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Tags: CRISPR/Cas, gene silencing, genetics, knockout, RNA interference, TALENs, zinc finger nuclease adeno-associated virus, Alzheimer's Disease, CRISPR, gene therapy, genetics, neurology, neuroscience, Parkinson's disease computational biology, genetics, Human Genome Project, non-coding RNA ideas the wired world in 2024

	Profile	Recent Articles on Subject
1	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 - 6 days ago
2	Amy Baxter Pharma Voice Scientist, inventor, former pediatrician. Atlanta, Georgia pain relieftechnologyinnovation	Lilly lays down $1B to be ‘first in biology’ with obesity gene therapies - 11 days ago To overcome barriers, cell and gene therapies need outside support - about 2 months ago
3	Jonathan Wosen STAT News West Coast Biotech Reporter. Formerly @sdut. Stanford PhD. UCSC alum. San Diego, California BiotechLife SciencesImmunology	STAT+: Gene therapy pioneer Jim Wilson believes he can commercialize rare-disease drugs in a tough climate - 29 days ago STAT+: Bone marrow transplant advance could widen use of this less buzzy cure for sickle cell disease - 9 months ago STAT+: Historic approval of sickle cell gene therapies met with cautious optimism by experts at ASH - 10 months ago
4	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: FDA rejects Rocket Pharmaceuticals’ gene therapy for ultra-rare condition, another setback for field - 3 months ago STAT+: Why the world’s most expensive drug might not be all that overpriced - 6 months ago STAT+: New gene therapy, to be priced at $4.25 million, has already transformed children’s lives - 6 months ago STAT+: FDA approves first gene therapy for fatal neuron disease in children - 6 months ago STAT+: Hemophilia gene therapies arrived after 40 years of struggle. Where are the patients? - 6 months ago STAT+: Doudna institute hatches plan to ‘cure hundreds of diseases’ left behind by CRISPR revolution - 8 months ago STAT+: Could sickle cell someday be treated not with CRISPR, but with a pill? - 9 months ago
5	<em>The Scientist</em> Staff The Scientist Exploring Life, Inspiring Innovation. scienceinnovation	Bringing Gene Therapy to the Brain - 3 months ago
6	Nicole Lou MedPage Today Medical reporter @medpagetoday. Bird advocate. undisclosed remote location medical reporting	Gene Therapy Allowing Heart to Grow New Blood Vessels Supported by Early Data - 5 months ago Milestone Gene Therapies for Sickle Cell Disease Greenlit by FDA - 10 months ago Promising Debut for CRISPR Gene Editing Therapy for LDL Lowering - 10 months ago
7	Meghana Keshavan STAT News Biotech nerd and writer @statnews. biotechwriting	How resurrecting extinct species might impact medicine - 6 months ago What happens when an approved drug doesn’t work? - 6 months ago Regeneron gene therapy improves hearing in child - 11 months ago
8	Emily Cooke Live Science Health reporter. London, United Kingdom healthscience	New mRNA therapy shows promise in treating 'ultrarare' inherited disease - 6 months ago
9	Andrew Joseph STAT News Reporter at STAT. Covers health, medicine in Europe. London, England health reportingmedicine	STAT+: Early data from rare-disease trial put spotlight on Moderna’s efforts to turn mRNA into medicines - 6 months ago STAT+: A gene therapy designed to heal skin wounds helped preserve a boy’s vision - 8 months ago STAT+: U.K. approves world’s first CRISPR-based medicine, giving greenlight to therapy for sickle cell, thalassemia - 10 months ago
10	Danielle Gerhard, PhD The Scientist Assistant Editor @TheScientistLLC. United Kingdom scienceediting	A Journey Into the Brain - 6 months ago

Journalists covering Gene therapy