E
Elizabeth M. Petty
Researcher at University of Michigan
Publications - 94
Citations - 5765
Elizabeth M. Petty is an academic researcher from University of Michigan. The author has contributed to research in topics: Gene & CHFR. The author has an hindex of 38, co-authored 93 publications receiving 5519 citations. Previous affiliations of Elizabeth M. Petty include Harvard University & Yale University.
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Journal ArticleDOI
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.
Lisa A. Cannon-Albright,David E. Goldgar,Laurence Meyer,Cathryn M. Lewis,David E. Anderson,Jane W. Fountain,Monika E. Hegi,Roger W. Wiseman,Elizabeth M. Petty,Allen E. Bale,Olufunmilayo I. Olopade,Manuel O. Diaz,David J. Kwiatkowski,Michael Piepkorn,John J. Zone,Mark H. Skolnick +15 more
TL;DR: Linkage analysis of Utah kindreds and one Texas kindred with multiple cases of cutaneous malignant melanoma provided evidence that a locus for familial melanoma susceptibility is in the chromosomal region 9p13-p22, previously implicated in homozygous deletions in melanoma tumors.
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PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.
Carol L. Rosenberg,Emily B. Wong,Elizabeth M. Petty,Allen E. Bale,Yoshihide Tsujimoto,Nanch L. Harris,Andrew Arnold +6 more
TL;DR: PRAD1 is an excellent candidate "BCL1 oncogene" and may be a key consequence of rearrangement of the BCL1 vicinity in B-cell neoplasms and a unifying pathogenetic feature in centrocytic lymphoma.
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Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.
Alain Colige,Aleksander Sieroń,Shi-Wu Li,Ulrike Schwarze,Elizabeth M. Petty,Wladimir Wertelecki,William R. Wilcox,Deborah Krakow,Daniel H. Cohn,W. Reardon,Peter H. Byers,Charles M. Lapière,Darwin J. Prockop,Betty Nusgens +13 more
TL;DR: The mutations that cause Ehlers-Danlos syndrome type VIIC are identified in the six known affected human individuals and also in one strain of dermatosparactic calf and used bovine cDNA to isolate human pNPI.
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Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.
Cornelius F. Boerkoel,Hiroshi Takashima,Joy John,Jiong Yan,Pawel Stankiewicz,Lisa Rosenbarker,Jean Luc André,Radovan Bogdanovic,Antoine Burguet,Sandra Cockfield,Isabel Cordeiro,Stefan Fründ,Friederike Illies,Mark Joseph,Ilkka Kaitila,Giuliana Lama,Chantal Loirat,D. Ross McLeod,David V. Milford,Elizabeth M. Petty,Francisco Rodrigo,Jorge M. Saraiva,Beate Schmidt,Graham Smith,Jürgen Spranger,Anja Stein,Hannelore Thiele,Jane Tizard,Rosanna Weksberg,James R. Lupski,David W. Stockton +30 more
TL;DR: Using genome-wide linkage mapping and a positional candidate approach, it is determined that mutations in SMARCAL1 (SWI/SNF2-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a–like 1), are responsible for SIOD.
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White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians.
Toby Epstein Jayaratne,Oscar Ybarra,Jane P. Sheldon,Tony Brown,Merle Feldbaum,Carla A. Pfeffer,Elizabeth M. Petty +6 more
TL;DR: The present research broadens the view of lay theories by showing how they support either prejudice or tolerance, depending on the target group, as well as reviewing the literature on essentialism and implicit theories of the malleability of traits.