Results 191 to 200 of about 128,632 (290)

Neurodevelopmental Disorders

, 2015
Stephan Heckers, Steven E. Hyman, Thomas Bourgeron, Bruce N. Cuthbert, Raquel E. Gur, Cynthia Joyce, Andreas Meyer-Lindenberg, Michael J. Owen, Matthew W. State   +8 more
openaire   +1 more source

Informational and Normative Influence on Conformity in Autism

Autism Research, EarlyView.
ABSTRACT This preregistered study examined whether adults with autism spectrum disorder (ASD) show reduced social conformity and whether any such reduction depends on the type of social influence. Social conformity—the tendency to adjust one's judgments to align with those of others—is typically driven by normative (acceptance‐seeking) and ...
Akiko Kobayashi, Takuya Makino, Yuka Mizuno, Hirotaka Kosaka, Keise Izuma   +4 more
wiley   +1 more source

Neurodevelopmental Disorders

, 2022
  +5 more sources

Episignature leads to diagnosis and reclassification of DYRK1A variant in a child with syndromic neurodevelopmental disorder: a case report. [PDF]

Front Genet
Al-Younis I, Basque L, Crapoulet N, Dyack S, Del Caño-Ochoa F, Ramón-Maiques S, MacKay SB, Rzasa J, Sadikovic B, McConkey H, Ben Amor M.   +10 more
europepmc   +1 more source

Does Ongoing Task Load Influence Prospective Remembering in Autism Spectrum Disorders?

Autism Research, EarlyView.
ABSTRACT Prospective memory (PM) refers to the cognitive ability to remember to carry out intended actions in the future. The present study investigated PM performance in autistic and non‐autistic adults as well as the impact of the cognitive load of the ongoing task on PM performance.
Daniela Nürnberg, Mareike Altgassen
wiley   +1 more source

Transcriptomic and phenotypic convergence of neurodevelopmental disorder risk genes in vitro and in vivo. [PDF]

Nat Neurosci
Fernandez Garcia M, Retallick-Townsley K, Pruitt A, Davidson EA, Balafkan N, Warrell J, Huang TC, Kibowen A, Chu Z, Dai Y, Fitzpatrick SE, Meng R, Sen A, Cohen S, Livoti O, Khan S, Becker C, Luiz Teles E Silva A, Liu J, Dossou G, Cheung J, Liu S, Ghorbani S, Deans PJM, DeCiucis M, Emani P, Gao H, Shen H, Gerstein M, Wang Z, Huckins LM, Hoffman EJ, Brennand K.   +32 more
europepmc   +1 more source

Lower Striatal and Cortical Calretinin Interneuron Density Associated With Altered Social Behavior in Cntnap2 Knockout Mice

Autism Research, EarlyView.
ABSTRACT Variants in the CNTNAP2 gene, encoding the cell adhesion molecule CASPR2, have been identified as genetic risk factors for autism spectrum disorder (ASD). However, the mechanisms through which CNTNAP2 dysfunction alters circuit function remain unknown.
Krisztina Sáfár, Vivien Szendi, Paulina Hoppa, Yutong Wang, Fanni Á. Seres, Szilvia Bartók, Tyler Teadora, Lei Shi, Árpád Dobolyi, Gina Puska, István Adorján   +10 more
wiley   +1 more source

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder. [PDF]

Am J Hum Genet
Planas-Serra L, Rodríguez-Ruiz M, Anderson EN, Rodríguez-Palmero A, Vélez-Santamaria V, Schlüter A, Verdura E, Gereñu G, Jiménez-Zúñiga A, Iñañez A, Casas J, Bech JJ, De Lima TB, De La Torre C, Martínez JJ, Ruiz M, Fourcade S, Iascone M, Tenconi R, Meier K, Diegmann S, Lee RHC, Beland B, Mir A, Darvish H, Chung W, Karimiani EG, Leal SM, Schrauwen I, Öhman S, Järvelä I, Granvik J, Reinson K, Kurvinen E, Õunap K, Schwan A, Platzer K, Kalayci T, Sharifi S, Korenke GC, Houlden H, Maroofian R, López de Munaín A, Casasnovas C, Pandey UB, Pujol A.   +45 more
europepmc   +1 more source

Beyond the Outburst: Charting a New Frontier for Understanding and Treating Irritability in Autistic Adults

Autism Research, EarlyView.
ABSTRACT Irritability is a prevalent and impairing feature associated with autism, yet remains poorly understood, particularly in adults. Drawing heavily on insights translated from pediatric and transdiagnostic literatures, we propose that irritability in autistic individuals often reflects a psychophysiological stress or threat response, rooted in a ...
Hsiang‐Yuan Lin, Arthur N. Westover, Amy S. F. Lutz, Manish K. Jha   +3 more
wiley   +1 more source

Expansion of the Phenotypic Spectrum of TNRC6B-Related Neurodevelopmental Disorder in a Three-Generation Family with 22q13.1 Deletion. [PDF]

Genes (Basel)
Archer J, O'Donnell S, Buckman M, Bain N, Goel H.   +4 more
europepmc   +1 more source