Remm 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: remm 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. Among authors: remm m. 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

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.

Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A. Patsalis PC, et al. Among authors: remm m. Eur J Hum Genet. 2007 Feb;15(2):162-72. doi: 10.1038/sj.ejhg.5201738. Epub 2006 Nov 22. Eur J Hum Genet. 2007. PMID: 17119536

4

Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.

Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A, Patsalis PC. Kousoulidou L, et al. Among authors: remm m. Nat Protoc. 2008;3(5):849-65. doi: 10.1038/nprot.2008.49. Nat Protoc. 2008. PMID: 18451793

5

Genetic structure of Europeans: a view from the North-East.

Nelis M, Esko T, Mägi R, Zimprich F, Zimprich A, Toncheva D, Karachanak S, Piskácková T, Balascák I, Peltonen L, Jakkula E, Rehnström K, Lathrop M, Heath S, Galan P, Schreiber S, Meitinger T, Pfeufer A, Wichmann HE, Melegh B, Polgár N, Toniolo D, Gasparini P, D'Adamo P, Klovins J, Nikitina-Zake L, Kucinskas V, Kasnauskiene J, Lubinski J, Debniak T, Limborska S, Khrunin A, Estivill X, Rabionet R, Marsal S, Julià A, Antonarakis SE, Deutsch S, Borel C, Attar H, Gagnebin M, Macek M, Krawczak M, Remm M, Metspalu A. Nelis M, et al. Among authors: remm m. PLoS One. 2009;4(5):e5472. doi: 10.1371/journal.pone.0005472. Epub 2009 May 8. PLoS One. 2009. PMID: 19424496 Free PMC article.

6

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications.

Scheler O, Glynn B, Parkel S, Palta P, Toome K, Kaplinski L, Remm M, Maher M, Kurg A. Scheler O, et al. Among authors: remm m. BMC Biotechnol. 2009 May 15;9:45. doi: 10.1186/1472-6750-9-45. BMC Biotechnol. 2009. PMID: 19445684 Free PMC article.

7

Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides.

Kaplinski L, Scheler O, Parkel S, Palta P, Toome K, Kurg A, Remm M. Kaplinski L, et al. Among authors: remm m. BMC Biotechnol. 2010 Apr 28;10:34. doi: 10.1186/1472-6750-10-34. BMC Biotechnol. 2010. PMID: 20426847 Free PMC article.

8

A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.

Männik K, Parkel S, Palta P, Zilina O, Puusepp H, Esko T, Mägi R, Nõukas M, Veidenberg A, Nelis M, Metspalu A, Remm M, Ounap K, Kurg A. Männik K, et al. Among authors: remm m. Eur J Med Genet. 2011 Mar-Apr;54(2):136-43. doi: 10.1016/j.ejmg.2010.11.005. Epub 2010 Nov 26. Eur J Med Genet. 2011. PMID: 21112420

9

Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes.

Scheler O, Kaplinski L, Glynn B, Palta P, Parkel S, Toome K, Maher M, Barry T, Remm M, Kurg A. Scheler O, et al. Among authors: remm m. BMC Biotechnol. 2011 Feb 28;11:17. doi: 10.1186/1472-6750-11-17. BMC Biotechnol. 2011. PMID: 21356118 Free PMC article.

10

No evidence of somatic DNA copy number alterations in eutopic and ectopic endometrial tissue in endometriosis.

Saare M, Sõritsa D, Vaidla K, Palta P, Remm M, Laan M, Karro H, Sõritsa A, Salumets A, D'Hooghe T, Peters M. Saare M, et al. Among authors: remm m. Hum Reprod. 2012 Jun;27(6):1857-64. doi: 10.1093/humrep/des125. Epub 2012 Apr 3. Hum Reprod. 2012. PMID: 22473391

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