Search Results - Goetz, Kerry

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  1. 1
    Molecular Docking Interaction Between Carotenoids and Curcumin and RAGE Receptor Prevents Diabetic Retinopathy Progression (P06-044-19)

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

    Published 2019
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  2. 2
    eyeGENE(R): a novel approach to combine clinical testing and researching genetic ocular disease

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

    Published 2012
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  3. 3
    Molecular Diagnostic Testing by eyeGENE: Analysis of Patients With Hereditary Retinal Dystrophy Phenotypes Involving Central Vision Loss

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

    Published 2014
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  4. 4
    Genotype-phenotype associations in a large PRPH2-related retinopathy cohort

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

    Published 2020
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  5. 5
    Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network

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

    Published 2020
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  6. 6
    Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa

    Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa by 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.

    Published 2013
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  7. 7
    Sample Confirmation Testing: A Short Tandem Repeat-Based Quality Assurance and Quality Control Procedure for the eyeGENE Biorepository

    Sample Confirmation Testing: A Short Tandem Repeat-Based Quality Assurance and Quality Control Procedure for the eyeGENE Biorepository by 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.

    Published 2016
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  8. 8
    Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy

    Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy by 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

    Published 2020
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  9. 9
    Improving the value of clinical research through the use of Common Data Elements (CDEs)

    Improving the value of clinical research through the use of Common Data Elements (CDEs) by 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

    Published 2016
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  10. 10
    Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases

    Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases by 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

    Published 2021
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  11. 11
    Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses

    Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses by 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.

    Published 2022
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  12. 12
    Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses

    Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses by 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.

    Published 2022
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  13. 13
    Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease

    Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease by 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

    Published 2022
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