Volume 5, issue 1, December 2013
32 articles in this issue
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Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome
Authors (first, second and last of 5)
- Akvile Lukoshe
- Tonya White
- Anita C Hokken-Koelega
- Content type: Research
- Open Access
- Published: 22 October 2013
- Article: 31
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A molecular genetic study of autism and related phenotypes in extended pedigrees
Authors (first, second and last of 10)
- Joseph Piven
- Veronica J Vieland
- Peter Szatmari
- Content type: Research
- Open Access
- Published: 05 October 2013
- Article: 30
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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Authors (first, second and last of 9)
- Elizabeth A Worthey
- Gordana Raca
- Lawrence D Shriberg
- Content type: Research
- Open Access
- Published: 02 October 2013
- Article: 29
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Eye tracking in early autism research
Authors
- Terje Falck-Ytter
- Sven Bölte
- Gustaf Gredebäck
- Content type: Review
- Open Access
- Published: 26 September 2013
- Article: 28
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Prevalence of selected clinical problems in older adults with autism and intellectual disability
Authors (first, second and last of 4)
- Dmitry Kats
- Leslie Payne
- Joseph Piven
- Content type: Research
- Open Access
- Published: 25 September 2013
- Article: 27
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Sensory and motor secondary symptoms as indicators of brain vulnerability
Authors
- Nava Levit-Binnun
- Michael Davidovitch
- Yulia Golland
- Content type: Review
- Open Access
- Published: 24 September 2013
- Article: 26
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The broad autism phenotype predicts child functioning in autism spectrum disorders
Authors (first, second and last of 5)
- Christina R Maxwell
- Julia Parish-Morris
- Robert T Schultz
- Content type: Research
- Open Access
- Published: 22 September 2013
- Article: 25
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Resting state EEG abnormalities in autism spectrum disorders
Authors (first, second and last of 6)
- Jun Wang
- Jamie Barstein
- John A Sweeney
- Content type: Review
- Open Access
- Published: 16 September 2013
- Article: 24
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Methotrexate treatment of FraX fibroblasts results in FMR1 transcription but not in detectable FMR1 protein levels
Authors (first, second and last of 5)
- Cornelia Brendel
- Benjamin Mielke
- Peter Huppke
- Content type: Research
- Open Access
- Published: 10 September 2013
- Article: 23
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Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders
Authors
- Yongjie Yang
- Haruki Higashimori
- Lydie Morel
- Content type: Review
- Open Access
- Published: 29 August 2013
- Article: 22
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Intracranial arachnoid cysts: impairment of higher cognitive functions and postoperative improvement
Authors (first, second and last of 4)
- Priyanthi B Gjerde
- Marit Schmid
- Knut Wester
- Content type: Research
- Open Access
- Published: 28 August 2013
- Article: 21
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Aberrant basal ganglia metabolism in fragile X syndrome: a magnetic resonance spectroscopy study
Authors (first, second and last of 10)
- Jennifer Lynn Bruno
- Elizabeth Walter Shelly
- Allan L Reiss
- Content type: Research
- Open Access
- Published: 28 August 2013
- Article: 20
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Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population
Authors (first, second and last of 9)
- Diane Mullins
- Eileen Daly
- Declan G Murphy
- Content type: Research
- Open Access
- Published: 20 August 2013
- Article: 19
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Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables
Authors (first, second and last of 5)
- Joseba Jauregi
- Virginie Laurier
- Denise Thuilleaux
- Content type: Research
- Open Access
- Published: 06 August 2013
- Article: 18
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The effect of chronic prenatal hypoxia on the development of mature neurons in the cerebellum
Authors (first, second and last of 5)
- Keumyoung So
- Yoonyoung Chung
- Yonghyun Jeon
- Content type: Research
- Open Access
- Published: 03 July 2013
- Article: 17
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Organization of brain networks governed by long-range connections index autistic traits in the general population
Authors (first, second and last of 9)
- Pablo Barttfeld
- LucÃa Amoruso
- Mariano Sigman
- Content type: Research
- Open Access
- Published: 27 June 2013
- Article: 16
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Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene
Authors
- Kimberly A Aldinger
- Jasmine T Plummer
- Pat Levitt
- Content type: Research
- Open Access
- Published: 11 June 2013
- Article: 15
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Working memory deficits in high-functioning adolescents with autism spectrum disorders: neuropsychological and neuroimaging correlates
Authors (first, second and last of 8)
- Evelien M Barendse
- Marc PH Hendriks
- Albert P Aldenkamp
- Content type: Review
- Open Access
- Published: 04 June 2013
- Article: 14
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Spontaneous and cued gaze-following in autism and Williams syndrome
Authors (first, second and last of 4)
- Deborah M Riby
- Peter JB Hancock
- Mary Hanley
- Content type: Research
- Open Access
- Published: 10 May 2013
- Article: 13
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Repetitive and self-injurious behaviors: associations with caudate volume in autism and fragile X syndrome
Authors (first, second and last of 5)
- Jason J Wolff
- Heather C Hazlett
- Joseph Piven
- Content type: Research
- Open Access
- Published: 02 May 2013
- Article: 12
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Autism and the broad autism phenotype: familial patterns and intergenerational transmission
Authors (first, second and last of 5)
- Noah J Sasson
- Kristen SL Lam
- Joseph Piven
- Content type: Research
- Open Access
- Published: 02 May 2013
- Article: 11
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Developmental patterns of DR6 in normal human hippocampus and in Down syndrome
Authors (first, second and last of 6)
- Anand Iyer
- Jackelien van Scheppingen
- Eleonora Aronica
- Content type: Research
- Open Access
- Published: 24 April 2013
- Article: 10
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A pilot open-label trial of minocycline in patients with autism and regressive features
Authors (first, second and last of 7)
- Carlos A Pardo
- Ashura Buckley
- Susan E Swedo
- Content type: Research
- Open Access
- Published: 08 April 2013
- Article: 9
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A quantitative homogeneous assay for fragile X mental retardation 1 protein
Authors (first, second and last of 6)
- Gabi Schutzius
- Dorothee Bleckmann
- Andreas Weiss
- Content type: New method
- Open Access
- Published: 02 April 2013
- Article: 8
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Social and emotional processing in Prader-Willi syndrome: genetic subtype differences
Authors
- Alexandra P Key
- Dorita Jones
- Elisabeth M Dykens
- Content type: Research
- Open Access
- Published: 27 March 2013
- Article: 7
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Neurodevelopmental alcohol exposure elicits long-term changes to gene expression that alter distinct molecular pathways dependent on timing of exposure
Authors (first, second and last of 4)
- Morgan L Kleiber
- Katarzyna Mantha
- Shiva M Singh
- Content type: Research
- Open Access
- Published: 13 March 2013
- Article: 6
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Journal of Neurodevelopmental Disorders reviewer acknowledgement 2012
Authors
- Joseph Piven
- Content type: Reviewer acknowledgement
- Open Access
- Published: 21 March 2013
- Article: 5
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Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
Authors
- Junlin Li
- Guifang Zhao
- Xiaocai Gao
- Content type: Review
- Open Access
- Published: 20 February 2013
- Article: 4
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Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalities
Authors (first, second and last of 4)
- Inês R Violante
- Maria J Ribeiro
- Miguel Castelo-Branco
- Content type: Research
- Open Access
- Published: 13 February 2013
- Article: 3
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The regulatory function of social referencing in preschoolers with Down syndrome or Williams syndrome
Authors
- Angela John Thurman
- Carolyn B Mervis
- Content type: Research
- Open Access
- Published: 13 February 2013
- Article: 2
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Using infrared eye-tracking to explore ordinal numerical processing in toddlers with Fragile X Syndrome
Authors
- Emily R Owen
- Heidi A Baumgartner
- Susan M Rivera
- Content type: Research
- Open Access
- Published: 12 February 2013
- Article: 1