TIAL1 c.130-1520A>G

Variant ID: 10-121343589-T-C

NM_003252.3(TIAL1):c.130-1520A>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Discovering the 3' UTR-mediated regulation of alpha-synuclein.

Nucleic Acids Research
Marchese, Domenica D; Botta-Orfila, Teresa T; Cirillo, Davide D; Rodriguez, Juan Antonio JA; Livi, Carmen Maria CM; Fernández-Santiago, Rubén R; Ezquerra, Mario M; Martí, Maria J MJ; Bechara, Elias E; Tartaglia, Gian Gaetano GG; ,
Publication Date: 2017-12-15

Variant appearance in text: rs10886515
PubMed Link: 29149290
Variant Present in the following documents:
  • gkx1048.pdf
View BVdb publication page



Establishing the role of rare coding variants in known Parkinson's disease risk loci.

Neurobiology Of Aging
Jansen, Iris E IE; Gibbs, J Raphael JR; Nalls, Mike A MA; Price, T Ryan TR; Lubbe, Steven S; van Rooij, Jeroen J; Uitterlinden, André G AG; Kraaij, Robert R; Williams, Nigel M NM; Brice, Alexis A; Hardy, John J; Wood, Nicholas W NW; Morris, Huw R HR; Gasser, Thomas T; Singleton, Andrew B AB; Heutink, Peter P; Sharma, Manu M; ,
Publication Date: 2017-11

Variant appearance in text: rs10886515
PubMed Link: 28867149
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide assessment of Parkinson's disease in a Southern Spanish population.

Neurobiology Of Aging
Bandrés-Ciga, Sara S; Price, Timothy Ryan TR; Barrero, Francisco Javier FJ; Escamilla-Sevilla, Francisco F; Pelegrina, Javier J; Arepalli, Sampath S; Hernández, Dena D; Gutiérrez, Blanca B; Cervilla, Jorge J; Rivera, Margarita M; Rivera, Alberto A; Ding, Jing-Hui JH; Vives, Francisco F; Nalls, Michael M; Singleton, Andrew A; Durán, Raquel R
Publication Date: 2016-09

Variant appearance in text: rs10886515
PubMed Link: 27393345
Variant Present in the following documents:
  • Main text
View BVdb publication page



Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Nature Genetics
Nalls, Mike A MA; Pankratz, Nathan N; Lill, Christina M CM; Do, Chuong B CB; Hernandez, Dena G DG; Saad, Mohamad M; DeStefano, Anita L AL; Kara, Eleanna E; Bras, Jose J; Sharma, Manu M; Schulte, Claudia C; Keller, Margaux F MF; Arepalli, Sampath S; Letson, Christopher C; Edsall, Connor C; Stefansson, Hreinn H; Liu, Xinmin X; Pliner, Hannah H; Lee, Joseph H JH; Cheng, Rong R; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; Ikram, M Arfan MA; Ioannidis, John P A JP; Hadjigeorgiou, Georgios M GM; Bis, Joshua C JC; Martinez, Maria M; Perlmutter, Joel S JS; Goate, Alison A; Marder, Karen K; Fiske, Brian B; Sutherland, Margaret M; Xiromerisiou, Georgia G; Myers, Richard H RH; Clark, Lorraine N LN; Stefansson, Kari K; Hardy, John A JA; Heutink, Peter P; Chen, Honglei H; Wood, Nicholas W NW; Houlden, Henry H; Payami, Haydeh H; Brice, Alexis A; Scott, William K WK; Gasser, Thomas T; Bertram, Lars L; Eriksson, Nicholas N; Foroud, Tatiana T; Singleton, Andrew B AB
Publication Date: 2014-09

Variant appearance in text: rs10886515
PubMed Link: 25064009
Variant Present in the following documents:
  • Main text
  • NIHMS610183-supplement-1.pdf
View BVdb publication page



Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

American Journal Of Human Genetics
Suarez, Brian K BK; Duan, Jubao J; Sanders, Alan R AR; Hinrichs, Anthony L AL; Jin, Carol H CH; Hou, Cuiping C; Buccola, Nancy G NG; Hale, Nancy N; Weilbaecher, Ann N AN; Nertney, Deborah A DA; Olincy, Ann A; Green, Susan S; Schaffer, Arthur W AW; Smith, Christopher J CJ; Hannah, Dominique E DE; Rice, John P JP; Cox, Nancy J NJ; Martinez, Maria M; Mowry, Bryan J BJ; Amin, Farooq F; Silverman, Jeremy M JM; Black, Donald W DW; Byerley, William F WF; Crowe, Raymond R RR; Freedman, Robert R; Cloninger, C Robert CR; Levinson, Douglas F DF; Gejman, Pablo V PV
Publication Date: 2006-02

Variant appearance in text: rs10886515
PubMed Link: 16400611
Variant Present in the following documents:
  • Main text
View BVdb publication page