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Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology
Elif Funda Sener, Halit Canatan, Yusuf Ozkul
Psychiatry Investig. 2016;13(3):255-264. Published online 2016 May 18 DOI: https://doi.org/10.4306/pi.2016.13.3.255
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Profile of psychotropic agents used in autism spectrum disorder according to comorbidities in Turkey: A 4-year evaluation
Yurdum Karabacak, Sureyya Barun, İsmail Mert Vural, Elif Vural, Elvan Iseri, Aybeniz Civan Kahve, Esra Şafak Yilmaz, Fatma Isli, Sena Turkes, Enes Ezber, Gokcen Paykal
International Clinical Psychopharmacology.2023; 38(4): 216. CrossRef SNAP-25 Polymorphisms in Autism Spectrum Disorder: A Pilot Study towards a Possible Endophenotype
Martina Maria Mensi, Franca Rosa Guerini, Michele Marchesi, Matteo Chiappedi, Elisabetta Bolognesi, Renato Borgatti
Pediatric Reports.2023; 15(4): 766. CrossRef Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder
Elif Funda Sener, Muge Gulcihan Onal, Fatma Dal, Ufuk Nalbantoglu, Yusuf Ozkul, Halit Canatan, Didem Behice Oztop
International Journal of Neuroscience.2022; 132(11): 1072. CrossRef Comparative analysis of the autism‑related variants between different autistic children in a family pedigree
Luxi Shen, Panyuan Li, Tianjin Zheng, Meichen Luo, Shao Zhang, Yuting Huang, Yongwu Hu, Hongzhi Li
Molecular Medicine Reports.2021;[Epub] CrossRef Molecular Dysregulation in Autism Spectrum Disorder
Pritmohinder S. Gill, Jeffery L. Clothier, Aravindhan Veerapandiyan, Harsh Dweep, Patricia A. Porter-Gill, G. Bradley Schaefer
Journal of Personalized Medicine.2021; 11(9): 848. CrossRef Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
Vanessa Aguiar-Pulido, Paul Wolujewicz, Alexander Martinez-Fundichely, Eran Elhaik, Gaurav Thareja, Alice Abdel Aleem, Nader Chalhoub, Tawny Cuykendall, Jamel Al-Zamer, Yunping Lei, Haitham El-Bashir, James M. Musser, Abdulla Al-Kaabi, Gary M. Shaw, Ekta
Proceedings of the National Academy of Sciences.2021;[Epub] CrossRef Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample
Jian Jiao, Manxue Zhang, Pingyuan Yang, Yan Huang, Xiao Hu, Jia Cai, Chan Yang, Mingjing Situ, Hui Zhang, Lei Fu, Kuifang Guo, Yi Huang
Journal of Molecular Neuroscience.2020; 70(2): 219. CrossRef Disregulation of Autophagy in the Transgenerational Cc2d1a Mouse Model of Autism
Halime Dana, Keziban Korkmaz Bayramov, Nesrin Delibaşı, Reyhan Tahtasakal, Ruslan Bayramov, Zuhal Hamurcu, Elif Funda Sener
NeuroMolecular Medicine.2020; 22(2): 239. CrossRef Genetic landscape of autism spectrum disorder in Vietnamese children
Kien Trung Tran, Vinh Sy Le, Hoa Thi Phuong Bui, Duong Huy Do, Ha Thi Thanh Ly, Hieu Thi Nguyen, Lan Thi Mai Dao, Thanh Hong Nguyen, Duc Minh Vu, Lien Thi Ha, Huong Thi Thanh Le, Arijit Mukhopadhyay, Liem Thanh Nguyen
Scientific Reports.2020;[Epub] CrossRef Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy
Junghan Lee, Sungji Ha, Seung-Tae Lee, Sung-Gyun Park, Saeam Shin, Jong Rak Choi, Keun-Ah Cheon
Frontiers in Pharmacology.2020;[Epub] CrossRef Prickle2 and Igsf9b Coordinately Regulate the Cytoarchitecture of the Axon Initial Segment
Md. Imrul Hasan Chowdhury, Tomoki Nishioka, Noriko Mishima, Toshihisa Ohtsuka, Kozo Kaibuchi, Daisuke Tsuboi
Cell Structure and Function.2020; 45(2): 143. CrossRef An Overview of the Main Genetic, Epigenetic and Environmental Factors Involved in Autism Spectrum Disorder Focusing on Synaptic Activity
Elena Masini, Eleonora Loi, Ana Florencia Vega-Benedetti, Marinella Carta, Giuseppe Doneddu, Roberta Fadda, Patrizia Zavattari
International Journal of Molecular Sciences.2020; 21(21): 8290. CrossRef NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families
Maryam Al Shehhi, Eva B. Forman, Jacqueline E. Fitzgerald, Veronica McInerney, Janusz Krawczyk, Sanbing Shen, David R. Betts, Linda Mc Ardle, Kathleen M. Gorman, Mary D. King, Andrew Green, Louise Gallagher, Sally A. Lynch
European Journal of Medical Genetics.2019; 62(3): 204. CrossRef Autism spectrum disorders: autistic phenotypes and complicated mechanisms
Xi-Cheng Zhang, Li-Qi Shu, Xing-Sen Zhao, Xue-Kun Li
World Journal of Pediatrics.2019; 15(1): 17. CrossRef Comorbidity between epilepsy and autism from the point of view of ontogenesis
G. V. Kuzmich, A. N. Sinelnikova
Russian Journal of Child Neurology.2019; 13(4): 40. CrossRef De novo Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
Aitana Alonso-Gonzalez, Cristina Rodriguez-Fontenla, Angel Carracedo
Frontiers in Genetics.2018;[Epub] CrossRef Progress in Genetic Studies of Tourette’s Syndrome
Yanjie Qi, Yi Zheng, Zhanjiang Li, Lan Xiong
Brain Sciences.2017; 7(12): 134. CrossRef Whole-exome sequencing identifies two novel missense mutations (p.L111P and p.R3048C) of RYR3 in a Vietnamese patient with autism spectrum disorders
Thu Hien Nguyen, Thi Thanh Ngan Nguyen, Bac Viet Le, Ngoc Minh Thanh, Thi Kim Lien Nguyen, Van Hai Nong, Huy Hoang Nguyen
Genes & Genomics.2017; 39(3): 301. CrossRef A role for the serotonin reuptake transporter in the brain and intestinal features of autism spectrum disorders and developmental antidepressant exposure
Kara Gross Margolis
Journal of Chemical Neuroanatomy.2017; 83-84: 36. CrossRef A preliminary study of the genes related to aggression and insensitivity to pain in autism spectrum disorders
Elif Funda Sener, Mustafa Caglar Sahin, Serpil Taheri, Keziban Korkmaz Bayramov, Mert Kahraman Marasli, Gokmen Zararsiz, Mehmet Canpolat, Nilfer Sahin, Didem Behice Oztop
Psychiatry and Clinical Psychopharmacology.2017; 27(1): 24. CrossRef
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