Valérie Cormier‐Daire
Hôpital Necker-Enfants Malades
ORCID: 0000-0002-2839-9856Also affiliated with Inserm, Université Paris Cité, Institut des Maladies Génétiques Imagine
Pilot corpus only
This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.
Indexed papers
Why this DataRank?
An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.
Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.
Read the full methodology →Top data-sharing exemplar
The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.
Carlos R. Ferreira, Geert Mortier, Houda Ali, Débora Romeo Bertola, Alistair Calder +16 more
Papers
Driven by 6 papers — median percentile 95. Top paper: “Nosology of genetic skeletal disorders: 2023 revision”.
Carlos R. Ferreira, Geert Mortier, Houda Ali, Débora Romeo Bertola, Alistair Calder +16 more
Valérie Cormier‐Daire, Xian Chen, Angelique W. Whitehurst, Becky Sinnott, Feng Yan +7 more
Phillip C. Aoto, Erik M.F. Machal, Ana Rivera‐Barahona, Patricia Soto‐Bielicka, Daniela Bertinetti +37 more
Kristina Cusmano‐Ozog, Rainer Koenig, Manuel Holtgrewe, Banu Nur, Ercan Mıhçı +16 more
Ramin Dubey, Annie Jen, Ganesh V. Pusapati, Bharti Singal, Evgenia Shishkova +7 more
Hannah McCurry, Amanda Girod, Madeline Hughes, Emma H. Wilcox, Mayher Patel +23 more