₂₂Jean-Pierre Fryns

This is an abridged 2007 data mining report for Jean-Pierre Fryns. 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: 2002, 2003, 2004.

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Summary for 2007 [at-glance overview of Jean-Pierre Fryns work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Jean-Pierre Fryns. According to available data, in 2007 Jean-Pierre Fryns published at least 22 articles. This work was completed in collaboration with several authors including Devriendt, Koen and Van Esch, Hilde. Many other authors have collaborated with Jean-Pierre Fryns as well. There is no information about the funding or the grants awarded to support this work.

Jean-Pierre Fryns is a key opinion leader on Phenotype, Mental Retardation, Abnormalities, Multiple, Chromosomes, Human, X. This author's highest rank is 1 when compared to all other authors using the keyword Phenotype. Analysis of the article abstracts and the titles suggests that Jean-Pierre Fryns professional interests are focused around "x-linked mental retardation", "hand foot malformations" and "array comparative genomic". These might also be referred to as "mental retardation", "x-linked mental" or "de novo". Statistical analysis shows that Jean-Pierre Fryns's writing is likely to contains terms "patients", "genes", "mutations", "gene", "syndrome" and "mental".

Unfortunately, there is not enough information to establish Jean-Pierre Fryns affiliation. Luckily, several email addresses are on file.

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Year 2007 Charts [Jean-Pierre Fryns frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Jean-Pierre Fryns publication and funding history for the range of years]

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