Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
7R01HD021244-04
Application #
3320052
Study Section
Human Embryology and Development Subcommittee 2 (HED)
Project Start
1988-10-01
Project End
1988-12-31
Budget Start
1988-10-01
Budget End
1988-12-31
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Sengupta, Subhajit; Gulukota, Kamalakar; Zhu, Yitan et al. (2016) Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samples. Nucleic Acids Res 44:e25
Burrows, Courtney K; Kosova, Gülüm; Herman, Catherine et al. (2016) Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes. PLoS Genet 12:e1005858
Livne, Oren E; Han, Lide; Alkorta-Aranburu, Gorka et al. (2015) PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population. PLoS Comput Biol 11:e1004139
Gao, Ziyue; Waggoner, Darrel; Stephens, Matthew et al. (2015) An estimate of the average number of recessive lethal mutations carried by humans. Genetics 199:1243-54
Kosova, Gülüm; Stephenson, Mary D; Lynch, Vincent J et al. (2015) Evolutionary forward genomics reveals novel insights into the genes and pathways dysregulated in recurrent early pregnancy loss. Hum Reprod 30:519-29
Campbell, Catarina D; Mohajeri, Kiana; Malig, Maika et al. (2014) Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. PLoS One 9:e104396
Kosova, Gülüm; Hotaling, James M; Ohlander, Samuel et al. (2014) Variants in DPF3 and DSCAML1 are associated with sperm morphology. J Assist Reprod Genet 31:131-7
Anderson, Rebecca L; Murray, Kathleen; Chong, Jessica X et al. (2014) Disclosure of genetic research results to members of a founder population. J Genet Couns 23:984-91
Bögershausen, Nina; Shahrzad, Nassim; Chong, Jessica X et al. (2013) Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. Am J Hum Genet 93:181-90
Gerull, Brenda; Kirchner, Florian; Chong, Jessica X et al. (2013) Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population. Circ Cardiovasc Genet 6:327-36

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