Manhattan Harvester and Cropper: a system for GWAS peak detection

por Haller, Toomas, Tasa, Tõnis, Metspalu, Andres
Publicado 2019

Locations of several novel 2'-O-methylated nucleotides in human 28S rRNA

por Rebane, Ana, Roomere, Hanno, Metspalu, Andres
Publicado 2002

Editorial: Can population health be personalized? Estonia and Finland as examples

por Kääriäinen, Helena, Metspalu, Andres, Perola, Markus
Publicado 2022

Oligonucleotide Array for Mutation Analysis in Familial Breast Cancer

por Metspalu, Andres, Kaasik, Krista, Tõnisson, Neeme, Kurg, Ants
Publicado 1999

A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line

por Tammur, Jaana, Sibul, Hiljar, Ustav, Ene, Ustav, Mart, Metspalu, Andres
Publicado 2002

A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line: Correction

por Tammur, Jaana, Sibul, Hiljar, Ustav, Ene, Ustav, Mart, Metspalu, Andres
Publicado 2002

Human basonuclin 2 up-regulates a cascade set of interferon-stimulated genes with anti-cancerous properties in a lung cancer model

por Urgard, Egon, Reigo, Anu, Reinmaa, Eva, Rebane, Ana, Metspalu, Andres
Publicado 2017

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores

por Läll, Kristi, Mägi, Reedik, Morris, Andrew, Metspalu, Andres, Fischer, Krista
Publicado 2017

Linking a Population Biobank with National Health Registries—The Estonian Experience

por Leitsalu, Liis, Alavere, Helene, Tammesoo, Mari-Liis, Leego, Erkki, Metspalu, Andres
Publicado 2015

Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort

por Aasmets, Oliver, Krigul, Kertu Liis, Lüll, Kreete, Metspalu, Andres, Org, Elin
Publicado 2022

Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

por Mägi, Reedik, Pfeufer, Arne, Nelis, Mari, Montpetit, Alexandre, Metspalu, Andres, Remm, Maido
Publicado 2007

Gene Expression-Based Approaches in Differentiation of Metastases and Second Primary Tumour

por Vooder, Tõnu, Välk, Kristjan, Kolde, Raivo, Roosipuu, Retlav, Vilo, Jaak, Metspalu, Andres
Publicado 2010

Within-Trait Heterogeneity in Age Group Differences in Personality Domains and Facets: Implications for the Development and Coherence of Personality Traits

por Mõttus, René, Realo, Anu, Allik, Jüri, Esko, Tõnu, Metspalu, Andres, Johnson, Wendy
Publicado 2015

Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples

por Pullat, Janne, Fleischer, Robert, Becker, Nikolaus, Beier, Markus, Metspalu, Andres, Hoheisel, Jörg D
Publicado 2007

In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes

por Ivanov, Maxim, Kals, Mart, Kacevska, Marina, Metspalu, Andres, Ingelman-Sundberg, Magnus, Milani, Lili
Publicado 2013

CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing

por Tserel, Liina, Limbach, Maia, Saare, Mario, Kisand, Kai, Metspalu, Andres, Milani, Lili, Peterson, Pärt
Publicado 2014

Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example

por Prins, Bram Peter, Leitsalu, Liis, Pärna, Katri, Fischer, Krista, Metspalu, Andres, Haller, Toomas, Snieder, Harold
Publicado 2021

BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia

por Tamboom, Kristiina, Kaasik, Krista, Aršavskaja, Jelena, Tekkel, Mare, Lilleorg, Aili, Padrik, Peeter, Metspalu, Andres, Veidebaum, Toomas
Publicado 2010

Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites

por Taba, Nele, Valge, Hanna-Kristel, Metspalu, Andres, Esko, Tõnu, Wilson, James F., Fischer, Krista, Pirastu, Nicola
Publicado 2021

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta

por Maasalu, Katre, Nikopensius, Tiit, Kõks, Sulev, Nõukas, Margit, Kals, Mart, Prans, Ele, Zhytnik, Lidiia, Metspalu, Andres, Märtson, Aare
Publicado 2015