Eric Moulton, OD, PhD
Profiles: Harvard Catalyst Profile Boston Children's Hospital Profile (Clinical) Boston Children's Hospital Profile (Research)
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ENT Forum & Networking Event
To Register: https://bit.ly/2HBIkKb Summary: Topics will cover residency, research, subspecialties, most treated conditions, work-life balance, interaction with other specialties and non-practitioners. Following a panel presentation, there will be an opportunity for a live Q&A, dinner, and...
NCFG Hands-on Training Sessions March 2019
The NCFG is hosting a Hands-On Training Session for Glycomics in March. For full details visit: https://ncfg.hms.harvard.edu/hands-training-sessions
Upcoming talk on mosaic chromosomal alterations
Po-Ru Loh will be speaking about phase-based detection of mosaic chromosomal alterations at the Gordon Research Conference on Quantitative Genetics and Genomics on Tue 2/12.
Gene Therapy Platform Developed by Neena Haider, PhD, Granted FDA Orphan Drug Designation
OCU400, a novel gene therapy platform developed by Neena Haider, PhD, Harvard Medical School Associate Professor of Ophthalmology and Associate Scientist at the Schepens Eye Research Institute of Mass. Eye and Ear, and licensed to biopharmaceutical company Ocugen, Inc., has been granted orphan drug...
Resources
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
Finucane, Hilary, Yakir Reshef, Verneri Anttila, Kamil Slowikowski, Alexander Gusev, Andrea Byrnes, Steven Gazal, et al. 2018. “Heritability Enrichment of Specifically Expressed Genes Identifies Disease-Relevant Tissues and Cell Types”. Nature Genetics 50 (4): 621-29.
High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction
Li, Gang, Marta Martínez-Bonet, Di Wu, Yu Yang, Jing Cui, Hung N. Nguyen, Pierre Cunin, et al. 2018. “High-Throughput Identification of Noncoding Functional SNPs via Type IIS Enzyme Restriction”. Nature Genetics 50 (8): 1180-88.
Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes
Westra, Harm-Jan#, Marta# Martínez-Bonet, Suna Onengut-Gumuscu, Anette Lee, Yang Luo, Nikola Teslovich, Jane Worthington, et al. 2018. “Fine-Mapping and Functional Studies Highlight Potential Causal Variants for Rheumatoid Arthritis and Type 1 Diabetes”. Nature Genetics 50 (10): 1366-74.
An Integrated Clinical Program and Crowdsourcing Strategy for Genomic Sequencing and Mendelian Disease Gene Discovery.
Haghighi, Alireza, Joel B. Krier, Agnes Tóth-Petróczy, Christopher A. Cassa, Natasha Y. Frank, Nikkola Carmichael, Eizabeth Fieg, et al. 2018. “An Integrated Clinical Program and Crowdsourcing Strategy for Genomic Sequencing and Mendelian Disease Gene Discovery.”. Npj Genomic Medicine 3: 21.