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Daniel J. Driscoll

Affiliations: 
Pediatrics University of Florida College of Medicine 
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"Daniel Driscoll"
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Parents

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Catherine Gardella Palmer grad student 1983 Indiana University Bloomington (GenetiTree)
 (CONSTITUTIVE HETEROCHROMATIN IN HUMAN MEIOSIS)

Children

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Amy Cristine Lossie grad student 1995-2001 University of Florida College of Medicine

Collaborators

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Publications

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Montes AS, Osann KE, Gold JA, et al. (2020) Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome. Genes. 11
Kimonis VE, Tamura R, Gold JA, et al. (2019) Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities. Genes. 10
Butler MG, Kimonis V, Dykens E, et al. (2019) Birth seasonality studies in a large Prader-Willi syndrome cohort. American Journal of Medical Genetics. Part A
Singh P, Mahmoud R, Gold JA, et al. (2018) Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome. Journal of Medical Genetics
Butler MG, Hartin SN, Hossain WA, et al. (2018) Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study. Journal of Medical Genetics
Singh P, Mahmoud R, Gold J, et al. (2018) Perinatal complications associated with Prader-Willi syndrome (PWS) – comparison to the general population and among the different genetic subtypes. Pediatrics. 142: 230-230
Butler MG, Kimonis V, Dykens E, et al. (2017) Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study. American Journal of Medical Genetics. Part A
Burnett LC, LeDuc CA, Sulsona CR, et al. (2016) Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome. The Journal of Clinical Investigation
Burnett LC, LeDuc CA, Sulsona CR, et al. (2016) Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS. Stem Cell Research. 17: 526-530
Manzardo AM, Johnson L, Miller JL, et al. (2016) Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls. American Journal of Medical Genetics. Part A
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