Hans‐Hilger Ropers
Reproducibility track record
2
assessed papers
96/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
0
total citations
flag rate:
0%
(0/2)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
—
Funders
—
Frequent co-authors
Georg Rosenberger 2Vera M. Kalscheuer 2Richard J. Sherins 1Reinhard Ullmann 1Gudrun Rappold 1Yasuhide Itokawa 1Friederike K Pientka 1Laurent Villard 1Kirsten Geider 1Cheol Yong Choi 1
Institutions
Max Planck Institute for Molecular Genetics 2Universität Hamburg 2University Medical Center Hamburg-Eppendorf 2Harvard University 1Augusta University 1Massachusetts General Hospital 1
Geography (author institutions)
DE 2US 1IN 1KR 1JP 1TR 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (2)
-
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
2010 L1 No computation
-
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
2010 96/100