Phenotype Similarity Regression for Identifying the Genetic Determinants of Rare Diseases

American Journal of Human Genetics

Volumn 98, Issue 3, 2016, Pages 490-499

  Greene, Daniel ^a,b   Richardson, Sylvia ^b   Turro, Ernest ^a,b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b MRC BIOSTATISTICS UNIT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ACTININ 1; DIAPH1 PROTEIN; PROTEIN; RASGRP2 PROTEIN; UNCLASSIFIED DRUG; ACTININ; ACTN1 PROTEIN, HUMAN; DIAPH1 PROTEIN, HUMAN; GUANINE NUCLEOTIDE EXCHANGE FACTOR; RASGRP2 PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ARTICLE; EXOME; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOME; GENOTYPE; INHERITANCE; MOLECULAR PATHOLOGY; PHENOTYPE; PREDICTIVE VALUE; PRIORITY JOURNAL; RARE DISEASE; SEQUENCE ANALYSIS; SIMULATION; BAYES THEOREM; BIOLOGICAL MODEL; GENETIC ASSOCIATION STUDY; GENETIC DATABASE; GENETICS; HUMAN; PROCEDURES; RARE DISEASES; STATISTICAL MODEL;

ACTININ; ADAPTOR PROTEINS, SIGNAL TRANSDUCING; BAYES THEOREM; DATABASES, GENETIC; GENETIC ASSOCIATION STUDIES; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMANS; LOGISTIC MODELS; MODELS, GENETIC; PHENOTYPE; RARE DISEASES;

EID: 84960117336     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2016.01.008     Document Type: Article

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