Serge Batalov
Affiliations: | 2016- | Rady Children's Hospital San Diego |
Area:
Genomics, Genetics, Human genetics, Computational Biology, PhysicsGoogle:
"Serge Batalov"Parents
Sign in to add mentor| Ruben Abagyan | research scientist | 1994-1999 | New York University School of Medicine (Computational Biology Tree) |
| Peter G. Schultz | research scientist | 1999-2015 | GNF Novartis (Chemistry Tree) |
Collaborators
Sign in to add collaborator| Eric Lander | collaborator | 2000-2004 | ||
| (RIKEN FANTOM consortium) | ||||
| Tim Jegla | collaborator | 1999-2015 | GNF Novartis (Neurotree) | |
| Tim Wiltshire | collaborator | 1999-2015 | GNF Novartis (Cell Biology Tree) | |
BETA: Related publications
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Publications
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| James KN, Chowdhury S, Ding Y, et al. (2023) Genome sequencing detects a wide range of clinically relevant copy number variants and other genomic alterations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101006 |
| Kingsmore SF, Smith LD, Kunard CM, et al. (2023) Response to Grosse et al. American Journal of Human Genetics. 110: 1017 |
| Owen MJ, Batalov S, Ellsworth KA, et al. (2023) Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Children. Methods in Molecular Biology (Clifton, N.J.). 2621: 217-239 |
| Ding Y, Owen M, Le J, et al. (2023) Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots. Npj Genomic Medicine. 8: 5 |
| Owen MJ, Wright MS, Batalov S, et al. (2023) Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing. Jama Network Open. 6: e2254069 |
| Vijayaraghavan P, Batalov S, Ding Y, et al. (2023) The Genomic landscape of short tandem repeats across multiple ancestries. Plos One. 18: e0279430 |
| Kingsmore SF, Smith LD, Kunard CM, et al. (2022) A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. American Journal of Human Genetics |
| Kingsmore SF, Smith LD, Kunard CM, et al. (2022) A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. Am J Hum Genet.. 109: 1605-1619 |
| Owen MJ, Lefebvre S, Hansen C, et al. (2022) An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases Nat Commun .. 13: 4057 |
| Owen MJ, Lefebvre S, Hansen C, et al. (2022) An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases. Nature Communications. 13: 4057 |