This is in progress. Below is a selection of co-authored articles. Eventually a CV will be here as well.

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.
Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST.
Eur J Hum Genet. 2010 Apr;18(4):448-56. Epub 2009 Nov 4.

Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?
Masny PS, Bengtsson U, Chung SA, Martin JH, van Engelen B, van der Maarel SM, Winokur ST.
Hum Mol Genet. 2004 Sep 1;13(17):1857-71. Epub 2004 Jul 6.

Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.
Winokur ST, Chen YW, Masny PS, Martin JH, Ehmsen JT, Tapscott SJ, van der Maarel SM, Hayashi Y, Flanigan KM.
Hum Mol Genet. 2003 Nov 15;12(22):2895-907. Epub 2003 Sep 30.

Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.
Winokur ST, Barrett K, Martin JH, Forrester JR, Simon M, Tawil R, Chung SA, Masny PS, Figlewicz DA.
Neuromuscul Disord. 2003 May;13(4):322-33.

A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.
McPherson JD, Apostol B, Wagner-McPherson CB, Hakim S, Del Mastro RG, Aziz N, Baer E, Gonzales G, Krane MC, Markovich R, Masny P, Ortega M, Vu J, Vujicic M, Church DM, Segal A, Grady DL, Moyzis RK, Spence MA, Lovett M, Wasmuth JJ.
Genome Res. 1997 Sep;7(9):897-909.