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J Cutler

Showing results (741-750 of 803) with videos related to

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Journal of Inherited Metabolic Disease|March 29, 2026
Heritability of Long-Term Complications in Classic GalactosemiaOlivia S Garrett, Nicole H Smith, David J Cutler, et al.
The Journal of Clinical Psychiatry|June 25, 2024
Efficacy and Safety of Esmethadone (REL-1017) in Patients With Major Depressive Disorder and Inadequate Response to Standard Antidepressants: A Phase 3 Randomized Controlled TrialMaurizio Fava, Stephen M Stahl, Luca Pani, et al.
Nature Genetics|September 6, 2005
Genomic alterations in cultured human embryonic stem cellsAnirban Maitra, Dan E Arking, Narayan Shivapurkar, et al.
Diabetes|February 25, 2014
A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetesRicardo C Ferreira, Hui Guo, Richard M R Coulson, et al.
Nature Microbiology|June 1, 2022
Genome-wide protein-DNA interaction site mapping in bacteria using a double-stranded DNA-specific cytosine deaminaseLarry A Gallagher, Elena Velazquez, S Brook Peterson, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Arthritis and Rheumatism|March 2, 2013
Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic lociSampath Prahalad, Karen N Conneely, Yunxuan Jiang, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genome Research|October 19, 2004
Generation of the Brucella melitensis ORFeome version 1.1Amélie Dricot, Jean-François Rual, Philippe Lamesch, et al.
Pageof 81

Showing results (741-750 of 803) with videos related to

Sort By:
Pageof 81
Journal of Inherited Metabolic Disease|March 29, 2026
Heritability of Long-Term Complications in Classic GalactosemiaOlivia S Garrett, Nicole H Smith, David J Cutler, et al.
The Journal of Clinical Psychiatry|June 25, 2024
Efficacy and Safety of Esmethadone (REL-1017) in Patients With Major Depressive Disorder and Inadequate Response to Standard Antidepressants: A Phase 3 Randomized Controlled TrialMaurizio Fava, Stephen M Stahl, Luca Pani, et al.
Nature Genetics|September 6, 2005
Genomic alterations in cultured human embryonic stem cellsAnirban Maitra, Dan E Arking, Narayan Shivapurkar, et al.
Diabetes|February 25, 2014
A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetesRicardo C Ferreira, Hui Guo, Richard M R Coulson, et al.
Nature Microbiology|June 1, 2022
Genome-wide protein-DNA interaction site mapping in bacteria using a double-stranded DNA-specific cytosine deaminaseLarry A Gallagher, Elena Velazquez, S Brook Peterson, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Arthritis and Rheumatism|March 2, 2013
Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic lociSampath Prahalad, Karen N Conneely, Yunxuan Jiang, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genome Research|October 19, 2004
Generation of the Brucella melitensis ORFeome version 1.1Amélie Dricot, Jean-François Rual, Philippe Lamesch, et al.
Pageof 81