Issue 1/2016
Content (47 Articles)
Mavoglurant in adolescents with fragile X syndrome: analysis of Clinical Global Impression-Improvement source data from a double-blind therapeutic study followed by an open-label, long-term extension study
Donald B. Bailey Jr., Elizabeth Berry-Kravis, Anne Wheeler, Melissa Raspa, Florence Merrien, Javier Ricart, Barbara Koumaras, Gerd Rosenkranz, Mark Tomlinson, Florian von Raison, George Apostol
Atypical functional connectivity in resting-state networks of individuals with 22q11.2 deletion syndrome: associations with neurocognitive and psychiatric functioning
Leah M. Mattiaccio, Ioana L. Coman, Matthew J. Schreiner, Kevin M. Antshel, Wanda P. Fremont, Carrie E. Bearden, Wendy R. Kates
Journal of Neurodevelopmental Disorders reviewer acknowledgement 2015
Joseph Piven
Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1
Satu Massinen, Jingwen Wang, Krista Laivuori, Andrea Bieder, Isabel Tapia Paez, Hong Jiao, Juha Kere
Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome
A. Ting Wang, Teresa Lim, Jesslyn Jamison, Lauren Bush, Latha V. Soorya, Teresa Tavassoli, Paige M. Siper, Joseph D. Buxbaum, Alexander Kolevzon
Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice
Remco T. Molenhuis, Hilgo Bruining, Esther Remmelink, Leonie de Visser, Maarten Loos, J. Peter H. Burbach, Martien J. H. Kas
Reduced engagement with social stimuli in 6-month-old infants with later autism spectrum disorder: a longitudinal prospective study of infants at high familial risk
E. J. H. Jones, K. Venema, R. Earl, R. Lowy, K. Barnes, A. Estes, G. Dawson, S. J. Webb
Erratum to: Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome
A. Ting Wang, Teresa Lim, Jesslyn Jamison, Lauren Bush, Latha V. Soorya, Teresa Tavassoli, Paige M. Siper, Joseph D. Buxbaum, Alexander Kolevzon
Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis complex (TSC): evidence from layer-specific marker expression
Angelika Mühlebner, Anand M. Iyer, Jackelien van Scheppingen, Jasper J. Anink, Floor E. Jansen, Tim J. Veersema, Kees P. Braun, Wim G. M. Spliet, Wim van Hecke, Figen Söylemezoğlu, Martha Feucht, Pavel Krsek, Josef Zamecnik, Christian G. Bien, Tilman Polster, Roland Coras, Ingmar Blümcke, Eleonora Aronica
Developmental trajectories of executive functions in 22q11.2 deletion syndrome
Johanna Maeder, Maude Schneider, Mathilde Bostelmann, Martin Debbané, Bronwyn Glaser, Sarah Menghetti, Marie Schaer, Stephan Eliez
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs
Madita Schumann, Andrea Hofmann, Sophia K. Krutzke, Alina C. Hilger, Florian Marsch, Dietlinde Stienen, Ulrich Gembruch, Michael Ludwig, Waltraut M. Merz, Heiko Reutter
Development, behavior, and biomarker characterization of Smith-Lemli-Opitz syndrome: an update
Audrey Thurm, Elaine Tierney, Cristan Farmer, Phebe Albert, Lisa Joseph, Susan Swedo, Simona Bianconi, Irena Bukelis, Courtney Wheeler, Geeta Sarphare, Diane Lanham, Christopher A. Wassif, Forbes D. Porter
An investigation of NFXL1, a gene implicated in a study of specific language impairment
Ron Nudel
Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus
Duncan Sinclair, Joseph Cesare, Mary McMullen, Greg C Carlson, Chang-Gyu Hahn, Karin E Borgmann-Winter
A functional neuroimaging study of fusiform response to restricted interests in children and adolescents with autism spectrum disorder
Jennifer H. Foss-Feig, Rankin W. McGugin, Isabel Gauthier, Lisa E. Mash, Pamela Ventola, Carissa J. Cascio
Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children
Renée J. Zwanenburg, Selma A.J. Ruiter, Edwin R. van den Heuvel, Boudien C.T. Flapper, Conny M.A. Van Ravenswaaij-Arts
Investigating the effects of copy number variants on reading and language performance
Alessandro Gialluisi, Alessia Visconti, Erik G. Willcutt, Shelley D. Smith, Bruce F. Pennington, Mario Falchi, John C. DeFries, Richard K. Olson, Clyde Francks, Simon E. Fisher
Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects
Carla Lintas, Roberto Sacco, Antonio M. Persico
Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome
Charlotte DiStefano, Amanda Gulsrud, Scott Huberty, Connie Kasari, Edwin Cook, Lawrence T. Reiter, Ronald Thibert, Shafali Spurling Jeste
Methods for acquiring MRI data in children with autism spectrum disorder and intellectual impairment without the use of sedation
Christine Wu Nordahl, Melissa Mello, Audrey M. Shen, Mark D. Shen, Laurie A. Vismara, Deana Li, Kayla Harrington, Costin Tanase, Beth Goodlin-Jones, Sally Rogers, Leonard Abbeduto, David G. Amaral
Persistence of self-injurious behaviour in autism spectrum disorder over 3 years: a prospective cohort study of risk markers
Caroline Richards, Jo Moss, Lisa Nelson, Chris Oliver
Complexities of X chromosome inactivation status in female human induced pluripotent stem cells—a brief review and scientific update for autism research
Mary G. Dandulakis, Kesavan Meganathan, Kristen L. Kroll, Azad Bonni, John N. Constantino
Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats
Yang Wu, Weiwei Zhong, Ningren Cui, Christopher M. Johnson, Hao Xing, Shuang Zhang, Chun Jiang
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
Kerry A. Pettigrew, Emily Frinton, Ron Nudel, May T. M. Chan, Paul Thompson, Marianna E. Hayiou-Thomas, Joel B. Talcott, John Stein, Anthony P. Monaco, Charles Hulme, Margaret J. Snowling, Dianne F. Newbury, Silvia Paracchini
Neural correlates of reward processing in adults with 22q11 deletion syndrome
Esther D. A. van Duin, Liesbet Goossens, Dennis Hernaus, Fabiana da Silva Alves, Nicole Schmitz, Koen Schruers, Therese van Amelsvoort
Sex bias in autism spectrum disorder in neurofibromatosis type 1
Shruti Garg, Hein Heuvelman, Susan Huson, Hannah Tobin, Jonathan Green, D. Gareth Evans, Elizabeth Howard, Emma Burkitt-Wright, Eileen Hupton, Sonia Patel, Judith Eelloo, Maria Gault, Grace Vasallo, Siobhan West, Vilka Kitching, Karen Tricker, Angus Dobbie, Ruth Drimer, Saghira Malik Sharif, Zahabiyah Bassi, Jamuna Acharya, Wayne Lam, Neil Harrower, Oliver Quarrell, Alyson Bradbury, Miranda Splitt, Susan Musson, Rachel Jones, Helen Bethell, Catherine Prem, Karen Horridge, Shaheena Anjum, Christine Steiger
A quantitative measure of restricted and repetitive behaviors for early childhood
Jason J. Wolff, Brian A. Boyd, Jed T. Elison
Cumulative life events, traumatic experiences, and psychiatric symptomatology in transition-aged youth with autism spectrum disorder
Julie Lounds Taylor, Katherine O. Gotham
Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders
Yukari Takarae, Savanna R. Sablich, Stormi P. White, John A. Sweeney
Visual perception and processing in children with 22q11.2 deletion syndrome: associations with social cognition measures of face identity and emotion recognition
Kathryn L. McCabe, Stuart Marlin, Gavin Cooper, Robin Morris, Ulrich Schall, Declan G. Murphy, Kieran C. Murphy, Linda E. Campbell
Erratum to: Neural correlates of reward processing in adults with 22q11 deletion syndrome
Esther D. A. Van Duin, Liesbet Goossens, Dennis Hernaus, Fabiana Da Silva Alves, Nicole Schmitz, Koen Schruers, Therese Van Amelsvoort
Comparing oxytocin and cortisol regulation in a double-blind, placebo-controlled, hydrocortisone challenge pilot study in children with autism and typical development
Blythe A. Corbett, Karen L. Bales, Deanna Swain, Kevin Sanders, Tamara A. R. Weinstein, Louis J. Muglia
Atypical audiovisual word processing in school-age children with a history of specific language impairment: an event-related potential study
Natalya Kaganovich, Jennifer Schumaker, Courtney Rowland
Automatic cortical representation of auditory pitch changes in Rett syndrome
John J. Foxe, Kelly M. Burke, Gizely N. Andrade, Aleksandra Djukic, Hans-Peter Frey, Sophie Molholm
The NIH Toolbox Cognitive Battery for intellectual disabilities: three preliminary studies and future directions
David Hessl, Stephanie M. Sansone, Elizabeth Berry-Kravis, Karen Riley, Keith F. Widaman, Leonard Abbeduto, Andrea Schneider, Jeanine Coleman, Dena Oaklander, Kelly C. Rhodes, Richard C. Gershon
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
Matthew J. Gazzellone, Mehdi Zarrei, Christie L. Burton, Susan Walker, Mohammed Uddin, S. M. Shaheen, Julie Coste, Rageen Rajendram, Reva J. Schachter, Marlena Colasanto, Gregory L. Hanna, David R. Rosenberg, Noam Soreni, Kate D. Fitzgerald, Christian R. Marshall, Janet A. Buchanan, Daniele Merico, Paul D. Arnold, Stephen W. Scherer
Effects of early-life exposure to THIP on phenotype development in a mouse model of Rett syndrome
Weiwei Zhong, Christopher Mychal Johnson, Yang Wu, Ningren Cui, Hao Xing, Shuang Zhang, Chun Jiang
Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome
Masahiro Hirai, Yukako Muramatsu, Seiji Mizuno, Naoko Kurahashi, Hirokazu Kurahashi, Miho Nakamura
Erratum to: Long-term alterations of striatal parvalbumin interneurons in a rat model of early exposure to alcohol
Andrea De Giorgio, Sara E. Comparini, Francesca Sangiuliano Intra, Alberto Granato
Developmental profiles of infants with an FMR1 premutation
Anne C. Wheeler, John Sideris, Randi Hagerman, Elizabeth Berry-Kravis, Flora Tassone, Donald B. Bailey Jr.
Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study
Mathilde Bostelmann, Maude Schneider, Maria Carmela Padula, Johanna Maeder, Marie Schaer, Elisa Scariati, Martin Debbané, Bronwyn Glaser, Sarah Menghetti, Stephan Eliez
Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome
A. Vangkilde, J. R. M. Jepsen, H. Schmock, C. Olesen, S. Arnarsdóttir, W. F. C. Baaré, K. J. Plessen, M. Didriksen, H. R. Siebner, T. Werge, L. Olsen
Postural orientation and equilibrium processes associated with increased postural sway in autism spectrum disorder (ASD)
Zheng Wang, Rami R. Hallac, Kaitlin C. Conroy, Stormi P. White, Alex A. Kane, Amy L. Collinsworth, John A. Sweeney, Matthew W. Mosconi
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder
Sara B. Estruch, Sarah A. Graham, Swathi M. Chinnappa, Pelagia Deriziotis, Simon E. Fisher
Wnt signaling networks in autism spectrum disorder and intellectual disability
Vickie Kwan, Brianna K. Unda, Karun K. Singh
Verbal labels increase the salience of novel objects for preschoolers with typical development and Williams syndrome, but not in autism
Giacomo Vivanti, Darren R. Hocking, Peter Fanning, Cheryl Dissanayake
A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome
Michelle Lee, Gary E. Martin, Elizabeth Berry-Kravis, Molly Losh