ScholarIQanswers from OpenAlex & ORCID
Marina Noris
ResearcherPublications, citations & collaboration network
Marina Noris is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Marina Noris have?
ScholarIQindexed works
Marina Noris has 351 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Marina Noris have?
ScholarIQcitation count
Marina Noris has 24,741 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Marina Noris?
ScholarIQh-index
Marina Noris has an h-index of 79 in OpenAlex.
What is the i10-index of Marina Noris?
ScholarIQi10-index
Marina Noris has an i10-index of 202 in OpenAlex.
What is the ORCID of Marina Noris?
ScholarIQorcid
The ORCID for Marina Noris is on the source record.
What is the OpenAlex record for Marina Noris?
ScholarIQopenalex
The OpenAlex for Marina Noris is on the source record.
What are the most-cited papers on Marina Noris?
ScholarIQmost cited works
Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype
Marina Noris, Jessica Caprioli, Elena Bresin, Chiara Mossali, Gaia Pianetti, Sara Gamba, Erica Daina, Chiara Fenili, Federica Castelletti, Annalisa Sorosina, Rossella Piras, Roberta Donadelli, Ramona Maranta, Irene van der Meer, Edward M. Conway, Peter F. Zipfel, Timothy H.J. Goodship, Giuseppe Remuzzi
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
Jessica Caprioli, Marina Noris, Simona Brioschi, Gaia Pianetti, Federica Castelletti, Paola Bettinaglio, Caterina Mele, Elena Bresin, Linda Cassis, Sara Gamba, Francesca Porrati, Sara Bucchioni, Giuseppe Monteferrante, Celia J. Fang, M. Kathryn Liszewski, David Kavanagh, John P. Atkinson, Giuseppe Remuzzi, for the International Registry of Recurrent and Familial HUS/TTP
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
Timothy H.J. Goodship, H. Terence Cook, Fádi Fakhouri, Fernando C. Fervenza, Véronique Frémeaux‐Bacchi, David Kavanagh, Carla Nester, Marina Noris, Matthew C. Pickering, Santiago Rodrı́guez de Córdoba, Lubka T. Roumenina, Sanjeev Sethi, Richard J. Smith, Charlie E. Alpers, Gerald B. Appel, Gianluigi Ardissino, Gema Ariceta, Mustafa Arıcı, Arvind Bagga, Ingeborg M. Bajema, Miguel Blasco, Linda Burke, Thomas Cairns, M.C. Carratalá, Vivette D. D’Agati, Mohamed R. Daha, An S. De Vriese, Marie‐Agnès Dragon‐Durey, Agnes B. Fogo, Miriam Galbusera, Daniel P. Gale, Hermann Haller, Sally Johnson, Mihály Józsi, Diana Karpman, Lynne D. Lanning, Moglie Le Quintrec, Christoph Licht, Chantal Loirat, Francisco Monfort, B. Paul Morgan, Laure-Hélène Noël, Michelle M. O’Shaughnessy, Marion Rabant, Éric Rondeau, Piero Ruggenenti, Neil Sheerin, Jenna L.H. Smith, Fabrizio Spoleti, Joshua M. Thurman, Nicole C. A. J. van de Kar, Marina Vivarelli, Peter F. Zipfel
C3 glomerulopathy — understanding a rare complement-driven renal disease
Richard J. Smith, Gerald B. Appel, Anna M. Blom, H. Terence Cook, Vivette D. D’Agati, Fádi Fakhouri, Véronique Frémeaux‐Bacchi, Mihály Józsi, David Kavanagh, John D. Lambris, Marina Noris, Matthew C. Pickering, Giuseppe Remuzzi, Santiago Rodrı́guez de Córdoba, Sanjeev Sethi, Johan van der Vlag, Peter F. Zipfel, Carla Nester
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome
Tamara Manuelian, Jens Hellwage, Seppo Meri, Jessica Caprioli, Marina Noris, Stefan Heinen, Mihály Józsi, Hartmut P.H. Neumann, Giuseppe Remuzzi, Peter F. Zipfel