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American Journal of Medical Genetics. Part A|February 5, 2016
ADAT3-related intellectual disability: Further delineation of the phenotypeAyman W El-Hattab, Mohammed A Saleh, Amal Hashem, et al.American Journal of Human Genetics|May 6, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen SyndromeNisha Patel, Hanan E Shamseldin, Nadia Sakati, et al.Nature|July 10, 2024
Dissociable hindbrain GLP1R circuits for satiety and aversionKuei-Pin Huang, Alisha A Acosta, Misgana Y Ghidewon, et al.Cell Reports|October 27, 2016
Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the RetinaHelen L May-Simera, Jessica D Gumerson, Chun Gao, et al.Blood Advances|November 8, 2023
Transient responses and significant toxicities of anti-CD30 CAR T cells for CD30+ lymphomas: results of a phase 1 trialJennifer N Brudno, Danielle A Natrakul, Jeremiah Karrs, et al.Medical Dosimetry : Official Journal of the American Association of Medical Dosimetrists|November 19, 2013
Bilateral implant reconstruction does not affect the quality of postmastectomy radiation therapyAlice Y Ho, Nisha Patel, Nisha Ohri, et al.Biorxiv : the Preprint Server for Biology|April 16, 2025
Molecular basis for multidrug efflux by an anaerobic RND transporterRyan Lawrence, Mohd Athar, Muhammad R Uddin, et al.Antioxidants (Basel, Switzerland)|October 26, 2024
PET Imaging with [18F]ROStrace Detects Oxidative Stress and Predicts Parkinson's Disease Progression in MiceYi Zhu, Neha Kohli, Anthony Young, et al.Nature Communications|December 3, 2025
Molecular basis for multidrug efflux by an anaerobic-associated RND transporterRyan Lawrence, Mohd Athar, Muhammad R Uddin, et al.Genome Biology|July 30, 2017
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutationNisha Patel, Arif O Khan, Maher Al-Saif, et al.Pageof 21