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Germline copy number variants and endometrial cancer risk

Human Genetics(2024)10.1007/s00439-024-02707-9Source: DataRank Database

Germline copy number variants and endometrial cancer risk is a research paper published in Human Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 3 times.

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Enrichment:Funding (54 grants)Impact (FWCI 1.16)OA: hybridTopics (60)IDs (PubMed, PMC, OpenAlex)Annotations (4)SDGs (1)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (50)

George A. R. Wiggins ORCID,V. Lau,Joe Dennis ORCID,Andrew N. Shelling ORCID,Michelle Wilson ORCID

Live enrichment

PubMed:39495297 PMC:PMC11576655 OpenAlex:https://openalex.org/W4404024219

Wellcome Trust

Grant: 090532

NCI NIH HHS

Grant: P30 CA015083

NCI NIH HHS

Grant: R01 CA192393

NCI NIH HHS

Grant: U01 CA164920

Health Research Council of New Zealand

Grant: #19/460

National Health and Medical Research Council

Grant: APP177524

National Health and Medical Research Council

Grant: APP1111246

NCI NIH HHS

Grant: R01 CA122443

NCI NIH HHS

Grant: R01 CA177150

European Research Council

Grant: 294576

Genetic and environmental risk factors for common malignant tumours especially breast cancer and melanoma.

National Institute for Health Research (NIHR)

Grant: NIHR203312

NCI NIH HHS

Grant: P50 CA116201

Cancer Research UK

Grant: PPRPGM-Nov20\100002

NCI NIH HHS

Grant: U19 CA148065

NCI NIH HHS

Grant: U19 CA148112

NCI NIH HHS

Grant: R01 CA097396

NCI NIH HHS

Grant: R01 CA140286

NCI NIH HHS

Grant: R35 CA253187

NCI NIH HHS

Grant: UM1 CA164920

NCI NIH HHS

Grant: P50 CA136393

NCI NIH HHS

Grant: R01 CA058598

NCI NIH HHS

Grant: R01 CA116167

NCI NIH HHS

Grant: R01 CA149429

NCI NIH HHS

Grant: R01 CA128931

NCI NIH HHS

Grant: R01 CA176785

Canadian Institutes of Health Research

Grant: unidentified

unidentified

National Health and Medical Research Council (NHMRC)

Grant: 209057

Epidemiology of Chronic Disease, Health Interventions and DNA Studies

National Institutes of Health

Grant: 1R01CA140286-01A1

Risk factors for breast cancer molecular subtypes

National Institutes of Health

Grant: 5R35CA253187-06

Resolving the cancer relevance of predisposition gene mutations

National Institutes of Health

Grant: 3U19CA148112-04S1

Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)

National Institutes of Health

Grant: 5UM1CA164920-03

Breast Cancer Family Registry Cohort

National Institutes of Health

Grant: 5R01CA192393-02

Risk and penetrance of mutations from breast cancer testing panels.

National Institutes of Health

Grant: 5R01CA176785-05

Identifying and validating novel susceptibility genes for breast cancer

National Institutes of Health

Grant: 5F32CA007491-03

EFFECT OF TRANSFORMATION ON REGULATION OF GM3 SYNTHETASE

National Health and Medical Research Council (NHMRC)

Grant: 1031333

Extension of a two-stage genome-wide association study of endometrial cancer: validation of endometrial cancer risk-associated alleles and identification of ‘multiple-cancer’ risk loci

National Institutes of Health

Grant: 5R01CA122443-06

Genetic Variation in the NF-kappaB Pathway and Ovarian Cancer Etiology

National Institutes of Health

Grant: 5R01CA128931-04

Identifying Genes for Mammographic Breast Density

National Institutes of Health

Grant: 5U19CA148065-04

Discovery Expansion and Replication

National Health and Medical Research Council (NHMRC)

Grant: 396414

The Health 2020 Cohort Study (Health 2020)

National Institutes of Health

Grant: 5P50CA116201-08

Career Development (Ingle)

National Institutes of Health

Grant: 1R01CA097396-01A1

A Mayo Cohort Study of Mammographic Breast Density

National Health and Medical Research Council (NHMRC)

Grant: 1074383

Linking lifestyle and molecular biology to inform "Precision Public Health" for major cancers

National Institutes of Health

Grant: 5R01CA149429-05

The Mitochondrial Genome and Ovarian Cancer Risk

National Institutes of Health

Grant: 5P50CA136393-10

Mayo Clinic Ovarian Cancer SPORE

National Institutes of Health

Grant: 1R01CA116167-01A1

BRCA2 missense mutations and breast cancer

National Health and Medical Research Council (NHMRC)

Grant: 1109286

Genetic epidemiology of endometrial cancer: towards understanding aetiology and improving risk prediction.

National Institutes of Health

Grant: 3P30CA015083-37S2

Mayo Comprehensive Cancer Center Grant

National Institutes of Health

Grant: 5R01CA177150-03

Automated Density Measures for Estimating Breast Cancer Risk and Therapy Response

National Health and Medical Research Council (NHMRC)

Grant: 1111246

Finding genetic risk markers for endometrial and other cancers

European Commission

Grant: 633784

Breast CAncer STratification: understanding the determinants of risk and prognosis of molecular subtypes

European Commission

Grant: 634935

Breast Cancer Risk after Diagnostic Gene Sequencing (BRIDGES)

National Institutes of Health

Grant: 5R01CA058598-05

COLLABORATIVE STUDY OF OVARIAN CANCER IN TWO RISK GROUPS

National Health and Medical Research Council (NHMRC)

Grant: 339435

Molecular Epidemiology of Endometrial Cancer

Wellcome Trust

FWCI

1.16

Citation Percentile

0.8%

Citation Trend

2025

2026

hybridLicense: cc-by

journalhttps://link.springer.com/content/pdf/10.1007/s00439-024-02707-9.pdf

publisherhttps://link.springer.com/content/pdf/10.1007/s00439-024-02707-9.pdf

journalhttps://doi.org/10.1007/s00439-024-02707-9

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39495297

repositoryhttps://research-repository.uwa.edu.au/en/publications/a0009253-d23c-4fe1-8d02-47af8bd077f4

Fields of Study

Genomic variations and chromosomal abnormalitiesCancer Genomics and DiagnosticsGenetic factors in colorectal cancer0301 basic medicine03 medical and health sciences

MeSH Terms

Chromosomes, Human, Pair 16FemaleHumansMiddle AgedRisk FactorsCase-Control StudiesEndometrial NeoplasmsGerm-Line MutationGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenome-Wide Association StudyDNA Copy Number Variations

Keywords

Endometrial cancerBiologyCopy-number variationGermlineGeneticsCancerGene duplicationCandidate geneHuman geneticsGermline mutationGeneGenome-wide association studyGene dosageGenomeSingle-nucleotide polymorphismGenotypeMutationEXPRESSIONDNA Copy Number VariationsABCTB InvestigatorsPolymorphism, Single Nucleotide3105 GeneticsRisk FactorsHumansGenetic Predisposition to DiseaseMETAANALYSISGerm-Line MutationOriginal InvestigationGenetics & Heredity0604 GeneticsScience & TechnologyDELETION SYNDROME3215 Reproductive medicineMiddle AgedEndometrial NeoplasmsASSOCIATION ANALYSISCase-Control Studies1114 Paediatrics and Reproductive MedicineFemale1104 Complementary and Alternative MedicineLife Sciences & BiomedicineINTEGRATIONChromosomes, Human, Pair 16

Sustainable Development Goals

SDG 0: Good health and well-being

Germline copy number variants and endometrial cancer risk

FAIR Checklist

Authors (50)

Funding (54 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)