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  1. 661
    A common MET polymorphism harnesses HER2 signaling to drive aggressive squamous cell carcinoma
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  2. 662
    Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients
    “... pes cavus deformity. SORD neuropathy is frequent in Czech patients and the third most common cause...”
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  3. 663
    Erratum: Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis
    por Solveig K. Sieberts, Fan Zhu, Javier García-García, Eli Stahl, Abhishek Pratap, Gaurav Pandey, Dimitrios Pappas, Daniel Aguilar, Bernat Anton, Jaume Bonet, Ridvan Eksi, Oriol Fornés, Emre Guney, Hongdong Li, Manuel Alejandro Marín, Bharat Panwar, Joan Planas-Iglesias, Daniel Poglayen, Jing Cui, Andre O. Falcao, Christine Suver, Bruce Hoff, Venkat S. K. Balagurusamy, Donna Dillenberger, Elias Chaibub Neto, Thea Norman, Tero Aittokallio, Muhammad Ammad-ud-din, Chloe-Agathe Azencott, Víctor Bellón, Valentina Boeva, Kerstin Bunte, Himanshu Chheda, Lu Cheng, Jukka Corander, Michel Dumontier, Anna Goldenberg, Peddinti Gopalacharyulu, Mohsen Hajiloo, Daniel Hidru, Alok Jaiswal, Samuel Kaski, Beyrem Khalfaoui, Suleiman Ali Khan, Eric R. Kramer, Pekka Marttinen, Aziz M. Mezlini, Bhuvan Molparia, Matti Pirinen, Janna Saarela, Matthias Samwald, Véronique Stoven, Hao Tang, Jing Tang, Ali Torkamani, Jean-Phillipe Vert, Bo Wang, Tao Wang, Krister Wennerberg, Nathan E. Wineinger, Guanghua Xiao, Yang Xie, Rae Yeung, Xiaowei Zhan, Cheng Zhao, Members of the Rheumatoid Arthritis Challenge Consortium, Jeff Greenberg, Joel Kremer, Kaleb Michaud, Anne Barton, Marieke Coenen, Xavier Mariette, Corinne Miceli, Nancy Shadick, Michael Weinblatt, Niek de Vries, Paul P. Tak, Danielle Gerlag, Tom W. J. Huizinga, Fina Kurreeman, Cornelia F. Allaart, S. Louis Bridges Jr., Lindsey Criswell, Larry Moreland, Lars Klareskog, Saedis Saevarsdottir, Leonid Padyukov, Peter K. Gregersen, Stephen Friend, Robert Plenge, Gustavo Stolovitzky, Baldo Oliva, Yuanfang Guan, Lara M. Mangravite
    Publicado 2016
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  4. 664
    Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting
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  5. 665
    Co-occurring expression and methylation QTLs allow detection of common causal variants and shared biological mechanisms
    “...Most expression QTLs (eQTLs) co-occur with a DNA methylation QTL (meQTL), suggesting a common...”
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  6. 666
    Common and cell-type specific responses to anti-cancer drugs revealed by high throughput transcript profiling
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  7. 667
    Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease
    por Eva Gonçalves Serra, Tobias Schwerd, Loukas Moutsianas, Athena Cavounidis, Laura Fachal, Sumeet Pandey, Jochen Kammermeier, Nicholas M. Croft, Carsten Posovszky, Astor Rodrigues, Richard K. Russell, Farah Barakat, Marcus K. H. Auth, Robert Heuschkel, Matthias Zilbauer, Krzysztof Fyderek, Christian Braegger, Simon P. Travis, Jack Satsangi, Miles Parkes, Nikhil Thapar, Helen Ferry, Julie C. Matte, Kimberly C. Gilmour, Andrzej Wedrychowicz, Peter Sullivan, Carmel Moore, Jennifer Sambrook, Willem Ouwehand, David Roberts, John Danesh, Toni A. Baeumler, Tudor A. Fulga, Mohammad Karaminejadranjbar, Ahmed Ahmed, Rachel Wilson, Jeffrey C. Barrett, Abdul Elkadri, Anne M. Griffiths, COLORS in IBD group investigators, Oxford IBD cohort study investigators, INTERVAL Study, Swiss IBD cohort investigators, UK IBD Genetics Consortium, NIDDK IBD Genetics Consortium, Scott B. Snapper, Neil Shah, Aleixo M. Muise, David C. Wilson, Holm H. Uhlig, Carl A. Anderson
    Publicado 2020
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  8. 668
    Global CO2 emissions from dry inland waters share common drivers across ecosystems
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  9. 669
    New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population
    por Ho-Sun Lee, Yongkang Kim, Taesung Park
    Publicado 2018
    “... variants for MetS, with its components, we performed multivariate analysis for common and rare associations...”
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  10. 670
    Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
    “...Epilepsies are common brain disorders and are classified based on clinical phenotyping, imaging...”
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  11. 671
    Common Inflammatory Mechanisms in COVID-19 and Parkinson’s Diseases: The Role of Microbiome, Pharmabiotics and Postbiotics in Their Prevention
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  12. 672
    Analysis of Common Pathways and Markers From Non-Alcoholic Fatty Liver Disease to Immune-Mediated Diseases
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  13. 673
    Microbiota in the coelomic fluid of two common coastal starfish species and characterization of an abundant Helicobacter-related taxon
    “... potentially impacts host health and disease. Here, we analysed the CF microbiota in two common coastal...”
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  14. 674
    Association of common TMPRSS6 and TF gene variants with hepcidin and iron status in healthy rural Gambians
    “... status. We sought to investigate the effects of common TMPRSS6 and TF gene SNPs on iron status indicators...”
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  15. 675
    MINFLUX nanometer-scale 3D imaging and microsecond-range tracking on a common fluorescence microscope
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  16. 676
    FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
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  17. 677
    COVID’s Razor: RAS Imbalance, the Common Denominator Across Disparate, Unexpected Aspects of COVID-19
    por Czick M, Shapter C, Shapter R
    Publicado 2020
    “... and unexpected aspects of COVID-19 share a common mechanism. Silent hypoxia, atypical acute respiratory distress...”
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  18. 678
    Some Characterizations for a Family of Nonexpansive Mappings and Convergence of a Generated Sequence to Their Common Fixed Point
    por Kazuhide Nakajo, Yasunori Kimura
    Publicado 2010
    “... of all common fixed points of a family of nonexpansive mappings by the notion of Mosco convergence...”
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  19. 679
    Origin of alkali-rich volcanic and alkali-poor intrusive carbonatites from a common parental magma
    “... are supposedly considered to originate via fractional crystallization of a “common parent” alkali-bearing Ca...”
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  20. 680
    Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
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