RORA c.167-95631G>A

Variant ID: 15-61066516-C-T

NM_134261.2(RORA):c.167-95631G>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


A systematic review of common genetic variation and biological pathways in autism spectrum disorder.

Bmc Neuroscience
Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C
Publication Date: 2021-10-09

Variant appearance in text: rs11639084
PubMed Link: 34627165
Variant Present in the following documents:
  • 12868_2021_662_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



RAR-related orphan receptor A: One gene with multiple functions related to migraine.

Cns Neuroscience & Therapeutics
Farahani, Sedigheh S; Solgi, Leila L; Bayat, Sahar S; Abedin Do, Atieh A; Zare-Karizi, Shohreh S; Safarpour Lima, Behnam B; Mirfakhraie, Reza R
Publication Date: 2020-12

Variant appearance in text: rs11639084
PubMed Link: 32892507
Variant Present in the following documents:
  • Main text
  • CNS-26-1315.pdf
View BVdb publication page



Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

American Journal Of Human Genetics
Guissart, Claire C; Latypova, Xenia X; Rollier, Paul P; Khan, Tahir N TN; Stamberger, Hannah H; McWalter, Kirsty K; Cho, Megan T MT; Kjaergaard, Susanne S; Weckhuysen, Sarah S; Lesca, Gaetan G; Besnard, Thomas T; Õunap, Katrin K; Schema, Lynn L; Chiocchetti, Andreas G AG; McDonald, Marie M; de Bellescize, Julitta J; Vincent, Marie M; Van Esch, Hilde H; Sattler, Shannon S; Forghani, Irman I; Thiffault, Isabelle I; Freitag, Christine M CM; Barbouth, Deborah Sara DS; Cadieux-Dion, Maxime M; Willaert, Rebecca R; Guillen Sacoto, Maria J MJ; Safina, Nicole P NP; Dubourg, Christèle C; Grote, Lauren L; Carré, Wilfrid W; Saunders, Carol C; Pajusalu, Sander S; Farrow, Emily E; Boland, Anne A; Karlowicz, Danielle Hays DH; Deleuze, Jean-François JF; Wojcik, Monica H MH; Pressman, Rena R; Isidor, Bertrand B; Vogels, Annick A; Van Paesschen, Wim W; Al-Gazali, Lihadh L; Al Shamsi, Aisha Mohamed AM; Claustres, Mireille M; Pujol, Aurora A; Sanders, Stephan J SJ; Rivier, François F; Leboucq, Nicolas N; Cogné, Benjamin B; Sasorith, Souphatta S; Sanlaville, Damien D; Retterer, Kyle K; Odent, Sylvie S; Katsanis, Nicholas N; Bézieau, Stéphane S; Koenig, Michel M; Davis, Erica E EE; Pasquier, Laurent L; Küry, Sébastien S
Publication Date: 2018-05-03

Variant appearance in text: rs11639084
PubMed Link: 29656859
Variant Present in the following documents:
  • Main text
View BVdb publication page



Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder.

Plos One
Lai, Yin-Chieh YC; Kao, Chung-Feng CF; Lu, Mong-Liang ML; Chen, Hsi-Chung HC; Chen, Po-Yu PY; Chen, Chien-Hsiun CH; Shen, Winston W WW; Wu, Jer-Yuarn JY; Lu, Ru-Band RB; Kuo, Po-Hsiu PH
Publication Date: 2015

Variant appearance in text: rs11639084
PubMed Link: 25789810
Variant Present in the following documents:
  • Main text
  • pone.0121245.pdf
View BVdb publication page