Clear Concepts
Genetics is complex, however we make it simple. Our team distills difficult topics into clear, digestible insights, perfect for students, clinicians, and curious minds alike.
Clinician-Curated
Every article is created by clinicians with real-world experience in medical genetics. No jargon, no fluff—just smart, accurate, and contextual information.
Open Access
Gene Commons is free, open, and community-driven. From deep-dives to quick guides, everything we publish is accessible to all, no paywalls, no ads.
Gene commons
Explore What Matters Most
At Gene Commons, we believe that clarity in genetics begins with curiosity.
Below are some of our most-read and thoughtfully curated categories, crafted for minds that seek both depth and direction.
Whether you’re here to learn, revisit, or discover something new, these are the topics worth your time.
Fetal medicine
Dive into prenatal scans, genetic testing in pregnancy, and the evaluation of fetal malformations.
Laboratory techniques
Learn how to interpret genetic tests like CMA, WES, MLPA, karyotyping, and more.
Syndromes
Explore detailed descriptions of genetic syndromes, their clinical features, and diagnostic approaches.
patient information
Simplified explanations of genetic conditions — written for families, patients, and anyone new to genetics.
About us
We’re a team of doctors and genetics enthusiasts who believe knowledge should be open, accurate, and compassionate. Gene Commons is our shared space to simplify complex genetics for students, families, and curious minds alike.
We’re not a company — we’re a mission.
We do this in our spare time, between clinics and classes, with the hope that no one feels alone or confused when facing a genetic diagnosis.
Why Gene Commons?
We believe no one should feel lost while navigating the maze of genetics.
Gene Commons was created by passionate clinicians who turn complex science into clarity — so that families, students, and young doctors can find comfort, answers, and hope.
Why Genetics is Hard to Grasp
Genetics is the blueprint of life—but decoding it is anything but simple.
Much of the information in this field is buried in technical jargon, published in research papers behind paywalls, or spread across expensive textbooks. Even for students and professionals, keeping up with rapidly evolving discoveries in genomics, bioinformatics, and molecular biology can be overwhelming.
Testimonials
Trusted by clinicians, students, and curious minds alike. Here’s what our readers say about Gene Commons:
Gene Commons website made by Dr. Sarath contains up to date well researched information presented in a lucid was that makes it extremely useful for any science enthusiast.
Dr. Soumalya
Unlocking the mysteries of DNA with sharper than a CRISPR cut. This site makes genetics, so fascinating, that even your double helix will want to unwind! A must read for budiing geneticists.
Dr. Ratna
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Dr. Praveen
What are you waiting for?
Curious about genetics? Need help decoding a report or understanding a rare disorder?
We’re here to make genetics simple, reliable, and accessible.
Reach out, we’d love to hear from you.
Our team
We are a team of geneticists, researchers, designers, and educators who believe that knowledge about our DNA should not be locked behind jargon or paywalls. We’re here to make genetics simple, open, and accessible for everyone.
Sarath
Founder
Olivia Rodriguez
Financial Analyst
Son Rodriguez
Financial Analyst
Our Impact in Numbers
Every number reflects a step toward making genetics easier to access, understand, and use in real life.
Articles
100
Doubts Cleared
110
Community reach
5,000
contributers
3
Explore Our Blog
Urine Reducing Substances: A Quick Bedside Clue Using Benedict’s Test
Learn how the Benedict’s test helps detect reducing substances in urine, including glucose, galactose, and fructose. Understand[…]
Designing Primers for PCR/Sanger Sequencing Using Ensembl and NCBI Primer-BLAST: Step-by-Step Guide
Learn how to design PCR/Sanger sequencing primers using Ensembl and NCBI Primer-BLAST with a real-life example. A[…]
Prenatal USG in Lethal Skeletal Dysplasias: A Clinical Geneticist’s Toolkit
Learn how clinical geneticists can interpret key ultrasound markers to identify lethal skeletal dysplasias early and accurately[…]
Contact us
Have questions, suggestions, or just want to say hi? We’d love to hear from you! Reach out to us anytime via email or social media. Your feedback helps us grow and serve better.