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Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
A transcriptomic approach to understand patient susceptibility to pneumonia after abdominal surgery
Study
EGAS00001007229
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
Ultra-fast deep-learned pediatric CNS tumor classification.
Study
EGAS00001007475
-
Multi-Layered Molecular Profiling Informs the Diagnosis and Targeted Therapy of Desmoplastic Small Round Cell Tumor
Study
EGAS00001007934
-
Multi-omic analysis of Down Syndrome in thyroid
Study
EGAS00001007677
-
A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Study
EGAS00001006547
-
Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers
Study
EGAS00001007242
-
Wistar PDX Development and Trial Center
Study
phs002432
-
Whole Exome Sequencing of Calcitonin Producing Pancreatic Neuroendocrine Neoplasms (CT-pNENs) Indicates a Unique Molecular Signature
Study
phs003060
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Uncovering RNA Signatures of C9orf72-Linked ALS and Related Disorders
Study
phs003065
-
Genetic defects in familial renal disorders
Study
phs000477
-
CaBagE: a Cas9-Based Background Elimination Strategy for Targeted, Long-Read DNA Sequencing
Study
phs002368
-
Prediction of Trastuzumab Benefit in Adjuvant Breast Cancer: Gene Expression Profiling in NSABP B31
Study
phs000826
-
Autism Sequencing Consortium (ASC)
Study
phs000298
-
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Study
phs000245
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs000379
-
Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC)
Study
phs003510
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts, Sub-types, and Subclinical Phenotypes - CIDR
Study
phs002815
-
Childhood Cancer Data Initiative (CCDI): Enhancement of Data Sharing in Pediatric, Adolescent and Young Adult Cancers
Study
phs002431
-
A Scalable, GMP-Compatible, Autologous Organotypic Cell Therapy for Dystrophic Epidermolysis Bullosa
Study
phs003271
-
Genomic Basis of Phenotypic Variability of Complex Disorders
Study
phs002450
-
Genomic Profiling of Pediatric Tumors by Cell Free DNA Sequencing
Study
EGAS50000000072