Baylor Genetics

Research facility

Location: Houston, TX

ISNI: -

Publications

(5)

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies. (2025) Kalanithy JC, Mingardo E, Stegmann JD, Dhakar R, Dakal TC, Rosenfeld JA, Tan WH, et al. Journal article Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders (2021) Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, et al. Journal article Pan-omics focused to Crick's central dogma (2020) Jaiswal AK, Tiwari S, Tavares GC, Da Silva WM, Oliveira LDC, Ibraim IC, Guimaraes LC, et al. Book chapter / Article in edited volumes Fruits of Genomic Match-making: De Novo Variants in PRR12 are Associated with a Spectrum of Eye and Neurodevelopmental Anomalies (2019) Balci TB, Wang L, Lalani S, Heide S, Keren B, Mignot C, Morley G, et al. Conference contribution Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features (2017) Stankiewicz P, Khan TN, Szafranski P, Slattery L, Streff H, Vetrini F, Bernstein JA, et al. Journal article