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Raoul C. M. Hennekam | ORCID 0000-0002-6745-1522 | ResearchHub

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Raoul C. M. Hennekam

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Researcher profile

Raoul C. M. Hennekam

ResearchHub researcher

University of Amsterdam ORCID

1

Publications

0

Citations

0

H-index

0

Recent H-index

2

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

Research identity

Research areas

Not available

Education

Not available

Research

Research outputs

Public works are drawn from admitted ResearchHub scholarly records.

Publications

Selected public works

Search public worksYearWork typeSort works

1 of 1 listed works

Exports contain available public metadata for the works currently shown.

Singleton-Merten Syndrome: a rare autoimmune disorder caused by a specific IFIH1 mutation

Molecular and Cellular Pediatrics · 2015 · journal-article

0 citations · 2 reads

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No public projects are available.

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Questions

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Not available

Impact

Measured impact

Publications: 1
Citations: 0
H-index: 0
Recent H-index: 0
Reads: 2

H-index follows the standard Hirsch definition: the largest h for which h publications each have at least h citations. Recent H-index applies the same calculation to the five most recent complete calendar years (2021-2025); the current year is excluded while incomplete.

Affiliations

Institutions

UUniversity of AmsterdamAffiliation

Identifiers

Scholarly links

ORCID: 0000-0002-6745-1522

Network

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0 followers

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Activity

Recent activity

Not available

Recognition

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Not available