Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity von Hopp, Katharina, Ward, Christopher J, Hommerding, Cynthia J, Nasr, Samih H, Tuan, Han-Fang, Gainullin, Vladimir G, Rossetti, Sandro, Torres, Vicente E, Harris, Peter C

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Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease von Rossetti, Sandro, Harris, Peter C

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Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease: A Biomarker of Disease Progression and Therapeutic Efficacy von Alam, Ahsan, MD, Dahl, Neera K., MD, Lipschutz, Joshua H., MD, Rossetti, Sandro, MD, Smith, Patricia, PhD, Sapir, Daniel, MD, Weinstein, Jordan, MD, McFarlane, Philip, MD, Bichet, Daniel G., MD

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Randomized Clinical Trial of Long-Acting Somatostatin for Autosomal Dominant Polycystic Kidney and Liver Disease von HOGAN, Marie C, MASYUK, Tetyana V, ROSSETTI, Sandro, HARRIS, Peter C, LARUSSO, Nicholas F, TORRES, Vicente E, PAGE, Linda J, KUBLY, Vickie J, BERGSTRALH, Eric J, XUJIAN LI, KIM, Bohyun, KING, Bernard F, GLOCKNER, James, HOLMES, David R

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Identification of Gene Mutations in Autosomal Dominant Polycystic Kidney Disease through Targeted Resequencing von ROSSETTI, Sandro, HOPP, Katharina, HARRIS, Peter C, SIKKINK, Robert A, SUNDSBAK, Jamie L, YEAN KIT LEE, KUBLY, Vickie, ECKLOFF, Bruce W, WARD, Christopher J, WINEARLS, Christopher G, TORRES, Vicente E

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Polycystin-2 mutations lead to impaired calcium cycling in the heart and predispose to dilated cardiomyopathy von Paavola, Jere, Schliffke, Simon, Rossetti, Sandro, Kuo, Ivana Y.-T, Yuan, Shiaulou, Sun, Zhaoxia, Harris, Peter C, Torres, Vicente E, Ehrlich, Barbara E

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Primary Hyperoxaluria Type III Gene HOGA1 (Formerly DHDPSL) as a Possible Risk Factor for Idiopathic Calcium Oxalate Urolithiasis von Monico, Carla G, Rossetti, Sandro, Belostotsky, Ruth, Cogal, Andrea G, Herges, Regina M, Seide, Barbara M, Olson, Julie B, Bergstrahl, Eric J, Williams, Hugh J, Haley, William E, Frishberg, Yaacov, Milliner, Dawn S

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Extended Follow-Up of Unruptured Intracranial Aneurysms Detected by Presymptomatic Screening in Patients with Autosomal Dominant Polycystic Kidney Disease von Irazabal, Maria V, Huston, 3rd, John, Kubly, Vickie, Rossetti, Sandro, Sundsbak, Jamie L, Hogan, Marie C, Harris, Peter C, Brown, Jr, Robert D, Torres, Vicente E

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The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein von Harris, Peter C, Ward, Christopher J, Hogan, Marie C, Rossetti, Sandro, Walker, Denise, Sneddon, Tam, Wang, Xiaofang, Kubly, Vicky, Cunningham, Julie M, Bacallao, Robert, Ishibashi, Masahiko, Milliner, Dawn S, Torres, Vicente E

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Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD) von Adeva, Magdalena, El-Youssef, Mounif, Rossetti, Sandro, Kamath, Patrick S., Kubly, Vickie, Consugar, Mark B., Milliner, Dawn M., King, Bernard F., Torres, Vicente E., Harris, Peter C.

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Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction von NAULI, Surya M, ROSSETTI, Sandro, KOLB, Robert J, ALENGHAT, Francis J, CONSUGAR, Mark B, HARRIS, Peter C, INGBER, Donald E, LOGHMAN-ADHAM, Mahmoud, JING ZHOU

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Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome von Consugar, Mark B., Wong, Wai C., Lundquist, Patrick A., Rossetti, Sandro, Kubly, Vickie J., Walker, Denise L., Rangel, Laureano J., Aspinwall, Richard, Niaudet, W. Patrick, Özen, Seza, David, Albert, Velinov, Milen, Bergstralh, Eric J., Bae, Kyongtae T., Chapman, Arlene B., Guay-Woodford, Lisa M., Grantham, Jared J., Torres, Vicente E., Sampson, Julian R., Dawson, Brian D., Harris, Peter C., for the CRISP Consortium

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Association of mutation position in polycystic kidney disease 1 ( PKD1) gene and development of a vascular phenotype von Rossetti, Sandro, Chauveau, Dominique, Kubly, Vickie, Slezak, Jeffrey M, Saggar-Malik, Anand K, Pei, York, Ong, Albert CM, Stewart, Fiona, Watson, Michael L, Bergstralh, Erik J, Winearls, Christopher G, Torres, Vicente E, Harris, Peter C

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A complete mutation screen of the ADPKD genes by DHPLC von Rossetti, Sandro, Chauveau, Dominique, Walker, Denise, Saggar-Malik, Anand, Winearls, Christopher G., Torres, Vicente E., Harris, Peter C.

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Management of Hyperphosphatemia in End-Stage Renal Disease: A New Paradigm von Rastogi, Anjay, Bhatt, Nisha, Rossetti, Sandro, Beto, Judith

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A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees von Rossetti, Sandro, Torra, Roser, Coto, Eliecer, Consugar, Mark, Kubly, Vickie, Málaga, Serafin, Navarro, Mercedes, El-Youssef, Mounif, Torres, Vicente E., Harris, Peter C.

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A telomerase immortalized human proximal tubule cell line with a truncation mutation (Q4004X) in polycystin-1 von Herbert, Brittney-Shea, Grimes, Brenda R, Xu, Wei Min, Werner, Michael, Ward, Christopher, Rossetti, Sandro, Harris, Peter, Bello-Reuss, Elsa, Ward, Heather H, Miller, Caroline, Gattone, 2nd, Vincent H, Phillips, Carrie L, Wandinger-Ness, Angela, Bacallao, Robert L

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Progression of autosomal dominant kidney disease: measurement of the stage transitions of chronic kidney disease von Blanchette, Christopher M, Liang, Caihua, Lubeck, Deborah P, Newsome, Britt, Rossetti, Sandro, Gu, Xiangmei, Gutierrez, Benjamin, Lin, Nancy D

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Investigation of Primary Cilia in the Pathogenesis of Biliary Atresia von Hartley, Jane L, O'Callaghan, Christopher, Rossetti, Sandro, Consugar, Mark, Ward, Christopher J, Kelly, Deirdre A, Harris, Peter C

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Mutation Analysis of the Entire PKD1 Gene: Genetic and Diagnostic Implications von Rossetti, Sandro, Strmecki, Lana, Gamble, Vicki, Burton, Sarah, Sneddon, Vicky, Peral, Belén, Roy, Sushmita, Bakkaloglu, Aysin, Komel, Radovan, Winearls, Christopher G., Harris, Peter C.

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