E. Petty

Donna M. Martin, S. Gebarski, E. Petty, 2003, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Dermatosparaxis in children. A case report and review of the newly recognized phenotype.

M. Seashore, E. Petty, I. Braverman, 1993, Archives of dermatology.

Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

M. Seashore, E. Petty, I. Braverman, 1992, American journal of human genetics.

Mutant deoxynucleotide carrier is associated with congenital microcephaly

Alejandro A. Schäffer, Richa Agarwala, Izabela Makalowska, 2002, Nature Genetics.

Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.

M. Skolnick, C. Lewis, O. Olopade, 1992, Science.

Loss of CHFR in human mammary epithelial cells causes genomic instability by disrupting the mitotic spindle assembly checkpoint.

E. Petty, Xiaochun Yu, H. N. Nguyen, 2008, Neoplasia.

High SEPT9_v1 Expression Is Associated with Poor Clinical Outcomes in Head and Neck Squamous Cell Carcinoma.

E. Petty, N. D’Silva, T. Carey, 2010, Translational oncology.

Molecular Genetic Diagnosis of Inherited Cancer Predisposition

E. Petty, B. Yashar, 2002 .

An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function1

E. Fearon, E. Stoffel, E. Petty, 2015, Neoplasia.

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy.

M. Seashore, E. Petty, T. Yang-Feng, 1992, American journal of medical genetics.

Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9.

E. Petty, T. Yang-Feng, A. Bale, 1993, American journal of medical genetics.

PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.

N. Harris, E. Petty, A. Arnold, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas.

E. Petty, G. Vassart, H. El Housni, 2001, Cancer research.

Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines.

E. Petty, M. Percy, C. Neeley, 2000, Cancer letters.

TRIM37 (tripartite motif-containing 37)

A. E. Erson, E. Petty, 2011 .

Up-regulation of SEPT9_v1 stabilizes c-Jun-N-terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells.

E. Petty, M. E. Gonzalez, Lisa M Privette, 2009, Cellular signalling.

Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed

E. Petty, L. Stanbery, 2012, Breast Cancer Research.

SEPT9_i1 and genomic instability: Mechanistic insights and relevance to tumorigenesis

E. Petty, H. Koçak, O. Makarova, 2011, Genes, chromosomes & cancer.

Direct molecular diagnosis of multiple endocrine neoplasia type 1.

E. Petty, A. Bale, M. Glynn, 2001, Methods in molecular medicine.

miRNAs and cancer: New research developments and potential clinical applications

A. E. Erson, E. Petty, 2009, Cancer biology & therapy.

Virtual genome scan: a tool for restriction landmark-based scanning of the human genome.

R. Kuick, J. Rouillard, A. E. Erson, 2001, Genome Research.

White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

Tony N. Brown, T. Brown, E. Petty, 2006, Group processes & intergroup relations : GPIR.

Mammalian septins nomenclature.

N. Zeleznik-Le, M. Kennedy, Y. Hayashi, 2002, Molecular biology of the cell.

BRCA1 mutation testing: controversies and challenges.

E. Petty, A. Killeen, 1997, Clinical chemistry.

USP32 is an active, membrane-bound ubiquitin protease overexpressed in breast cancers

A. E. Erson, E. Petty, H. B. Akman, 2010, Mammalian Genome.

Spontaneous direct carotid-cavernous fistula in Ehlers-Danlos syndrome type IV: two case reports and a review of the literature.

P. Byers, E. Petty, J. Trobe, 2002, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Perceived Changes to Obstetric Care and the Integration of Personal and Professional Life as a Pregnant Prenatal Genetic Counselor

E. Petty, Laura E. Birkeland, Jennifer L. Rietzler, 2018, Journal of Genetic Counseling.

Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric community.

E. Petty, K. Milner, T. Han, 1999, Genetic testing.

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.

E. Petty, L. Kalikin, H. Sims, 2000, Genomics.

The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis.

P. Hedera, E. Petty, J. Fink, 2003, Archives of neurology.

A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors

K. Cooney, E. Petty, T. Frank, 1997, Oncogene.

Genetic Counseling Graduate Student Debt: Impact on Program, Career and Life Choices

E. Petty, J. Eickhoff, C. Reiser, 2014, Journal of Genetic Counseling.

Malignant triton tumor in a patient with Li‐Fraumeni syndrome and a novel TP53 mutation

E. Petty, W. Kohlmann, J. Levine, 2007, Pediatric blood & cancer.

Localization of the human estrogen-responsive finger protein (EEP) gene (ZNF147) within a YAC contig containing the myeloperoxidase (MPO) gene.

E. Petty, D. J. Law, Y. Lee, 1995, Genomics.

Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells

E. Petty, S. Ethier, M. Percy, 2000, Genes, chromosomes & cancer.

CHFR binds to and regulates MAD2 in the spindle checkpoint through its cysteine-rich domain.

E. Petty, Jennifer A Keller, 2011, Biochemical and biophysical research communications.

The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay

E. Petty, J. Iruretagoyena, Laura E. Birkeland, 2021, Journal of Community Genetics.

CHFR‐associated early G2/M checkpoint defects in breast cancer cells

A. E. Erson, E. Petty, Elizabeth M. Petty, 2004, Molecular carcinogenesis.

Exploring empathy in genetic counseling students and new genetic counselors

E. Petty, Amy B. Zelenski, Jonica L. Richards, 2020, Journal of genetic counseling.

Attitudes of young adults to prenatal screening and genetic correction for human attributes and psychiatric conditions.

E. Petty, K. Milner, G. Connors, 1998, American journal of medical genetics.

Counseling Close to Home: Genetic Counselors’ Experiences with their own Family Members

E. Petty, C. Reiser, Laura M Rust, 2018, Journal of Genetic Counseling.

Petty–Laxova–Wiedemann progeroid syndrome: Further phenotypical delineation and confirmation of a rare syndrome of premature aging

E. Petty, A. Morales-Machín, William Zabala-Fernández, 2009, American journal of medical genetics. Part A.

Previously unrecognized congenital progeroid disorder.

E. Petty, R. Laxová, H. Wiedemann, 1990, American journal of medical genetics.

The Perennial Debate: Nature, Nurture, or Choice? Black and White Americans’ Explanations for Individual Differences

S. Gelman, S. Kardia, E. Petty, 2009, Review of general psychology : journal of Division 1, of the American Psychological Association.

Vive La Difference? Genetic Explanations for Perceived Gender Differences in Nurturance

E. Petty, E. Cole, T. Jayaratne, 2007 .

Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1

P. Hedera, E. Petty, H. Toriello, 2002, Journal of medical genetics.

Novel autosomal dominant mandibulofacial dysostosis with ptosis : clinical description and exclusion of TCOF 1 P Hedera

P. Hedera, E. Petty, H. Toriello, 2002 .

Airway obstruction caused by PTEN hamartoma (Bannayan-Riley-Ruvalcaba) syndrome.

E. Petty, M. Lesperance, Manish R Sharma, 2007, Archives of otolaryngology--head & neck surgery.

Working with the Hmong Population in a Genetics Setting: an Interpreter Perspective

E. Petty, C. Reiser, Meghan Krieger, 2018, Journal of Genetic Counseling.

White Americans' Genetic Explanations for a Perceived Race Difference in Athleticism: The Relation to Prejudice toward and Stereotyping of Blacks

E. Petty, T. Jayaratne, Toby E. Jayaratne, 2007 .

Working with the Hmong Population in a Genetics Setting: Genetic Counselor Perspectives

E. Petty, C. Reiser, Jennifer L. Rietzler, 2017, Journal of Genetic Counseling.

Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

S. Kardia, E. Petty, T. Jayaratne, 2010, Public Health Genomics.

Applications and Implications of Advances in Human Genetics: Perspectives from a Group of Black Americans

E. Petty, C. Dinardo, Jane P. Sheldon, 2007, Public Health Genomics.

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors.

J. F. Burrows, J. Weissenbach, P. Johnston, 2000, Cancer research.

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.

H. Mefford, E. Eichler, K. Buysse, 2009, Human molecular genetics.

High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes.

E. Petty, M. E. Gonzalez, Lisa M Privette, 2007, Cancer research.

A pulsed-field gel electrophoresis (PFGE) map of twelve loci on chromosome 11q11-q13.

E. Petty, A. Arnold, S. Marx, 1993, Genomics.

CHFR (checkpoint with fork-head associated and ring finger)

E. Petty, A. E. Erson-Bensan, H. B. Akman, 2011 .

Altered expression of the early mitotic checkpoint protein, CHFR, in breast cancers: implications for tumor suppression.

E. Petty, L. Ding, C. Kleer, 2007, Cancer research.

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).

E. Petty, W. R. Breg, T. Yang-Feng, 1993, American journal of medical genetics.

Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

E. Petty, L. Kalikin, Jr. Robert H. Lyons, 2001, Mammalian Genome.

Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin

E. Petty, W. Trimble, L. Kalikin, 2007, Mammalian Genome.

Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: Implications for tumorigenesis

D. Beer, M. Orringer, E. Petty, 1998, Molecular carcinogenesis.

Alternative option labeling impacts decision‐making in noninvasive prenatal screening

B. Zikmund‐Fisher, E. Petty, C. Palmer, 2019, Journal of genetic counseling.

Uva-dare (digital Academic Repository) Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (myh7) Cause Laing Early-onset Distal Myopathy (mpd1)

F. Mastaglia, P. Hedera, N. Laing, 2022 .

Genetic counselor workforce generational diversity: Millennials to Baby Boomers

E. Petty, C. Reiser, Victoria Van Vreede, 2019, Journal of genetic counseling.

Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records

M. Brilliant, E. Petty, Jinkuk Hong, 2017, Journal of Genetic Counseling.

Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records

M. Brilliant, E. Petty, Jinkuk Hong, 2017, Journal of Genetic Counseling.

The role of steroid hormones in the NF1 phenotype: Focus on pregnancy

E. Petty, K. Barald, Therese M. Roth, 2008, American journal of medical genetics. Part A.

Advances in Brief Isolation and Mapping of a Human Septin Gene to a Region on Chromosome 17 q , Commonly Deleted in Sporadic Epithelial Ovarian Tumors 1

J. F. Burrows, J. Weissenbach, P. Johnston, 2000 .

Isolation and Mapping of a Human SeptinGene to a Region on Chromosome 17q, Commonly Deleted in Sporadic Epithelial Ovarian Tumors

J. F. Burrows, J. Weissenbach, E. Petty, 2000 .

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.

H. Mefford, E. Eichler, K. Buysse, 2009, Human molecular genetics.

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on l7q25

E. Petty, D. J. Law, R. Caduff, 1996, Genes, chromosomes & cancer.