Daniel S. Lieber, Ph.D.

2013 Systems Biology Harvard University, Cambridge, MA, United States 
Genetics, Systematic Biology, Bioinformatics Biology
"Daniel Lieber"


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Vamsi Mootha grad student 2013 Harvard
 (Computational and experimental approaches for evaluating the genetic basis of mitochondrial disorders.)
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Chennagiri N, White EJ, Frieden A, et al. (2016) Orthogonal NGS for High Throughput Clinical Diagnostics. Scientific Reports. 6: 24650
Lieber DS, Hershman SG, Slate NG, et al. (2014) Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency. Bmc Medical Genetics. 15: 30
Hildick-Smith GJ, Cooney JD, Garone C, et al. (2013) Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4. American Journal of Human Genetics. 93: 906-14
Lieber DS, Calvo SE, Shanahan K, et al. (2013) Targeted exome sequencing of suspected mitochondrial disorders. Neurology. 80: 1762-70
Calvo SE, Compton AG, Hershman SG, et al. (2012) Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. Science Translational Medicine. 4: 118ra10
Lieber DS, Vafai SB, Horton LC, et al. (2012) Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial disease. Bmc Medical Genetics. 13: 3
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