Lukas Lange

@thisislukasl

CEO & Co-Founder | alumni | Genetics PhD cand. at | scholar

Oxford, England
probablygenetic.com
Vrijeme pridruživanja: travanj 2011.
4 fotografije ili videozapisa Fotografije i videozapisi

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  1. 23. sij

    Worked for and looking for a gig in genetics with the potential to help 200 million rare genetic disease patients? Hmu, DMs are open!

    23andMe laying off 14% of employees amid falling spit kit sales
    3 proslijeđena tweeta 10 korisnika označava da im se sviđa
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  2. proslijedio/la je Tweet
    23. sij

    "I visited over 40 doctors as well as health care practitioners & had what seems like dozens of doctor’s visits. Why did it take years for me to be diagnosed? Why didn’t my doctors believe me when I told them something was wrong?"

    25 proslijeđenih tweetova 53 korisnika označavaju da im se sviđa
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  3. 23. sij

    We're excited to work with to help his family find answers!

    . is helping me with my oldest, who suffers from multiple rare genetic diseases. If you're in need of whole genome sequencing, but haven't been able to, please check them out. They can help. Use code "theautismdad100" and save $100.
    4 proslijeđena tweeta 8 korisnika označava da im se sviđa
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  4. 25. pro 2019.

    Happy holidays from the team 🎄 🎅🏽 🎉!!

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  5. 18. pro 2019.

    If you're a disease patient, parent or care for someone on the , get in touch!

    4 proslijeđena tweeta 7 korisnika označava da im se sviđa
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  6. 18. pro 2019.

    None of this would have been possible without the mentorship of

    1 reply 7 korisnika označava da im se sviđa
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  7. 18. pro 2019.

    I couldn't be more proud of our amazing team and am so grateful to everyone who has supported us along the way

    1 reply 2 proslijeđena tweeta 5 korisnika označava da im se sviđa
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  8. 18. pro 2019.

    1 long year of work and we're finally there! We just launched the best value clinical-grade genetic test on the market & will keep working tirelessly to make a difference for the patients world-wide. Get yours now at

    In the last year we’ve talked with hundreds of families about their struggles getting access to care and meaningful answers about their (or their children’s) conditions. It’s amazing how broken this system is…(1/7)
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    1 reply 6 proslijeđenih tweetova 18 korisnika označava da im se sviđa
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  9. 11. pro 2019.

    🙌

    . is TIME's 2019 Person of the Year
    1 korisnik označava da mu se sviđa
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  10. proslijedio/la je Tweet
    3. pro 2019.
    Odgovor korisniku/ci

    Thank you for your leadership you are a pioneer in improving the diagnostic odyssey.

    2 proslijeđena tweeta 3 korisnika označavaju da im se sviđa
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  11. 12. stu 2019.

    Another story about the Vega family She began to talk — then mysteriously fell silent. Months later her parents learned why (2/2)

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  12. 12. stu 2019.

    What the diagnostic odyssey looks like, all the best to the Bruner family (1/2) Praying for a cure: Genetic test uncovers Florida girl's extremely rare disorder

    1 reply 1 korisnik označava da mu se sviđa
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  13. 9. stu 2019.

    How many rare diseases are there? Latest estimates suggest ~10,000, with rare disease patients constituting up to 10% of the population

    1 reply 23 proslijeđena tweeta 29 korisnika označava da im se sviđa
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  14. 23. lis 2019.

    Cc

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  15. 23. lis 2019.

    twitter: who are the best for you know? Looking for someone w/ empathy & intuition for how to communicate results to rare Moms

    6 replies 2 proslijeđena tweeta 8 korisnika označava da im se sviđa
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  16. proslijedio/la je Tweet
    10. lis 2019.

    My University was going to throw away what I think was the first Illumina HiSeq 1000 shipped to Europe. I moved the HiSeq in my office, and transformed it in the most expensive (and technologically advanced, although a little noisy) refrigerator I ever had.

    60 replies 508 proslijeđenih tweetova 3.490 korisnika označava da im se sviđa
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  17. proslijedio/la je Tweet
    8. lis 2019.

    Mama bear thread: Last night, ⁦⁩ aired a beautiful interview, conducted by ⁦⁩, with our family. For the first time, on camera, we shared that our baby girl is dying. 1/

    38 replies 27 proslijeđenih tweetova 315 korisnika označava da im se sviđa
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  18. 18. ruj 2019.

    Super excited to read ‘s new book! 💥🤓🎊🎉

    2 proslijeđena tweeta 5 korisnika označava da im se sviđa
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  19. proslijedio/la je Tweet
    16. ruj 2019.

    New blog post alert!💫"How Social Media Helps the Rare Disease Community" is up on our Medium publication and ready for you to read and share.

    7 proslijeđenih tweetova 13 korisnika označava da im se sviđa
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  20. proslijedio/la je Tweet
    14. ruj 2019.

    Rare genetic conditions can take up to 7 years to identify. During the , patients are often misdiagnosed and left searching for answers. How long was your diagnostic odyssey?

    5 proslijeđenih tweetova 7 korisnika označava da im se sviđa
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