Ren C - Search Results

1

MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway.

Gong M, Li J, Qin Z, Machado Bressan Wilke MV, Liu Y, Li Q, Liu H, Liang C, Morales-Rosado JA, Cohen ASA, Hughes SS, Sullivan BR, Waddell V, van den Boogaard MH, van Jaarsveld RH, van Binsbergen E, van Gassen KL, Wang T, Hiatt SM, Amaral MD, Kelley WV, Zhao J, Feng W, Ren C, Yu Y, Boczek NJ, Ferber MJ, Lahner C, Elliott S, Ruan Y, Mignot C, Keren B, Xie H, Wang X, Popp B, Zweier C, Piard J, Coubes C, Mau-Them FT, Safraou H, Innes AM, Gauthier J, Michaud JL, Koboldt DC, Sylvie O, Willems M, Tan WH, Cogne B, Rieubland C, Braun D, McLean SD, Platzer K, Zacher P, Oppermann H, Evenepoel L, Blanc P, El Khattabi L, Haque N, Dsouza NR, Zimmermann MT, Urrutia R, Klee EW, Shen Y, Du H, Rappaport L, Liu CM, Chen X. Gong M, et al. Among authors: ren c. Am J Hum Genet. 2024 Nov 7;111(11):2392-2410. doi: 10.1016/j.ajhg.2024.09.006. Epub 2024 Oct 16. Am J Hum Genet. 2024. PMID: 39419027 Free PMC article.

2

Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis.

Ren XT, Wang XH, Ding CH, Shen X, Zhang H, Zhang WH, Li JW, Ren CH, Fang F. Ren XT, et al. Front Genet. 2019 Apr 25;10:370. doi: 10.3389/fgene.2019.00370. eCollection 2019. Front Genet. 2019. PMID: 31105743 Free PMC article.

3

Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy.

Liu Z, Zhang L, Ren C, Xu M, Li S, Ban R, Wu Y, Chen L, Sun S, Elstner M, Shimura M, Ogawa-Tominaga M, Murayama K, Shi T, Prokisch H, Fang F. Liu Z, et al. Among authors: ren c. J Med Genet. 2022 Apr;59(4):351-357. doi: 10.1136/jmedgenet-2020-107383. Epub 2021 Apr 2. J Med Genet. 2022. PMID: 33811136 Free PMC article.

4

Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.

Zhang W, Ren C, Wang X, Li J, Ding C, Han T, Lv J, Chen C, Gong S, Xiuwei Z, Dai L, Feng W, Yang X, Zhang S, Zhou J, Ren H, Guan H, Ren X, Fang F. Zhang W, et al. Among authors: ren h, ren x, ren c. Eur J Paediatr Neurol. 2021 Sep;34:67-73. doi: 10.1016/j.ejpn.2021.07.004. Epub 2021 Jul 9. Eur J Paediatr Neurol. 2021. PMID: 34399369

5

Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome.

Wang J, Liu Z, Xu M, Han X, Ren C, Yang X, Zhang C, Fang F. Wang J, et al. Among authors: ren c. Front Pharmacol. 2021 Mar 8;12:605803. doi: 10.3389/fphar.2021.605803. eCollection 2021. Front Pharmacol. 2021. PMID: 33762937 Free PMC article.

6

Case Report: Autoimmune Encephalitis Associated With Anti-glutamic Acid Decarboxylase Antibodies: A Pediatric Case Series.

Ren C, Ren H, Ren X, Zhang W, Li J, Dai L, Guan H, Fang F. Ren C, et al. Among authors: ren h, ren x. Front Neurol. 2021 Apr 12;12:641024. doi: 10.3389/fneur.2021.641024. eCollection 2021. Front Neurol. 2021. PMID: 33912125 Free PMC article.

7

Autoimmune Basal Ganglia Encephalitis Associated With Anti-N-methyl-d-Aspartate Receptor Antibodies in Children.

Zhang W, Ren C, Wu Y. Zhang W, et al. Among authors: ren c. Pediatr Neurol. 2024 Apr;153:65-67. doi: 10.1016/j.pediatrneurol.2024.01.012. Epub 2024 Jan 17. Pediatr Neurol. 2024. PMID: 38325023 No abstract available.

8

Encephalitis is an Important Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Diseases: A Single-Center Cohort Study.

Ren C, Zhou A, Zhou J, Zhuo X, Dai L, Tian X, Yang X, Gong S, Ding C, Fang F, Ren X, Zhang W. Ren C, et al. Among authors: ren x. Pediatr Neurol. 2024 Mar;152:98-106. doi: 10.1016/j.pediatrneurol.2023.12.018. Epub 2023 Dec 28. Pediatr Neurol. 2024. PMID: 38242024

9

Anti-Purkinje Cell Cytoplasmic Antibody Type 2-Associated Autoimmune Cerebellar Degeneration in Children: A Different Phenotype From Adults.

Zhou A, Ren H, Fu L, Ren C, Zhou J, Guan H, Ren X, Zhang W. Zhou A, et al. Among authors: ren h, ren x, ren c. Pediatr Neurol. 2024 Nov;160:26-29. doi: 10.1016/j.pediatrneurol.2024.07.004. Epub 2024 Jul 11. Pediatr Neurol. 2024. PMID: 39178650

10

Clinical Presentation, Management, and Diagnostic Performance of 2021 Criteria for Paraneoplastic Neurologic Syndromes in Childhood.

Zhou J, Jin M, Su Y, Zhuo X, Fu L, Ren X, Ren C, Zhou A, Li J, Zhang W. Zhou J, et al. Among authors: ren x, ren c. Neurol Neuroimmunol Neuroinflamm. 2024 May;11(3):e200242. doi: 10.1212/NXI.0000000000200242. Epub 2024 Apr 24. Neurol Neuroimmunol Neuroinflamm. 2024. PMID: 38657195 Free PMC article.

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