Automated Organization ProfileInstitute of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark
Institute of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets in this organization
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the organization's datasets
Total Mentions
Total mentions of the organization's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 3.6 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Supplementary table 1. Mean expression levels of genes in the IGF family and common proliferation markers across five time points before and up to 36 h after ovulation trigger.These supplementary data belong to the manuscript entitled "Dynamics of IGF signalling during the ovulatory peak in women undergoing ovarian stimulation" published in The Journal of Clinical Endocrinology & Metabolism (JCEM) (04 March 2024). This manuscript describes the expression of the insulin-like growth factor (IGF) system during the ovulatory peak in women and suggests that downregulation of IGF signalling is crucial for the sudden cessation in granulosa cell proliferation and onset of differentiation during this critical time course.This table shows data extracted from a microarray analysis of key IGF family members and common proliferation markers in granulosa cells collected from five different time-points (0 h (n =17), 12 h (n =7), 17 h (n =6), 32 h (n =9) and 36 h (n=44) after ovulation trigger), during the ovulatory peak from fifty women receiving fertility treatment at the Fertility Clinic, Department of Gynaecology and Obstetrics, Holbæk Hospital, Denmark. Differential expression with a false discovery rate (FDR)<0.01 combined with a gene expression fold change >2 was considered significant. For further details please read the full manuscript published at JCEM following the DOI: https://doi.org/10.1210/clinem/dgae132.
Authors
- Bøtkjær, Jane Alrø ;
- Poulsen, Liv la Cour ;
- Noer, Pernille Rimmer ;
- Grøndahl, Marie Louise ;
- Mikkelsen, Anne Lis ;
- Franks, Stephen ;
- Hardy, Kate ;
- Oxvig, Claus ;
- Andersen, Claus Yding
Supplementary table 1. Mean expression levels of genes in the IGF family and common proliferation markers across five time points before and up to 36 h after ovulation trigger.These supplementary data belong to the manuscript entitled "Dynamics of IGF signalling during the ovulatory peak in women undergoing ovarian stimulation" published in The Journal of Clinical Endocrinology & Metabolism (JCEM) (04 March 2024). This manuscript describes the expression of the insulin-like growth factor (IGF) system during the ovulatory peak in women and suggests that downregulation of IGF signalling is crucial for the sudden cessation in granulosa cell proliferation and onset of differentiation during this critical time course.This table shows data extracted from a microarray analysis of key IGF family members and common proliferation markers in granulosa cells collected from five different time-points (0 h (n =17), 12 h (n =7), 17 h (n =6), 32 h (n =9) and 36 h (n=44) after ovulation trigger), during the ovulatory peak from fifty women receiving fertility treatment at the Fertility Clinic, Department of Gynaecology and Obstetrics, Holbæk Hospital, Denmark. Differential expression with a false discovery rate (FDR)<0.01 combined with a gene expression fold change >2 was considered significant. For further details please read the full manuscript published at JCEM following the DOI: https://doi.org/10.1210/clinem/dgae132.
Authors
- Bøtkjær, Jane Alrø ;
- Poulsen, Liv la Cour ;
- Noer, Pernille Rimmer ;
- Grøndahl, Marie Louise ;
- Mikkelsen, Anne Lis ;
- Franks, Stephen ;
- Hardy, Kate ;
- Oxvig, Claus ;
- Andersen, Claus Yding