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 *

482 related articles for article (PubMed ID: 9345087)

  • 21. Alström syndrome: further evidence for linkage to human chromosome 2p13.
    Collin GB; Marshall JD; Boerkoel CF; Levin AV; Weksberg R; Greenberg J; Michaud JL; Naggert JK; Nishina PM
    Hum Genet; 1999 Nov; 105(5):474-9. PubMed ID: 10598815
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Model-Free Linkage Analysis of a Binary Trait.
    Xu W; Ma J; Greenwood CMT; Paterson AD; Bull SB
    Methods Mol Biol; 2017; 1666():343-373. PubMed ID: 28980254
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of a new candidate locus for uric acid nephrolithiasis.
    Ombra MN; Forabosco P; Casula S; Angius A; Maestrale G; Petretto E; Casu G; Colussi G; Usai E; Melis P; Pirastu M
    Am J Hum Genet; 2001 May; 68(5):1119-29. PubMed ID: 11309680
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The role of meta-analysis in linkage studies of complex traits.
    Rice JP
    Am J Med Genet; 1997 Feb; 74(1):112-4. PubMed ID: 9034017
    [No Abstract]   [Full Text] [Related]  

  • 25. Power comparison of parametric and nonparametric linkage tests in small pedigrees.
    Sham PC; Lin MW; Zhao JH; Curtis D
    Am J Hum Genet; 2000 May; 66(5):1661-8. PubMed ID: 10762550
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.
    Arcos-Burgos M; Castellanos FX; Pineda D; Lopera F; Palacio JD; Palacio LG; Rapoport JL; Berg K; Bailey-Wilson JE; Muenke M
    Am J Hum Genet; 2004 Dec; 75(6):998-1014. PubMed ID: 15497111
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Calculation of multipoint likelihoods using flanking marker data: a simulation study.
    George AW; Mangin LA; Bartlett CW; Logue MW; Segre AM; Vieland VJ
    BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S44. PubMed ID: 16451655
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes.
    Wiltshire S; Frayling TM; Hattersley AT; Hitman GA; Walker M; Levy JC; O'Rahilly S; Groves CJ; Menzel S; Cardon LR; McCarthy MI
    Am J Hum Genet; 2002 Feb; 70(2):543-6. PubMed ID: 11753821
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.
    Hodge SE; Anderson CE; Neiswanger K; Sparkes RS; Rimoin DL
    Am J Hum Genet; 1983 Nov; 35(6):1139-55. PubMed ID: 6580815
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Evaluating the results of genomewide linkage scans of complex traits by locus counting.
    Wiltshire S; Cardon LR; McCarthy MI
    Am J Hum Genet; 2002 Nov; 71(5):1175-82. PubMed ID: 12355401
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic Analysis Workshop II: results of incorporating a linkage disequilibrium parameter.
    Goldgar DE; Fain PR
    Genet Epidemiol; 1984; 1(2):179-82. PubMed ID: 14971367
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evidence against linkage of schizophrenia to chromosome 5q11-q13 markers in systematically ascertained families.
    Hallmayer J; Maier W; Ackenheil M; Ertl MA; Schmidt S; Minges J; Lichtermann D; Wildenauer D
    Biol Psychiatry; 1992 Jan; 31(1):83-94. PubMed ID: 1543800
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Linkage analyses in type I diabetes mellitus using CASPAR, a software and statistical program for conditional analysis of polygenic diseases.
    Buhler J; Owerbach D; Schäffer AA; Kimmel M; Gabbay KH
    Hum Hered; 1997; 47(4):211-22. PubMed ID: 9239508
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.
    Nance MA; Raabe WA; Midani H; Kolodny EH; David WS; Megna L; Pericak-Vance MA; Haines JL
    Hum Hered; 1998; 48(3):169-78. PubMed ID: 9618065
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.
    Pankratz N; Nichols WC; Uniacke SK; Halter C; Rudolph A; Shults C; Conneally PM; Foroud T;
    Am J Hum Genet; 2002 Jul; 71(1):124-35. PubMed ID: 12058349
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.
    Harrap SB; Zammit KS; Wong ZY; Williams FM; Bahlo M; Tonkin AM; Anderson ST
    Arterioscler Thromb Vasc Biol; 2002 May; 22(5):874-8. PubMed ID: 12006406
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM.
    Elbein SC; Hoffman M; Ridinger D; Otterud B; Leppert M
    Diabetes; 1994 Aug; 43(8):1061-5. PubMed ID: 7913686
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Treatment of uninformative families in mean allele sharing tests for linkage.
    Mukhopadhyay I; Feingold E; Wang T; Elston RC; Weeks DE
    Stat Appl Genet Mol Biol; 2006; 5():Article13. PubMed ID: 17049024
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Distribution of lod scores in oligogenic linkage analysis.
    Williams JT; North KE; Martin LJ; Comuzzie AG; Göring HH; Blangero J
    Genet Epidemiol; 2001; 21 Suppl 1():S805-10. PubMed ID: 11793782
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Corrections to the parameterization of constraints on allele sharing in sibling pairs alter covariate-parameter estimates but not sharing-probability estimates or power of tests for linkage.
    Greenwood CM; Bull SB
    Am J Hum Genet; 2005 Jan; 76(1):187-9. PubMed ID: 15580549
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.