, C; Ebner, T; Tiemann-Boege, I; Hudson, RR; Przeworski, M Evaluating the evidence for transmission distortion in human pedigrees.
Genetics. 2012; 191(1): 215-232. [OPEN ACCESS]
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2010

Freitag, CM; Agelopoulos, K; Huy, E; Rothermundt, M; Krakowitzky, P; Meyer, J; Deckert, J; von Gontard, A; Hohoff, C Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder.
Eur Child Adolesc Psychiatry. 2010; 19(1):67-74
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2009

Marschik, PB; Einspieler, C; Oberle, A; Laccone, F; Prechtl, HF Case report: Retracing atypical development: a preserved speech variant of Rett syndrome.
J Autism Dev Disord. 2009; 39(6): 958-961. [OPEN ACCESS]
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Vincent, JB; Noor, A; Windpassinger, C; Gianakopoulos, PJ; Schwarzbraun, T; Alfred, SE; Stachowiak, B; Scherer, SW; Roberts, W; Wagner, K; Kroisel, PM; Petek, E Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.
Am J Med Genet B Neuropsychiatr Genet. 2009; 150B(6):817-826
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2008

Phagava, H; Muratori, F; Einspieler, C; Maestro, S; Apicella, F; Guzzetta, A; Prechtl, HF; Cioni, G General movements in infants with autism spectrum disorders.
Georgian Med News. 2008; 94(156):100-105
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2007

Petek, E; Schwarzbraun, T; Noor, A; Patel, M; Nakabayashi, K; Choufani, S; Windpassinger, C; Stamenkovic, M; Robertson, MM; Aschauer, HN; Gurling, HM; Kroisel, PM; Wagner, K; Scherer, SW; Vincent, JB Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.
Mol Genet Genomics. 2007; 277(1):71-81
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2003

Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; Parker-Katiraee, L; Skaug, J; Khaja, R; Zhang, J; Hudek, AK; Li, M; Haddad, M; Duggan, GE; Fernandez, BA; Kanematsu, E; Gentles, S; Christopoulos, CC; Choufani, S; Kwasnicka, D; Zheng, XH; Lai, Z; Nusskern, D; Zhang, Q; Gu, Z; Lu, F; Zeesman, S; Nowaczyk, MJ; Teshima, I; Chitayat, D; Shuman, C; Weksberg, R; Zackai, EH; Grebe, TA; Cox, SR; Kirkpatrick, SJ; Rahman, N; Friedman, JM; Heng, HH; Pelicci, PG; Lo-Coco, F; Belloni, E; Shaffer, LG; Pober, B; Morton, CC; Gusella, JF; Bruns, GA; Korf, BR; Quade, BJ; Ligon, AH; Ferguson, H; Higgins, AW; Leach, NT; Herrick, SR; Lemyre, E; Farra, CG; Kim, HG; Summers, AM; Gripp, KW; Roberts, W; Szatmari, P; Winsor, EJ; Grzeschik, KH; Teebi, A; Minassian, BA; Kere, J; Armengol, L; Pujana, MA; Estivill, X; Wilson, MD; Koop, BF; Tosi, S; Moore, GE; Boright, AP; Zlotorynski, E; Kerem, B; Kroisel, PM; Petek, E; Oscier, DG; Mould, SJ; Döhner, H; Döhner, K; Rommens, JM; Vincent, JB; Venter, JC; Li, PW; Mural, RJ; Adams, MD; Tsui, LC Human chromosome 7: DNA sequence and biology.
Science. 2003; 300(5620):767-772 [OPEN ACCESS]
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2002

Vincent, JB; Petek, E; Thevarkunnel, S; Kolozsvari, D; Cheung, J; Patel, M; Scherer, SW The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.
Genomics. 2002; 80(3):283-294
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2001

Cheung, J; Petek, E; Nakabayashi, K; Tsui, LC; Vincent, JB; Scherer, SW Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Genomics. 2001; 78(1-2):7-11
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Petek, E; Windpassinger, C; Vincent, JB; Cheung, J; Boright, AP; Scherer, SW; Kroisel, PM; Wagner, K Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
Am J Hum Genet. 2001; 68(4):848-858 (- Case Report) [OPEN ACCESS]
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