Saunders CJ, Farrow EG, and Rush ET. Variant Reinterpretation: Examining Clinical Practices of Returning Genetic Test Results. Next Generation Dx Summit. Washington, DC. 22 August 2018.
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Rush ET. X-linked Hypophosphatemia. AACE Regional Conference. Tulsa, OK. 10 August 2018.
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Rush ET. What we have learned about Treatment of Osteogenesis Imperfecta in the Past 20 Years. Bacon Endocrinology Distinguished Lecture, University of Michigan. Ann Arbor, MI. 1 May 2018.
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Rush ET. Overview of Hypophosphatasia and CNS Pathology. Neurology in Hypophosphatasia Meeting. Boston, MA. 14 October 2017.
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Rush ET. Genetic Approach to Skeletal Dysplasias. Perinatology-Neonatology Conference. Children’s Mercy Kansas City. Kansas City, MO. 9 October 2017.
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Rush ET. Genetic Testing for the Busy Clinician. Department of Internal Medicine Grand Rounds. University of Kansas Medical Center. Kansas City, KS. 6 September 2017.
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Rush ET. Bone Disease in Zellweger Spectrum Disorders. United Leukodystrophies Foundation Annual Meeting. Omaha, NE. 29 July 2016.
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Rush ET. Bone Disease in Zellweger Spectrum Disorders. Global Foundation for Peroxisomal Disorders Board Meeting. Baltimore, MD. 5 June 2016.
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Rush ET. Genetic Disorders after Birth. 42nd Annual Perinatal Conference. St. Luke’s Hospital, Sioux City, IA. 11 May 2016.
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Rush ET. Diagnosis and Management of Adult Genetic Disorders. Prevention Genetics Noon Conference Series, Marshfield, WI. 18 May 2016.
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Rush ET. A Crash Course in Modern Genetics and Genomics. Hospital Administrators Roundtable. University of Nebraska Medical Center. Omaha, NE. 29 April 2016.
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Rush ET, Goodwin JL, Kreikemeier RM, Li L, Craft M, Danford DA, and Kutty S. Echocardiography of Pediatric Patients with Osteogenesis Imperfecta Shows Early Changes of Aortic Dilation. Presented at the OI Scientific Meeting. 2016 14 April; Chicago, IL.
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Kishnani P, Rush ET, and Case L. Hypophosphatasia – Emerging Therapies and Clinical Implications. American College of Medical Genetics Annual Meeting. Tampa, FL. 8-12 March 2016
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Rush ET. The Future of Genetic Medicine. 19th Annual Practical Pediatrics: 2016 Update Conference. Omaha, NE. 4 March 2016.
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Recent Publications
Tam A, Chen S, Schauer E, Grafe I, Bandi V, Shapiro JR, Steiner RD, Smith PA, Bober MB, Hart T, Cuthbertson D, Krischer J, Mullins M, Byers PH, Sandhaus RA, Durigova M, Glorieux FH, Rauch F, Sutton VR, Lee B; Members of the Brittle Bone Disorders Consortium., Rush ET, Nagamani SCS. A Multicenter Study to Evaluate Pulmonary Function in Osteogenesis Imperfecta. Clin Genet. 2018 Sep 24.
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Rush ET. Childhood hypophosphatasia: to treat or not to treat. Orphanet J Rare Dis. 2018 Jul 16;13(1):116.
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Ross M, Sofronsecu AG, Rush E, and Goldner W. Spurious Testosterone Laboratory Results in a Patient Taking Synthetic Alkaline Phosphatase (Asfotase alfa). Clin Biochem. 2018 Aug;58:118-121.
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Wu C, Econs MJ, DiMeglio LA, Insogna KL, Levine MA, Orchard PJ, Miller WP, Petryk A, Rush ET, Shoback DM, Ward LM, Polgreen LE. Diagnosis and Management of Osteopetrosis: Consensus Guidelines from the Osteopetrosis Working Group. J Clin Endocrinol Metab. 2017 Sep 1;102(9):3111-3123.
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Kishnani PS, Rush ET, Arundel P, Dahir K, Fraser W, Harmatz P, Linlart A, Munns CF, Nunes ME, Saal HM, Seefried L, and Ozono K. Monitoring Guidance for Patients With Hypophosphatasia Treated With Asfotase Alfa. Mol Genet Metab. 2017 Sep;122(1-2):4-17
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Rush ET, Baker CV, and Rizzo WB. Dolichol Kinase Deficiency (DOLK-CDG): Two New Cases and Expansion of Phenotype. Am J Med Genet A. 2017 Sep;173(9):2428-2434.
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Kreikemeier RM, Gosnell HN, Halbur L, Rush ET. Retrospective Review of Initial Bisphosphonate Infusion in Inpatient versus Outpatient Setting for Bisphosphonate Naïve Patients. J Pediatr Endocrinol Metab. 2017 Oct 26;30(10):1105-1110.
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Fadus MC, Rush ET, and Lettieri CK. Syndrome of Progressive Bone Marrow Failure and Pancreatic Insufficiency Remains Cryptic Despite Whole Exome Sequencing: Variant of Schwachman-Diamond Syndrome or New Condition? Clin Case Rep. 2017 Apr 4;5(6):748-752.
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Bhatti D, Balasetti V, Malgireddy K, Rush ET, Torres-Russotto D. Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at Chromosome 18q22.1 and Chromosome 13q12.3-q13.1. Parkinsonism Relat Disord. 2016 Sep 4. pii: S1353-8020(16)30327-3.
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Rush ET, Goodwin JL, Kreikemeier RM, Li L, Craft M, Danford DA, and Kutty S. Echocardiographic phenotype in osteogenesis imperfecta varies with disease severity. Heart. 2016 Sep 19. pii: heartjnl-2016-310099.​
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Rush ET, Goodwin JL, Braverman NE, and Rizzo WB. Osteoporosis is a Common Feature of Peroxisomal Biogenesis Disorders. Molecular Genetics and Metabolism. 2016;117(1):33-37.
Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines. Mol Genet Metab. 2016 Mar;117(3):313-21.
Newton LE, Abdessalam SF, Raynor SC, Lyden ER, Rush ET, Needelman H, Cusick RA. Neurodevelopmental outcomes of tracheoesophageal fistulas. J Pediatr Surg. 2016 May;51(5):743-7.
Rush ET, Goodwin JL, Braverman NE, Rizzo WB. Reply: Low bone mineral density is a common feature of Zellweger spectrum disorders. Mol Genet Metab Rep. 2016 May 23;7:94-5.
Rush ET. Atypical presentation of mucopolysaccharidosis type IVA. Mol Genet Metab Rep. 2016 Jun 7;8:8-12.
Azzam KA, Rush ET, Nabower AM, Burke B, and Esposito PW. Mid-term results of Percutaneous Osteotomies and Fassier-Duval Nailing in Children with Osteogenesis Imperfecta. J Pediatr Orthop. 2016 Jul 2.
Grossman LS, Harlan A, Rush ET, Goodwin JL, and Esposito PW. Initial Experience with Percutaneous IM Rodding of Humeri in Children with Osteogenesis Imperfecta. J Pediatr Orthop. 2016 Sep 22.
Nampoothiri S, Fernandez-Rebollo E, Yesodharan D, Rush ET, Langman CB, and Jüppner HW. Jansen’s metaphyseal chondrodysplasia due to a heterozygous PTH/PTHrP receptor mutation (H223R) in a mother and her two children: radiographic findings from infancy to adulthood. J Clin Endocrinol Metab. 2016 Jul 13:jc20162054.
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