Torthaí cuardaigh - Nurlan Kerimov
- 1 - 9 toradh as 9 á dtaispeáint
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1
Co-expression analysis reveals interpretable gene modules controlled by trans-acting genetic variants de réir Liis Kolberg, Nurlan Kerimov, Hedi Peterson, Kaur Alasoo
Foilsithe / Cruthaithe 2020Artigo -
2
eQTL Catalogue: a compendium of uniformly processed human gene expression and splicing QTLs de réir Nurlan Kerimov, James Hayhurst, Kateryna Peikova, Jonathan Manning, Peter Walter, Liis Kolberg, Marija Samoviča, Manoj Pandian Sakthivel, Ivan Kuzmin, Stephen J. Trevanion, Tony Burdett, Simon Jupp, Helen Parkinson, Irene Papatheodorou, Andrew Yates, Daniel R. Zerbino, Kaur Alasoo
Foilsithe / Cruthaithe 2020Pré-impressão -
3
A compendium of uniformly processed human gene expression and splicing quantitative trait loci de réir Nurlan Kerimov, James Hayhurst, Kateryna Peikova, Jonathan Manning, Peter Walter, Liis Kolberg, Marija Samoviča, Manoj Pandian Sakthivel, Ivan Kuzmin, Stephen J. Trevanion, Tony Burdett, Simon Jupp, Helen Parkinson, Irene Papatheodorou, Andrew Yates, Daniel R. Zerbino, Kaur Alasoo
Foilsithe / Cruthaithe 2021Artigo -
4
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs de réir Nurlan Kerimov, Ralf Tambets, James Hayhurst, Ida Rahu, Peep Kolberg, Uku Raudvere, Ivan Kuzmin, Anshika Chowdhary, Andreas Vija, Hans Teras, Masahiro Kanai, Jacob C. Ulirsch, Mina Ryten, John Hardy, Sebastian Guelfi, Daniah Trabzuni, Sarah Kim-Hellmuth, William Rayner, Hilary K. Finucane, Hedi Peterson, Abayomi Mosaku, Helen Parkinson, Kaur Alasoo
Foilsithe / Cruthaithe 2023Artigo -
5
Metabolomic and genomic prediction of common diseases in 477,706 participants in three national biobanks de réir Jeffrey C. Barrett, Tõnu Esko, Krista Fischer, Luke Jostins-Dean, Pekka Jousilahti, Heli Julkunen, Tuija Jääskeläinen, Nurlan Kerimov, Sini Kerminen, Anastassia Kolde, Harri Koskela, Jaanika Kronberg, Sara Lundgren, Annamari Lundqvist, Valtteri Mäkelä, Kristian Nybo, Markus Perola, Veikko Salomaa, Kirsten Schut, Maiju Soikkeli, Pasi Soininen, Mika Tiainen, Taavi Tillmann, Peter Würtz
Foilsithe / Cruthaithe 2023Pré-impressão -
6
Metabolomic and genomic prediction of common diseases in 700,217 participants in three national biobanks de réir Jeffrey C. Barrett, Tõnu Esko, Krista Fischer, Luke Jostins-Dean, Pekka Jousilahti, Heli Julkunen, Tuija Jääskeläinen, Antti J. Kangas, Nurlan Kerimov, Sini Kerminen, Anastassia Kolde, Harri Koskela, Jaanika Kronberg, Sara Lundgren, Annamari Lundqvist, Valtteri Mäkelä, Kristian Nybo, Markus Perola, Veikko Salomaa, Kirsten Schut, Maiju Soikkeli, Pasi Soininen, Mika Tiainen, Taavi Tillmann, Peter Würtz
Foilsithe / Cruthaithe 2024Artigo -
7
Insights from complex trait fine-mapping across diverse populations de réir Masahiro Kanai, Jacob C. Ulirsch, Juha Karjalainen, Mitja Kurki, Konrad J. Karczewski, Eric B. Fauman, Qingbo Wang, Hannah Jacobs, François Aguet, Kristin Ardlie, Nurlan Kerimov, Kaur Alasoo, Christian Benner, Kazuyoshi Ishigaki, Saori Sakaue, Steven K. Reilly, Yoichiro Kamatani, Koichi Matsuda, Aarno Palotie, Benjamin M. Neale, Ryan Tewhey, Pardis C. Sabeti, Yukinori Okada, Mark J. Daly, Hilary K. Finucane
Foilsithe / Cruthaithe 2021Pré-impressão -
8
FinnGen: Unique genetic insights from combining isolated population and national health register data de réir Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipilä, Kati Kristiansson, Kati Donner, Mary Pat Reeve, Hannele Laivuori, Mervi Aavikko, Mari Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, Arto Lehistö, Masahiro Kanai, Nina Mars, Joel Rämö, Tuomo Kiiskinen, Henrike Heyne, Kumar Veerapen, Sina Rüeger, Susanna Lemmelä, Wei Zhou, Sanni Ruotsalainen, Kalle Pärn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari, Mari Niemi, Marianna Niemi
Foilsithe / Cruthaithe 2022Pré-impressão -
9
FinnGen provides genetic insights from a well-phenotyped isolated population de réir Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipilä, Kati Kristiansson, Kati Donner, Mary Pat Reeve, Hannele Laivuori, Mervi Aavikko, Mari Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, Arto Lehistö, Masahiro Kanai, Nina Mars, Joel Rämö, Tuomo Kiiskinen, Henrike Heyne, Kumar Veerapen, Sina Rüeger, Susanna Lemmelä, Wei Zhou, Sanni Ruotsalainen, Kalle Pärn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Graham J. Mann, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari
Foilsithe / Cruthaithe 2023Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Genotype
Single-nucleotide polymorphism
Biobank
Computational biology
Genome-wide association study
Quantitative trait locus
Expression quantitative trait loci
Medicine
Computer science
Disease
Environmental health
Genetic association
Internal medicine
Population
Allele
Allele frequency
Archaeology
Bioinformatics
Compendium
Genome
Metabolomics
Minor allele frequency
Programming language
RNA
RNA splicing
Trait
1000 Genomes Project