| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yoshihiko Saito, Eri Takeshita, Hirofumi Komaki, Ichizo Nishino, Masayuki Sasak. Determining neurodevelopmental manifestations in Duchenne muscular dystrophy using a battery of brief tests. Journal of the neurological sciences. vol 440. 2022-07-19. PMID:35849899. |
we report neurodevelopmental manifestations in boys with duchenne muscular dystrophy (dmd) and evaluate the correlations between mutation location and three neurodevelopmental abnormalities: intellectual disability, autism spectrum disorder, and attentional problems. |
2022-07-19 |
2023-08-14 |
Not clear |
| Illana Goze. From the Desk of the Editor‑in‑Chief: Excerpts from the Society for Neurochemistry (ESN) Future Perspectives for European Neurochemistry Highlighting the Symposium Asking "Autism, Epilepsy, Intellectual Disability Where Do These All Meet?" Journal of molecular neuroscience : MN. 2022-07-07. PMID:35796943. |
from the desk of the editor‑in‑chief: excerpts from the society for neurochemistry (esn) future perspectives for european neurochemistry highlighting the symposium asking "autism, epilepsy, intellectual disability where do these all meet?" |
2022-07-07 |
2023-08-14 |
Not clear |
| Tomoya Hirota, Tomoko Nishimura, Misaki Mikami, Manabu Saito, Kazuhiko Nakamur. The Role of the Maternal and Child Health Handbook in Developmental Surveillance: The Exploration of Milestone Attainment Trajectories. Frontiers in psychiatry. vol 13. 2022-07-05. PMID:35782444. |
in class 3, 90% of children were diagnosed with at least one ndds at age 5 and approximately 65% of children had autism spectrum disorder and/or intellectual disability, the rate of which was higher than that in the other two classes. |
2022-07-05 |
2023-08-14 |
Not clear |
| Megan Conrow-Graham, Jamal B Williams, Jennifer Martin, Ping Zhong, Qing Cao, Benjamin Rein, Zhen Ya. A convergent mechanism of high risk factors ADNP and POGZ in neurodevelopmental disorders. Brain : a journal of neurology. 2022-07-01. PMID:35775424. |
adnp and pogz are two top-ranking risk factors for autism spectrum disorder and intellectual disability, but how they are linked to these neurodevelopmental disorders is largely unknown. |
2022-07-01 |
2023-08-14 |
mouse |
| Megan Conrow-Graham, Jamal B Williams, Jennifer Martin, Ping Zhong, Qing Cao, Benjamin Rein, Zhen Ya. A convergent mechanism of high risk factors ADNP and POGZ in neurodevelopmental disorders. Brain : a journal of neurology. 2022-07-01. PMID:35775424. |
these findings have uncovered the convergent functions of two top risk factors for autism spectrum disorder and intellectual disability in prefrontal cortex, providing a mechanism linking chromatin, transcriptional and synaptic dysregulation to cognitive deficits associated with neurodevelopmental disorders. |
2022-07-01 |
2023-08-14 |
mouse |
| Wenbo Zhang, P Joel Ross, James Ellis, Michael W Salte. Targeting NMDA receptors in neuropsychiatric disorders by drug screening on human neurons derived from pluripotent stem cells. Translational psychiatry. vol 12. issue 1. 2022-06-10. PMID:35680847. |
nmda receptors (nmdars), a prominent subtype of glutamatergic receptors, are implicated in the pathogenesis and development of neuropsychiatric disorders such as epilepsy, intellectual disability, autism spectrum disorder, and schizophrenia, and are therefore a potential therapeutic target in treating these disorders. |
2022-06-10 |
2023-08-14 |
human |
| Youngshin Lim, Il-Taeg Cho, Jeffrey A Golden, Ginam Ch. Generation of FLAG-tagged Arx knock-in mouse model. Genesis (New York, N.Y. : 2000). 2022-06-03. PMID:35656878. |
patients with mutations in arx have a spectrum of neurodevelopmental disorders such as epilepsy, intellectual disability, and autism spectrum disorder, with or without structural abnormalities of the brain such as lissencephaly (smooth brain), microcephaly (small brain), and/or agenesis of the corpus callosum. |
2022-06-03 |
2023-08-14 |
mouse |
| Ernest V Pedapati, Lauren M Schmitt, Lauren E Ethridge, Makoto Miyakoshi, John A Sweeney, Rui Liu, Elizabeth Smith, Rebecca C Shaffer, Kelli C Dominick, Donald L Gilbert, Steve W Wu, Paul S Horn, Devin K Binder, Martine Lamy, Megan Axford, Craig A Erickso. Neocortical localization and thalamocortical modulation of neuronal hyperexcitability contribute to Fragile X Syndrome. Communications biology. vol 5. issue 1. 2022-05-13. PMID:35546357. |
fragile x syndrome (fxs) is a monogenetic form of intellectual disability and autism in which well-established knockout (ko) animal models point to neuronal hyperexcitability and abnormal gamma-frequency physiology as a basis for key disorder features. |
2022-05-13 |
2023-08-13 |
Not clear |
| Sahar Javadi, Yue Li, Jie Sheng, Lucy Zhao, Yao Fu, Daifeng Wang, Xinyu Zha. Sustained correction of hippocampal neurogenic and cognitive deficits after a brief treatment by Nutlin-3 in a mouse model of fragile X syndrome. BMC medicine. vol 20. issue 1. 2022-05-13. PMID:35549943. |
fragile x syndrome (fxs), the most prevalent inherited intellectual disability and one of the most common monogenic forms of autism, is caused by a loss of fragile x messenger ribonucleoprotein 1 (fmr1). |
2022-05-13 |
2023-08-13 |
mouse |
| Jessica L Armstrong, Clinton E Cana. Targeting 5-HT FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 36 Suppl 1. 2022-05-13. PMID:35554052. |
targeting 5-ht fragile x syndrome (fxs), caused by fmr1gene silencing and subsequent loss of the rna-binding protein fmrp, is the leading monogenic cause of intellectual disability and autism spectrum disorder, characterized by social deficits and repetitive behaviors. |
2022-05-13 |
2023-08-13 |
mouse |
| Kellan Weston, Xiaoyi Gao, Jinghan Zhao, Kwang-Soo Kim, Joseph S Harrison, Kuen-Phon Wu, Jason Y. UBE3A Hyperactivity as a Driver of Neurodevelopmental Disease. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. vol 36 Suppl 1. 2022-05-13. PMID:35555767. |
the ube3agene is of unique interest for its gene dosage-dependent effect in the developing brain: precise deletion or null mutation of the maternal copy of ube3a causes a severe intellectual disability known as angelman syndrome; meanwhile, duplication or triplication of the gene region in which ube3a resides is linked to a prevalent syndromic form of autism known as dup15q syndrome. |
2022-05-13 |
2023-08-13 |
mouse |
| Ai Zhang, Irina Sokolova, Alain Domissy, Joshua Davis, Lee Rao, Kagistia Hana Utami, Yanling Wang, Randi J Hagerman, Mahmoud A Pouladi, Pietro Sanna, Michael J Boland, Jeanne F Lorin. Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells. Stem cells translational medicine. 2022-05-13. PMID:35556144. |
fragile x syndrome (fxs), the leading monogenic cause of intellectual disability and autism spectrum disorder, is caused by expansion of a cgg trinucleotide repeat in the 5'-utr of the fragile x mental retardation-1 (fmr1) gene. |
2022-05-13 |
2023-08-13 |
human |
| Elise Ng-Cordell, Anna Kolesnik-Taylor, Sinéad O'Brien, Duncan Astle, Gaia Scerif, Kate Bake. Social and emotional characteristics of girls and young women with DDX3X-associated intellectual disability: a descriptive and comparative study. Journal of autism and developmental disorders. 2022-05-10. PMID:35536379. |
ddx3x variants are a common cause of intellectual disability (id) in females, and have been associated with autism spectrum disorder and emotional-behavioural difficulties. |
2022-05-10 |
2023-08-13 |
Not clear |
| Markus Wöhr, Wendy M Fong, Justyna A Janas, Moritz Mall, Christian Thome, Madhuri Vangipuram, Lingjun Meng, Thomas C Südhof, Marius Werni. Myt1l haploinsufficiency leads to obesity and multifaceted behavioral alterations in mice. Molecular autism. vol 13. issue 1. 2022-05-10. PMID:35538503. |
moreover, human genetics studies found myt1l mutations to cause intellectual disability and autism spectrum disorder often coupled with obesity. |
2022-05-10 |
2023-08-13 |
mouse |
| Scott H Yamamoto, Charlotte Y Alverso. Post-high school outcomes of students with autism spectrum disorder and students with intellectual disability: Utilizing predictive analytics and state data for decision making. Journal of intellectual disabilities : JOID. 2022-05-09. PMID:35533266. |
post-high school outcomes of students with autism spectrum disorder and students with intellectual disability: utilizing predictive analytics and state data for decision making. |
2022-05-09 |
2023-08-13 |
Not clear |
| Olivier Perche, Fabien Lesne, Alain Patat, Susanne Raab, Roy Twyman, Robert H Ring, Sylvain Briaul. Large-conductance calcium-activated potassium channel haploinsufficiency leads to sensory deficits in the visual system: a case report. Journal of medical case reports. vol 16. issue 1. 2022-05-05. PMID:35509069. |
mutations in the genes encoding the large-conductance calcium-activated potassium channel, especially kcnma1 encoding its α-subunit, have been linked to several neurological features, including intellectual disability or autism. |
2022-05-05 |
2023-08-13 |
Not clear |
| Michal Icht, Gil Zukerman, Esther Ben-Itzchak, Boaz M Ben-Davi. Response to McKenzie et al. 2021: Keep It Simple; Young Adults With Autism Spectrum Disorder Without Intellectual Disability Can Process Basic Emotions. Journal of autism and developmental disorders. 2022-05-04. PMID:35507295. |
2021: keep it simple; young adults with autism spectrum disorder without intellectual disability can process basic emotions. |
2022-05-04 |
2023-08-13 |
Not clear |
| Michal Icht, Gil Zukerman, Esther Ben-Itzchak, Boaz M Ben-Davi. Response to McKenzie et al. 2021: Keep It Simple; Young Adults With Autism Spectrum Disorder Without Intellectual Disability Can Process Basic Emotions. Journal of autism and developmental disorders. 2022-05-04. PMID:35507295. |
namely, these papers suggest that young adults with autism spectrum disorder without intellectual disability can successfully recruit their cognitive abilities to distinguish between different simple spoken emotions, but may still face difficulties processing complex, subtle emotions. |
2022-05-04 |
2023-08-13 |
Not clear |
| Lottie D Morison, Ruth O Braden, David J Amor, Amanda Brignell, Bregje W M van Bon, Angela T Morga. Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments. European journal of human genetics : EJHG. 2022-04-19. PMID:35437318. |
moderate to severe intellectual disability (id), autism spectrum disorder (asd), vision, motor and feeding impairments were common, alongside epilepsy in a third of cases. |
2022-04-19 |
2023-08-13 |
human |
| Masuhiko Sano, Tetsu Hirosawa, Mitsuru Kikuchi, Chiaki Hasegawa, Sanae Tanaka, Yuko Yoshimur. Relation between acquisition of lexical concept and joint attention in children with autism spectrum disorder without severe intellectual disability. PloS one. vol 17. issue 4. 2022-04-14. PMID:35421165. |
relation between acquisition of lexical concept and joint attention in children with autism spectrum disorder without severe intellectual disability. |
2022-04-14 |
2023-08-13 |
Not clear |