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

Completed2
Terminated3
Other1

Role Distribution

Other Roles6

Activity Timeline

Clinical Trials (6)

NCT04925804Completed
Unraveling Genetics of HypoPhosPhatasia (HPP Genetics)
Hypophosphatasia
StudychairStart date: 2021-06-02
Biomarker for Friedreich's Ataxia (BioFridA)
FRDAFXN GeneHereditary Diseases
StudychairStart date: 2020-07-01
NCT04098198Completed
Biomarkers for Inborn Errors of Metabolism
BiomarkerInborn Errors of Metabolism
StudychairStart date: 2019-08-01
NCT02710383Terminated
Biomarker for Cystic Fibrosis
BreathlessnessChronic Nasal CongestionClubbing Toes+4 more
StudychairStart date: 2018-08-20
NCT02718027Terminated
Biomarker for Alport Syndrome (BioAlport)
Hematuria-Nephropathy-Deafness SyndromeNephritis, Hereditary
StudychairStart date: 2018-08-20
NCT03651245Terminated
European Alpha-Mannosidosis Participant
DeafnessFacial DysmorphismGingival Hypertrophy+3 more
StudychairStart date: 2018-08-20

Research Network

Collaboration Network

1 collaborators·0 connections
Network Legend
KOL
Current Investigator
CO
High-influence Collaborator
CO
Collaborator
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Research Areas & Affiliations

Similar Key Opinion Leaders

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10 similar investigators found

Publications (0)

No publications found for this investigator.

Clinical Trials (6)

Showing 6 of 6 trials

NCT04925804StudyChair

Unraveling Genetics of HypoPhosPhatasia (HPP Genetics)

Hypophosphatasia
Completed
NCT04548921StudyChair

Biomarker for Friedreich's Ataxia (BioFridA)

FRDAFXN GeneHereditary Diseases
Unknown
NCT04098198StudyChair

Biomarkers for Inborn Errors of Metabolism

BiomarkerInborn Errors of Metabolism
Completed
NCT02710383StudyChair

Biomarker for Cystic Fibrosis

BreathlessnessChronic Nasal CongestionClubbing Toes+4 more
Terminated
NCT02718027StudyChair

Biomarker for Alport Syndrome (BioAlport)

Hematuria-Nephropathy-Deafness SyndromeNephritis, Hereditary
Terminated
NCT03651245StudyChair

European Alpha-Mannosidosis Participant

DeafnessFacial DysmorphismGingival Hypertrophy+3 more
Terminated

All 6 trials loaded