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	Profile	Recent Articles on Subject
1	Emily Cooke Live Science Health reporter. London, United Kingdom healthscience	Argyria: The rare disease that turns people blue - 6 days ago Stone man disease: A rare condition that causes a person to grow a second skeleton - about 2 months ago New mRNA therapy shows promise in treating 'ultrarare' inherited disease - 10 months ago
2	Nicoletta Lanese Live Science Science journalist. New York, USA sciencehealthjournalism	Some schizophrenia cases stem from malformations of the skull, study suggests - 30 days ago Gene variant guards against Parkinson's and could lead to therapies - about 1 year ago
3	Adam Feuerstein STAT News Reporter at STATnews. Dog lover. Polk Award winner. Boston, Massachusetts biotech reporting	STAT+: Biotech companies detail emerging efforts to ease ‘conditioning’ before genetic treatments - about 1 month ago Sanofi advances a drug for a rare, platelet-destroying disease - about 2 months ago
4	The Conversation Science Alert Science news. Official account. Australia science news	Mysterious Fatal 'Disease X' Outbreak in Congo Still Can't Be Explained - about 1 month ago Many Dementia Cases Could Actually Be a Hidden Form of Liver Disease - 11 months ago
5	Jonathan Wosen STAT News West Coast Biotech Reporter. Formerly @sdut. Stanford PhD. UCSC alum. San Diego, California BiotechLife SciencesImmunology	Sanofi advances a drug for a rare, platelet-destroying disease - about 2 months ago STAT+: Gene therapy pioneer Jim Wilson believes he can commercialize rare-disease drugs in a tough climate - 5 months ago
6	Frank Vinluan MedCity News Medical innovation tracker. MedCity, USA medicalinnovation	Applied Therapeutics Drug Is Denied FDA Approval in Rare Inherited Metabolic Disease - about 2 months ago AstraZeneca’s Rare Disease Pipeline Notches Another FDA Approval - 10 months ago
7	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: Sarepta, Arrowhead Pharmaceuticals partner to advance RNA-based drugs in rare diseases - about 2 months ago STAT+: A rare disease program, portrayed as both lifeline and pharma handout, is set to expire - 4 months ago STAT+: FDA rejects Rocket Pharmaceuticals’ gene therapy for ultra-rare condition, another setback for field - 7 months ago STAT+: Doudna institute hatches plan to ‘cure hundreds of diseases’ left behind by CRISPR revolution - about 1 year ago STAT+: Peter Marks on creating Operation Warp Speed, but for rare diseases - over 1 year ago
8	Ashley Gallagher, Associate Editor Pharmacy Times One of Cabra girls on GoggleboxIRL. Dublin City, Ireland televisionentertainment	FDA Grants Rare Pediatric Disease Designation for Treatment of Neonatal SP-B Deficiency - 2 months ago FDA Grants Orphan Drug Designation to RAG-18 for Duchenne, Becker Muscular Dystrophy - 5 months ago Moderna Announces Expansion of mRNA Research Across Respiratory, Oncology, Rare Disease Franchises - over 1 year ago
9	Meagan Parrish Pharma Voice Senior editor @industrydive. Pharma world follower. Wisconsin, USA pharmaceuticalsjournalismparenting	2024 PharmaVoice 100s: Rare Disease Warriors - 3 months ago Behind a big-name rare disease biotech, an exec draws from personal experience - 11 months ago
10	Randy Dotinga MedPage Today Indie scribbler, advocate. Board member, @ahcj. San Diego WritingAdvocacy	Gene Therapy Shows Promise in Rare Eye Disease That Causes Early Blindness - 4 months ago

Journalists covering Rare Diseases