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Dolores A. Fici
Researcher at Harvard University
Publications - 19
Citations - 409
Dolores A. Fici is an academic researcher from Harvard University. The author has contributed to research in topics: Haplotype & Linkage disequilibrium. The author has an hindex of 11, co-authored 19 publications receiving 401 citations. Previous affiliations of Dolores A. Fici include Boston Children's Hospital & Massachusetts Institute of Technology.
Papers
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Journal ArticleDOI
The Haplotype Structure of the Human Major Histocompatibility Complex
Chester A. Alper,Chester A. Alper,Charles E. Larsen,Charles E. Larsen,Devendra P. Dubey,Zuheir L. Awdeh,Dolores A. Fici,Edmond J. Yunis,Edmond J. Yunis +8 more
TL;DR: The results suggest that the human genome, including the major histocompatibility complex (MHC), consists largely of 5- to 200-kb blocks of sequence fixity between which random recombination occurs, and the use of statistical analysis rather than direct haplotype determination and counting fails to reveal the details of haplotype structure essential for gene localization.
Journal ArticleDOI
Molecular analysis of major histocompatibility complex allelic associations with systemic lupus erythematosus in Taiwan
Ling-Ying Lu,Wei-Zi Ding,Dolores A. Fici,Richard Deulofeut,He-Hsiung Cheng,Ching‐Cheng Cheu,Ping-Kuang Sung,Peter H. Schur,Patricia A. Fraser +8 more
TL;DR: Although no HLA-DRB1 allele was found to be significantly associated with SLE, the associations with DQB1*0501 and TNF2 suggest that DQB 1 and tumor necrosis factor a may be important genetic factors in SLE susceptibility in the Chinese population in Taiwan.
Journal ArticleDOI
A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease.
Z Awdeh,Edmond J. Yunis,Mark J. Audeh,Dolores A. Fici,Alberto Pugliese,Charles E. Larsen,Chester A. Alper +6 more
TL;DR: The hypothesis that parents originated from previously isolated populations that had selected against different critical susceptibility genes for a polygenic disease, their offspring could have a greater risk of that disease than either parent is explained explains some seemingly disconnected puzzling phenomena.
Patent
Colloid compositions for solid phase biomolecular analytical, preparative and identification systems
TL;DR: In this article, a liquid composition comprising a colloidal suspension of a biomolecule-binding matrix material (preferably nitrocellulose) dispersed in a liquid, with particles of the matrix material being of a defined particle size, is disclosed.
Journal ArticleDOI
Genetic Fixity in the Human Major Histocompatibility Complex and Block Size Diversity in the Class I Region Including HLA-E
Viviana Romero,Charles E. Larsen,Charles E. Larsen,Jonathan S. Duke-Cohan,Edward A. Fox,T. Romero,Olga P. Clavijo,Dolores A. Fici,Zaheed Husain,Zaheed Husain,Ingrid Almeciga,Dennis R. Alford,Zuheir L. Awdeh,Joaquín Zúñiga,Lama El-Dahdah,Chester A. Alper,Chester A. Alper,Edmond J. Yunis +17 more
TL;DR: It is concluded that to generate high-resolution maps for relating MHC haplotypes to disease susceptibility, both SNP and MHC allele analysis must be conducted as complementary techniques.