Rezultati pretrage - Dimitrios Vitsios
- Prikaz rezultata 1 – 19 od 19
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Mirnovo: genome-free prediction of microRNAs from small RNA sequencing data and single-cells using decision forests od Dimitrios Vitsios, Elissavet Kentepozidou, Leonor Quintais, Èlia Benito‐Gutiérrez, Stijn van Dongen, Matthew P. Davis, Anton J. Enright
Izdano 2017Artigo -
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Cancer-driving mutations are enriched in genic regions intolerant to germline variation od Dimitrios Vitsios, Ryan S. Dhindsa, Dorota Matelska, Jonathan Mitchell, Xuequing Zou, Joshua Armenia, Fengyuan Hu, Quanli Wang, Ben S. Sidders, Andrew R. Harper, Slavé Petrovski
Izdano 2022Artigo -
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mRNA 3′ uridylation and poly(A) tail length sculpt the mammalian maternal transcriptome od Marcos Morgan, Christian Much, Monica Di Giacomo, Chiara Azzi, Ivayla Ivanova, Dimitrios Vitsios, Jelena Pistolic, Paul Collier, Pedro N. Moreira, Vladimı́r Beneš, Anton J. Enright, Dónal O’Carroll
Izdano 2017Artigo -
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Diverse ancestral representation improves genetic intolerance metrics od Alexander Han, Chloe F. Sands, Dorota Matelska, Jessica C. Butts, Vida Ravanmehr, Fengyuan Hu, Esmeralda Villavicencio Gonzalez, Nicholas Katsanis, Carlos D. Bustamante, Quanli Wang, Slavé Petrovski, Dimitrios Vitsios, Ryan S. Dhindsa
Izdano 2024Pré-impressão -
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A programmed wave of uridylation-primed mRNA degradation is essential for meiotic progression and mammalian spermatogenesis od Marcos Morgan, Yuka Kabayama, Christian Much, Ivayla Ivanova, Monica Di Giacomo, Tatsiana Auchynnikava, Jack Monahan, Dimitrios Vitsios, Lina Vasiliauskaitė, Stefano Comazzetto, Juri Rappsilber, Robin C. Allshire, Bo Porse, Anton J. Enright, Dónal O’Carroll
Izdano 2019Artigo -
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Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank od Abhishek Nag, Ryan S. Dhindsa, Lawrence Middleton, Xiao Jiang, Dimitrios Vitsios, Eleanor M. Wigmore, Erik L. Allman, Anna Reznichenko, Keren Carss, Katherine R. Smith, Quanli Wang, Benjamin Challis, Dirk S. Paul, Andrew R. Harper, Slavé Petrovski
Izdano 2023Artigo -
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Disease prediction with multi-omics and biomarkers empowers case–control genetic discoveries in the UK Biobank od Manik Garg, Marcin Karpiński, Dorota Matelska, Lawrence Middleton, Oliver S. Burren, Fengyuan Hu, Eleanor Wheeler, Katherine R. Smith, Margarete A. Fabre, Jonathan Mitchell, Amanda O’Neill, Euan A. Ashley, Andrew R. Harper, Quanli Wang, Ryan S. Dhindsa, Slavé Petrovski, Dimitrios Vitsios
Izdano 2024Artigo -
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Exome-Based Rare-Variant Analyses in CKD od Sophia Cameron‐Christie, Charles J. Wolock, Emily Groopman, Slavé Petrovski, Sitharthan Kamalakaran, Gundula Povysil, Dimitrios Vitsios, Mengqi Zhang, Jan Fleckner, Ruth March, Sahar Gelfman, Maddalena Marasà, Yifu Li, Simone Sanna‐Cherchi, Krzysztof Kiryluk, Andrew S. Allen, Bengt Fellström, Carolina Haefliger, Adam Platt, David B. Goldstein, Ali G. Gharavi
Izdano 2019Artigo -
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Identification of plasma proteomic markers underlying polygenic risk of type 2 diabetes and related comorbidities od Douglas P. Loesch, Manik Garg, Dorota Matelska, Dimitrios Vitsios, Xiao Jiang, Scott C. Ritchie, Benjamin B. Sun, Heiko Runz, Christopher D. Whelan, Rury R. Holman, Robert J. Mentz, Filipe A. Moura, Stephen D. Wiviott, Marc S. Sabatine, Miriam S. Udler, I Gause-Nilsson, Slavé Petrovski, Jan Oscarsson, Abhishek Nag, Dirk S. Paul, Michael Inouye
Izdano 2025Artigo -
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Influences of rare protein-coding genetic variants on the human plasma proteome in 50,829 UK Biobank participants od Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, Bram P. Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A. Hristova, Katherine R. Smith, Keren Carss, Sebastian Wasilewski, Andrew R. Harper, Dirk S. Paul, Margarete A. Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, Dimitrios Vitsios, Euan A. Ashley, Christopher D. Whelan, Menelas N. Pangalos, Quanli Wang, Slavé Petrovski
Izdano 2022Pré-impressão -
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Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis od Ryan S. Dhindsa, Johan Mattsson, Abhishek Nag, Quanli Wang, Louise V. Wain, Richard J. Allen, Eleanor M. Wigmore, Kristina Ibáñez, Dimitrios Vitsios, Sri V. V. Deevi, Sebastian Wasilewski, Maria Karlsson, Glenda Lassi, Henric Olsson, Daniel Muthas, Susan J. Monkley, Alex Mackay, Lynne A. Murray, Simon Young, Carolina Haefliger, Toby M. Maher, Maria G. Belvisi, Gisli Jenkins, Philip L. Molyneaux, Adam Platt, Slavé Petrovski
Izdano 2021Artigo -
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Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease od Thomas P Spargo, Chloe F. Sands, Isabella R. Juan, Jonathan Mitchell, Vida Ravanmehr, Jessica C. Butts, Ruth B. De-Paula, Young-Doo Kim, Fengyuan Hu, Quanli Wang, Dimitrios Vitsios, Manik Garg, Lawrence Middleton, Michal Tyrlik, Mirko Messa, Guillermo del Angel, Daniel G. Calame, Hiba Saade, Laurie Robak, Ben Hollis, Vishnu Anand Cuddapah, Huda Y. Zoghbi, Joshua M. Shulman, Slavé Petrovski, Ismael Al‐Ramahi, Ioanna Tachmazidou, Ryan S. Dhindsa
Izdano 2025Artigo -
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Spontaneous Coronary Artery Dissection od Keren Carss, Anna Baranowska, Javier Armisen, Tom R. Webb, Stephen E. Hamby, Diluka Premawardhana, Abtehale Al-Hussaini, Alice Wood, Quanli Wang, Sri V. V. Deevi, Dimitrios Vitsios, Samuel H. Lewis, Deevia Kotecha, Nabila Bouatia‐Naji, Stephanie Hesselson, Siiri E. Iismaa, Ingrid Tarr, Lucy McGrath‐Cadell, David W.M. Muller, Sally L. Dunwoodie, Diane Fatkin, Robert M. Graham, Eleni Giannoulatou, Nilesh J. Samani, Slavé Petrovski, Carolina Haefliger, David Adlam
Izdano 2020Artigo -
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Rare variant contribution to human disease in 281,104 UK Biobank exomes od Quanli Wang, Ryan S. Dhindsa, Keren Carss, Andrew R. Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V. V. Deevi, Alex Mackay, Daniel Muthas, Michael Hühn, Susan J. Monkley, Henric Olsson, Bastian R. Angermann, Ronen Artzi, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Oliver S. Burren, Lisa Buvall, Benjamin Challis, Sophia Cameron‐Christie, E. Suzanne Cohen, Andrew Davis, Regina Fritsche Danielson, Brian Dougherty, Benjamin Georgi, Zara Ghazoui, Pernille Hansen, Fengyuan Hu, Magda Jeznach, Xiao Jiang, Chanchal Kumar, Zhongwu Lai, Glenda Lassi, Samuel H. Lewis, Bolan Linghu, Kieren Lythgow, Peter Maccallum, Carla Martins, Athena Matakidou, Erik Michaëlsson, Sven Moosmang, Sean M. O’Dell, Yoichiro Ohne, Joel Okae, Amanda O’Neill, Dirk S. Paul, Anna Reznichenko, Michael Snowden, Anna Walentinsson, Jorge Zeron, Menelas N. Pangalos, Sebastian Wasilewski, Katherine R. Smith, Ruth March, Adam Platt, Carolina Haefliger, Slavé Petrovski
Izdano 2021Artigo -
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Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences od Oliver S. Burren, Ryan S. Dhindsa, Sri V. V. Deevi, Sean Wen, Abhishek Nag, Jonathan Mitchell, Fengyuan Hu, Douglas P. Loesch, Katherine R. Smith, Neetu Razdan, Henric Olsson, Adam Platt, Dimitrios Vitsios, Qiang Wu, Rasmus Ågren, Lauren Anderson-Dring, Santosh S. Atanur, David H. Baker, Maria G. Belvisi, Mohammad Bohlooly‐Y, Lisa Buvall, Sophia Cameron‐Christie, E. Suzanne Cohen, Regina Fritsche Danielson, Shikta Das, Andrew Davis, Guillermo del Angel, Wei Ding, Brian Dougherty, Zammy Fairhurst-Hunter, Manik Garg, Benjamin Georgi, Carmen Guerrero Rangel, Andrew R. Harper, Carolina Haefliger, Mårten Hammar, Richard N. Hanna, Pernille Hansen, Jennifer Harrow, Ian Henry, Sonja Hess, Ben Hollis, Jiang Xiao, Kousik Kundu, Zhongwu Lai, Mark Lal, Glenda Lassi, Yupu Liang, Margarida Lopes, Eagle Lou, Kieren Lythgow, Stewart MacArthur, Meeta Maisuria-Armer, Ruth March, Carla Martins, Dorota Matelska, Karyn Mégy, Robert Menzies, Erik Michaëlsson, Fiona K. Middleton, Bill Mowrey, Daniel Muthas, Sean M. O’Dell, Erin Oerton, Yoichiro Ohne, Henric Olsson, Amanda O’Neill, Kristoffer Ostridge, Dirk S. Paul, Bram P. Prins, Benjamin Pullman, William Rae, Arwa Bin Raies, Anna Reznichenko, Xavier Romero Ros, Hitesh J. Sanganee, Ben S. Sidders, Mike Snowden, Stasa Stankovic, Helen Stevens, Ioanna Tachmazidou, Haeyam Taiy, Lifeng Tian, Christina Underwood, Coralie Viollet, Anna Walentinsson, Lily Wang, Qing‐Dong Wang, Eleanor Wheeler, Ahmet Zehir, Zoe Zou, Veryan Codd, Christopher P. Nelson, Nilesh J. Samani, Ruth March, Sebastian Wasilewski, Keren Carss, Margarete A. Fabre, Quanli Wang, Menelas N. Pangalos
Izdano 2024Artigo -
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Rare variant associations with plasma protein levels in the UK Biobank od Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, Bram P. Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A. Hristova, Katherine R. Smith, Keren Carss, Sebastian Wasilewski, Andrew R. Harper, Dirk S. Paul, Margarete A. Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, Rasmus Ågren, Lauren Anderson-Dring, Santosh S. Atanur, David H. Baker, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Lisa Buvall, Niedzica Camacho, Lisa H. Cazares, Sophia Cameron‐Christie, Morris Chen, E. Suzanne Cohen, Regina Fritsche Danielson, Shikta Das, Andrew Davis, Sri Vishnu Vardhan Deevi, Wei Ding, Brian Dougherty, Zammy Fairhurst-Hunter, Manik Garg, Benjamin Georgi, Carmen Guerrero Rangel, Carolina Haefliger, Mårten Hammar, Richard N. Hanna, Pernille Hansen, Jennifer Harrow, Ian Henry, Sonja Hess, Ben Hollis, Fengyuan Hu, Xiao Jiang, Kousik Kundu, Zhongwu Lai, Mark Lal, Glenda Lassi, Yupu Liang, Margarida Lopes, Kieren Lythgow, Stewart MacArthur, Meeta Maisuria-Armer, Ruth March, Carla Martins, Karyn Mégy, Robert Menzies, Erik Michaëlsson, Fiona K. Middleton, Bill Mowrey, Daniel Muthas, Abhishek Nag, Sean M. O’Dell, Yoichiro Ohne, Henric Olsson, Amanda O’Neill, Kristoffer Ostridge, Benjamin Pullman, William Rae, Arwa Bin Raies, Anna Reznichenko, Xavier Romero Ros, Maria Ryaboshapkina, Hitesh J. Sanganee, Ben S. Sidders, Mike Snowden, Stasa Stankovic, Helen Stevens, Ioanna Tachmazidou, Haeyam Taiy, Lifeng Tian, Christina Underwood, Anna Walentinsson, Qing‐Dong Wang, Ahmet Zehir, Zoe Zou, Dimitrios Vitsios, Euan A. Ashley, Christopher D. Whelan, Menelas N. Pangalos, Quanli Wang, Slavé Petrovski
Izdano 2023Artigo
Alati za pretragu:
Povezani predmeti
Biology
Gene
Genetics
Computational biology
Internal medicine
Medicine
Biobank
Bioinformatics
Disease
Exome sequencing
Genome
Exome
Phenotype
Genome-wide association study
Genotype
Single-nucleotide polymorphism
Endocrinology
Genetic association
Computer science
Genomics
Mutation
Proteomics
Small RNA
microRNA
Cell biology
Deep sequencing
Evolutionary biology
Gene expression
Messenger RNA
MiRBase