ResearcherUniversity of Southern DenmarkNo recent work listed
Maiken Thyregod Jøergensen
Matched on OpenAlex author ID A5112315443. Sources: OpenAlex.
Their work
- Papers
- 7 (first author 1, last author 5)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 6
2013: 1 paper · 2014: none · 2015: none · 2016: 1 paper · 2017: none · 2018: none · 2019: none · 2020: 1 paper · 2021: 3 papers · 2022: 1 paper
Papers 7
- Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. Last author DOI 10.1111/ahg.12464↗
- Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. Last author DOI 10.1080/00365521.2021.1937697↗
- Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients. Last author DOI 10.1111/cge.14038↗
- Heritability of familial pancreatic cancer in a Danish national family cohort Last author DOI 10.21203/rs.3.rs-141845/v1↗
- Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. Last author DOI 10.1089/pancan.2020.0007↗
- Is screening for pancreatic cancer in high-risk groups cost-effective? - Experience from a Danish national screening program. Co-author DOI 10.1016/j.pan.2016.03.013↗
- Cell-free plasma microRNA in pancreatic ductal adenocarcinoma and disease controls. First author DOI 10.1097/mpa.0b013e318296bb34↗
Closest collaborators
The 6 strongest of 6 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Ove B. Schaffalitzky de Muckadell · 7 shared papers, 2013–2022 · strength 0.92
- Paper Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. DOI 10.1089/pancan.2020.0007↗
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Ming Tan · 5 shared papers, 2020–2022 · strength 0.80
- Paper Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. DOI 10.1089/pancan.2020.0007↗
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Michael Bau Mortensen · 5 shared papers, 2016–2022 · strength 0.68
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Paper Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of… DOI 10.1111/cge.14038↗
- Sönke Detlefsen · 4 shared papers, 2021–2022 · strength 0.61
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Paper Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of… DOI 10.1111/cge.14038↗
- Niels H. H. Heegaard · 1 shared paper, 2013 · strength 0.05
- Anting Liu Carlsen · 1 shared paper, 2013 · strength 0.05
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.