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Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
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- Nature Genetics, 2014, v. 46, n. 5, p. 498, doi. 10.1038/ng.2957
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- Article
Common and low-frequency variants associated with genome-wide recombination rate.
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- Nature Genetics, 2014, v. 46, n. 1, p. 11, doi. 10.1038/ng.2833
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Detection of sharing by descent, long-range phasing and haplotype imputation.
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- Nature Genetics, 2008, v. 40, n. 9, p. 1068, doi. 10.1038/ng.216
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Recombination rate and reproductive success in humans.
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- Nature Genetics, 2004, v. 36, n. 11, p. 1203, doi. 10.1038/ng1445
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The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.
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- Nature Genetics, 2004, v. 36, n. 3, p. 233, doi. 10.1038/ng1311
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- Article
A high-resolution recombination map of the human genome.
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- Nature Genetics, 2002, v. 31, n. 3, p. 241, doi. 10.1038/ng917
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- Article
Allegro, a new computer program for multipoint linkage analysis.
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- Nature Genetics, 2000, v. 25, n. 1, p. 12, doi. 10.1038/75514
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- Article
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06920-9
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- Article
Support for involvement of the AHI1 locus in schizophrenia.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 988, doi. 10.1038/sj.ejhg.5201848
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- Article
A genome-wide scan for preeclampsia in the Netherlands.
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- European Journal of Human Genetics, 2001, v. 9, n. 10, p. 758, doi. 10.1038/sj.ejhg.5200706
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- Article
Fine-scale recombination rate differences between sexes, populations and individuals.
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- Nature, 2010, v. 467, n. 7319, p. 1099, doi. 10.1038/nature09525
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Parental origin of sequence variants associated with complex diseases.
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- Nature, 2009, v. 462, n. 7275, p. 868, doi. 10.1038/nature08625
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Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
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- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0857-9
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- Article
Reproductive fitness and genetic risk of psychiatric disorders in the general population.
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- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15833
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- Article
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.
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- Nature Communications, 2017, v. 8, n. 2, p. 14265, doi. 10.1038/ncomms14265
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- Article
Epigenetic and genetic components of height regulation.
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- Nature Communications, 2016, v. 7, n. 11, p. 13490, doi. 10.1038/ncomms13490
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- Article
A susceptibility gene for late-onset idiopathic Parkinson's disease.
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- Annals of Neurology, 2002, v. 52, n. 5, p. 549, doi. 10.1002/ana.10324
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- Article
Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2.
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- PLoS Biology, 2003, v. 1, n. 3, p. 351, doi. 10.1371/journal.pbio.0000069
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Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2.
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- PLoS Biology, 2003, v. 1, n. 11, p. 1, doi. 10.1371/journal.pbio.0000069
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- Article
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
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- Nature, 2013, v. 497, n. 7450, p. 517, doi. 10.1038/nature12124
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- Article
Rate of de novo mutations and the importance of father's age to disease risk.
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- Nature, 2012, v. 488, n. 7412, p. 471, doi. 10.1038/nature11396
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Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05428-6
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- Article
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.
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- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1799, doi. 10.1093/hmg/8.9.1799
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The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland.
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- Arthritis & Rheumatology, 2021, v. 73, n. 11, p. 2025, doi. 10.1002/art.41793
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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19733-6
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- Article