David R Deyle, MD

  • 518 Citations
  • 10 Scopus h-Index
20042020
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Fingerprint Dive into the research topics where David R Deyle is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Induced Pluripotent Stem Cells Medicine & Life Sciences
Mesenchymal Stromal Cells Medicine & Life Sciences
Gene Targeting Medicine & Life Sciences
Dependovirus Medicine & Life Sciences
Ehlers-Danlos Syndrome Medicine & Life Sciences
Spumavirus Medicine & Life Sciences
Osteogenesis Imperfecta Medicine & Life Sciences
Virus Integration Medicine & Life Sciences

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Projects 2008 2020

Gene Targeting
Bone Diseases
Osteogenesis
Bone and Bones
Collagen
Osteogenesis Imperfecta
Pluripotent Stem Cells
Mutation
Induced Pluripotent Stem Cells
Gene Targeting
Osteogenesis Imperfecta
Dependovirus
Gene Targeting
Genes
Genetic Therapy

Research Output 2004 2019

  • 518 Citations
  • 10 Scopus h-Index
  • 24 Article
  • 3 Chapter
  • 1 Review article

Fracture incidence in Ehlers-Danlos syndrome – A population-based case-control study

Rolfes, M. C., Deyle, D. R., King, K. S., Hand, J. L., Graff, A. H. & Derauf, C., May 1 2019, In : Child Abuse and Neglect. 91, p. 95-101 7 p.

Research output: Contribution to journalArticle

Ehlers-Danlos Syndrome
Case-Control Studies
Incidence
Population
Medical Record Linkage

Oncolytic Measles Virotherapy and Opposition to Measles Vaccination

Russell, S. J., Babovic-Vuksanovic, D., Bexon, A., Cattaneo, R., Dingli, D., Dispenzieri, A., Deyle, D. R., Federspiel, M. J., Fielding, A., Galanis, E., Lacy, M., Leibovich, B., Liu, M. C., Muñoz-Alía, M., Miest, T. C., Molina, J. R., Mueller, S., Okuno, S. H., Packiriswamy, N., Peikert, T. & 6 others, Raffel, C., Van Rhee, F., Ungerechts, G., Young, P. R., Zhou, Y. & Peng, K. W., Jan 1 2019, In : Mayo Clinic proceedings.

Research output: Contribution to journalReview article

Open Access
Oncolytic Virotherapy
Measles
Vaccination
Measles virus
Immunity
2 Citations (Scopus)

Aortic Root Dilation: Do Patients With Marfan Syndrome Fare Worse Than Those With Marfanoid Features?

Helder, M. R. K., Schaff, H. V., Foley, T. A., Anavekar, N. S., Deyle, D. R., Pochettino, A. & Connolly, H. M., Jan 1 2018, (Accepted/In press) In : Mayo Clinic Proceedings.

Research output: Contribution to journalArticle

Marfan Syndrome
Dilatation
Dissection
Genetic Testing
4 Citations (Scopus)

Arterial tortuosity syndrome: 40 new families and literature review

Beyens, A., Albuisson, J., Boel, A., Al-Essa, M., Al-Manea, W., Bonnet, D., Bostan, O., Boute, O., Busa, T., Canham, N., Cil, E., Coucke, P. J., Cousin, M. A., Dasouki, M., De Backer, J., De Paepe, A., De Schepper, S., De Silva, D., Devriendt, K., De Wandele, I. & 44 others, Deyle, D. R., Dietz, H., Dupuis-Girod, S., Fontenot, E., Fischer-Zirnsak, B., Gezdirici, A., Ghoumid, J., Giuliano, F., Diéz, N. B., Haider, M. Z., Hardin, J. S., Jeunemaitre, X., Klee, E. W., Kornak, U., Landecho, M. F., Legrand, A., Loeys, B., Lyonnet, S., Michael, H., Moceri, P., Mohammed, S., Muiño-Mosquera, L., Nampoothiri, S., Pichler, K., Prescott, K., Rajeb, A., Ramos-Arroyo, M., Rossi, M., Salih, M., Seidahmed, M. Z., Schaefer, E., Steichen-Gersdorf, E., Temel, S., Uysal, F., Vanhomwegen, M., Van Laer, L., Van Maldergem, L., Warner, D., Willaert, A., Collins, T. R., Taylor, A., Davis, E. C., Zarate, Y. & Callewaert, B., Oct 1 2018, In : Genetics in Medicine. 20, 10, p. 1236-1245 10 p.

Research output: Contribution to journalArticle

Blood Vessels
Skin
Newborn Respiratory Distress Syndrome
Electron Microscopy
Diaphragmatic Hernia

Correction to: Arterial tortuosity syndrome: 40 new families and literature review (GENETICS in MEDICINE, (2018), 10.1038/gim.2017.253)

Beyens, A., Albuisson, J., Boel, A., Al-Essa, M., Al-Manea, W., Bonnet, D., Bostan, O., Boute, O., Busa, T., Canham, N., Cil, E., Coucke, P. J., Cousin, M. A., Dasouki, M., De Backer, J., De Paepe, A., De Schepper, S., De Silva, D., Devriendt, K., De Wandele, I. & 44 others, Deyle, D. R., Dietz, H., Dupuis-Girod, S., Fontenot, E., Fischer-Zirnsak, B., Gezdirici, A., Ghoumid, J., Giuliano, F., Baena, N., Haider, M. Z., Hardin, J. S., Jeunemaitre, X., Klee, E. W., Kornak, U., Landecho, M. F., Legrand, A., Loeys, B., Lyonnet, S., Michael, H., Moceri, P., Mohammed, S., Muiño-Mosquera, L., Nampoothiri, S., Pichler, K., Prescott, K., Rajeb, A., Ramos-Arroyo, M., Rossi, M., Salih, M., Seidahmed, M. Z., Schaefer, E., Steichen-Gersdorf, E., Temel, S., Uysal, F., Vanhomwegen, M., Van Laer, L., Van Maldergem, L., Warner, D., Willaert, A., Collins, T. R., Taylor, A., Davis, E. C., Zarate, Y. & Callewaert, B., Jan 1 2018, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalArticle

Names
Arterial Tortuosity Syndrome