Founding Fellow (American College of Medical Genetics and Genomics, 1995 - Present)
member (American Society of Human Genentics, 1984 - Present)
Recent Publications
Toriello HV, Erick M, Alessandri JL, Bailey D, Brunetti-Pierri N, Cox H, Fryer A, Marty D, McCurdy C, Mulliken JB, Murphy H, Omlor J, Pauli RM, Ranells JD, Sanchez-Valle A, Tobiasz A, Van Maldergem L, Lin AE. Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease.American Journal of Medical Genetics. Part A. 161A(3) : 417-29, 2013.
Russell Z, Kontopoulos EV, Quintero RA, DeBauche DM, Ranells JD. Prenatal diagnosis of a 4q33-4qter deletion in a fetus with hydrops.Fetal diagnosis and therapy. 24(3) : 250-3, 2008.
Lacson AG, Donaldson G, Barness EG, Ranells JD, Pomerance HH. Infant with high arched palate, bell-shaped chest, joint contractures, and intrauterine fractures.Pediatric pathology & molecular medicine. 21(6) : 569-84, 2002.
Sutcliffe MJ, Mueller OT, Kousseff BG, Dumont DP, McFarland JA, Mawani F, Conforto D, Ranells JD. Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX.American journal of medical genetics. 102(2) : 192-9, 2001.