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Brendan Lee

Affiliations: 
Chair of Genetics Baylor College of Medicine, Houston, TX 
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"Brendan Lee"
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Parents

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Gerard Karsenty post-doc Baylor College of Medicine
Francesco Ramirez post-doc Mount Sinai School of Medicine

Children

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Feyza Engin post-doc University of Wisconsin School of Medicine and Public Health
Roy Morello post-doc UAMS

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Publications

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Couasnay G, Madel MB, Lim J, et al. (2021) Sites of Cre-recombinase activity in mouse lines targeting skeletal cells. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research
Rauch D, Robinson ME, Seiltgens C, et al. (2020) Assessment of Longitudinal Bone Growth in Osteogenesis Imperfecta Using Metacarpophalangeal Pattern Profiles. Bone. 115547
Stroup BM, Marom R, Li X, et al. (2020) A Global Slc7a7 Knockout Mouse Model Demonstrates Characteristic Phenotypes of Human Lysinuric Protein Intolerance. Human Molecular Genetics
Samsa WE, Mamidi MK, Bashur LA, et al. (2020) The crucial p53-dependent oncogenic role of JAB1 in osteosarcoma in vivo. Oncogene
Chung HL, Wangler MF, Marcogliese PC, et al. (2020) Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron
Ortinau LC, Wang H, Lei K, et al. (2019) Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells. Cell Stem Cell. 25: 784-796.e5
Cho KY, Kelley BP, Monier D, et al. (2019) Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion. Frontiers in Physiology. 10: 513
Kruger KM, Caudill A, Rodriguez Celin M, et al. (2019) Mobility in osteogenesis imperfecta: a multicenter North American study. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Burrage LC, Reynolds JJ, Baratang NV, et al. (2019) Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. American Journal of Human Genetics
Retrouvey JM, Taqi D, Tamimi F, et al. (2018) Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V. European Journal of Medical Genetics
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