Division of Pediatric Nephrology and Hypertension

Displaying 1 - 17 of 17CSV
Flatow, J. S., Byfield, R., Singer, J., Chang, M. J., Schwartz, J. E., Shimbo, D., & Kronish, I. M. (2024). Clinical Inertia in the Diagnosis and Management of Hypertension Following Ambulatory Blood Pressure Monitoring. American Journal of Hypertension. https://doi.org/10.1093/ajh/hpae157
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Liu, J., Brettler, J., Ramirez, U. A., Walsh, S., Sangapalaarachchi, D., Narita, K., Byfield, R. L., Reynolds, K., & Shimbo, D. (2024). Home Blood Pressure Monitoring. American Journal of Hypertension. https://doi.org/10.1093/ajh/hpae151
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South, A. M., Giammattei, V. C., Bagley, K. W., Bakhoum, C. Y., Beasley, W. H., Bily, M. B., Biswas, S., Bridges, A. M., Byfield, R. L., Campbell, J. F., Chanchlani, R., Chen, A., D’Agostino McGowan, L., Downs, S. M., Fergeson, G. M., Greenberg, J. H., Hill-Horowitz, T. A., Jensen, E. T., Kallash, M., … Weaver, D. J. (2024). The Study of the Epidemiology of Pediatric Hypertension Registry (SUPERHERO): rationale and methods. American Journal of Epidemiology, 193(12), 1650–1661. https://doi.org/10.1093/aje/kwae116
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Weiss, R., Milo Rasouly, H., Marasa, M., Fernandez, H., Lin, F., & Sabatello, M. (2024). Nephrologists’ Views on a Workflow for Returning Genetic Results to Research Participants. Kidney International Reports, 9(11), 3278–3289. https://doi.org/10.1016/j.ekir.2024.08.026
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Fernandez, H. E., Lipton, M., Balderes, O., Lin, F., Marasa, M., Milo Rasouly, H., & Sabatello, M. (2024). Pediatric nephrologists’ perspectives and clinical practices related to genetic testing and education. Pediatric Nephrology. https://doi.org/10.1007/s00467-024-06539-7
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Gupta, Y., Friedman, D. J., McNulty, M. T., Khan, A., Lane, B., Wang, C., Ke, J., Jin, G., Wooden, B., Knob, A. L., Lim, T. Y., Appel, G. B., Huggins, K., Liu, L., Mitrotti, A., Stangl, M. C., Bomback, A., Westland, R., Bodria, M., … Sanna-Cherchi, S. (2023). Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-43020-9
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Barry, A., McNulty, M. T., Jia, X., Gupta, Y., Debiec, H., Luo, Y., Nagano, C., Horinouchi, T., Jung, S., Colucci, M., Ahram, D. F., Mitrotti, A., Sinha, A., Teeninga, N., Jin, G., Shril, S., Caridi, G., Bodria, M., Lim, T. Y., … Sampson, M. G. (2023). Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-37985-w
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Marasa, M., Ahram, D. F., Rehman, A. U., Mitrotti, A., Abhyankar, A., Jain, N. G., Weng, P. L., Piva, S. E., Fernandez, H. E., Uy, N. S., Chatterjee, D., Kil, B. H., Nestor, J. G., Felice, V., Robinson, D., Whyte, D., Gharavi, A. G., Appel, G. B., Radhakrishnan, J., … Sanna-Cherchi, S. (2023). Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease. Kidney International Reports, 8(8), 1638–1647. https://doi.org/10.1016/j.ekir.2023.05.021
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Ahram, D. F., Lim, T. Y., Ke, J., Jin, G., Verbitsky, M., Bodria, M., Kil, B. H., Chatterjee, D., Piva, S. E., Marasa, M., Zhang, J. Y., Cocchi, E., Caridi, G., Gucev, Z., Lozanovski, V. J., Pisani, I., Izzi, C., Savoldi, G., Gnutti, B., … Sanna-Cherchi, S. (2023). Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. Journal of the American Society of Nephrology, 34(6), 1105–1119. https://doi.org/10.1681/asn.0000000000000132
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Donovan, D. J., Jain, N. G., Feygina, V. M., Fernandez, H. E., & Zuckerman, W. A. (2023). A novel approach to pediatric cardiorenal syndrome. Progress in Pediatric Cardiology, 69, 101635. https://doi.org/10.1016/j.ppedcard.2023.101635
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Rasouly, H. M., Balderes, O., Marasa, M., Fernandez, H., Lipton, M., Lin, F., Gharavi, A. G., & Sabatello, M. (2023). The effect of genetic education on the referral of patients to genetic evaluation: Findings from a national survey of nephrologists. Genetics in Medicine, 25(5), 100814. https://doi.org/10.1016/j.gim.2023.100814
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Jain, N. G., Ahram, D. F., Marasa, M., Rehman, A. U., May, H. J., Zacharoulis, S., Revah-Politi, A., Florido, M. E., Whittemore, G. B., Aggarwal, V. S., Hargus, G., Anyane-Yeboa, K., D’Agati, V. D., Lin, F., Jobanputra, V., & Sanna-Cherchi, S. (2022). Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple Malignancies. Kidney International Reports, 7(10), 2312–2316. https://doi.org/10.1016/j.ekir.2022.07.174
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Kavanagh, C. R., Zanoni, F., Leal, R., Jain, N. G., Stack, M. N., Vasilescu, E.-R., Serban, G., Shaut, C., Kamal, J., Kudose, S., Martinho, A., Alves, R., Santoriello, D., Canetta, P. A., Cohen, D., Radhakrishnan, J., Appel, G. B., Stokes, M. B., Markowitz, G. S., … Batal, I. (2021). Clinical Predictors and Prognosis of Recurrent IgA Nephropathy in the Kidney Allograft. Glomerular Diseases, 2(1), 42–53. Portico. https://doi.org/10.1159/000519834
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Shen, T. H., Stauber, J., Xu, K., Jacunski, A., Paragas, N., Callahan, M., Banlengchit, R., Levitman, A. D., Desanti De Oliveira, B., Beenken, A., Grau, M. S., Mathieu, E., Zhang, Q., Li, Y., Gopal, T., Askanase, N., Arumugam, S., Mohan, S., Good, P. I., … Barasch, J. (2022). Snapshots of nascent RNA reveal cell- and stimulus-specific responses to acute kidney injury. JCI Insight, 7(6). https://doi.org/10.1172/jci.insight.146374
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Jain, N. G., Chen, J. K., Mahajan, R., Kehoe, J., Singer, P., Whyte, D., & Bomback, A. S. (2021). Use of ofatumumab and eplerenone in post‐transplant recurrence of FSGS. Pediatric Transplantation, 26(2). Portico. https://doi.org/10.1111/petr.14191
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