Abstract

The Administrative Core of the Boston Children's Hospital / Harvard Medical School IDDRC enhances research and promotes the development of new therapies by supporting outstanding research focused on problems relevant to intellectual and developmental disabilities. The Core supports the financial and administrative management of core facilities, provides core services to aid in the training of young investigators and their trainees, and fosters overall ?centerness? to enhance and encourage collaboration between IDDRC investigators. Through active engagement with other IDDRC cores and investigators throughout the national IDDRC network, the core services provided by our IDDRC promote collaboration outside the institution to speed the development of effective clinical interventions in intellectual and developmental disabilities.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HD090255-05
Application #
10003041
Study Section
Special Emphasis Panel (ZHD1)
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost

  Institution

Name
Boston Children's Hospital
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115

  Publications

Marsh, Ashley P L; Edwards, Timothy J; Galea, Charles et al. (2018) DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome. Hum Mutat 39:23-39
Sveinsdóttir, Kristbjörg; Ley, David; Hövel, Holger et al. (2018) Relation of Retinopathy of Prematurity to Brain Volumes at Term Equivalent Age and Developmental Outcome at 2 Years of Corrected Age in Very Preterm Infants. Neonatology 114:46-52
Schwartz, Talia S; Wojcik, Monica H; Pelletier, Renee C et al. (2018) Expanding the phenotypic spectrum associated with OPHN1 variants. Eur J Med Genet :
Sourati, Jamshid; Gholipour, Ali; Dy, Jennifer G et al. (2018) Active Deep Learning with Fisher Information for Patch-wise Semantic Segmentation. Deep Learn Med Image Anal Multimodal Learn Clin Decis Support ( 11045:83-91
Koczkowska, Magdalena; Chen, Yunjia; Callens, Tom et al. (2018) Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848. Am J Hum Genet 102:69-87
Sieberg, Christine B; Taras, Caitlin; Gomaa, Aya et al. (2018) Neuropathic pain drives anxiety behavior in mice, results consistent with anxiety levels in diabetic neuropathy patients. Pain Rep 3:e651
Torres, Alcy; Brownstein, Catherine A; Tembulkar, Sahil K et al. (2018) De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome. Mol Genet Metab Rep 16:23-29
Shannon, Morgan L; Fame, Ryann M; Chau, Kevin F et al. (2018) Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors. Am J Pathol 188:1334-1344
Liang, Liang; Fratzl, Alex; Goldey, Glenn et al. (2018) A Fine-Scale Functional Logic to Convergence from Retina to Thalamus. Cell 173:1343-1355.e24
Chau, Kevin F; Shannon, Morgan L; Fame, Ryann M et al. (2018) Downregulation of ribosome biogenesis during early forebrain development. Elife 7:

Showing the most recent 10 out of 498 publications