Automated Author ProfileRiemann, Burkhard
Riemann, Burkhard
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author'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: 11.5 (sum of 17 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Supplementary to the publication mentioned above
Authors
- Hescheler, Daniel A. ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane Josephine ;
- Alakus, Hakan ;
- Chiapponi, Costanza
Supplementary to the publication mentioned above
Authors
- Hescheler, Daniel A. ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane Josephine ;
- Alakus, Hakan ;
- Chiapponi, Costanza
Supplementary to the publication mentioned above
Authors
- Hescheler, Daniel A. ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane Josephine ;
- Alakus, Hakan ;
- Chiapponi, Costanza
Supplementary to the publication mentioned above
Authors
- Hescheler, Daniel A. ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane Josephine ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome. Finally, 129 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 128 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action. Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB were mined.
Authors
- Hescheler, Daniel ;
- Riemann, Burkhard ;
- Hartmann, Milan ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, first all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome (database query 09/2021). Unspecific drugs such as Tretinoin or Cabazitaxel were excluded (Supplementary Table 1). Finally, 155 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 136 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action (Supplementary Table 1). Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB (Supplementary Table 2) were mined.
Authors
- Hescheler, Daniel ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, first all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome (database query 09/2021). Unspecific drugs such as Tretinoin or Cabazitaxel were excluded (Supplementary Table 1(11)). Finally, 155 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 136 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action (Supplementary Table 1). Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB (Supplementary Table 2) were mined. @font-face {font-family:"Cambria Math"; panose-1:2 4 5 3 5 4 6 3 2 4; mso-font-charset:0; mso-generic-font-family:roman; mso-font-pitch:variable; mso-font-signature:-536870145 1107305727 0 0 415 0;}@font-face {font-family:Calibri; panose-1:2 15 5 2 2 2 4 3 2 4; mso-font-charset:0; mso-generic-font-family:swiss; mso-font-pitch:variable; mso-font-signature:-536859905 -1073732485 9 0 511 0;}p.MsoNormal, li.MsoNormal, div.MsoNormal {mso-style-unhide:no; mso-style-qformat:yes; mso-style-parent:""; margin-top:0cm; margin-right:0cm; margin-bottom:10.0pt; margin-left:0cm; line-height:115%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri",sans-serif; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:Calibri; mso-fareast-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi; mso-ansi-language:DE; mso-fareast-language:EN-US;}.MsoChpDefault {mso-style-type:export-only; mso-default-props:yes; font-size:11.0pt; mso-ansi-font-size:11.0pt; mso-bidi-font-size:11.0pt; font-family:"Calibri",sans-serif; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:Calibri; mso-fareast-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi; mso-ansi-language:DE; mso-fareast-language:EN-US;}.MsoPapDefault {mso-style-type:export-only; margin-bottom:10.0pt; line-height:115%;}div.WordSection1 {page:WordSection1;}
Authors
- Hescheler, Daniel ;
- Riemann, Burkhard ;
- Hartmann, Milan ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, first all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome (database query 09/2021). Unspecific drugs such as Tretinoin or Cabazitaxel were excluded (Supplementary Table 1). Finally, 155 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 136 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action (Supplementary Table 1). Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB (Supplementary Table 2) were mined.
Authors
- Hescheler, Daniel ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, first all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome (database query 09/2021). Unspecific drugs such as Tretinoin or Cabazitaxel were excluded (Supplementary Table 1). Finally, 155 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 136 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action (Supplementary Table 1). Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB (Supplementary Table 2) were mined.
Authors
- Hescheler, Daniel ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza
In order to find new therapeutic options in anaplastic thyroid cancer, first all FDA-approved drugs for any cancer therapy were identified by searching the databases of National Cancer Institute and MyCancerGenome (database query 09/2021). Unspecific drugs such as Tretinoin or Cabazitaxel were excluded (Supplementary Table 1). Finally, 155 FDA/EMA-approved drugs targeting cancer genetic alterations were included. These drug lists were linked to 136 genes by querying databases of MD Anderson Cancer Center and Drugbank, which encode the potential sites of binding and action (Supplementary Table 1). Moreover, special attention was given to specific genetic alterations resulting in either drug sensitivity or drug resistance of targeted therapy. Hereby the expert-crowdsourced, publication-based databases from MyCancerGenome, CIViC, TARGET and OncoKB (Supplementary Table 2) were mined.
Authors
- Hescheler, Daniel ;
- Hartmann, Milan ;
- Riemann, Burkhard ;
- Michel, Maximilian ;
- Bruns, Christiane ;
- Alakus, Hakan ;
- Chiapponi, Costanza