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Clinical Assistant Professor

Division Chief Medical Genetics and Genomics

Spectrum Health Helen DeVos Children's Hospital

Email
 

Education & Training

Medical Genetics Residency, Greenwood Genetic Center, Greenwood, SC, USA (2012 - 2014)

Pediatrics Residency, University of Louisville, Louisville, KY, USA (2009 - 2012)

MD, University of Toledo, Toledo, OH, USA (2005 - 2009)

BS, Grove City College, Grove City, PA, USA (2001- 2005)



    Selected Grants

    Children's Foundation - Rapid Whole Genome Sequencing

    Selected Peer-Reviewed Publications

    Bupp C, Schultz CR, Uhl KL, Rajasekaran S, Bachmann AS.  Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features.  American Journal of Medical Genetics – accepted for publication

    Prokop JW, May T, Strong K, Bilinovich SM, Bupp C, Rajasekaran S, Worthey EA, Lazar J.  Genome Sequencing in the Clinic: The Past, Present, and Future of Genomic Medicine. Physiological Genomics, 2018.

    Spellicy CJ, Norris J, Bend R, Bupp C, Mester P, Reynolds T, Dean J, Peng Y, Alexov E, Schwartz CE, Stevenson RSJ Friez M. Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects. European Journal of Human Genetics, 2018.

    Anazi S, Maddirevula S, Salpietro V, Asi YT, Alsahli S, Alhashem A, Shamseldin HE, AlZahrani F, Patel N, Ibrahim N, Abdulwahab FM, Hashem M, Alhashmi N, Al Murshedi F, Al Kindy A, Alshaer A, Rumayyan A, Al Tala S, Kurdi W, Alsaman A, Alasmari A, Banu S, Sultan T, Saleh MM, Alkuraya H, Salih MA, Aldhalaan H, Ben-Omran T, Al Musafri F, Ali R, Suleiman J, Tabarki B, El-Hattab AW, Bupp C, Alfadhel M, Al Tassan N, Monies D, Arold ST, Abouelhoda M, Lashley T, Houlden H, Faqeih E, Alkuraya FS. Expanding the genetic heterogeneity of intellectual disability. Human Genetics, 2017.

    Ma L, Bayram Y, McLaughlin HM, Cho MT, Krokosky A, Turner CE, Lindstrom K, Bupp CP, Mayberry K, Mu W, Bodurtha J, Weinstein V, Zadeh N, Alcaraz W, Powis Z, Shao Y, Scott DA, Lewis AM, White JJ, Jhangiani SN, Gulec EY, Lalani SR, Lupski JR, Retterer K, Schnur RE, Wentzensen IM, Bale S, Chung WK. De novo missense variants in PPP1CB are associated with intellectual disabilities and congenital heart disease. Human Genetics, 2016.

    Bupp CP, Sarasua SM, Dean JH, Stevenson RE.  When folic acid fails: Insights from 20 years of neural tube defect surveillance in South Carolina.  American Journal of Medical Genetics, 2015. Article featured on cover.

    Bupp CP, Demmer LA, Saul RA.  Surveying the current landscape of clinical genetics residency training. Genetics in Medicine, 2015.

    Lindy AS, Bupp CP, McGee SJ, Basehore MJ, Stevenson RE, Friez MJ.  Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndrome.  American Journal of Medical Genetics, 2014.