PRRT2 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "PRRT2" in English language version.

Last modified: 05:49:46, 8 September 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

98nih.gov

5^th place

62ensembl.org

630^th place

326^th place

44doi.org

2^nd place

33semanticscholar.org

15^th place

8^th place

11ucl.ac.uk

1,187^th place

756^th place

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

Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, et al. (November 2011). "Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia". Nature Genetics. 43 (12): 1252–1255. doi:10.1038/ng.1008. PMID 22101681. S2CID 16129198.
Li J, Zhu X, Wang X, Sun W, Feng B, Du T, et al. (February 2012). "Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis". Journal of Medical Genetics. 49 (2): 76–78. doi:10.1136/jmedgenet-2011-100635. PMC 3261727. PMID 22131361.
Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA (February 2020). "The expanding spectrum of movement disorders in genetic epilepsies". Developmental Medicine and Child Neurology. 62 (2): 178–191. doi:10.1111/dmcn.14407. PMID 31784983. S2CID 208498567.
Riant F, Roos C, Roubertie A, Barbance C, Hadjadj J, Auvin S, et al. (January 2022). "Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study". Neurology. 98 (1): e51–e61. doi:10.1212/WNL.0000000000012947. PMID 34649875. S2CID 245539537.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000167371 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000045114 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

ncbi.nlm.nih.gov

"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: Proline-rich transmembrane protein 2". Retrieved 2011-11-26.
Li J, Zhu X, Wang X, Sun W, Feng B, Du T, et al. (February 2012). "Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis". Journal of Medical Genetics. 49 (2): 76–78. doi:10.1136/jmedgenet-2011-100635. PMC 3261727. PMID 22131361.

pubmed.ncbi.nlm.nih.gov

Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, et al. (November 2011). "Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia". Nature Genetics. 43 (12): 1252–1255. doi:10.1038/ng.1008. PMID 22101681. S2CID 16129198.
Li J, Zhu X, Wang X, Sun W, Feng B, Du T, et al. (February 2012). "Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis". Journal of Medical Genetics. 49 (2): 76–78. doi:10.1136/jmedgenet-2011-100635. PMC 3261727. PMID 22131361.
Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA (February 2020). "The expanding spectrum of movement disorders in genetic epilepsies". Developmental Medicine and Child Neurology. 62 (2): 178–191. doi:10.1111/dmcn.14407. PMID 31784983. S2CID 208498567.
Riant F, Roos C, Roubertie A, Barbance C, Hadjadj J, Auvin S, et al. (January 2022). "Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study". Neurology. 98 (1): e51–e61. doi:10.1212/WNL.0000000000012947. PMID 34649875. S2CID 245539537.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, et al. (November 2011). "Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia". Nature Genetics. 43 (12): 1252–1255. doi:10.1038/ng.1008. PMID 22101681. S2CID 16129198.
Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA (February 2020). "The expanding spectrum of movement disorders in genetic epilepsies". Developmental Medicine and Child Neurology. 62 (2): 178–191. doi:10.1111/dmcn.14407. PMID 31784983. S2CID 208498567.
Riant F, Roos C, Roubertie A, Barbance C, Hadjadj J, Auvin S, et al. (January 2022). "Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study". Neurology. 98 (1): e51–e61. doi:10.1212/WNL.0000000000012947. PMID 34649875. S2CID 245539537.

ucl.ac.uk (Global: 1,187^th place; English: 756^th place)

discovery.ucl.ac.uk

Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA (February 2020). "The expanding spectrum of movement disorders in genetic epilepsies". Developmental Medicine and Child Neurology. 62 (2): 178–191. doi:10.1111/dmcn.14407. PMID 31784983. S2CID 208498567.

PRRT2 (English Wikipedia)

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

ensembl.org (Global: 630th place; English: 326th place)