Connection

HUDA ZOGHBI to Syndrome

This is a "connection" page, showing publications HUDA ZOGHBI has written about Syndrome.
Connection Strength

0.385
  1. Lessons learned from studying syndromic autism spectrum disorders. Nat Neurosci. 2016 10 26; 19(11):1408-1417.
    View in: PubMed
    Score: 0.101
  2. Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome. Nat Genet. 2012 Jan 08; 44(2):206-11.
    View in: PubMed
    Score: 0.072
  3. Mental retardation: X marks the spot. Neurology. 2003 Jul 22; 61(2):156-7.
    View in: PubMed
    Score: 0.040
  4. Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations. Nat Commun. 2018 08 13; 9(1):3225.
    View in: PubMed
    Score: 0.029
  5. Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22. Genomics. 1998 Jul 15; 51(2):251-61.
    View in: PubMed
    Score: 0.028
  6. Cloning and characterization of a novel rho-type GTPase-activating protein gene (ARHGAP6) from the critical region for microphthalmia with linear skin defects. Genomics. 1997 Dec 01; 46(2):268-77.
    View in: PubMed
    Score: 0.027
  7. Molecular genetics and neurobiology of neurodegenerative and neurodevelopmental disorders. Pediatr Res. 1997 May; 41(5):722-6.
    View in: PubMed
    Score: 0.026
  8. Genetic aspects of Rett syndrome. J Child Neurol. 1988; 3 Suppl:S76-8.
    View in: PubMed
    Score: 0.014
  9. Reduction of biogenic amine levels in the Rett syndrome. N Engl J Med. 1985 Oct 10; 313(15):921-4.
    View in: PubMed
    Score: 0.012
  10. Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome. Hum Mol Genet. 2002 Dec 01; 11(25):3237-48.
    View in: PubMed
    Score: 0.010
  11. A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22. Hum Mol Genet. 1994 Jul; 3(7):1155-61.
    View in: PubMed
    Score: 0.005
  12. Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. Am J Med Genet. 1994 Jan 15; 49(2):229-34.
    View in: PubMed
    Score: 0.005
  13. Neuropathology of Rett syndrome. Acta Neuropathol. 1988; 76(2):142-58.
    View in: PubMed
    Score: 0.003
  14. Rett syndrome: qualitative and quantitative differentiation from autism. J Child Neurol. 1988; 3 Suppl:S65-7.
    View in: PubMed
    Score: 0.003
  15. Rett's syndrome: characterization of respiratory patterns and sleep. Ann Neurol. 1987 Apr; 21(4):377-82.
    View in: PubMed
    Score: 0.003
  16. Rett syndrome: discrimination of typical and variant forms. Brain Dev. 1987; 9(5):458-61.
    View in: PubMed
    Score: 0.003
  17. Rett syndrome: initial experience with an emerging clinical entity. Brain Dev. 1985; 7(3):300-4.
    View in: PubMed
    Score: 0.003
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.