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1. Full Text Common genetic variants influence human subcortical brain structures
by Hibar, Derrek and Stein, J.L and Rentería, Miguel and Arias-Vásquez, Alejano and Desrivières, Sylvane and Jahanshad, Neda and Toro, Roberto and Wittfeld, Katharina and Abramovic, Lucija and Andersson, Micael and Aribisala, Benjamin and Armstrong, Nicola J and Bernard, Manon and Bohlken, Marc M and Boks, Marco and Bralten, Linda and Brown, Anew and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher and Cuellar-Partida, Gabriel and Braber, Anouk and Giddaluru, Sudheer and Goldman, Aaron L and Grimm, Oliver and Guadalupe, Tulio and Hass, Johanna and Woldehawariat, Girma and Holmes, Avram and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Kim, Shinseog and Klein, Marieke and Kraemer, Bernd and Lee, Phil H and Olde Loohuis, Loes M and Luciano, Michelle and MacAre, Christine and Mather, R and Mattheisen, Manuel and Milaneschi, Yuri and Nho, Kwangsik and Papmeyer, Martina and Ramasamy, Adaikalavan and Risacher, Shannon and Roiz-Santiañez, Roberto and Rose, Emma and Salami, Alireza and Sämann, Philipp and Schmaal, Lianne and Schork, Nicholas and Shin, Jean and Strike, Vanessa and Teumer, Alexander and Van Donkelaar, Marjolein M. J and Eijk, Kristel and Walters, Raymond and Westlye, Lars and Whelan, Christopher and Winkler, Anderson and Zwiers, Marcel and Alhusaini, Saud and Athanasiu, Lavinia and Ehrlich, Stefan and Hakobjan, Marina and Hartberg, Cecilie B and Haukvik, Unn and Heister, Angelien J. G. A. M and Hoehn, David and Kasperaviciute, Dalia and Liewald, David C and Lopez, Lorna and Makkinje, Remco R. R and Matarin, Mar and Naber, Marlies A. M and Reese McKay, D and Needham, Margaret and Nugent, Allison and Pütz, Benno and Royle, Natalie and Shen, Li and Sprooten, Roy and Trabzuni, Danyah and Van Der Marel, Saskia S. L and Van Hulzen, Kimm J. E and Walton, Esther and Björnsson, Asgeir and Almasy, Laura and Ames, David and Arepalli, Sampath and Assareh, A.A and Bastin, Mark and Brodaty, Henry and Bulayeva, Kazima and Carless, Melanie and Cichon, Sven and Corvin, Aiden and Curran, Joanne and Czisch, Michael and ... and EPIGEN and SYS and Alzheimers Dis Neuroimaging and CHARGE Consortium and IMAGEN and Alzheimer’s Disease Neuroimaging Initiative and The Alzheimer’s Disease Neuroimaging Initiative and The CHARGE Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 04/2015, Volume 520, Issue 7546, pp. 224 - 229
textabstractThe highly complex structure of the human brain is strongly shaped by genetic influences. Subcortical brain regions form circuits with cortical... 
EVOLUTION | CHROMATIN | BASAL GANGLIA | MULTIDISCIPLINARY SCIENCES | HIPPOCAMPAL | DYNAMICS | IDENTIFICATION | EXPRESSION | KINECTIN | STRIATUM | GENOME-WIDE ASSOCIATION | Caudate Nucleus - anatomy & histology | Brain - anatomy & histology | Humans | Middle Aged | Genetic Loci - genetics | Gene Expression Regulation, Developmental - genetics | Apoptosis - genetics | Male | Young Adult | Putamen - anatomy & histology | Aging - genetics | Organ Size - genetics | Aged, 80 and over | Adult | Female | Child | Genome-Wide Association Study | Membrane Proteins - genetics | Sex Characteristics | Magnetic Resonance Imaging | Skull - anatomy & histology | Adolescent | Aged | Genetic Variation - genetics | Hippocampus - anatomy & histology | Genetic research | Brain | Genetic aspects | Brain research | Research | Genetic variation | Genomics | Genomes | Epigenetics | Genes | Index Medicus | Neuroscience | Cognitive science | Biological Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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2. Full Text Transethnic differences in GWAS signals: A simulation study
by Zanetti, Daniela and Weale, Michael E
Annals of Human Genetics, ISSN 0003-4800, 09/2018, Volume 82, Issue 5, pp. 280 - 286
Genome‐wide association studies (GWASs) have allowed researchers to identify thousands of single nucleotide polymorphisms (SNPs) and other variants associated... 
genome‐wide association studies | Causal SNP | complex human diseases | transethnic differences | genome-wide association studies | METAANALYSIS | SUSCEPTIBILITY | GENETIC ARCHITECTURE | LOCI | ANCESTRY | INDIVIDUALS | PROVIDES INSIGHTS | REPLICATION | DIVERSE POPULATIONS | GENETICS & HEREDITY | GENOME-WIDE ASSOCIATION | Medicine, Experimental | Medical research | Single nucleotide polymorphisms | Chromosomes | Analysis | Genomics | Gene frequency | Linkage disequilibrium | Alleles | Single-nucleotide polymorphism | Genomes | Gene mapping | Polymorphism
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3. Full Text Identification of common variants associated with human hippocampal and intracranial volumes
by Stein, J.L and Medland, S.E and Arias Vasquez, A and Hibar, D.P and Senstad, R.E and Winkler, A.M and Toro, R and Appel, K and Bartecek, R and Bergmann, O and Bernard, M and Brown, A.A and Cannon, D.M and Chakravarty, M.M and Christoforou, A and Domin, M and Grimm, O and Hollinshead, M and Holmes, A.J and Homuth, G and Hottenga, J.J and Langan, C and Lopez, L.M and Hansell, N.K and Hwang, K.S and Kim, S and Laje, G and Lee, P.H and Liu, X and Loth, E and Lourdusamy, A and Mattingsdal, M and Mohnke, S and Maniega, S.M and Nho, K and Nugent, A.C and O'Brien, C and Papmeyer, M and Putz, B and Ramasamy, A and Rasmussen, J and Rijpkema, M.J.P and Risacher, S.L and Roddey, J.C and Rose, E.J and Ryten, M and Shen, L and Sprooten, E and Strengman, E and Teumer, A and Trabzuni, D and Turner, J and Eijk, K. van and Erp, T.G. van and Tol, M.J. van and Wittfeld, K and Wolf, C. de and Woudstra, S and Aleman, A and Alhusaini, S and Almasy, L and Binder, E.B and Brohawn, D.G and Cantor, R.M and Carless, M.A and Corvin, A and Czisch, M and Curran, J.E and Davies, G and Almeida, M.A. de and Delanty, N and Depondt, C and Duggirala, R and Dyer, T.D and Erk, S and Fagerness, J and Fox, P.T and Freimer, N.B and Gill, M and Goring, H.H and Hagler, D.J and Hoehn, D and Holsboer, F and Hoogman, M and Hosten, N and Jahanshad, N and Johnson, M.P and Kasperaviciute, D and Kent Jr., J.W and Kochunov, P and Lancaster, J.L and Lawrie, S.M and Liewald, D.C and Mandl, R.C.W and Matarin, M and Mattheisen, M and Meisenzahl, E and Melle, I and Moses, E.K and Muhleisen, T.W and ... and Cohorts Heart Aging Res Genomic Ep and EPIGEN Consortium and ADNI and Saguenay Youth Study Grp SYS and IMAGEN Consortium and Enhancing Neuro Imaging Genetics M and Alzheimer's Disease Neuroimaging Initiative and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and Saguenay Youth Study Group and Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium and the Alzheimer's Disease Neuroimaging Initiative (ADNI) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and Saguenay Youth Study Group (SYS) and for the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 552 - 561
Identifying genetic variants influencing human brain structures may reveal new biological mechanisms underlying cognition and neuropsychiatric illness. The... 
AUTOMATED SEGMENTATION | HUMAN HEIGHT | FUNCTIONAL IMPLICATIONS | TEMPORAL-LOBE EPILEPSY | UNIFIED APPROACH | GENOTYPE IMPUTATION | ALZHEIMERS-DISEASE | GENETICS & HEREDITY | BRAIN VOLUME | NA+/H+ EXCHANGER | GENOME-WIDE ASSOCIATION | Neuroimaging | Genome-Wide Association Study | Meta-Analysis as Topic | Brain - physiopathology | Humans | Polymorphism, Single Nucleotide - genetics | Genetic Loci | Genetic Markers | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Head | Genetic aspects | Hippocampus (Brain) | Genetic variation | Identification and classification | Body size | Studies | Haplotypes | Neurology | Brain | Genealogy | Statistical analysis | Quality control | Genetics | Genomes | Meta-analysis | Index Medicus | Life Sciences | Neurons and Cognition
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4. Full Text Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
by Franke, Barbara and Stein, Jason L and Ripke, Stephan and Anttila, Verneri and Hibar, Derrek P and van Hulzen, Kimm J. E and Arias-Vasquez, Alejano and Smoller, Jordan W and Nichols, Thomas E and Neale, Michael C and McIntosh, Anew M and Lee, Phil and McMahon, Francis J and Meyer-Lindenberg, Aneas and Mattheisen, Manuel and Aneassen, Ole A and Gruber, Oliver and Sachdev, Perminder S and Roiz-Santiañez, Roberto and Saykin, Anew J and Ehrlich, Stefan and Mather, Karen A and Turner, Jessica A and Schwarz, Emanuel and Thalamuthu, Anbupalam and Yao, Yin and Ho, Yvonne Y. W and Martin, Nicholas G and Wright, Margaret J and O'Donovan, Michael C and Thompson, Paul M and Neale, Benjamin M and Medland, Sarah E and Sullivan, Patrick F and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William F and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberley D and Chan, Raymond C. K and Chen, Eric Y. H and Chen, Ronald Y. L and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and DeLisi, Lynn E and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and ... and ENIGMA Consortium and Psychiat Genomics Consortium and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Enigma Consortium
Nature neuroscience, ISSN 1097-6256, 2016, Volume 19, Issue 3, pp. 420 - +
Schizophrenia is a devastating psychiatric illness with high heritability. Brain structure and function differ, on average, between people with schizophrenia... 
INDIVIDUALS | METAANALYSIS | PERSPECTIVE | RELATIVES | VARIANTS | DISORDERS | PHENOTYPES | NEUROSCIENCES | ENDOPHENOTYPE | DISCOVERY | GENOME-WIDE ASSOCIATION | Neuroimaging | Magnetic Resonance Imaging | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Schizophrenia - genetics | Endophenotypes | Humans | Brain - pathology | Organ Size | Polymorphism, Single Nucleotide - genetics | Schizophrenia - pathology | Linkage Disequilibrium | Genome-wide association studies | Phenotype | Schizophrenia | Disease susceptibility | Genetic aspects | Identification and classification | Health aspects | Methods | Index Medicus | Neuroscience | Cognitive science
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5. Full Text The transcriptional landscape of age in human peripheral blood
by Peters, Marjolein and Joehanes, Roby and Pilling, Luke and Schurmann, Claudia and Conneely, Karen N and Powell, Joseph and Reinmaa, Eva and Sutphin, George L and Zhernakova, Alexana and Schramm, Katharina and Wilson, Yana A and Kobes, Sayuko and Tukiainen, Taru and Ramos, Yolande and Göring, Harald H and Fornage, Myriam and Liu, Yongmei and Gharib, Sina and Stranger, Barbara and Jager, Philip and Aviv, Abraham and Levy, Daniel and Murabito, Joanne and Munson, Peter J and Huan, Tianxiao and Hofman, Albert and Uitterlinden, Ané and Rivadeneira Ramirez, Fernando and van Rooij, Jeroen and Stolk, Lisette and Broer, Linda and Verbiest, Michael and Jhamai, Mila and Arp, Pascal and Metspalu, Anes and Tserel, Liina and Milani, Lili and Samani, Nilesh and Peterson, Pärt and Kasela, Silva and Codd, Veryan and Peters, Annette and Ward-Caviness, Cavin K and Herder, Christian and Waldenberger, Melanie and Roden, Michael and Singmann, Paula and Zeilinger, Sonja and Illig, Thomas and Homuth, Georg and Grabe, Hans Jörgen and Völzke, Henry and Steil, Leif and Kocher, Thomas and Murray, Anna and Melzer, David and Yaghootkar, Hanieh and Bandinelli, S and Moses, Eric and Kent, Jack and Curran, Joanne and Johnson, Matthew and Williams-Blangero, Sarah and Westra, Harm-Jan and McRae, Allan F and Smith, Jennifer A and Kardia, Sharon and Hovatta, Iiris and Perola, Markus and Ripatti, Samuli and Salomaa, Veikko and Henders, Anjali and Martin, Nicholas and Smith, Alicia K and Mehta, Divya and Binder, Elisabeth B and Nylocks, K. Maria and Kennedy, Elizabeth M and Klengel, Torsten and Ding, Jingzhong and Suchy-Dicey, Astrid and Enquobahrie, D and Brody, Jennifer and Rotter, Jerome I and Chen, Yii-Der I and Houwing-Duistermaat, Jeanine and Kloppenburg, Margreet and Slagboom, Eline and Helmer, Quinta and Hollander, Wouter and Bean, Shannon and Raj, Towfique and Bakhshi, Noman and Wang, Qiao Ping and Oyston, Lisa J and Psaty, Bruce and Tracy, Russell and Montgomery, Grant and Turner, Stephen and Blangero, John and ... and NABEC UKBEC Consortium and NABEC/UKBEC Consortium
Nature Communications, ISSN 2041-1723, 10/2015, Volume 6, Issue 1, pp. 8570 - 8570
textabstractDisease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately... 
LIFE-SPAN | OXIDATIVE STRESS | METHYLATION | PROFILES | GLYCOSAMINOGLYCANS | HUMAN LONGEVITY | DROSOPHILA-MELANOGASTER | MULTIDISCIPLINARY SCIENCES | PATTERNS | GENE-EXPRESSION CHANGES | GENOME-WIDE ASSOCIATION | Aging - blood | DNA Methylation | Humans | Transcriptome | European Continental Ancestry Group | Gene Expression Profiling | Biomarkers - blood | Index Medicus
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