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Linkage analysis

Identification of a KEAP1 Germline Mutation in a Family with Multinodular Goitre

Risa Teshiba, Tatsuro Tajiri, [ ... ], Ken Yamamoto

Evaluating Power and Type 1 Error in Large Pedigree Analyses of Binary Traits

Anna C. Cummings, Eric Torstenson, [ ... ], Jonathan L. Haines

A PLSPM-Based Test Statistic for Detecting Gene-Gene Co-Association in Genome-Wide Association Study with Case-Control Design

Xiaoshuai Zhang, Xiaowei Yang, [ ... ], Fuzhong Xue

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

Christina A. Markunas, Karen Soldano, [ ... ], Allison E. Ashley-Koch

The 3D Organization of the Yeast Genome Correlates with Co-Expression and Reflects Functional Relations between Genes

Dirar Homouz, Andrzej S. Kudlicki

Linkage Replication for Chromosomal Region 13q32 in Schizophrenia: Evidence from a Brazilian Pilot Study on Early Onset Schizophrenia Families

Ary Gadelha, Vanessa Kiyomi Ota, [ ... ], Gerome Breen

A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers

Minna K. Karjalainen, Johanna M. Huusko, [ ... ], Mikko Hallman

The Genetic Basis of Natural Variation in Oenological Traits in Saccharomyces cerevisiae

Francisco Salinas, Francisco A. Cubillos, [ ... ], Claudio Martinez

Identification of a Potential Susceptibility Locus for Macular Telangiectasia Type 2

Nancy L. Parmalee, Carl Schubert, [ ... ], for the MacTel Project

Sex-Specific Regulation of Mitochondrial DNA Levels: Genome-Wide Linkage Analysis to Identify Quantitative Trait Loci

Sonia López, Alfonso Buil, [ ... ], Jose Manuel Soria

Genome-Wide Linkage and Association Analysis Identifies Major Gene Loci for Guttural Pouch Tympany in Arabian and German Warmblood Horses

Julia Metzger, Bernhard Ohnesorge, Ottmar Distl

The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

Lisa J. Strug, Laura Addis, [ ... ], Deb K. Pal

A Novel Autosomal Dominant Inclusion Body Myopathy Linked to 7q22.1-31.1

Yan Lu, Xingang Li, [ ... ], Jianping Jia

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