Laan M - Search Results

1

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.

2

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.

3

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.

4

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.

5

Dissecting initiation of gene conversion events.

Laan M. Laan M. Hum Mutat. 2009 Aug;30(8):v. doi: 10.1002/humu.21084. Hum Mutat. 2009. PMID: 19626717 No abstract available.

6

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.

7

WITHDRAWN: TNF-Related Apoptosis-Inducing Ligand TRAIL as a Potential Biomarker for Early Pregnancy Complications.

Rull K, Tomberg K, Kõks S, Männik J, Möls M, Sirotkina M, Värv S, Laan M. Rull K, et al. Among authors: laan m. J Clin Endocrinol Metab. 2012 Jun 14. doi: 10.1210/jc.2011-3192. Online ahead of print. J Clin Endocrinol Metab. 2012. PMID: 22419717

8

Genetics of recurrent miscarriage: challenges, current knowledge, future directions.

Rull K, Nagirnaja L, Laan M. Rull K, et al. Among authors: laan m. Front Genet. 2012 Mar 19;3:34. doi: 10.3389/fgene.2012.00034. eCollection 2012. Front Genet. 2012. PMID: 22457663 Free PMC article.

9

Structural and functional analysis of rare missense mutations in human chorionic gonadotrophin β-subunit.

Nagirnaja L, Venclovas Č, Rull K, Jonas KC, Peltoketo H, Christiansen OB, Kairys V, Kivi G, Steffensen R, Huhtaniemi IT, Laan M. Nagirnaja L, et al. Among authors: laan m. Mol Hum Reprod. 2012 Aug;18(8):379-90. doi: 10.1093/molehr/gas018. Epub 2012 May 3. Mol Hum Reprod. 2012. PMID: 22554618 Free PMC article.

10

Mid-gestational gene expression profile in placenta and link to pregnancy complications.

Uusküla L, Männik J, Rull K, Minajeva A, Kõks S, Vaas P, Teesalu P, Reimand J, Laan M. Uusküla L, et al. Among authors: laan m. PLoS One. 2012;7(11):e49248. doi: 10.1371/journal.pone.0049248. Epub 2012 Nov 7. PLoS One. 2012. PMID: 23145134 Free PMC article.

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