Research output per year
Research output per year
Personal profile
Research interests
Molecular genetic mechanisms of developmental birth defects
Clinical interests
Congenital birth defects, genetic disorders, transport medicine
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Dive into the research topics where Scott Saunders is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Potential risk modifiers for severe intraventricular hemorrhage in very low birthweight infants requiring transport
Morris, H., Magers, N., Saunders, S. & Vesoulis, Z., 2022, In: Journal of Maternal-Fetal and Neonatal Medicine. 35, 15, p. 2988-2991 4 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Addressing medically underserved populations through maternal-fetal transport: a geographic analysis
Rosenbloom, J. I., Nelson, D. M., Saunders, S., Cole, F. S., Chandarlis, J., Macones, G. A. & Cahill, A. G., Sep 1 2020, In: Journal of Maternal-Fetal and Neonatal Medicine. 33, 17, p. 2913-2917 5 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Implementation of Telemedicine in Pediatric and Neonatal Transport
Curfman, A., Groenendyk, J., Markham, C., Quayle, K., Turmelle, M., Tieken, B., Brancato, C. & Saunders, S., Jul 1 2020, In: Air Medical Journal. 39, 4, p. 271-275 5 p.Research output: Contribution to journal › Article › peer-review
14 Scopus citations -
Wise regulates bone deposition through genetic interactions with Lrp5
Ellies, D. L., Economou, A., Viviano, B., Rey, J. P., Paine-Saunders, S., Krumlauf, R. & Saunders, S., May 1 2014, In: PloS one. 9, 5, e96257.Research output: Contribution to journal › Article › peer-review
Open Access17 Scopus citations -
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are Likely Mediated by Complex Low-Copy Repeats
Stankiewicz, P., Kulkarni, S., Dharmadhikari, A. V., Sampath, S., Bhatt, S. S., Shaikh, T. H., Xia, Z., Pursley, A. N., Cooper, M. L., Shinawi, M., Paciorkowski, A. R., Grange, D. K., Noetzel, M. J., Saunders, S., Simons, P., Summar, M., Lee, B., Scaglia, F., Fellmann, F., Martinet, D., & 33 others, Jan 2012, In: Human mutation. 33, 1, p. 165-179 15 p.Research output: Contribution to journal › Article › peer-review
Open Access33 Scopus citations