Eric W. Klee, Ph.D.
Affiliations: | 2005 | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Molecular BiologyGoogle:
"Eric Klee"Parents
Sign in to add mentor| Lynda B. M. Ellis | grad student | 2005 | UMN | |
| (Computational prediction of cotranslational translocated proteins in expressed sequence tag assemblies.) | ||||
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Publications
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| Bowles B, Clark K, Klee E. (2021) 95233 Analysis of 5'UTR Variation in Rare Disease Patients Reveals Variants of Potential Disease Relevance Journal of Clinical and Translational Science. 5: 101-101 |
| Schultz-Rogers L, Masuho I, Pinto E Vairo F, et al. (2020) Haploinsufficiency as a disease mechanism in GNB1-associated neurodevelopmental disorder. Molecular Genetics & Genomic Medicine. e1477 |
| Muthusamy K, Macke EL, Klee EW, et al. (2020) Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. American Journal of Medical Genetics. Part A |
| Kennedy J, Goudie D, Blair E, et al. (2020) Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Pinto E Vairo F, Kroc SA, Bertsch NL, et al. (2020) Biallelic variants in PROZ as a cause of hypercoagulability and livedo racemosa. Thrombosis Research. 195: 187-189 |
| Trost B, Engchuan W, Nguyen CM, et al. (2020) Genome-wide detection of tandem DNA repeats that are expanded in autism. Nature |
| Schultz-Rogers L, Lach FP, Rickman KA, et al. (2020) Homozygous missense variant in UBE2T is associated with mild Fanconi anemia phenotype. Haematologica |
| Morales-Rosado JA, Goel K, Zhang L, et al. (2020) Next-Generation Sequencing of CYP2C19 in Stent Thrombosis: Implications for Clopidogrel Pharmacogenomics. Cardiovascular Drugs and Therapy |
| Morales-Rosado JA, Macke EL, Cousin MA, et al. (2020) Interpretation challenges of novel dual-class missense and splice-impacting variant in POLR3A-related late-onset hereditary spastic ataxia. Molecular Genetics & Genomic Medicine. e1341 |
| Drivas TG, Li D, Nair D, et al. (2020) A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome. European Journal of Human Genetics : Ejhg |