Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Scientist Development Award (K21)
Project #
5K21MH001338-02
Application #
2032872
Study Section
Epidemiology and Genetics Review Committee (EPI)
Project Start
1995-08-01
Project End
2000-07-31
Budget Start
1996-09-30
Budget End
1997-07-31
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Tufts University
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02111
Wassink, Thomas H; Piven, Joseph; Vieland, Veronica J et al. (2005) Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene. Am J Med Genet B Neuropsychiatr Genet 136B:36-44
Wassink, Thomas H; Piven, Joseph; Vieland, Veronica J et al. (2002) Evaluation of FOXP2 as an autism susceptibility gene. Am J Med Genet 114:566-9
Collaborative Linkage Study of Autism (2001) An autosomal genomic screen for autism. Am J Med Genet 105:609-15
Collaborative Linkage Study of Autism (2001) Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet 105:539-47
Van Eerdewegh, P; Dowd, M; Dupuis, J et al. (2001) On the detection of linkage in multiple data sets: a comparison of various statistical approaches. Genet Epidemiol 21 Suppl 1:S67-72
Wassink, T H; Piven, J; Vieland, V J et al. (2001) Evidence supporting WNT2 as an autism susceptibility gene. Am J Med Genet 105:406-13
Wassink, T H; Piven, J; Patil, S R (2001) Chromosomal abnormalities in a clinic sample of individuals with autistic disorder. Psychiatr Genet 11:57-63
Bradford, Y; Haines, J; Hutcheson, H et al. (2001) Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet 105:539-47
Folstein, S E; Santangelo, S L; Gilman, S E et al. (1999) Predictors of cognitive test patterns in autism families. J Child Psychol Psychiatry 40:1117-28
Van Eerdewegh, P; Dupuis, J; Santangelo, S L et al. (1999) The importance of watching our weights: how the choice of weights for non-independent sib pairs can dramatically alter results. Genet Epidemiol 17 Suppl 1:S373-8

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