Výsledky vyhledávání - Priit Palta
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A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling Autor Christine Clark, Priit Palta, Christopher J. Joyce, Carol Scott, Elin Grundberg, Panos Deloukas, Aarno Palotie, Alison J. Coffey
Vydáno 2012Artigo -
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Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type–specific hypomethylated regions Autor Matthias Zilbauer, Tim F. Rayner, Christine Clark, Alison J. Coffey, Chris J. Joyce, Priit Palta, Aarno Palotie, Paul Lyons, Kenneth G. C. Smith
Vydáno 2013Artigo -
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GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer Autor Mariann Koel, Urmo Võsa, Maarja Jõeloo, Kristi Läll, Natàlia Pujol‐Gualdo, Hannele Laivuori, Susanna Lemmelä, Mark J. Daly, Priit Palta, Reedik Mägi, Triin Laisk
Vydáno 2023Artigo -
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Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel Autor Mario Mitt, Mart Kals, Kalle Pärn, Stacey Gabriel, Eric S. Lander, Aarno Palotie, Samuli Ripatti, Andrew P. Morris, Andres Metspalu, Tõnu Esko, Reedik Mägi, Priit Palta
Vydáno 2017Artigo -
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Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies Autor Samuel Lessard, Michael J. Chao, Kadri Reis, Mathieu Beauvais, Deepak K. Rajpal, Jennifer Sloane, Priit Palta, K. Klinger, Emanuele de Rinaldis, Khader Shameer, Clément Chatelain
Vydáno 2024Artigo -
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Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom Autor Himanshu Chheda, Priit Palta, Matti Pirinen, Shane McCarthy, Klaudia Walter, Seppo Koskinen, Veikko Salomaa, Mark J. Daly, Richard Durbin, Aarno Palotie, Tero Aittokallio, Samuli Ripatti
Vydáno 2017Artigo -
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Targeted gene expression profiling for accurate endometrial receptivity testing Autor Alvin Meltsov, Merli Saare, Hindrek Teder, Priit Paluoja, Riikka K. Arffman, Terhi Piltonen, Piotr Laudański, Mirosław Wielgoś, Luca Gianaroli, Mariann Koel, Maire Peters, Andres Salumets, Kaarel Krjutškov, Priit Palta
Vydáno 2023Artigo -
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The GENCODE exome: sequencing the complete human exome Autor Alison J Coffey, Felix Kokocinski, Maria S Calafato, Carol Scott, Priit Palta, Eleanor Drury, Christopher J. Joyce, Emily M LeProust, Jennifer Harrow, Sarah Hunt, Anna-Elina Lehesjoki, Daniel J. Turner, Tim Hubbard, Aarno Palotie
Vydáno 2011Artigo -
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Polygenic Hyperlipidemias and Coronary Artery Disease Risk Autor Pietari Ripatti, Joel Rämö, Nina Mars, Yu Fu, Jake Lin, Sanni Söderlund, Christian Benner, Ida Surakka, Tuomo Kiiskinen, Aki S. Havulinna, Priit Palta, Nelson B. Freimer, Elisabeth Widén, Veikko Salomaa, Taru Tukiainen, Matti Pirinen, Aarno Palotie, Marja‐Riitta Taskinen, Samuli Ripatti
Vydáno 2020Artigo -
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Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health Autor Satu Strausz, Sanni Ruotsalainen, Hanna M. Ollila, Juha Karjalainen, Tuomo Kiiskinen, Mary Pat Reeve, Mitja Kurki, Nina Mars, Aki S. Havulinna, Elina Luonsi, Dina Mansour Aly, Emma Ahlqvist, Maris Teder‐Laving, Priit Palta, Leif Groop, Reedik Mägi, Antti Mäkitie, Veikko Salomaa, Adel Bachour, Jaakko Tuomilehto, Aarno Palotie, Tuula Palotie, Samuli Ripatti
Vydáno 2020Artigo -
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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms Autor Michael H. Guo, Satish K. Nandakumar, Jacob C. Ulirsch, Seyedeh M. Zekavat, Jason D. Buenrostro, Pradeep Natarajan, Rany M. Salem, Roberto Chiarle, Mario Mitt, Mart Kals, Kalle Pärn, Krista Fischer, Lili Milani, Reedik Mägi, Priit Palta, Stacey Gabriel, Andres Metspalu, Eric S. Lander, Sekar Kathiresan, Joel N. Hirschhorn, Tõnu Esko, Vijay G. Sankaran
Vydáno 2016Artigo -
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Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations Autor Yali Xue, Massimo Mezzavilla, Marc Haber, Shane McCarthy, Yuan Chen, Vagheesh M. Narasimhan, Arthur Gilly, Qasim Ayub, Vincenza Colonna, Lorraine Southam, Chris Finan, Andrea Massaia, Himanshu Chheda, Priit Palta, Graham R. S. Ritchie, Jennifer L. Asimit, George Dedoussis, Paolo Gasparini, Aarno Palotie, Samuli Ripatti, Nicole Soranzo, Daniela Toniolo, James F. Wilson, Richard Durbin, Chris Tyler‐Smith, Eleftheria Zeggini
Vydáno 2017Artigo -
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Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes Autor Amanda Elliott, Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jacqueline I. Goldstein, Mary Pat Reeve, Harri Siirtola, Susanna Lemmelä, Patrick Turley, Elisa Lahtela, Juha Mehtonen, Kadri Reis, Abdelrahman G. Elnahas, Anu Reigo, Priit Palta, Tõnu Esko, Reedik Mägi, Andres Metspalu, Mari Nelis, Lili Milani, Georgi Hudjashov, Haari Siirtola, Elisa Lahtinen, Aarno Palotie, Mark J. Daly, Elisabeth Widén
Vydáno 2024Artigo -
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High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene Autor Fedik Rahimov, Pekka Nieminen, Priyanka Kumari, Emma Juuri, Tiit Nikopensius, Kitt Paraiso, J German, Antti Karvanen, Mart Kals, Abdelrahman G. Elnahas, Juha Karjalainen, Mitja Kurki, Aarno Palotie, Arja Heliövaara, Tõnu Esko, Sakari Jukarainen, Priit Palta, Andrea Ganna, Anjali P. Patni, Daniel Mar, Karol Bomsztyk, Julie Mathieu, Hannele Ruohola‐Baker, Axel Visel, Walid D. Fakhouri, Brian C. Schutte, Robert A. Cornell, David Rice
Vydáno 2024Artigo -
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De novo mutations in schizophrenia implicate synaptic networks Autor Menachem Fromer, Andrew Pocklington, David H. Kavanagh, Hywel Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M. Ruderfer, Noa Carrera, Isla Humphreys, Jessica Johnson, Panos Roussos, Douglas Barker, Eric Banks, Vihra Milanova, Seth G. N. Grant, Eilís Hannon, Samuel A. Rose, Kimberly Chambert, Milind Mahajan, Edward M. Scolnick, Jennifer L. Moran, George Kirov, Aarno Palotie, Steven A. McCarroll, Peter Holmans, Pamela Sklar, Michael J. Owen, Shaun Purcell, Michael O’Donovan
Vydáno 2014Artigo -
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Genetic analysis for a shared biological basis between migraine and coronary artery disease Autor Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik, Padhraig Gormley, Verneri Anttila, Jason Vander Heiden, Katherine S. Elliott, L.M. Jacobsen, Priit Palta, Najaf Amin, Boukje de Vries, Eija Hämäläinen, Tobias Freilinger, M. Arfan Ikram, Thorsten Kessler, Markku Koiranen, Lannie Ligthart, George McMahon, Linda M. Pedersen, Christina Willenborg, Hong‐Hee Won, Jes Olesen, Ville Artto, Themistocles L. Assimes, Stefan Blankenberg, Dorret I. Boomsma, Lynn Cherkas, George Davey Smith, Stephen E. Epstein, Jeanette Erdmann, Michel D. Ferrari, Hartmut Göbel, Alistair S. Hall, Marjo‐Riitta Järvelin, Mikko Kallela, Jaakko Kaprio, Sekar Kathiresan, Terho Lehtimäki, Ruth McPherson, Winfried März, Dale R. Nyholt, Christopher J. O’Donnell, Lydia Quaye, Daniel J. Rader, Olli T. Raitakari, Robert J. Roberts, Heribert Schunkert, Markus Schürks, Alexandre F.R. Stewart, Gisela M. Terwindt, Unnur Þorsteinsdóttir, Arn M. J. M. van den Maagdenberg, Cornelia M. van Duijn, Maija Wessman, Tobias Kurth, Christian Kubisch, Martin Dichgans, Daniel I. Chasman, Chris Cotsapas, John‐Anker Zwart, Nilesh J. Samani, Aarno Palotie, Leonore J. Launer, George Davey Smith, George McMahon, Dale R. Nyholt, Alfons Macaya, Patricia Pozo‐Rosich, Bru Cormand, Jessica Fernandez, Marta Vila‐Pueyo, Cèlia Sintas, Jes Olesen, Anne Francke Christensen, Ann-Louise Esserlind, Najaf Amin, Tõnu Esko, Aarno Palotie, Mikko Kallela, Maija Wessman, Ville Artto, Verneri Anttila, Eija Hämäläinen, Priit Palta, Padhraig Gormley, E Garcia Cuenca, Jaakko Kaprio, Martin Dichgans, Hartmut Göbel, Christian Kubisch, Tobias Freilinger, Rainer Malik, Bertram Müller‐Myhsok, John‐Anker Zwart, Bendik S. Winsvold, L.M. Jacobsen, Linda M. Pedersen, Alice Pressman, Arn van den Maagdenberg, Gisela M. Terwindt
Vydáno 2015Artigo -
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The Estonian Biobank’s journey from biobanking to personalized medicine Autor Lili Milani, Maris Alver, Sven Laur, Sulev Reisberg, Toomas Haller, Oliver Aasmets, Erik Abner, Helene Alavere, Annely Allik, Tarmo Annilo, Krista Fischer, Robin J. Hofmeister, Georgi Hudjashov, Maarja Jõeloo, Mart Kals, Liis Karo-Astover, Silva Kasela, Anastassia Kolde, Kristi Krebs, Kertu Liis Krigul, Jaanika Kronberg, Karoliina Kruusmaa, Viktorija Kukuškina, Kadri Kõiv, Kelli Lehto, Liis Leitsalu, Sirje Lind, Laura Birgit Luitva, Kristi Läll, Kreete Lüll, Kristjan Metsalu, Mait Metspalu, René Mõttus, Mari Nelis, Tiit Nikopensius, Miriam Nurm, Margit Nõukas, Marek Oja, Elin Org, Marili Palover, Priit Palta, Vasili Pankratov, Kateryna Pantiukh, Natalia Pervjakova, Natàlia Pujol‐Gualdo, Anu Reigo, Ene Reimann, Steven Smit, Diana Rogozina, Dage Särg, Nele Taba, Harry-Anton Talvik, Maris Teder‐Laving, Neeme Tönisson, Mariliis Vaht, Uku Vainik, Urmo Võsa, Burak Yelmen, Tõnu Esko, Raivo Kolde, Reedik Mägi, Jaak Vilo, Triin Laisk, Andres Metspalu
Vydáno 2025Revisão -
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Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population Autor Elaine T. Lim, Peter Würtz, Aki S. Havulinna, Priit Palta, Taru Tukiainen, Karola Rehnström, Tõnu Esko, Reedik Mägi, Michael Inouye, Tuuli Lappalainen, Yingleong Chan, Rany M. Salem, Monkol Lek, Jason Flannick, Xueling Sim, Alisa K. Manning, Claes Ladenvall, Suzannah Bumpstead, Eija Hämäläinen, Kristiina Aalto, Mikael Maksimow, Marko Salmi, Stefan Blankenberg, Diego Ardissino, Svati H. Shah, Benjamin D. Horne, Ruth McPherson, Gerald K. Hovingh, Muredach P. Reilly, Hugh Watkins, Anuj Goel, Martin Farrall, Domenico Girelli, Alex P. Reiner, Nathan O. Stitziel, Sekar Kathiresan, Stacey Gabriel, Jeffrey C. Barrett, Terho Lehtimäki, Markku Laakso, Leif Groop, Jaakko Kaprio, Markus Perola, Mark I. McCarthy, Michael Boehnke, David Altshuler, Cecilia M. Lindgren, Joel N. Hirschhorn, Andres Metspalu, Nelson B. Freimer, Tanja Zeller, Sirpa Jalkanen, Seppo Koskinen, Olli T. Raitakari, Richard Durbin, Daniel G. MacArthur, Veikko Salomaa, Samuli Ripatti, Mark J. Daly, Aarno Palotie
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Internal medicine
Computational biology
Genetic association
Bioinformatics
Genome
Population
Allele frequency
Biobank
Environmental health
Migraine
Allele
Computer science
Phenotype
Disease
Endocrinology
Genetic variants
Demography
Gene expression
Heritability
Mendelian randomization
Minor allele frequency
Sociology
1000 Genomes Project