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 *

84 related articles for article (PubMed ID: 3374730)

  • 1. Genetic analysis of late-onset diseases using first-degree relatives.
    Sobel E; Davanipour Z; Alter M
    Neuroepidemiology; 1988; 7(2):81-8. PubMed ID: 3374730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.
    Jimenez-Escrig A; Gomez-Tortosa E; Baron M; Rabano A; Arcos-Burgos M; Palacios LG; Yusta A; Anta P; Perez I; Hierro M; Munoz DG; Barquero S
    Brain; 2005 Jul; 128(Pt 7):1707-15. PubMed ID: 15843424
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease.
    Larner AJ; Ray PS; Doran M
    J Neurol Sci; 2007 Jan; 252(2):173-6. PubMed ID: 17188713
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correcting for Ascertainment.
    Ewens W; Elston RC
    Methods Mol Biol; 2017; 1666():211-232. PubMed ID: 28980248
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The genetics of Alzheimer's disease].
    Pinessi L; Rainero I; Brunetti E; Cerrato P; Cosentino N; Martino C; Vaula G; Bergamini L
    Minerva Psichiatr; 1992; 33(3):159-64. PubMed ID: 1474878
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new Italian pedigree with early-onset Alzheimer's disease.
    Rainero I; Bergamini L; Bruni AC; Ferini-Strambi L; Foncin JF; Gei G; Macciardi F; Montesi MP; Pinessi L; Vaula G
    J Geriatr Psychiatry Neurol; 1994; 7(1):28-32. PubMed ID: 8192827
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variability of familial risk of Alzheimer disease across the late life span.
    Silverman JM; Ciresi G; Smith CJ; Marin DB; Schnaider-Beeri M
    Arch Gen Psychiatry; 2005 May; 62(5):565-73. PubMed ID: 15867110
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.
    Martinez M; Campion D; Babron MC; Hannequin D; Agid Y; Bellis M; Brice A; Mallet J; Michon A; Thomas-Anterion C; Clerget-Darpoux F
    Am J Med Genet; 1996 Feb; 67(1):9-12. PubMed ID: 8678122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of sequential and fixed-structure sampling of pedigrees in complex segregation analysis of a quantitative trait.
    Boehnke M; Young MR; Moll PP
    Am J Hum Genet; 1988 Sep; 43(3):336-43. PubMed ID: 3414688
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ascertainment in the sequential sampling of pedigrees.
    Cannings C; Thompson EA
    Clin Genet; 1977 Oct; 12(4):208-12. PubMed ID: 334399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS
    Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The inheritance of Alzheimer's disease: a new interpretation.
    Fitch N; Becker R; Heller A
    Ann Neurol; 1988 Jan; 23(1):14-9. PubMed ID: 2964224
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial risks for Alzheimer disease from a population-based series.
    Hirst C; Yee IM; Sadovnick AD
    Genet Epidemiol; 1994; 11(4):365-74. PubMed ID: 7813898
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A bivariate problem in human genetics: ascertainment of families through a correlated trait.
    Dawson DV; Elston RC
    Am J Med Genet; 1984 Jul; 18(3):435-48. PubMed ID: 6476005
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical features of a neuropathologically verified familial Alzheimer's cohort with onset in the fourth decade: comparison with senile onset Alzheimer's disease and etiopathogenic implications.
    Reisberg B; Ferris SH; Franssen E; Jenkins EC; Wisniewski KE
    Prog Clin Biol Res; 1989; 317():43-54. PubMed ID: 2690108
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inherent intractability of the ascertainment problem for pedigree data: a general likelihood framework.
    Vieland VJ; Hodge SE
    Am J Hum Genet; 1995 Jan; 56(1):33-43. PubMed ID: 7825595
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial Alzheimer's disease. Evidences for clinical and genetic heterogeneity.
    Bergamini L; Pinessi L; Rainero I; Brunetti E; Cerrato P; Cosentino L; Vaula G; Bruni AC; Ermio C; Gei G
    Acta Neurol (Napoli); 1991 Dec; 13(6):534-8. PubMed ID: 1805554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heritability of plasma amyloid beta in typical late-onset Alzheimer's disease pedigrees.
    Ertekin-Taner N; Graff-Radford N; Younkin LH; Eckman C; Adamson J; Schaid DJ; Blangero J; Hutton M; Younkin SG
    Genet Epidemiol; 2001 Jul; 21(1):19-30. PubMed ID: 11443731
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The essence of single ascertainment.
    Hodge SE; Vieland VJ
    Genetics; 1996 Nov; 144(3):1215-23. PubMed ID: 8913762
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Pedigree study of pathological myopia].
    Yu ZQ; Fu CW; Shen FM; Chu RY
    Yi Chuan Xue Bao; 2005 Feb; 32(2):130-5. PubMed ID: 15759859
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.