Copy number profiling of 556 high-risk neuroblastoma patients using aCGH or SNP arrays

Allelic Imbalances in bladder tumors based on high-density SNP array

Affymetrix 100K SNP array data-

Genome-wide SNP Microarray Mapping in Basal Cell Carcinomas Unveils Uniparental Disomy as a Key Somatic Event.

Human Breast Tumor SNPs

Genomic and expression profiling identifies Syk as a possible therapeutic target in mantle cell lymphoma

Global variation of copy number in the human genome_EA

SNP Analysis of Primary Glioblastoma Cell Lines

Global variation of copy number in the human genome_COMM

High Resolution Copy Number Analysis of Paraffin Embedded Archival Tissue Using SNP BeadArrays

Genes regulating B cell development are mutated in acute lymphoid leukaemia

High-resolution Global Genomic Survey of 178 Gliomas

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

SCLC cell line profiling on 100K arrays

Pancreatic cancer_Affymetrix 100K SNP arrays

Relapse versus diagnostic acute myeloid leukaemia samples analysed using Affymetrix 10K SNP array

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Genomic profiling data of 40 childhood leukemia patients

Genome-wide detection of recurring sites of uniparental disomy in folicular and transformed follicular lymphoma

Frequent Partial Uniparental Disomy Due to Somatic Recombination in Acute Myeloid Leukemias