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• 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)
• 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)
• 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 !)
• 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)
• 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 !)
• 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 !)
• 09:38, 26 July 2023 Homo sapiens:TAR syndrome‎ (Ontology Term : 'disease pathway' added !)
• 09:37, 26 July 2023 Homo sapiens:TAR syndrome‎ (Modified description)
• 09:30, 26 July 2023 Homo sapiens:TAR syndrome‎ (corrections and updates (done))
• 07:47, 26 July 2023 Homo sapiens:TAR syndrome‎ (update in progress)
• 06:54, 26 July 2023 Homo sapiens:TAR syndrome‎ (update in progress)
• 13:11, 24 July 2023 Homo sapiens:TAR syndrome‎ (update)
• 12:36, 24 July 2023 Homo sapiens:TAR syndrome‎ (upgrade)
• 12:00, 24 July 2023 Homo sapiens:TAR syndrome‎ (upgrade)
• 10:08, 24 July 2023 Homo sapiens:1p36 copy number variation syndrome‎ (Modified description)
• 10:06, 24 July 2023 Homo sapiens:1p36 copy number variation syndrome‎ (update and corrections)
• 13:17, 5 June 2023 Homo sapiens:NF1 copy number variation syndrome ‎ (Ontology Term : 'disease pathway' added !)
• 13:17, 5 June 2023 Homo sapiens:NF1 copy number variation syndrome ‎ (Ontology Term : 'neurofibromatosis 1' added !)
• 09:04, 30 May 2023 Homo sapiens:1p36 copy number variation syndrome‎ (Converted interaction to graphical line)
• 08:59, 30 May 2023 Homo sapiens:1p36 copy number variation syndrome‎ (graphical update)
• 08:38, 30 May 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome‎ (Graphical update)
• 11:40, 4 May 2023 RareDisease/News‎ (top)
• 15:21, 6 April 2023 Homo sapiens:1p36 copy number variation syndrome‎ (Modified title)
• 15:19, 6 April 2023 Homo sapiens:11p11.2 copy number variation syndrome ‎ (Ontology Term : 'disease pathway' added !)
• 15:18, 6 April 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 15:17, 6 April 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome‎ (Modified title)

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