Automated Author Profile

Riemann, Burkhard

Current S-Index

11.5

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.7

Average Dataset Index per dataset

Total Datasets

17

Total datasets for this author

Average FAIR Score

22.2%

Average FAIR Score per dataset

Total Citations

10

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Targeted therapy for adrenocortical carcinoma: a genomic-based search for available and emerging options.

Supplementary to the publication mentioned above

Authors

  • Hescheler, Daniel A. ;
  • Hartmann, Milan ;
  • Riemann, Burkhard ;
  • Michel, Maximilian ;
  • Bruns, Christiane Josephine ;
  • Alakus, Hakan ;
  • Chiapponi, Costanza
1 Citation0 Mentions85% FAIR2.2 Dataset Index
10.6084/m9.figshare.19531561January 2022

Targeted therapy for adrenocortical carcinoma: a genomic-based search for available and emerging options.

Supplementary to the publication mentioned above

Authors

  • Hescheler, Daniel A. ;
  • Hartmann, Milan ;
  • Riemann, Burkhard ;
  • Michel, Maximilian ;
  • Bruns, Christiane Josephine ;
  • Alakus, Hakan ;
  • Chiapponi, Costanza
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.19531561.v3January 2022

Targeted therapy for adrenocortical carcinoma: a genomic-based search for available and emerging options.

Supplementary to the publication mentioned above

Authors

  • Hescheler, Daniel A. ;
  • Hartmann, Milan ;
  • Riemann, Burkhard ;
  • Michel, Maximilian ;
  • Bruns, Christiane Josephine ;
  • Alakus, Hakan ;
  • Chiapponi, Costanza
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.19531561.v2January 2022

Targeted therapy for adrenocortical carcinoma: a genomic-based search for available and emerging options.

Supplementary to the publication mentioned above

Authors

  • Hescheler, Daniel A. ;
  • Hartmann, Milan ;
  • Riemann, Burkhard ;
  • Michel, Maximilian ;
  • Bruns, Christiane Josephine ;
  • Alakus, Hakan ;
  • Chiapponi, Costanza
0 Citations0 Mentions85% FAIR1.8 Dataset Index
10.6084/m9.figshare.19531561.v1January 2022

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.14937117.v1January 2021

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
2 Citations0 Mentions13% FAIR1.1 Dataset Index
10.6084/m9.figshare.14937117January 2021

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.14937117.v2January 2021

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.14937117.v3January 2021

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.14937117.v4January 2021

Limitations and Options for Targeted Therapy of Anaplastic Thyroid Cancer: a Novel genome-based Approach. Supplementary

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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.14937117.v5January 2021