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Suzanne Schubbert, Ph.D. - Publications

Affiliations: 
2007 Biomedical Sciences University of California, San Francisco, San Francisco, CA 
Area:
Cell Biology, Molecular Biology
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15 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
2010 Rauen KA, Schoyer L, McCormick F, Lin AE, Allanson JE, Stevenson DA, Gripp KW, Neri G, Carey JC, Legius E, Tartaglia M, Schubbert S, Roberts AE, Gelb BD, Shannon K, et al. Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back. American Journal of Medical Genetics. Part A. 152: 4-24. PMID 20014119 DOI: 10.1002/Ajmg.A.33183  0.619
2009 Søvik O, Schubbert S, Houge G, Steine SJ, Norgård G, Engelsen B, Njølstad PR, Shannon K, Molven A. De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Bmj Case Reports. 2009. PMID 21686750 DOI: 10.1136/Bcr.07.2008.0550  0.724
2008 Denayer E, Parret A, Chmara M, Schubbert S, Vogels A, Devriendt K, Frijns JP, Rybin V, de Ravel TJ, Shannon K, Cools J, Scheffzek K, Legius E. Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation. Human Mutation. 29: 232-9. PMID 17979197 DOI: 10.1002/Humu.20616  0.693
2007 Schubbert S, Bollag G, Lyubynska N, Nguyen H, Kratz CP, Zenker M, Niemeyer CM, Molven A, Shannon K. Biochemical and functional characterization of germ line KRAS mutations. Molecular and Cellular Biology. 27: 7765-70. PMID 17875937 DOI: 10.1128/Mcb.00965-07  0.723
2007 Søvik O, Schubbert S, Houge G, Steine SJ, Norgård G, Engelsen B, Njølstad PR, Shannon K, Molven A. De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Journal of Medical Genetics. 44: e84. PMID 17601930 DOI: 10.1136/Jmg.2007.049361  0.721
2007 Schubbert S, Shannon K, Bollag G. Hyperactive Ras in developmental disorders and cancer Nature Reviews Cancer. 7: 295-308. PMID 17384584 DOI: 10.1038/Nrc2109  0.701
2007 Schubbert S, Bollag G, Shannon K. Deregulated Ras signaling in developmental disorders: new tricks for an old dog Current Opinion in Genetics and Development. 17: 15-22. PMID 17208427 DOI: 10.1016/J.Gde.2006.12.004  0.723
2007 Schubbert S, Shannon K, Bollag G. Erratum: Hyperactive Ras in developmental disorders and cancer Nature Reviews Cancer. 7: 564-564. DOI: 10.1038/Nrc2175  0.535
2006 Kratz CP, Schubbert S, Bollag G, Niemeyer CM, Shannon KM, Zenker M. Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders. Cell Cycle (Georgetown, Tex.). 5: 1607-11. PMID 16921267 DOI: 10.4161/Cc.5.15.3128  0.747
2006 Schubbert S, Zenker M, Rowe SL, Böll S, Klein C, Bollag G, van der Burgt I, Musante L, Kalscheuer V, Wehner LE, Nguyen H, West B, Zhang KY, Sistermans E, Rauch A, et al. Germline KRAS mutations cause Noonan syndrome. Nature Genetics. 38: 331-6. PMID 16474405 DOI: 10.1038/Ng1748  0.73
2006 Schubbert S, Sovik O, Bollag G, Nguyen H, Rowe SL, Kratz C, Zenker MM, Niemeyer CM, Molven A, Shannon K. Biochemical and Functional Analysis of Germline KRAS Mutations That Cause Disorders of the Noonan Syndrome Spectrum. Blood. 108: 1431-1431. DOI: 10.1182/Blood.V108.11.1431.1431  0.692
2006 Schubbert S, Zenker M, Rowe SL, Böll S, Klein C, Bollag G, Burgt Ivd, Musante L, Kalscheuer V, Wehner L, Nguyen H, West B, Zhang KYJ, Sistermans E, Rauch A, et al. Corrigendum: Germline KRAS mutations cause Noonan syndrome Nature Genetics. 38: 598. DOI: 10.1038/Ng0506-598  0.655
2005 Schubbert S, Lieuw K, Rowe SL, Lee CM, Li X, Loh ML, Clapp DW, Shannon KM. Functional analysis of leukemia-associated PTPN11 mutations in primary hematopoietic cells. Blood. 106: 311-7. PMID 15761018 DOI: 10.1182/Blood-2004-11-4207  0.701
2005 Schubbert S, Zenker M, Rowe SL, Böll S, Klein C, Burgt Ivd, Musante L, Nguyen H, West B, Bollag G, Niemeyer CM, Shannon KM, Kratz CP. Novel Germ Line Mutations in the KRAS2 Gene Cause Noonan Syndrome and Deregulate Hematopoietic Cell Growth. Blood. 106: 1602-1602. DOI: 10.1182/Blood.V106.11.1602.1602  0.739
2004 Loh ML, Vattikuti S, Schubbert S, Reynolds MG, Carlson E, Lieuw KH, Cheng JW, Lee CM, Stokoe D, Bonifas JM, Curtiss NP, Gotlib J, Meshinchi S, Le Beau MM, Emanuel PD, et al. Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis. Blood. 103: 2325-31. PMID 14644997 DOI: 10.1182/Blood-2003-09-3287  0.732
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