Steve Scherer, Ph.D.

Professor, Department of Molecular and Human Genetics

image: Steve Scherer, Ph.D.Contact information

sscherer@bcm.edu

Publications

2015
Sadd BM, Barribeau SM, Bloch G, de Graaf DC, Dearden P, Elsik CG, et al.. The genomes of two key bumblebee species with primitive eusocial organization. Genome Biol. 2015;16:76.

2014
Rasmussen-Torvik LJ, Stallings SC, Gordon AS, Almoguera B, Basford MA, Bielinski SJ, et al.. Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems. Clin Pharmacol Ther. 2014;96(4):482-9.

Chipman AD, Ferrier DEK, Brena C, Qu J, Hughes DST, Schröder R, et al.. The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima. PLoS Biol. 2014;12(11):e1002005.

Chen Z-X, Sturgill D, Qu J, Jiang H, Park S, Boley N, et al.. Comparative validation of the D. melanogaster modENCODE transcriptome annotation. Genome Res. 2014;24(7):1209-23.

2009
Birney E, Hudson TJ, Green ED, Gunter C, Eddy S, Rogers J, et al.. Prepublication data sharing. Nature. 2009;461(7261):168-70.

Guo D-chuan, Papke CL, Tran-Fadulu V, Regalado ES, Avidan N, Johnson RJay, et al.. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Am J Hum Genet. 2009;84(5):617-27.

Hampton OA, Hollander PDen, Miller CA, Delgado DA, Li J, Coarfa C, et al.. A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome. Genome Res. 2009;19(2):167-77.

Cotton RT, Li D, Scherer SE, Muzny DM, Hodges SE, Catania RL, et al.. Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma. HPB (Oxford). 2009;11(5):435-44.

2008
Ding L, Getz G, Wheeler DA, Mardis ER, McLellan MD, Cibulskis K, et al.. Somatic mutations affect key pathways in lung adenocarcinoma. Nature. 2008;455(7216):1069-75.

Majewski T, Lee S, Jeong J, Yoon D-S, Kram A, Kim M-S, et al.. Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy. Lab Invest. 2008;88(7):694-721.

Richards S, Gibbs RA, Weinstock GM, Brown SJ, Denell R, Beeman RW, et al.. The genome of the model beetle and pest Tribolium castaneum. Nature. 2008;452(7190):949-55.

2007
Pannu H, Tran-Fadulu V, Papke CL, Scherer SE, Liu Y, Presley C, et al.. MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II. Hum Mol Genet. 2007;16(20):2453-62.

Guo D-chuan, Pannu H, Tran-Fadulu V, Papke CL, Yu RK, Avidan N, et al.. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. Nat Genet. 2007;39(12):1488-93.

Lee S, Jeong J, Majewski T, Scherer SE, Kim M-S, Tuziak T, et al.. Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Proc Natl Acad Sci U S A. 2007;104(34):13732-7.

2006
Yang Z, Bowles NE, Scherer SE, Taylor MD, Kearney DL, Ge S, et al.. Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circ Res. 2006;99(6):646-55.

Johnson ME, Cheng Z, V Morrison A, Scherer SE, Ventura M, Gibbs RA, et al.. Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A. 2006;103(47):17626-31.

Scherer SE, Muzny DM, Buhay CJ, Chen R, Cree A, Ding Y, et al.. The finished DNA sequence of human chromosome 12. Nature. 2006;440(7082):346-51.

Kim M-S, Jeong J, Majewski T, Kram A, Yoon D-S, Zhang R-D, et al.. Evidence for alternative candidate genes near RB1 involved in clonal expansion of in situ urothelial neoplasia. Lab Invest. 2006;86(2):175-90.

Muzny DM, Scherer SE, Kaul R, Wang J, Yu J, Sudbrak R, et al.. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 2006;440(7088):1194-8.

2005
Ross MT, Grafham DV, Coffey AJ, Scherer SE, McLay K, Muzny DM, et al.. The DNA sequence of the human X chromosome. Nature. 2005;434(7031):325-37.