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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 Lee, Sven and Adams, Hieab and Reitz, Christiane and Hofman, A and Rivadeneira, F and Uitterlinden, Ané and Ikram, Arfan and Launer, Lenore and Amin, Najaf and Duijn, Cornelia and EADI and GERAD PERADES and ARUKConsortium and CHARGE and ADGC and GERAD/PERADES, CHARGE, ADGC, EADI and ARUK Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
markdownabstractWe identified rare coding variants associated with Alzheimer's disease in a three-stage case-control study of 85,133 subjects. In stage 1, we... 
COMMON VARIANTS | IDENTIFIES VARIANTS | METAANALYSIS | GENOTYPE IMPUTATION | LOW-FREQUENCY | SUSCEPTIBILITY | GENETICS & HEREDITY | RISK | LOCI | WAVE2 COMPLEX | GENOME-WIDE ASSOCIATION | Amino Acid Sequence | Microglia - metabolism | Genetic Predisposition to Disease - genetics | Gene Frequency | Humans | Immunity, Innate - genetics | Genotype | Gene Expression Profiling | Case-Control Studies | Linkage Disequilibrium | Membrane Glycoproteins - genetics | Sequence Homology, Amino Acid | Exome - genetics | Protein Interaction Maps - genetics | Adaptor Proteins, Signal Transducing - genetics | Phospholipase C gamma - genetics | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Odds Ratio | Receptors, Immunologic - genetics | Immune response | Genetic variation | Physiological aspects | Development and progression | Genetic aspects | Research | Alzheimer's disease | Neurodegenerative diseases | Genes | Genomics | Health risks | Innate immunity | Genomes | Disease control | Immunity | Microglia | Proteins | Studies | Consortia | DNA microarrays | Genotyping | Gene frequency | DNA methylation | Alzheimers disease | Protein interaction | Bioinformatics | Genotypes | Immune system | Biological Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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2. Full Text Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates A beta, tau, immunity and lipid processing
by Kunkle, BW and Grenier-Boley, B and Sims, R and Bis, JC and Damotte, V and Naj, AC and Boland, A and Vronskaya, M and van der Lee, SJ and Amlie-Wolf, A and Bellenguez, C and Frizatti, A and Chouraki, V and Martin, ER and Sleegers, K and Badarinarayan, N and Jakobsdottir, J and Hamilton-Nelson, KL and Moreno-Grau, S and Olaso, R and Raybould, R and Chen, YN and Kuzma, AB and Hiltunen, M and Morgan, T and Ahmad, S and Vardarajan, BN and Epelbaum, J and Hoffmann, P and Boada, M and Beecham, GW and Garnier, JG and Harold, D and Fitzpatrick, AL and Valladares, O and Moutet, ML and Gerrish, A and Smith, AV and Qu, LM and Bacq, D and Denning, N and Jian, XQ and Zhao, Y and Del Zompo, M and Fox, NC and Choi, SH and Mateo, I and Hughes, JT and Adams, HH and Malamon, J and Sanchez-Garcia, F and Patel, Y and Brody, JA and Dombroski, BA and Naranjo, MCD and Daniilidou, M and Eiriksdottir, G and Mukherjee, S and Wallon, D and Uphill, J and Aspelund, T and Cantwell, LB and Garzia, F and Galimberti, D and Hofer, E and Butkiewicz, M and Fin, B and Scarpini, E and Sarnowski, C and Bush, WS and Meslage, S and Kornhuber, J and White, CC and Song, Y and Barber, RC and Engelborghs, S and Sordon, S and Voijnovic, D and Adams, PM and Vandenberghe, R and Mayhaus, M and Cupples, LA and Albert, MS and De Deyn, PP and Gu, W and Himali, JJ and Beekly, D and Squassina, A and Hartmann, AM and Orellana, A and Blacker, D and Rodriguez-Rodriguez, E and Lovestone, S and Garcia, ME and Doody, RS and Munoz-Fernadez, C and Sussams, R and Lin, HH and Fairchild, TJ and Benito, YA and ... and Cohorts Heart Aging Res Genomic Ep and Alzheimer Dis Genetics Consortium and European Alzheimers Dis Initiative and Genetic Environm Risk AD Defining and Alzheimer Disease Genetics Consortium (ADGC) and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE) and European Alzheimer’s Disease Initiative (EADI) and Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES) and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
NATURE GENETICS, ISSN 1061-4036, 03/2019, Volume 51, Issue 3, pp. 414 - 414
Risk for late-onset Alzheimer's disease (LOAD), the most prevalent dementia, is partially driven by genetics. To identify LOAD risk loci, we performed a large... 
COMMON VARIANTS | GENOTYPE IMPUTATION | AMYLOID-BETA | GENETICS & HEREDITY | DOMAIN-CONTAINING OXIDOREDUCTASE | MUTATIONS | ANGIOTENSIN-CONVERTING ENZYME | TRANSCRIPTION FACTOR | ONSET | GENOME-WIDE ASSOCIATION | APOLIPOPROTEIN-E | Genetic Predisposition to Disease - genetics | Lipids - genetics | Humans | Genetic Loci - genetics | Male | Genetic Testing - methods | Case-Control Studies | Haplotypes - genetics | tau Proteins - genetics | Amyloid beta-Peptides - genetics | Female | Lipid Metabolism - genetics | Aged | Alzheimer Disease - genetics | Genome-Wide Association Study - methods | Immunity - genetics | Ontology | Genomics | Genes | Lipids | Genomes | Mapping | Family medical history | Immunity | Risk factors | Protein turnover | Datasets | Proteins | Consortia | Genetic analysis | Dementia disorders | Genetics | Lipid metabolism | Alzheimer's disease | Age | ADAMTS-1 protein | Neurodegenerative diseases | Health risks | Metabolism | Risk analysis | Amyloid precursor protein | Meta-analysis | White blood cells | Genetic variance | Tau protein | Histocompatibility antigen HLA | Gene loci | Gene mapping | Alzheimers disease | Secretase | Dementia | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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3. Full Text Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
by Berndt, Sonja I and Camp, Nicola J and Skibola, Christine F and Vijai, Joseph and Wang, Zhaoming and Gu, Jian and Nieters, Alexana and Kelly, Rachel S and Smedby, Karin E and Monnereau, Alain and Cozen, Wendy and Cox, Angela and Wang, Sophia S and Lan, Qing and Teras, Lauren R and Machado, Moara and Yeager, Meredith and Brooks-Wilson, Angela R and Hartge, Patricia and Purdue, Mark P and Birmann, Brenda M and Vajdic, Claire M and Cocco, Pierluigi and Zhang, Yawei and Giles, Graham G and Zeleniuch-Jacquotte, Anne and Lawrence, Charles and Montalvan, Rebecca and Burdett, Laurie and Hutchinson, Amy and Ye, Yuanqing and Call, Timothy G and Shanafelt, Tait D and Novak, Anne J and Kay, Neil E and Liebow, Mark and Cunningham, Julie M and Allmer, Cristine and Hjalgrim, Henrik and Adami, Hans-Olov and Melbye, Mads and Glimelius, Bengt and Chang, Ellen T and Glenn, Martha and Curtin, Karen and Cannon-Albright, Lisa A and Diver, W Ryan and Link, Brian K and Weiner, George J and Conde, Lucia and Bracci, Paige M and Riby, Jacques and Arnett, Donna K and Zhi, Degui and Leach, Justin M and Holly, Elizabeth A and Jackson, Rebecca D and Tinker, Lesley F and Benavente, Yolanda and Sala, Núria and Casabonne, Delphine and Becker, Nikolaus and Boffetta, Paolo and Brennan, Paul and Foretova, Lenka and Maynadie, Marc and McKay, James and Staines, Anthony and Chaffee, Kari G and Achenbach, Sara J and Vachon, Celine M and Goldin, Lynn R and Strom, Sara S and Leis, Jose F and Weinberg, J Brice and Caporaso, Neil E and Norman, Aaron D and De Roos, Anneclaire J and Morton, Lindsay M and Severson, Richard K and Riboli, Elio and Vineis, Paolo and Kaaks, Rudolph and Masala, Giovanna and Weiderpass, Elisabete and Chirlaque, María-Dolores and Vermeulen, Roel C H|info:eu-repo/dai/nl/216532620 and Travis, Ruth C and Southey, Melissa C and Milne, Roger L and Albanes, Demetrius and Virtamo, Jarmo and Weinstein, Stephanie and Clavel, Jacqueline and Zheng, Tongzhang and Holford, Theodore R and Villano, Danylo J and Maria, Ann and Spinelli, John J and Gascoyne, Randy D and ... and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet and Experimentell och klinisk onkologi
Nature Communications [E], ISSN 2041-1723, 2016, Volume 7, Issue 1, p. 10933
Chronic lymphocytic leukemia (CLL) is a common lymphoid malignancy with strong heritability. To further understand the genetic susceptibility for CLL and... 
Membrane Proteins | Adaptor Proteins, Signal Transducing | Genetic Predisposition to Disease | Genome-Wide Association Study | Apoptosis Regulatory Proteins | Humans | Serpins | European Continental Ancestry Group | Polymorphism, Single Nucleotide | Proto-Oncogene Proteins | T-Box Domain Proteins | Leukemia, Lymphocytic, Chronic, B-Cell | VARIANTS | BANK1 | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | RISK | CLASSIFICATION | FAS GENE-MUTATIONS | FOLLICULAR LYMPHOMA | PRIORITIZATION | COMMON VARIATION | IDENTIFICATION | European Continental Ancestry Group - genetics | Serpins - genetics | Membrane Proteins - genetics | Proto-Oncogene Proteins - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | T-Box Domain Proteins - genetics | Bcl-2-Like Protein 11 | Adaptor Proteins, Signal Transducing - genetics | Apoptosis Regulatory Proteins - genetics | Chronic lymphatic leukemia | Leukemia | Agent orange | Genomes | Single-nucleotide polymorphism | Malignancy | Lymphatic leukemia | Chromosome 4 | Chromosome 3 | Loci | Chromosome 2 | Heritability | Apoptosis | Samfunnsmedisin, sosialmedisin: 801 | Community medicine, Social medicine: 801 | VDP | Helsefag: 800 | Health sciences: 800 | Medisinske Fag: 700 | Medical disciplines: 700 | Life Sciences | Hematology | Human health and pathology | Medical and Health Sciences | Medicin och hälsovetenskap
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4. Full Text Africa's ICT infrastructure
: building on the mobile revolution
by Williams, Mark D. J., 1972 and Mayer, Rebecca and Minges, Michael and Foster, Vivien, 1968 and Briceño-Garmendia, Cecilia and World Bank
2011, Directions in development, infrastructure, ISBN 082138676X, xxv, 279
Information and communication technologies (ICTs) have been a remarkable success in Africa. In just 10 years—dating from the end of the 1990s—mobile network... 
Telecommunication | Information technology | Economic assistance | Africa | GEOTHERMAL POWER | ELECTRICITY SERVICES | COSTS OF POWER | GLOBAL CARBON DIOXIDE EMISSIONS | LEASE CONTRACTS | AVERAGE TARIFF | POWER PRODUCTION | POWER PROJECT | POWER CORPORATION | PRICE OF OIL | REVENUE COLLECTION | PRICE DIFFERENTIAL | PUBLIC INFRASTRUCTURE | EMISSIONS REDUCTIONS | LOWER TARIFFS | FARES | DISTRIBUTION NETWORK | NUCLEAR POWER | TRANSMISSION CAPACITY | WIND | ECONOMIC GROWTH | TRANSMISSION GRID | VEHICLE | INTERNATIONAL ENERGY | WEATHER PATTERNS | POWER PLANTS | INVESTMENT CLIMATE | GENERATION | FOSSIL | GRID POWER | PETROLEUM | RENEWABLE ENERGY RESOURCES | FUEL OIL | POWER SECTOR PLANNING | CLIMATE CHANGE | SANITATION | CAPITAL INVESTMENTS | INFRASTRUCTURE INVESTMENT | POWER SUPPLY | TRADING PATTERNS | KEROSENE | ELECTRICAL POWER | THERMAL ENERGY | POWER SYSTEMS | HOUSEHOLD CONSUMPTION | REDUCTION IN EMISSIONS | TRANSPORTATION | BORDER TRANSMISSION | POWER COSTS | POWER | POWER PRICES | GEOTHERMAL PLANTS | OIL PRODUCTION | PREPAYMENT | AVAILABILITY | POWER MARKETS | POWER OUTAGES | TIN | POWER TRADE | ENVIRONMENTAL BENEFITS | HOUSEHOLD BUDGETS | COMPENSATION MECHANISMS | GROWTH RATES | DIESEL POWER | THERMAL CAPACITY | DIESEL GENERATORS | ENVIRONMENTAL IMPACTS | GOVERNMENT POLICY | OIL PRICES | UTILITY BILL | GLOBAL CARBON DIOXIDE | INVESTMENT COSTS | POWER STATIONS | RENEWABLE ENERGY | ELECTRICITY TARIFF | THERMAL POWER | CAPACITY EXPANSION | CERTIFIED EMISSION REDUCTION | POWER PROJECTS | PUBLIC PRIVATE INFRASTRUCTURE | ENERGY RESOURCES | BORDER TRADE | POWER GENERATION CAPACITY | GAS | CARBON DIOXIDE EMISSIONS | URANIUM | GENERATION CAPACITY | OIL RESERVES | GREENHOUSE | PROFIT MARGIN | BLACKOUTS | THERMAL POWER PLANTS | RESIDENTIAL CUSTOMERS | INFRASTRUCTURE SERVICES | ELECTRICITY DEMAND | POWER GRID | ACCESS TO ELECTRICITY | EMISSIONS SAVINGS | ECONOMIC DEVELOPMENT | CAPITAL EXPENDITURES | GAS PRODUCTION | POWER SYSTEM | HEAT PRODUCTION | TARIFF STRUCTURES | PRIVATE SECTOR PARTICIPATION | APPROACH | INFRASTRUCTURE FUNDING | DRIVING | MANAGEMENT CONTRACTS | POWER CAPACITY | INFRASTRUCTURE COSTS | ELECTRICITY GENERATION | BORDER INFRASTRUCTURE | POWER DEVELOPMENT | ALUMINUM | GAS RESOURCES | UTILITIES | POWER SECTOR | POWER SECTOR REFORM | CARBON DIOXIDE | DAMS | POWER SUPPLIES | BACKUP POWER | GROSS DOMESTIC PRODUCT | CAPITAL INVESTMENT | HEAVY FUEL OIL | GREENHOUSE GASES | ELECTRICITY PRODUCTION | GREENHOUSE GAS | DEMAND FOR POWER | BLOCK TARIFF | POWER SHORTAGES | ROUTES | PROPANE | ELECTRIC POWER | GENERATING CAPACITY | ELECTRICITY SUPPLY | GENERATION COSTS | POWER CRISIS | KILOWATT-HOUR | NUCLEAR POWER PLANT | POWER TRADING | INVESTMENT REQUIREMENTS | VOLTAGE | INFRASTRUCTURE FINANCING | POWER POOLS | HYDROPOWER GENERATION | HYDROPOWER | PERFORMANCE INDICATORS | INFRASTRUCTURE DEVELOPMENT | GENERATION OF ELECTRICITY | NATURAL GAS | FOSSIL FUELS | FUELS | CARBON | COST RECOVERY | DOMESTIC ENERGY | ENERGY POLICY | WATER RESOURCE MANAGEMENT | TOTAL EMISSIONS | GREENHOUSE GAS EMISSIONS | CAPITAL COSTS | O&M | REGIONAL INFRASTRUCTURE | ANNUAL CARBON DIOXIDE EMISSIONS | ECONOMIC COSTS | SURPLUS POWER | COAL | DROUGHT | INFRASTRUCTURE SPENDING | MARGINAL COST OF ELECTRICITY | MARGINAL COSTS | DOMESTIC ENERGY RESOURCES | METHANE | LOAD SHEDDING | FUEL | TRANSPORT POLICY | TRANSMISSION SYSTEM | COLORS | POWER CONSUMPTION | ELECTRICITY PRICES | HYDROELECTRIC PLANTS | POWER GENERATION | GASOLINE | EXCESS CAPACITY | SHIPPING CONTAINERS | OIL | CAR | POWER DEMAND | EMISSION | CONCESSIONS | RURAL ELECTRIFICATION | CONSUMPTION OF ELECTRICITY | COST OF POWER | PRICE OF POWER | HEAT | TRANSPORT | FUEL PRICES | ELECTRICITY SECTOR | SERVICE EXPANSION | ECONOMIES OF SCALE | EMISSION REDUCTION CREDIT | ELECTRICITY CONSUMPTION | COAL RESERVES | DIESEL | DOMINANT FUEL | ECONOMIC INTEGRATION | UTILITY LOAD | KILOWATT HOUR
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5. Full Text Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia
by Martin, Elodie and Martin, Jean-Jacques and Schüle, Rebecca and Smets, Katrien and Rastetter, Agnès and Boukhris, Amir and Loureiro, José L and Gonzalez, Michael A and Mundwiller, Emeline and Deconinck, Tine and Wessner, Marc and Jornea, Ludmila and Oteyza, Andrés Caballero and Durr, Alexandra and Schöls, Ludger and Mhiri, Chokri and Lamari, Foudil and Züchner, Stephan and De Jonghe, Peter and Kabashi, Edor and Brice, Alexis and Stevanin, Giovanni
The American Journal of Human Genetics, ISSN 0002-9297, 02/2013, Volume 92, Issue 2, pp. 238 - 244
refers to a locus mapped to chromosome 9 that accounts for a complicated autosomal-recessive form of hereditary spastic paraplegia (HSP). With next-generation... 
BETA-GLUCOSIDASE-2 | ZEBRAFISH | GENETICS & HEREDITY | AUTOSOMAL-DOMINANT | HUMAN LIVER | GENERATION | ACID BETA-GLUCOSIDASE | NONLYSOSOMAL GLUCOSYLCERAMIDASE | DNA-SEQUENCING DATA | AXON OUTGROWTH | GAUCHER-DISEASE | Neuroimaging | Spastic Paraplegia, Hereditary - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Zebrafish | Mutation - genetics | Motor Neurons - pathology | Young Adult | Animals | Pedigree | beta-Glucosidase - genetics | Adolescent | Brain - pathology | Adult | Family | Female | Aged | Zebrafish Proteins - genetics | Spastic Paraplegia, Hereditary - enzymology | Child | Motor neurons | Gene mutations | Genetic variation | Paralysis, Spastic | Physiological aspects | Causes of | Genetic aspects | Research | Enzyme activation | Glucose metabolism | Enzymes | Molecular genetics | RNA | Neurons | Heat shock proteins | Glucose | Dextrose | Deoxycholic acid | Report
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6. Full Text Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
by Lambert, Jean-Charles and Ibrahim-Verbaas, Carla A and Harold, Denise and Naj, Adam C and Sims, Rebecca and Bellenguez, Céline and Jun, Gyungah and DeStefano, Anita L and Bis, Joshua C and Beecham, Gary W and Grenier-Boley, Benjamin and Russo, Giancarlo and Thornton-Wells, Tricia A and Jones, Nicola and Smith, Albert V and Chouraki, Vincent and Thomas, Charlene and Ikram, M. Arfan and Zelenika, Diana and Vardarajan, Badri N and Kamatani, Yoichiro and Lin, Chiao-Feng and Gerrish, Amy and Schmidt, Helena and Kunkle, Brian and Fiévet, Nathalie and Amouyel, Philippe and Pasquier, Florence and Deramecourt, Vincent and De Bruijn, Renee F.A.G and Amin, Najaf and Hofman, Albert and Van Duijn, Cornelia M and Dunstan, Melanie L and Hollingworth, Paul and Owen, Michael J and O'Donovan, Michael C and Jones, Lesley and Holmans, Peter A and Moskvina, Valentina and Williams, Julie and Baldwin, Clinton and Farrer, Lindsay A and Choi, Seung-Hoan and Lunetta, Kathryn L and Fitzpatrick, Annette L and Harris, Tamara B and Psaty, Bruce M and Gilbert, John R and Hamilton-Nelson, Kara L and Martin, Eden R and Kunkle, Brian and Haines, Jonathan L and Gudnason, Vilmundur and Jonsson, Palmi V and Eiriksdottir, Gudny and Bihoreau, Marie-Thérèse and Lathrop, Mark and Valladares, Otto and Cantwell, Laura B and Wang, Li-San and Schellenberg, Gerard D and Ruiz, Agustin and Boada, Mercè and Reitz, Christiane and Mayeux, Richard and Ramirez, Alfredo and Maier, Wolfgang and Hanon, Olivier and Kukull, Walter A and Buxbaum, Joseph D and Campion, Dominique and Wallon, David and Hannequin, Didier and Crane, Paul K and Larson, Eric B and Becker, Tim and Cruchaga, Carlos and Goate, Alison M and Craig, David and Johnston, Janet A and Mc-Guinness, Bernadette and Todd, Stephen and Passmore, Peter and Berr, Claudine and Ritchie, Karen and Lopez, Oscar L and De Jager, Philip L and Evans, Denis and Lovestone, Simon and Proitsi, Petroula and Powell, John F and Letenneur, Luc and Barberger-Gateau, Pascale and Dufouil, Carole and Dartigues, Jean-François and Morón, Francisco J and Rubinsztein, David C and St. George-Hyslop, Peter and Sleegers, Kristel and ... and EADI and CHARGE and ADGC and GERAD and Cohorts for Heart and Aging Research in Genomic Epidemiology and Genetic and Environmental Risk in Alzheimer's Disease and Alzheimer's Disease Genetic Consortium and European Alzheimer's Disease Initiative (EADI) and Alzheimer's Disease Genetic Consortium (ADGC) and Genetic and Environmental Risk in Alzheimer's Disease (GERAD) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 12/2013, Volume 45, Issue 12, pp. 1452 - 1458
Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous studies; however, a large portion of the genetic risk for this... 
GENOTYPES | COMMON VARIANTS | IMPUTATION | GENETIC RISK | SEQUENCE | GENETICS & HEREDITY | NEURONS | RECEPTOR | MUTATIONS | CD33 | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Genetic Loci | Genome-Wide Association Study - statistics & numerical data | Case-Control Studies | Age of Onset | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Cohort Studies | Quantitative trait loci | Genetic aspects | Research | Genetic susceptibility | Alzheimer's disease | Identification and classification | Genealogy | Genomics | Genes | Quality control | Aging | Genomes | Alzheimers disease | Health risk assessment | Meta-analysis | Genetik | Biological Sciences | Genetics | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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7. Full Text The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8
by Jahic, A and Khundadze, M and Jaenisch, N and Schuuele, R and Klimpe, S and Klebe, S and Frahm, C and Kassubek, J and Stevanin, G and Schols, L and Brice, A and Hubner, CA and Beetz, C
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 11/2015, Volume 10, Issue 147, p. 147
Background: The hereditary spastic paraplegias (HSPs) are rare neurodegenerative gait disorders which are genetically highly heterogeneous. For each single... 
MEDICINE, RESEARCH & EXPERIMENTAL | PROTEIN | KIAA0196 | SPG8 | TRAFFICKING | RETROMER COMPLEX | Knockout | FAMILY | Hereditary spastic paraplegia | GENE | WASH COMPLEX | DISEASE | GENETICS & HEREDITY | Mouse model | Strumpellin | ASSOCIATION | Spastic Paraplegia, Hereditary - genetics | Spastic Paraplegia, Hereditary - diagnosis | Humans | Paraplegia - genetics | Paraplegia - diagnosis | Male | Mice, 129 Strain | Mutation - genetics | Mice, Knockout | Proteins - genetics | Animals | Female | Genetic Variation - genetics | Mice | Gene mutations | Paralysis, Spastic | Development and progression | Genetic aspects | Gene expression | Identification and classification | Health aspects | Life Sciences | Genetics | Neurons and Cognition
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8. Full Text Rebecca Gilbert January 18, 1897. -- Ordered to be printed
by Brice, Calvin Stewart and Vilas, William Freeman
1897, United States congressional serial set, Volume serial set no. 3474, 1
Legislative Report - Private Bills | Claims | Survivors' benefits | Mexican War (1846-1848) | United States | Military pensions | Lester, William | Gilbert, Rebecca
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9. Full Text Common Variants at Abca7, Ms4A6A/Ms4A4E, Epha1, Cd33 and Cd2Ap Are Associated with Alzheimer'S Disease
by Hollingworth, P and Harold, D and Sims, R and Gerrish, A and Lambert, J.C and Carrasquillo, M.M and Abraham, R and Hamshere, M.L and Pahwa, J.S and Moskvina, V and Dowzell, K and Jones, N and Stretton, A and Thomas, C and Richards, A and Ivanov, D and Widdowson, C and Chapman, J and Lovestone, S and Powell, J and Proitsi, P and Lupton, M.K and Brayne, C and Rubinsztein, D.C and Gill, M and Lawlor, B and Lynch, A and Brown, K.S and Passmore, P.A and Craig, D and McGuinness, B and Todd, S and Holmes, C and Mann, D and Smith, A.D and Beaumont, H and Warden, D and Wilcock, G and Love, S and Kehoe, P.G and Hooper, N.M and Vardy, E.R.L.C and Hardy, J and Mead, S and Fox, N.C and Rossor, M and Collinge, J and Maier, W and Jessen, F and Ruther, E and Schurmann, B and Heun, R and Kolsch, H and van den Bussche, H and Heuser, I and Kornhuber, J and Wiltfang, J and Dichgans, M and Frolich, L and Hampel, H and Gallacher, J and Hull, M and Rujescu, D and Giegling, I and Goate, A.M and Kauwe, J.S.K and Cruchaga, C and Nowotny, P and Morris, J.C and Mayo, K and Sleegers, K and Bettens, K and Engelborghs, S and de Deyn, P.P and Van Broeckhoven, C and Livingston, G and Bass, N.J and Gurling, H and McQuillin, A and Gwilliam, R and Deloukas, P and Al-Chalabi, A and Shaw, C.E and Tsolaki, M and Singleton, A.B and Guerreiro, R and Muhleisen, T. W and Nothen, M. M and Moebus, S and Jockel, K.H and Klopp, N and Wichmann, H. E and Pankratz, V.S and Sando, S.B and Aasly, J.O and Barcikowska, M and Wszolek, Z.K and Dickson, D.W and Graff-Radford, N.R. and others and Alzheimer's Dis Neuroimaging and EADI1 Consortium and CHARGE Consortium and the Alzheimer's Disease Neuroimaging Initiative and EADI1 consortium and CHARGE consortium
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 5, pp. 429 - 435
We sought to identify new susceptibility loci for Alzheimer's disease through a staged association study (GERAD+) and by testing suggestive loci reported by... 
IDENTIFIES VARIANTS | GENETICS & HEREDITY | GENE-EXPRESSION | RISK | LOCI | APOE | CR-1 | CLU | RECEPTOR TYROSINE KINASE | GENOME-WIDE ASSOCIATION | PICALM | Usage | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Drug therapy | Alzheimer's disease | Health aspects | Risk factors | Genomes | Medical imaging | Biomedical research | Alzheimers disease | Genes
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