Výsledky vyhledávání - Goetz, Kerry
- Zobrazuji výsledky 1 - 13 z 13
-
1
-
2
-
3
Molecular Diagnostic Testing by eyeGENE: Analysis of Patients With Hereditary Retinal Dystrophy Phenotypes Involving Central Vision Loss Autor Alapati, Akhila, Goetz, Kerry, Suk, John, Navani, Mili, Al-Tarouti, Amani, Jayasundera, Thiran, Tumminia, Santa J., Lee, Pauline, Ayyagari, Radha
Vydáno 2014Text -
4
-
5
Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network Autor Goetz, Kerry E., Reeves, Melissa J., Gagadam, Shaina, Blain, Delphine, Bender, Chelsea, Lwin, Cara, Naik, Amelia, Tumminia, Santa J., Hufnagel, Robert B.
Vydáno 2020Text -
6
Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa Autor 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.
Vydáno 2013Text -
7
Sample Confirmation Testing: A Short Tandem Repeat-Based Quality Assurance and Quality Control Procedure for the eyeGENE Biorepository Autor 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.
Vydáno 2016Text -
8
Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy Autor 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
Vydáno 2020Text -
9
Improving the value of clinical research through the use of Common Data Elements (CDEs) Autor 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
Vydáno 2016Text -
10
Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases Autor 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
Vydáno 2021Text -
11
Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses Autor 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.
Vydáno 2022Text -
12
Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses Autor 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.
Vydáno 2022Text -
13
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease Autor 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
Vydáno 2022Text