These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome. Dentici ML; Barresi S; Nardella M; Bellacchio E; Alfieri P; Bruselles A; Pantaleoni F; Danieli A; Iarossi G; Cappa M; Bertini E; Tartaglia M; Zanni G Gene; 2017 Sep; 628():141-145. PubMed ID: 28698159 [TBL] [Abstract][Full Text] [Related]
5. Additional features of Gillespie syndrome in two Brazilian siblings with a novel ITPR1 homozygous pathogenic variant. Carvalho DR; Medeiros JEG; Ribeiro DSM; Martins BJAF; Sobreira NLM Eur J Med Genet; 2018 Mar; 61(3):134-138. PubMed ID: 29169895 [TBL] [Abstract][Full Text] [Related]
6. A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. McEntagart M; Williamson KA; Rainger JK; Wheeler A; Seawright A; De Baere E; Verdin H; Bergendahl LT; Quigley A; Rainger J; Dixit A; Sarkar A; López Laso E; Sanchez-Carpintero R; Barrio J; Bitoun P; Prescott T; Riise R; McKee S; Cook J; McKie L; Ceulemans B; Meire F; Temple IK; Prieur F; Williams J; Clouston P; Németh AH; Banka S; Bengani H; Handley M; Freyer E; Ross A; ; van Heyningen V; Marsh JA; Elmslie F; FitzPatrick DR Am J Hum Genet; 2016 May; 98(5):981-992. PubMed ID: 27108798 [TBL] [Abstract][Full Text] [Related]
7. Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome. Gerber S; Alzayady KJ; Burglen L; Brémond-Gignac D; Marchesin V; Roche O; Rio M; Funalot B; Calmon R; Durr A; Gil-da-Silva-Lopes VL; Ribeiro Bittar MF; Orssaud C; Héron B; Ayoub E; Berquin P; Bahi-Buisson N; Bole C; Masson C; Munnich A; Simons M; Delous M; Dollfus H; Boddaert N; Lyonnet S; Kaplan J; Calvas P; Yule DI; Rozet JM; Fares Taie L Am J Hum Genet; 2016 May; 98(5):971-980. PubMed ID: 27108797 [TBL] [Abstract][Full Text] [Related]
8. Gillespie syndrome in a South Asian child: a case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features. De Silva D; Williamson KA; Dayasiri KC; Suraweera N; Quinters V; Abeysekara H; Wanigasinghe J; De Silva D; De Silva H BMC Pediatr; 2018 Sep; 18(1):308. PubMed ID: 30249237 [TBL] [Abstract][Full Text] [Related]
9. Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design. Tolonen JP; Parolin Schnekenberg R; McGowan S; Sims D; McEntagart M; Elmslie F; Shears D; Stewart H; Tofaris GK; Dabir T; Morrison PJ; Johnson D; Hadjivassiliou M; Ellard S; Shaw-Smith C; Znaczko A; Dixit A; Suri M; Sarkar A; Harrison RE; Jones G; Houlden H; Ceravolo G; Jarvis J; Williams J; Shanks ME; Clouston P; Rankin J; Blumkin L; Lerman-Sagie T; Ponger P; Raskin S; Granath K; Uusimaa J; Conti H; McCann E; Joss S; Blakes AJM; Metcalfe K; Kingston H; Bertoli M; Kneen R; Lynch SA; Martínez Albaladejo I; Moore AP; Jones WD; ; Becker EBE; Németh AH Mov Disord; 2024 Jan; 39(1):141-151. PubMed ID: 37964426 [TBL] [Abstract][Full Text] [Related]
10. Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review. Stendel C; Wagner M; Rudolph G; Klopstock T Neuropediatrics; 2019 Dec; 50(6):382-386. PubMed ID: 31340402 [TBL] [Abstract][Full Text] [Related]
11. The genetic architecture of aniridia and Gillespie syndrome. Hall HN; Williamson KA; FitzPatrick DR Hum Genet; 2019 Sep; 138(8-9):881-898. PubMed ID: 30242502 [TBL] [Abstract][Full Text] [Related]
12. ITPR1: The missing gene in miosis-ataxia syndrome? Chesneau B; Calvas P; Cassagne M; Varenne F; Rozet JM; Bonneville F; Chassaing N; Fournié P; Fares-Taie L; Plaisancié J Am J Med Genet A; 2024 Sep; 194(9):e63655. PubMed ID: 38711238 [TBL] [Abstract][Full Text] [Related]
13. Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias. Hsiao CT; Liu YT; Liao YC; Hsu TY; Lee YC; Soong BW PLoS One; 2017; 12(11):e0187503. PubMed ID: 29186133 [TBL] [Abstract][Full Text] [Related]
14. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Glaser T; Ton CC; Mueller R; Petzl-Erler ML; Oliver C; Nevin NC; Housman DE; Maas RL Genomics; 1994 Jan; 19(1):145-8. PubMed ID: 8188215 [TBL] [Abstract][Full Text] [Related]
15. Missense mutation in the ITPR1 gene presenting with ataxic cerebral palsy: Description of an affected family and literature review. Das J; Lilleker J; Shereef H; Ealing J Neurol Neurochir Pol; 2017; 51(6):497-500. PubMed ID: 28826917 [TBL] [Abstract][Full Text] [Related]
17. Retrocollis as the cardinal feature in a de novo ITRP1 variant. Zachou A; Palaiologou D; Kanavakis E; Anagnostou E Brain Dev; 2022 May; 44(5):347-352. PubMed ID: 35148930 [TBL] [Abstract][Full Text] [Related]
18. Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. van de Leemput J; Chandran J; Knight MA; Holtzclaw LA; Scholz S; Cookson MR; Houlden H; Gwinn-Hardy K; Fung HC; Lin X; Hernandez D; Simon-Sanchez J; Wood NW; Giunti P; Rafferty I; Hardy J; Storey E; Gardner RJ; Forrest SM; Fisher EM; Russell JT; Cai H; Singleton AB PLoS Genet; 2007 Jun; 3(6):e108. PubMed ID: 17590087 [TBL] [Abstract][Full Text] [Related]
19. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities. Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613 [TBL] [Abstract][Full Text] [Related]