MitziLeahMurrayMD

PubMed

• 22 citations
  Somatic PDGFRB Activating Variants in Fusiform Cerebral Aneurysms
  Yigit Karasozen, Joshua W. Osbun, Carolina Parada, Tina Busald, Philip D. Tatman, Luis F. Gonzalez-Cuyar, Christopher J. Hale, Diana Alcantara, Mark O'Driscoll, Willia...> ;American Journal of Human Genetics. 2019 May 2
• 10 citations
  Endovascular Repair of Internal Mammary Artery Aneurysms in 2 Sisters with SMAD3 Mutation.
  Daiva Nevidomskyte, Sherene Shalhub, Gabriel S. Aldea, Peter H. Byers, Ulrike Schwarze, Mitzi L. Murray, Benjamin W. Starnes> ;Annals of Vascular Surgery. 2017 May 1
• 6 citations
  Current Practices and the Provider Perspectives on Inconclusive Genetic Test Results for Osteogenesis Imperfecta in Children with Unexplained Fractures: ELSI Implicati...
  Emily Youngblom, Mitzi L. Murray, Peter H. Byers> ;The Journal of Law, Medicine & Ethics. 2016 Sep 1
• 49 citations
  The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories
  Melanie Pepin, Mitzi L. Murray, Samuel S. Bailey, Dru Leistritz-Kessler, Ulrike Schwarze, Peter H. Byers> ;Genetics in Medicine. 2016 Jan 1
• 267 citations
  Actionable exomic incidental findings in 6503 participants: challenges of variant classification
  Laura M. Amendola, Michael O. Dorschner, Peggy D. Robertson, Joseph Salama, Ragan Hart, Brian H. Shirts, Mitzi L. Murray, Mari Tokita, Carlos J. Gallego, Daniel Seung ...> ;Genome Research. 2015 Mar 1
• 22 citations
  FKBP14-related Ehlers-Danlos syndrome: Expansion of the phenotype to include vascular complications
  Mitzi L. Murray, Margaret H. Yang, Christine Fauth, Peter H. Byers> ;American Journal of Medical Genetics. Part A. 2014 Jul 1
• 85 citations
  Pregnancy-related deaths and complications in women with vascular Ehlers–Danlos syndrome
  Mitzi L. Murray, Melanie Pepin, Suzanne Peterson, Peter H. Byers> ;Genetics in Medicine. 2014 Jun 12
• 39 citations
  Ehlers-Danlos syndrome: a showcase of conditions that lead to understanding matrix biology.
  Peter H. Byers, Mitzi L. Murray> ;Matrix Biology. 2014 Jan 1
• 92 citations
  The genetic basis of DOORS syndrome: an exome-sequencing study.
  Philippe M. Campeau, Dalia Kasperaviciute, James T. Lu, Lindsay C. Burrage, Choel Kim, Mutsuki Hori, Berkley R. Powell, Fiona Stewart, Têmis Maria Félix, Jenneke van d...> ;The Lancet. Neurology. 2014 Jan 1
• Heritable collagen disorders: the paradigm of the ehlers-danlos syndrome.
  Byers, P. H., Murray, M. L.> ;J Invest Dermatol. 2012 Nov
• 98 citations
  Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions
  Mitzi L. Murray, Felecia Cerrato, Robin L. Bennett, Gail P. Jarvik> ;Genetics in Medicine. 2011 Dec 1
• 18 citations
  Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III
  Gordana Juric-Sekhar, Raj P. Kapur, Ian A. Glass, Mitzi L. Murray, Shawn E. Parnell, Robert F. Hevner> ;Acta Neuropathologica. 2011 Apr 1
• 49 citations
  Phenotypic and genotypic analyses of genetic skin disease through the Online Mendelian Inheritance in Man (OMIM) database.
  Jamison D. Feramisco, Ruslan I. Sadreyev, Mitzi L. Murray, Nick V. Grishin, Hensin Tsao> ;The Journal of Investigative Dermatology. 2009 Nov 1
• 308 citations
  Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
  Pawel Stankiewicz, Partha Sen, Samarth Bhatt, Mekayla Storer, Zhilian Xia, Bassem A. Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J. Driscoll, Juan Bolivar, Mislen ...> ;American Journal of Human Genetics. 2009 Jun 12
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