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

Logo MUG-Forschungsportal

Publikationen

Suchbegriffe: DEVELOPMENTAL DISORDERS, . Treffer: 24

2020

Pokorny, FB; Bartl-Pokorny, KD; Zhang, DJ; Marschik, PB; Schuller, D; Schuller, BW Efficient Collection and Representation of Preverbal Data in Typical and Atypical Development
J NONVERBAL BEHAV. 2020; [OPEN ACCESS]
Web of Science FullText FullText_MUG

 

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]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Lang, S; Bartl-Pokorny, KD; Pokorny, FB; Garrido, D; Mani, N; Fox-Boyer, AV; Zhang, D; Marschik, PB Canonical Babbling: A Marker for Earlier Identification of Late Detected Developmental Disorders?
Curr Dev Disord Rep. 2019; 6(3): 111-118. [OPEN ACCESS]
PubMed PUBMED Central FullText FullText_MUG

 

Papuc, SM; Abela, L; Steindl, K; Begemann, A; Simmons, TL; Schmitt, B; Zweier, M; Oneda, B; Socher, E; Crowther, LM; Wohlrab, G; Gogoll, L; Poms, M; Seiler, M; Papik, M; Baldinger, R; Baumer, A; Asadollahi, R; Kroell-Seger, J; Schmid, R; Iff, T; Schmitt-Mechelke, T; Otten, K; Hackenberg, A; Addor, MC; Klein, A; Azzarello-Burri, S; Sticht, H; Joset, P; Plecko, B; Rauch, A The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.
Eur J Hum Genet. 2019; 27(3):408-421 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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
Web of Science PubMed FullText FullText_MUG

 

Bolte, S; Tomalski, P; Marschik, PB; Berggren, S; Norberg, J; Falck-Ytter, T; Pokorska, O; Jones, EJH; Charman, T; Roeyers, H; Kostrzewa, E Challenges and Inequalities of Opportunities in European Psychiatry Research The Example of Psychodiagnostic Tool Availability in Research on Early Autism Identification
EUR J PSYCHOL ASSESS. 2018; 34(4): 270-277.
Web of Science FullText FullText_MUG

 

Davies, G; Lam, M; Harris, SE; Trampush, JW; Luciano, M; Hill, WD; Hagenaars, SP; Ritchie, SJ; Marioni, RE; Fawns-Ritchie, C; Liewald, DCM; Okely, JA; Ahola-Olli, AV; Barnes, CLK; Bertram, L; Bis, JC; Burdick, KE; Christoforou, A; DeRosse, P; Djurovic, S; Espeseth, T; Giakoumaki, S; Giddaluru, S; Gustavson, DE; Hayward, C; Hofer, E; Ikram, MA; Karlsson, R; Knowles, E; Lahti, J; Leber, M; Li, S; Mather, KA; Melle, I; Morris, D; Oldmeadow, C; Palviainen, T; Payton, A; Pazoki, R; Petrovic, K; Reynolds, CA; Sargurupremraj, M; Scholz, M; Smith, JA; Smith, AV; Terzikhan, N; Thalamuthu, A; Trompet, S; van der Lee, SJ; Ware, EB; Windham, BG; Wright, MJ; Yang, J; Yu, J; Ames, D; Amin, N; Amouyel, P; Andreassen, OA; Armstrong, NJ; Assareh, AA; Attia, JR; Attix, D; Avramopoulos, D; Bennett, DA; Böhmer, AC; Boyle, PA; Brodaty, H; Campbell, H; Cannon, TD; Cirulli, ET; Congdon, E; Conley, ED; Corley, J; Cox, SR; Dale, AM; Dehghan, A; Dick, D; Dickinson, D; Eriksson, JG; Evangelou, E; Faul, JD; Ford, I; Freimer, NA; Gao, H; Giegling, I; Gillespie, NA; Gordon, SD; Gottesman, RF; Griswold, ME; Gudnason, V; Harris, TB; Hartmann, AM; Hatzimanolis, A; Heiss, G; Holliday, EG; Joshi, PK; Kähönen, M; Kardia, SLR; Karlsson, I; Kleineidam, L; Knopman, DS; Kochan, NA; Konte, B; Kwok, JB; Le Hellard, S; Lee, T; Lehtimäki, T; Li, SC; Liu, T; Koini, M; London, E; Longstreth, WT; Lopez, OL; Loukola, A; Luck, T; Lundervold, AJ; Lundquist, A; Lyytikäinen, LP; Martin, NG; Montgomery, GW; Murray, AD; Need, AC; Noordam, R; Nyberg, L; Ollier, W; Papenberg, G; Pattie, A; Polasek, O; Poldrack, RA; Psaty, BM; Reppermund, S; Riedel-Heller, SG; Rose, RJ; Rotter, JI; Roussos, P; Rovio, SP; Saba, Y; Sabb, FW; Sachdev, PS; Satizabal, CL; Schmid, M; Scott, RJ; Scult, MA; Simino, J; Slagboom, PE; Smyrnis, N; Soumaré, A; Stefanis, NC; Stott, DJ; Straub, RE; Sundet, K; Taylor, AM; Taylor, KD; Tzoulaki, I; Tzourio, C; Uitterlinden, A; Vitart, V; Voineskos, AN; Kaprio, J; Wagner, M; Wagner, H; Weinhold, L; Wen, KH; Widen, E; Yang, Q; Zhao, W; Adams, HHH; Arking, DE; Bilder, RM; Bitsios, P; Boerwinkle, E; Chiba-Falek, O; Corvin, A; De Jager, PL; Debette, S; Donohoe, G; Elliott, P; Fitzpatrick, AL; Gill, M; Glahn, DC; Hägg, S; Hansell, NK; Hariri, AR; Ikram, MK; Jukema, JW; Vuoksimaa, E; Keller, MC; Kremen, WS; Launer, L; Lindenberger, U; Palotie, A; Pedersen, NL; Pendleton, N; Porteous, DJ; Räikkönen, K; Raitakari, OT; Ramirez, A; Reinvang, I; Rudan, I; Dan Rujescu, I; Schmidt, R; Schmidt, H; Schofield, PW; Schofield, PR; Starr, JM; Steen, VM; Trollor, JN; Turner, ST; Van Duijn, CM; Villringer, A; Weinberger, DR; Weir, DR; Wilson, JF; Malhotra, A; McIntosh, AM; Gale, CR; Seshadri, S; Mosley, TH; Bressler, J; Lencz, T; Deary, IJ Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Nat Commun. 2018; 9(1):2098-2098 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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
Web of Science PubMed FullText FullText_MUG

 

Marschik, PB; Pokorny, FB; Peharz, R; Zhang, D; O'Muircheartaigh, J; Roeyers, H; Bölte, S; Spittle, AJ; Urlesberger, B; Schuller, B; Poustka, L; Ozonoff, S; Pernkopf, F; Pock, T; Tammimies, K; Enzinger, C; Krieber, M; Tomantschger, I; Bartl-Pokorny, KD; Sigafoos, J; Roche, L; Esposito, G; Gugatschka, M; Nielsen-Saines, K; Einspieler, C; Kaufmann, WE; BEE-PRI Study Group A Novel Way to Measure and Predict Development: A Heuristic Approach to Facilitate the Early Detection of Neurodevelopmental Disorders.
Curr Neurol Neurosci Rep. 2017; 17(5):43-43 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Marschik, PB; Zhang, DJ; Esposito, G; Bolte, S; Einspieler, C; Sigafoos, J Same or different: Common pathways of behavioral biomarkers in infants and children with neurodevelopmental disorders?
BEHAV BRAIN SCI. 2017; 40: e64
Web of Science PubMed FullText FullText_MUG

 

Zhang, D; Kaufmann, WE; Sigafoos, J; Bartl-Pokorny, KD; Krieber, M; Marschik, PB; Einspieler, C Parents' initial concerns about the development of their children later diagnosed with fragile X syndrome.
J Intellect Dev Disabil. 2017; 42(2):114-122 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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
Web of Science PubMed FullText FullText_MUG

 

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]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

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
Web of Science PubMed FullText FullText_MUG

 

Einspieler, C; Sigafoos, J; Bölte, S; Bratl-Pokorny, KD; Landa, R; Marschik, PB 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 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Marschik, PB; Kaufmann, WE; Bolte, S; Sigafoos, J; Einspieler, C En route to disentangle the impact and neurobiological substrates of early vocalizations: Learning from Rett syndrome
BEHAV BRAIN SCI. 2014; 37(6):
Web of Science PubMed FullText FullText_MUG

 

Reinthaler, EM; Lal, D; Lebon, S; Hildebrand, MS; Dahl, HH; Regan, BM; Feucht, M; Steinböck, H; Neophytou, B; Ronen, GM; Roche, L; Gruber-Sedlmayr, U; Geldner, J; Haberlandt, E; Hoffmann, P; Herms, S; Gieger, C; Waldenberger, M; Franke, A; Wittig, M; Schoch, S; Becker, AJ; Hahn, A; Männik, K; Toliat, MR; Winterer, G; 16p11.2 European Consortium; Lerche, H; Nürnberg, P; Mefford, H; Scheffer, IE; Berkovic, SF; Beckmann, JS; EPICURE Consortium; EuroEPINOMICS Consortium; Sander, T; Jacquemont, S; Reymond, A; Zimprich, F; Neubauer, BA 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
Hum Mol Genet. 2014; 23(22):6069-6080 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Roche, L; Sigafoos, J; Lancioni, GE; O'Reilly, MF; Schlosser, RW; Stevens, M; van der Meer, L; Achmadi, D; Kagohara, D; James, R; Carnett, A; Hodis, F; Green, VA; Sutherland, D; Lang, R; Rispoli, M; Machalicek, W; Marschik, PB An evaluation of speech production in two boys with neurodevelopmental disorders who received communication intervention with a speech-generating device.
Int J Dev Neurosci. 2014; 38(2):10-16
Web of Science PubMed FullText FullText_MUG

 

2013

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]
Web of Science PubMed FullText FullText_MUG

 

2012

Horak, F; Fazekas, T; Zacharasiewicz, A; Eber, E; Kiss, H; Lichtenschopf, A; Neuberger, M; Schmitzberger, R; Simma, B; Wilhelm-Mitteräcker, A; Riedler, J The Fetal Tobacco Syndrome - A statement of the Austrian Societies for General- and Family Medicine (GAM), Gynecology and Obstetrics (GGG), Hygiene, Microbiology and Preventive Medicine (GHMP), Pediatrics and Adolescence Medicine (GKJ) as well as Pneumology (GP)
Wien Klin Wochenschr. 2012; 124(5-6):129-145
Web of Science PubMed FullText FullText_MUG

 

2003

Kreuzer, C; Urlesberger, B; Maurer, U; Müller, W Transient periventricular echodensities (TPE) in preterm infants under 1500 gramms: an analysis of the outcome of the last 10 years
Klin Padiatr. 2003; 215(5):252-256
Web of Science PubMed FullText FullText_MUG

 

2001

Stefan, H; Feichtinger, M; Pauli, E; Schäfer, I; Eberhardt, KW; Kasper, BS; Hopp, P; Buchfelder, M; Huk, J; Paulus, W Magnetic resonance spectroscopy and histopathological findings in temporal lobe epilepsy.
Epilepsia. 2001; 42(1):41-46
Web of Science PubMed FullText FullText_MUG

 

© Med Uni Graz Impressum