Discrete domains of gene expression in germinal layers distinguish the development of gyrencephalyEMBO JOURNALIF8.32015-04-27133OAAI
The Murine Model for Hantaan Virus-Induced Lethal Disease Shows Two Distinct Paths in Viral Evolutionary Trajectory with and without Ribavirin TreatmentJOURNAL OF VIROLOGYIF3.82013-10-1520OAAI
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysisENDOCRINE-RELATED CANCERIF4.62010-09-0129OAAI
Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferretVIROLOGY JOURNALIF3.82010-07-0915OAAI
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progressionEUROPEAN JOURNAL OF HUMAN GENETICSIF4.62010-01-0645OAAI
Transcriptome sequencing and development of an expression microarray platform for the domestic ferretBMC GENOMICSIF3.72010-01-0130OAAI
Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC arrayNEURO-ONCOLOGYIF13.42009-12-0151OAAI
Somatic mosaicism for copy number variation in differentiated human tissuesHUMAN MUTATIONIF3.72008-09-01194OAAI
Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseasesJOURNAL OF AUTOIMMUNITYIF72008-06-0114PREAI
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 KBAC-clone-based arrayHUMAN MUTATIONIF3.72008-03-0144OAAI
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesAMERICAN JOURNAL OF HUMAN GENETICSIF8.12008-03-01453OAAI
Growth hormone overexpression in the central nervous system results in hyperphagia-induced obesity associated with insulin resistance and dyslipidemiaDIABETESIF7.52005-01-0169OAAI
Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular diseaseEXPERIMENTAL CELL RESEARCHIF3.52004-11-0115PREAI
NF2 tumor suppressor gene -: A comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGHNEUROMOLECULAR MEDICINEIF3.92003-01-0112PREAI
Fine mapping of the constitutional translocation t(11;22)(q23;q11)HUMAN GENETICSIF3.62000-04-2023PREAI
A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 geneHUMAN GENETICSIF3.61999-06-0227PREAI
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?GENES CHROMOSOMES & CANCERIF2.81999-06-0138PREAI