Works matching IS 09646906 AND DT 2025 AND VI 34 AND IP 3

Results: 7

Genetic architecture of RNA editing, splicing and gene expression in schizophrenia.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 277, doi. 10.1093/hmg/ddae172

By:

Choudhury, Mudra;
Yamamoto, Ryo;
Xiao, Xinshu

Publication type:

Article

Development of a riboflavin-responsive model of riboflavin transporter deficiency in zebrafish.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 265, doi. 10.1093/hmg/ddae171

By:

Choueiri, Catherine M;
Lau, Jarred;
O'Connor, Emily;
DiBattista, Alicia;
Wong, Brittany Y;
Spendiff, Sally;
Horvath, Rita;
Pena, Izabella;
MacKenzie, Alexander;
Lochmüller, Hanns

Publication type:

Article

Constructing methylation-driven ceRNA networks unveil tumor heterogeneity and predict patient prognosis.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 251, doi. 10.1093/hmg/ddae176

By:

Li, Xinyu;
Peng, Chuo;
Liu, Hongyu;
Dong, Mingjie;
Li, Shujuan;
Liang, Weixin;
Li, Xia;
Bai, Jing

Publication type:

Article

Dysregulation of alternative splicing is a transcriptomic feature of patient-derived fibroblasts from CAG repeat expansion spinocerebellar ataxias.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 239, doi. 10.1093/hmg/ddae174

By:

Aliyeva, Asmer;
Lennon, Claudia D;
Cleary, John D;
Shorrock, Hannah K;
Berglund, J Andrew

Publication type:

Article

Recruitment of chromatin remodelers by XIST B-repeat region is variably dependent on HNRNPK.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 229, doi. 10.1093/hmg/ddae173

By:

Navarro-Cobos, Maria Jose;
Brown, Carolyn J

Publication type:

Article

The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 207, doi. 10.1093/hmg/ddae169

By:

Faber, Benjamin G;
Frysz, Monika;
Zheng, Jaiyi;
Lin, Huandong;
Flynn, Kaitlyn A;
Ebsim, Raja;
Saunders, Fiona R;
Beynon, Rhona;
Gregory, Jennifer S;
Aspden, Richard M;
Harvey, Nicholas C;
Lindner, Claudia;
Cootes, Timothy;
Evans, David M;
Smith, George Davey;
Gao, Xin;
Wang, Sijia;
Kemp, John P;
Tobias, Jonathan H

Publication type:

Article

The role of complement factor I rare genetic variants in age related macular degeneration in Finland.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 3, p. 218, doi. 10.1093/hmg/ddae165

By:

Andreadi, Anneliza;
Hallam, Thomas M;
Brocklebank, Vicky;
Sharp, Scott J;
Walsh, Patrick R;
Southerington, Tom;
Hautalahti, Marco;
Steel, David H;
Lotery, Andrew J;
Harris, Claire L;
Marchbank, Kevin J;
Kavanagh, David;
Jones, Amy V

Publication type:

Article