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American Journal of Human Genetics|November 4, 2022
Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discoveryKym M Boycott, Taila Hartley, Kristin D Kernohan, et al.American Journal of Human Genetics|October 20, 2022
Liability-scale heritability estimation for biobank studies of low-prevalence diseaseSven E Ojavee, Zoltan Kutalik, Matthew R RobinsonAmerican Journal of Human Genetics|October 5, 2022
MagicalRsq: Machine-learning-based genotype imputation quality calibrationQuan Sun, Yingxi Yang, Jonathan D Rosen, et al.American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.American Journal of Human Genetics|October 7, 2022
FastRNA: An efficient solution for PCA of single-cell RNA-sequencing data based on a batch-accounting count modelHanbin Lee, Buhm HanAmerican Journal of Human Genetics|August 1, 1987
Genetic studies of human apolipoproteins. I. Polymorphism of apolipoprotein A-IVM I Kamboh, R E FerrellAmerican Journal of Human Genetics|July 1, 1987
Inheritance of total serum IgE (basal levels) in manD A Meyers, T H Beaty, L R Freidhoff, et al.American Journal of Human Genetics|March 24, 2021
Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithmValentina Favalli, Giulia Tini, Emanuele Bonetti, et al.American Journal of Human Genetics|May 21, 2011
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2Jessica C de Greef, Jun Wang, Judit Balog, et al.American Journal of Human Genetics|May 3, 2011
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesisMehmet Bakircioglu, Ofélia P Carvalho, Maryam Khurshid, et al.Pageof 979