Caylor, Raymond

Assistant Director, Molecular Diagnostic Laboratory

Caylor, Raymond

Dr. Caylor joined the Greenwood Genetic Center as Assistant Director of the Molecular Diagnostic Laboratory in 2018. Before coming to the Greenwood Genetic Center, Dr. Caylor completed his Clinical Molecular Genetics and Genomics fellowship training at Children’s Mercy Hospital, Kansas City, MO. He is a member of the American College of Medical Genetics and Genomics, the American Society of Human Genetics, and the European Society of Human Genetics.

Contact Information

Office: (864) 941-8171
Fax: (864) 941-8141
rcaylor@ggc.org

Education

  • B.S. (Health Science) Valley City State University, Valley City, ND, 2007 
  • Ph.D. (Molecular, Cellular, and Developmental Biology) University of Kansas, 2014
  • Postdoctoral Fellow, Department of Molecular Biosciences, University of Kansas, 2015
  • Clinical Molecular Genetics and Genomics Fellow – Children’s Mercy Hospital, Kansas City, MO, 2016-2018
  • Assistant Director, Molecular Diagnostic Laboratory, Greenwood Genetic Center, 2018

Selected Publications

  • Isabelle Thiffault, Maxime Cadieux-Dion, Emily Farrow, Raymond Caylor, Neil Miller, Sarah Soden, Carol Saunders (Accepted: Human Mutation). On the verge of diagnosis: Detection, reporting, and investigation of de novo variants in novel genes by clinical sequencing.
  • Isabelle Thiffault, Emily Farrow, Lee Zellmer, Courtney Berrios, Neil Miller, Margaret Gibson, Raymond Caylor, Janda Jenkins, Deb Faller, Sarah Soden, Carol Saunders (Published online: Genetics in Medicine). Clinical Whole Genome Sequencing in an Unbiased Pediatric Cohort.
  • R.C. Caylor, L. Grote, I. Thiffault, E. Farrow, L. Willig, S. Soden, S.M. Amudhavalli, A.J. Nopper, K.A. Horii, E. Fleming, J. Jenkins, H. Welsh, M. Ilyas, K. Engleman, A. Abdelmoity and C. Saunders (Published online: neurogenetics). Tuberous sclerosis as an atypical or incidental diagnosis in three families.
  • Caylor, R.C., Jin, Y., & Ackley, B. D. (2013). The Caenorhabditis elegans voltage-gated calcium channel subunits UNC-2 and UNC-36 and the calcium-dependent kinase UNC-43/CaMKII regulate neuromuscular junction morphology. Neural Dev, 8, 10. doi: 10.1186/1749-8104-8-10

 

Meet The Jones Family

Meet The Jones Family

The journey to becoming parents did not start as an easy one for my husband and I. We suffered the heartache of miscarriage and the unimaginable pain of burying our first born child. Our son, sweet 1 lb 1.4 ounce, 12 inches long, teeny, tiny little Joseph “Hamilton” Jones was born with spina bifida, hydrocephalus, and a heart defect. It tore our hearts out leaving the hospital without him, knowing our dreams and hope for the future were shattered. ...

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