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Bai-Lin Wu, Ph.D., M.Med.

Co-Author

This page shows the publications co-authored by Bai-Lin Wu and James Gusella.
Connection Strength

0.832
  1. Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs. Am J Hum Genet. 2013 Mar 07; 92(3):375-86.
    View in: PubMed
    Score: 0.136
  2. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 2012 Apr 27; 149(3):525-37.
    View in: PubMed
    Score: 0.128
  3. Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar; 156(2):225-32.
    View in: PubMed
    Score: 0.117
  4. Large-scale medical resequencing for X-linked mental retardation. Clin Chem. 2010 Mar; 56(3):339-41.
    View in: PubMed
    Score: 0.109
  5. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet. 2009 Apr; 46(4):242-8.
    View in: PubMed
    Score: 0.100
  6. Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance. Clin Chem. 2007 Dec; 53(12):2051-9.
    View in: PubMed
    Score: 0.093
  7. Detection of copy number variants reveals association of cilia genes with neural tube defects. PLoS One. 2013; 8(1):e54492.
    View in: PubMed
    Score: 0.034
  8. Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. Am J Hum Genet. 2011 Oct 07; 89(4):551-63.
    View in: PubMed
    Score: 0.031
  9. Age- and gender-dependent obesity in individuals with 16p11.2 deletion. J Genet Genomics. 2011 Sep 20; 38(9):403-9.
    View in: PubMed
    Score: 0.031
  10. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 05; 153B(4):937-47.
    View in: PubMed
    Score: 0.028
  11. Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med. 2008 Feb 14; 358(7):667-75.
    View in: PubMed
    Score: 0.024
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.