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Adam J de Smith

Showing results (21-30 of 106) with videos related to

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Plos One|September 5, 2008
Small deletion variants have stable breakpoints commonly associated with alu elementsAdam J de Smith, Robin G Walters, Lachlan J M Coin, et al.
HGG Advances|September 15, 2023
Evaluating genomic polygenic risk scores for childhood acute lymphoblastic leukemia in LatinosSoyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood|November 9, 2013
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALLKyle M Walsh, Adam J de Smith, Anand P Chokkalingam, et al.
Neuro-Oncology Advances|May 16, 2022
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastomaShaobo Li, Xiaowu Gai, Swe Swe Myint, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Hypothesis-generating analysis of mutational signatures in childhood B-cell acute lymphoblastic leukemia in relation to socio-demographic, genetic, and environmental factors: A report from the Children's Oncology GroupCassandra J Clark, Zhanni Lu, Nathan Anderson, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in LatinosSoyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood Advances|February 22, 2020
Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemiaPeleg Winer, Ivo S Muskens, Kyle M Walsh, et al.
Neuro-Oncology Advances|September 1, 2020
Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysisIvo S Muskens, Qianxi Feng, Stephen S Francis, et al.
Neuro-Oncology|January 24, 2020
Germline cancer predisposition variants and pediatric glioma: a population-based study in CaliforniaIvo S Muskens, Adam J de Smith, Chenan Zhang, et al.
Human Molecular Genetics|December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletionKristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Pageof 11

Showing results (21-30 of 106) with videos related to

Sort By:
Pageof 11
Plos One|September 5, 2008
Small deletion variants have stable breakpoints commonly associated with alu elementsAdam J de Smith, Robin G Walters, Lachlan J M Coin, et al.
HGG Advances|September 15, 2023
Evaluating genomic polygenic risk scores for childhood acute lymphoblastic leukemia in LatinosSoyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood|November 9, 2013
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALLKyle M Walsh, Adam J de Smith, Anand P Chokkalingam, et al.
Neuro-Oncology Advances|May 16, 2022
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastomaShaobo Li, Xiaowu Gai, Swe Swe Myint, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Hypothesis-generating analysis of mutational signatures in childhood B-cell acute lymphoblastic leukemia in relation to socio-demographic, genetic, and environmental factors: A report from the Children's Oncology GroupCassandra J Clark, Zhanni Lu, Nathan Anderson, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in LatinosSoyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood Advances|February 22, 2020
Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemiaPeleg Winer, Ivo S Muskens, Kyle M Walsh, et al.
Neuro-Oncology Advances|September 1, 2020
Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysisIvo S Muskens, Qianxi Feng, Stephen S Francis, et al.
Neuro-Oncology|January 24, 2020
Germline cancer predisposition variants and pediatric glioma: a population-based study in CaliforniaIvo S Muskens, Adam J de Smith, Chenan Zhang, et al.
Human Molecular Genetics|December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletionKristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Pageof 11