Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01MH105666-04S1
Application #
9644736
Study Section
Program Officer
Addington, Anjene M
Project Start
2014-09-23
Project End
2019-07-31
Budget Start
2018-04-24
Budget End
2019-07-31
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
Ganna, Andrea; Satterstrom, F Kyle; Zekavat, Seyedeh M et al. (2018) Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. Am J Hum Genet 102:1204-1211
Gormley, Padhraig; Kurki, Mitja I; Hiekkala, Marjo Eveliina et al. (2018) Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron 98:743-753.e4
Short, Patrick J; McRae, Jeremy F; Gallone, Giuseppe et al. (2018) De novo mutations in regulatory elements in neurodevelopmental disorders. Nature 555:611-616
Sanders, Stephan J; Neale, Benjamin M; Huang, Hailiang et al. (2017) Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nat Neurosci 20:1661-1668
Singh, Tarjinder; Walters, James T R; Johnstone, Mandy et al. (2017) The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nat Genet 49:1167-1173
Ganna, Andrea; Genovese, Giulio; Howrigan, Daniel P et al. (2016) Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neurosci 19:1563-1565