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NEW BRAIN TUMOR DATASET AVAILABLE Learn More

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THE VALUE OF KIDS FIRST

KIDS COME FIRST IN SCIENTIFIC RESEARCH

Thousands of children are diagnosed with cancer and congenital disorders each year, impacting families emotionally and financially. The Gabriella Miller Kids First Pediatric Research Program (Kids First), funded  and administered by the National Institutes of Health (NIH) Common Fund, aims to alleviate some of that hardship by improving how we diagnose, treat, and eventually eliminate these threats. This program is a valuable resource for researchers and is a critical investment in pediatric research.

The Kids First Data Resource Center (Kids First DRC) provides robust genetic and clinical data for pediatric cancer and congenital disorders. Kids First data is accessible to researchers worldwide, free of charge, to help us understand these diseases better.

While this valuable program is funded through 2024, Kids First needs continued support to pursue its essential work well into the future.

DISCOVER A NEW APPROACH TO RESEARCH

Kids First is the leading global contributor of pediatric studies for research

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35
STUDIES
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550
DATA ACCESS REQUESTS
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6,500
ANNUAL USER SESSIONS
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100
SAMPLES
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188
FILES
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27000
PATIENT AND FAMILY PARTICIPANTS
Gabriella Miller

STOP TALKING, START DOING

Gabriella’s Story

The Gabriella Miller Kids First Research Act was enacted in April 2014, less than six months after 10-year-old child cancer research advocate Gabriella Miller died from an inoperable brain tumor.

Her efforts to raise childhood cancer awareness, and its connection to congenital disorders, raised hundreds of thousands of dollars for children’s cancer charities. Through her passionate advocacy, Congress passed the Gabriella Miller Kids First Research Act to direct funding into the NIH Common Fund over ten years to support pediatric research.

Gabriella’s mother, Ellyn Miller, continues her daughter’s work to demand better treatments and cures for kids through the Smashing Walnuts Foundation.

GET THE LATEST KIDS FIRST STUDIES

Sign up to receive updates and new data announcements from the Gabriella Miller Kids First Data Resource Center

JOIN OUR ONLINE COMMUNITY

Check out the latest news and updates from the Kids First DRC

Follow @kidsfirstdrc

Email info@kidsfirstdrc.org

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News & Articles

October 15, 2024 in Press

Children’s Brain Tumor Network Dataset Now Accessible on Kids First Data Resource Center Portal

View this press release on PR Newswire  The Gabriella Miller Kids First Data Resource Center (Kids First DRC) announces the addition of the full Children’s Brain Tumor Network (CBTN) dataset…
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September 6, 2024 in Press

NIH Kids First Program announces the release of three new pediatric research datasets exploring childhood rare disease

These new datasets further support the effort to understand the genetic causes and links between childhood cancers and congenital disorders. WHO: The Gabriella Miller Kids First Pediatric Research Program (Kids…
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June 13, 2024 in Articles

Revolutionizing Pediatric Research: Unveiling the Enhanced Beta Portal

A New Chapter in Pediatric Research In a landmark move poised to transform research for rare congenital disorders and childhood cancers, the Gabriella Miller Kids First Pediatric Research Program Data…
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January 28, 2024 in Articles

NCI Pre-Application Webinar for RFA-CA-19-033: Improving Outcomes for Pediatric, Adolescent and Young Adult Cancer Survivors

On January 31, 2019 from 1:00 to 2:00 p.m. EST, the National Cancer Institute’s (NCI) Division of Cancer Control and Population Sciences (DCCPS) will host a webinar to discuss the Funding…
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