1539 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by SNP array
GSE169469
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
  • Genome variation profiling by SNP array
2 Xuejiao Chen Mar 24, 2021
GSE162283
14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia
42 Danika Di Giacomo Sep 05, 2021
GSE20368
1q gain clinical impact in Ewing's Sarcoma: role of DTL
94 Carlos Mackintosh Aug 01, 2011
GSE53021
250K SNP array data for 40 high-grade myogenic cancers
47 Jonathan A Fletcher May 02, 2014
GSE13813
50K SNP Copy Number Analysis of Ovarian Carcinomas
  • Genome variation profiling by SNP array
118 Dariush Etemadmoghadam Feb 17, 2009
GSE63058
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages
139 Giuseppe Testa Dec 15, 2014
GSE63028
7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages (aCGH)
  • Genome variation profiling by SNP array
34 Giuseppe Testa Dec 15, 2014
GSE118648
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS)
31 Cristina Mecucci Sep 01, 2019
GSE65777
A Genome Wide Association Study Reveals Genetic Predisposition for Bortezomib-Induced Peripheral Neuropathy in Multiple Myeloma by Variation in the PREP1-CBS locus.
469 Wilfried Gouraud Nov 23, 2016
GSE85594
A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population
47 Lynn Jorde Aug 16, 2016
GSE34678
A Genome-wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Possibilities for Future Personalized Treatment
172 Muhammad Ghulam Kibriya Dec 19, 2014
GSE54504
A Genomic Portrait of Resectable Hepatocellular Carcinomas: Implications of RB1 and FGF19 Aberrations for Patient Stratification.
  • Genome variation profiling by SNP array
462 Farhan Haq May 01, 2014
GSE34573
A Global View of the Oncogenic Landscape in Nasopharyngeal Carcinoma:An Integrated Analysis at the Genetic and Expression Levels
64 Wenbin Wei Dec 10, 2012
GSE59150
A High-Resolution Copy Number Variation Resource for Clinical Genetics
873 Stephen W Scherer Jul 24, 2014
GSE30481
A Map of Copy Number Variations in Chinese Populations
  • Genome variation profiling by SNP array
155 Haiyi Lou Dec 31, 2011
GSE133063
A Novel Silent Mutation in the L1CAM Gene causing Fetal Hydrocephalus
  • Genome variation profiling by SNP array
1 yixi sun Jul 16, 2019
GSE16122
A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma
203 Luca Agnelli May 16, 2009
GSE14845
A Whole Genome Approach to Characterising a Novel Immunodeficiency Disorder
4 Michael Richard Green Apr 01, 2009
GSE99221
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth and senescence escape via regulation of MITF
126 Jiyeon Choi Jul 01, 2017
GSE7822
A comparison of DNA copy number profiling platforms using a panel of melanoma cell lines
151 Joel Greshock Nov 02, 2007