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Genomics
(15)
Unknown
(10)
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Homo sapiens
(15)
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EGA
(15)
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Illumina 15K
(8)
Illumina_670k - Illuminus, Affymetrix 6.0, Illumina 1.2M
(1)
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2025
(2)
2024
(2)
2022
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2018
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CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML.
Not available
S-EPMC4911865
|
biostudies-literature
Cite
The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Not available
S-EPMC5907936
|
biostudies-literature
Cite
Integrated stem cell signature and cytomolecular risk determination in pediatric acute myeloid leukemia.
Not available
S-EPMC9485122
|
biostudies-literature
Cite
AS
WTCCC2 project samples from Ankylosing spondylitis Cohort
EGAD00010000150
|
EGA
Cite
Genomewide association studies in ankylosing spondylitis
The aim of this study was to identify genes associated with ankylosing spondylitis susceptibility in British and Australian individuals of European descent.
EGAS00000000104
|
EGA
Cite
ATD
WTCCC1 project Autoimmune Thyroid Disease (ATD) samples
EGAD00000000011
|
EGA
Cite
BC
WTCCC1 project Breast cancer (BC) samples
EGAD00000000013
|
EGA
Cite
MS
WTCCC1 project Multiple Sclerosis (MS) samples
EGAD00000000012
|
EGA
Cite
WTCCC2 Ankylosing spondylitis cases - individual
WTCCC1 project Ankylosing Spondylitis (AS) samples
EGAD00000000010
|
EGA
Cite
58C
WTCCC1 project samples from 1958 British Birth Cohort
EGAD00000000014
|
EGA
Cite
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