AJHG

The American Journal of Human Genetics

[From the Labs at Baylor College of Medicine @BCMFromtheLabs]

Researchers have identified new genetic candidates that help explain why #autism is diagnosed about four times more often in boys than in girls. H Zoghbi, @RMeyerSchuman et al explain their findings in @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics https://t.co/rO7JXpMtzh

[From the Labs at Baylor College of Medicine @BCMFromtheLabs]

New genetic candidates help explain why #autism affects males more often than females. H. Zoghbi, @RMeyerSchuman explain their findings in this interview.https://t.co/Y2xk64TJDw @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics @EurekAlertAAAS

[Rebecca Meyer-Schuman @RMeyerSchuman]

I'm excited to finally publish my postdoctoral work in
@AJHGNews! This work was motivated by two big mysteries in autism research: 1) where and what are the undiscovered genetic components of autism, and 2) why are males diagnosed with autism more frequently than females?

[ASHG @GeneticsSociety]

Meet AJHG (@AJHGNews) author and researcher Sarah Vergult, PhD. Learn about their experience of publishing in AJHG and their research: https://t.co/jpmUPPRT5Q #ASHG #HumanGenetics

[Cell Press @CellPressNews]

How to create personalized gene editing platforms: Next steps toward interventional genetics by @AhrensNicklas and @kiranmusunuru https://t.co/ujQdzBX0NU
@AJHGNews (@GeneticsSociety) highlight from the best of collection 2025-2026

[AJHG @AJHGNews]

🧬New from Meyer-Schuman et al!
📄A massively parallel reporter assay of MECP2cis-regulatory elements reveals genetic candidates for male-biased autism
https://t.co/Q68GrwTv5c

[ASHG @GeneticsSociety]

.@konradjk & colleagues of @AJHGNews' latest article introduce ALLSPICE, a new framework for identifying cross-phenotype effect-size heterogeneity and resolving the architecture of rare variant pleiotropy: https://t.co/NpXnk7aLFU #ASHG #humangenetics #geneticsdiscoveries

[Cell Press @CellPressNews]

Explore a selection of best papers from 2025-26 from @AJHGNews and @HGGAdvances showcasing influential discoveries and emerging technologies that are shaping the future of human genetics, precision diagnostics, and equitable genomic care.
https://t.co/ocsCZvLOjx
@GeneticsSociety

[Sinai Health @SinaiHealth]

🧬 An expert team led by Sinai Health's Dr. Jordan Lerner-Ellis has released recommendations in @AJHGNews to align genetic data sharing across Canadian clinical labs, strengthening patient privacy and professional trust.

Read the paper ➡️ https://t.co/FWnDgnxtLW

[AJHG @AJHGNews]

🧬New from Lin et al!
📄Hypomorphic IDUA genotypes are associated with retinitis pigmentosa in individuals without syndromic mucopolysaccharidosis type I
https://t.co/0r2rycapWs

[ASHG @GeneticsSociety]

.@AJHGNews is a home for discoveries, statistical methods, & ideas that move the field forward. Hear from Editorial Board member @LoicYengo, on why AJHG is a trusted destination for readers & researchers alike. Learn more & submit your work: https://t.co/JZAEc4BFxA #ASHG

[Konrad Platzer @platzer_k]

This sounds really helpful for the genetics community diagnosing patients on cancer susceptibility genes. @AJHGNews 👌 👇

https://t.co/B0ecEv2tTe

[ASHG @GeneticsSociety]

In @AJHGNews latest article, @ZornitzaS & colleagues highlight recent progress integrating genomics into newborn screening programs & discuss persistent challenges in standardization, scale, and equity: https://t.co/BU9wTYYtRK #ASHG #humangenetics #geneticsdiscoveries

[AJHG @AJHGNews]

Our October issue is online--check it out!
https://t.co/yT3q5AtRaa

[AJHG @AJHGNews]

🧬New Research Letter!
📄MMACHC burden variants are associated with higher circulating vitamin B12 in the @AllofUsResearch cohort

https://t.co/Orngnj5k7l

[AJHG @AJHGNews]

🧬New today from Lu et al!
📄Effect heterogeneity reveals complex pleiotropic effects of rare coding variants
https://t.co/70rux1ufPC
🖥️https://t.co/69brLKtisA

[AJHG @AJHGNews]

🧬New from Macintosh et al!
📄Integrating clinical diagnostics with #interventionalgenetics for neurodevelopmental disorders
https://t.co/UkvTJcEn2F

[From the Labs at Baylor College of Medicine @BCMFromtheLabs]

A novel approach to diagnose rare, complex #neurodevelopmentalDisorders has brought answers to undiagnosed families. H. Bellen, M. Deng, @mfwangler et al. @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics #BRSK1 #fruitfly @genengnews https://t.co/qRGSPgFcIs

[From the Labs at Baylor College of Medicine @BCMFromtheLabs]

Together human #genetics, #AI and animal studies provide diagnosis for rare, complex #neurodevelopmentalDisorder. H. Bellen, M. Deng, @mfwangler et al. @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics #BRSK1 #fruitfly https://t.co/oTgrpEm5MR

[AJHG @AJHGNews]

🧬🪰 New from Deng et al!
📄Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy
https://t.co/TaqIOcRrHg