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Human Genomics|July 27, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disordersWenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.Human Genomics|July 27, 2022
Epigenetics may characterize asymptomatic COVID-19 infectionCosby G Arnold, Iain Konigsberg, Jason Y Adams, et al.Human Genomics|July 15, 2022
Human adaptation to high altitude: a review of convergence between genomic and proteomic signaturesVandana Sharma, Rajeev Varshney, Niroj Kumar SethyHuman Genomics|July 29, 2022
Identification of the ataxin-1 interaction network and its impact on spinocerebellar ataxia type 1Jiu-Ming Chen, Shi-Kai Chen, Pei-Pei Jin, et al.Human Genomics|April 15, 2018
Public attitudes in Japan toward participation in whole genome sequencing studiesTaketoshi Okita, Noriko Ohashi, Daijiro Kabata, et al.Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.Human Genomics|August 22, 2025
Flu-CNN: identifying host specificity of Influenza A virus using convolutional networksMingda Hu, Nan Luo, Boqian Wang, et al.Human Genomics|March 24, 2023
Pharmacy students' attitudes and intentions of pursuing postgraduate studies and training in pharmacogenomics and personalised medicineDimitra Makrygianni, Margarita-Ioanna Koufaki, George P Patrinos, et al.Human Genomics|March 6, 2023
Controlling the confounding effect of metabolic gene expression to identify actual metabolite targets in microsatellite instability cancersChung-I Li, Yu-Min Yeh, Yi-Shan Tsai, et al.Human Genomics|February 28, 2023
Computational and mitochondrial functional studies of novel compound heterozygous variants in SPATA5 gene support a causal link with epileptogenic encephalopathyVíctor Raggio, Martín Graña, Erik Winiarski, et al.Pageof 112