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Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review.
Eur J Med Genet. 2022 May;65(5):104477. doi: 10.1016/j.ejmg.2022.104477. Epub 2022 Mar 18.
Eur J Med Genet. 2022.
PMID: 35314380
Review.
Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants.
Leitsalu L, Palover M, Sikka TT, Reigo A, Kals M, Pärn K, Nikopensius T, Esko T, Metspalu A, Padrik P, Tõnisson N.
Leitsalu L, et al. Among authors: palover m.
Eur J Hum Genet. 2021 Mar;29(3):471-481. doi: 10.1038/s41431-020-00760-2. Epub 2020 Nov 23.
Eur J Hum Genet. 2021.
PMID: 33230308
Free PMC article.
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Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.
Jürgens H, Roht L, Leitsalu L, Nõukas M, Palover M, Nikopensius T, Reigo A, Kals M, Kallak K, Kütner R, Budrikas K, Kuusk S, Valvere V, Laidre P, Toome K, Rekker K, Tooming M, Ülle Murumets, Kahre T, Kruuv-Käo K, Õunap K, Padrik P, Metspalu A, Esko T, Fischer K, Tõnisson N.
Jürgens H, et al. Among authors: palover m.
Front Genet. 2022 Jul 22;13:881100. doi: 10.3389/fgene.2022.881100. eCollection 2022.
Front Genet. 2022.
PMID: 35938029
Free PMC article.
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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification.
Läll K, Lepamets M, Palover M, Esko T, Metspalu A, Tõnisson N, Padrik P, Mägi R, Fischer K.
Läll K, et al. Among authors: palover m.
BMC Cancer. 2019 Jun 10;19(1):557. doi: 10.1186/s12885-019-5783-1.
BMC Cancer. 2019.
PMID: 31182048
Free PMC article.
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Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia.
Alver M, Palover M, Saar A, Läll K, Zekavat SM, Tõnisson N, Leitsalu L, Reigo A, Nikopensius T, Ainla T, Kals M, Mägi R, Gabriel SB, Eha J, Lander ES, Irs A, Philippakis A, Marandi T, Natarajan P, Metspalu A, Kathiresan S, Esko T.
Alver M, et al. Among authors: palover m.
Genet Med. 2019 May;21(5):1173-1180. doi: 10.1038/s41436-018-0311-2. Epub 2018 Oct 1.
Genet Med. 2019.
PMID: 30270359
Free PMC article.
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Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia.
Nurm M, Reigo A, Nõukas M, Leitsalu L, Nikopensius T, Palover M, Annilo T, Alver M, Saar A, Marandi T, Ainla T, Metspalu A, Esko T, Tõnisson N.
Nurm M, et al. Among authors: palover m.
Front Genet. 2022 Jul 19;13:936131. doi: 10.3389/fgene.2022.936131. eCollection 2022.
Front Genet. 2022.
PMID: 35928446
Free PMC article.
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Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.
Leitsalu L, Reigo A, Palover M, Nikopensius T, Läll K, Krebs K, Reisberg S, Mägi R, Kals M, Alavere H, Nõukas M, Kolk A, Normet I, Tammesoo ML, Käärik E, Puusepp M, Metsalu K, Allik A, Milani L, Fischer K, Tõnisson N, Metspalu A.
Leitsalu L, et al. Among authors: palover m.
Eur J Hum Genet. 2023 Sep;31(9):1048-1056. doi: 10.1038/s41431-022-01196-6. Epub 2022 Oct 3.
Eur J Hum Genet. 2023.
PMID: 36192438
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Disclosing genetic information to family members without consent: Five Australian case studies.
Tiller J, Bilkey G, Macintosh R, O'Sullivan S, Groube S, Palover M, Pachter N, Rothstein M, Lacaze P, Otlowski M.
Tiller J, et al. Among authors: palover m.
Eur J Med Genet. 2020 Nov;63(11):104035. doi: 10.1016/j.ejmg.2020.104035. Epub 2020 Aug 14.
Eur J Med Genet. 2020.
PMID: 32805446
Review.
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