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Adam J de Smith

Showing results (81-90 of 106) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The impact of Indigenous American-like ancestry on risk of acute lymphoblastic leukemia in Hispanic/Latino childrenJalen Langie, Tsz Fung Chan, Wenjian Yang, et al.
Neuro-Oncology|February 22, 2023
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locusJon Foss-Skiftesvik, Shaobo Li, Adam Rosenbaum, et al.
HGG Advances|November 20, 2025
The impact of Indigenous American-like ancestry on the risk of acute lymphoblastic leukemia in Hispanic/Latino childrenJalen Langie, Tsz Fung Chan, Wenjian Yang, et al.
Genes, Chromosomes & Cancer|May 19, 2019
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in childrenAdam J de Smith, Geneviève Lavoie, Kyle M Walsh, et al.
Cancer Epidemiology|June 13, 2024
Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populationsSydney E Lucas, Tianzhong Yang, Courtney E Wimberly, et al.
Human Molecular Genetics|June 6, 2009
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadismAdam J de Smith, Carolin Purmann, Robin G Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Genome-wide association studies of Down syndrome associated congenital heart defectsElizabeth R Feldman, Yunqi Li, David J Cutler, et al.
Nature Communications|May 19, 2015
PDGFRα demarcates the cardiogenic clonogenic Sca1+ stem/progenitor cell in adult murine myocardiumMichela Noseda, Mutsuo Harada, Sara McSweeney, et al.
Cancer Research|November 4, 2015
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal EvolutionKyle M Walsh, Adam J de Smith, Helen M Hansen, et al.
Genetic Epidemiology|May 23, 2025
Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DSElizabeth R Feldman, Yunqi Li, David J Cutler, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The impact of Indigenous American-like ancestry on risk of acute lymphoblastic leukemia in Hispanic/Latino childrenJalen Langie, Tsz Fung Chan, Wenjian Yang, et al.
Neuro-Oncology|February 22, 2023
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locusJon Foss-Skiftesvik, Shaobo Li, Adam Rosenbaum, et al.
HGG Advances|November 20, 2025
The impact of Indigenous American-like ancestry on the risk of acute lymphoblastic leukemia in Hispanic/Latino childrenJalen Langie, Tsz Fung Chan, Wenjian Yang, et al.
Genes, Chromosomes & Cancer|May 19, 2019
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in childrenAdam J de Smith, Geneviève Lavoie, Kyle M Walsh, et al.
Cancer Epidemiology|June 13, 2024
Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populationsSydney E Lucas, Tianzhong Yang, Courtney E Wimberly, et al.
Human Molecular Genetics|June 6, 2009
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadismAdam J de Smith, Carolin Purmann, Robin G Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Genome-wide association studies of Down syndrome associated congenital heart defectsElizabeth R Feldman, Yunqi Li, David J Cutler, et al.
Nature Communications|May 19, 2015
PDGFRα demarcates the cardiogenic clonogenic Sca1+ stem/progenitor cell in adult murine myocardiumMichela Noseda, Mutsuo Harada, Sara McSweeney, et al.
Cancer Research|November 4, 2015
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal EvolutionKyle M Walsh, Adam J de Smith, Helen M Hansen, et al.
Genetic Epidemiology|May 23, 2025
Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DSElizabeth R Feldman, Yunqi Li, David J Cutler, et al.
Pageof 11