KELVIN: A Software Package for Rigorous Measurement of Statistical Evidence in Human Genetics

Where’s the Evidence?

(2011) Veronica J. Vieland   HUMAN HEREDITY

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

(2011) Veronica J. Vieland et al.   Journal of Neurodevelopmental Disorders

Association statistics under the PPL framework

(2010) Yungui Huang et al.   GENETIC EPIDEMIOLOGY

Expected Monotonicity – A Desirable Property for Evidence Measures

(2010) Susan E. Hodge et al.   HUMAN HEREDITY

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

(2010) A. T. Pagnamenta et al.   JOURNAL OF MEDICAL GENETICS

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci

(2010) Judy F. Flax et al.   Journal of Neurodevelopmental Disorders

Identification of a Schizophrenia-Associated Functional Noncoding Variant inNOS1AP

(2009) Naomi S. Wratten et al.   AMERICAN JOURNAL OF PSYCHIATRY

Fast and Accurate Calculation of a Computationally Intensive Statistic for Mapping Disease Genes

(2009) Sang-Cheol Seok et al.   JOURNAL OF COMPUTATIONAL BIOLOGY

A Multilocus Model of the Genetic Architecture of Autoimmune Thyroid Disorder, with Clinical Implications

(2008) Veronica J. Vieland et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Practical Considerations for Dividing Data into Subsets Prior to PPL Analysis

(2008) M. Govil et al.   HUMAN HEREDITY