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genetics (2) 2
adaptor proteins, signal transducing (1) 1
alzheimer disease (1) 1
alzheimer's disease; genome-wide association studies (1) 1
amino acid sequence (1) 1
aruk consortium (1) 1
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1. Full Text Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
by Sims, Rebecca and van der Lee, Sven J and Naj, Adam C and Bellenguez, Céline and Badarinarayan, Nandini and Jakobsdottir, Johanna and Kunkle, Brian W and Boland, Anne and Raybould, Rachel and Bis, Joshua C and Martin, Eden R and Grenier-Boley, Benjamin and Heilmann-Heimbach, Stefanie and Chouraki, Vincent and Kuzma, Amanda B and Sleegers, Kristel and Vronskaya, Maria and Ruiz, Agustin and Graham, Robert R and Olaso, Robert and Hoffmann, Per and Grove, Megan L and Vardarajan, Badri N and Hiltunen, Mikko and Nöthen, Markus M and White, Charles C and Hamilton-Nelson, Kara L and Epelbaum, Jacques and Maier, Wolfgang and Choi, Seung-Hoan and Beecham, Gary W and Dulary, Cécile and Herms, Stefan and Smith, Albert V and Funk, Cory C and Derbois, Céline and Forstner, Andreas J and Ahmad, Shahzad and Li, Hongdong and Bacq, Delphine and Harold, Denise and Satizabal, Claudia L and Valladares, Otto and Squassina, Alessio and Thomas, Rhodri and Brody, Jennifer A and Qu, Liming and Sánchez-Juan, Pascual and Morgan, Taniesha and Wolters, Frank J and Zhao, Yi and Garcia, Florentino Sanchez and Denning, Nicola and Fornage, Myriam and Malamon, John and Naranjo, Maria Candida Deniz and Majounie, Elisa and Mosley, Thomas H and Dombroski, Beth and Wallon, David and Lupton, Michelle K and Dupuis, Josée and Whitehead, Patrice and Fratiglioni, Laura and Medway, Christopher and Jian, Xueqiu and Mukherjee, Shubhabrata and Keller, Lina and Brown, Kristelle and Lin, Honghuang and Cantwell, Laura B and Panza, Francesco and McGuinness, Bernadette and Moreno-Grau, Sonia and Burgess, Jeremy D and Solfrizzi, Vincenzo and Proitsi, Petra and Adams, Hieab H and Allen, Mariet and Seripa, Davide and Pastor, Pau and Cupples, L Adrienne and Price, Nathan D and Hannequin, Didier and Frank-García, Ana and Levy, Daniel and Chakrabarty, Paramita and Caffarra, Paolo and Giegling, Ina and Beiser, Alexa S and Giedraitis, Vilmantas and Hampel, Harald and Garcia, Melissa E and Wang, Xue and Lannfelt, Lars and Mecocci, Patrizia and Eiriksdottir, Gudny and Crane, Paul K and Pasquier, Florence and Boccardi, Virginia and ... and Medicinska fakulteten and Geriatrik and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 9, p. 1373
We identified rare coding variants associated with Alzheimer's disease in a three-stage case-control study of 85,133 subjects. In stage 1, we genotyped 34,174... 
Amino Acid Sequence | Genetic Predisposition to Disease | GERAD/PERADES, CHARGE, ADGC, EADI | ARUK Consortium | Humans | Gene Frequency | Genotype | Gene Expression Profiling | Alzheimer Disease | Immunity, Innate | Case-Control Studies | Microglia | Linkage Disequilibrium | Protein Interaction Maps | Sequence Homology, Amino Acid | Exome | Adaptor Proteins, Signal Transducing | Phospholipase C gamma | Receptors, Immunologic | Polymorphism, Single Nucleotide | Membrane Glycoproteins | Odds Ratio | Genetik | Biological Sciences | Genetics | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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2. Full Text Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease
by Baker, Emily and Sims, Rebecca and Leonenko, Ganna and Frizzati, Aura and Harwood, Janet C and Grozeva, Detelina and Morgan, Kevin and Passmore, Peter and Holmes, Clive and Powell, John and Brayne, Carol and Gill, Michael and Mead, Simon and Bossù, Paola and Spalletta, Gianfranco and Goate, Alison M and Cruchaga, Carlos and Maier, Wolfgang and Heun, Reinhard and Jessen, Frank and Peters, Oliver and Dichgans, Martin and FröLich, Lutz and Ramirez, Alfredo and Jones, Lesley and Hardy, John and Ivanov, Dobril and Hill, Matthew and Holmans, Peter and Allen, Nicholas D and Morgan, B. Paul and Seshadri, Sudha and Schellenberg, Gerard D and Amouyel, Philippe and Williams, Julie and Escott-Price, Valentina and GERAD/PERADES and EADI and CHARGE and ADGC and IGAP consortia
PLOS ONE, ISSN 1932-6203, 07/2019, Volume 14, Issue 7, p. e0218111
Late onset Alzheimer’s disease is the most common form of dementia for which about 30 susceptibility loci have been reported. The aim of the current study is... 
Energy metabolism | Neurosciences | Laboratories | Genomics | Genes | DNA damage | Psychotherapy | Genomes | Single-nucleotide polymorphism | Nucleotides | DNA repair | Gene polymorphism | Consortia | Proteins | Neurodegeneration | Dementia disorders | Genetics | Life sciences | Lipid metabolism | Genotypes | Deoxyribonucleic acid--DNA | Public health | Plaques | Circadian rhythms | Medical research | Signs and symptoms | Centrosomes | Rhythm | Metabolism | Gene expression | Loci | Cholesterol | Medicine | Neurology | Hospitals | Councils | Psychiatry | Polymorphism | Dementia | Deoxyribonucleic acid | DNA
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