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Combined display of all available logs of Compendium of Cancer Genome Aberrations. You can narrow down the view by selecting a log type, the username (case-sensitive), or the affected page (also case-sensitive).
(newest | oldest) View (newer 50 | older 50) (20 | 50 | 100 | 250 | 500)- 13:51, 25 February 2024 Jennelleh talk contribs moved page Diffuse Midline Glioma, H3 K27-Altered to CNS5:Diffuse midline glioma, H3 K27-altered without leaving a redirect (Move to CNS5)
- 13:50, 25 February 2024 Jennelleh talk contribs moved page Diffuse Astrocytoma, MYB- or MYBL1-Altered to CNS5:Diffuse astrocytoma, MYB- or MYBL1-altered without leaving a redirect (Move to CNS5)
- 13:50, 25 February 2024 Jennelleh talk contribs moved page Glioblastoma, IDH-Wildtype to CNS5:Glioblastoma, IDH-wildtype without leaving a redirect (Move to CNS5)
- 13:49, 25 February 2024 Jennelleh talk contribs moved page Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted to CNS5:Oligodendroglioma, IDH-mutant and 1p/19q-codeleted without leaving a redirect (Move to CNS5)
- 13:48, 25 February 2024 Jennelleh talk contribs moved page Astrocytoma, IDH-Mutant to CNS5:Astrocytoma, IDH-mutant without leaving a redirect (Move to CNS5)
- 13:44, 25 February 2024 Jennelleh talk contribs moved page DICER1-Related Tumour Predisposition Syndrome (DICER1) to GTS5:DICER1-related tumour predisposition syndrome (DICER1) without leaving a redirect (Move to GTS5)
- 13:43, 25 February 2024 Jennelleh talk contribs moved page CHEK2-Related Hereditary (Breast) Cancer Predisposition Syndrome (CHEK2) to GTS5:CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2) without leaving a redirect (Move to GTS5)
- 13:42, 25 February 2024 Jennelleh talk contribs moved page Ataxia-Telangiectasia Syndrome (ATM) to GTS5:Ataxia-telangiectasia syndrome (ATM) without leaving a redirect (Move to GTS5)
- 13:42, 25 February 2024 Jennelleh talk contribs moved page PALB2-Related Cancer Predisposition Syndrome (PALB2) to GTS5:PALB2-related cancer predisposition syndrome (PALB2) without leaving a redirect (Move to GTS5)
- 13:41, 25 February 2024 Jennelleh talk contribs moved page BRCA-Related Cancer Predisposition Syndrome (BRCA1, BRCA2) to GTS5:BRCA-related cancer predisposition syndrome (BRCA1, BRCA2) without leaving a redirect (Move to GTS5)
- 13:41, 25 February 2024 Jennelleh talk contribs moved page Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome (MLH1, PMS2, MSH2, MSH6) to GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) without leaving a redirect (Move to GTS5)
- 13:39, 25 February 2024 Jennelleh talk contribs moved page Li-Fraumeni Syndrome (TP53) to GTS5:Li-Fraumeni syndrome (TP53) without leaving a redirect (Move to GTS5)
- 13:38, 25 February 2024 Jennelleh talk contribs moved page Hereditary Gastric and Breast Cancer Syndrome (CDH1, CTNNA1) to GTS5:Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1) without leaving a redirect (Move to GTS5)
- 13:37, 25 February 2024 Jennelleh talk contribs moved page Peutz-Jeghers Syndrome (STK11) to GTS5:Peutz-Jeghers syndrome (STK11) without leaving a redirect (Move to GTS5)
- 13:34, 25 February 2024 Jennelleh talk contribs moved page Familial Adenomatous Polyposis (APC) to GTS5:Familial adenomatous polyposis (APC) without leaving a redirect (Move to GTS5)
- 13:33, 25 February 2024 Jennelleh talk contribs moved page Neurofibromatosis Type 1 (NF1) to GTS5:Neurofibromatosis type 1 (NF1) without leaving a redirect (Moved to GTS5 version)
- 11:50, 25 February 2024 Jennelleh talk contribs moved page STBT:Ewing sarcoma to STBT5:Ewing sarcoma without leaving a redirect
- 11:49, 25 February 2024 Jennelleh talk contribs deleted page Ewing Sarcoma (Moved to STBT5:Ewing sarcoma)
- 11:49, 25 February 2024 Jennelleh talk contribs created page STBT:Ewing sarcoma (Created page with "==Primary Author(s)*== Put your text here ==Cancer Category/Type== Put your text here ==Cancer Sub-Classification / Subtype== Put your text here ==Definition / Description of...")
- 11:47, 25 February 2024 Jennelleh talk contribs deleted page NTRK-Rearranged Spindle Cell Neoplasm (Moved to STBT5:NTRK-rearranged spindle cell neoplasm (emerging))
- 11:47, 25 February 2024 Jennelleh talk contribs created page STBT5:NTRK-rearranged spindle cell neoplasm (emerging) (Created page with "==Primary Author(s)*== James Solomon, MD, PhD, Weill Cornell Medicine ==Cancer Category/Type== Put your text here ==Cancer Sub-Classification / Subtype== Put your text here ==...") Tag: Visual edit
- 13:09, 23 February 2024 User account Reba.Daniel talk contribs was created by Jennelleh talk contribs (New user)
- 11:18, 23 February 2024 Jennelleh talk contribs created page STBT5:Solitary fibrous tumour (Created page with "<span style="color:#0070C0"> (''General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease type. Use [https://www...")
- 10:28, 23 February 2024 Jennelleh talk contribs uploaded a new version of File:Disease or Entity-Specific Template Word Version with Instructions.docx
- 13:19, 22 February 2024 Bailey.Glen talk contribs created page HAEM5:Edittest12 (Created page with "test") Tag: Visual edit
- 13:17, 22 February 2024 Jennelleh talk contribs created page HAEM5:Edittesttest (Created page with "test") Tag: Visual edit
- 13:16, 22 February 2024 Bailey.Glen talk contribs deleted page HAEM5:Edittest (content was: "test more testing <br />", and the only contributor was "TestEditor" (talk))
- 13:15, 22 February 2024 Bailey.Glen talk contribs deleted page Edittest (content was: "test more testing <br />", and the only contributor was "TestEditor" (talk))
- 13:13, 22 February 2024 TestEditor talk contribs created page Edittest (Created page with "test") Tag: Visual edit
- 13:12, 22 February 2024 TestEditor talk contribs created page HAEM5:Edittest (Created page with "test") Tag: Visual edit
- 06:32, 22 February 2024 Dan talk contribs created page HAEM5:Test (Created page with "test")
- 14:20, 21 February 2024 User account TestEditor talk contribs was created by Bailey.Glen talk contribs
- 10:04, 17 February 2024 User account Molly.Walkenhorst talk contribs was created by Jennelleh talk contribs (New user)
- 15:26, 9 February 2024 User account Constance.Albarracin talk contribs was created by Jennelleh talk contribs (New user)
- 11:16, 9 February 2024 User account LiaoJun talk contribs was created by Dan talk contribs and password was sent by email
- 13:17, 1 February 2024 Jennelleh talk contribs created page Disease-Specific Template with Instructions (Created page with "<span style="color:#0070C0">(''General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease type. Use [https://www....") Tag: Visual edit
- 10:47, 29 January 2024 Jennelleh talk contribs moved page Cowden Syndrome to Cowden syndrome without leaving a redirect (Fix capitalization in title)
- 11:40, 26 January 2024 Bailey.Glen talk contribs created page User:Bailey.Glen (Created page with "Plasma_cell_neoplasms_with_associated_paraneoplastic_syndrome")
- 14:25, 30 December 2023 Jennelleh talk contribs created page Cowden Syndrome (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...") Tag: Visual edit
- 14:19, 30 December 2023 Jennelleh talk contribs created page Peutz-Jeghers Syndrome (STK11) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...")
- 14:16, 30 December 2023 Jennelleh talk contribs created page PALB2-Related Cancer Predisposition Syndrome (PALB2) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...")
- 14:13, 30 December 2023 Jennelleh talk contribs created page Hereditary Gastric and Breast Cancer Syndrome (CDH1, CTNNA1) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...")
- 14:09, 30 December 2023 Jennelleh talk contribs created page CHEK2-Related Hereditary (Breast) Cancer Predisposition Syndrome (CHEK2) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...")
- 14:05, 30 December 2023 Jennelleh talk contribs created page Li-Fraumeni Syndrome (TP53) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...") Tag: Visual edit
- 13:59, 30 December 2023 Jennelleh talk contribs created page Ataxia-Telangiectasia Syndrome (ATM) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...") Tag: Visual edit
- 13:49, 30 December 2023 Jennelleh talk contribs created page BRCA-Related Cancer Predisposition Syndrome (BRCA1, BRCA2) (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...") Tag: Visual edit
- 13:18, 30 December 2023 Jennelleh talk contribs created page Polygenic Component of Breast Cancer Susceptibility (Created page with "{{Under Construction}}<span style="color:#0070C0">(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease typ...") Tag: Visual edit
- 10:04, 25 December 2023 Jennelleh talk contribs created page Old (not for use) Volunteer Assignments and Opportunities (Created page with "Welcome! *For assignments, please see the "Author" column below. If no name is present, volunteer to create content! *We will be creating content for all entities with genet...") Tag: Visual edit
- 22:40, 24 December 2023 Jennelleh talk contribs created page DIG5:Volunteer Assignments and Opportunities (Created page with "Welcome! For assignments, please see the "Author" column below (highlighted blue). If empty (no name is present), please volunteer to create content for that disease! To vo...") Tag: Visual edit
- 22:39, 24 December 2023 Jennelleh talk contribs created page THOR5:Volunteer Assignments and Opportunities (Created page with "Welcome! For assignments, please see the "Author" column below (highlighted blue). If empty (no name is present), please volunteer to create content for that disease! To vo...") Tag: Visual edit