Simone Sanna‐Cherchi

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

0.113Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

RESOLVE: Recurrence Posttransplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change Disease

Glomerular Diseases(2024)10.1159/000542839

Top 72%

0.113DataRank

Top 72%1 citations

A. M. Rahimi, Hailey Desmond, Nathaniel Putnam, Elena Martinelli, Elizabeth Hendren +8 more

Papers

Driven by 34 papers — median percentile 28. 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

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2022)10.1016/j.kint.2022.03.019

N/A

4.5DataRank · unranked

193 citations

Émilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew Mallett, Rulan S. Parekh +57 more

Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

Journal of the American Society of Nephrology(2024)10.1681/asn.0000000501

N/A

0.709DataRank · unranked

16 citations

Andrew Beenken, Elena Martinelli, Ken Saida, Andrea L. Knob, Juntao Ke +45 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

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

RESOLVE: Recurrence Posttransplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change Disease

Glomerular Diseases(2024)10.1159/000542839

Top 72%

0.113DataRank

Top 72%1 citations

A. M. Rahimi, Hailey Desmond, Nathaniel Putnam, Elena Martinelli, Elizabeth Hendren +8 more

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

European Urology Open Science(2022)10.1016/j.euros.2022.08.004

N/A

0DataRank · unranked

12 citations

Tze Yin Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum +31 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

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008

N/A

0DataRank · unranked

27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 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

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis

Journal of Clinical Investigation(2023)10.1172/jci165019

N/A

0DataRank · unranked

43 citations

Museer A. Lone, Winston Lee, Laura Capolupo, Sylvia Ho, Adekemi M. Adeyemi +80 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

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

Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families

Pediatric Nephrology(2023)10.1007/s00467-023-06134-2

N/A

0DataRank · unranked

5 citations

Nils D. Mertens, Ronen Schneider, Selina Hölzel, Jameela A. Kari, Sherif El Desoky +6 more

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome

Kidney International(2020)10.1016/j.kint.2020.04.045

N/A

0DataRank · unranked

35 citations

Nan Wu, Shuangshuang Dong, Ling Zhang, Yanxue Zhao, Wei‐Sheng Chen +25 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

Pre-transplant anti-nephrin antibodies are specific predictors of recurrent diffuse podocytopathy in the kidney allograft

Kidney International(2024)10.1016/j.kint.2024.07.022

N/A

0DataRank · unranked

50 citations

Andrew Watts, Jean‐Baptiste Gibier, Aghilès Hamroun, Isabelle Top, François Provôt +15 more

Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

Blood(2024)10.1182/blood.2023023326

N/A

0DataRank · unranked

24 citations

Joel Rämö, Sean J. Jurgens, Teemu Niiranen, Simone Sanna‐Cherchi, Kenneth A. Bauer +7 more

Type IV Collagen Mutations in Familial IgA Nephropathy

Kidney International Reports(2020)10.1016/j.ekir.2020.04.011

N/A

0DataRank · unranked

43 citations

Emily Groopman, Vivette D. D’Agati, Sindhuri Prakash, Junying Zhang, Małgorzata Mizerska-Wasiak +13 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

N/A

0DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

APOL1 genotyping is incomplete without testing for the protective M1 modifier p.N264K variant

Glomerular Diseases(2024)10.1159/000537948

N/A

0DataRank · unranked

15 citations

Elena Martinelli, Yask Gupta, David J. Friedman, Matthew G. Sampson, Martin R. Pollak +2 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

The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease

Prenatal Diagnosis(2024)10.1002/pd.6527

N/A

0DataRank · unranked

10 citations

Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David E. Solowiejczyk, Neeta L. Vora +9 more

The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event

G3 Genes Genomes Genetics(2024)10.1093/g3journal/jkae290

N/A

0DataRank · unranked

8 citations

Michelle T. McNulty, Yask Gupta, Giulio Genovese, Matthew G. Sampson, Simone Sanna‐Cherchi +3 more

Loss of function in protein Z (PROZ) is associated with increased risk of ischemic stroke in the UK Biobank

Journal of Thrombosis and Haemostasis(2024)10.1016/j.jtha.2024.09.016

N/A

0DataRank · unranked

6 citations

Justine Ryu, Sean J. Jurgens, Sharjeel Chaudhry, Satoshi Koyama, Xin Wang +7 more

Prevalence and Impact of APOL1 Kidney Risk Variants in West Africa

Journal of the American Society of Nephrology(2024)10.1681/asn.0000000587

N/A

0DataRank · unranked

3 citations

Rik Westland, Opeyemi A. Olabisi, Simone Sanna‐Cherchi, Elena Martinelli

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

Population-scale analysis reveals inherited C1-inhibitor deficiency is a polyphenotypic thrombotic disorder

Blood Advances(2025)10.1182/bloodadvances.2025017220

N/A

0DataRank · unranked

2 citations

Amelia K. Haj, Sean J. Jurgens, Harish Eswaran, Linda Sundler Björkman, Justine Ryu +11 more

Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral reflux

JCI Insight(2025)10.1172/jci.insight.199689

N/A

0DataRank · unranked

1 citations

Pavan Khosla, Daniel L. Bivona, Atlas Khan, Yask Gupta, Heekuk Park +19 more

Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome

medRxiv(2025)10.1101/2025.08.01.25332825

N/A

0DataRank · unranked

1 citations

Alejandro Ochoa, Amika Sood, Ashley Drabik, Megan Chryst-Stangl, Brandon M. Lane +43 more

Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations

Kidney International(2021)10.1016/j.kint.2021.09.034

N/A

0DataRank · unranked

27 citations

Dina Ahram, Yangfan P. Liu, Rik Westland, Rosemary V. Sampogna, Nicholas Katsanis +3 more

Association of Collapsing Glomerulopathy with Donor Apolipoprotein L1 Risk Variants in Kidney Allografts from Black Donors

Clinical Journal of the American Society of Nephrology(2025)10.2215/cjn.0000000778

N/A

0DataRank · unranked

0 citations

Alexei Mikhailov, S. Ali Husain, Rachel A. Nuccitelli, Francesca Zanoni, Lili Liu +17 more

Simone Sanna‐Cherchi

Indexed papers

Top data-sharing exemplar

Papers