Modifier locus of the skeletal muscle involvement in Emery–Dreifuss muscular dystrophy

Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits

(2010) Elisabeth A. Rosenthal et al.   GENETIC EPIDEMIOLOGY

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

(2010) Ellen M. Wijsman et al.   HUMAN GENETICS

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

(2009) Lucie Gueneau et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Disruption of Striated Preferentially Expressed Gene Locus Leads to Dilated Cardiomyopathy in Mice

(2009) Xiaoli Liu et al.   CIRCULATION

A Genomewide Assessment of Inbreeding Depression: Gene Number, Function, and Mode of Action

(2009) JULIEN F. AYROLES et al.   CONSERVATION BIOLOGY

Extreme phenotypic diversity and nonpenetrance in families with theLMNA gene mutation R644C

(2008) Julia Rankin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Identifying Modifier Loci in Existing Genome Scan Data

(2008) E. W. Daw et al.   ANNALS OF HUMAN GENETICS

Identifying modifier genes of monogenic disease: strategies and difficulties

(2008) Emmanuelle Génin et al.   HUMAN GENETICS

Overdominance in the Human Genome and Olfactory Receptor Activity

(2008) S. Alonso et al.   MOLECULAR BIOLOGY AND EVOLUTION

Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation

(2008) Nicola Carboni et al.   NEUROMUSCULAR DISORDERS

Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis

(2007) Robert P. Igo et al.   GENETIC EPIDEMIOLOGY