₁Marie-Cécile Aubry

This is an abridged 2007 data mining report for Marie-Cécile Aubry. The complete report is available only to the community members. As a guest user you can access the free unabridged reports for this author for the years prior to 2005: 2003, 2004.

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Summary for 2007 [at-glance overview of Marie-Cécile Aubry work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Marie-Cécile Aubry. According to available data, in 2007 Marie-Cécile Aubry published at least 1 articles. This work was completed in collaboration with several authors including Vekemans, Michel and Attié-Bitach, Tania. Several other authors have collaborated with Marie-Cécile Aubry as well. There is no information about the funding or the grants awarded to support this work.

Analysis of the article abstracts and the titles suggests that Marie-Cécile Aubry professional interests are focused around "supporting autosomal recessive", "exclusion fgf10 fgfr2" and "syndrome report cases". These might also be referred to as "matthew-wood syndrome", "fgf10 fgfr2" or "supporting autosomal". Statistical analysis shows that Marie-Cécile Aubry's writing is likely to contains terms "cases", "matthew-wood", "syndrome", "fgf10", "fgfr2" and "supporting".

The majority of Marie-Cécile Aubry articles are affiliated with Assistance Publique - Hôpitaux de Paris, Hôpital Necker - Enfants Malades, Department of Genetics, Embryo-Fetal Pathology Unit, Paris, France. Luckily, one email address is on file.

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Year 2007 Charts [Marie-Cécile Aubry frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Marie-Cécile Aubry publication and funding history for the range of years]

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