The genomic landscape of familial glioma is a research paper published in Science Advances (2023). On theSindex it has a DataRank of 0. It has been cited 50 times.
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Medical Research Council
Grant: MR/M009203/1
NCI NIH HHS
Grant: R01 CA217105
NHGRI NIH HHS
Grant: U54 HG003273
Cancer Research UK
Grant: 25514
National Institute for Health Research (NIHR)
Grant: NF-SI-0617-10154
NHLBI NIH HHS
Grant: T32 HL092332
Medical Research Council
Grant: MR/T028068/1
NCI NIH HHS
Grant: R01 CA139020
Medical Research Council
Grant: MC_EX_MR/M009203/1
NHGRI NIH HHS
Grant: UM1 HG008898
Medical Research Council
Grant: MC_PC_14089
National Institute for Health Research (NIHR)
Grant: NF-SI-0512-10113
NCI NIH HHS
Grant: R01 CA119215
National Institutes of Health
Grant: 5R01LM013039-02
HealthyMe/MiSalud Smartphone Application: Identifying Mechanisms to Engage African Americans and Hispanics in Personal Health Libraries
National Institutes of Health
Grant: 7R01CA119215-06
Genetic Epidemiology of Glioma International Consortium
National Institutes of Health
Grant: 1R01CA139020-01A1
International Case Control Study of Malignant Glioma
Wellcome Trust
Grant: unidentified
unidentified
National Institutes of Health
Grant: 3U54HG003273-04S1
Genomes and Genetics at the BCM-HGSC
National Institutes of Health
Grant: 5R01CA217105-06
Discovery, Biology and Risk of Inherited Variants in Glioma
National Institutes of Health
Grant: 3UM1HG008898-01S3
Genomic Architecture of Common Disease in Diverse Populations
Wellcome Trust
MeSH Terms
Keywords
Additional file 2 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 2 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 1 of Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Additional file 1 of Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Additional file 2 of Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Additional file 2 of Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Additional file 3 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 3 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 4 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 4 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 5 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 5 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 6 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 6 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 8 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 8 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 9 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 9 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 7 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model
Additional file 7 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model