Bergamaschi et al.

iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72–polymorphic p53

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Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule

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Nucleosome positions predicted through comparative genomics

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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

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Padiath et al.

Lamin B1 duplications cause autosomal dominant leukodystrophy

Zara et al.

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract

Manak et al.

Biological function of unannotated transcription during the early development of Drosophila melanogaster

Lee et al.

Indian hedgehog is a major mediator of progesterone signaling in the mouse uterus

Chan et al.

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

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Maller et al.

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

Li et al.

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

Ramsey et al.

Dual feedback loops in the GAL regulon suppress cellular heterogeneity in yeast

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Knight et al.

Unraveling adaptive evolution: how a single point mutation affects the protein coregulation network

Carter et al.

A signature of chromosomal instability inferred from gene expression profiles predicts clinical outcome in multiple human cancers

Burdick et al.

In silico method for determining genotypes in pedigrees

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Koolen et al.

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

Shaw-Smith et al.

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Sharp et al.

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

Dierick & Greenspan

Molecular analysis of flies selected for aggressive behavior

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Ruderfer et al.

Population genomic analysis of outcrossing and recombination in yeast

Shi et al.

JAK signaling globally counteracts heterochromatic gene silencing

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Hsien-Hsien Lei has been moderating a very interesting interview series at Genetics and Health, and now has posted a Q & A with yours truly. Topics include the Nature Publishing Group, peer review, blogs, open access, and others.

Pickersgill et al.

Characterization of the Drosophila melanogaster genome at the nuclear lamina

Dews et al.

Augmentation of tumor angiogenesis by a Myc-activated microRNA cluster

Mahadevan et al.

Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy

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Price et al.

Principal components analysis corrects for stratification in genome-wide association studies

Liu et al.

Candidate lung tumor susceptibility genes identified through whole-genome association analyses in inbred mice

Lei & Corces

RNA interference machinery influences the nuclear organization of a chromatin insulator

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Crow et al.

Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

Crow et al.

Mutations in the gene encoding the 3’-5’ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

Lehner et al.

Systematic mapping of genetic interactions in Caenorhabditis elegans identifies common modifiers of diverse signaling pathways

Ozaki et al.

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

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