Laan M - Search Results

1

X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations.

Laan M, Wiebe V, Khusnutdinova E, Remm M, Pääbo S. Laan M, et al. Eur J Hum Genet. 2005 Apr;13(4):452-62. doi: 10.1038/sj.ejhg.5201340. Eur J Hum Genet. 2005. PMID: 15657606 Free PMC article.

2

Demographic history and linkage disequilibrium in human populations.

Laan M, Pääbo S. Laan M, et al. Nat Genet. 1997 Dec;17(4):435-8. doi: 10.1038/ng1297-435. Nat Genet. 1997. PMID: 9398845

3

Mapping genes through the use of linkage disequilibrium generated by genetic drift: 'drift mapping' in small populations with no demographic expansion.

Terwilliger JD, Zöllner S, Laan M, Pääbo S. Terwilliger JD, et al. Among authors: laan m. Hum Hered. 1998 May-Jun;48(3):138-54. doi: 10.1159/000022794. Hum Hered. 1998. PMID: 9618061 Review.

4

Mapping genes by drift-generated linkage disequilibrium.

Laan M, Pääbo S. Laan M, et al. Am J Hum Genet. 1998 Aug;63(2):654-6. doi: 10.1086/301972. Am J Hum Genet. 1998. PMID: 9683603 Free PMC article. No abstract available.

5

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo.

Varilo T, Laan M, Hovatta I, Wiebe V, Terwilliger JD, Peltonen L. Varilo T, et al. Among authors: laan m. Eur J Hum Genet. 2000 Aug;8(8):604-12. doi: 10.1038/sj.ejhg.5200482. Eur J Hum Genet. 2000. PMID: 10951523

6

Extensive linkage disequilibrium in small human populations in Eurasia.

Kaessmann H, Zöllner S, Gustafsson AC, Wiebe V, Laan M, Lundeberg J, Uhlén M, Pääbo S. Kaessmann H, et al. Among authors: laan m. Am J Hum Genet. 2002 Mar;70(3):673-85. doi: 10.1086/339258. Epub 2002 Jan 28. Am J Hum Genet. 2002. PMID: 11813132 Free PMC article.

7

Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin beta gene cluster.

Hallast P, Nagirnaja L, Margus T, Laan M. Hallast P, et al. Among authors: laan m. Genome Res. 2005 Nov;15(11):1535-46. doi: 10.1101/gr.4270505. Genome Res. 2005. PMID: 16251463 Free PMC article.

8

Complex signatures of locus-specific selective pressures and gene conversion on Human Growth Hormone/Chorionic Somatomammotropin genes.

Sedman L, Padhukasahasram B, Kelgo P, Laan M. Sedman L, et al. Among authors: laan m. Hum Mutat. 2008 Oct;29(10):1181-93. doi: 10.1002/humu.20767. Hum Mutat. 2008. PMID: 18473352 Free PMC article.

9

Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans.

Putku M, Kepp K, Org E, Sõber S, Comas D, Viigimaa M, Veldre G, Juhanson P, Hallast P, Tõnisson N; HYPertension in ESTonia (HYPEST); Shaw-Hawkins S, Caulfield MJ; BRItish Genetics of HyperTension (BRIGHT); Khusnutdinova E, Kožich V, Munroe PB, Laan M. Putku M, et al. Among authors: laan m. Hum Mutat. 2011 Jul;32(7):806-14. doi: 10.1002/humu.21508. Epub 2011 May 10. Hum Mutat. 2011. PMID: 21520334 Free PMC article.

10

Structural genomic variation as risk factor for idiopathic recurrent miscarriage.

Nagirnaja L, Palta P, Kasak L, Rull K, Christiansen OB, Nielsen HS, Steffensen R, Esko T, Remm M, Laan M. Nagirnaja L, et al. Among authors: laan m. Hum Mutat. 2014 Aug;35(8):972-82. doi: 10.1002/humu.22589. Epub 2014 Jun 24. Hum Mutat. 2014. PMID: 24827138 Free PMC article.

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