Harvard Catalyst Profiles

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Christopher A. Walsh, M.D., Ph.D.

Co-Author

This page shows the publications co-authored by Christopher Walsh and Bernard Chang.
Connection Strength

3.991
  1. A structural basis for reading fluency: white matter defects in a genetic brain malformation. Neurology. 2007 Dec 04; 69(23):2146-54.
    View in: PubMed
    Score: 0.380
  2. The role of RELN in lissencephaly and neuropsychiatric disease. . 2007 Jan 05; 144B(1):58-63.
    View in: PubMed
    Score: 0.356
  3. A familial syndrome of unilateral polymicrogyria affecting the right hemisphere. Neurology. 2006 Jan 10; 66(1):133-5.
    View in: PubMed
    Score: 0.333
  4. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology. 2005 Mar 08; 64(5):799-803.
    View in: PubMed
    Score: 0.314
  5. Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation. Neurology. 2004 May 25; 62(10):1722-8.
    View in: PubMed
    Score: 0.297
  6. Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations. Epilepsy Behav. 2003 Dec; 4(6):618-25.
    View in: PubMed
    Score: 0.287
  7. Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Ann Neurol. 2003 May; 53(5):596-606.
    View in: PubMed
    Score: 0.276
  8. Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations. Am J Med Genet A. 2018 02; 176(2):337-350.
    View in: PubMed
    Score: 0.192
  9. Cover Image, Volume 176A, Number 2, February 2018. Am J Med Genet A. 2018 Feb; 176(2):i.
    View in: PubMed
    Score: 0.192
  10. Somatic mutations in cerebral cortical malformations. N Engl J Med. 2014 Aug 21; 371(8):733-43.
    View in: PubMed
    Score: 0.151
  11. Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. Science. 2014 Feb 14; 343(6172):764-8.
    View in: PubMed
    Score: 0.146
  12. Schizencephaly: association with young maternal age, alcohol use, and lack of prenatal care. J Child Neurol. 2013 Feb; 28(2):198-203.
    View in: PubMed
    Score: 0.135
  13. Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. Am J Med Genet A. 2010 Nov; 152A(11):2736-42.
    View in: PubMed
    Score: 0.116
  14. Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nat Genet. 2010 Mar; 42(3):245-9.
    View in: PubMed
    Score: 0.110
  15. The syndrome of perisylvian polymicrogyria with congenital arthrogryposis. Brain Dev. 2010 Aug; 32(7):550-5.
    View in: PubMed
    Score: 0.107
  16. Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. Hum Mutat. 2008 Nov; 29(11):E231-41.
    View in: PubMed
    Score: 0.101
  17. A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome. . 2007 Aug 01; 143A(15):1692-8.
    View in: PubMed
    Score: 0.093
  18. Comprehensive EMX2 genotyping of a large schizencephaly case series. . 2007 Jun 15; 143A(12):1313-6.
    View in: PubMed
    Score: 0.092
  19. Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. Ann Neurol. 2005 Nov; 58(5):680-7.
    View in: PubMed
    Score: 0.082
  20. EMX2-independent familial schizencephaly: clinical and genetic analyses. . 2005 Jun 01; 135(2):166-70.
    View in: PubMed
    Score: 0.080
  21. Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome. . 2005 Feb 15; 133A(1):53-7.
    View in: PubMed
    Score: 0.078
  22. G protein-coupled receptor-dependent development of human frontal cortex. Science. 2004 Mar 26; 303(5666):2033-6.
    View in: PubMed
    Score: 0.073
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.