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Chad D Huff

Showing results (61-70 of 88) with videos related to

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Cancer Epidemiology|January 23, 2025
Risk of carcinomas among children and adolescents with birth defectsJeremy M Schraw, Ji Yun Tark, Tania A Desrosiers, et al.
Journal of the National Cancer Institute|March 23, 2023
Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology GroupBailey A Martin-Giacalone, Melissa A Richard, Michael E Scheurer, et al.
Leukemia|September 20, 2022
Impact of conditioning chemotherapy on lymphocyte kinetics and outcomes in LBCL patients treated with CAR T-cell therapyPaolo Strati, Andrew P Jallouk, Ryan Sun, et al.
HGG Advances|June 11, 2025
The Impact of Genetic Ancestry on Survival Outcomes in Pediatric Rhabdomyosarcoma: A Report from the Children's Oncology GroupEkene A Onwuka, Christina L Magyar, Bailey A Martin-Giacalone, et al.
Nature Genetics|July 28, 2025
Large-scale genome-wide analyses of stutteringHannah G Polikowsky, Alyssa C Scartozzi, Douglas M Shaw, et al.
Human Mutation|June 27, 2019
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancerAlin Voskanian, Panagiotis Katsonis, Olivier Lichtarge, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2022
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignanciesJian Tu, Zijun Huo, Yao Yu, et al.
Human Molecular Genetics|January 10, 2019
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sampleLauren E Petty, Heather M Highland, Eric R Gamazon, et al.
JAMA Oncology|June 21, 2019
Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live BirthsPhilip J Lupo, Jeremy M Schraw, Tania A Desrosiers, et al.
American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Cancer Epidemiology|January 23, 2025
Risk of carcinomas among children and adolescents with birth defectsJeremy M Schraw, Ji Yun Tark, Tania A Desrosiers, et al.
Journal of the National Cancer Institute|March 23, 2023
Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology GroupBailey A Martin-Giacalone, Melissa A Richard, Michael E Scheurer, et al.
Leukemia|September 20, 2022
Impact of conditioning chemotherapy on lymphocyte kinetics and outcomes in LBCL patients treated with CAR T-cell therapyPaolo Strati, Andrew P Jallouk, Ryan Sun, et al.
HGG Advances|June 11, 2025
The Impact of Genetic Ancestry on Survival Outcomes in Pediatric Rhabdomyosarcoma: A Report from the Children's Oncology GroupEkene A Onwuka, Christina L Magyar, Bailey A Martin-Giacalone, et al.
Nature Genetics|July 28, 2025
Large-scale genome-wide analyses of stutteringHannah G Polikowsky, Alyssa C Scartozzi, Douglas M Shaw, et al.
Human Mutation|June 27, 2019
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancerAlin Voskanian, Panagiotis Katsonis, Olivier Lichtarge, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2022
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignanciesJian Tu, Zijun Huo, Yao Yu, et al.
Human Molecular Genetics|January 10, 2019
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sampleLauren E Petty, Heather M Highland, Eric R Gamazon, et al.
JAMA Oncology|June 21, 2019
Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live BirthsPhilip J Lupo, Jeremy M Schraw, Tania A Desrosiers, et al.
American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Pageof 9