User contributions
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- 16:07, 2 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 15:03, 2 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (corrections in progress)
- 14:41, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (Ontology Term : 'disease pathway' added !)
- 14:40, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (Modified description)
- 14:35, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (work in progress)
- 12:16, 2 August 2023 N Homo sapiens:7q11.23 distal copy number variation (New pathway)
- 11:35, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'Down syndrome' added !) (top)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'melanocortin system pathway' added !)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'leptin system pathway' added !)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'disease pathway' added !)
- 11:32, 2 August 2023 N Homo sapiens:6q16 copy number variation (New pathway)
- 10:48, 2 August 2023 Homo sapiens:5q35 copy number variation (Ontology Term : 'disease pathway' added !)
- 10:48, 2 August 2023 Homo sapiens:5q35 copy number variation (Ontology Term : 'Sotos syndrome' added !)
- 10:47, 2 August 2023 Homo sapiens:5q35 copy number variation (Modified description)
- 10:42, 2 August 2023 Homo sapiens:5q35 copy number variation (correction)
- 10:00, 2 August 2023 Homo sapiens:5q35 copy number variation (correction and update in progress)
- 14:01, 1 August 2023 Homo sapiens:5q35 copy number variation (update and correction in progress)
- 10:24, 1 August 2023 Homo sapiens:5q35 copy number variation (correcton and update in progress)
- 16:37, 27 July 2023 Homo sapiens:Smith-Magenis and Potocki-Lupski syndrome copy number variation (correction and update in progress)
- 16:17, 27 July 2023 Homo sapiens:Smith-Magenis and Potocki-Lupski syndrome copy number variation (Ontology Term : 'disease pathway' added !)
- 13:02, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 12:20, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 11:33, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 11:25, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 10:18, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 09:49, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 09:11, 27 July 2023 Homo sapiens:4p16.3 copy number variation (Modified description)
- 09:06, 27 July 2023 Homo sapiens:4p16.3 copy number variation (Ontology Term : 'disease pathway' added !)
- 09:04, 27 July 2023 Homo sapiens:4p16.3 copy number variation (correction and updates)
- 08:45, 27 July 2023 Homo sapiens:4p16.3 copy number variation (correction and updates)
- 15:58, 26 July 2023 Homo sapiens:2q37 copy number variation syndrome (Modified description) (top)
- 15:56, 26 July 2023 Homo sapiens:2q37 copy number variation syndrome (Added information on chromosomal location found in the Kirov et al. 2014 paper)
- 15:48, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (Modified description) (top)
- 15:47, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (corrected legend position)
- 15:46, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (correcting starting positions according to Kirov et al 2014 in addition to Gimelli et al.)
- 15:18, 26 July 2023 Homo sapiens:NPHP1 deletion syndrome (Ontology Term : 'disease pathway' added !) (top)
- 15:18, 26 July 2023 Homo sapiens:NPHP1 deletion syndrome (Ontology Term : 'nephronophthisis 3' added !)
- 15:16, 26 July 2023 N Homo sapiens:NPHP1 deletion syndrome (New pathway)
- 14:44, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (Update to GRCh37 numbers) (top)
- 14:38, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (Reverted to version '12:56, 7 May 2022' by <a href="/index.php/User:Fehrhart" title="User:Fehrhart">Fehrhart</a>)
- 11:00, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (correction of chr numbers)
- 10:48, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (update to GRCh37)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'paranoid schizophrenia' added !) (top)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'autism spectrum disorder' added !)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'schizophrenia pathway' added !)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'disease pathway' added !)
- 10:13, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Modified description)
- 10:12, 26 July 2023 N Homo sapiens:NRXN1 deletion syndrome (New pathway)
- 09:38, 26 July 2023 Homo sapiens:TAR syndrome (Ontology Term : 'Disease' added !) (top)
- 09:38, 26 July 2023 Homo sapiens:TAR syndrome (Ontology Term : 'disease pathway' added !)
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