These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 9679319)

  • 1. Models for haplotype evolution in a nonstationary population.
    Fan R; Lange K
    Theor Popul Biol; 1998 Jun; 53(3):184-98. PubMed ID: 9679319
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Branching process models for mutant genes in nonstationary populations.
    Lange K; Fan RZ
    Theor Popul Biol; 1997 Apr; 51(2):118-33. PubMed ID: 9169237
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.
    Hästbacka J; de la Chapelle A; Kaitila I; Sistonen P; Weaver A; Lander E
    Nat Genet; 1992 Nov; 2(3):204-11. PubMed ID: 1345170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.
    Zhang K; Sun F; Zhao H
    Bioinformatics; 2005 Jan; 21(1):90-103. PubMed ID: 15231536
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High frequencies of human genetic diseases: founder effect with genetic drift or selection?
    Zlotogora J
    Am J Med Genet; 1994 Jan; 49(1):10-3. PubMed ID: 8172234
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recovering haplotype structure through recombination and gene conversion.
    Lajoie M; El-Mabrouk N
    Bioinformatics; 2005 Sep; 21 Suppl 2():ii173-9. PubMed ID: 16204098
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Classifying disease chromosomes arising from multiple founders, with application to fine-scale haplotype mapping.
    Yu K; Martin RB; Whittemore AS
    Genet Epidemiol; 2004 Nov; 27(3):173-81. PubMed ID: 15389930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Waiting with and without recombination: the time to production of a double mutant.
    Christiansen FB; Otto SP; Bergman A; Feldman MW
    Theor Popul Biol; 1998 Jun; 53(3):199-215. PubMed ID: 9679320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.
    Garner C; Slatkin M
    Genet Epidemiol; 2003 Jan; 24(1):57-67. PubMed ID: 12508256
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype trees and modern human origins.
    Templeton AR
    Am J Phys Anthropol; 2005; Suppl 41():33-59. PubMed ID: 16369961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Haplotypes vs single marker linkage disequilibrium tests: what do we gain?
    Akey J; Jin L; Xiong M
    Eur J Hum Genet; 2001 Apr; 9(4):291-300. PubMed ID: 11313774
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage disequilibrium mapping in populations of variable size using the decay of haplotype sharing and a stepwise-mutation model.
    Zhang S; Zhao H
    Genet Epidemiol; 2000; 19 Suppl 1():S99-105. PubMed ID: 11055377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Likelihood-based disequilibrium mapping for two-marker haplotype data.
    Garner C; Slatkin M
    Theor Popul Biol; 2002 Mar; 61(2):153-61. PubMed ID: 11969387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes.
    Yu K; Gu CC; Province M; Xiong CJ; Rao DC
    Genet Epidemiol; 2004 Nov; 27(3):182-91. PubMed ID: 15389925
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene mapping of a simulated complex disease.
    Newman B; Lee M; Stillman L; Louie L; Anderson L; King MC
    Prog Clin Biol Res; 1989; 329():171-6. PubMed ID: 2622949
    [No Abstract]   [Full Text] [Related]  

  • 16. Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring.
    Van der Meulen MA; te Meerman GJ
    Genet Epidemiol; 1997; 14(6):915-20. PubMed ID: 9433600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
    Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA
    Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies.
    Bessant DA; Payne AM; Plant C; Bird AC; Swaroop A; Bhattacharya SS
    Eur J Hum Genet; 2000 Oct; 8(10):783-7. PubMed ID: 11039579
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Finnish disease heritage].
    Kestilä M; Ikonen E; Lehesjoki AE
    Duodecim; 2010; 126(19):2311-20. PubMed ID: 21086689
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Power calculations for a general class of tests of linkage and association that use nuclear families with affected and unaffected sibs.
    Kaplan NL; Martin ER
    Theor Popul Biol; 2001 Nov; 60(3):193-201. PubMed ID: 11855953
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.