Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Y Y, Shugart"'
Publikováno v:
Annals of Oncology. 13:30-33
Although the occurrence of familial Hodgkin's lymphoma (HL) is a rare event, genetic susceptibility as a cause of HL and its influence on treatment outcome may not be rare. However, results obtained from the analysis of HL families will probably have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48676abce534b0590fcde16a61c982a0
https://doi.org/10.1093/annonc/13.s1.30
https://doi.org/10.1093/annonc/13.s1.30
Autor:
M. Le Merrer, Eileen M. Shore, Michel Fardeau, Y Y Shugart, James T. Triffitt, David L. Glaser, J. M. Connor, Roger Smith, J. A. Urtizberea, Frederick S. Kaplan, George J. Feldman, Meiqi Xu
Publikováno v:
Clinical Genetics. 58:291-298
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare and disabling genetic disorder characterized by congenital malformation of the great toes and by progressive heterotopic endochondral ossification in predictable anatomical patterns. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0fdd186f18dc149777bb29bdca86d99
https://doi.org/10.1034/j.1399-0004.2000.580407.x
https://doi.org/10.1034/j.1399-0004.2000.580407.x
Autor:
T. Conrad Gilliam, Penchaszadeh Gk, Barbara Ross, P. Banerjee, Y Y Shugart, Patrick W. Kleyn, James A. Knowles, Samuel G. Jacobson, Jurg Ott, Charles A. Lewis
Publikováno v:
Genomics. 48:171-177
Retinitis pigmentosa (RP) is a heterogeneous genetic disorder with autosomal dominant, autosomal recessive, and X-linked forms. We previously mapped an additional arRP locus to chromosome 6p21 (RP14) in a single extended kinship from the Dominican Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::835d55d9a4977815b1127ba24bdac600
https://doi.org/10.1006/geno.1997.5174
https://doi.org/10.1006/geno.1997.5174
Autor:
D T, Chen, X, Jiang, N, Akula, Y Y, Shugart, J R, Wendland, C J M, Steele, L, Kassem, J-H, Park, N, Chatterjee, S, Jamain, A, Cheng, M, Leboyer, P, Muglia, T G, Schulze, S, Cichon, M M, Nöthen, M, Rietschel, F J, McMahon, A, Farmer, P, McGuffin, I, Craig, C, Lewis, G, Hosang, S, Cohen-Woods, J B, Vincent, J L, Kennedy, Thomas G, Schulze
Publikováno v:
Molecular psychiatry. 18(2)
Meta-analyses of bipolar disorder (BD) genome-wide association studies (GWAS) have identified several genome-wide significant signals in European-ancestry samples, but so far account for little of the inherited risk. We performed a meta-analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce0989cb997025f762cc42843d6a7f14
https://pubmed.ncbi.nlm.nih.gov/22182935
https://pubmed.ncbi.nlm.nih.gov/22182935
Publikováno v:
Genetic epidemiology. 17
The analysis of a complex disease such as alcohol dependence requires a more precise definition of affection status. Collaborative Study on the Genetics of Alcoholism (COGA) provided a variety of qualitative and quantitative measures as well as genot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00fe2f394dc3db333238b5c0cabbf7ac
https://pubmed.ncbi.nlm.nih.gov/10597428
https://pubmed.ncbi.nlm.nih.gov/10597428
Publikováno v:
Genetic epidemiology. 17
For the analysis of complex traits, it is of interest to compare a few nonparametric methods such as affected-sib-pair (ASP) analyses and transmission/disequilibrium tests (TDT). The affected-sib-pair approaches we have examined here are ASP and ALL-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e33c3dd84d43ccf26b4040cbd25a627b
https://pubmed.ncbi.nlm.nih.gov/10597521
https://pubmed.ncbi.nlm.nih.gov/10597521
Autor:
Y Y, Shugart, D E, Goldgar
Publikováno v:
Genetic epidemiology. 14(6)
This paper summarizes the results of searching for evidence of loci contributing to simulated quantitative traits which are associated with a common genetic disease using two multipoint identity by descent (IBD) sharing methods: MIM and MAPMAKER/SIBS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3f9f46340b9c14a3055c4b88dc51719
https://pubmed.ncbi.nlm.nih.gov/9433597
https://pubmed.ncbi.nlm.nih.gov/9433597
Autor:
Y Y, Shugart
Publikováno v:
Genetic epidemiology. 12(6)
Sample sizes may greatly affect the accuracy of estimates of marker heterozygosities. Therefore, indicating the precision of these estimates is strongly recommended. A computer program HETMAX was written and used to obtain unbiased estimates of heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b17a7963e1061387581b27bd2d2e9e5
https://pubmed.ncbi.nlm.nih.gov/8787992
https://pubmed.ncbi.nlm.nih.gov/8787992
Publikováno v:
Genetic epidemiology. 10(3)
The results of classical segregation analysis on 159 families with polycystic kidney disease (PKD) are presented. It had been previously estimated that about 95% of autosomal dominant PKD (ADPKD) families have PKD1, the gene localized to chromosome 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f5f9f5fe70f76ada55b70f017df7584
https://pubmed.ncbi.nlm.nih.gov/8349100
https://pubmed.ncbi.nlm.nih.gov/8349100
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