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1دورية أكاديمية
المؤلفون: Labreche, K, Kinnersley, B, Berzero, G, Di Stefano, AL, Rahimian, A, Detrait, I, Marie, Y, Grenier-Boley, B, Hoang-Xuan, K, Delattre, J-Y, Idbaih, A, Houlston, RS, Sanson, M
المساهمون: Kinnersley, Benjamin, Houlston, Richard
مصطلحات موضوعية: Chromosomes, Human, Pair 1, Pair 19, Humans, Glioma, Brain Neoplasms, Genetic Predisposition to Disease, Isocitrate Dehydrogenase, Telomerase, Proto-Oncogene Proteins c-myc, RNA, Messenger, Case-Control Studies, Mutation, Polymorphism, Single Nucleotide, European Continental Ancestry Group, Stathmin, Promoter Regions, Genetic, Genetic Loci, Genetic Association Studies, Preliminary Data
وصف الملف: Print-Electronic; 755; application/pdf
العلاقة: Acta neuropathologica, 2018, 135 (5), pp. 743 - 755; https://repository.icr.ac.uk/handle/internal/1624Test
الإتاحة: https://doi.org/10.1007/s00401-018-1825-zTest
https://repository.icr.ac.uk/handle/internal/1624Test -
2دورية أكاديمية
المؤلفون: Liu, Fan, Duffy, David L., Hysi, Pirro G., Jacobs, Leonie C., Lao, Oscar, Zhong, Kaiyin, Walsh, Susan, Chaitanya, Lakshmi, Wollstein, Andreas, Zhu, Gu, Montgomery, Grant W., Henders, Anjali K., Mangino, Massimo, Glass, Daniel, Bataille, Veronique, Sturm, Richard A., Rivadeneira, Fernando, Hofman, Albert, van IJcken, Wilfred F. J., Uitterlinden, André G., Palstra, Robert‑Jan T. S., Spector, Timothy D.
المساهمون: Department of Biology, School of Science
المصدر: PMC
مصطلحات موضوعية: Agouti Signaling Protein -- genetics, Antigens, Neoplasm -- genetics, Chromosomes, Human -- genetics, European Continental Ancestry Group -- genetics, Guanine Nucleotide Exchange Factors -- genetics, Interferon Regulatory Factors -- genetics, Membrane Transport Proteins -- genetics, Polymorphism, Single Nucleotide
وصف الملف: application/pdf
العلاقة: Human Genetics; Liu, F., Visser, M., Duffy, D. L., Hysi, P. G., Jacobs, L. C., Lao, O., … Kayser, M. (2015). Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Human Genetics, 134(8), 823–835. http://doi.org/10.1007/s00439-015-1559-0Test; https://hdl.handle.net/1805/8073Test
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المؤلفون: Anna C. Need, Katri Räikkönen, Edythe D. London, Jari Lahti, Aiden Corvin, Antony Payton, Russell A. Poldrack, Nikolaos Smyrnis, Matthew C. Keller, Ian J. Deary, Aarno Palotie, Deborah K. Attix, Srdjan Djurovic, Elisabeth Widen, John M. Starr, Fred W. Sabb, Kjetil Sundet, Stella G. Giakoumaki, David C. Liewald, Daniel R. Weinberger, Neil Pendleton, Panos Bitsios, Jin Yu, Ole A. Andreassen, Bettina Konte, Alex Hatzimanolis, William E R Ollier, Johan G. Eriksson, Ina Giegling, Emma Knowles, Dwight Dickinson, Elizabeth T. Cirulli, David C. Glahn, Nelson A. Freimer, Panos Roussos, Aristotle N. Voineskos, Thomas Espeseth, Joey W. Trampush, Dan E. Arking, Gary Davies, Nicholas C. Stefanis, Dan Rujescu, Derek W. Morris, Gary Donohoe, Vidar M. Steen, S. Le Hellard, Anil K. Malhotra, Astri J. Lundervold, Todd Lencz, Ornit Chiba-Falek, Andrea Christoforou, Matthew A. Scult, Emily Drabant Conley, Michael A Horan, Ingrid Melle, M. Gill, Robert M. Bilder, Katherine E. Burdick, Ivar Reinvang, M. L. Z. Yang, Eliza Congdon, Tyrone D. Cannon, Richard E. Straub, Pamela DeRosse, Ahmad R. Hariri, Dimitrios Avramopoulos
المساهمون: Medicum, Behavioural Sciences, Institute for Molecular Medicine Finland, Elisabeth Ingrid Maria Widen / Principal Investigator, Clinicum, Aarno Palotie / Principal Investigator, Department of Medical and Clinical Genetics, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Helsinki Collegium for Advanced Studies, Developmental Psychology Research Group, Genomics of Neurological and Neuropsychiatric Disorders, Genomic Discoveries and Clinical Translation
المصدر: Molecular Psychiatry
Trampush, J W, Zhan Yang, M L, Knowles, E, Davies, G, Liewald, D, Starr, J, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, Derosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N B, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I, Glahn, D C, Malhotra, A K & Lencz, T 2017, ' GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function : A report from the COGENT consortium ', Molecular Psychiatry, vol. 22, pp. 336-345 . https://doi.org/10.1038/mp.2016.244Test
Molecular psychiatry, vol 22, iss 3
Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E D, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K & Lencz, T 2017, ' GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function : a report from the COGENT consortium ', Molecular psychiatry, vol. 22, no. 3, pp. 336-345 . https://doi.org/10.1038/mp.2016.244Test, https://doi.org/10.1038/mp.2016.244Test
Molecular psychiatry, vol 22, iss 11مصطلحات موضوعية: 0301 basic medicine, Male, Multifactorial Inheritance, Genome-wide association study, Cathie Marsh Institute, Medical and Health Sciences, 3124 Neurology and psychiatry, 0302 clinical medicine, Cognition, Gene Frequency, 2.1 Biological and endogenous factors, provides insights, Aetiology, Genetics, Psychiatry, scottish mental survey, 11 Medical And Health Sciences, Single Nucleotide, Biological Sciences, Middle Aged, educational-attainment, developmental delay, Psychiatry and Mental health, uk biobank n=112151, Mental Health, intellectual disability, Female, Psychology, Corrigendum, Biotechnology, Adult, ability, 515 Psychology, human intelligence, European Continental Ancestry Group, Neurocognitive Disorders, Single-nucleotide polymorphism, Basic Behavioral and Social Science, Polymorphism, Single Nucleotide, White People, 17 Psychology And Cognitive Sciences, 03 medical and health sciences, Cellular and Molecular Neuroscience, Clinical Research, Behavioral and Social Science, Journal Article, SNP, Humans, Genetic Predisposition to Disease, Allele, Polymorphism, Molecular Biology, Allele frequency, Alleles, Genetic Association Studies, Genetic association, Prevention, Human Genome, Psychology and Cognitive Sciences, Genetic Variation, 06 Biological Sciences, Minor allele frequency, 030104 developmental biology, executive function, Genetic Loci, ResearchInstitutes_Networks_Beacons/cathie_marsh_institute, genome-wide association, 1182 Biochemistry, cell and molecular biology, Immediate Communication, Neurocognitive, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec26100056b46b727e48a65987866d2Test
https://hdl.handle.net/1956/19271Test -
4دورية أكاديمية
المؤلفون: Zhao, Z, Wen, W, Michailidou, K, Bolla, MK, Wang, Q, Zhang, B, Long, J, Shu, X-O, Schmidt, MK, Milne, RL, García-Closas, M, Chang-Claude, J, Lindstrom, S, Bojesen, SE, Ahsan, H, Aittomäki, K, Andrulis, IL, Anton-Culver, H, Arndt, V, Beckmann, MW, Beeghly-Fadiel, A, Benitez, J, Blomqvist, C, Bogdanova, NV, Børresen-Dale, A-L, Brand, J, Brauch, H, Brenner, H, Burwinkel, B, Cai, Q, Casey, G, Chenevix-Trench, G, Couch, FJ, Cox, A, Cross, SS, Czene, K, Dörk, T, Dumont, M, Fasching, PA, Figueroa, J, Flesch-Janys, D, Fletcher, O, Flyger, H, Fostira, F, Gammon, M, Giles, GG, Guénel, P, Haiman, CA, Hamann, U, Harrington, P, Hartman, M, Hooning, MJ, Hopper, JL, Jakubowska, A, Jasmine, F, John, EM, Johnson, N, Kabisch, M, Khan, S, Kibriya, M, Knight, JA, Kosma, V-M, Kriege, M, Kristensen, V, Le Marchand, L, Lee, E, Li, J, Lindblom, A, Lophatananon, A, Luben, R, Lubinski, J, Malone, KE, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, McLean, C, Meijers-Heijboer, H, Meindl, A, Miao, H, Muir, K, Neuhausen, SL, Nevanlinna, H, Neven, P, Olson, JE, Perkins, B, Peterlongo, P, Phillips, K-A, Pylkäs, K, Rudolph, A, Santella, R, Sawyer, EJ, Schmutzler, RK, Schoemaker, M, Shah, M, Shrubsole, M, Southey, MC, Swerdlow, AJ, Toland, AE, Tomlinson, I, Torres, D, Truong, T, Ursin, G, Van Der Luijt, RB, Verhoef, S, Wang-Gohrke, S, Whittemore, AS, Winqvist, R, Pilar Zamora, M, Zhao, H, Dunning, AM, Simard, J, Hall, P, Kraft, P, Pharoah, P, Hunter, D, Easton, DF, Zheng, W
المساهمون: Fletcher, Olivia, Schoemaker, Minouk, Swerdlow, Anthony
مصطلحات موضوعية: Humans, Breast Neoplasms, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, Odds Ratio, Risk Factors, Case-Control Studies, Polymorphism, Single Nucleotide, Middle Aged, European Continental Ancestry Group, Ethnic Groups, Female, Genetic Variation
وصف الملف: Print-Electronic; 693; application/pdf
العلاقة: Cancer causes & control : CCC, 2016, 27 (5), pp. 679 - 693; https://repository.icr.ac.uk/handle/internal/147Test
الإتاحة: https://doi.org/10.1007/s10552-016-0741-6Test
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5دورية أكاديمية
المؤلفون: Adhikari, Kaustubh, Reales, Guillermo, Smith, Andrew J. P., Konka, Esra, Palmen, Jutta, Quinto-Sanchez, Mirsha, Acuna-Alonzo, Victor, Jaramillo, Claudia, Arias, William, Fuentes, Macarena, Pizarro, Maria, Barquera Lozano, Rodrigo, Macin Perez, Gaston, Gomez-Valdes, Jorge, Villamil-Ramirez, Hugo, Hunemeier, Tabita, Ramallo, Virginia, Silva de Cerqueira, Caio C., Hurtado, Malena, Villegas, Valeria, Granja, Vanessa, Gallo, Carla, Poletti, Giovanni, Schuler-Faccini, Lavinia, Salzano, Francisco M., Bortolini, Maria-Catira, Canizales-Quinteros, Samuel, Rothhammer, Francisco, Bedoya, Gabriel, Calderon, Rosario, Rosique, Javier, Cheeseman, Michael, Bhutta, Mahmood F., Humphries, Steve E., Gonzalez-Jose, Rolando, Headon, Denis, Balding, David, Ruiz-Linares, Andres
مصطلحات موضوعية: Adolescent, Adult, Female, Humans, Male, Young Adult, Latin America, Animals, Phenotype, Genotype, Genome-Wide Association Study, Cell Line, Tumor, American Native Continental Ancestry Group/genetics, European Continental Ancestry Group/genetics, Mice, Edar Receptor/genetics, Polymorphism, Single Nucleotide, Ear Auricle/anatomy & histology/embryology, Homeodomain Proteins/metabolism, Morphogenesis/genetics, T-Box Domain Proteins/genetics/metabolism, https://purl.org/pe-repo/ocde/ford#3.02.00Test, https://purl.org/pe-repo/ocde/ford#1.06.03Test, https://purl.org/pe-repo/ocde/ford#1.04.00Test, https://purl.org/pe-repo/ocde/ford#1.03.00Test
العلاقة: urn:issn:2041-1723; https://hdl.handle.net/20.500.12866/5370Test; https://doi.org/10.1038/ncomms8500Test
الإتاحة: https://doi.org/20.500.12866/5370Test
https://doi.org/10.1038/ncomms8500Test
https://hdl.handle.net/20.500.12866/5370Test -
6دورية أكاديمية
المؤلفون: Zamudio, Roxana, Pereira, Latife, Rocha, Carolina D., Berg, Douglas E., Muniz-Queiroz, Thais, Sant Anna, Hanaisa P., Cabrera, Lilia, Combe, Juan M., Herrera, Phabiola, Jahuira, Martha H., Leao, Felipe B., Lyon, Fernanda, Prado, William A., Rodrigues, Maira R., Rodrigues-Soares, Fernanda, Santolalla, Meddly L., Zolini, Camila, Silva, Aristobolo M., Gilman, Robert H., Tarazona-Santos, Eduardo, Kehdy, Fernanda S. G.
مصطلحات موضوعية: Humans, Peru/epidemiology, Case-Control Studies, Risk Factors, Phenotype, Computational Biology, African Continental Ancestry Group/genetics, European Continental Ancestry Group/genetics, Ancestry, Amerindians, Polymorphism, Single Nucleotide, Genetic Predisposition to Disease, Adenocarcinoma/ethnology/genetics/metabolism, Asian Continental Ancestry Group/genetics, Association studies, Binding Sites, Biomarkers, Tumor/genetics, Cyclooxygenase 2/genetics, Forkhead Box Protein O3, Forkhead Transcription Factors/genetics/metabolism, Gastric cancer, Gene Expression Regulation, Neoplastic, Gene Frequency, Genetic Association Studies, Haplotypes, HEK293 Cells, Indians
العلاقة: urn:issn:1573-2568; https://hdl.handle.net/20.500.12866/5303Test; https://doi.org/10.1007/s10620-015-3859-6Test
الإتاحة: https://doi.org/20.500.12866/5303Test
https://doi.org/10.1007/s10620-015-3859-6Test
https://hdl.handle.net/20.500.12866/5303Test