Education

Medical School
School of Medicine. National University of Colombia, Bogota, Colombia, 1999
Residency
Winthrop University Hospital, General Pediatrics Residency, Mineola, New York, 2006-2009
Fellowship
Winthrop University Hospital, Pediatric Endocrinology, Mineola, New York, 2009-2012
Fellowship
University of Alabama at Birmingham Clinical Genetics Fellowship, Birmingham, Alabama, 2012- 2014

Publications

Publication Information

Hnatow T, Rubio N, Evangelista M, Rodriguez-Buritica D, Yafi M. A case of X-linked adrenoleukodystrophy. Colsultant 360. August 24, 2017.

Aggarwal A, Nguyen J, Rivera-Davila M, Rodriguez-Buritica D. Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation. Eur J Med Genet. 2017 Jul;60(7):391-394. doi: 10.1016/j.ejmg.2017.04.012. Epub 2017 Apr 24. PubMed PMID: 28442439.

Aggarwal A, Rodriguez-Buritica DF, Northrup H. Wiedemann-Steiner syndrome: Novel pathogenic variant and review of literature. Eur J Med Genet. 2017 Jun; 60(6):285-288. doi: 10.1016/j.ejmg.2017.03.006. Epub 2017 Mar 27. Review. PubMed PMID: 28359930.

Gabriele M, Vulto-van Silfhout AT, Germain PL, Vitriolo A, Kumar R, Douglas E, Haan E, Kosaki K, Takenouchi T, Rauch A, Steindl K, Frengen E, Misceo D, Pedurupillay CRJ, Stromme P, Rosenfeld JA, Shao Y, Craigen WJ, Schaaf CP, Rodriguez-Buritica D, Farach L, Friedman J, Thulin P, McLean SD, Nugent KM, Morton J, Nicholl J, Andrieux J, Stray-Pedersen A, Chambon P, Patrier S, Lynch SA, Kjaergaard S, Tørring PM, Brasch-Andersen C, Ronan A, van Haeringen A, Anderson PJ, Powis Z, Brunner HG, Pfundt R, Schuurs-Hoeijmakers JHM, van Bon BWM, Lelieveld S, Gilissen C, Nillesen WM, Vissers LELM, Gecz J, Koolen DA, Testa G, de Vries BBA. YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. Am J Hum Genet. 2017 Jun 1;100(6):907-925. doi: 10.1016/j.ajhg.2017.05.006. PubMed PMID: 28575647; PubMed Central PMCID: PMC5473733.

Bashamboo A, Eozenou C, Jorgensen A, Bignon-Topalovic J, Siffroi JP, Hyon C, Tar A, Nagy P, Sólyom J, Halász Z, Paye-Jaouen A, Lambert S, Rodriguez-Buritica D, Bertalan R, Martinerie L, Rajpert-De Meyts E, Achermann JC, McElreavey K. Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. Am J Hum Genet. 2018 Mar 1;102(3):487-493. doi: 10.1016/j.ajhg.2018.01.021. Epub 2018 Feb 22. PubMed PMID: 29478779; PubMed Central PMCID: PMC5985285

Certifications

American Board of Pediatrics, 2010
American Board of Genetics and Genomics, 2015                                                                                                                                                                                    American Board of Pediatrics, Pediatric Endocrinology, 2015