Daniel S. Lieber, Ph.D.

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

Parents

Sign in to add mentor
Vamsi Mootha grad student 2013 Harvard
 (Computational and experimental approaches for evaluating the genetic basis of mitochondrial disorders.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...