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Sara T. Winokur

Observed names: S T Winokur, S. T. Winokur, S. Winokur, S.T. Winokur, ST Winokur, Sara T Winokur, Sara Winokur, SaraT. Winokur
Observed institutions: Los Alamos National Laboratory, Emory University, University of California, San Francisco, University of California, Irvine, University of Iowa Hospitals and Clinics, University of California San Diego, RIKEN, Massachusetts Institute of Technology
OpenAlex ID: A5110132363
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
1994 · Rita Shiang, Leslie M. Thompson, et al. · Cell · 1,341
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
2003 · Petra G M van Overveld, Richard J F L Lemmers, et al. · Nature Genetics · 436
DUX4 , a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
2007 · Manjusha Dixit, Eugénie Ansseau, et al. · Proceedings of the National Academy of Sciences · 399
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration
2006 · Marina Bakay, Zuyi Wang, et al. · Brain · 338
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Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD)
2009 · Weihua Zeng, Jessica C. de Greef, et al. · PLoS Genetics · 280
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Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
2003 · S. T. Winokur · Human Molecular Genetics · 239
Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice
2017 · Ryan G Lim, Lisa L Salazar, et al. · Nature Neuroscience · 228
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RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy
2009 · Lauren Snider, Amy Asawachaicharn, et al. · Human Molecular Genetics · 228
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Actinin-associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs
1997 · Houhui Xia, Sara T. Winokur, et al. · The Journal of Cell Biology · 222
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Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress
2003 · Sara T Winokur, Kathy Barrett, et al. · Neuromuscular Disorders · 158
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
1994 · Sara T. Winokur, Ulla Bengtsson, et al. · Chromosome Research · 158
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy
2005 · Petra G. M. Van Overveld, Leo Enthoven, et al. · Annals of Neurology · 155
The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus
1998 · S. T. Winokur, R. Shiang · Human Molecular Genetics · 87
The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: Distribution in human fetal fibroblasts
2000 · Missag H. Parseghian, Robert L. Newcomb, et al. · Chromosome Research · 76
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA
2006 · Vassilios Alexiadis, Mary E. Ballestas, et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 72
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region [published erratum appears in Hum Mol Genet 1997 Mar;6(3):502]
1996 · S. Winokur · Human Molecular Genetics · 66
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events
1993 · B. Weiffenbach, J. Dubois, et al. · Nature Genetics · 56
Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei
2009 · Peter S Masny, On Ying A Chan, et al. · European Journal of Human Genetics · 46
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Methylation of the FSHD Syndrome-Linked Subtelomeric Repeat in Normal and FSHD Cell Cultures and Tissues
2001 · Fern Tsien, Baodong Sun, et al. · Molecular Genetics and Metabolism · 44
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus
1993 · Cisca Wijmenga, SaraT. Winokur, et al. · Human Genetics · 34
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
1994 · Ulla Bengtsson, Michael R. Altherr, et al. · Human Molecular Genetics · 32
Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy
1995 · Michael R. Altherr, Ulla Bengtsson, et al. · Muscle & Nerve · 28
A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
1993 · S T Winokur, B Schutte, et al. · PubMed · 27
Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus
1993 · Y. Haraguchi, A.B. Chung, et al. · Genomics · 25
Gene Selection for Multiclass Prediction by Weighted Fisher Criterion
2007 · Jianhua Xuan, Yue Wang, et al. · EURASIP Journal on Bioinformatics and Systems Biology · 23
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Works count: 35
Citation count: 4,849
H-index: 24
I10-index: 28
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