Year |
Citation |
Score |
2020 |
Boskovski MT, Homsy J, Nathan M, Sleeper LA, Morton S, Manheimer KB, Tai A, Gorham J, Lewis M, Swartz M, Alfieris GM, Bacha EA, Karimi M, Meyer D, Nguyen K, et al. De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease. Circulation. Genomic and Precision Medicine. 13: e002836. PMID 32812804 DOI: 10.1161/CIRCGEN.119.002836 |
0.509 |
|
2018 |
Manheimer KB, Patel N, Richter F, Gorham J, Tai AC, Homsy J, Boskovski MT, Parfenov M, Goldmuntz E, Chung WK, Brueckner M, Tristani-Firouzi M, Srivastava D, Seidman JG, Seidman CE, et al. Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors. Human Mutation. PMID 29527824 DOI: 10.1002/Humu.23419 |
0.497 |
|
2018 |
Manheimer KB, Richter F, Edelmann LJ, D'Souza SL, Shi L, Shen Y, Homsy J, Boskovski MT, Tai AC, Gorham J, Yasso C, Goldmuntz E, Brueckner M, Lifton RP, Chung WK, et al. Robust identification of mosaic variants in congenital heart disease. Human Genetics. PMID 29417219 DOI: 10.1007/S00439-018-1871-6 |
0.529 |
|
2013 |
Boskovski MT, Yuan S, Pedersen NB, Goth CK, Makova S, Clausen H, Brueckner M, Khokha MK. The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality. Nature. 504: 456-9. PMID 24226769 DOI: 10.1038/Nature12723 |
0.501 |
|
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