₂₆Alexis Brice

Summary for 2009 [at-glance overview of Alexis Brice work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Alexis Brice. According to available data, in 2009 Alexis Brice published at least 26 articles. This work was completed in collaboration with several authors including Dürr, Alexandra and Stevanin, Giovanni. Many other authors have collaborated with Alexis Brice as well. There is no information about the funding or the grants awarded to support this work.

Alexis Brice is a key opinion leader in numerous areas including DNA Mutational Analysis, Ubiquitin-Protein Ligases, Spastic Paraplegia, Hereditary, Point Mutation, Parkinsonian Disorders. This author's highest rank is 1 when compared to all other authors using the keyword Spastic Paraplegia, Hereditary. Analysis of the article abstracts and the titles suggests that Alexis Brice professional interests are focused around "hereditary spastic paraplegia", "parkinson disease pd" and "alpha-synuclein gene snca". These might also be referred to as "parkinson disease", "spastic paraplegia" or "hereditary spastic". Statistical analysis shows that Alexis Brice's writing is likely to contains terms "mutations", "gene", "patients", "disease", "parkin" and "association".

The affiliations of Alexis Brice vary, with INSERM, UMR_S679, Paris, France being the most prominent. Luckily, several email addresses are on file.

ENFRESRU

make correctionleave commentask question

Images [images we found on the Internet for Alexis Brice]

loading...

Do you know Alexis Brice who matches the profile above? Click the photo and let us know!

Alternative names (1) [other authors with names similar to Alexis Brice]

• ₁₃₈Brice, A