Elizabeth M. Petty - Publications

University of Michigan, Ann Arbor, Ann Arbor, MI 
Cell Biology, Genetics, Oncology

53 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
2016 Doyle DL, Awwad RI, Austin JC, Baty BJ, Bergner AL, Brewster SJ, Erby LA, Franklin CR, Greb AE, Grubs RE, Hooker GW, Noblin SJ, Ormond KE, Palmer CG, Petty EM, et al. 2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling. Journal of Genetic Counseling. PMID 27333894 DOI: 10.1007/s10897-016-9984-3  0.76
2013 Murray B, Yashar BM, Uhlmann WR, Clauw DJ, Petty EM. Ehlers-Danlos syndrome, hypermobility type: A characterization of the patients' lived experience. American Journal of Medical Genetics. Part A. 161: 2981-8. PMID 24254846 DOI: 10.1002/Ajmg.A.36293  0.76
2012 Huismann DJ, Sheldon JP, Yashar BM, Amburgey K, Dowling JJ, Petty EM. Quality of life and autonomy in emerging adults with early-onset neuromuscular disorders. Journal of Genetic Counseling. 21: 713-25. PMID 22367485 DOI: 10.1007/S10897-012-9492-Z  0.76
2012 Stanbery L, Petty EM. Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed. Breast Cancer Research : Bcr. 14: 101. PMID 22236777 DOI: 10.1186/bcr3056  0.4
2011 Peterson EA, Stanbery L, Li C, Kocak H, Makarova O, Petty EM. SEPT9_i1 and genomic instability: mechanistic insights and relevance to tumorigenesis. Genes, Chromosomes & Cancer. 50: 940-9. PMID 21910160 DOI: 10.1002/Gcc.20916  0.76
2011 Keller JA, Petty EM. CHFR binds to and regulates MAD2 in the spindle checkpoint through its cysteine-rich domain. Biochemical and Biophysical Research Communications. 409: 389-93. PMID 21575600 DOI: 10.1016/J.Bbrc.2011.04.143  0.76
2011 Potti TA, Petty EM, Lesperance MM. A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD). Human Mutation. 32: 877-86. PMID 21538686 DOI: 10.1002/Humu.21515  0.76
2011 Marvin ML, Mazzoni SM, Herron CM, Edwards S, Gruber SB, Petty EM. AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. American Journal of Medical Genetics. Part A. 155: 898-902. PMID 21416598 DOI: 10.1002/Ajmg.A.33927  0.76
2011 Erson AE, Petty EM. Kidney: Nephroblastoma (Wilms tumor) Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/38390  0.92
2011 Erson AE, Petty EM. TRIM37 (tripartite motif-containing 37) Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/38349  0.92
2011 Erson-Bensan AE, Akman HB, Petty EM. CHFR (checkpoint with fork-head associated and ring finger) Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/38099  0.36
2010 Keller JA, Erson-Bensan AE, Petty EM. Connections between CHFR, the cell cycle, and chemosensitivity: Are they critical in cancer? Cancer Biology & Therapy. 10: 942-4. PMID 21057211 DOI: 10.4161/Cbt.10.9.13876  0.76
2010 Stanbery L, D'Silva NJ, Lee JS, Bradford CR, Carey TE, Prince ME, Wolf GT, Worden FP, Cordell KG, Petty EM. High SEPT9_v1 Expression Is Associated with Poor Clinical Outcomes in Head and Neck Squamous Cell Carcinoma. Translational Oncology. 3: 239-45. PMID 20689765 DOI: 10.1593/Tlo.10109  0.76
2010 Akhavantabasi S, Akman HB, Sapmaz A, Keller J, Petty EM, Erson AE. USP32 is an active, membrane-bound ubiquitin protease overexpressed in breast cancers. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 388-97. PMID 20549504 DOI: 10.1007/S00335-010-9268-4  0.92
2010 Peterson EA, Petty EM. Conquering the complex world of human septins: implications for health and disease. Clinical Genetics. 77: 511-24. PMID 20236126 DOI: 10.1111/J.1399-0004.2010.01392.X  0.76
2009 Erson AE, Petty EM. miRNAs and cancer: New research developments and potential clinical applications. Cancer Biology & Therapy. 8: 2317-22. PMID 20168083 DOI: 10.4161/Cbt.8.24.10765  0.92
2009 Jayaratne TE, Gelman SA, Feldbaum M, Sheldon JP, Petty EM, Kardia SL. The Perennial Debate: Nature, Nurture, or Choice? Black and White Americans' Explanations for Individual Differences. Review of General Psychology : Journal of Division 1, of the American Psychological Association. 13: 24-33. PMID 20072661 DOI: 10.1037/A0014227  0.76
2009 Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, et al. Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Human Molecular Genetics. 18: 1200-8. PMID 19139049 DOI: 10.1093/Hmg/Ddp014  0.76
2009 Gonzalez ME, Makarova O, Peterson EA, Privette LM, Petty EM. Up-regulation of SEPT9_v1 stabilizes c-Jun-N-terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells. Cellular Signalling. 21: 477-87. PMID 19071215 DOI: 10.1016/J.Cellsig.2008.11.007  0.76
2008 Erson AE, Petty EM. MicroRNAs in development and disease. Clinical Genetics. 74: 296-306. PMID 18713256 DOI: 10.1111/J.1399-0004.2008.01076.X  0.92
2008 Privette LM, Petty EM. CHFR: A Novel Mitotic Checkpoint Protein and Regulator of Tumorigenesis. Translational Oncology. 1: 57-64. PMID 18633460 DOI: 10.1593/Tlo.08109  1
2008 Privette LM, Weier JF, Nguyen HN, Yu X, Petty EM. Loss of CHFR in human mammary epithelial cells causes genomic instability by disrupting the mitotic spindle assembly checkpoint. Neoplasia (New York, N.Y.). 10: 643-52. PMID 18592005 DOI: 10.1593/Neo.08176  1
2007 Sharma MR, Petty EM, Lesperance MM. Airway obstruction caused by PTEN hamartoma (Bannayan-Riley-Ruvalcaba) syndrome. Archives of Otolaryngology--Head & Neck Surgery. 133: 1157-60. PMID 18025323 DOI: 10.1001/Archotol.133.11.1157  0.76
2007 Peterson EA, Kalikin LM, Steels JD, Estey MP, Trimble WS, Petty EM. Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 796-807. PMID 17922164 DOI: 10.1007/S00335-007-9065-X  0.76
2007 Gonzalez ME, Peterson EA, Privette LM, Loffreda-Wren JL, Kalikin LM, Petty EM. High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes. Cancer Research. 67: 8554-64. PMID 17875694 DOI: 10.1158/0008-5472.Can-07-1474  0.76
2007 Privette LM, González ME, Ding L, Kleer CG, Petty EM. Altered expression of the early mitotic checkpoint protein, CHFR, in breast cancers: implications for tumor suppression. Cancer Research. 67: 6064-74. PMID 17596595 DOI: 10.1158/0008-5472.Can-06-4109  1
2007 Chao MM, Levine JE, Ruiz RE, Kohlmann WK, Bower MA, Petty EM, Mody RJ. Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation Pediatric Blood and Cancer. 49: 1000-1004. PMID 16333835 DOI: 10.1002/Pbc.20700  0.76
2007 Cole ER, Jayaratne TE, Cecchi LA, Feldbaum M, Petty EM. Vive la difference? Genetic explanations for perceived gender differences in nurturance Sex Roles. 57: 211-222. DOI: 10.1007/S11199-007-9248-7  0.76
2006 Jayaratne TE, Ybarra O, Sheldon JP, Brown TN, Feldbaum M, Pfeffer C, Petty EM. White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians. Group Processes & Intergroup Relations : Gpir. 9. PMID 24260013 DOI: 10.1177/1368430206059863  0.76
2004 Probst FJ, Hedera P, Sclafani AM, Pomponi MG, Neri G, Tyson J, Douglas JA, Petty EM, Martin DM. Skewed X-inactivation in carriers establishes linkage in an X-linked deafness-mental retardation syndrome. American Journal of Medical Genetics. Part A. 131: 209-12. PMID 15389700 DOI: 10.1002/Ajmg.A.30308  0.76
2004 Erson AE, Petty EM. CHFR-associated early G2/M checkpoint defects in breast cancer cells. Molecular Carcinogenesis. 39: 26-33. PMID 14694445 DOI: 10.1002/Mc.10161  0.92
2003 Hedera P, Petty EM, Bui MR, Blaivas M, Fink JK. The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis. Archives of Neurology. 60: 1321-5. PMID 12975303 DOI: 10.1001/Archneur.60.9.1321  0.76
2003 Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Gebarski SS, Lesperance MM. Characterization of a stapes ankylosis family with a NOG mutation. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 24: 210-5. PMID 12621334 DOI: 10.1097/00129492-200303000-00014  0.76
2002 Macara IG, Baldarelli R, Field CM, Glotzer M, Hayashi Y, Hsu SC, Kennedy MB, Kinoshita M, Longtine M, Low C, Maltais LJ, McKenzie L, Mitchison TJ, Nishikawa T, Noda M, ... Petty EM, et al. Mammalian septins nomenclature. Molecular Biology of the Cell. 13: 4111-3. PMID 12475938 DOI: 10.1091/Mbc.E02-07-0438  0.76
2002 Rosenberg MJ, Agarwala R, Bouffard G, Davis J, Fiermonte G, Hilliard MS, Koch T, Kalikin LM, Makalowska I, Morton DH, Petty EM, Weber JL, Palmieri F, Kelley RI, Schäffer AA, et al. Mutant deoxynucleotide carrier is associated with congenital microcephaly. Nature Genetics. 32: 175-9. PMID 12185364 DOI: 10.1038/Ng948  0.76
2002 Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin. American Journal of Human Genetics. 71: 618-24. PMID 12089654 DOI: 10.1086/342067  0.76
2002 Boerkoel CF, Takashima H, John J, Yan J, Stankiewicz P, Rosenbarker L, André JL, Bogdanovic R, Burguet A, Cockfield S, Cordeiro I, Fründ S, Illies F, Joseph M, Kaitila I, ... ... Petty EM, et al. Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia. Nature Genetics. 30: 215-20. PMID 11799392 DOI: 10.1038/Ng821  0.76
2001 Erson AE, Niell BL, DeMers SK, Rouillard JM, Hanash SM, Petty EM. Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells Neoplasia. 3: 521-526. PMID 11774034 DOI: 10.1038/Sj.Neo.7900187  0.76
2001 Rouillard JM, Erson AE, Kuick R, Asakawa J, Wimmer K, Muleris M, Petty EM, Hanash S. Virtual genome scan: a tool for restriction landmark-based scanning of the human genome. Genome Research. 11: 1453-9. PMID 11483587 DOI: 10.1101/Gr.181601  0.92
2001 Martin DM, Gencyuz CF, Petty EM. Systemic lupus erythematosus in a man with Noonan syndrome American Journal of Medical Genetics. 102: 59-62. PMID 11471173 DOI: 10.1002/1096-8628(20010722)102:1<59::Aid-Ajmg1351>3.0.Co;2-O  0.76
2000 Petty EM, Yanik GA, Hutchinson RJ, Alter BP, Schmalstieg FC, Levine JE, Ginsburg D, Robillard JE, Castle VP. Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia Journal of Pediatrics. 137: 882-886. PMID 11113849 DOI: 10.1067/Mpd.2000.109147  0.76
2000 Martin DM, Probst FJ, Camper SA, Petty EM. Characterisation and genetic mapping of a new X linked deafness syndrome. Journal of Medical Genetics. 37: 836-41. PMID 11073537 DOI: 10.1136/Jmg.37.11.836  0.76
2000 Kalikin LM, Sims HL, Petty EM. Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors. Genomics. 63: 165-72. PMID 10673329 DOI: 10.1006/Geno.1999.6077  0.48
1999 Kalikin LM, George RA, Keller MP, Bort S, Bowler NS, Law DJ, Chance PF, Petty EM. An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci. Genomics. 57: 36-42. PMID 10191081 DOI: 10.1006/Geno.1998.5740  0.76
1998 Petty EM, Kalikin LM, Orringer MB, Beer DG. Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: implications for tumorigenesis. Molecular Carcinogenesis. 22: 222-8. PMID 9726814 DOI: 10.1002/(Sici)1098-2744(199808)22:4<222::Aid-Mc3>3.0.Co;2-L  0.48
1997 Kalikin LM, Frank TS, Svoboda-Newman SM, Wetzel JC, Cooney KA, Petty EM. A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors. Oncogene. 14: 1991-4. PMID 9150366 DOI: 10.1038/Sj.Onc.1201013  0.76
1996 Kalikin LM, Qu X, Frank TS, Caduff RF, Svoboda SM, Law DJ, Petty EM. Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25. Genes, Chromosomes & Cancer. 17: 64-8. PMID 8889509 DOI: 10.1002/(Sici)1098-2264(199609)17:1<64::Aid-Gcc10>3.0.Co;2-H  0.76
1996 Merajver SD, Petty EM. Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancer Clinics in Laboratory Medicine. 16: 139-167. PMID 8867588 DOI: 10.1016/S0272-2712(18)30292-0  0.76
1995 Law DJ, Prasad MA, King SE, Spranger KD, Lee YH, Fox RE, Collins EE, Gebuhr TC, Miller DE, Petty EM. Localization of the human estrogen-responsive finger protein (EEP) gene (ZNF147) within a YAC contig containing the myeloperoxidase (MPO) gene. Genomics. 28: 361-3. PMID 8530055 DOI: 10.1006/Geno.1995.1160  0.76
1993 Petty EM, Arnold A, Marx SJ, Bale AE. A pulsed-field gel electrophoresis (PFGE) map of twelve loci on chromosome 11q11-q13 Genomics. 15: 423-425. PMID 8449512 DOI: 10.1006/Geno.1993.1080  0.76
1993 Rosen CL, Novotny EJ, D'Andrea LA, Petty EM. Klippel-Feil sequence and sleep-disordered breathing in two children American Review of Respiratory Disease. 147: 202-204. PMID 8420417 DOI: 10.1164/ajrccm/147.1.202  0.76
1993 Petty EM, Seashore MR, Braverman IM, Spiesel SZ, Smith LT, Milstone LM. Dermatosparaxis in children. A case report and review of the newly recognized phenotype. Archives of Dermatology. 129: 1310-5. PMID 8215497 DOI: 10.1001/archderm.1993.01680310080014  0.76
1992 Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, Hegi ME, Wiseman RW, Petty EM, Bale AE, Olopade OI, Diaz MO, Kwiatkowski DJ, Piepkorn MW, Zone JJ, et al. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22 Science. 258: 1148-1152. PMID 1439824 DOI: 10.1126/Science.1439824  0.76
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