Simons Simplex Collection

Oligogenic combinations of rare variants influence specific phenotypes in complex disorders.

Genetic counseling as preventive intervention: Toward individual specification of transgenerational autism risk.

Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions.

The impact of birth order on language development in autistic children from Simplex families.

Rates of contributory de novo mutation in high and low-risk autism families.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders.

Advancing methodologies to improve RRB outcome measures in autism research: Evaluation of the RBS-R.

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

“Guilt by association” is not competitive with genetic association for identifying autism risk genes.

Genetic correlates of phenotypic heterogeneity in autism.

• Previous Page
• Viewing Page 1 of 37 Page 2 of 37 Page 3 of 37 Page 4 of 37 Page 5 of 37 Page 6 of 37 Page 7 of 37 Page 8 of 37 Page 9 of 37 Page 10 of 37 Page 11 of 37 Page 12 of 37 Page 13 of 37 Page 14 of 37 Page 15 of 37 Page 16 of 37 Page 17 of 37 Page 18 of 37 Page 19 of 37 Page 20 of 37 Page 21 of 37 Page 22 of 37 Page 23 of 37 Page 24 of 37 Page 25 of 37 Page 26 of 37 Page 27 of 37 Page 28 of 37 Page 29 of 37 Page 30 of 37 Page 31 of 37 Page 32 of 37 Page 33 of 37 Page 34 of 37 Page 35 of 37 Page 36 of 37 Page 37 of 37
• Page 1 of 37 Page 2 of 37 Page 3 of 37 Page 4 of 37 Page 5 of 37 Page 6 of 37 Page 7 of 37 Page 8 of 37 Page 9 of 37 Page 10 of 37 Page 11 of 37 Page 12 of 37 Page 13 of 37 Page 14 of 37 Page 15 of 37 Page 16 of 37 Page 17 of 37 Page 18 of 37 Page 19 of 37 Page 20 of 37 Page 21 of 37 Page 22 of 37 Page 23 of 37 Page 24 of 37 Page 25 of 37 Page 26 of 37 Page 27 of 37 Page 28 of 37 Page 29 of 37 Page 30 of 37 Page 31 of 37 Page 32 of 37 Page 33 of 37 Page 34 of 37 Page 35 of 37 Page 36 of 37 Page 37 of 37
• Next Page