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Elizabeth Petty

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Darcy J Huismann; Kimberly Amburgey; James Dowling; Jane P Sheldon; Beverly M Yashar; Elizabeth M Petty
Quality of life and autonomy in emerging adults with early-onset neuromuscular disorders.
Laura Stanbery; Elizabeth M Petty
Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed.
Esther A Peterson; Hande Kocak; Christina Li; Olga Makarova; Laura Stanbery; Elizabeth M Petty
SEPT9_i1 and genomic instability: mechanistic insights and relevance to tumorigenesis.

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All Publications

2012: Darcy J Huismann; Kimberly Amburgey; James Dowling; Jane P Sheldon; Beverly M Yashar; Elizabeth M Petty
Quality of life and autonomy in emerging adults with early-onset neuromuscular disorders.
Journal of genetic counseling 2012;21(5):713-25.
2012: Laura Stanbery; Elizabeth M Petty
Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed.
Breast cancer research : BCR 2012;14(1):101.
2011: Esther A Peterson; Hande Kocak; Christina Li; Olga Makarova; Laura Stanbery; Elizabeth M Petty
SEPT9_i1 and genomic instability: mechanistic insights and relevance to tumorigenesis.
Genes, chromosomes & cancer 2011;50(11):940-9.
2011: Tommy A Potti; Elizabeth M Petty; Marci M Lesperance
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 2011;32(8):877-86.
2011: Jennifer A Keller; Elizabeth M Petty
CHFR binds to and regulates MAD2 in the spindle checkpoint through its cysteine-rich domain.
Biochemical and biophysical research communications 2011;409(3):389-93.
2011: Monica L Marvin; Serina M Mazzoni; Casey M Herron; Sean Edwards; Stephen B Gruber; Elizabeth M Petty
AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome.
American journal of medical genetics. Part A 2011;155A(4):898-902.
2010: Jennifer A Keller; Ayse Elif Erson-Bensan; Elizabeth M Petty
Connections between CHFR, the cell cycle, and chemosensitivity: Are they critical in cancer?
Cancer biology & therapy 2010;10(9):942-4.
2010: Shiva Akhavantabasi; Hesna B Akman; Aysegul Sapmaz; Jennifer Keller; Elizabeth M Petty; Ayse E Erson
USP32 is an active, membrane-bound ubiquitin protease overexpressed in breast cancers.
Mammalian genome : official journal of the International Mammalian Genome Society 2010;21(7-8):388-97.
2010: E A Peterson; Elizabeth M Petty
Conquering the complex world of human septins: implications for health and disease.
Clinical genetics 2010;77(6):511-24.
2010: Laura Stanbery; Nisha J D'Silva; Julia S Lee; Carol R Bradford; Thomas Carey; Mark E Prince; Gregory T Wolf; Francis P Worden; Kitrina G Cordell; Elizabeth M Petty
High SEPT9_v1 Expression Is Associated with Poor Clinical Outcomes in Head and Neck Squamous Cell Carcinoma.
Translational oncology 2010;3(4):239-45.
2010: K D Christensen; T E Jayaratne; J Scott Roberts; S L R Kardia; Elizabeth M Petty
Understandings of basic genetics in the United States: results from a national survey of black and white men and women.
Public health genomics 2010;13(7-8):467-76.
2009: Ayse E Erson; Elizabeth M Petty
miRNAs and cancer: New research developments and potential clinical applications.
Cancer biology & therapy 2009;8(24):2317-22.
2009: Wilmer Delgado Luengo; Elizabeth M Petty; Ernesto Solís-Añez; Orlando Römel; Juana Delgado Luengo; María Luisa Hernández; Alisandra Morales-Machín; Lisbeth Borjas-Fuentes; William Zabala-Fernández; Sandra González Ferrer; Lennie Pineda Bernal; Tatiana Pardo-Govea; María Caridad Martínez-Basalo; Richard González; Karelis Urdaneta; Jenny Cañizales; Herminia Fleitas-Cabello
Petty-Laxova-Wiedemann progeroid syndrome: further phenotypical delineation and confirmation of a rare syndrome of premature aging.
American journal of medical genetics. Part A 2009;149A(10):2200-5.
2009: Megan L Landsverk; Elizabeth K Ruzzo; Heather C Mefford; Karen Buysse; Jillian G Buchan; Evan E Eichler; Elizabeth M Petty; Esther A Peterson; Dana M Knutzen; Karen Barnett; Martin R Farlow; Judy Caress; Gareth J Parry; Dianna Quan; Kathy L Gardner; Ming Hong; Zachary Simmons; Thomas D Bird; Phillip F Chance; Mark C Hannibal
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.
Human molecular genetics 2009;18(7):1200-8.
2009: Maria E Gonzalez; Olga Makarova; Esther A Peterson; Lisa M Privette; Elizabeth M Petty
Up-regulation of SEPT9_v1 stabilizes c-Jun-N-terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells.
Cellular signalling 2009;21(4):477-87.
2009: Gyorgyi Csankovszki; Karishma Collette; Karin Spahl; James Carey; Martha Snyder; Elizabeth M Petty; Uchita Patel; Tomoko Tabuchi; Hongbin Liu; Ian McLeod; James Thompson; Ali Sarkeshik; Ali Sarkesik; John Yates; Barbara J Meyer; Kirsten Hagstrom
Three distinct condensin complexes control C. elegans chromosome dynamics.
Current biology : CB 2009;19(1):9-19.
2008: Lisa M Privette; Elizabeth M Petty
CHFR: A Novel Mitotic Checkpoint Protein and Regulator of Tumorigenesis.
Translational oncology 2008;1(2):57-64.
2008: Lisa M Privette; Jingly Fung Weier; Ha Nam Nguyen; Xiaochun Yu; Elizabeth M Petty
Loss of CHFR in human mammary epithelial cells causes genomic instability by disrupting the mitotic spindle assembly checkpoint.
Neoplasia (New York, N.Y.) 2008;10(7):643-52.
2008: Therese Roth; Elizabeth M Petty; Kate F Barald
The role of steroid hormones in the NF1 phenotype: focus on pregnancy.
American journal of medical genetics. Part A 2008;146A(12):1624-33.
2007: Mwe Mwe Chao; John E Levine; Robert E Ruiz; Wendy Kohlmann; Matthew A Bower; Elizabeth M Petty; Rajen J Mody
Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation.
Pediatric blood & cancer 2007;49(7):1000-4.
2007: Manish R Sharma; Elizabeth M Petty; Marci M Lesperance
Airway obstruction caused by PTEN hamartoma (Bannayan-Riley-Ruvalcaba) syndrome.
Archives of otolaryngology--head & neck surgery 2007;133(11):1157-60.
2007: Esther A Peterson; Linda M Kalikin; Jonathan D Steels; Mathew P Estey; William S Trimble; Elizabeth M Petty
Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(11):796-807.
2007: Maria E Gonzalez; Esther A Peterson; Lisa M Privette; Janice L Loffreda-Wren; Linda M Kalikin; Elizabeth M Petty
High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes.
Cancer research 2007;67(18):8554-64.
2007: Lisa M Privette; Maria E González; Lei Ding; Celina G Kleer; Elizabeth M Petty
Altered expression of the early mitotic checkpoint protein, CHFR, in breast cancers: implications for tumor suppression.
Cancer research 2007;67(13):6064-74.
2007: Jane P Sheldon; Carla A Pfeffer; Toby Epstein Jayaratne; Merle Feldbaum; Elizabeth M Petty
Beliefs about the etiology of homosexuality and about the ramifications of discovering its possible genetic origin.
Journal of homosexuality 2007;52(3-4):111-50.
2007: Jane P Sheldon; Toby Epstein Jayaratne; Merle Feldbaum; Courtney D DiNardo; Elizabeth M Petty
Applications and implications of advances in human genetics: perspectives from a group of Black Americans.
Community genetics 2007;10(2):82-92.
2004: Frank J Probst; Peter Hedera; Anthony M Sclafani; Maria Grazia Pomponi; Giovanni Neri; Jessica Tyson; Julie A Douglas; Elizabeth M Petty; Donna M Martin
Skewed X-inactivation in carriers establishes linkage in an X-linked deafness-mental retardation syndrome.
American journal of medical genetics. Part A 2004;131(2):209-12.
2004: Christopher Meredith; Ralf Herrmann; Cheryl Parry; Khema Liyanage; Danielle E Dye; Hayley J Durling; Rachael M Duff; Kaye Beckman; Marianne de Visser; Maaike M van der Graaff; Peter Hedera; John K Fink; Elizabeth M Petty; Phillipa Lamont; Vicki Fabian; Leslie Bridges; Thomas Voit; Frank L Mastaglia; Nigel G Laing
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
American journal of human genetics 2004;75(4):703-8.
2004: Angela D Lanie; Toby Epstein Jayaratne; Jane P Sheldon; Sharon L R Kardia; Elizabeth S Anderson; Merle Feldbaum; Elizabeth M Petty
Exploring the public understanding of basic genetic concepts.
Journal of genetic counseling 2004;13(4):305-20.
2004: Ayse E Erson; Elizabeth M Petty
CHFR-associated early G2/M checkpoint defects in breast cancer cells.
Molecular carcinogenesis 2004;39(1):26-33.
2003: Peter Hedera; Elizabeth M Petty; Melanie R Bui; Mila Blaivas; John K Fink
The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis.
Archives of neurology 2003;60(9):1321-5.
2003: David J Brown; Theresa B Kim; Elizabeth M Petty; Catherine A Downs; Donna M Martin; Peter J Strouse; Sayoko E Moroi; Stephen S Gebarski; Marci M Lesperance
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 2003;24(2):210-5.
2002: Ian G Macara; Richard Baldarelli; Christine M Field; Michael Glotzer; Yasuhide Hayashi; Shu-Chan Hsu; Mary B Kennedy; Makoto Kinoshita; Mark S Longtine; Claudia Low; Lois J Maltais; Louise McKenzie; Timothy J Mitchison; Toru Nishikawa; Makoto Noda; Elizabeth M Petty; Mark Peifer; John R Pringle; Phillip J Robinson; Dagmar Roth; S E Hilary Russell; Heidi Stuhlmann; Manami Tanaka; Tomoo Tanaka; William S Trimble; Jerry Ware; Nancy J Zeleznik-Le; Barbara Zieger
Mammalian septins nomenclature.
Molecular biology of the cell 2002;13(12):4111-3.
2002: Marjorie J Rosenberg; Richa Agarwala; Gerald Bouffard; Joie Davis; Giuseppe Fiermonte; Mark S Hilliard; Thorsten Koch; Linda M Kalikin; Izabela Makalowska; D Holmes Morton; Elizabeth M Petty; James L Weber; Ferdinando Palmieri; Richard I Kelley; Alejandro A Schäffer; Leslie G Biesecker
Mutant deoxynucleotide carrier is associated with congenital microcephaly.
Nature genetics 2002;32(1):175-9.
2002: David J Brown; Theresa B Kim; Elizabeth M Petty; Catherine A Downs; Donna M Martin; Peter J Strouse; Sayoko E Moroi; Jeff M Milunsky; Marci M Lesperance
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 2002;71(3):618-24.
2002: Peter Hedera; H V Toriello; Elizabeth M Petty
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1.
Journal of medical genetics 2002;39(7):484-8.
2002: Hideki Chuman; Jonathan D Trobe; Elizabeth M Petty; Ulrike Schwarze; Melanie Pepin; Peter H Byers; John P Deveikis
Spontaneous direct carotid-cavernous fistula in Ehlers-Danlos syndrome type IV: two case reports and a review of the literature.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2002;22(2):75-81.
2001: Linda M Kalikin; E M Bugeaud; Phillip L Palmbos; Robert H Lyons Jr; Elizabeth M Petty
Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(12):925-9.
2001: Ayse E Erson; Bethany L Niell; S K DeMers; Jean-Marie Rouillard; Samir M Hanash; Elizabeth M Petty
Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells.
Neoplasia (New York, N.Y.) 2001;3(6):521-6.
2001: Ulrike Schwarze; W I Schievink; Elizabeth M Petty; M R Jaff; D Babovic-Vuksanovic; K J Cherry; Melanie Pepin; Peter H Byers
Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV.
American journal of human genetics 2001;69(5):989-1001.
2001: Jean-Marie Rouillard; Ayse E Erson; Rork Kuick; Jun-ichi Asakawa; Katharina Wimmer; Martine Muleris; Elizabeth M Petty; Samir Hanash
Virtual genome scan: a tool for restriction landmark-based scanning of the human genome.
Genome research 2001;11(8):1453-9.
2001: Donna M Martin; Charisse Feli Gencyuz; Elizabeth M Petty
Systemic lupus erythematosus in a man with Noonan syndrome.
American journal of medical genetics 2001;102(1):59-62.
2001: Elizabeth M Petty; M Glynn; A E Bale
Direct molecular diagnosis of multiple endocrine neoplasia type 1.
Methods in molecular medicine 2001;49():227-42.
2000: Elizabeth M Petty; Gregory Yanik; Raymond J Hutchinson; BLANCHE ALTER; Frank C Schmalstieg; John E Levine; David Ginsburg; J E Robillard; Valerie P Castle
Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia.
The Journal of pediatrics 2000;137(6):882-6.
2000: M J Percy; K A Myrie; Chris K Neeley; James N Azim III; Stephen Ethier; Elizabeth M Petty
Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells.
Genes, chromosomes & cancer 2000;29(4):356-62.
2000: Donna M Martin; Frank J Probst; Sally A Camper; Elizabeth M Petty
Characterisation and genetic mapping of a new X linked deafness syndrome.
Journal of medical genetics 2000;37(11):836-41.
2000: S E Hilary Russell; Michael A McIlhatton; J F Burrows; Paul Donaghy; Severine Chanduloy; Elizabeth M Petty; Linda M Kalikin; S W Church; S McIlroy; D Paul Harkin; G W Keilty; A N Cranston; J Weissenbach; I Hickey; Patrick G Johnston
Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors.
Cancer research 2000;60(17):4729-34.
2000: K A Myrie; M J Percy; James N Azim III; Chris K Neeley; Elizabeth M Petty
Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines.
Cancer letters 2000;152(2):193-9.
2000: Linda M Kalikin; H L Sims; Elizabeth M Petty
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 2000;63(2):165-72.
1999: Alain Colige; A L Sieron; Shi-Wu Li; Ulrike Schwarze; Elizabeth M Petty; W Wertelecki; William R Wilcox; Deborah Krakow; Daniel H Cohn; W Reardon; Peter H Byers; Charles M Lapière; Darwin J Prockop; Betty Nusgens
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.
American journal of human genetics 1999;65(2):308-17.
1999: Kathleen Cooney; HC Tsou; Elizabeth M Petty; Susan Miesfeldt; XL Ping; AC Gruener; M Peacocke
Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 1999;5(6):1387-91.
1999: Linda M Kalikin; R A George; MP Keller; S Bort; N S Bowler; D J Law; Phillip F Chance; Elizabeth M Petty
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci.
Genomics 1999;57(1):36-42.
1999: Karen K Milner; T Han; Elizabeth M Petty
Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric community.
Genetic testing 1999;3(3):279-86.
1998: Dianna M Milewicz; H Chen; ES Park; Elizabeth M Petty; H Zaghi; G Shashidhar; Marcia C Willing; Vijaykumar Surendrakant Patel
Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections.
The American journal of cardiology 1998;82(4):474-9.
1998: Elizabeth M Petty; Linda M Kalikin; Mark B Orringer; David G Beer
Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: implications for tumorigenesis.
Molecular carcinogenesis 1998;22(4):222-8.
1998: Karen K Milner; E E Collins; G R Connors; Elizabeth M Petty
Attitudes of young adults to prenatal screening and genetic correction for human attributes and psychiatric conditions.
American journal of medical genetics 1998;76(2):111-9.
1997: Linda M Kalikin; TS Frank; SM Svoboda-Newman; J C Wetzel; Kathleen Cooney; Elizabeth M Petty
A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors.
Oncogene 1997;14(16):1991-4.
1996: Linda M Kalikin; X Qu; T S Frank; RF Caduff; S M Svoboda; David J Law; Elizabeth M Petty
Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25.
Genes, chromosomes & cancer 1996;17(1):64-8.
1996: Sofia D Merajver; Elizabeth M Petty
Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancer.
Clinics in laboratory medicine 1996;16(1):139-67.
1996: Elizabeth M Petty; Diane E Miller; A L Grant; E E Collins; Thomas W Glover; David J Law
FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors.
Cytogenetics and cell genetics 1996;72(4):319-21.
1995: David J Law; M A Prasad; S E King; K D Spranger; Y H Lee; R E Fox; E E Collins; T C Gebuhr; Diane E Miller; Elizabeth M Petty
Localization of the human estrogen-responsive finger protein (EEP) gene (ZNF147) within a YAC contig containing the myeloperoxidase (MPO) gene.
Genomics 1995;28(2):361-3.
1994: Elizabeth M Petty; J S Green; S J Marx; R T Taggart; N Farid; Allen E Bale
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.
American journal of human genetics 1994;54(6):1060-6.
1993: Elizabeth M Petty; Margretta R Seashore; I M Braverman; S Z Spiesel; Lynne T Smith; L M Milstone
Dermatosparaxis in children. A case report and review of the newly recognized phenotype.
Archives of dermatology 1993;129(10):1310-5.
1993: Elizabeth M Petty; L H Gibson; JW Fountain; Jean L Bolognia; TL Yang-Feng; D E Housman; Allen E Bale
Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).
American journal of human genetics 1993;53(1):96-104.
1993: Elizabeth M Petty; L H Gibson; W R Breg; J P Burns; TL Yang-Feng
Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
American journal of medical genetics 1993;45(6):770-3.
1993: Elizabeth M Petty; A Arnold; S J Marx; Allen E Bale
A pulsed-field gel electrophoresis (PFGE) map of twelve loci on chromosome 11q11-q13.
Genomics 1993;15(2):423-5.
1993: C L Rosen; E J Novotny; L A D'Andrea; Elizabeth M Petty
Klippel-Feil sequence and sleep-disordered breathing in two children.
The American review of respiratory disease 1993;147(1):202-4.
1993: Elizabeth M Petty; Jean L Bolognia; Allen E Bale; TL Yang-Feng
Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9.
American journal of medical genetics 1993;45(1):77-80.
1992: Elizabeth M Petty; E Gold; Allen E Bale
DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508.
Clinical chemistry 1992;38(12):2422-5.
1992: Lisa A Cannon-Albright; David E Goldgar; Laurence J Meyer; C M Lewis; D E Anderson; JW Fountain; M E Hegi; R W Wiseman; Elizabeth M Petty; Allen E Bale
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.
Science (New York, N.Y.) 1992;258(5085):1148-52.
1992: S P Lin; Elizabeth M Petty; L H Gibson; J Inserra; Margretta R Seashore; TL Yang-Feng
Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy.
American journal of medical genetics 1992;44(4):500-2.
1992: Lynne T Smith; W Wertelecki; L M Milstone; Elizabeth M Petty; Margretta R Seashore; I M Braverman; T G Jenkins; Peter H Byers
Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.
American journal of human genetics 1992;51(2):235-44.
1991: C L Rosenberg; E Wong; Elizabeth M Petty; Allen E Bale; Y Tsujimoto; N L Harris; A Arnold
PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(21):9638-42.
1991: Elizabeth M Petty; R Carstens; Allen E Bale
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site.
Nucleic acids research 1991;19(3):690.