RNA-Seq DE Genes on Glioblastoma Using Non Linear SVM and Pathway Analysis of NOG and ASCL5 von Binoy, Sandra, Biju, Vinai George, Basilia, Cynthia, Mathew, Blessy B., Prashanth, C. M.

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Role of Arterial Lactate and Lactate Clearance in Risk Stratification of Patients with Upper Gastrointestinal Bleeding Presenting to the Emergency Department for use at Primary Hea... von Kaliparambil, Binoy Xavier, Maprani, Jobin Jose, Paulson, Sandra

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2021 Asia‐Pacific League of Associations for Rheumatology clinical practice guideline for treatment of gout von Lorenzo, Jose Paulo P., Sollano, Ma. Hanna Monica Z., Salido, Evelyn O., Li‐Yu, Julie, Tankeh‐Torres, Sandra A., Wulansari Manuaba, Ida Ayu Ratih, Rahman, Md Mujibur, Paul, Binoy J., Mok, Mo Yin, De Silva, Monika, Padhan, Prasanta, Lim, Ai Lee, Marcial, Melvin, Vicera, Jennifer Jeanne, Haq, Syed Atiqul, Salman, Sami, Liyanage, Chiranthi K., Keen, Helen I., Yew Kuang, Cheng, Wei, James Cheng‐Chung, Hellmi, Rakhma Yanti, Chan, Charlie E., Louthrenoo, Worawit

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Endothelial-to-Mesenchymal Transition in Human and Murine Models of Congenital Diaphragmatic Hernia von Gilley, Jamie, Hanneman, Sandra K., Ottosen, Madelene J., Shivanna, Binoy, Keswani, Sundeep

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Metabolome and microbiome multi-omics integration from a murine lung inflammation model of bronchopulmonary dysplasia von El Saie, Ahmed, Fu, Chenlian, Grimm, Sandra L., Robertson, Matthew J., Hoffman, Kristi, Putluri, Vasanta, Ambati, Chandra Shekar R., Putluri, Nagireddy, Shivanna, Binoy, Coarfa, Cristian, Pammi, Mohan

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Leveraging Integrated RNA Sequencing to Decipher Adrenomedullin's Protective Mechanisms in Experimental Bronchopulmonary Dysplasia von Palit, Subarna, Shrestha, Amrit Kumar, Thapa, Shyam, L Grimm, Sandra, Coarfa, Cristian, Theis, Fabian, Simon, Lukas M, Shivanna, Binoy

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Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31 von Appukuttan, Binoy, Gillanders, Elizabeth, Juo, Suh-Hang, Freas-Lutz, Diana, Ott, Sandra, Sood, Raman, Van Auken, Ann, Bailey-Wilson, Joan, Wang, Xiaoguang, Patel, Reshma J., Robbins, Christiane M., Chung, Mina, Annett, Geralyn, Weinberg, Kenneth, Borchert, Mark S., Trent, Jeffrey M., Brownstein, Michael J., Stout, J. Timothy

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DNA-based diagnosis of the von Hippel–Lindau syndrome von Patel, Reshma J, Appukuttan, Binoy, Ott, Sandra, Wang, Xiaoguang, Stout, J.Timothy

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Exclusion of candidate genetic loci for Duane retraction syndrome von Ott, Sandra, Borchert, Mark, Chung, Mina, Appukuttan, Binoy, Wang, Xiaoguang, Weinberg, Kenneth, Stout, J.Timothy

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A novel mutation in the Norrie disease gene von Ott, Sandra, Patel, Reshma J., Appukuttan, Binoy, Wang, Xiaoguang, Stout, J.Timothy

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Isolation and characterization of the human homeobox gene HOX D1 von Appukuttan, B, Sood, R, Ott, S, Makalowska, I, Patel, R J, Wang, X, Robbins, C M, Brownstein, M J, Stout, J T

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Cliical phenotype associated with the arg 141 his mutation in the x-linkd retinoschisis gene von Park, Jeong-Hee C, Ott, Sandra H, Wang, Xiaoguang, Appukuttan, Binoy

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Clinical Phenotype Associated With the Arg141His Mutation in the X-linked Retinoschisis Gene von Park, Jeong-Hee C, Ott, Sandra H, Wang, Xiaoguang, Appukuttan, Binoy, Patel, Reshma J, Van Boemel, Gretchen B, Stout, J. Timothy

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