Transcriptional Regulatory Elements in the Human GenomeThe Ciliopathies: An Emerging Class of Human Genetic DisordersR ACE , A NCESTRY , AND G ENES : Implications for Defining Disease RiskH UMAN M IGRATIONS AND P OPULATION S TRUCTURE : What We Know and Why it MattersThe human microbiome: our second genomeThe tension between data sharing and the protection of privacy in genomics researchMendelian disorders of the epigenetic machinery: tipping the balance of chromatin statesThe genetics of substance dependenceThe RASopathiesReturn of individual research results and incidental findings: facing the challenges of translational scienceApolipoprotein E: far more than a lipid transport proteinCongenital disorders of glycosylationPeroxisome biogenesis disordersDeciphering the genetic basis of Alzheimer's diseasePredicting the effects of amino acid substitutions on protein functionBiased gene conversion and the evolution of mammalian genomic landscapesAdvances in Skeletal Dysplasia GeneticsNext-generation DNA sequencing methodsThe neutral theory of molecular evolution in the genomic eraAdmixture mapping comes of ageGene duplication: a drive for phenotypic diversity and cause of human diseaseLINE-1 elements in structural variation and diseaseThe power of meta-analysis in genome-wide association studiesAfrican genetic diversity: implications for human demographic history, modern human origins, and complex disease mappingPatents in genomics and human geneticsGenotype imputationA new approach to decoding life: systems biologyMammalian circadian biology: elucidating genome-wide levels of temporal organizationStructuring the universe of proteins.Cystic Fibrosis and Its Management Through Established and Emerging Therapies.Sharing Data to Build a Medical Information Commons: From Bermuda to the Global Alliance.Stewardship of human biospecimens, DNA, genotype, and clinical data in the GWAS era.Participatory Genomic Research: Ethical Issues from the Bottom Up to the Top Down.How many genes can make a cell: the minimal-gene-set concept.Advances in chemical genetics.The patterns of natural variation in human genes.Chromosomes, conflict, and epigenetics: chromosomal speciation revisited.Syndromes of telomere shorteningThe posttranslational processing of prelamin A and disease.Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.
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P1433
description
Wissenschaftliche Fachzeitschrift
@de
revista científica
@es
rivista scientifica
@it
scientific journal
@en
vědecký časopis
@cs
wetenschappelijk tijdschrift van Annual Reviews
@nl
науковий журнал
@uk
वैज्ञानिक पत्रिका
@hi
英语期刊
@zh
name
Annual Review of Genomics and Human Genetics
@ast
Annual Review of Genomics and Human Genetics
@de
Annual Review of Genomics and Human Genetics
@en
Annual Review of Genomics and Human Genetics
@es
Annual Review of Genomics and Human Genetics
@it
Annual Review of Genomics and Human Genetics
@nl
type
label
Annual Review of Genomics and Human Genetics
@ast
Annual Review of Genomics and Human Genetics
@de
Annual Review of Genomics and Human Genetics
@en
Annual Review of Genomics and Human Genetics
@es
Annual Review of Genomics and Human Genetics
@it
Annual Review of Genomics and Human Genetics
@nl
altLabel
Annu Rev Genomics Hum Genet
@de
Annu. Rev. Genomics Hum. Genet.
@de
Annu.Rev.Genomics Hum.Genet.
@de
prefLabel
Annual Review of Genomics and Human Genetics
@ast
Annual Review of Genomics and Human Genetics
@de
Annual Review of Genomics and Human Genetics
@en
Annual Review of Genomics and Human Genetics
@es
Annual Review of Genomics and Human Genetics
@it
Annual Review of Genomics and Human Genetics
@nl
P3181
P1055
P1156
P123
P1277
P1476
Annual Review of Genomics and Human Genetics
@en