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Shanxiang Zhang, Ph.D. - Publications

Affiliations: 
2001 Ohio State University, Columbus, Columbus, OH 
Area:
Genetics
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2004 Grewal RP, Zhang S, Ma W, Rosenberg M, Krahe R. Clinical and genetic analysis of a family with PROMM. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 11: 603-5. PMID 15261229 DOI: 10.1016/J.Jocn.2003.09.014  0.537
2004 Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscular Disorders : Nmd. 14: 274-83. PMID 15019706 DOI: 10.1016/J.Nmd.2004.01.002  0.544
2003 Meola G, Sansone V, Perani D, Scarone S, Cappa S, Dragoni C, Cattaneo E, Cotelli M, Gobbo C, Fazio F, Siciliano G, Mancuso M, Vitelli E, Zhang S, Krahe R, et al. Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2). Neuromuscular Disorders : Nmd. 13: 813-21. PMID 14678804 DOI: 10.1016/S0960-8966(03)00137-8  0.494
2003 Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, Thornton CA, Moxley RT, Harper PS, Rogers MT, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, ... ... Zhang S, et al. Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect. American Journal of Human Genetics. 73: 835-48. PMID 12970845 DOI: 10.1086/378566  0.558
2003 Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, Mancinelli E, Rouche A, Hogrel JY, Laforêt P, Maisonobe T, Pellissier JF, Krahe R, Eymard B, Udd B. Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology. 60: 1854-7. PMID 12796551 DOI: 10.1212/01.Wnl.0000065898.61358.09  0.495
2002 Zhang S, Krahe R. Physical and transcript map of a 2-Mb region in Xp22.1 containing candidate genes for X-linked mental retardation and short stature. Genomics. 79: 274-7. PMID 11863356 DOI: 10.1006/Geno.2002.6702  0.476
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