Computational framework for targeted high-coverage sequencing based NIPT

Por Teder, Hindrek, Paluoja, Priit, Rekker, Kadri, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit
Publicado no PLoS One (2019)

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

Por Kaplinski, Lauris, Scheler, Ott, Parkel, Sven, Palta, Priit, Toome, Kadri, Kurg, Ants, Remm, Maido
Publicado em 2010

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

Por Kaplinski Lauris, Toome Kadri, Palta Priit, Parkel Sven, Glynn Barry, Scheler Ott, Remm Maido, Maher Majella, Kurg Ants
Publicado em 2009-05-01

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

Por Scheler, Ott, Glynn, Barry, Parkel, Sven, Palta, Priit, Toome, Kadri, Kaplinski, Lauris, Remm, Maido, Maher, Majella, Kurg, Ants
Publicado em 2009

A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip(®) for Methylome Profiling

Por Clark, Christine, Palta, Priit, Joyce, Christopher J., Scott, Carol, Grundberg, Elin, Deloukas, Panos, Palotie, Aarno, Coffey, Alison J.
Publicado em 2012

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

Por Scheler, Ott, Kaplinski, Lauris, Glynn, Barry, Palta, Priit, Parkel, Sven, Toome, Kadri, Maher, Majella, Barry, Thomas, Remm, Maido, Kurg, Ants
Publicado em 2011

Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families

Por Palta, Priit, Kaplinski, Lauris, Nagirnaja, Liina, Veidenberg, Andres, Möls, Märt, Nelis, Mari, Esko, Tõnu, Metspalu, Andres, Laan, Maris, Remm, Maido
Publicado no PLoS One (2015)

Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage

Por Nagirnaja, Liina, Palta, Priit, Kasak, Laura, Rull, Kristiina, Christiansen, Ole B, Nielsen, Henriette S, Steffensen, Rudi, Esko, Tõnu, Remm, Maido, Laan, Maris
Publicado no Hum Mutat (2014)

Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type–specific hypomethylated regions

Por Zilbauer, Matthias, Rayner, Tim F., Clark, Christine, Coffey, Alison J., Joyce, Chris J., Palta, Priit, Palotie, Aarno, Lyons, Paul A., Smith, Kenneth G. C.
Publicado em 2013

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

Por Chheda, Himanshu, Palta, Priit, Pirinen, Matti, McCarthy, Shane, Walter, Klaudia, Koskinen, Seppo, Salomaa, Veikko, Daly, Mark, Durbin, Richard, Palotie, Aarno, Aittokallio, Tero, Ripatti, Samuli
Publicado no Eur J Hum Genet (2017)

Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

Por Mitt, Mario, Kals, Mart, Pärn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tõnu, Mägi, Reedik, Palta, Priit
Publicado no Eur J Hum Genet (2017)

TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting

Por Teder, Hindrek, Koel, Mariann, Paluoja, Priit, Jatsenko, Tatjana, Rekker, Kadri, Laisk-Podar, Triin, Kukuškina, Viktorija, Velthut-Meikas, Agne, Fjodorova, Olga, Peters, Maire, Kere, Juha, Salumets, Andres, Palta, Priit, Krjutškov, Kaarel
Publicado no NPJ Genom Med (2018)

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

Por Sauk, Martin, Žilina, Olga, Kurg, Ants, Ustav, Eva-Liina, Peters, Maire, Paluoja, Priit, Roost, Anne Mari, Teder, Hindrek, Palta, Priit, Brison, Nathalie, Vermeesch, Joris R., Krjutškov, Kaarel, Salumets, Andres, Kaplinski, Lauris
Publicado no Sci Rep (2018)

The GENCODE exome: sequencing the complete human exome

Por Coffey, Alison J, Kokocinski, Felix, Calafato, Maria S, Scott, Carol E, Palta, Priit, Drury, Eleanor, Joyce, Christopher J, LeProust, Emily M, Harrow, Jen, Hunt, Sarah, Lehesjoki, Anna-Elina, Turner, Daniel J, Hubbard, Tim J, Palotie, Aarno
Publicado em 2011

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

Por Ripatti, Pietari, Rämö, Joel T., Mars, Nina J., Fu, Yu, Lin, Jake, Söderlund, Sanni, Benner, Christian, Surakka, Ida, Kiiskinen, Tuomo, Havulinna, Aki S., Palta, Priit, Freimer, Nelson B., Widén, Elisabeth, Salomaa, Veikko, Tukiainen, Taru, Pirinen, Matti, Palotie, Aarno, Taskinen, Marja-Riitta, Ripatti, Samuli
Publicado no Circ Genom Precis Med (2020)

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

Por Guo, Michael H., Nandakumar, Satish K., Ulirsch, Jacob C., Zekavat, Seyedeh M., Buenrostro, Jason D., Natarajan, Pradeep, Salem, Rany M., Chiarle, Roberto, Mitt, Mario, Kals, Mart, Pärn, Kalle, Fischer, Krista, Milani, Lili, Mägi, Reedik, Palta, Priit, Gabriel, Stacey B., Metspalu, Andres, Lander, Eric S., Kathiresan, Sekar, Hirschhorn, Joel N., Esko, Tõnu, Sankaran, Vijay G.
Publicado no Proc Natl Acad Sci U S A (2017)

Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

Por Xue, Yali, Mezzavilla, Massimo, Haber, Marc, McCarthy, Shane, Chen, Yuan, Narasimhan, Vagheesh, Gilly, Arthur, Ayub, Qasim, Colonna, Vincenza, Southam, Lorraine, Finan, Christopher, Massaia, Andrea, Chheda, Himanshu, Palta, Priit, Ritchie, Graham, Asimit, Jennifer, Dedoussis, George, Gasparini, Paolo, Palotie, Aarno, Ripatti, Samuli, Soranzo, Nicole, Toniolo, Daniela, Wilson, James F., Durbin, Richard, Tyler-Smith, Chris, Zeggini, Eleftheria
Publicado no Nat Commun (2017)

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

Por Tabassum, Rubina, Rämö, Joel T., Ripatti, Pietari, Koskela, Jukka T., Kurki, Mitja, Karjalainen, Juha, Palta, Priit, Hassan, Shabbeer, Nunez-Fontarnau, Javier, Kiiskinen, Tuomo T. J., Söderlund, Sanni, Matikainen, Niina, Gerl, Mathias J., Surma, Michal A., Klose, Christian, Stitziel, Nathan O., Laivuori, Hannele, Havulinna, Aki S., Service, Susan K., Salomaa, Veikko, Pirinen, Matti, Jauhiainen, Matti, Daly, Mark J., Freimer, Nelson B., Palotie, Aarno, Taskinen, Marja-Riitta, Simons, Kai, Ripatti, Samuli
Publicado no Nat Commun (2019)

De novo mutations in schizophrenia implicate synaptic networks

Por Fromer, Menachem, Pocklington, Andrew J., Kavanagh, David H., Williams, Hywel J., Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas M., Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter, Sklar, Pamela, Owen, Michael J., Purcell, Shaun M., O’Donovan, Michael C.
Publicado no Nature (2014)

Common variant burden contributes to the familial aggregation of migraine in 1,589 families

Por Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Nissilä, Markku, Säkö, Erkki, Sumelahti, Marja-Liisa, Liukkonen, Jarmo, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Lehtimäki, Terho, Raitakari, Olli, Männikkö, Minna, Ran, Caroline, Belin, Andrea Carmine, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Färkkilä, Markus, Runz, Heiko, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno
Publicado no Neuron (2018)