Albers S, Waisbren SE, Ampola MG, Brewster TG, Burke LW, Demmer LA, Filiano J, Greenstein RM, Ingham CL, Korson MS, Marsden D, Schwartz RC, Seashore MR, Shih VE, Levy HL. (2001) New England Consortium: a model for medical evaluation of expanded newborn screening with tandem mass spectrometry. J Inherit Metab Dis. 24:303-204.

Pilarski R, Greenstein RM. (1998) Cancer gene testing? Conn Med. 62:248.

Pilarski RT, Greenstein RM, Benn P. (1995) Developing a role for genetics within a cancer program. Ann N Y Acad Sci. 768:258-60.

Benn PA, Horne D, Briganti S, Greenstein RM. (1995) Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome. Am J Obstet Gynecol. 173:496-501.

Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA. (1994) Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome. Am J Med Genet. 52:85-91.