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Connection

Edward Ip to DiGeorge Syndrome

This is a "connection" page, showing publications Edward Ip has written about DiGeorge Syndrome.
Connection Strength

0.407
  1. Shashi V, Francis A, Hooper SR, Kranz PG, Zapadka M, Schoch K, Ip E, Tandon N, Howard TD, Keshavan MS. Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. Eur J Hum Genet. 2012 Oct; 20(10):1051-7.
    View in: PubMed
    Score: 0.105
  2. Schoch K, Harrell W, Hooper SR, Ip EH, Saldana S, Kwapil TR, Shashi V. Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome. J Learn Disabil. 2014 Mar-Apr; 47(2):153-66.
    View in: PubMed
    Score: 0.104
  3. Das Chakraborty R, Chakraborty D, Bernal AJ, Schoch K, Howard TD, Ip EH, Hooper SR, Keshavan MS, Jirtle RL, Shashi V. Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome. Transl Psychiatry. 2012 Apr 24; 2:e105.
    View in: PubMed
    Score: 0.103
  4. Veerapandiyan A, Blalock D, Ghosh S, Ip E, Barnes C, Shashi V. The role of cephalometry in assessing velopharyngeal dysfunction in velocardiofacial syndrome. Laryngoscope. 2011 Apr; 121(4):732-7.
    View in: PubMed
    Score: 0.095
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.