PRICKLE1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "PRICKLE1" in English language version.

refsWebsite

Global rank English rank

4^th place

2^nd place

1,626^th place

1,007^th place

doi.org (Global: 2^nd place; English: 2^nd place)

Algahtani, Hussein; Al-Hakami, Fahad; Al-Shehri, Mohammed; Shirah, Bader; Al-Qahtani, Mohammad H; Abdulkareem, Angham Abdulrahman; Naseer, Muhammad Imran (July 2019). "A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene". Seizure. 69: 133–39. doi:10.1016/j.seizure.2019.04.016. PMID 31035234.
Todd, Brittany P; Bassuk, Alexander G (December 2018). "A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder". Journal of Neurogenetics. 32 (4): 313–15. doi:10.1080/01677063.2018.1473862. PMC 6251753. PMID 29790814.
Ban, Yue; Yu, Ting; Wang, Jingyi; Wang, Xiaojia; Liu, Can; Baker, Clayton; Zou, Yimin (January 2022). "Mutation of the murine Prickle1 (R104Q) causes phenotypes analogous to human symptoms of epilepsy and autism". Experimental Neurology. 347 113880. doi:10.1016/j.expneurol.2021.113880. PMC 8718102. PMID 34597683.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Prickle planar cell polarity protein 1". Retrieved 2017-08-08.
Todd, Brittany P; Bassuk, Alexander G (December 2018). "A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder". Journal of Neurogenetics. 32 (4): 313–15. doi:10.1080/01677063.2018.1473862. PMC 6251753. PMID 29790814.
Ban, Yue; Yu, Ting; Wang, Jingyi; Wang, Xiaojia; Liu, Can; Baker, Clayton; Zou, Yimin (January 2022). "Mutation of the murine Prickle1 (R104Q) causes phenotypes analogous to human symptoms of epilepsy and autism". Experimental Neurology. 347 113880. doi:10.1016/j.expneurol.2021.113880. PMC 8718102. PMID 34597683.

Algahtani, Hussein; Al-Hakami, Fahad; Al-Shehri, Mohammed; Shirah, Bader; Al-Qahtani, Mohammad H; Abdulkareem, Angham Abdulrahman; Naseer, Muhammad Imran (July 2019). "A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene". Seizure. 69: 133–39. doi:10.1016/j.seizure.2019.04.016. PMID 31035234.
Todd, Brittany P; Bassuk, Alexander G (December 2018). "A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder". Journal of Neurogenetics. 32 (4): 313–15. doi:10.1080/01677063.2018.1473862. PMC 6251753. PMID 29790814.
Ban, Yue; Yu, Ting; Wang, Jingyi; Wang, Xiaojia; Liu, Can; Baker, Clayton; Zou, Yimin (January 2022). "Mutation of the murine Prickle1 (R104Q) causes phenotypes analogous to human symptoms of epilepsy and autism". Experimental Neurology. 347 113880. doi:10.1016/j.expneurol.2021.113880. PMC 8718102. PMID 34597683.