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Andrew Jenkinson

Showing results (21-30 of 32) with videos related to

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Obesity Surgery|July 26, 2018
Is Pre-operation Social Connectedness Associated with Weight Loss up to 2 Years Post Bariatric Surgery?Urszula Tymoszuk, Meena Kumari, Andrea Pucci, et al.
JAMA Surgery|July 26, 2023
Safety and Efficacy of Liraglutide, 3.0 mg, Once Daily vs Placebo in Patients With Poor Weight Loss Following Metabolic Surgery: The BARI-OPTIMISE Randomized Clinical TrialJessica Mok, Mariam O Adeleke, Adrian Brown, et al.
Nature Medicine|May 22, 2026
Semaglutide versus placebo in individuals with poor weight loss after bariatric surgery: a double-blinded, randomized, placebo-controlled trialChloe Stanley, Ritwika Mallik, Nausheen Hamid, et al.
Nature Communications|May 15, 2023
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetesLiam McAllan, Damir Baranasic, Sergio Villicaña, et al.
Nature|July 9, 2025
Selective remodelling of the adipose niche in obesity and weight lossAntonio M A Miranda, Liam McAllan, Guianfranco Mazzei, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Nature Genetics|August 21, 2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationPatrick S Tarpey, F Lucy Raymond, Lam S Nguyen, et al.
Nucleic Acids Research|November 13, 2009
Ensembl's 10th yearPaul Flicek, Bronwen L Aken, Benoit Ballester, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Obesity Surgery|July 26, 2018
Is Pre-operation Social Connectedness Associated with Weight Loss up to 2 Years Post Bariatric Surgery?Urszula Tymoszuk, Meena Kumari, Andrea Pucci, et al.
JAMA Surgery|July 26, 2023
Safety and Efficacy of Liraglutide, 3.0 mg, Once Daily vs Placebo in Patients With Poor Weight Loss Following Metabolic Surgery: The BARI-OPTIMISE Randomized Clinical TrialJessica Mok, Mariam O Adeleke, Adrian Brown, et al.
Nature Medicine|May 22, 2026
Semaglutide versus placebo in individuals with poor weight loss after bariatric surgery: a double-blinded, randomized, placebo-controlled trialChloe Stanley, Ritwika Mallik, Nausheen Hamid, et al.
Nature Communications|May 15, 2023
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetesLiam McAllan, Damir Baranasic, Sergio Villicaña, et al.
Nature|July 9, 2025
Selective remodelling of the adipose niche in obesity and weight lossAntonio M A Miranda, Liam McAllan, Guianfranco Mazzei, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Nature Genetics|August 21, 2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationPatrick S Tarpey, F Lucy Raymond, Lam S Nguyen, et al.
Nucleic Acids Research|November 13, 2009
Ensembl's 10th yearPaul Flicek, Bronwen L Aken, Benoit Ballester, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Pageof 4