The Genome of the Netherlands: design, and project goals
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Pieter B. T. Neerincx | Jeroen F. J. Laros | David van Enckevort | A. Hofman | A. Uitterlinden | J. Hehir-Kwa | C. Wijmenga | Jun Wang | Yingrui Li | Qibin Li | Ning Li | P. D. de Bakker | K. Ye | J. Houwing-Duistermaat | G. Willemsen | H. Cao | P. de Knijff | D. Boomsma | M. Swertz | S. Pulit | J. Hottenga | M. Beekman | A. D. de Craen | L. Karssen | E. V. van Leeuwen | C. V. van Duijn | G. van Ommen | K. Estrada | J. D. den Dunnen | E. Slagboom | A. Abdellaoui | V. Guryev | M. Vermaat | F. van Dijk | L. Francioli | Ruoyan Chen | Yuanping Du | S. Cao | J. van Setten | A. Menelaou | C. Elbers | H. Byelas | Patrick Deelen | M. Dijkstra | V. Koval | A. Kanterakis | Hailiang Mai | M. Kattenberg | B. Oostra | Fernanodo Rivadeneira | E. Suchiman | B. Wolffenbuttel | Clara C Elbers | J. Laros | Yingrui Li | F. Rivadeneira | A. Uitterlinden | A. Hofman | B. Oostra | C. V. van Duijn | D. Boomsma
[1] H. Ostrer,et al. Founder mutations among the Dutch , 2004, European Journal of Human Genetics.
[2] Marian Beekman,et al. Evidence of genetic enrichment for exceptional survival using a family approach: the Leiden Longevity Study , 2006, European Journal of Human Genetics.
[3] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[4] D. Postma,et al. Universal risk factors for multifactorial diseases , 2007, European Journal of Epidemiology.
[5] K. Shianna,et al. Long-range LD can confound genome scans in admixed populations. , 2008, American journal of human genetics.
[6] Monique M. B. Breteler,et al. The Rotterdam Study: 2016 objectives and design update , 2015, European Journal of Epidemiology.
[7] Kai Ye,et al. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads , 2009, Bioinform..
[8] P. Visscher,et al. Common SNPs explain a large proportion of heritability for human height , 2011 .
[9] T. Lehner,et al. The Netherlands Twin Register Biobank: A Resource for Genetic Epidemiological Studies , 2010, Twin Research and Human Genetics.
[10] W. G. Hill,et al. Genome partitioning of genetic variation for complex traits using common SNPs , 2011, Nature Genetics.
[11] Gonçalo R. Abecasis,et al. Fine Mapping of Five Loci Associated with Low-Density Lipoprotein Cholesterol Detects Variants That Double the Explained Heritability , 2011, PLoS genetics.
[12] Sarah Edkins,et al. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease , 2011, Nature Genetics.
[13] Si Quang Le,et al. SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples. , 2011, Genome research.
[14] M. Arfan Ikram,et al. The Rotterdam Study: 2012 objectives and design update , 2011, European journal of epidemiology.
[15] Hon-Cheong So,et al. Uncovering the total heritability explained by all true susceptibility variants in a genome‐wide association study , 2011, Genetic epidemiology.
[16] Joshua M. Korn,et al. Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease , 2011, Nature Genetics.
[17] P. Sham,et al. Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases , 2011, Genetic epidemiology.
[18] S. Steinberg,et al. Rate of de novo mutations and the importance of father’s age to disease risk , 2012, Nature.
[19] Jacob A. Tennessen,et al. Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes , 2012, Science.
[20] L. Kiemeney,et al. How to kickstart a national biobanking infrastructure – experiences and prospects of BBMRI-NL , 2012 .
[21] Paul Scheet,et al. A Genome-Wide Association Scan on the Levels of Markers of Inflammation in Sardinians Reveals Associations That Underpin Its Complex Regulation , 2012, PLoS genetics.
[22] B. Penninx,et al. Estimating the Genetic Variance of Major Depressive Disorder Due to All Single Nucleotide Polymorphisms , 2012, Biological Psychiatry.
[23] Claudio J. Verzilli,et al. An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People , 2012, Science.
[24] P. Visscher,et al. Five years of GWAS discovery. , 2012, American journal of human genetics.
[25] Tanya M. Teslovich,et al. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes , 2012, Nature Genetics.
[26] P. Scheet,et al. The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children , 2012, Twin Research and Human Genetics.
[27] H. M. Draisma,et al. The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection , 2013, Twin Research and Human Genetics.
[28] P. Sullivan,et al. Population structure, migration, and diversifying selection in the Netherlands , 2013, European Journal of Human Genetics.