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by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and The EPIC-InterAct Consortium and CHD Exome+ Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Journal Article
Journal Article
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1802, pp. 49 - 62
The allele frequency net database (AFND, http://www.allelefrequencies.net ) is an online web-based repository that contains information on the frequencies of... 
Immunogenetics | Frequencies | HLA | Polymorphisms | Population genetics | Geography | Genetics, Population | Haplotypes - genetics | Gene Frequency | Humans | Alleles | Databases, Genetic | HLA Antigens - genetics | Internet | Epitopes - genetics | Index Medicus
Journal Article
Circulation Research, ISSN 0009-7330, 01/2019, Volume 124, Issue 1, pp. 114 - 120
RATIONALE:Ischemic stroke is among the leading causes of adult disability. Part of the variability in functional outcome after stroke has been attributed to... 
CARDIAC & CARDIOVASCULAR SYSTEMS | GENETICS | allele | genome-wide association study | PERIPHERAL VASCULAR DISEASE | genetic variant | SCALE | HEMATOLOGY | genetic loci | ischemic stroke | Stroke (Disease) | Genome-wide association studies | Phenotype | Analysis | Patient outcomes | Genetic aspects | Research | Meta-analysis
Journal Article
by Huang, Jie and Howie, Bryan and McCarthy, Shane and Memari, Yasin and Walter, Klaudia and Min, Josine L and Danecek, Petr and Malerba, Giovanni and Trabetti, Elisabetta and Zheng, Hou-Feng and Gambaro, Giovanni and Richards, Brent and Durbin, Richard and Timpson, Nicholas and Marchini, Jonathan and Soranzo, Nicole and Al Turki, Saeed and Amuzu, Antoinette and Anderson, Carl and Anney, Richard and Antony, Dinu and Artigas, M.S and Ayub, Muhammad and Bala, Senduran and Barrett, Jeffrey and Barroso, Inês and Beales, Philip and Benn, Marianne and Bentham, Jamie and Bhattacharya, Shoumo and Birney, Ewan and Blackwood, Douglas and Bobrow, Martin and Bochukova, Elena and Bolton, Patrick F and Bounds, Rebecca and Boustred, Chris and Breen, Gerome and Calissano, Mattia and Carss, Keren and Casas, Juan Pablo and Chambers, John C and Charlton, Ruth and Chatterjee, Krishna and Chen, Lu and Ciampi, Antonio and Cirak, Sebahattin and Clapham, Peter and Clement, Gail and Coates, Guy and Cocca, Massimiliano and Collier, David and Cosgrove, Catherine and Cox, Tony and Craddock, Nick and Crooks, Lucy and Curran, Sarah and Curtis, David and Daly, Allan and Day, Ian N.M and Day-Williams, Aaron and Dedoussis, George and Down, Thomas and Du, Yuanping and Duijn, Cornelia and Dunham, Ian and Edkins, Ted and Ekong, Rosemary and Ellis, Peter and Evans, David and Farooqi, I. Sadaf and Fitzpatrick, David R and Flicek, Paul and Floyd, James and Foley, A. Reghan and Franklin, Christopher S and Futema, Marta and Gallagher, Louise and Gasparini, Paolo and Gaunt, Tom and Geihs, Matthias and Geschwind, Daniel and Greenwood, Celia and Griffin, Heather and Grozeva, Detelina and Guo, Xiaosen and Guo, Xueqin and Gurling, Hugh and Hart, Deborah and Henicks, Auey E and Holmans, Peter A and Huang, Liren and Hubbard, Tim and Humphries, Steve E and Hurles, Matthew and Hysi, Pirro and Iotchkova, Valentina and Isaacs, Aaron and Jackson, David K and Jamshidi, Yalda and ... and UK10K Consortium
Nature Communications, ISSN 2041-1723, 09/2015, Volume 6, Issue 1, pp. 8111 - 8111
textabstractImputing genotypes from reference panels created by whole-genome sequencing (WGS) provides a cost-effective strategy for augmenting the... 
TWINSUK | GENOTYPE IMPUTATION | FORMAT | MULTIDISCIPLINARY SCIENCES | Index Medicus
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 4583 - 9
As the number of genes identified for linkage to hearing loss has been increasing and more public databases have become available, we aimed to systematically... 
DATABASE | IDENTIFICATION | MULTIDISCIPLINARY SCIENCES | INTERPRETATION GUIDELINES | Pathogenicity | Hearing | Databases | Gene frequency | Benign | Alleles | Hearing impairment | Population genetics | Hearing loss
Journal Article