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Hakon Hakonarson

Showing results (71-80 of 950) with videos related to

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Bone|December 13, 2016
Late-onset hereditary hypophosphatemic rickets with hypercalciuria (HHRH) due to mutation of SLC34A3/NPT2cGauri Dhir, Dong Li, Hakon Hakonarson, et al.
Lancet (London, England)|February 1, 2011
Structural variations in attention-deficit hyperactivity disorderJosephine Elia, Xaiowu Gai, Hakon Hakonarson, et al.
Scientific Reports|May 2, 2025
Role of genetic modifiers on pulmonary consequences of cancer therapy in childrenShoshana Leftin Dobkin, Xiao Chang, Frank Mentch, et al.
Nucleic Acids Research|February 15, 2011
Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forestUsman Roshan, Satish Chikkagoudar, Zhi Wei, et al.
Current Diabetes Reports|November 6, 2019
The Genetic Contribution to Type 1 DiabetesMarina Bakay, Rahul Pandey, Struan F A Grant, et al.
European Journal of Human Genetics : EJHG|December 6, 2017
Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk lociYu Zhang, Lifeng Tian, Patrick Sleiman, et al.
Genome Research|February 27, 2023
Complex hierarchical structures in single-cell genomics data unveiled by deep hyperbolic manifold learningTian Tian, Cheng Zhong, Xiang Lin, et al.
Genes & Diseases|June 16, 2025
Data-informed insights into sex differences in peripheral blood mononuclear cells from single-cell transcriptomicsHui-Qi Qu, Joseph T Glessner, Charlly Kao, et al.
Biological Psychiatry|October 21, 2023
A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number VariationsXiao Chang, Huiqi Qu, Yichuan Liu, et al.
Nature Communications|March 26, 2021
Model-based deep embedding for constrained clustering analysis of single cell RNA-seq dataTian Tian, Jie Zhang, Xiang Lin, et al.
Pageof 95

Showing results (71-80 of 950) with videos related to

Sort By:
Pageof 95
Bone|December 13, 2016
Late-onset hereditary hypophosphatemic rickets with hypercalciuria (HHRH) due to mutation of SLC34A3/NPT2cGauri Dhir, Dong Li, Hakon Hakonarson, et al.
Lancet (London, England)|February 1, 2011
Structural variations in attention-deficit hyperactivity disorderJosephine Elia, Xaiowu Gai, Hakon Hakonarson, et al.
Scientific Reports|May 2, 2025
Role of genetic modifiers on pulmonary consequences of cancer therapy in childrenShoshana Leftin Dobkin, Xiao Chang, Frank Mentch, et al.
Nucleic Acids Research|February 15, 2011
Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forestUsman Roshan, Satish Chikkagoudar, Zhi Wei, et al.
Current Diabetes Reports|November 6, 2019
The Genetic Contribution to Type 1 DiabetesMarina Bakay, Rahul Pandey, Struan F A Grant, et al.
European Journal of Human Genetics : EJHG|December 6, 2017
Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk lociYu Zhang, Lifeng Tian, Patrick Sleiman, et al.
Genome Research|February 27, 2023
Complex hierarchical structures in single-cell genomics data unveiled by deep hyperbolic manifold learningTian Tian, Cheng Zhong, Xiang Lin, et al.
Genes & Diseases|June 16, 2025
Data-informed insights into sex differences in peripheral blood mononuclear cells from single-cell transcriptomicsHui-Qi Qu, Joseph T Glessner, Charlly Kao, et al.
Biological Psychiatry|October 21, 2023
A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number VariationsXiao Chang, Huiqi Qu, Yichuan Liu, et al.
Nature Communications|March 26, 2021
Model-based deep embedding for constrained clustering analysis of single cell RNA-seq dataTian Tian, Jie Zhang, Xiang Lin, et al.
Pageof 95