检索结果 - Goetz, Kerry

Molecular Docking Interaction Between Carotenoids and Curcumin and RAGE Receptor Prevents Diabetic Retinopathy Progression (P06-044-19) 由 Sriramoju, Swetha, Goetz, Kerry

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eyeGENE(R): a novel approach to combine clinical testing and researching genetic ocular disease 由 Goetz, Kerry E., Reeves, Melissa J., Tumminia, Santa J., Brooks, Brian P.

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Molecular Diagnostic Testing by eyeGENE: Analysis of Patients With Hereditary Retinal Dystrophy Phenotypes Involving Central Vision Loss 由 Alapati, Akhila, Goetz, Kerry, Suk, John, Navani, Mili, Al-Tarouti, Amani, Jayasundera, Thiran, Tumminia, Santa J., Lee, Pauline, Ayyagari, Radha

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Genotype-phenotype associations in a large PRPH2-related retinopathy cohort 由 Reeves, Melissa J., Goetz, Kerry E., Guan, Bin, Ullah, Ehsan, Blain, Delphine, Zein, Wadih M., Tumminia, Santa J., Hufnagel, Robert B.

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Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network 由 Goetz, Kerry E., Reeves, Melissa J., Gagadam, Shaina, Blain, Delphine, Bender, Chelsea, Lwin, Cara, Naik, Amelia, Tumminia, Santa J., Hufnagel, Robert B.

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Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa 由 Sullivan, Lori S., Bowne, Sara J., Reeves, Melissa J., Blain, Delphine, Goetz, Kerry, NDifor, Vida, Vitez, Sally, Wang, Xinjing, Tumminia, Santa J., Daiger, Stephen P.

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Sample Confirmation Testing: A Short Tandem Repeat-Based Quality Assurance and Quality Control Procedure for the eyeGENE Biorepository 由 Parrish, Rebecca S., Garafalo, Alexandra V., Ndifor, Vida, Goetz, Kerry E., Reeves, Melissa J., Yim, Annette, Cooper, Remy C., Iano-Fletcher, Jemma, Wang, Xinjing, Tumminia, Santa J.

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Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy 由 Xu, Shunbin, Coku, Ardian, Muraleedharan, Chithra K., Harajli, Ali, Mishulin, Eric, Dahabra, Chafic, Choi, Joanne, Garcia, William J., Webb, Kaylie, Birch, David, Goetz, Kerry, Li, Weifeng

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Improving the value of clinical research through the use of Common Data Elements (CDEs) 由 Sheehan, Jerry, Hirschfeld, Steven, Foster, Erin, Ghitza, Udi, Goetz, Kerry, Karpinski, Joanna, Lang, Lisa, Moser, Richard P., Odenkirchen, Joanne, Reeves, Dianne, Rubinstein, Yaffa, Werner, Ellen, Huerta, Michael

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Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases 由 Qian, Xinye, Wang, Jun, Wang, Meng, Igelman, Austin D., Jones, Kaylie D., Li, Yumei, Wang, Keqing, Goetz, Kerry E., Birch, David G., Yang, Paul, Pennesi, Mark E., Chen, Rui

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Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses 由 Madlock-Brown, Charisse, Wilkens, Ken, Weiskopf, Nicole, Cesare, Nina, Bhattacharyya, Sharmodeep, Riches, Naomi O., Espinoza, Juan, Dorr, David, Goetz, Kerry, Phuong, Jimmy, Sule, Anupam, Kharrazi, Hadi, Liu, Feifan, Lemon, Cindy, Adams, William G.

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Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses 由 Madlock-Brown, Charisse, Wilkens, Ken, Weiskopf, Nicole, Cesare, Nina, Bhattacharyya, Sharmodeep, Riches, Naomi O., Espinoza, Juan, Dorr, David, Goetz, Kerry, Phuong, Jimmy, Sule, Anupam, Kharrazi, Hadi, Liu, Feifan, Lemon, Cindy, Adams, William G.

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Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease 由 Zernant, Jana, Lee, Winston, Wang, Jun, Goetz, Kerry, Ullah, Ehsan, Nagasaki, Takayuki, Su, Pei-Yin, Fishman, Gerald A., Tsang, Stephen H., Tumminia, Santa J., Brooks, Brian P., Hufnagel, Robert B., Chen, Rui, Allikmets, Rando

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