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Xu M, Ouyang Q., Gong J., Pescosolido M.F., Pruett B.S., Mishra S., Schmidt M., Jones R.N., Gamsiz Uzun E.D., Lizarraga S.B., Morrow E.M.
"Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome." e-neuro, vol. 4, no. 6, 2017.
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Gamsiz ED, Sciarra LN, Maguire AM, Pescosolido MF, van Dyck LI, Morrow EM.
"Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms." Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, vol. 12, no. 3, 2015, pp. 553-71.
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Harrison, Ashley J., Gamsiz, Ece D., Berkowitz, Isaac C., Nagpal, Shailender, Jerskey, Beth A.
"Genetic variation in the oxytocin receptor gene is associated with a social phenotype in autism spectrum disorders." Am. J. Med. Genet., vol. 168, no. 8, 2015, pp. 720-729.
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Pescosolido, Matthew F, Schwede, Matthew, Johnson Harrison, Ashley, Schmidt, Michael, Gamsiz, Ece D, Chen, Wendy S, Donahue, John P, Shur, Natasha, Jerskey, Beth A, Phornphutkul, Chanika, Morrow, Eric M.
"Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein." Journal of Medical Genetics, vol. 51, no. 9, 2014, pp. 587-9.
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Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.
"Distribution of Disease-Associated Copy Number Variants Across Distinct Disorders of Cognitive Development." Journal of the American Academy of Child & Adolescent Psychiatry, vol. 52, no. 4, 2013, pp. 414-430.e14.
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Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M; Simons Simplex Collection Genetics Consortium, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH Jr, Devlin B, Morrow EM.
"Intellectual disability is associated with increased runs of homozygosity in simplex autism." American Journal of Human Genetics, vol. 93, no. 1, 2013, pp. 103-9.
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Gamsiz, Ece D., Thombre, Avinash G., Ahmed, Imran, Carrier, Rebecca L.
"Model predicting impact of complexation with cyclodextrins on oral absorption." Biotechnology and Bioengineering, vol. 110, no. 9, 2013, pp. 2536-2547.
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Gamsiz ED, Ouyang Q, Schmidt M, Nagpal S, Morrow EM.
"Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing." Genomics, vol. 99, no. 1, 2012, pp. 44-51.
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Gamsiz, Ece Dilber, Thombre, Avinash G., Ahmed, Imran, Carrier, Rebecca Lyn.
"Drug Salts and Solubilization: Modeling the Influence of Cyclodextrins on Oral Absorption." Annals of Biomedical Engineering, vol. 39, no. 1, 2010, pp. 455-468.
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Gamsiz, Ece Dilber, Miller, Lee, Thombre, Avinash G., Ahmed, Imran, Carrier, Rebecca Lyn.
"Modeling the influence of cyclodextrins on oral absorption of low solubility drugs: II. Experimental validation." Biotechnology and Bioengineering, vol. 105, no. 2, 2010, pp. 421-430.
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Gamsiz, Ece Dilber, Miller, Lee, Thombre, Avinash G., Ahmed, Imran, Carrier, Rebecca Lyn.
"Modeling the influence of cyclodextrins on oral absorption of low-solubility drugs: I. Model development." Biotechnology and Bioengineering, vol. 105, no. 2, 2010, pp. 409-420.
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Gamsiz, Ece Dilber, Ashtikar, Mukul, Crison, John, Woltosz, Walt, Bolger, Michael B., Carrier, Rebecca Lyn.
"Predicting the Effect of Fed-State Intestinal Contents on Drug Dissolution." Pharmaceutical Research, vol. 27, no. 12, 2010, pp. 2646-2656.
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Ece Gamsiz, D., Shah, Lipa K., Devalapally, Harikrishna, Amiji, Mansoor M., Carrier, Rebecca L.
"A model predicting delivery of saquinavir in nanoparticles to human monocyte/macrophage (Mo/Mac) cells." Biotechnology and Bioengineering, vol. 101, no. 5, 2008, pp. 1072-1082.
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DNA markers in low-IQ autism suggest heredity
