93 related articles for article (PubMed ID: 17044871)
1. Ignoring distant genealogic loops leads to false-positives in homozygosity mapping.
Liu F; Elefante S; van Duijn CM; Aulchenko YS
Ann Hum Genet; 2006 Nov; 70(Pt 6):965-70. PubMed ID: 17044871
[TBL] [Abstract][Full Text] [Related]
2. An approach for cutting large and complex pedigrees for linkage analysis.
Liu F; Kirichenko A; Axenovich TI; van Duijn CM; Aulchenko YS
Eur J Hum Genet; 2008 Jul; 16(7):854-60. PubMed ID: 18301450
[TBL] [Abstract][Full Text] [Related]
3. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
[TBL] [Abstract][Full Text] [Related]
4. The genealogic approach to human genetics of disease.
Gulcher J; Kong A; Stefansson K
Cancer J; 2001; 7(1):61-8. PubMed ID: 11269649
[TBL] [Abstract][Full Text] [Related]
5. Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.
Kruglyak L; Daly MJ; Lander ES
Am J Hum Genet; 1995 Feb; 56(2):519-27. PubMed ID: 7847388
[TBL] [Abstract][Full Text] [Related]
6. The impact of some parameters on linkage analysis of Alzheimer's disease.
Xu JF; Taylor EW; Lung FW; Chung AS; Chase GA; Maestri NE; Meyers DA
Genet Epidemiol; 1993; 10(6):407-12. PubMed ID: 8314035
[TBL] [Abstract][Full Text] [Related]
7. Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease.
Sillén A; Andrade J; Lilius L; Forsell C; Axelman K; Odeberg J; Winblad B; Graff C
Eur J Hum Genet; 2008 Feb; 16(2):202-8. PubMed ID: 17957224
[TBL] [Abstract][Full Text] [Related]
8. Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages.
Ayub M; Irfan M; Maclean A; Naeem F; MacGregor S; Visscher PM; Muir W; Blackwood D
Hum Hered; 2008; 66(3):190-8. PubMed ID: 18506107
[TBL] [Abstract][Full Text] [Related]
9. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
[TBL] [Abstract][Full Text] [Related]
10. A locus for Fanconi anemia on 16q determined by homozygosity mapping.
Gschwend M; Levran O; Kruglyak L; Ranade K; Verlander PC; Shen S; Faure S; Weissenbach J; Altay C; Lander ES; Auerbach AD; Botstein D
Am J Hum Genet; 1996 Aug; 59(2):377-84. PubMed ID: 8755924
[TBL] [Abstract][Full Text] [Related]
11. Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.
Gelernter J; Panhuysen C; Weiss R; Brady K; Poling J; Krauthammer M; Farrer L; Kranzler HR
Biol Psychiatry; 2007 Jan; 61(1):119-26. PubMed ID: 17081504
[TBL] [Abstract][Full Text] [Related]
12. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
Knight HM; Maclean A; Irfan M; Naeem F; Cass S; Pickard BS; Muir WJ; Blackwood DH; Ayub M
Eur J Hum Genet; 2008 Jun; 16(6):750-8. PubMed ID: 18322454
[TBL] [Abstract][Full Text] [Related]
13. Inferential testing for linkage with GENEHUNTER-MODSCORE: the impact of the pedigree structure on the null distribution of multipoint MOD scores.
Mattheisen M; Dietter J; Knapp M; Baur MP; Strauch K
Genet Epidemiol; 2008 Jan; 32(1):73-83. PubMed ID: 17849490
[TBL] [Abstract][Full Text] [Related]
14. Model-based linkage analysis with imprinting for quantitative traits: ignoring imprinting effects can severely jeopardize detection of linkage.
Sung YJ; Rao DC
Genet Epidemiol; 2008 Jul; 32(5):487-96. PubMed ID: 18366130
[TBL] [Abstract][Full Text] [Related]
15. Modeling the effect of inbreeding among founders in linkage analysis.
Hössjer O
Theor Popul Biol; 2006 Sep; 70(2):146-63. PubMed ID: 16828135
[TBL] [Abstract][Full Text] [Related]
16. Complex trait mapping in isolated populations: Are specific statistical methods required?
Bourgain C; Génin E
Eur J Hum Genet; 2005 Jun; 13(6):698-706. PubMed ID: 15785775
[TBL] [Abstract][Full Text] [Related]
17. Breaking loops in large complex pedigrees.
Axenovich TI; Zorkoltseva IV; Liu F; Kirichenko AV; Aulchenko YS
Hum Hered; 2008; 65(2):57-65. PubMed ID: 17898536
[TBL] [Abstract][Full Text] [Related]
18. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.
Uyguner O; Kayserili H; Li Y; Karaman B; Nürnberg G; Hennies H; Becker C; Nürnberg P; Başaran S; Apak MY; Wollnik B
Clin Genet; 2007 Mar; 71(3):212-9. PubMed ID: 17309643
[TBL] [Abstract][Full Text] [Related]
19. Autosomal dominant moyamoya disease maps to chromosome 17q25.3.
Mineharu Y; Liu W; Inoue K; Matsuura N; Inoue S; Takenaka K; Ikeda H; Houkin K; Takagi Y; Kikuta K; Nozaki K; Hashimoto N; Koizumi A
Neurology; 2008 Jun; 70(24 Pt 2):2357-63. PubMed ID: 18463369
[TBL] [Abstract][Full Text] [Related]
20. Linkage replication of the MYP12 locus in common myopia.
Chen CY; Stankovich J; Scurrah KJ; Garoufalis P; Dirani M; Pertile KK; Richardson AJ; Baird PN
Invest Ophthalmol Vis Sci; 2007 Oct; 48(10):4433-9. PubMed ID: 17898262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
