Works matching IS 09646906 AND DT 2024 AND VI 33 AND IP 14

Results: 9

Correction to: G2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain.

Published in:: Human Molecular Genetics, 2024, v. 33, n. 14, p. 1277, doi. 10.1093/hmg/ddae093
Publication type:: Article

Genetic susceptibility to chronic diseases leads to heart failure among Europeans: the influence of leukocyte telomere length.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1262, doi. 10.1093/hmg/ddae063

By:

Wong, Jason Y Y;
Blechter, Batel;
Liu, Zhonghua;
Shi, Jianxin;
Roger, Véronique L

Publication type:

Article

Correction to: Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation.

Published in:: Human Molecular Genetics, 2024, v. 33, n. 14, p. 1273, doi. 10.1093/hmg/ddae091
Publication type:: Article

A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1A.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1229, doi. 10.1093/hmg/ddae070

By:

Bhattacharya, Aniket;
Parlanti, Paola;
Cavallo, Luca;
Farrow, Edward;
Spivey, Tyler;
Renieri, Alessandra;
Mari, Francesca;
Manzini, M Chiara

Publication type:

Article

Predicting prognosis and immunotherapy response in colorectal cancer by pericytes insights from single-cell RNA sequencing.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1215, doi. 10.1093/hmg/ddae064

By:

Wei, Chen;
Wang, Weikai;
Hu, Zhihao;
Huang, Zhuoli;
Lu, Ye;
Zhou, Wenwen;
Liu, Xiaoying;
Jin, Xin;
Yin, Jianhua;
Li, Guibo

Publication type:

Article

Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1195, doi. 10.1093/hmg/ddae061

By:

McKaige, Emily A;
Lee, Clara;
Calcinotto, Vanessa;
Giri, Saveen;
Crawford, Simon;
McGrath, Meagan J;
Ramm, Georg;
Bryson-Richardson, Robert J

Publication type:

Article

Impact of the inaccessible genome on genotype imputation and genome-wide association studies.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1207, doi. 10.1093/hmg/ddae062

By:

König, Eva;
Mitchell, Jonathan Stewart;
Filosi, Michele;
Fuchsberger, Christian

Publication type:

Article

Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1250, doi. 10.1093/hmg/ddae060

By:

Alpaslan, Murat;
Fastré, Elodie;
Mestre, Sandrine;
Haeringen, Arie van;
Repetto, Gabriela M;
Keymolen, Kathelijn;
Boon, Laurence M;
Belva, Florence;
Giacalone, Guido;
Revencu, Nicole;
Sznajer, Yves;
Riches, Katie;
Keeley, Vaughan;
Mansour, Sahar;
Gordon, Kristiana;
Martin-Almedina, Silvia;
Dobbins, Sara;
Ostergaard, Pia;
Quere, Isabelle;
Brouillard, Pascal

Publication type:

Article

Genetic correlation between circulating cytokines and risk of three ophthalmic diseases: a bidirectional two-sample Mendelian randomization study.

Published in:

Human Molecular Genetics, 2024, v. 33, n. 14, p. 1241, doi. 10.1093/hmg/ddae041

By:

Zhang, Xin;
Fu, Qiangqiang;
Cai, Yuying;
Li, Xianglian;
Chen, Li;
Jiang, Yaping;
Chen, Yihui

Publication type:

Article