Rezultati - Ene Reimann

  • Showing 1 - 20 results of 20
Refine Results
  1. 1
    Whole exome sequencing of a single osteosarcoma case—integrative analysis with whole transcriptome RNA-seq data

    Whole exome sequencing of a single osteosarcoma case—integrative analysis with whole transcriptome RNA-seq data od Ene Reimann, Sulev Kõks, Xuan Dung Ho, Katre Maasalu, Aare Märtson

    Izdano 2014
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  2. 2
    Transcriptional landscape of psoriasis identifies the involvement of IL36 and IL36RN

    Transcriptional landscape of psoriasis identifies the involvement of IL36 and IL36RN od Maris Keermann, Sulev Kõks, Ene Reimann, Ele Prans, Kristi Abram, Külli Kingo

    Izdano 2015
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  3. 3
    Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients

    Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients od Lidiia Zhytnik, Katre Maasalu, Ene Reimann, Ele Prans, Sulev Kõks, Aare Märtson

    Izdano 2017
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  4. 4
    Smoking-Induced Expression of the GPR15 Gene Indicates Its Potential Role in Chronic Inflammatory Pathologies

    Smoking-Induced Expression of the GPR15 Gene Indicates Its Potential Role in Chronic Inflammatory Pathologies od Gea Kõks, Mari‐Liis Uudelepp, Maia Limbach, Pärt Peterson, Ene Reimann, Sulev Kõks

    Izdano 2015
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    The Genetics and Functional Genomics of Osteoarthritis

    The Genetics and Functional Genomics of Osteoarthritis od Ana Luiza Arruda, Georgia Katsoula, Shibo Chen, Ene Reimann, Peter Kreitmaier, Eleftheria Zeggini

    Izdano 2024
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  6. 6
    Looking beyond the brain to improve the pathogenic understanding of Parkinson’s disease: implications of whole transcriptome profiling of Patients’ skin

    Looking beyond the brain to improve the pathogenic understanding of Parkinson’s disease: implications of whole transcriptome profiling of Patients’ skin od Anu Planken, Lille Kurvits, Ene Reimann, Liis Kadastik‐Eerme, Külli Kingo, Sulev Kõks, Pille Taba

    Izdano 2017
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  7. 7
    COL1A1/2 Pathogenic Variants and Phenotype Characteristics in Ukrainian Osteogenesis Imperfecta Patients

    COL1A1/2 Pathogenic Variants and Phenotype Characteristics in Ukrainian Osteogenesis Imperfecta Patients od Lidiia Zhytnik, Katre Maasalu, Andrey Pashenko, Sergey Khmyzov, Ene Reimann, Ele Prans, Sulev Kõks, Aare Märtson

    Izdano 2019
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  8. 8
    Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta

    Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta od Binh Ho Duy, Lidiia Zhytnik, Katre Maasalu, Ivo Kändla, Ele Prans, Ene Reimann, Aare Märtson, Sulev Kõks

    Izdano 2016
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  9. 9
    Melanocytes in the Skin – Comparative Whole Transcriptome Analysis of Main Skin Cell Types

    Melanocytes in the Skin – Comparative Whole Transcriptome Analysis of Main Skin Cell Types od Paula Reemann, Ene Reimann, Sten Ilmjärv, Orm Porosaar, Helgi Silm, Viljar Jaks, Eero Vasar, Külli Kingo, Sulev Kõks

    Izdano 2014
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  10. 10
    Polymorphisms in the ATG16L1 Gene are Associated with Psoriasis Vulgaris

    Polymorphisms in the ATG16L1 Gene are Associated with Psoriasis Vulgaris od Konstantinos Douroudis, Külli Kingo, Tanel Traks, Ene Reimann, Kristi Raud, Ranno Rätsep, Rotraut Mößner, Helgi Silm, Eero Vasar, Sulev Kõks

    Izdano 2012
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  11. 11
    Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis

    Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis od Eeva Sliz, Laura Huilaja, Anu Pasanen, Triin Laisk, Ene Reimann, Reedik Mägi, Katariina Hannula-Jouppi, Sirkku Peltonen, Teea Salmi, Leena Koulu, Kaisa Tasanen, Johannes Kettunen

    Izdano 2021
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  12. 12
    Whole transcriptome analysis identifies differentially regulated networks between osteosarcoma and normal bone samples

    Whole transcriptome analysis identifies differentially regulated networks between osteosarcoma and normal bone samples od Xuan Dung Ho, Phuong Phung, Van Quang Le, Văn Hiếu Nguyễn, Ene Reimann, Ele Prans, Gea Kõks, Katre Maasalu, Nghi T. N. Le, Le Huy Trinh, hoang Gia Nguyen, Aare Märtson, Sulev Kõks

    Izdano 2017
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  13. 13
    Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

    Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta od Tauno Metsalu, Triin Viltrop, Airi Tiirats, Balaji Rajashekar, Ene Reimann, Sulev Kõks, Kristiina Rull, Lili Milani, Ganesh Acharya, Purusotam Basnet, Jaak Vilo, Reedik Mägi, Andres Metspalu, Maire Peters, Kadri Haller‐Kikkatalo, Andres Salumets

    Izdano 2014
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  14. 14
    Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma

    Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma od Xuan Dung Ho, hoang Gia Nguyen, Le Huy Trinh, Ene Reimann, Ele Prans, Gea Kõks, Katre Maasalu, Van Quang Le, Văn Hiếu Nguyễn, Nghi T. N. Le, Phuong Phung, Aare Märtson, Freddy Lättekivi, Sulev Kõks

    Izdano 2017
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  15. 15
    Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study

    Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study od Maria Nethander, Eivind Coward, Ene Reimann, Louise Grahnemo, Maiken E. Gabrielsen, Carl Wibom, Reedik Mägi, Thomas Funck‐Brentano, Mari Hoff, Arnulf Langhammer, U. Pettersson, Kristian Hveem, Claes Ohlsson, Mari Nelis, Lili Milani, Tõnu Esko, Andres Metspalu

    Izdano 2022
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  16. 16
    Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study

    Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study od Yongmei Zhao, Li Tai Fang, Tsai-Wei Shen, Sulbha Choudhari, Keyur Talsania, Xiongfong Chen, Jyoti Shetty, Yuliya Kriga, Bao Tran, Bin Zhu, Zhong Chen, Wanqiu Chen, Charles Wang, Erich Jaeger, Daoud Meerzaman, Charles Lu, Kenneth B. Idler, Luyao Ren, Yuanting Zheng, Leming Shi, Virginie Petitjean, Marc Sultan, Tiffany Hung, Eric Peters, Jir̆ı́ Drábek, Petr Vojta, Roberta Maestro, Daniela Gasparotto, Sulev Kõks, Ene Reimann, Andreas Scherer, Jessica Nordlund, Ulrika Liljedahl, Jonathan Foox, Christopher E. Mason, Chunlin Xiao, Huixiao Hong, Wenming Xiao

    Izdano 2021
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  17. 17
    The Estonian Biobank’s journey from biobanking to personalized medicine

    The Estonian Biobank’s journey from biobanking to personalized medicine od 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

    Izdano 2025
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  18. 18
    Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

    Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing od Wenming Xiao, Luyao Ren, Zhong Chen, Li Tai Fang, Yongmei Zhao, Justin Lack, Meijian Guan, Bin Zhu, Erich Jaeger, Liz Kerrigan, Thomas Blomquist, Tiffany Hung, Marc Sultan, Kenneth B. Idler, Charles Lu, Andreas Scherer, Rebecca Kusko, Malcolm Moos, Chunlin Xiao, Stephen T. Sherry, Ogan D. Abaan, Wanqiu Chen, Xin Chen, Jessica Nordlund, Ulrika Liljedahl, Roberta Maestro, Maurizio Polano, Jir̆ı́ Drábek, Petr Vojta, Sulev Kõks, Ene Reimann, Bindu Swapna Madala, Tim R. Mercer, Chris Miller, Howard J. Jacob, Tiffany Truong, Ali Moshrefi, Aparna Natarajan, Ana Granat, Gary P. Schroth, Rasika Kalamegham, Eric Peters, Virginie Petitjean, Ashley Walton, Tsai-Wei Shen, Keyur Talsania, Cristobal Juan Vera, Kurt J. Langenbach, Maryellen de Mars, Jennifer Hipp, James C. Willey, Jing Wang, Jyoti Shetty, Yuliya Kriga, Arati Raziuddin, Bao Tran, Yuanting Zheng, Ying Yu, Margaret C. Cam, Parthav Jailwala, Cu Nguyen, Daoud Meerzaman, Qingrong Chen, Chunhua Yan, Ben Ernest, Urvashi Mehra, Roderick V. Jensen, Wendell Jones, Jian‐Liang Li, Brian N. Papas, Mehdi Pirooznia, Yunching Chen, Fayaz Seifuddin, Zhipan Li, Xue‐Lu Liu, Wolfgang Resch, Jingya Wang, Leihong Wu, Gökhan Yavaş, Corey J. Miles, Baitang Ning, Weida Tong, Christopher E. Mason, Eric Donaldson, Samir Lababidi, Louis M. Staudt, Živana Težak, Huixiao Hong, Charles Wang, Leming Shi

    Izdano 2021
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  19. 19
    Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

    Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing od Li Tai Fang, Bin Zhu, Yongmei Zhao, Wanqiu Chen, Zhaowei Yang, Liz Kerrigan, Kurt J. Langenbach, Maryellen de Mars, Charles Lu, Kenneth B. Idler, Howard J. Jacob, Yuanting Zheng, Luyao Ren, Ying Yu, Erich Jaeger, Gary P. Schroth, Ogan D. Abaan, Keyur Talsania, Justin Lack, Tsai-Wei Shen, Zhong Chen, Seta Stanbouly, Bao Tran, Jyoti Shetty, Yuliya Kriga, Daoud Meerzaman, Cu Nguyen, Virginie Petitjean, Marc Sultan, Margaret C. Cam, Monika Mehta, Tiffany Hung, Eric Peters, Rasika Kalamegham, Sayed Mohammad Ebrahim Sahraeian, Marghoob Mohiyuddin, Yunfei Guo, Lijing Yao, Lei Song, Hugo Y. K. Lam, Jir̆ı́ Drábek, Petr Vojta, Roberta Maestro, Daniela Gasparotto, Sulev Kõks, Ene Reimann, Andreas Scherer, Jessica Nordlund, Ulrika Liljedahl, Roderick V. Jensen, Mehdi Pirooznia, Zhipan Li, Chunlin Xiao, Stephen T. Sherry, Rebecca Kusko, Malcolm Moos, Eric Donaldson, Živana Težak, Baitang Ning, Weida Tong, Jing Li, Penelope Duerken-Hughes, Claudia Catalanotti, Shamoni Maheshwari, Joe Shuga, Winnie S. Liang, Jonathan J. Keats, Jonathan Adkins, Erica E. Tassone, Victoria Zismann, Timothy K. McDaniel, Jeffrey M. Trent, Jonathan Foox, Daniel Butler, Christopher E. Mason, Huixiao Hong, Leming Shi, Charles Wang, Wenming Xiao, Ogan D. Abaan, Meredith Ashby, Ozan Aygün, Xiaopeng Bian, Thomas M. Blomquist, Pierre R. Bushel, Margaret C. Cam, Fabien Campagne, Qingrong Chen, Tao Chen, Xin Chen, Yunching Chen, Han‐Yu Chuang, Maryellen de Mars, Youping Deng, Eric Donaldson, Jir̆ı́ Drábek, Ben Ernest, Jonathan Foox, Don Freed, Paul G. Giresi

    Izdano 2021
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  20. 20
    Translational genomics of osteoarthritis in 1,962,069 individuals

    Translational genomics of osteoarthritis in 1,962,069 individuals od Konstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefánsdóttir, Cindy G. Boer, Merry‐Lynn McDonald, J. Patrick Pett, Young‐Chan Park, Margo Tuerlings, Rick Mulders, Andrei Barysenka, Ana Luiza Arruda, Vinicius Tragante, Alison Rocco, Norbert Bittner, Shibo Chen, Susanne Horn, Vinodh Srinivasasainagendra, Ken To, Georgia Katsoula, Peter Kreitmaier, Amabel Tenghe, Arthur Gilly, Liubov Arbeeva, Lane G. Chen, Agathe de Pins, Daniel Dochtermann, Cecilie Henkel, Jonas Höijer, Shuji Ito, Penelope A. Lind, Bitota Lukusa-Sawalena, Aye Ko Ko Minn, Marina Mola-Caminal, Akira Narita, Chelsea Nguyen, Ene Reimann, Micah Silberstein, Anne Heidi Skogholt, Hemant K. Tiwari, Michelle S. Yau, Ming Yue, Wei Zhao, Jin Zhou, George Alexiadis, Karina Banasik, Søren Brunak, Archie Campbell, Jackson T S Cheung, Joseph Dowsett, Tariq Faquih, Jessica D. Faul, Lijiang Fei, Anne Marie Fenstad, Takamitsu Funayama, Maiken E. Gabrielsen, Chinatsu Gocho, Kirill Gromov, Thomas Hansen, Georgi Hudjashov, Þorvaldur Ingvarsson, Jessica Johnson, Helgi Jónsson, Saori Kakehi, Juha Karjalainen, Elisa Kasbohm, Susanna Lemmelä, Kuang Lin, Xiaoxi Liu, M. Loef, Massimo Mangino, Daniel L. McCartney, Iona Y. Millwood, Joshua Richman, Mary B. Roberts, Kathleen A. Ryan, Dino Samartzis, Manu Shivakumar, Søren Thorgaard Skou, Sachiyo Sugimoto, Ken Suzuki, Hiroshi Takuwa, Maris Teder‐Laving, Laurent F. Thomas, Kohei Tomizuka, Constance Turman, Stefan Weiß, Tian Wu, Eleni Zengini, Yanfei Zhang, Manuel A. R. Ferreira, George C. Babis, Aris Baras, Tyler Barker, David J. Carey, Kathryn S.E. Cheah, Zhengming Chen, Jason Pui Yin Cheung, Mark Daly, Renée de Mutsert, Charles B. Eaton

    Izdano 2025
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: