Jennelle C. Hodge, Ph.D.
Affiliations: | 2003 | Medical College of Wisconsin, Milwaukee, WI, United States |
Area:
Molecular Biology, Cell BiologyGoogle:
"Jennelle Hodge"Parents
Sign in to add mentor| Paul Lindholm | grad student | 2003 | Medical College of Wisconsin | |
| (Interaction of RhoA and NF-kappaB in the induction of human prostate cancer invasion.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Hodge JC, Cooley L, Chen H, et al. (2018) 5. Progress and future of the compendium of Cancer Genome Aberrations (CCGA) Cancer Genetics and Cytogenetics. 37-38 |
| Redin C, Brand H, Collins RL, et al. (2016) The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature Genetics |
| Hodge JC, Bedroske PB, Pearce KE, et al. (2016) Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors: Discovery of Genetic Complexity by Fluorescence in Situ Hybridization. The Journal of Molecular Diagnostics : Jmd |
| Schoolmeester JK, Sciallis AP, Greipp PT, et al. (2015) Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall. International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists. 34: 576-83 |
| Mitchell E, Douglas A, Kjaegaard S, et al. (2015) Recurrent duplications of 17q12 associated with variable phenotypes. American Journal of Medical Genetics. Part A |
| Brand H, Collins RL, Hanscom C, et al. (2015) Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. American Journal of Human Genetics. 97: 170-6 |
| Cuturilo G, Hodge JC, Runke CK, et al. (2015) Phenotype analysis impacts testing strategy in patients with Currarino syndrome. Clinical Genetics |
| Hand JL, Runke CK, Hodge JC. (2015) The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray. Journal of the American Academy of Dermatology. 72: 617-27 |
| Chen X, Wang J, Mitchell E, et al. (2014) Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks. Bmc Medical Genetics. 15: 90 |
| Hodge JC, Pearce KE, Clayton AC, et al. (2014) Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity. American Journal of Obstetrics and Gynecology. 210: 572.e1-7 |