JessicaRoseDuisMD

PubMed

• A novel remote monitoring device recapitulates sleep patterns in angelman syndrome.
  Molly M Crenshaw, Talia Thompson, Robert Carson, Stacey L Simon, Shital Patel, Tal Klap, Jessica Duis> ;Sleep Medicine. 2023 Oct 1
• 2 citations
  Communication practices of parents and unaffected sibling needs in families impacted by a diagnosis of Angelman syndrome.
  Abigail Turnwald, Talia Thompson, Kelly Nori, Jessica Duis> ;American Journal of Medical Genetics. Part A. 2022 Jul 1
• 5 citations
  Neuropsychiatric features of Prader-Willi syndrome.
  Emily Shelkowitz, Marie G Gantz, Ty A Ridenour, Ann O Scheimann, Theresa Strong, Jessica Bohonowych, Jessica Duis> ;American Journal of Medical Genetics. Part A. 2022 May 1
• 1 citations
  Pharmacodynamic Gene Testing in Prader-Willi Syndrome.
  Janice L. Forster, Jessica Duis, Merlin G. Butler> ;Frontiers in Genetics. 2020 Nov 20
• 17 citations
  Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches.
  Merlin G. Butler, Jessica Duis> ;Frontiers in Pediatrics. 2020 May 12
• 12 citations
  Mirtazapine for sleep disturbances in Angelman syndrome: a retrospective chart review of 8 pediatric cases.
  Emily Hanzlik, Sarah A Klinger, Robert P. Carson, Jessica Duis> ;Journal of Clinical Sleep Medicine. 2020 Apr 15
• 39 citations
  Limitations of exome sequencing in detecting rare and undiagnosed diseases
  Kendall J. Burdick, Joy D. Cogan, Lynette Rives, Amy K. Robertson, Mary Koziura, Elly Brokamp, Laura Duncan, Vickie L. Hannig, Jean P. Pfotenhauer, Rena Vanzo, Michael...> ;American Journal of Medical Genetics. Part A. 2020 Mar 19
• 7 citations
  Evaluation of the safety and tolerability of a nutritional Formulation in patients with ANgelman Syndrome (FANS): study protocol for a randomized controlled trial.
  Donna L. Herber, Edwin J. Weeber, Dominic P. D’Agostino, Jessica Duis> ;Trials. 2020 Jan 9
• 12 citations
  Preserved expressive language as a phenotypic determinant of Mosaic Angelman Syndrome
  Robert P. Carson, Lynne M. Bird, Anna Childers, Ferrin C. Wheeler, Jessica Duis> ;Molecular Genetics & Genomic Medicine. 2019 Aug 10
• 4 citations
  Juvenile idiopathic arthritis associated with a mutation in GATA3.
  Anna E. Patrick, Wei Wang, Elly Brokamp, Thomas Brent Graham, Thomas M. Aune, Jessica Duis> ;Arthritis Research & Therapy. 2019 Jun 25
• 40 citations
  A multidisciplinary approach to the clinical management of Prader-Willi syndrome.
  Jessica Duis, Pieter Joost van Wattum, Ann O. Scheimann, Parisa Salehi, Elly Brokamp, Laura Fairbrother, Anna Childers, Althea Robinson Shelton, Nathan C. Bingham, Ash...> ;Molecular Genetics & Genomic Medicine. 2019 Jan 29
• 9 citations
  A closer look at ARSA activity in a patient with metachromatic leukodystrophy.
  Kathleen M. Doherty, S. Barron Frazier, Matthew Clark, Anna Childers, Sumit Pruthi, David A. Wenger, Jessica Duis> ;Molecular Genetics and Metabolism Reports. 2019 Feb 20
• 8 citations
  Effect of Genotype and Maternal Affective Disorder on Intronic Methylation of FK506 Binding Protein 5 in Cord Blood DNA.
  Jessica Duis, Olivia Cox, Yuelong Ji, Fayaz Seifuddin, Richard S. Lee, Xiaobin Wang> ;Frontiers in Genetics. 2018 Dec 17
• 9 citations
  Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1A.
  Katia M. Perez, Evon B. Lee, Sachini Kahanda, Jessica Duis, Monica Reyes, Harald Jüppner, Ashley H. Shoemaker> ;American Journal of Medical Genetics. Part A. 2018 Feb 1
• Premature Identical Twin Neonates With Sleep Apnea.
  Anirudh Ramesh, Johanna Diaz, Lawrence M. Nogee, Jessica Duis, Dae Song Jang, Cathleen Lawson, Gustavo Maegawa> ;Clinical Pediatrics. 2017 Mar 20
• 38 citations
  KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction.
  Jessica Duis, Shannon L. Dean, Carolyn D. Applegate, Amy Harper, Rui Xiao, Weimin He, James D. Dollar, Lisa R. Sun, Marta Biderman Waberski, Thomas O. Crawford, Ada Ha...> ;Annals of Neurology. 2016 Aug 24
• 5 citations
  The management of pregnancy and delivery in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
  Angela Pipitone, Donna B. Raval, Jessica Duis, Hilary J. Vernon, Regina Martin, Ada Hamosh, David Valle, Meral Gunay-Aygun> ;American Journal of Medical Genetics. Part A. 2016 Jun 1
• 79 citations
  Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations
  Seema R. Lalani, Pengfei Liu, Jill A. Rosenfeld, Levi B. Watkin, Theodore Chiang, Magalie S. Leduc, Wenmiao Zhu, Yan Ding, Shujuan Pan, Francesco Vetrini, Christina Y....> ;American Journal of Human Genetics. 2016 Feb 4
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