Research Impact

h-index

N/A

Research impact score

Publications

0

Total publications

Trial Results

0

Published trial results

Citations

0

Total citations

Analytics

Trial Phases

No phase data

Trial Status

Completed4
Terminated1

Role Distribution

Principal Investigator5
PI Rate100%

Activity Timeline

Clinical Trials (5)

NCT02124109Completed
The Genetic Basis of Acquired Heart Disease in Africa
Acquired Heart DiseaseEndomyocardial FibrosisRheumatic Fever+1 more
PrincipalinvestigatorStart date: 2014-04-03
NCT01629095Terminated
Genetic Studies of Non-Alcoholic Fatty Liver Disease
Liver CirrhosisNon-Alcoholic Fatty Liver DiseaseNon-Alcoholic Steato-Hepatitis
PrincipalinvestigatorStart date: 2013-04-23
NCT01294345Completed
Personalized Genomic Research
Birth DefectsGenetic DiseaseGenetic Linkage+2 more
PrincipalinvestigatorStart date: 2011-01-24
NCT00106977Completed
Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis)
CraniosynostosisMuenke Syndrome
PrincipalinvestigatorStart date: 2005-03-31
NCT00088426Completed
Clinical and Genetic Studies on Holoprosencephaly
Brain DisordersDevelopmental Delay DisordersHoloprosencephaly+1 more
PrincipalinvestigatorStart date: 2004-01-23

Research Network

Collaboration Network

1 collaborators·0 connections
Network Legend
KOL
Current Investigator
CO
High-influence Collaborator
CO
Collaborator
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Publications (0)

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Clinical Trials (5)

Showing 5 of 5 trials

NCT02124109PrincipalInvestigator

The Genetic Basis of Acquired Heart Disease in Africa

Acquired Heart DiseaseEndomyocardial FibrosisRheumatic Fever+1 more
Completed
NCT01629095PrincipalInvestigator

Genetic Studies of Non-Alcoholic Fatty Liver Disease

Liver CirrhosisNon-Alcoholic Fatty Liver DiseaseNon-Alcoholic Steato-Hepatitis
Terminated
NCT01294345PrincipalInvestigator

Personalized Genomic Research

Birth DefectsGenetic DiseaseGenetic Linkage+2 more
Completed
NCT00106977PrincipalInvestigator

Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis)

CraniosynostosisMuenke Syndrome
Completed
NCT00088426PrincipalInvestigator

Clinical and Genetic Studies on Holoprosencephaly

Brain DisordersDevelopmental Delay DisordersHoloprosencephaly+1 more
Completed

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