Issue 1/2014
Content (46 Articles)
Journal of Neurodevelopmental Disorders reviewer acknowledgement 2013
Joseph Piven
Associations of HLA alleles with specific language impairment
Ron Nudel, Nuala H Simpson, Gillian Baird, Anne O’Hare, Gina Conti-Ramsden, Patrick F Bolton, Elizabeth R Hennessy, Anthony P Monaco, Julian C Knight, Bruce Winney, Simon E Fisher, Dianne F Newbury
Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
Yael Schonherz, Maayan Davidov, Ariel Knafo, Hadas Zilkha, Gal Shoval, Gil Zalsman, Amos Frisch, Abraham Weizman, Doron Gothelf
Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits
Maria J Ribeiro, Otília C d’Almeida, Fabiana Ramos, Jorge Saraiva, Eduardo D Silva, Miguel Castelo-Branco
Neonatal exposure to permethrin pesticide causes lifelong fear and spatial learning deficits and alters hippocampal morphology of synapses
Cinzia Nasuti, Patrizia Fattoretti, Manuel Carloni, Donatella Fedeli, Massimo Ubaldi, Roberto Ciccocioppo, Rosita Gabbianelli
Differences in age-related effects on brain volume in Down syndrome as compared to Williams syndrome and typical development
Mary Ellen I Koran, Timothy J Hohman, Courtney M Edwards, Jennifer N Vega, Jennifer R Pryweller, Laura E Slosky, Genea Crockett, Lynette Villa de Rey, Shashwath A Meda, Nathan Dankner, Suzanne N Avery, Jennifer U Blackford, Elisabeth M Dykens, Tricia A Thornton-Wells
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Julie Lauzon, Rachel Laframboise, Joo Wook Ahn, Caroline Mackie Ogilvie, Anath C Lionel, Christian R Marshall, Andrea K Vaags, Bita Hashemi, Karine Boisvert, Géraldine Mathonnet, Frédérique Tihy, Joyce So, Stephen W Scherer, Emmanuelle Lemyre, Dimitri J Stavropoulos
Self-injury and aggression in tuberous sclerosis complex: cross syndrome comparison and associated risk markers
Kate E Eden, Petrus J de Vries, Jo Moss, Caroline Richards, Chris Oliver
Motor function and perception in children with neuropsychiatric and conduct problems: results from a population based twin study
Peik Gustafsson, Nóra Kerekes, Henrik Anckarsäter, Paul Lichtenstein, Christopher Gillberg, Maria Råstam
Inaugural Christianson Syndrome Association conference: families meeting for the first time
David M Stein, Alan Gerber, Eric M Morrow
Robust features for the automatic identification of autism spectrum disorder in children
Justin Eldridge, Alison E Lane, Mikhail Belkin, Simon Dennis
Reactivity to fearful expressions of familiar and unfamiliar people in children with autism: an eye-tracking pupillometry study
Heather J Nuske, Giacomo Vivanti, Cheryl Dissanayake
Neural synchrony examined with magnetoencephalography (MEG) during eye gaze processing in autism spectrum disorders: preliminary findings
Renée Lajiness-O’Neill, Annette E Richard, John E Moran, Amy Olszewski, Lesley Pawluk, Daniel Jacobson, Alfred Mansour, Kelly Vogt, Laszlo A Erdodi, Aimee M Moore, Susan M Bowyer
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder
Elena Bacchelli, Fabiola Ceroni, Dalila Pinto, Silvia Lomartire, Maila Giannandrea, Patrizia D'Adamo, Elena Bonora, Piero Parchi, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini
The neural correlates of visuo-spatial working memory in children with autism spectrum disorder: effects of cognitive load
Vanessa M Vogan, Benjamin R Morgan, Wayne Lee, Tamara L Powell, Mary Lou Smith, Margot J Taylor
Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients
Hannah Broadbent, Emily K Farran, Esther Chin, Kay Metcalfe, May Tassabehji, Peter Turnpenny, Francis Sansbury, Emma Meaburn, Annette Karmiloff-Smith
Developmental delay in Rett syndrome: data from the natural history study
Jeffrey L Neul, Jane B Lane, Hye-Seung Lee, Suzanne Geerts, Judy O Barrish, Fran Annese, Lauren McNair Baggett, Katherine Barnes, Steven A Skinner, Kathleen J Motil, Daniel G Glaze, Walter E Kaufmann, Alan K Percy
Visual motion processing deficits in infants with the fragile X premutation
Pamela K Gallego, Jessica L Burris, Susan M Rivera
Associated features in females with an FMR1 premutation
Anne C Wheeler, Donald B Bailey Jr, Elizabeth Berry-Kravis, Jan Greenberg, Molly Losh, Marsha Mailick, Montserrat Milà, John M Olichney, Laia Rodriguez-Revenga, Stephanie Sherman, Leann Smith, Scott Summers, Jin-Chen Yang, Randi Hagerman
Late, not early mismatch responses to changes in frequency are reduced or deviant in children with dyslexia: an event-related potential study
Lorna F Halliday, Johanna G Barry, Mervyn J Hardiman, Dorothy VM Bishop
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, Montserrat Naudo, Jordi Genoves, Alessandra Murgia, Roberta Polli, Lili Zhou, Deborah Barbouth, Abigail Rupchock, Brenda Finucane, Gary J Latham, Andrew Hadd, Elizabeth Berry-Kravis, Flora Tassone
Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome
Robert F Berman, Ronald AM Buijsen, Karen Usdin, Elizabeth Pintado, Frank Kooy, Dalyir Pretto, Isaac N Pessah, David L Nelson, Zachary Zalewski, Nicholas Charlet-Bergeurand, Rob Willemsen, Renate K Hukema
The cognitive neuropsychological phenotype of carriers of the FMR1 premutation
Jim Grigsby, Kim Cornish, Darren Hocking, Claudine Kraan, John M Olichney, Susan M Rivera, Andrea Schneider, Stephanie Sherman, Jun Yi Wang, Jin-Chen Yang
Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)
Stephanie L Sherman, Eliza C Curnow, Charles A Easley, Peng Jin, Renate K Hukema, Maria Isabel Tejada, Rob Willemsen, Karen Usdin
Emerging topics in FXTAS
Deborah A Hall, Rachael C Birch, Mathieu Anheim, Aia E Jønch, Elizabeth Pintado, Joanne O’Keefe, Julian N Trollor, Glenn T Stebbins, Randi J Hagerman, Stanley Fahn, Elizabeth Berry-Kravis, Maureen A Leehey
Copy number variation in Han Chinese individuals with autism spectrum disorder
Matthew J Gazzellone, Xue Zhou, Anath C Lionel, Mohammed Uddin, Bhooma Thiruvahindrapuram, Shuang Liang, Caihong Sun, Jia Wang, Mingyang Zou, Kristiina Tammimies, Susan Walker, Thanuja Selvanayagam, John Wei, Zhuozhi Wang, Lijie Wu, Stephen W Scherer
Eye-voice span during rapid automatized naming: evidence of reduced automaticity in individuals with autism spectrum disorder and their siblings
Abigail L Hogan-Brown, Renske S Hoedemaker, Peter C Gordon, Molly Losh
Examining the relationship between face processing and social interaction behavior in children with and without autism spectrum disorder
Blythe A Corbett, Cassandra Newsom, Alexandra P Key, Lydia R Qualls, E Kale Edmiston
PreImplantation factor (PIF*) promotes embryotrophic and neuroprotective decidual genes: effect negated by epidermal growth factor
Christina M Duzyj, Michael J Paidas, Lellean Jebailey, Jing Shun Huang, Eytan R Barnea
Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS)
Kathryn Louise McCabe, Rebbekah Josephine Atkinson, Gavin Cooper, Jessica Lauren Melville, Jill Harris, Ulrich Schall, Carmel Maree Loughland, Renate Thienel, Linda Elisabet Campbell
Enhanced parietal cortex activation during location detection in children with autism
Thomas P DeRamus, Briley S Black, Mark R Pennick, Rajesh K Kana
EEG hyper-connectivity in high-risk infants is associated with later autism
Elena V Orekhova, Mayada Elsabbagh, Emily JH Jones, Geraldine Dawson, Tony Charman, Mark H Johnson
Social (pragmatic) communication disorder: a research review of this new DSM-5 diagnostic category
Lauren B Swineford, Audrey Thurm, Gillian Baird, Amy M Wetherby, Susan Swedo
The relationship between sleep and behavior in autism spectrum disorder (ASD): a review
Simonne Cohen, Russell Conduit, Steven W Lockley, Shantha MW Rajaratnam, Kim M Cornish
An investigation of the middle and late behavioural phenotypes of Mucopolysaccharidosis Type-III
Elaine M Cross, Sheena Grant, Simon Jones, Brian W Bigger, James E Wraith, Louise V Mahon, Michelle Lomax, Dougal J Hare
Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring
Alexander Kolevzon, Benjamin Angarita, Lauren Bush, A Ting Wang, Yitzchak Frank, Amy Yang, Robert Rapaport, Jeffrey Saland, Shubhika Srivastava, Cristina Farrell, Lisa J Edelmann, Joseph D Buxbaum
Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome
Thomas H Wassink, Heather C Hazlett, Lea K Davis, Allan L Reiss, Joseph Piven
The multiple molecular facets of fragile X-associated tremor/ataxia syndrome
Chantal Sellier, Karen Usdin, Chiara Pastori, Veronica J Peschansky, Flora Tassone, Nicolas Charlet-Berguerand
Genomic studies in fragile X premutation carriers
Reymundo Lozano, Randi J Hagerman, Michael Duyzend, Dejan B Budimirovic, Evan E Eichler, Flora Tassone
A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation
Ling M Wong, Naomi J Goodrich-Hunsaker, Yingratana A McLennan, Flora Tassone, Susan M Rivera, Tony J Simon
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
Andrea I Quintero, Elliott A Beaton, Danielle J Harvey, Judith L Ross, Tony J Simon
Improving IQ measurement in intellectual disabilities using true deviation from population norms
Stephanie M Sansone, Andrea Schneider, Erika Bickel, Elizabeth Berry-Kravis, Christina Prescott, David Hessl
Facial emotion recognition in agenesis of the corpus callosum
Matthew W Bridgman, Warren S Brown, Michael L Spezio, Matthew K Leonard, Ralph Adolphs, Lynn K Paul
Hippocampal glutamate-glutamine (Glx) in adults with Down syndrome: a preliminary study using in vivo proton magnetic resonance spectroscopy (1H MRS)
Giles MY Tan, Felix Beacher, Eileen Daly, Jamie Horder, Verinder Prasher, Maria-Luisa Hanney, Robin Morris, Simon Lovestone, Kieran C Murphy, Andrew Simmons, Declan GM Murphy
Event-related potentials to repeated speech in 9-month-old infants at risk for autism spectrum disorder
Anne Seery, Helen Tager-Flusberg, Charles A Nelson