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Human Genomics|March 11, 2018
2-deoxy-2-[18]fluoro-D-glucose PET/CT (18FDG PET/CT) may not be a viable biomarker in Pompe diseaseU Plöckinger, V Prasad, A Ziagaki, et al.Human Genomics|March 2, 2018
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative featuresGeorgios Kellaris, Kamal Khan, Shahid M Baig, et al.Human Genomics|November 16, 2017
Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadismAbdulaziz Alsemari, Banan Al-Younes, Ewa Goljan, et al.Human Genomics|January 10, 2019
The X chromosome and sex-specific effects in infectious disease susceptibilityHaiko Schurz, Muneeb Salie, Gerard Tromp, et al.Human Genomics|May 11, 2021
Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery diseaseVíctor Raggio, Nicolas Dell'Oca, Camila Simoes, et al.Human Genomics|August 29, 2021
Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's diseaseSungjae Kim, Jong-Yeon Shin, Nak-Jung Kwon, et al.Human Genomics|May 13, 2020
Identification of rare and common variants in BNIP3L: a schizophrenia susceptibility geneJuan Zhou, Chuanchuan Ma, Ke Wang, et al.Human Genomics|October 23, 2019
Prediction of microbial communities for urban metagenomics using neural network approachGuangyu Zhou, Jyun-Yu Jiang, Chelsea J-T Ju, et al.Human Genomics|October 23, 2019
A semi-supervised machine learning framework for microRNA classificationMohsen Sheikh Hassani, James R GreenHuman Genomics|October 23, 2019
Robust hypergraph regularized non-negative matrix factorization for sample clustering and feature selection in multi-view gene expression dataNa Yu, Ying-Lian Gao, Jin-Xing Liu, et al.Pageof 112