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gene expression (3) 3
humans (3) 3
life sciences & biomedicine (3) 3
science & technology (3) 3
adolescent (2) 2
aged (2) 2
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brain (2) 2
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genomes (2) 2
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gene expression profiling - methods (1) 1
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histocompatibility antigens class i - genetics (1) 1
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1. Full Text Gene co-expression networks shed light into diseases of brain iron accumulation
by Bettencourt, Conceição and Forabosco, Paola and Wiethoff, Sarah and Heidari, Moones and Johnstone, Daniel M and Botía, Juan A and Collingwood, Joanna F and Hardy, John and Milward, Elizabeth A and Ryten, Mina and Houlden, Henry and for the UK Brain Expression Consortium (UKBEC) and UKBEC and UK Brain Expression Consortium (UKBEC)
Neurobiology of disease, ISSN 0969-9961, 2015, Volume 87, pp. 59 - 68
Neurology | Human brain | Whole-transcriptome analysis | NBIA | Iron metabolism | WGCNA | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurons - pathology | White Matter - metabolism | Hemochromatosis Protein | Humans | Basal Ganglia - metabolism | Transcriptome | Child, Preschool | Infant | Male | Histocompatibility Antigens Class I - metabolism | Young Adult | Aged, 80 and over | Female | Membrane Proteins - metabolism | Neurons - metabolism | Receptors, Transferrin - genetics | Neuroaxonal Dystrophies - pathology | Child | Disease Models, Animal | Membrane Proteins - genetics | Gene Expression Profiling - methods | Mice, Transgenic | Basal Ganglia - pathology | Histocompatibility Antigens Class I - genetics | Iron - metabolism | Receptors, Transferrin - metabolism | White Matter - pathology | Animals | Neuroaxonal Dystrophies - metabolism | Adolescent | Iron Metabolism Disorders - metabolism | Aged | Iron Metabolism Disorders - pathology | Gene expression | Nervous system diseases | Genes | Index Medicus
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2. Full Text Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
by Wain, Louise V, PhD and Shrine, Nick, PhD and Miller, Suzanne, PhD and Jackson, Victoria E, MSc and Ntalla, Ioanna, PhD and Artigas, María Soler, PhD and Billington, Charlotte K, PhD and Kheirallah, Abdul Kader, BSc and Allen, Richard, MSc and Cook, James P, PhD and Probert, Kelly, BSc and Obeidat, Ma'en, PhD and Bossé, Yohan, PhD and Hao, Ke, ScD and Postma, Dirkje S, Prof and Paré, Peter D, MD and Ramasamy, Adaikalavan, DPhil and Mägi, Reedik, PhD and Mihailov, Evelin, MSc and Reinmaa, Eva, MSc and Melén, Erik, MD and O'Connell, Jared, DPhil and Frangou, Eleni, MSc[Res] and Delaneau, Olivier, PhD and Freeman, Colin, PhD and Petkova, Desislava, PhD and McCarthy, Mark, Prof and Sayers, Ian, PhD and Deloukas, Panos, Prof and Hubbard, Richard, Prof and Pavord, Ian, FMedSci and Hansell, Anna L, MBBChir and Thomson, Neil C, Prof and Zeggini, Eleftheria, PhD and Morris, Andrew P, Prof and Marchini, Jonathan, Prof and Strachan, David P, Prof and Tobin, Martin D, Prof and Hall, Ian P, Prof and OxGSK Consortium and UK Brain Expression Consortium (UKBEC) and UKBEC
The lancet respiratory medicine, ISSN 2213-2600, 2015, Volume 3, Issue 10, pp. 769 - 781
Pulmonary/Respiratory | METAANALYSIS | 17Q21.31 MICRODELETION SYNDROME | VARIANTS | INVERSION POLYMORPHISM | SUSCEPTIBILITY LOCI | ASTHMA | KANSL1 CAUSE | MUTATIONS | EXPRESSION | GENOME-WIDE ASSOCIATION | Respiratory System | Life Sciences & Biomedicine | Critical Care Medicine | General & Internal Medicine | Science & Technology | Forced Expiratory Volume - genetics | Genetic Association Studies | Humans | Middle Aged | Risk Factors | Male | Smoking - genetics | United Kingdom | Lung - physiopathology | Case-Control Studies | Young Adult | Biological Specimen Banks | Adolescent | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Pulmonary Disease, Chronic Obstructive - genetics | Index Medicus | Medicin och hälsovetenskap
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3. Full Text Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
by D’Sa, Karishma and Botía, Juan A and Vandrovcova, Jana and Reynolds, Regina H and Zhang, David and Trabzuni, Daniah and Thomason, Andrew and Nalls, Mike A and Noyce, Alastair J and Nicolas, Aude and Cookson, Mark R and Bandres-Ciga, Sara and Gibbs, J. Raphael and Hernandez, Dena G and Singleton, Andrew B and Reed, Xylena and Blauwendraat, Cornelis and Bras, Jose and Guerreiro, Rita and Tucci, Arianna and Wood, Nicholas W and R’Bibo, Lea and Chelban, Viorica and Tan, Manuela and Middlehurst, Ben and Quinn, John and Lewis, Patrick and Williams, Nigel and Foltynie, Thomas and Lesage, Suzanne and Corvol, Jean-Christophe and Martinez, Maria and Giri, Anamika and Schulte, Claudia and Brockmann, Kathrin and Simón-Sánchez, Javier and Heutink, Peter and Gasser, Thomas and Rizzu, Patrizia and Shulman, Joshua M and Robak, Laurie and Lubbe, Steven and Lungu, Codrin and Scholz, Sonja W and Gan-Or, Ziv and Rouleau, Guy A and Krohan, Lynne and van Hilten, Jacobus J and Marinus, Johan and Carrillo, Fátima and Carrión-Claro, Mario and Gómez-Garre, Pilar and Jesús, Silvia and Méndez-del-Barrio, Carlota and Periñán-Tocino, Teresa and Diez-Fairen, Monica and Aguilar, Miquel and Alvarez, Ignacio and Boungiorno, María Teresa and Carcel, Maria and Alvarez, Victoria and González, Manuel Menéndez and Blazquez, Marta and Garcia, Ciara and Suarez-Sanmartin, Esther and Barrero, Francisco Javier and Arregui, Adolfo López de Munain and Ruiz-Martínez, Javier and Cerdan, Debora and Clarimón, Jordi and Dols-Icardo, Oriol and Infante, Jon and Kulisevsky, Jaime and Pagonabarraga, Javier and Gonzalez-Aramburu, Isabel and Rodriguez, Antonio Sanchez and Sierra, María and Duran, Raquel and Vives, Francisco and Escamilla-Sevilla, Francisco and Cámara, Ana and Compta, Yaroslau and Ezquerra, Mario and Marti, Maria Jose and Fernández-Santiago, Rubén and Tolosa, Eduard and Valldeoriola, Francesc and Heredia, Maria Jose Gomez and Hoenicka, Janet and Martínez-Castrillo, Juan Carlos and Lopez-Sendon, Jose Luis and Pihlstrom, Lasse and Koks, Sulev and Taba, Pille and Forabosco, Paola and Walker, Robert and Smith, Colin and Ramasamy, Adaikalavan and Hardy, John and Weale, Michael E and International Parkinson’s Disease Genomics Consortium (IPDGC) and UK Brain Expression Consortium (UKBEC)
Nature communications, ISSN 2041-1723, 12/2020, Volume 11, Issue 1, pp. 1041 - 1041
Genome-Wide Association Study | Reproducibility of Results | Putamen - physiology | Humans | Gene Expression Regulation | Transcriptome | Parkinson Disease - genetics | Nervous System Diseases - genetics | RNA Splicing | Schizophrenia - genetics | Alleles | Neurons - physiology | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Substantia Nigra - physiology | Enrichment | Brain | Basal ganglia | Splicing | Mental disorders | Genetic control | Substantia nigra | Health risks | Genomes | Gene expression | Servers | Disease control | Putamen | Loci | Ganglia | Quantitative trait loci | Genetic variance | Annotations | Internet | Gene mapping | RNA processing | Index Medicus | RNA sequencing | Genetics of the nervous system | Gene regulation | RNA splicing
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4. Full Text Characterizing the relation between expression QTLs and complex traits: exploring the role of tissue specificity
by Ip, Hill F and Jansen, Rick and Abdellaoui, Abdel and Bartels, Meike and Boomsma, Dorret I and Nivard, Michel G and Consortium, UK Brain Expression
Behavior genetics, ISSN 0001-8244, 2018, Volume 48, Issue 5, pp. 374 - 385
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5. Full Text Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue
by Bhalala, Oneil G and Nath, Artika P and Inouye, Michael and Sibley, Christopher R and UK Brain Expression Consortium
PLoS genetics, ISSN 1553-7390, 08/2018, Volume 14, Issue 8, pp. e1007607 - e1007607
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Quantitative trait loci | Brain | Schizophrenia | Genetic aspects | Research | Single nucleotide polymorphisms | Gene expression | Health aspects | Risk factors | Heart | Tibial nerve | Mental disorders | Genomics | Bipolar disorder | Genomes | Single-nucleotide polymorphism | Primary care | Morbidity | Studies | Consortia | Missense mutation | Affective disorders | Autopsy | Coding | DNA methylation | Software | Diabetes | Psychiatry | Public health | Methods | Index Medicus
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