Results 231 to 240 of about 523,896 (324)

Genomic prediction for Nordic Red Cattle using one-step and selection index blending [PDF]

, 2012
Gloria H. Su, Per Madsen, U. Nielsen, Esa Mäntysaari, Gert Pedersen Aamand, Ole Fredslund Christensen, Mogens Sandø Lund   +6 more
openalex   +1 more source

CSF Levels of NPTX2 Are Associated With Less Brain Atrophy Over Time in Cognitively Unimpaired Individuals

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez, Corinne Pettigrew, Yuxin Zhu, Claire Anderson, Guray Erus, Christos Davatzikos, Michael Miller, Abhay Moghekar, Sungtaek Oh, Chan‐Hyun Na, Marilyn Albert, Paul Worley, Anja Soldan   +12 more
wiley   +1 more source

Disentangling soybean GxE effects in an integrated genomic prediction and machine learning-GWAS workflow. [PDF]

Plant Methods
Verbrigghe N, Muylle H, Pegard M, Rietman H, Đorđević V, Ćeran M, Roldán-Ruiz I.   +6 more
europepmc   +1 more source

Data mining of high density genomic variant data for prediction of Alzheimer's disease risk [PDF]

, 2012
Natalia Briones, Valentin Dinu
openalex   +1 more source

Genomic prediction of health traits in humans: demonstrating the value of marker selection. [PDF]

, 2014
Agakov, Felix, Bermingham, Mairead, Campbell, Harry, Haley, Chris, Hayward, Caroline, Navarro, Pau, Pong-Wong, Ricardo, Rudan, Igor, Spiliopoulou, Athina, Wilson, Jim, Wright, Alan   +10 more
core  

Nationwide Characterization of MFN2‐Related CMT in 176 Japanese Patients: Clinical and Genetic Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando, Yujiro Higuchi, Jun‐Hui Yuan, Akiko Yoshimura, Chikashi Yano, Takahiro Hobara, Fumikazu Kojima, Yu Hiramatsu, Satoshi Nozuma, Tomonori Nakamura, Yusuke Sakiyama, Jun Mitsui, Shoji Tsuji, Hiroshi Takashima   +13 more
wiley   +1 more source

Transferability of genomic prediction models across market segments in potato and the effect of selection. [PDF]

Theor Appl Genet
Thelen K, Wu PY, Baig N, Prigge V, Bruckmüller J, Muders K, Truberg B, Hartje S, Renner J, Van Inghelandt D, Stich B.   +10 more
europepmc   +1 more source

IMP: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks [PDF]

, 2012
Aaron K. Wong, Christopher Y. Park, Casey S. Greene, Lars Ailo Bongo, Yuanfang Guan, Olga G. Troyanskaya   +5 more
openalex   +1 more source

Impact of APOE ε4 Genotype Load on Cognitive Function and Lipid Metabolism in Patients With Cerebral Small Vessel Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Apolipoprotein ε4 (APOE ε4) is a potent genetic risk factor for Alzheimer's disease (AD). However, its role in cerebral small vessel disease (CSVD) remains unclear. Given the clinical and pathological similarities between CSVD and AD, this study aimed to investigate the associations of APOE ε4 gene dosage with cognitive function and
Tingru Jin, Haocheng Yang, Feng Liu, Sihao Lin, Junru Hu, Jian Wang, Yulan Gou   +6 more
wiley   +1 more source

A Self-Supervised Pre-Trained Transformer Model for Accurate Genomic Prediction of Swine Phenotypes. [PDF]

Animals (Basel)
Xiang W, Li Z, Sun Q, Chai X, Sun T.
europepmc   +1 more source