| Year |
Citation |
Score |
| 2017 |
Krupp DR, Barnard RA, Duffourd Y, Evans SA, Mulqueen RM, Bernier R, Rivière JB, Fombonne E, O'Roak BJ. Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder. American Journal of Human Genetics. PMID 28867142 DOI: 10.1016/J.Ajhg.2017.07.016 |
0.478 |
|
| 2015 |
Kraus WE, Muoio DM, Stevens R, Craig D, Bain JR, Grass E, Haynes C, Kwee L, Qin X, Slentz DH, Krupp D, Muehlbauer M, Hauser ER, Gregory SG, Newgard CB, et al. Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Plos Genetics. 11: e1005553. PMID 26540294 DOI: 10.1371/Journal.Pgen.1005553 |
0.491 |
|
| 2015 |
Shah AA, Gregory SG, Krupp D, Feng S, Dorogi A, Haynes C, Grass E, Lin SS, Hauser ER, Kraus WE, Shah SH, Hughes GC. Epigenetic Profiling Identifies Novel Genes for Ascending Aortic Aneurysm Formation with Bicuspid Aortic Valves. The Heart Surgery Forum. 18: E134-9. PMID 26334848 DOI: 10.1532/Hsf.1247 |
0.481 |
|
| 2014 |
Krupp DR, Soldano KL, Garrett ME, Cope H, Ashley-Koch AE, Gregory SG. Missing genetic risk in neural tube defects: can exome sequencing yield an insight? Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 642-6. PMID 25044326 DOI: 10.1002/bdra.23276 |
0.499 |
|
| 2012 |
Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG. Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 683-92. PMID 22806986 DOI: 10.1002/Bdra.23040 |
0.481 |
|
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