LGLesley Georger

Lesley Georger

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Lesley Georger has a total of 10 co-authors. Here are the top co-authors by number of shared publications:

  • Alan Posner

    Department of Molecular Biology, Adelson School of Medicine, Ariel University, Ariel 40700, Israel

    1 shared publication
  • Albert Pinhasov

    Department of Molecular Biology, Adelson School of Medicine, Ariel University, Ariel 4070000, Israel

    1 shared publication
  • Colin Hanna

    Behavioral Neuropharmacology and Neuroimaging Laboratory on Addictions, Department of Pharmacology and Toxicology, Clinical Research Institute on Addictions, Jacobs School of Medicine and Biosciences, University at Buffalo, Buffalo, NY 14203, USA

    1 shared publication
  • Fiona Comstock

    Behavioral Neuropharmacology and Neuroimaging Laboratory on Addictions, Department of Pharmacology and Toxicology, Clinical Research Institute on Addictions, Jacobs School of Medicine and Biosciences, University at Buffalo, Buffalo, NY 14203, USA

    1 shared publication
  • John Butsch

    Department of Surgery, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA

    1 shared publication
  • Kenneth Blum

    Department of Molecular Biology, Adelson School of Medicine, Ariel University, Ariel 40700, Israel

    1 shared publication

Latest Publications

  • Open Access

    A Personalized Medicine Approach: Psychosocial and Genetic Risk Assessments Predictors of Bariatric Surgery Outcomes After 3 Years

    by Panayotis K. Thanos, Shtakshe Chatrath, Colin Hanna, Fiona Comstock, John Butsch, Kenneth Blum, Albert Pinhasov, Lucy Mastrandrea, Teresa Quattrin, Lesley Georger, et al.

    Background: This study aimed to further explore the application of genetic risk assessments in 24 metabolic bariatric surgery (MBS) patients to predict weight loss outcomes three years after the procedure. Methods: Participants were assessed using the Genetic Addiction Risk Severity (GARS) test, which evaluates neurogenic polymorphisms linked to addiction and reward deficiency. Genetic and psychosocial data collected prior to surgery were analyzed in relation to post-operative weight loss measures, including weight change, body mass index (BMI), percentage of total weight loss (%TWL), and percentage of expected weight loss (%EWL). The analysis examined associations between specific genetic risk alleles, weight-related outcomes at three to four years post-surgery, and psychosocial trait scores. Results: Spearman’s correlations revealed that the DRD2 risk allele is negatively correlated with 3-year BMI (rs = −0.481, p < 0.05, 95% CI: –0.746 to –0.083). One-way ANOVA indicated that there is a significant difference in 3-year BMI (p = 0.018) between 0 and 1 DRD2 risk allele copy. There is also a significant difference in ∆weight (p = 0.022), ∆BMI (p = 0.014), and %EWL (p = 0.032) among the different SNP expression values of the MAOA risk allele. In addition, Spearman’s correlation revealed that FCQ scores are negatively correlated with ∆BMI (rs = −0.470, p < 0.05, 95% CI: −0.767, −0.005), %TWL (rs = −0.561, p < 0.05, 95% CI: −0.814, −0.129), and %EWL (rs = −0.533, p < 0.05, 95% CI: −0.800, −0.090) at 3 years post-surgery and positively correlated with 3-year weight (rs = 0.576, p < 0.05, 95% CI: 0.151, 0.821) and 3-year BMI (rs = 0.552, p < 0.05, 95% CI: 0.117, 0.810). Lastly, GARS scores are positively correlated with 3-year ∆weight (rs = 0.422, p < 0.05, 95% CI: 0.010, 0.712).