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Heredity

rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants

Jürgen Glas, Julia Seiderer, [ ... ], Stephan Brand

Development of Sensory, Motor and Behavioral Deficits in the Murine Model of Sanfilippo Syndrome Type B

Coy D. Heldermon, Anne K. Hennig, [ ... ], Mark S. Sands

Combining Phylogeography with Distribution Modeling: Multiple Pleistocene Range Expansions in a Parthenogenetic Gecko from the Australian Arid Zone

Jared L. Strasburg, Michael Kearney, Craig Moritz, Alan R. Templeton

Haplotyping a Quantitative Trait with a High-Density Map in Experimental Crosses

Wei Hou, John Stephen F. Yap, [ ... ], Rongling Wu

Wolbachia-Induced Unidirectional Cytoplasmic Incompatibility and Speciation: Mainland-Island Model

Arndt Telschow, Matthias Flor, [ ... ], John H. Werren

Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene

Andre Franke, Jochen Hampe, [ ... ], Stefan Schreiber

In Vitro Human Keratinocyte Migration Rates Are Associated with SNPs in the KRT1 Interval

Heng Tao, Anthony J. Berno, David R. Cox, Kelly A. Frazer

An Ultra-High Discrimination Y Chromosome Short Tandem Repeat Multiplex DNA Typing System

Erin K. Hanson, Jack Ballantyne

Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy

Andrew Orr, Marie-Pierre Dubé, [ ... ], Mark Samuels

HLA-A Confers an HLA-DRB1 Independent Influence on the Risk of Multiple Sclerosis

Boel Brynedal, Kristina Duvefelt, [ ... ], Jan Hillert

Large-Scale In Silico Mapping of Complex Quantitative Traits in Inbred Mice

Pengyuan Liu, Haris Vikis, [ ... ], Ming You

Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression

Fanny Mochel, Perrine Charles, [ ... ], Alexandra Durr

Common HLA Alleles Associated with Health, but Not with Facial Attractiveness

Vinet Coetzee, Louise Barrett, [ ... ], Ahmed A. Wadee

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