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1. Full Text GWAS for executive function and processing speed suggests involvement of the CADM2 gene
by Ibrahim-Verbaas, Carla and Bressler, Jan and Debette, Stéphanie and Schuur, Maaike and Smith, Albert and Bis, Joshua and Davies, Gail and Trompet, Stella and Smith, J.A and Björnsson, Asgeir and Chibnik, Lori and Liu, Y and Vitart, Veronique and Kirin, Mirna and Petrovic, Katja and Polasek, Ozren and Zgaga, Lina and Fawns-Ritchie, C and Hoffmann, Per and Karjalainen, Juha and Lahti, J and Llewellyn, D.J and Schmidt, Carsten O and Mather, R and Chouraki, Vincent and Sun, Q and Resnick, Susan and Rose, Lynda and Oldmeadow, Christopher and Stewart, M and Smith, B.H and Gudnason, Vilmundur and Yang, Qiong and Mirza, Saira and Jukema, J.W and DeJager, Philip L and Harris, Tamara and Liewald, David C and Amin, Najaf and Coker, Laura and Stegle, Oliver and Lopez, O.L and Schmidt, R and Teumer, Alexander and Ford, I and Karbalai, Nazanin and Becker, James and Jonsdottir, Maria K and Au, Rhoda and Fehrmann, Rudolf and Herms, Stefan and Nalls, Michael and Zhao, W and Turner, Stephen and Yaffe, K and Lohman, Kurt and Swieten, John and Kardia, Sharon L.r and Knopman, David and Meeks, William and Heiss, Gerardo and Holliday, Elizabeth and Schofield, P.W and Tanaka, Toshiko and Stott, David J and Wang, Jing and Ridker, Paul and Gow, A.J and Pattie, Alison and Starr, John and Hocking, L.J and Armstrong, Nicola and McLachlan, Stela and Shulman, J.M and Pilling, Luke and Eiriksdottir, Gudny and Scott, Rodney and Kochan, Nicole A and Palotie, Aarno and Hsieh, Yi-Chen and Eriksson, Johan G and Penman, Alan and Gottesman, Rebecca and Oostra, Ben and Yu, Lei and DeStefano, Anita and Beiser, Alexa and Garcia, M and Rotter, Jerome I and Nöthen, Markus M and Hofman, Albert and Slagboom, Eline and Westendorp, R.G.J and Buckley, Brendan M and Wolf, P.A and Uitterlinden, Ané and Psaty, Bruce and Grabe, Hans Jörgen and Bandinelli, Stefania and Chasman, Daniel and ... and Generation Scotland and on behalf of Generation Scotland
Molecular psychiatry, ISSN 1359-4184, 02/2016, Volume 21, Issue 2, pp. 189 - 197
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | gamma-Aminobutyric Acid | Cell Adhesion Molecules - genetics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Cell Adhesion Molecules - physiology | Genetic Association Studies | Introns | Genomics | Humans | Middle Aged | Male | Executive Function - physiology | Neuropsychological Tests | Aged, 80 and over | Cognition - physiology | Female | Aged | Genetic Variation - genetics | Polymorphism, Single Nucleotide | Cohort Studies | GABA | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Research | Diagnosis | Dementia | Index Medicus
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2. Full Text Genetic contributions to variation in general cognitive function: A meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)
by Davies, Gail and Armstrong, Nicola and Bis, Joshua and Bressler, Jan and Chouraki, Vincent and Giddaluru, Sudheer and Hofer, E and Ibrahim-Verbaas, Carla and Kirin, Mirna and Lahti, J and Lee, Sven and Le Hellard, Stephanie and Liu, T and Marioni, Riccardo and Oldmeadow, Christopher and Postmus, Douwe and Smith, Davey and Smith, Jennifer A and Thalamuthu, Anbupalam and Thomson, Russell and Vitart, Veronique and Wang, J and Yu, L and Zgaga, Lina and Zhao, Wei and Boxall, Ruth and Harris, Sarah and Hill, W. David and Liewald, David C and Luciano, Michelle and Adams, Hieab and Ames, David and Amin, Najaf and Amouyel, Philippe and Assareh, A.A and Au, R and Becker, James and Beiser, A and Berr, Claudine and Bertram, Lars and Boerwinkle, Eric and Buckley, Brendan M and Campbell, Harry and Corley, Janie and De Jager, P.L and Dufouil, Carole and Eriksson, Johan G and Espeseth, Thomas and Faul, J.D and Ford, I and Scotland, Generation and Gottesman, Rebecca and Griswold, Michael and Gudnason, Vilmundur and Harris, T.B and Heiss, Gerardo and Hofman, Albert and Holliday, Elizabeth and Huffman, Jennifer and Kardia, Sharon and Kochan, Nicole A and Knopman, David and Kwok, J.B and Lambert, J.-C and Lee, T and Li, G and Li, S.-C and Loitfelder, Marisa and Lopez, Oscar and Lundervold, A.J and Lundqvist, A and Mather, R and Mirza, Saira and Nyberg, L and Oostra, Ben and Palotie, Aarno and Papenberg, G and Pattie, Alison and Petrovic, Katja and Polasek, Ozren and Psaty, Bruce and Redmond, Paul and Reppermund, S and Rotter, J.I and Schmidt, Reinhold and Schuur, Maaike and Schofield, P.W and Scott, R.J and Steen, Vidar and Stott, David J and Swieten, John and Taylor, Kent and Trollor, J and Trompet, Stella and Uitterlinden, Ané and Weinstein, G and Widen, Elisabeth and Windham, B Gwen and Jukema, Jan Wouter and Wright, Alan and ... and Generation Scotland
Molecular psychiatry, ISSN 1359-4184, 01/2015, Volume 20, Issue 2, pp. 183 - 192
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | HMGN1 Protein - genetics | Humans | Middle Aged | Atherosclerosis - complications | Male | Scotland | Cognition Disorders - genetics | Neuropsychological Tests | Phenotype | Cognition Disorders - etiology | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Female | Aged | Cohort Studies | Cognition | Genetic aspects | Research | Single nucleotide polymorphisms | Index Medicus | Immediate Communication | Medicin och hälsovetenskap
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3. Full Text Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
by Davies, Gail and Lam, M and Harris, Sarah and Trampush, J.W and Luciano, Michelle and Hill, W.D and Hagenaars, Saskia and Ritchie, S.J and Marioni, Riccardo and Fawns-Ritchie, C and Liewald, D.C.M and Okely, J.A and Ahola-Olli, A.V and Barnes, C.L.K and Bertram, Lars and Bis, Joshua and Burdick, K.E and Christoforou, Anea and Derosse, P and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, S and Giddaluru, Sudheer and Gustavson, D.E and Hayward, Caroline and Hofer, Edith and Ikram, Arfan and Karlsson, Robert and Knowles, E and Lahti, Jari and Leber, Isabelle and Li, S and Mather, R and Melle, Ingrid and Morris, D and Oldmeadow, Christopher and Palviainen, T and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, C and Sargurupremraj, M and Scholz, Markus and Smith, Jennifer A and Smith, Albert and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and Lee, Sven and Ware, Erin B and Windham, B Gwen and Wright, M.J and Yang, J and Yu, J and Ames, David and Amin, Najaf and Amouyel, Philippe and Aneassen, Ole and Armstrong, Nicola J and Assareh, A.A and Attia, John and Attix, D and Avramopoulos, D and Bennett, David and Böhmer, Marcel and Boyle, P.A and Brodaty, Henry and Campbell, Harry and Cannon, T.D and Cirulli, E.T and Congdon, E and Conley, E.D and Corley, Janie and Cox, Simon R and Dale, Anders and Dehghan, Abbas and Dick, D and Dickinson, D and Hagen, Knut and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, N.A and Gao, H and Giegling, Ina and Gillespie, N.A and Gordon, Scott D and Gottesman, Rebecca and Griswold, Michael and Gudnason, V and Harris, Tamara and Hartmann, Annette M and Hatzimanolis, A and Heiss, Gerardo and Holliday, Elizabeth and Joshi, Peter and Kähönen, Mika and Kardia, S.L.R and Karlsson, I and Kleineidam, L and ...
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | Index Medicus | Medicin och hälsovetenskap
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4. Full Text Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
by Wain, Louise V and Vaez, Ahmad and Jansen, Rick and Joehanes, Roby and van der Most, Peter J and Erzurumluoglu, A Mesut and O'Reilly, Paul F and Cabrera, Claudia P and Warren, Helen R and Rose, Lynda M and Verwoert, Germaine C and Hottenga, Jouke-Jan and Strawbridge, Rona J and Esko, Tonu and Arking, Dan E and Hwang, Shih-Jen and Guo, Xiuqing and Kutalik, Zoltan and Trompet, Stella and Shrine, Nick and Teumer, Alexander and Ried, Janina S and Bis, Joshua C and Smith, Albert V and Amin, Najaf and Nolte, Ilja M and Lyytikäinen, Leo-Pekka and Mahajan, Anubha and Wareham, Nicholas J and Hofer, Edith and Joshi, Peter K and Kristiansson, Kati and Traglia, Michela and Havulinna, Aki S and Goel, Anuj and Nalls, Mike A and Sõber, Siim and Vuckovic, gana and Luan, Jian'an and Del Greco M, Fabiola and Ayers, Kristin L and Marrugat, Jaume and Ruggiero, Daniela and Lopez, Lorna M and Niiranen, Teemu and Enroth, Stefan and Jackson, Anne U and Nelson, Christopher P and Huffman, Jennifer E and Zhang, Weihua and Marten, Jonathan and Gandin, Ilaria and Harris, Sarah E and Zemunik, Tatijana and Lu, Yingchang and Evangelou, Evangelos and Shah, Nabi and de Borst, Martin H and Mangino, Massimo and Prins, Bram P and Campbell, Archie and Li-Gao, Ruifang and Chauhan, Ganesh and Oldmeadow, Christopher and Abecasis, Gonçalo and Abedi, Maryam and Barbieri, Caterina M and Barnes, Michael R and Batini, Chiara and Beilby, John and Blake, Tineka and Boehnke, Michael and Bottinger, Erwin P and Braund, Peter S and Brown, Morris and Brumat, Marco and Campbell, Harry and Chambers, John C and Cocca, Massimiliano and Collins, Francis and Connell, John and Cordell, Heather J and Damman, Jeffrey J and Davies, Gail and de Geus, Eco J and de Mutsert, Renée and Deelen, Joris and Demirkale, Yusuf and Doney, Alex S F and Dörr, Marcus and Farrall, Martin and Ferreira, Teresa and Frånberg, Mattias and Gao, He and Gieaitis, Vilmantas and Gieger, Christian and Giulianini, Franco and Gow, Alan J and Hamsten, Anders and Harris, Tamara B and ... and Lifelines Cohort Study and Understanding Soc Sci Grp and BIOS Consortium and Understanding Society Scientific Group
Hypertension (Dallas, Tex. 1979), ISSN 0194-911X, 09/2017, Volume 70, Issue 3, pp. E4 - +
TARGET | blood pressure | COMMON VARIANTS | GWAS | METAANALYSIS | complex traits | PERIPHERAL-BLOOD | PULSE PRESSURE | INDIVIDUALS | CENTRIC ARRAY | cardiovascular risk | TRAITS | NETHERLANDS | hypertension | eSNP | Peripheral Vascular Disease | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Medicin och hälsovetenskap
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5. Full Text Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
by Warren, Helen R and Evangelou, Evangelos and Cabrera, Claudia P and Gao, He and Ren, Meixia and Mifsud, Borbala and Ntalla, Ioanna and Surenan, Praveen and Liu, Chunyu and Cook, James P and Kraja, Aldi T and nos, Fotios and Loh, Marie and Verweij, Niek and Marten, Jonathan and Karaman, Ibrahim and Lepe, Marcelo P. Segura and O'Reilly, Paul F and Knight, Joanne and Snieder, Harold and Kato, Norihiro and He, Jiang and Tai, E. Shyong and Said, M. Abdullah and Porteous, David and Alver, Maris and Poulter, Neil and Farrall, Martin and Gansevoort, Ron T and Padmanabhan, Sandosh and Magi, Reedik and Stanton, Alice and Connell, John and Bakker, Stephan J. L and Metspalu, Anes and Shields, Denis C and Thom, Simon and Brown, Morris and Sever, Peter and Esko, Tonu and Hayward, Caroline and van der Harst, Pim and Saleheen, Danish and Chowdhury, Rajiv and Chambers, John C and Chasman, Daniel I and Chakravarti, Aravinda and Newton-Cheh, Christopher and Lindgren, Cecilia M and Levy, Daniel and Kooner, Jaspal S and Keavney, Bernard and Tomaszewski, Maciej and Samani, Nilesh J and Howson, Joanna M. M and Tobin, Martin D and Munroe, Patricia B and Ehret, Georg B and Wain, Louise V and Barnes, Michael R and Tzoulaki, Joanna and Caulfield, Mark J and Elliott, Paul and Vaez, Ahmad and Jansen, Rick and Joehanes, Roby and van der Most, Peter J and Erzurumluoglu, A. Mesut and O'Reilly, Paul and Rose, Lynda M and Verwoert, Germaine C and Hottenga, Jouke-Jan and Strawbridge, Rona J and Arking, Dan E and Hwang, Shih-Jen and Guo, Xiuqing and Kutalik, Zoltan and Trompet, Stella and Shrine, Nick and Teumer, Alexander and Ried, Janina S and Bis, Joshua C and Smith, Albert V and Amin, Najaf and Nolte, Ilja M and Lyytikainen, Leo-Pekka and Mahajan, Anubha and Wareham, Nicholas J and Hofer, Edith and Joshi, Peter K and Kristiansson, Kati and Traglia, Michela and Havulinna, Aki S and Goel, Anuj and Nalls, Mike A and Sober, Siim and Vuckovic, gana and Luan, Jian'an and del Greco, Fabiola M and Ayers, Kristin L and ... and CHARGE BP Exome Consortium and UK Biobank CardioMetab Consortium and GoT2D Genes Consortium and Understanding Soc Sci Grp and Lifelines Cohort Study and Int Consortium Blood Pressure ICBP and BIOS Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-GENES Consortium and iGEN-BP Consortium and International Consortium of Blood Pressure (ICBP) 1000G Analyses and Understanding Society Scientific group and CHD Exome+ Consortium and Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and International Genomics of Blood Pressure (iGEN-BP) Consortium and UK Biobank CardioMetabolic Consortium BP working group and GoT2DGenes Consortium and The CHD Exome+ Consortium and The International Consortium of Blood Pressure (ICBP) 1000G Analyses and The International Genomics of Blood Pressure (iGEN-BP) Consortium and The UK Biobank CardioMetabolic Consortium BP working group and The Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and The GoT2DGenes Consortium and The ExomeBP Consortium and The T2D-GENES Consortium
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 3, pp. 403 - 415
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Blood Pressure - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Cardiovascular Diseases - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Hypertension - genetics | Genome-Wide Association Study - methods | Genotype | Genetic aspects | Single nucleotide polymorphisms | Cardiovascular diseases | Health aspects | Risk factors | Hypertension | Studies | Consortia | Medical research | Genealogy | Biomedical research | Councils | Cardiovascular disease | Genomes | Gene expression | Research centers | Meta-analysis | Index Medicus | Medicin och hälsovetenskap
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6. Full Text Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases
by Tajuddin, Salman M and Schick, Ursula M and Eicher, John D and Chami, Nathalie and Giri, Ayush and Brody, Jennifer A and Hill, W. David and Kacprowski, Tim and Li, Jin and Lyytikäinen, Leo-Pekka and Manichaikul, Ani and Mihailov, Evelin and O’Donoghue, Michelle L and Pankratz, Nathan and Pazoki, Raha and Polfus, Linda M and Smith, Albert Vernon and Schurmann, Claudia and Vacchi-Suzzi, Caterina and Waterworth, Dawn M and Evangelou, Evangelos and Yanek, Lisa R and Burt, Amber and Chen, Ming-Huei and van Rooij, Frank J.A and Floyd, James S and Greinacher, Andreas and Harris, Tamara B and Highland, Heather M and Lange, Leslie A and Liu, Yongmei and Mägi, Reedik and Nalls, Mike A and Mathias, Rasika A and Nickerson, Deborah A and Nikus, Kjell and Starr, John M and Tardif, Jean-Claude and Tzoulaki, Ioanna and Velez Edwards, Digna R and Wallentin, Lars and Bartz, Traci M and Becker, Lewis C and Denny, Joshua C and Raffield, Laura M and Rioux, John D and Friedrich, Nele and Fornage, Myriam and Gao, He and Hirschhorn, Joel N and Liewald, David C.M and Rich, Stephen S and Uitterlinden, Andre and Bastarache, Lisa and Becker, Diane M and Boerwinkle, Eric and de Denus, Simon and Bottinger, Erwin P and Hayward, Caroline and Hofman, Albert and Homuth, Georg and Lange, Ethan and Launer, Lenore J and Lehtimäki, Terho and Lu, Yingchang and Metspalu, Andres and O’Donnell, Chris J and Quarells, Rakale C and Richard, Melissa and Torstenson, Eric S and Taylor, Kent D and Vergnaud, Anne-Claire and Zonderman, Alan B and Crosslin, David R and Deary, Ian J and Dörr, Marcus and Elliott, Paul and Evans, Michele K and Gudnason, Vilmundur and Kähönen, Mika and Psaty, Bruce M and Rotter, Jerome I and Slater, Andrew J and Dehghan, Abbas and White, Harvey D and Ganesh, Santhi K and Loos, Ruth J.F and Esko, Tõnu and Faraday, Nauder and Wilson, James G and Cushman, Mary and Johnson, Andrew D and Edwards, Todd L and Zakai, Neil A and Lettre, Guillaume and Reiner, Alex P and Auer, Paul L
American journal of human genetics, ISSN 0002-9297, 07/2016, Volume 99, Issue 1, pp. 22 - 39
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Exome - genetics | Genome-Wide Association Study | Immune System Diseases - genetics | Humans | Genetic Loci - genetics | Genetic Pleiotropy | Blood Cell Count | Leukocytes - cytology | Quality Control | Quantitative trait loci | Genome-wide association studies | Genetic aspects | Leukocytes | Autoimmune diseases | Health aspects | Leucocytes | Genotype & phenotype | Transcription factors | Genomes | Meta-analysis | Index Medicus
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