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Inflammatory Bowel Diseases|October 13, 2017
Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel DiseaseMáire A Conrad, Noor Dawany, Kathleen E Sullivan, et al.Genetics|July 21, 2025
Quantile-specific confounding: correction for subtle population stratification via quantile regressionChen Wang, Marco Masala, Edoardo Fiorillo, et al.Investigative Ophthalmology & Visual Science|June 28, 2005
Identification of a novel locus on 2q for autosomal dominant high-grade myopiaPrasuna C Paluru, Sudha Nallasamy, Marcella Devoto, et al.Genetic Epidemiology|March 26, 2003
A general class of association tests for family-based data using weight functionsXin Liu, Derek GordonHuman Mutation|January 12, 2005
A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expressionPaola Griseri, Tiziana Bachetti, Francesca Puppo, et al.Human Heredity|July 8, 2011
Genome-wide linkage analysis to identify genetic modifiers of ALK mutation penetrance in familial neuroblastomaMarcella Devoto, Claudia Specchia, Marci Laudenslager, et al.Cancer Chemotherapy and Pharmacology|September 13, 2019
A reliable method to determine which candidate chemotherapeutic drugs effectively inhibit tumor growth in patient-derived xenografts (PDX) in single mouse trialsDerek Gordon, David E AxelrodThe Journal of Clinical Investigation|June 3, 2005
Factors affecting statistical power in the detection of genetic associationDerek Gordon, Stephen J FinchClinical Immunology (Orlando, Fla.)|May 25, 2022
Clinical and laboratory predictors of monogenic very early onset inflammatory bowel diseaseJudith Kelsen, Noor Dawany, Maire Conrad, et al.BMC Bioinformatics|August 25, 2009
Computing power of quantitative trait locus association mapping for haploid lociDerek Gordon, Andrew R ZinnPageof 21