Alessandra Renieri

Also affiliated with Azienda Ospedaliera Universitaria Senese

Biochemistry, Genetics and Molecular BiologyMedicine

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 16 papers. Top paper: “SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect”.

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Brain(2020)10.1093/brain/awaa176

N/A

0DataRank · unranked

49 citations

Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian +15 more

Human CRY1 variants associate with attention deficit/hyperactivity disorder

Journal of Clinical Investigation(2020)10.1172/jci135500

N/A

0DataRank · unranked

47 citations

Meltem Ece Kars, Şeref Gül, Kaya Bilgüvar, Yiming Wu, Ayşe Özhan +13 more

Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study

medRxiv(2020)10.1101/2020.09.08.20190975

N/A

0DataRank · unranked

30 citations

Tomoko Nakanishi, Vincent Mooser, David Morrison, Tala Abdullah, Olumide Adeleye +11 more

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

Journal of Clinical Investigation(2021)10.1172/jci152386

N/A

0DataRank · unranked

124 citations

Sara Pigazzini, Frauke Degenhardt, Mattia Cordioli, Guillaume Butler‐Laporte, Douglas Maya-Miles +42 more

Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study

PLoS Medicine(2021)10.1371/journal.pmed.1003605

N/A

0DataRank · unranked

123 citations

Tomoko Nakanishi, Vincent Mooser, David Morrison, Tala Abdullah, Olumide Adeleye +11 more

The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males

Autophagy(2021)10.1080/15548627.2021.1995152

N/A

0DataRank · unranked

43 citations

Mary Anna Venneri, Stefania Mantovani, Chiara Fallerini, Elisa Benetti, Nicola Picchiotti +28 more

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

medRxiv(2021)10.1101/2021.03.07.21252875

N/A

0DataRank · unranked

29 citations

Sara Pigazzini, Frauke Degenhardt, Mattia Cordioli, Guillaume Butler‐Laporte, Douglas Maya‐Miles +44 more

Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity

medRxiv(2021)10.1101/2021.06.15.21258703

N/A

0DataRank · unranked

7 citations

Johnathan Cooper‐Knock, Annika K. Weimer, Calum Harvey, Thomas Julian, Cheng Wang +18 more

Cryptic pathogen-sugar interactions revealed by universal saturation transfer analysis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.14.439284

N/A

0DataRank · unranked

5 citations

Ben Gaunt, Peter J. Harrison, Yun Yang, Jiwei Liu, Aziz Khan +32 more

The 2019 and 2021 International Workshops on Alport Syndrome

European Journal of Human Genetics(2022)10.1038/s41431-022-01075-0

N/A

0DataRank · unranked

37 citations

Jie Ding, Constantinos Deltas, Judy Savige, Beata S. Lipska‐Ziętkiewicz, Julia Hoefele +21 more

Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity

Cell Systems(2022)10.1016/j.cels.2022.05.007

N/A

0DataRank · unranked

37 citations

Johnathan Cooper‐Knock, Annika K. Weimer, Minyi Shi, Lina Kozhaya, Derya Unutmaz +15 more

HLA‐DPB113:01 associates with enhanced, and KIR2DS4001 with diminished protection from developing severe COVID‐19

HLA(2023)10.1111/tan.15251

N/A

0DataRank · unranked

15 citations

Silvia Brugiapaglia, Susanna Croci, Paola Magistroni, Claudia Curcio, Kristina Zguro +19 more

Limited overlap between genetic effects on disease susceptibility and disease survival

medRxiv(2023)10.1101/2023.10.10.23296544

N/A

0DataRank · unranked

5 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +19 more

A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

Research Square(2023)10.21203/rs.3.rs-3316459/v1

N/A

0DataRank · unranked

0 citations

Francesca Minnai, Filippo Biscarini, Martina Esposito, Tommaso A. Dragani, Luís Bujanda +14 more

ARID1B-related disorder in 87 adults: Natural history and self-sustainability

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101873

N/A

0DataRank · unranked

6 citations

M. Gösgens, Alexander J.M. Dingemans, P. Striano, Antonella Riva, C. Mignot +81 more

Limited overlap between genetic effects on disease susceptibility and disease survival

Nature Genetics(2025)10.1038/s41588-025-02342-8

N/A

0DataRank · unranked

16 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +20 more