Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
2T32GM007748-16
Application #
2166869
Study Section
Genetic Basis of Disease Review Committee (GBD)
Project Start
1979-07-01
Project End
1999-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
16
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Harvard University
Department
Genetics
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Rohanizadegan, Mersedeh (2018) Analysis of circulating tumor DNA in breast cancer as a diagnostic and prognostic biomarker. Cancer Genet 228-229:159-168
Demirbas, Didem; Brucker, William J; Berry, Gerard T (2018) Inborn Errors of Metabolism with Hepatopathy: Metabolism Defects of Galactose, Fructose, and Tyrosine. Pediatr Clin North Am 65:337-352
Schwartz, Talia S; Wojcik, Monica H; Pelletier, Renee C et al. (2018) Expanding the phenotypic spectrum associated with OPHN1 variants. Eur J Med Genet :
Zhu, Qihui; High, Frances A; Zhang, Chengsheng et al. (2018) Systematic analysis of copy number variation associated with congenital diaphragmatic hernia. Proc Natl Acad Sci U S A 115:5247-5252
Stachler, Matthew D; Camarda, Nicholas D; Deitrick, Christopher et al. (2018) Detection of Mutations in Barrett's Esophagus Before Progression to High-Grade Dysplasia or Adenocarcinoma. Gastroenterology 155:156-167
Srivastava, Siddharth; Desai, Sonal; Cohen, Julie et al. (2018) Monogenic disorders that mimic the phenotype of Rett syndrome. Neurogenetics 19:41-47
Wojcik, Monica H; Brodsky, Dara; Stewart, Jane E et al. (2018) Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology. J Perinatol 38:1125-1134
Guissart, Claire; Latypova, Xenia; Rollier, Paul et al. (2018) Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia. Am J Hum Genet 102:744-759
Takeda, David Y; Spisák, Sándor; Seo, Ji-Heui et al. (2018) A Somatically Acquired Enhancer of the Androgen Receptor Is a Noncoding Driver in Advanced Prostate Cancer. Cell 174:422-432.e13
Rohanizadegan, Mersedeh; Sacharow, Stephanie (2018) Desmosterolosis presenting with multiple congenital anomalies. Eur J Med Genet 61:152-156

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