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Jennelle C. Hodge, Ph.D. - Publications

Affiliations: 
2003 Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Molecular Biology, Cell Biology
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32 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
2018 Hodge JC, Cooley L, Chen H, Yang F, Pitel B, Sathanoori M, Davis B, Corboy G, Griffith O, Baughn L, Newman S, Wolff DJ. 5. Progress and future of the compendium of Cancer Genome Aberrations (CCGA) Cancer Genetics and Cytogenetics. 37-38. DOI: 10.1016/J.Cancergen.2018.04.066  0.308
2016 Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, et al. The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature Genetics. PMID 27841880 DOI: 10.1038/Ng.3720  0.382
2016 Hodge JC, Bedroske PB, Pearce KE, Sukov WR. 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. PMID 27154512 DOI: 10.1016/J.Jmoldx.2016.02.001  0.344
2015 Schoolmeester JK, Sciallis AP, Greipp PT, Hodge JC, Dal Cin P, Keeney GL, Nucci MR. 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. PMID 26444253 DOI: 10.1097/Pgp.0000000000000187  0.332
2015 Mitchell E, Douglas A, Kjaegaard S, Callewaert B, Vanlander A, Janssens S, Lawson Yuen A, Skinner C, Failla P, Alberti A, Avola E, Fichera M, Kibaek M, Digilio MC, Hannibal MC, ... ... Hodge JC, et al. Recurrent duplications of 17q12 associated with variable phenotypes. American Journal of Medical Genetics. Part A. PMID 26420380 DOI: 10.1002/Ajmg.A.37351  0.381
2015 Brand H, Collins RL, Hanscom C, Rosenfeld JA, Pillalamarri V, Stone MR, Kelley F, Mason T, Margolin L, Eggert S, Mitchell E, Hodge JC, Gusella JF, Sanders SJ, Talkowski ME. Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. American Journal of Human Genetics. 97: 170-6. PMID 26094575 DOI: 10.1016/J.Ajhg.2015.05.012  0.324
2015 Cuturilo G, Hodge JC, Runke CK, Thorland EC, Al-Owain MA, Ellison JW, Babovic-Vuksanovic D. Phenotype analysis impacts testing strategy in patients with Currarino syndrome. Clinical Genetics. PMID 25691298 DOI: 10.1111/Cge.12572  0.361
2015 Hand JL, Runke CK, Hodge JC. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray. Journal of the American Academy of Dermatology. 72: 617-27. PMID 25659225 DOI: 10.1016/J.Jaad.2014.12.020  0.349
2014 Chen X, Wang J, Mitchell E, Guo J, Wang L, Zhang Y, Hodge JC, Shen Y. 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. PMID 25135225 DOI: 10.1186/S12881-014-0090-9  0.348
2014 Hodge JC, Pearce KE, Clayton AC, Taran FA, Stewart EA. Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity. American Journal of Obstetrics and Gynecology. 210: 572.e1-7. PMID 24412114 DOI: 10.1016/J.Ajog.2014.01.011  0.321
2014 Lionel AC, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B, Fagerberg C, Laulund LW, Pellecchia G, ... ... Hodge JC, et al. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Human Molecular Genetics. 23: 2752-68. PMID 24381304 DOI: 10.1093/Hmg/Ddt669  0.353
2014 Mullegama SV, Rosenfeld JA, Orellana C, van Bon BW, Halbach S, Repnikova EA, Brick L, Li C, Dupuis L, Rosello M, Aradhya S, Stavropoulos DJ, Manickam K, Mitchell E, Hodge JC, et al. Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder. European Journal of Human Genetics : Ejhg. 22: 57-63. PMID 23632792 DOI: 10.1038/Ejhg.2013.67  0.394
2014 Hodge JC, Mitchell E, Pillalamarri V, Toler TL, Bartel F, Kearney HM, Zou YS, Tan WH, Hanscom C, Kirmani S, Hanson RR, Skinner SA, Rogers RC, Everman DB, Boyd E, et al. Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities. Molecular Psychiatry. 19: 368-79. PMID 23587880 DOI: 10.1038/Mp.2013.42  0.393
2013 Schoolmeester JK, Sukov WR, Maleszewski JJ, Bedroske PP, Folpe AL, Hodge JC. JAZF1 rearrangement in a mesenchymal tumor of nonendometrial stromal origin: report of an unusual ossifying sarcoma of the heart demonstrating JAZF1/PHF1 fusion. The American Journal of Surgical Pathology. 37: 938-42. PMID 23629446 DOI: 10.1097/Pas.0B013E318282Da9D  0.309
2013 Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, ... ... Hodge JC, et al. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Human Molecular Genetics. 22: 2055-66. PMID 23393157 DOI: 10.1093/Hmg/Ddt056  0.304
2013 Handrigan GR, Chitayat D, Lionel AC, Pinsk M, Vaags AK, Marshall CR, Dyack S, Escobar LF, Fernandez BA, Stegman JC, Rosenfeld JA, Shaffer LG, Goodenberger M, Hodge JC, Cain JE, et al. Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation. Journal of Medical Genetics. 50: 163-73. PMID 23335808 DOI: 10.1136/Jmedgenet-2012-101288  0.365
2013 Hoppman-Chaney N, Wain K, Seger P, Superneau D, Hodge J. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype. Clinical Genetics. 83: 345-351. PMID 22775350 DOI: 10.1111/J.1399-0004.2012.01925.X  0.383
2012 Ernst C, Marshall CR, Shen Y, Metcalfe K, Rosenfeld J, Hodge JC, Torres A, Blumenthal I, Chiang C, Pillalamarri V, Crapper L, Diallo AB, Ruderfer D, Pereira S, Sklar P, et al. Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. Archives of General Psychiatry. 69: 1238-46. PMID 23044507 DOI: 10.1001/Archgenpsychiatry.2012.660  0.334
2012 Sukov WR, Hodge JC, Lohse CM, Akre MK, Leibovich BC, Thompson RH, Cheville JC. ALK alterations in adult renal cell carcinoma: frequency, clinicopathologic features and outcome in a large series of consecutively treated patients. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 25: 1516-25. PMID 22743654 DOI: 10.1038/Modpathol.2012.107  0.364
2012 Graham RP, Hodge JC, Folpe AL, Oliveira AM, Meyer KJ, Jenkins RB, Sim FH, Sukov WR. A cytogenetic analysis of 2 cases of phosphaturic mesenchymal tumor of mixed connective tissue type. Human Pathology. 43: 1334-8. PMID 22503486 DOI: 10.1016/J.Humpath.2011.11.020  0.341
2012 Sukov WR, Hodge JC, Lohse CM, Leibovich BC, Thompson RH, Pearce KE, Wiktor AE, Cheville JC. TFE3 rearrangements in adult renal cell carcinoma: clinical and pathologic features with outcome in a large series of consecutively treated patients. The American Journal of Surgical Pathology. 36: 663-70. PMID 22498819 DOI: 10.1097/Pas.0B013E31824Dd972  0.343
2012 Hodge JC, Kim TM, Dreyfuss JM, Somasundaram P, Christacos NC, Rousselle M, Quade BJ, Park PJ, Stewart EA, Morton CC. Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profilingof the t(12;14) and evidence in support of predisposing genetic heterogeneity. Human Molecular Genetics. 21: 2312-29. PMID 22343407 DOI: 10.1093/Hmg/Dds051  0.336
2012 Hodge JC, Hulshizer RL, Seger P, St Antoine A, Bair J, Kirmani S. Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: a skin biopsy should remain the diagnostic gold standard. American Journal of Medical Genetics. Part A. 158: 669-73. PMID 22315202 DOI: 10.1002/Ajmg.A.35209  0.31
2012 Vaags AK, Lionel AC, Sato D, Goodenberger M, Stein QP, Curran S, Ogilvie C, Ahn JW, Drmic I, Senman L, Chrysler C, Thompson A, Russell C, Prasad A, Walker S, ... ... Hodge JC, et al. Rare deletions at the neurexin 3 locus in autism spectrum disorder. American Journal of Human Genetics. 90: 133-41. PMID 22209245 DOI: 10.1016/J.Ajhg.2011.11.025  0.334
2012 Hoppman-Chaney N, Jang JS, Jen J, Babovic-Vuksanovic D, Hodge JC. In-frame multi-exon deletion of SMC1A in a severely affected female with Cornelia de Lange Syndrome. American Journal of Medical Genetics. Part A. 158: 193-8. PMID 22106055 DOI: 10.1002/Ajmg.A.34360  0.351
2012 Xiang B, Leon A, Li MM, Iqbal AM, Li P, Li S, Papenhausen PR, Schwartz S, Zhang X, Geiersbach KB, South S, Gu G, Batanian JR, Lu X, Wolff DJ, ... ... Hodge JC, et al. Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database Cancer Genetics. 205: 420. DOI: 10.1016/J.Cancergen.2012.07.005  0.379
2009 Hodge JC, Park PJ, Dreyfuss JM, Assil-Kishawi I, Somasundaram P, Semere LG, Quade BJ, Lynch AM, Stewart EA, Morton CC. Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis. Genes, Chromosomes & Cancer. 48: 865-85. PMID 19603527 DOI: 10.1002/Gcc.20692  0.394
2009 Hodge JC, T Cuenco K, Huyck KL, Somasundaram P, Panhuysen CI, Stewart EA, Morton CC. Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele. Human Genetics. 125: 257-63. PMID 19132395 DOI: 10.1007/S00439-008-0621-6  0.315
2008 Hodge JC, Quade BJ, Rubin MA, Stewart EA, Dal Cin P, Morton CC. Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids. The American Journal of Pathology. 172: 1403-10. PMID 18403592 DOI: 10.2353/Ajpath.2008.071102  0.337
2007 Hodge JC, Morton CC. Genetic heterogeneity among uterine leiomyomata: insights into malignant progression. Human Molecular Genetics. 16: R7-13. PMID 17613550 DOI: 10.1093/Hmg/Ddm043  0.423
2006 Hwang YS, Hodge JC, Sivapurapu N, Lindholm PF. Lysophosphatidic acid stimulates PC-3 prostate cancer cell Matrigel invasion through activation of RhoA and NF-kappaB activity. Molecular Carcinogenesis. 45: 518-29. PMID 16402387 DOI: 10.1002/Mc.20183  0.573
2003 Hodge JC, Bub J, Kaul S, Kajdacsy-Balla A, Lindholm PF. Requirement of RhoA activity for increased nuclear factor kappaB activity and PC-3 human prostate cancer cell invasion. Cancer Research. 63: 1359-64. PMID 12649199  0.568
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