المؤلفون: Adhikari, K., Mendoza-Revilla, J., Sohail, A., Fuentes-Guajardo, M., Lampert, J., Chacón-Duque, J.C., Hurtado, M., Villegas, V., Granja, V., Acuña-Alonzo, V., Jaramillo, C., Arias, W., Lozano, R.B., Everardo, P., Gómez-Valdés, J., Villamil-Ramírez, H., Silva de Cerqueira, C.C., Hunemeier, T., Ramallo, V., Schuler-Faccini, L., Salzano, F.M., Gonzalez-José, R., Bortolini, M.-C., Canizales-Quinteros, S., Gallo, C., Poletti, G., Bedoya, G., Rothhammer, F., Tobin, D.J., Fumagalli, M., Balding, D., Ruiz-Linares, A.

مصطلحات موضوعية: allele, Alleles, amino acid substitution, Article, Asian continental ancestry group, binding site, Biological Evolution, carrier protein, Caucasian, chromosome 1q, chromosome 20q, chromosome 22q, controlled study, convergent evolution, epistasis, Genetic, ethnic group, Ethnic Groups, European Continental Ancestry Group, evolution, exon, eye color, female, gene expression, gene frequency, gene linkage disequilibrium, gene locus, genetic association, genetics, Population

العلاقة: urn:issn:2041-1723; https://hdl.handle.net/20.500.12866/7500Test; https://doi.org/10.1038/s41467-018-08147-0Test

الإتاحة: https://doi.org/20.500.12866/7500Test
https://doi.org/10.1038/s41467-018-08147-0Test
https://hdl.handle.net/20.500.12866/7500Test

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 11

مصطلحات 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

المؤلفون: Ugur Ozbek, Muge Aydin-Sayitoglu, Sema Sirma, Cemaliye B Akyerli, Tayfun Ozcelik

المصدر: Journal of Cancer Research and Clinical Oncology

مصطلحات موضوعية: Cancer Research, Protein MYH, Unclassified drug, Turkey, Glycine, DNA repair, Childhood leukemia, Major clinical study, Myh gene, Biology, Acute lymphoblastic leukemia, Gene, White People, Article, Turkey (republic), DNA Glycosylases, Mismatch repair, Cancer risk, MUTYH, Humans, Missense mutation, Cysteine, Child, Priority journal, Genetics, DNA, neoplasm, Genetic variants, Leukemia, myelocytic, acute, DNA, Neoplasm, General Medicine, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Acute granulocytic leukemia, Leukemia, Myeloid, Acute, Oncology, DNA glycosylases, United kingdom, Mutation, Aspartic acid, Tyrosine, Excision repair, Mutant protein, Leukemia, lymphocytic, acute, Controlled study, Human, European continental ancestry group

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e87374daa711ee6dc03d1c2f162398aTest
https://hdl.handle.net/11693/24423Test