Masny PS, Bengtsson U, Chung SA, Martin JH, Van Engelen B, Van Der Maarel SM, Winokur ST (2004) Localization of 4q35.2 to the nuclear periphery: Is FSHD a nuclear envelope disease? Hum Mol Genet. 13(17):1857-1871 
Sara Winokur, Yi- Wen Chen (2004) "Expression Profiling Of FSHD"
Book: Facioscapulohumeral Muscular Dystrophy (FSHD): Clinical Medicine and Molecular Cell Biology.
Editors: M. Upadhyaya & D.N. Cooper
Petra G M van Overveld,
Richard J F L Lemmers, Lodewijk A Sandkuijl, Leo Enthoven, Sara
T Winokur, Floor Bakels, George
W Padberg,
Gert-Jan B van Ommen, Rune R Frants & Silvère M van der
Maarel (2003) Hypomethylation of D4Z4 in 4q-linked and non-4q-linked
facioscapulohumeral muscular dystrophy. Nat Genet. 35(4):315-7
Winokur
ST,
Chen Y-W, Masny P, Martin JH, Ehmsen
JE, Tapscott SJ, van der Maarel SM, Hayashi
Y, and Flanigan KM (2003) Expression profiling of FSHD muscle supports
a defect in specific stages
of myogenic differentiation. Hum Mol Genet. 12(22):2895-907 ...... 
Winokur ST,
Barrett K, Martin JH, Forrester JR, Simon M, Tawil R, Chung S-A,
Masny PS and Figlewicz DA (2003) Facioscapulohumeral muscular dystrophy
(FSHD) myoblasts demonstrate increased susceptibility to
oxidative
stress. Neuromuscular Disorders 13(4):322-33 ------
Tsien F, Sun B, Hopkins
NE, Vedanarayanan V, Figlewicz D, Winokur S, and
Ehrlich M (2001) Hypermethylation of the FSHD syndrome-associated
D4Z4 repeat in normal and FSHD somatic cell populations but not in
ICF
syndrome cells. Molecular Genetics and Metabolism 74(3):322-31
Nishizuka, S, Winokur,
ST, Simon, M, Martin, JH, Tsujimoto H and Stanbridge EJ
(2001) Gene expression profiling using synthetic oligonucleotide
arrays
in tumorigenic and non tumorigenic HeLa x human fibroblasts. Cancer
Letters 165 201-209
Parseghian MH, Newcomb
RL, Winokur
ST, Hamkalo BA (2000) The distribution
of somatic H1 subtypes is non-random on active vs. inactive chromatin:
distribution in human fetal fibroblasts.
Chromosome Res8(5):405-24
Winokur,
ST and Shiang
R (1998) The Treacher Collins syndrome (TCOF1) gene product, treacle,
is localized to the nucleolus by signals in its carboxy terminus. Hum
Molecular Genetics 7 (12): 1947-52
Xia H, Winokur,
ST,
Kuo W-L, and Bredt (1997) Actinin-associated LIM protein: identification
of a domain interaction between PDZ and spectrin-like repeat motifs.
J. Cell Biology 139(2):507-15
Winokur,
ST, Bengtsson
U, Vargas JC, Wasmuth JJ and Altherr MR (1996) The evolutionary distribution
and structural organization of the homeobox-containing repeat D4Z4
indicates a functional role for the ancestral copy in the FSHD region.
Hum Molecular Genetics 5:1567-1575
Altherr MR, Bengtsson,
U, Makovich RP and Winokur, ST (1995) Efforts towards
understanding the molecular basis of facioscapulohumeral muscular dystrophy.
Muscle
and Nerve S2: S73-78
Weiffenbach B, Dubois
J, Manning S, Ma NS, Schutte BC, Winokur, ST, Altherr
MR, Jacobsen SJ, Stanton VP Jr,Yokoyama K and Moir D (1994) YAC contigs
for 4q35
in the region of the facioscapulohumeral muscular dystrophy (FSHD)
gene. Genomics 19: 532-541
Bengtsson U, Wasmuth
JJ, Altherr MA and Winokur, ST (1994) High resolution
fluorescence in situ hybridization to linearly extended DNA visually
maps a tandem
repeat associated with facioscapulohumeral muscular dystrophy immediately
adjacent to the telomere of 4q. Human Molecular Genetics 3: 1801-1805
Shiang R, Thompson
LM, Zhu Y-Z, Church DM, Fielder TJ, Bocian M, Winokur, ST and
Wasmuth JJ (1994) Mutations in the transmembrane domain of fibroblast
growth
factor receptor 3 (FGFR3) cause the most common genetic form of dwarfism,
achondroplasia. Cell 78:335-342
Winokur,
ST, Bengtsson
U, Feddersen J, Mathews KD, Markovich R, Weiffenbach B, Bailey H, Murray
JC, Wasmuth JJ, Altherr MR and Schutte BC (1994) The DNA rearrangement
associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated
repetitive element: Implications for a role of chromatin structure
in the pathogenesis of the disease. Chromosome Research 2: 225-234
Weiffenbach B, Dubois
J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell
JR, Winokur, ST, Altherr MR, Schultz P, Olandt S,
Frants RR, Pericak-Vance M and Griggs RC (1993) Recombination events
at 4q35 complicate efforts
to localize the FSHD gene. Nature Genetics 4(2):165-9
Wijmenga C, Winokur,
ST, Frants RR, Scholte HR, Van den Bogert C, Skraastad MI,
Altherr MR, Wasmuth JJ, Murray JC, Hofker MH and Padberg GW (1993)
The human
skeletal muscle adenine nucleotide translocator gene maps to chromosome
4q35 in the region of the facioscapulohumeral muscular dystrophy locus.
Human Genetics 92: 198-203
Winokur,
ST, Schutte
B, Weiffenbach B, Washington S, Chakravarti A, Wasmuth JJ and Altherr
MR (1993) A radiation hybrid map of fifteen loci on the distal long
arm of chromosome 4, the region containing the gene responsible for
facioscapulohumeral muscular dystrophy. American Journal of Human Genetics
53: 874-880
