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You Searched For "genetic editing" and got 19 results


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3 mins read

What is the Y chromosome and what does its shrinkage mean for humans?

The Y chromosome, critical for male traits, has been shrinking over millions of years, raising ques…

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15 mins read

Williams syndrome is the genetic condition that makes people pathologically friendly in a lonely world

Living with Williams syndrome makes people hypersocial in a world where loneliness is an epidemic. …

Hayley Cuccinello   


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4 mins read

Lauren Ruotolo has a rare genetic disease that warps her bones. The experience inspired her to start a size-inclusive shoe line.

Lauren Ruotolo uses crutches and stilettos to get around. She said, "Might as well give them someth…

Andrea Michelson   


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3 mins read

My dad's frontotemporal dementia left me traumatized. Genetic testing revealed I have a 99% chance of developing FTD too.

My dad's frontotemporal dementia diagnosis came at 38. Genetic tests show I'll likely develop FTD t…

Kelly Burch   


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4 mins read

Pros and cons of GMOs: An evidence-based comparison of genetically modified foods

GMO crops have had their DNA altered to be more resistant to pesticides and less expensive to produ…

Madeline Kennedy,Samantha Cas…   


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2 mins read

Scientists are studying twins to understand a type of eating disorder linked to anxiety. It could be genetic.

Researchers are studying twins to learn more about an eating disorder that largely affects people w…

Andrea Michelson   


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3 mins read

I'm an Ancestry exec who plans my day based on my genetics. Here's my daily routine and productivity hacks.

Ancestry CCO Brian Donnelly said he sets up his whole day to play to his genetic and behavioral str…

Robin Madell   


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3 mins read

I've got more than 100 tumors in my body. They are benign and caused by a rare genetic disorder.

Michele Holbrook has schwannomatosis. The condition, a type of neurofibromatosis, has resulted in h…

Jane Ridley   


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3 mins read

My daughter has a rare seizure-inducing condition. She wasn't diagnosed until insurance agreed to pay for genetic testing.

After trying to push aside concerns, a new mom realized she needed more testing to find the correct…

Kelly Burch   


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2 mins read

My children have the same degenerative condition. I wish I had gotten genetic-carrier screening earlier to get them treated faster.

When her son wasn't walking by 18 months, the author decided to look for answers. She took a geneti…

Kelly Burch   


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2 mins read

Israeli scientists inch closer to developing a genetic treatment to cure AIDS

The one time injection technique utilises type B white blood cells that would be genetically engine…

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2 mins read

China is launching a probe into Chinese researcher’s claim of creating the world’s first ‘genetically edited’ babies

Jiankui has alleged that the girls had their embryos modified in order to give them an advantage…

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3 mins read

My baby was diagnosed with a rare genetic disorder. I learned a cure might be available but could cost $2.5 million to develop.

The 17-month-old has a condition that fewer than 50 people in the world have. Her parents, both doc…

Kelly Burch   


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2 mins read

Kate Hull   


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4 mins read

23andMe connected me with a half-brother I didn't know about. He made me realize I could pass a rare genetic mutation to my kids.

It was only when Meghan Thomas struggled to have a baby of her own that her mom said she was donor-…

Jane Ridley   


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3 mins read

At 63, I'm one of the oldest women living with my rare genetic condition. I'm also a musician, and thanks to new treatments, I'm going on tour.

After being diagnosed as a child and going through multiple failed treatments, she found a treatmen…

Kelly Burch   


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3 mins read

How a gene-editing breakthrough from a Harvard lab saved the life of a girl with leukemia

A 13-year-old girl became the first-ever patient to receive a base-editing therapy, and her leukemi…

Andrew Dunn   


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2 mins read

Gabrielle Bienasz   


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3 mins read

I was told my daughter would never walk because of a rare genetic disease. We just strolled down the catwalk together at New York Fashion Week.

When my child was diagnosed with spinal muscular atrophy, I was told she'd never walk. Four years l…

Kelly Burch