Maddalena Marasà

Mario Negri Institute for Pharmacological Research

Also affiliated with Istituti di Ricovero e Cura a Carattere Scientifico

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 7%percentile

0.104Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Challenges associated with diagnostic exome sequencing in liver diseases

medRxiv(2022)10.1101/2022.06.21.22276400

Top 78%

0.104DataRank

Top 78%1 citations

Kelsie Bogyo, Sheena Kapoor, Emily Groopman, Amanda Thomas‐Wilson, Enrico Cocchi +15 more

Papers

Driven by 19 papers — median percentile 22. Top paper: “The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis”.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

Nature Communications(2020)10.1038/s41467-020-15383-w

N/A

4.6DataRank · unranked

223 citations

Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang +95 more

The Clinical Utility of Genetic Testing in the Diagnosis and Management of Adults with Chronic Kidney Disease

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000249

N/A

0.685DataRank · unranked

95 citations

Michelle S. Bloom, Fouad T. Chebib, Dinah Clark, Maggie Westemeyer, Sara Jandeska +14 more

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

Nature Communications(2023)10.1038/s41467-023-43020-9

N/A

0.637DataRank · unranked

69 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

An electronic health record (EHR) log analysis shows limited clinician engagement with unsolicited genetic test results

JAMIA Open(2021)10.1093/jamiaopen/ooab014

N/A

0.385DataRank · unranked

12 citations

Alexander Fedotov, David Fasel, Maddalena Marasà, Hila Milo Rasouly, Julia Wynn +7 more

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Nature Communications(2025)10.1038/s41467-025-62319-3

N/A

0.345DataRank · unranked

9 citations

Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Miguel Verbitsky +95 more

Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease

Kidney International Reports(2023)10.1016/j.ekir.2023.05.021

N/A

0.241DataRank · unranked

4 citations

Dina Ahram, Atteeq U. Rehman, Adele Mitrotti, Avinash Abhyankar, Namrata G. Jain +20 more

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

medRxiv(2023)10.1101/2023.08.02.23293554

N/A

0.208DataRank · unranked

3 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Challenges associated with diagnostic exome sequencing in liver diseases

medRxiv(2022)10.1101/2022.06.21.22276400

Top 78%

0.104DataRank

Top 78%1 citations

Kelsie Bogyo, Sheena Kapoor, Emily Groopman, Amanda Thomas‐Wilson, Enrico Cocchi +15 more

Age of Onset and Disease Course in Biopsy-Proven Minimal Change Disease: An Analysis From the Cure Glomerulonephropathy Network

American Journal of Kidney Diseases(2023)10.1053/j.ajkd.2022.11.012

N/A

0DataRank · unranked

12 citations

Margaret Helmuth, Abigail R. Smith, Pietro A. Canetta, Isabelle Ayoub, Krzysztof Mucha +95 more

Increased risk of kidney failure in patients with genetic kidney disorders

Journal of Clinical Investigation(2024)10.1172/jci178573

N/A

0DataRank · unranked

12 citations

Natalie Vena, Maddalena Marasà, Enrico Cocchi, Shiraz Bheda, Kelsie Bogyo +27 more

Genome-wide studies define new genetic mechanisms of IgA vasculitis

medRxiv(2024)10.1101/2024.10.10.24315041

N/A

0DataRank · unranked

5 citations

Li Zhu, Sara Monteiro-Martins, Aaron T. Griffin, Lukas Vlahos, Masashi Fujita +88 more

Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy

Journal of Clinical Investigation(2025)10.1172/jci181164

N/A

0DataRank · unranked

15 citations

Nicholas J. Steers, Yifu Li, Elena Sánchez, Miguel Verbitsky, Isabel Robbins +30 more

GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing

Journal of Genetic Counseling(2020)10.1002/jgc4.1364

N/A

0DataRank · unranked

33 citations

Nicole Cuneo, Maddalena Marasà, Natalia DeMaria, Debanjana Chatterjee, Jacqueline J. Thompson +8 more

Pilot Study of Return of Genetic Results to Patients in Adult Nephrology

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.12481019

N/A

0DataRank · unranked

47 citations

Maddalena Marasà, Hila Milo Rasouly, Emily Groopman, S. Ali Husain, Sumit Mohan +19 more

Improving data quality in observational research studies: Report of the Cure Glomerulonephropathy (CureGN) network

Contemporary Clinical Trials Communications(2021)10.1016/j.conctc.2021.100749

N/A

0DataRank · unranked

9 citations

Louis‐Philippe Laurin, Dawn Zinsser, Richard Lafayette, Maddalena Marasà, Scott E. Wenderfer +18 more

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(2022)10.1016/j.ekir.2022.07.174

N/A

0DataRank · unranked

3 citations

Dina Ahram, Maddalena Marasà, Ateeq Ur Rehman, Halie May, Stergios Zacharoulis +11 more

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Nature Communications(2023)10.1038/s41467-023-37985-w

N/A

0DataRank · unranked

50 citations

Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Dêbiec, Yang Luo +65 more

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(2023)10.1681/asn.0000000000000132

N/A

0DataRank · unranked

15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

Association of COVID-19 Versus COVID-19 Vaccination With Kidney Function and Disease Activity in Primary Glomerular Disease: A Report of the Cure Glomerulonephropathy Study

American Journal of Kidney Diseases(2023)10.1053/j.ajkd.2023.07.008

N/A

0DataRank · unranked

13 citations

Dorey A. Glenn, Margaret Helmuth, Abigail R. Smith, Andrew S. Bomback, Pietro A. Canetta +95 more

Maddalena Marasà

Indexed papers

Top data-sharing exemplar

Papers