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A second generation human haplotype map of over 3.1 million SNPs.

• Authors : Frazer KA; Ballinger DG; Cox DR ...

Subjects: Haplotypes/Haplotypes/Haplotypes/*genetics ; Polymorphism, Single Nucleotide/Polymorphism, Single Nucleotide/Polymorphism, Single Nucleotide/*genetics; Female

• Source: Nature [Nature] 2007 Oct 18; Vol. 449 (7164), pp. 851-61.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium:

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Genome-wide detection and characterization of positive selection in human populations.

• Authors : Sabeti PC; Varilly P ...

Subjects: Selection, Genetic*; Genome, Human/Genome, Human/Genome, Human/*genetics; Antiporters/Antiporters/Antiporters/genetics

• Source: Nature [Nature] 2007 Oct 18; Vol. 449 (7164), pp. 913-8.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium:

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Variation near complement factor I is associated with risk of advanced AMD.

• Authors : Fagerness JA; Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, USA.; Maller JB

Subjects: Polymorphism, Single Nucleotide*; Complement Factor I/Complement Factor I/Complement Factor I/*genetics ; Macular Degeneration/Macular Degeneration/Macular Degeneration/*genetics

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2009 Jan; Vol. 17 (1), pp. 100-4. Date of Electronic Publication: 2008 Aug 06.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited

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Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach.

• Authors : Sobrin L; Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA.; Maller JB

Subjects: Genetic Predisposition to Disease* ; Genetic Testing*; Macular Degeneration/Macular Degeneration/Macular Degeneration/*genetics

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Apr; Vol. 18 (4), pp. 496-501. Date of Electronic Publication: 2009 Oct 21.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

• Authors : Craddock N; Hurles ME; Cardin N ...

Subjects: Disease* ; Genome-Wide Association Study*; DNA Copy Number Variations/DNA Copy Number Variations/DNA Copy Number Variations/*genetics

• Source: Nature [Nature] 2010 Apr 01; Vol. 464 (7289), pp. 713-20.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium:

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Bayesian refinement of association signals for 14 loci in 3 common diseases

• Authors : Maller, Julian; McVean, Gilean; Byrnes, Jake

Subjects: Bayes theorem; CDKAL1 gene; CTLA-4 Antigen

• Source: Nature Genetics

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The Genotype-Tissue Expression (GTEx) project

• Authors : Lonsdale, John; Thomas, Emile; Salvatore, Mike ...

Subjects: [SDV.SA]Life Sciences [q-bio]/Agricultural sciences; [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology; [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie

• Source: ISSN: 1061-4036.

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Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

• Authors : Yang, Jialiang; Huang, Tao; Petralia, Francesca

• Source: Yang, J., T. Huang, F. Petralia, Q. Long, B. Zhang, C. Argmann, Y. Zhao, et al. 2015. “Synchronized age-related gene expression changes across multiple tissues in human and the link to complex

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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

• Authors : Romagnoni, Alberto; Jégou, Simon; van Steen, Kristel ...

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

• Authors : Demontis, Ditte; Walters, Raymond K.; Martin, Joanna

Subjects: Trastorns per dèficit d'atenció amb hiperactivitat en els infants; Trastorns per dèficit d'atenció amb hiperactivitat en els adults; Genoma humà

• Source: Articles publicats en revistes (Genètica, Microbiologia i Estadística)

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