James L. Resnick

University of Florida — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

29h-index3.6kcitations62works2.32yr avg
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Research Topics

Genetic Syndromes and Imprinting(33), Epigenetics and DNA Methylation(26), Prenatal Screening and Diagnostics(10), Genetics and Neurodevelopmental Disorders(10), Pluripotent Stem Cells Research(8)

Publications62 total

The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome
2025· 1 citedOpen Access
A novel early onset spinocerebellar ataxia 13 BAC mouse model with cerebellar atrophy, tremor, and ataxic gait
EXPERIMENTAL ANIMALS·2025Open Access
A Novel Early Onset Spinocerebellar Ataxia 13 BAC Mouse Model with Cerebellar Hypoplasia, Tremor, and Ataxic Gait
2024Open Access
Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2024· 8 citedOpen Access
Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
2023Open Access
RF17 | PMON27 Genetic Subtype Differences in Relation to Health Problems Among Adults With Prader-Willi Syndrome
Journal of the Endocrine Society·2022Open Access
Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature
Journal of Clinical Medicine·2022· 21 citedOpen Access
Genetic subtype differences in relation to health problems among adults with Prader-Willi syndrome
Endocrine Abstracts·2022
Towards the Use of Primordial Germ Cells for Germline Modification
2022· 2 cited
The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature
Genes·2021· 33 citedOpen Access
Role of Epigenetic Mechanisms in Transmitting the Effects of Neonatal Sevoflurane Exposure to the Next Generation of Male, but not Female, Rats
Obstetric Anesthesia Digest·2019· 2 cited
A mouse model of Angelman syndrome imprinting defects
Human Molecular Genetics·2018· 20 citedOpen Access
Prader–Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN
Human Molecular Genetics·2018· 25 citedOpen Access
Role of epigenetic mechanisms in transmitting the effects of neonatal sevoflurane exposure to the next generation of male, but not female, rats
British Journal of Anaesthesia·2018· 60 cited
Prader-Willi locus <i>Snord116</i> RNA processing requires an active endogenous allele and neuron-specific splicing by <i>Rbfox3/NeuN</i>
2018Open Access
Paradoxical leanness in the imprinting-centre deletion mouse model for Prader–Willi syndrome
Journal of Endocrinology·2016· 21 citedOpen Access
The imprinted ncRNA, UBE3A-ATS regulates the chromatin architecture of MAGEL2 and NDN locus over long distance.
日本分子生物学会/日本生化学会·2015
Correction for Lewis et al., Angelman syndrome imprinting center encodes a transcriptional promoter
Proceedings of the National Academy of Sciences·2015· 2 citedOpen Access
Angelman syndrome imprinting center encodes a transcriptional promoter
Proceedings of the National Academy of Sciences·2014· 40 citedOpen Access
Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain
Epigenetics·2014· 15 citedOpen Access
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Frequent Co-authors

Karen A. Johnstone(9), Peter J. Donovan(7), Camilynn I. Brannan(6), Amanda J. DuBose(6), Emily Y. Smith(5), Thomas P. Yang(5), Raquel Sussman(5), Linzhao Cheng(3), Danielle M. Maatouk(3), Michael W. Lewis(3), Jason O. Brant(3), Douglas E. Williams(2), Mary K. Ernst(2), Leslie F. Lock(2), Stewart D. Lyman(2), Rachel Wevrick(2), Marisa S. Bartolomei(2), B A Boyd(2), Christopher R. Futtner(2), Michael D. Elmore(2)