
The Department of Molecular and Human Genetics at @BCMHouston is transforming medicine, research, and education in genetics and genomics.
Houston, TX
Joined September 2021
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.@BCMHouston has received more than $6M from @NIH to lead the new Peroxisomal Disorders Consortium. Led by Dr. Michael Wangler @mfwangler, it will advance research into rare genetic disorders affecting multiple organ systems. bit.ly/3WE3yhg
Got a Variant? Watch the video to learn how the @BCMHouston Center for Precision Medicine Models helps #undiagnosed individuals find answers by developing models to investigate genetic variants to better understand their role in disease. youtube.com/watch?v=yAdof0ZZ…
New research from Dr. Seema Lalani, Blake Vuocolo, et. al. shows how virtual genetic evaluation & genome sequencing has helped to uncover genetic causes of hearing loss in children along the Texas–Mexico border. texaschildrens.org/content/r…
Read more about Blake Vuocolo's presentation on the @GeneticsSociety web site: ashg.org/publications-news/p…
BCM Department of Molecular and Human Genetics retweeted
At #ASHG26, Baylor Genetics is presenting research on the diagnostic utility of genome sequencing, developmental and epileptic encephalopathy, and clinical mitochondrial testing.
Visit booth #500 to connect with our team and learn more: baylorgenetics.com/conferenc…
@GeneticsSociety
BCM Department of Molecular and Human Genetics retweeted
Every discovery can expand our understanding of rare & complex genetic conditions. At #ASHG26, Baylor Genetics is presenting research on how advanced genomic technologies can improve diagnosis & inform clinical care.
Visit booth #500: baylorgenetics.com/conferenc…
@GeneticsSociety
BCM Department of Molecular and Human Genetics retweeted
I am very excited we are starting this NIH funded research project. It is a solemn privilege to do this work. I’ve been working on diseases of the Peroxisome for nearly 20 years now. We have so far to go in terms of treating these disorders. I have met many remarkable patients, families, doctors and scientists. Now a group of us can formally organize clinical research in centers from east to west, and give families hubs to share data centralize samples and move forward towards better treatment.
.@BCMHouston has received more than $6M from @NIH to lead the new Peroxisomal Disorders Consortium. Led by Dr. Michael Wangler @mfwangler, it will advance research into rare genetic disorders affecting multiple organ systems. bit.ly/3WE3yhg
BCM Department of Molecular and Human Genetics retweeted
Researchers uncovered how two major cellular signaling pathways cooperate to fuel #kidneycyst formation and #tumor development. #KidneyCancer @bcmhouston @TexasChildrens #TFEB #TFE3 Find the paper here: nature.com/articles/s41418-0… @bcmgenetics texaschildrens.org/content/r…
BCM Department of Molecular and Human Genetics retweeted
H. Zoghbi, @RMeyerSchuman et al explain how their findings can help explain the predominance of #autism in males vs females @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics bcm.edu/news/new-genetic-can…
BCM Department of Molecular and Human Genetics retweeted
New genetic candidates help explain why #autism affects males more often than females. H. Zoghbi, @RMeyerSchuman explain their findings in this interview.eurekalert.org/news-releases… @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics @EurekAlertAAAS
Congratulations to Dr. Huda Zoghbi on being named the 2026 recipient of the Mendel Medal! Read more about the award from @VillanovaU villanova.edu/university/med…
Villanova University has named renowned molecular geneticist Huda Zoghbi, MD, the 2026 recipient of the Mendel Medal, recognizing her groundbreaking research into the genetic causes of neurological disorders.
Read more: villanova.edu/university/med…
BCM Department of Molecular and Human Genetics retweeted
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 genengnews.com/topics/omics/…
BCM Department of Molecular and Human Genetics retweeted
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 bcm.edu/news/together-human-…
BCM Department of Molecular and Human Genetics retweeted
Kevin Mitchell @WiringTheBrain talks with Huda Zoghbi about her work identifying the #MECP2 gene, its role in the brain and therapies to address its dysfunction. @bcmhouston @bcmgenetics thetransmitter.org/spectrum/…
BCM Department of Molecular and Human Genetics retweeted
Celebrate #NationalPostdocAppreciationWeek @bcmhouston! Take a look at a sample of the work conducted by #Baylor #postdocs. #PAW26 @Evelin_Y_ @bcmgenetics @BCMDeptMedicine @BCMCancerCenter @TexasChildrens blogs.bcm.edu/2026/09/24/nat…
Congratulations to Yichi Niu of the Zong Lab on receiving the 2026 Shan and Lee-Jun Wong Fellowship for the project, "Investigating mtDNA Mutations and Heteroplasmy in Mitochondrial Disease at Single-Cell Resolution."
Congratulations to the 2026 Rolanette & Berdon Lawrence Family Achievement Award in Genetics Winners: Dr. Chonghui Cheng (Faculty), Betty Fernandini (Administrative/Clinical Staff), Rebecca Maywald (Scientific Staff) and Yan Li (Trainee).
Don't forget! Our next Evenings with Genetics webinar is less than a week away. We hope you will join us next Tuesday, Sept. 29 at 7 p.m. to learn more about the Undiagnosed Disease Network. Sign up today: bit.ly/3RKROb0 #undiagnoseddisease #raredisease
Searching for answers? Join us Sept. 29 at 7 p.m. CST for a free Evenings with Genetics webinar to learn how the Undiagnosed Diseases Network (UDN) helps families pursue answers through genetic evaluation and collaborative research. Register: bit.ly/3RKROb0
BCM Department of Molecular and Human Genetics retweeted
How do alterations to an #ionChannel that governs neuronal excitability may result in pervasive alterations in spontaneous #behavior? Check the new paper by V. Krishnan, AD Mazumder, J Noebels et al in #Brain @OUPAcademic @bcmhouston @bcmneurology academic.oup.com/brain/advan…
BCM Department of Molecular and Human Genetics retweeted
A new rare genetic variant has been identified as a new cause of #neurodevelopmentalDisorders. #BMPR2 S. Yamamoto, @DamianYoung29, @mfwangler, H. Bellen et al. @AJHGNews @bcmhouston @TexasChildrens @bcmgenetics @bcm_neurosci bcm.edu/news/researchers-ide…




















