Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
2019 · Genetics in Medicine · 615 citations
https://doi.org/10.1038/s41436-019-0596-9
D
Deepak Vangala
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Deepak Vangala is an academic researcher from Universitätsklinikum Knappschaftskrankenhaus Bochum. The author has contributed to research in topics: Genetic factors in colorectal cancer & Cancer Genomics and Diagnostics & Colorectal Cancer Screening and Detection. The author has an h-index of 19, co-authored 76 publications.
ORCID: 0000-0002-4175-5683Papers by this author
worksVariation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
2021 · The Lancet Oncology · 112 citations
https://doi.org/10.1016/s1470-2045(21)00189-3
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
2023 · EClinicalMedicine · 97 citations
https://doi.org/10.1016/j.eclinm.2023.101909
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
2019 · Hereditary Cancer in Clinical Practice · 62 citations
https://doi.org/10.1186/s13053-019-0106-8
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
2022 · Hereditary Cancer in Clinical Practice · 54 citations
https://doi.org/10.1186/s13053-022-00241-1
Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study
2020 · BMC Cancer · 49 citations
https://doi.org/10.1186/s12885-020-06926-x
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