Report date: Nov 6,2024
Conflict count: 361874
Publisher: Wiley (Blackwell Publishing)
Title count: 475
Conflict count: 16773


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Created: 2023-10-11 13:53:12
ConfID: 6960727
CauseID: 1592611436
OtherID: 138686763
JT: Clinical Genetics
MD: ,65,1,1,2004,The dichotomy of causation vs consequence in ID
DOI: 10.1111/j..2004.0195a.x(Journal) (6960727-N)
DOI: 10.1111/j..2004.0195b.x(Journal)
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Created: 2023-10-11 13:58:36
ConfID: 6960912
CauseID: 1592613332
OtherID: 138686326
JT: Clinical Genetics
MD: Nasir,63,1,11,2003,Hotspots
DOI: 10.1034/j.1399-0004.2002.6105022.x(Journal) (6960912-N)
DOI: 10.1034/j.1399-0004.2002.610502.x-i3(Journal)
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Created: 2023-10-11 13:58:36
ConfID: 6960913
CauseID: 1592613332
OtherID: 138686326
JT: Clinical Genetics
MD: Nasir,63,1,13,2003,Hotspots
DOI: 10.1034/j.1399-0004.2002.6105023.x(Journal) (6960913-N)
DOI: 10.1034/j.1399-0004.2002.620417.x-i1(Journal)
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Created: 2023-10-15 17:03:42
ConfID: 6961658
CauseID: 1593115137
OtherID: 138685487
JT: Clinical Genetics
MD: Hackam,59,3,152,2001,Silencing the quiet
DOI: 10.1034/j.1399-0004.2001.590302.2.x(Journal) (6961658-N)
DOI: 10.1111/j.1399-0004.2001.590302.2.x(Journal)
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Created: 2023-10-15 17:03:42
ConfID: 6961659
CauseID: 1593115137
OtherID: 138685487
JT: Clinical Genetics
MD: Hackam,59,3,153,2001,A phosphatase mutation implicated in multiple sclerosis
DOI: 10.1034/j.1399-0004.2001.590302.3.x(Journal) (6961659-N)
DOI: 10.1111/j.1399-0004.2001.590302.3.x(Journal)
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Created: 2023-10-16 05:09:20
ConfID: 6961729
CauseID: 1593167425
OtherID: 3141
JT: Clinical Genetics
MD: Lewis,59,6,389,2001,Hammerhead ribozyme as a therapeutic agent for hyperlipidemia: Production of truncated apolipoprotein B and hypolipidemic effects in a dyslipidemia murine model
DOI: 10.1034/j.1399-0004.2001.590602.3.x(Journal) (6961729-N)
DOI: 10.1111/j.1399-0004.2001.590602.3.x(Journal)
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Created: 2023-10-16 00:59:14
ConfID: 6962648
CauseID: 1593143652
OtherID: 3148
JT: Clinical Genetics
MD: Devon,60,2,99,2001,HotSpots
DOI: 10.1034/j.1399-0004.2001.600202.1.x(Journal) (6962648-N)
DOI: 10.1034/j.1399-0004.2001.6002021.x(Journal)
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Created: 2023-10-16 00:59:14
ConfID: 6962649
CauseID: 1593143652
OtherID: 3148
JT: Clinical Genetics
MD: Devon,60,2,100,2001,HotSpots
DOI: 10.1034/j.1399-0004.2001.600202.2.x(Journal) (6962649-N)
DOI: 10.1034/j.1399-0004.2001.6002022.x(Journal)
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Created: 2023-10-16 00:59:14
ConfID: 6962647
CauseID: 1593143652
OtherID: 3148
JT: Clinical Genetics
MD: Devon,60,2,102,2001,HotSpots
DOI: 10.1034/j.1399-0004.2001.600202.3.x(Journal) (6962647-N)
DOI: 10.1034/j.1399-0004.2001.6002023.x(Journal)
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Created: 2020-09-09 07:01:21
ConfID: 5657722
CauseID: 1477374665
OtherID: 1477370995
JT: Clinical Genetics
MD: ,58,2,156,2000,Errata
DOI: 10.1034/j.1399-0004.2000.580213.x(Journal) (5657722-N)
DOI: 10.1034/j.1399-0004.2000.580214.x(Journal)