204 related articles for article (PubMed ID: 25324312)
1. EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.
Ran X; Li J; Shao Q; Chen H; Lin Z; Sun ZS; Wu J
Nucleic Acids Res; 2015 Jan; 43(Database issue):D893-9. PubMed ID: 25324312
[TBL] [Abstract][Full Text] [Related]
2. Epilepsy-associated genes.
Wang J; Lin ZJ; Liu L; Xu HQ; Shi YW; Yi YH; He N; Liao WP
Seizure; 2017 Jan; 44():11-20. PubMed ID: 28007376
[TBL] [Abstract][Full Text] [Related]
3. IDGenetics: a comprehensive database for genes and mutations of intellectual disability related disorders.
Chen C; Chen D; Xue H; Liu X; Zhang T; Tang S; Li W; Xu X
Neurosci Lett; 2018 Oct; 685():96-101. PubMed ID: 30144540
[TBL] [Abstract][Full Text] [Related]
4. dbCPG: A web resource for cancer predisposition genes.
Wei R; Yao Y; Yang W; Zheng CH; Zhao M; Xia J
Oncotarget; 2016 Jun; 7(25):37803-37811. PubMed ID: 27192119
[TBL] [Abstract][Full Text] [Related]
5. Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
Chow J; Jensen M; Amini H; Hormozdiari F; Penn O; Shifman S; Girirajan S; Hormozdiari F
Genome Med; 2019 Oct; 11(1):65. PubMed ID: 31653223
[TBL] [Abstract][Full Text] [Related]
6. HCSGD: An integrated database of human cellular senescence genes.
Dong Q; Han H; Liu X; Wei L; Zhang W; Zhao Z; Zhang MQ; Wang X
J Genet Genomics; 2017 May; 44(5):227-234. PubMed ID: 28529078
[TBL] [Abstract][Full Text] [Related]
7. 'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.
Ran X; Cai WJ; Huang XF; Liu Q; Lu F; Qu J; Wu J; Jin ZB
Database (Oxford); 2014; 2014():. PubMed ID: 24939193
[TBL] [Abstract][Full Text] [Related]
8. piRBase: integrating piRNA annotation in all aspects.
Wang J; Shi Y; Zhou H; Zhang P; Song T; Ying Z; Yu H; Li Y; Zhao Y; Zeng X; He S; Chen R
Nucleic Acids Res; 2022 Jan; 50(D1):D265-D272. PubMed ID: 34871445
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
[TBL] [Abstract][Full Text] [Related]
10. Heredity in epilepsy: neurodevelopment, comorbidity, and the neurological trait.
Johnson MR; Shorvon SD
Epilepsy Behav; 2011 Nov; 22(3):421-7. PubMed ID: 21890419
[TBL] [Abstract][Full Text] [Related]
11. Inherited disorder phenotypes: controlled annotation and statistical analysis for knowledge mining from gene lists.
Masseroli M; Galati O; Manzotti M; Gibert K; Pinciroli F
BMC Bioinformatics; 2005 Dec; 6 Suppl 4(Suppl 4):S18. PubMed ID: 16351744
[TBL] [Abstract][Full Text] [Related]
12. ORegAnno: an open-access community-driven resource for regulatory annotation.
Griffith OL; Montgomery SB; Bernier B; Chu B; Kasaian K; Aerts S; Mahony S; Sleumer MC; Bilenky M; Haeussler M; Griffith M; Gallo SM; Giardine B; Hooghe B; Van Loo P; Blanco E; Ticoll A; Lithwick S; Portales-Casamar E; Donaldson IJ; Robertson G; Wadelius C; De Bleser P; Vlieghe D; Halfon MS; Wasserman W; Hardison R; Bergman CM; Jones SJ;
Nucleic Acids Res; 2008 Jan; 36(Database issue):D107-13. PubMed ID: 18006570
[TBL] [Abstract][Full Text] [Related]
13. A curated online resource for SOX10 and pigment cell molecular genetic pathways.
Baxter LL; Moreland RT; Nguyen AD; Wolfsberg TG; Pavan WJ
Database (Oxford); 2010 Oct; 2010():baq025. PubMed ID: 20974870
[TBL] [Abstract][Full Text] [Related]
14. BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.
Stryke D; Kawamoto M; Huang CC; Johns SJ; King LA; Harper CA; Meng EC; Lee RE; Yee A; L'Italien L; Chuang PT; Young SG; Skarnes WC; Babbitt PC; Ferrin TE
Nucleic Acids Res; 2003 Jan; 31(1):278-81. PubMed ID: 12520002
[TBL] [Abstract][Full Text] [Related]
15. PolyMAPr: programs for polymorphism database mining, annotation, and functional analysis.
Freimuth RR; Stormo GD; McLeod HL
Hum Mutat; 2005 Feb; 25(2):110-7. PubMed ID: 15643605
[TBL] [Abstract][Full Text] [Related]
16. Prioritization of epilepsy associated candidate genes by convergent analysis.
Jia P; Ewers JM; Zhao Z
PLoS One; 2011 Feb; 6(2):e17162. PubMed ID: 21390307
[TBL] [Abstract][Full Text] [Related]
17. Skeleton Genetics: a comprehensive database for genes and mutations related to genetic skeletal disorders.
Chen C; Jiang Y; Xu C; Liu X; Hu L; Xiang Y; Chen Q; Chen D; Li H; Xu X; Tang S
Database (Oxford); 2016; 2016():. PubMed ID: 27580923
[TBL] [Abstract][Full Text] [Related]
18. Dlg4 and Vamp2 are involved in comorbid epilepsy and attention-deficit hyperactivity disorder: A microarray data study.
Xi XJ; Tang JH; Zhang BB; Xiao X; Hu XY; Wan Y; Zhou C; Lin H
Epilepsy Behav; 2020 Sep; 110():107192. PubMed ID: 32580088
[TBL] [Abstract][Full Text] [Related]
19. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort.
Symonds JD; Zuberi SM; Stewart K; McLellan A; O'Regan M; MacLeod S; Jollands A; Joss S; Kirkpatrick M; Brunklaus A; Pilz DT; Shetty J; Dorris L; Abu-Arafeh I; Andrew J; Brink P; Callaghan M; Cruden J; Diver LA; Findlay C; Gardiner S; Grattan R; Lang B; MacDonnell J; McKnight J; Morrison CA; Nairn L; Slean MM; Stephen E; Webb A; Vincent A; Wilson M
Brain; 2019 Aug; 142(8):2303-2318. PubMed ID: 31302675
[TBL] [Abstract][Full Text] [Related]
20. The comprehensive microbial resource.
Davidsen T; Beck E; Ganapathy A; Montgomery R; Zafar N; Yang Q; Madupu R; Goetz P; Galinsky K; White O; Sutton G
Nucleic Acids Res; 2010 Jan; 38(Database issue):D340-5. PubMed ID: 19892825
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]