The New York Times, March 22, 2018

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Nearly two decades ago, the rumors began: In the Atacama Desert of northern Chile, someone had discovered a tiny mummified alien.

An amateur collector exploring a ghost town was said to have come across a white cloth in a leather pouch. Unwrapping it, he found a six-inch-long skeleton.

Despite its size, the skeleton was remarkably complete. It even had hardened teeth. And yet there were striking anomalies: it had 10 ribs instead of the usual 12, giant eye sockets and a long skull that ended in a point.

Continue reading “Was a Tiny Mummy in the Atacama an Alien? No, but the Real Story Is Almost as Strange”

The New York Times, March 20, 2018

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BOSTON — David Reich wore a hooded, white suit, cream-colored clogs, and a blue surgical mask. Only his eyes were visible as he inspected the bone fragments on the counter.

Dr. Reich, a geneticist at Harvard Medical School, pointed out a strawberry-sized chunk: “This is from a 4,000-year-old site in Central Asia — from Uzbekistan, I think.”

He moved down the row. “This is a 2,500-year-old sample from a site in Britain. This is Bronze Age Russian, and these are Arabian samples. These people would have never met each other in time or space.”

Continue reading “David Reich Unearths Human History Etched in Bone”

The New York Times, March 15, 2018

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Gregor Mendel discovered fundamental rules of genetics by raising pea plants. He realized that hidden factors — we now know them to be genes — were passed down from parents to offspring.

It wasn’t until the early 1900s, long after Mendel’s death, that doctors discovered that humans weren’t so very different. Some diseases, it turns out, are inherited — they’re Mendelian.

Today, scientists have identified over 7,000 Mendelian diseases, and many are discovered with screenings of children and adults. But a new study suggests that many disorders go undetected.

Continue reading “What’s Behind Many Mystery Ailments? Genetic Mutations, Study Finds”

Tracing Diseases to Their Dawns

One of the great milestones of medicine, as I write in my new book She Has Her Mother’s Laugh, was the discovery that some diseases are inherited–even when the parents of sick children seem perfectly healthy.

These hereditary diseases, known as recessive disorders, manifest themselves when both copies of a gene carry a disabling mutation. They include cystic fibrosis and Tay-Sachs disease. But the most striking of them all is sickle cell anemia. An unusually high number of people in some parts of the world are carriers of the disease, because having a single copy of the sickle cell mutation can actually be good for your health. Continue reading “Friday’s Elk, March 10, 2018”

The New York Times, March 8, 2018

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Thousands of years ago, a special child was born in the Sahara. At the time, this was not a desert; it was a green belt of savannas, woodlands, lakes and rivers. Bands of hunter-gatherers thrived there, catching fish and spearing hippos.

A genetic mutation had altered the child’s hemoglobin, the molecule in red blood cells that ferries oxygen through the body. It was not harmful; there are two copies of every gene, and the child’s other hemoglobin gene was normal. The child survived, had a family and passed down the mutation to future generations.

Continue reading “How One Child’s Sickle Cell Mutation Helped Protect the World From Malaria”