Results 181 to 190 of about 790,983 (253)

Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome

, 2010
Julien Barc, François Briec, Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, C Vieyres, Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott   +12 more
openalex   +1 more source

Missing in Plain Sight No More? Copy Number Variation in Monogenic Kidney Disease. [PDF]

Kidney Int Rep
Jefferis J, Mallett AJ.
europepmc   +1 more source

Whole-genome sequencing of copy number variation analysis in Ethiopian cattle reveals adaptations to diverse environments. [PDF]

BMC Genomics
Ayalew W, Xiaoyun W, Tarekegn GM, Tessema TS, Chu M, Liang C, Naboulsi R, Van Damme R, Bongcam-Rudloff E, Ping Y.   +9 more
europepmc   +1 more source

Association of GSTM1 and GSTT1 Copy Number Variation with Chromosomal Aberrations in Nuclear Power Plant Workers Exposed to Occupational Ionizing Radiation. [PDF]

Toxics
Lee JW, Lee Y, Kim YJ.
europepmc   +1 more source

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells. [PDF]

Mov Disord
Wang H, Chang TS, Dombroski BA, Cheng PL, Si YQ, Tucci A, Patil V, Valiente-Banuet L, Li C, Farrell K, Mclean C, Molina-Porcel L, Rajput A, De Deyn PP, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, de Yébenes JG, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Le Ber I, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL, Morris HR, de Silva R, Crary JF, Goate AM, Friedman JS, Compta Y, Leung YY, Coppola G, Naj AC, Wang LS, PSP Genetics Study Group, Dalgard C, Dickson DW, Höglinger GU, Tzeng JY, Geschwind DH, Schellenberg GD, Lee WP.   +66 more
europepmc   +1 more source

A clinically feasible algorithm for the parallel detection of glioma-associated copy number variation markers based on shallow whole genome sequencing. [PDF]

J Pathol Clin Res
Wu S, Ma C, Cai J, Yang C, Liu X, Luo C, Yang J, Xiong Z, Cao D, Chen H.   +9 more
europepmc   +1 more source

Novel Association Strategy with Copy Number Variation for Identifying New Risk Loci of Human Diseases

, 2010
Xianfeng Chen, Xinlei Li, Ping Wang, Yang Liu, Zhenguo Zhang, Guoping Zhao, Haiming Xu, Jun Zhu, Xueying Qin, Suchao Chen, Landian Hu, Xiangyin Kong   +11 more
openalex   +2 more sources

Copy number variation and population-specific immune genes in the model vertebrate zebrafish. [PDF]

Elife
Schäfer Y, Palitzsch K, Leptin M, Whiteley AR, Wiehe T, Suurväli J.   +5 more
europepmc   +1 more source

Comprehensive analysis of flavohemoprotein copy number variation in Giardia intestinalis: exploring links to metronidazole resistance. [PDF]

Parasit Vectors
Korenková V, Weisz F, Perglerová A, Cacciò SM, Nohýnková E, Tůmová P.   +5 more
europepmc   +1 more source