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by Pers, Tune H and Karjalainen, Juha M and Chan, Yingleong and Westra, Harm-Jan and Wood, Anew R and Yang, Jian and Lui, Julian C and Vedantam, Sailaja and Gustafsson, Stefan and Esko, Tonu and Frayling, Tim and Speliotes, Elizabeth K and Boehnke, Michael and Raychaudhuri, Soumya and Fehrmann, Rudolf S. N and Hirschhorn, Joel N and Franke, Lude and Chu, Auey Y and Estrada, Karol and Luan, Jian'an and Kutalik, Zoltán and Amin, Najaf and Buchkovich, Martin L and Croteau-Chonka, Damien C and Day, Felix R and Duan, Yanan and Fall, Tove and Fehrmann, Rudolf and Ferreira, Teresa and Jackson, Anne U and Karjalainen, Juha and Lo, Ken Sin and Locke, Adam E and Mägi, Reedik and Mihailov, Evelin and Porcu, Eleonora and Randall, Joshua C and Scherag, Ané and Vinkhuyzen, Anna A. E and Winkler, Thomas W and Workalemahu, Tsegaselassie and Zhao, Jing Hua and Absher, Devin and Albrecht, Eva and Anderson, Denise and Baron, Jeffrey and Beekman, Marian and Demirkan, Ayse and Ehret, Georg B and Feenstra, Bjarke and Feitosa, Mary F and Fischer, Krista and Fraser, Ross M and Goel, Anuj and Gong, Jian and Justice, E and Kanoni, Stavroula and Kleber, Marcus E and Kristiansson, Kati and Lim, Unhee and Lotay, Vaneet and Mangino, Massimo and Mateo Leach, Irene and Medina-Gomez, Carolina and Nalls, Michael A and Nyholt, Dale R and Palmer, Cameron D and Pasko, Dorota and Pechlivanis, Sonali and Prokopenko, Inga and Ried, Janina S and Ripke, Stephan and Shungin, Dmitry and Stancáková, Alena and Strawbridge, Rona J and Sung, Yun Ju and Tanaka, Toshiko and Teumer, Alexander and Trompet, Stella and van der Laan, Sander W and van Setten, Jessica and van Vliet-Ostaptchouk, Jana V and Wang, Zhaoming and Yengo, Loïc and Zhang, Weihua and Afzal, Uzma and Ärnlöv, Johan and Arscott, Gillian M and Bandinelli, Stefania and Barrett, Amy and Bellis, Claire and Bennett, Amanda J and Berne, Christian and Blüher, Matthias and Bolton, Jennifer L and Böttcher, Yvonne and Boyd, Heather A and Bruinenberg, Marcel and Buckley, Brendan M and Buyske, Steven and ... and Genetic Invest ANthropometric Trai and Genetic Investigation of ANthropometric Traits (GIANT) Consortium and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, p. 5890
The main challenge for gaining biological insights from genetic associations is identifying which genes and pathways explain the associations. Here we present... 
NETWORK | INTEGRATION | MULTIDISCIPLINARY SCIENCES | CANDIDATE GENES | DISEASE | ARCHITECTURE | COMMON | LOCI | IDENTIFICATION | HEIGHT | DATA SETS | Genome-Wide Association Study - methods | Software | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 7, p. e1004494
Exome sequencing studies in complex diseases are challenged by the allelic heterogeneity, large number and modest effect sizes of associated variants on... 
PROFILE | GENE | MUTATION | DISEASE | GENETICS & HEREDITY | LEVEL | ASSOCIATION | CARDIOVASCULAR RISK | Physiological aspects | Genetic research | Genome-wide association studies | Research | Lipoprotein A | Heart attacks | Disease | Genomics | Genes | Biomarkers | Medical records | Population | Grants
Journal Article
Nature Neuroscience, ISSN 1097-6256, 09/2017, Volume 20, Issue 9, pp. 1217 - 1224
Journal Article
Nature Biotechnology, ISSN 1087-0156, 07/2018, Volume 36, Issue 6, pp. 540 - 546
Journal Article
by Joshi, Peter K and Esko, Tonu and Mattsson, Hannele and Eklund, Niina and Gandin, Ilaria and Nutile, Teresa and Jackson, Anne U and Schurmann, Claudia and Smith, Albert V and Zhang, Weihua and Okada, Yukinori and Stancakova, Alena and Faul, Jessica D and Zhao, Wei and Bartz, Traci M and Concas, Maria Pina and Franceschini, Nora and Enroth, Stefan and Vitart, Veronique and Trompet, Stella and Guo, Xiuqing and Chasman, Daniel I and O'Connel, Jeffrey R and Corre, Tanguy and Nongmaithem, Suraj S and Chen, Yuning and Mangino, Massimo and Ruggiero, Daniela and Traglia, Michela and Farmaki, Aliki-Eleni and Kacprowski, Tim and Bjonnes, Anew and van der Spek, Ashley and Wu, Ying and Giri, Anil K and Yanek, Lisa R and Wang, Lihua and Hofer, Edith and Rietveld, Cornelius A and McLeod, Olga and Cornelis, Marilyn C and Pattaro, Cristian and Verweij, Niek and Baumbach, Clemens and Abdellaoui, Abdel and Warren, Helen R and Vuckovic, gana and Mei, Hao and Bouchard, Claude and Perry, John R. B and Cappellani, Stefania and Mirza, Saira S and Benton, Miles C and Broeckel, Ulrich and Medland, Sarah E and Lind, PenelopeA and Malerba, Giovanni and ng, Alexander and Yengo, Loic and Bielak, Lawrence F and Zhi, Degui and van der Most, Peter J and Shriner, Daniel and Maegi, Reedik and Hemani, Gibran and Karaderi, Tugce and Wang, Zhaoming and Liu, Tian and Demuth, Ilja and Zhao, Jing Hua and Meng, Weihua and Lataniotis, Lazaros and van der Laan, Sander W and Bradfield, Jonathan P and Wood, Anew R and Bonnefond, Amelie and Ahluwalia, Tarunveer S and Hall, LeanneM and Salvi, Erika and Yazar, Seyhan and Carstensen, Lisbeth and de Haan, Hugoline G and Abney, Mark and Afzal, Uzma and Allison, Matthew A and Amin, Najaf and Asselbergs, Folkert W and Bakker, Stephan J. L and Barr, R. Graham and Baumeister, Sebastian E and Benjamin, Daniel J and Bergmann, Sven and Boerwinkle, Eric and Bottinger, Erwin P and Campbell, Archie and Chakravarti, Aravinda and Chan, Yingleong and Chanock, Stephen J and Chen, Constance and Chen, Y. -D. Ida and ... and BioBank Japan Project and The BioBank Japan Project
Nature, ISSN 0028-0836, 07/2015, Volume 523, Issue 7561, pp. 459 - U176
Homozygosity has long been associated with rare, often devastating, Mendelian disorders(1), and Darwin was one of the first to recognize that inbreeding... 
INTELLIGENCE | HOMOZYGOSITY | MULTIDISCIPLINARY SCIENCES | ARCHITECTURE | GENETIC-VARIANTS | TRAITS | ASSOCIATION | BLOOD-PRESSURE | Studies | Cognition & reasoning | Disease | Genomics | Cognitive ability | Genomes | Educational attainment
Journal Article
Genome Medicine, ISSN 1756-994X, 04/2018, Volume 10, Issue 1, pp. 1 - 11
We describe a method that enables the multiplex screening of a pool of many different donor cell lines. Our method accurately predicts each donor proportion... 
Multiplexed testing | Barcode free method | Next-generation sequencing | Single nucleotide polymorphisms | Expectation maximization algorithm | Personal Genome Project | VULNERABILITIES | OVARIAN-CANCER | HEIGHT | LINES | RESPONSES | WIDE ANALYSIS | GENETICS & HEREDITY | PCR | Genetic variation | Analysis | Research | Nucleotide sequencing | Chromosomes | DNA sequencing
Journal Article
Scientific Reports, ISSN 2045-2322, 04/2017, Volume 7, p. 46148
The Personal Genome Project (PGP) is an effort to enroll many participants to create an open-access repository of genome, health and trait data for research.... 
UNITED-STATES | GENOTYPES | DESIGN | QUANTITATIVE TRAITS | DATABASE | GENOMES | DBGAP | MULTIDISCIPLINARY SCIENCES | POWER | LINKAGE | COMPLEX TRAITS | Geography | Phenotype | Algorithms | Disease | Quantitative Trait, Heritable | United States | Humans | Female | Male | Surveys and Questionnaires | Genome, Human | Cohort Studies | Genomes | Open access | Demography
Journal Article
Genome medicine, ISSN 1756-994X, 04/2018, Volume 10, Issue 1, p. 31
We describe a method that enables the multiplex screening of a pool of many different donor cell lines. Our method accurately predicts each donor proportion... 
Genomes | Biology | Single nucleotide polymorphisms | Expectation-maximization algorithms
Journal Article