Aurora Pujol

Institució Catalana de Recerca i Estudis Avançats

Also affiliated with Instituto de Salud Carlos III, Institut d'Investigació Biomédica de Bellvitge, Centre for Biomedical Network Research on Rare Diseases

Agricultural and Biological SciencesBiochemistry, 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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 29 papers. Top paper: “Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19”.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Genome Medicine(2023)10.1186/s13073-023-01173-8

N/A

1.5DataRank · unranked

78 citations

Estelle Talouarn, Astrid Marchal, Peng Zhang, Jérémy Manry, Yoann Seeleuthner +95 more

Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

The Journal of Experimental Medicine(2022)10.1084/jem.20220258

N/A

1.3DataRank · unranked

47 citations

Paul Bastard, Pascal Chappert, Giovanna Barba–Spaeth, Slim Fourati, Alexis Vanderberghe +47 more

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Nature(2023)10.1038/s41586-023-06034-3

N/A

0.795DataRank · unranked

199 citations

Konrad Rawlik, Andrew D. Bretherick, Ting Qi, Yang Wu, Isar Nassiri +3013 more

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

Science Immunology(2021)10.1126/sciimmunol.abl4348

N/A

0DataRank · unranked

421 citations

Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada‐Vélez, Majistor Raj Luxman Maglorius Renkilaraj +95 more

SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

The Journal of Experimental Medicine(2021)10.1084/jem.20210446

N/A

0DataRank · unranked

150 citations

Petter Brodin, Aurélie Cobat, Catherine M. Biggs, Julie Toubiana, C. Lucas +95 more

Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain

Journal of Clinical Immunology(2021)10.1007/s10875-021-01036-0

N/A

0DataRank · unranked

139 citations

Paul Bastard, Laura Planas‐Serra, Pablo Ryan, Montserrat Ruíz, María de Carranza +6 more

A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

Nature Immunology(2021)10.1038/s41590-021-01030-z

N/A

0DataRank · unranked

72 citations

Laurent Abel, Donald C. Vinh, Elżbieta Kaja, Beth A. Drolet, Qian Zhang +51 more

Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β

Journal of Clinical Immunology(2021)10.1007/s10875-021-01068-6

N/A

0DataRank · unranked

45 citations

Laurent Abel, Paul Bastard, Matthew P. Cheng, Antônio Condino‐Neto, Peter K. Gregersen +30 more

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

Nature Communications(2021)10.1038/s41467-021-22627-w

N/A

0DataRank · unranked

52 citations

Deepa Rajan, Tyler R. Fortuna, Eric N. Anderson, Caroline Ward, Youngha Lee +65 more

From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio

Journal of Investigative Dermatology(2021)10.1016/j.jid.2021.05.024

N/A

0DataRank · unranked

28 citations

John J. Moon, Jennifer M. Tran, Samira Asgari, Cliona O’Farrelly, Jean-Laurent Casanova +54 more

Anti-oxidant MitoQ rescue of AWB chemosensory neuron impairment in a C. elegans model of X-linked Adrenoleukodystrophy

PubMed(2021)10.17912/micropub.biology.000346

N/A

0DataRank · unranked

2 citations

Aurora Pujol, Esther Dalfó, Sanjib Guha

Human genetic and immunological determinants of critical COVID-19 pneumonia

Nature(2022)10.1038/s41586-022-04447-0

N/A

0DataRank · unranked

393 citations

Paul Bastard, COVID Human Genetic Effort, Adem Karbuz, Adrian Gervais, Ahmad Abou Tayoun +95 more

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Science(2022)10.1126/science.abo3627

N/A

0DataRank · unranked

168 citations

Jérémie Le Pen, Ahmad Yatim, Beihua Dong, Yann Aquino, Masato Ogishi +95 more

Autoantibodies against type I IFNs in patients with critical influenza pneumonia

The Journal of Experimental Medicine(2022)10.1084/jem.20220514

N/A

0DataRank · unranked

130 citations

Andrés Pizzorno, Lisa Miorin, Paul Bastard, Adrian Gervais, Tom Le Voyer +95 more

Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

Science Immunology(2022)10.1126/sciimmunol.abp8966

N/A

0DataRank · unranked

77 citations

Sara E. Vazquez, Jamin Liu, Matthew T. Laurie, Chung‐Yu Wang, Adrian Gervais +95 more

Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.11.010

N/A

0DataRank · unranked

41 citations

Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Saleh Al‐Muhsen, Fahd Al‐Mulla +63 more

Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy

Brain(2022)10.1093/brain/awac110

N/A

0DataRank · unranked

20 citations

Johanne Dubail, Sergio Aguilera, Chiara Paganini, Catherine Vanhulle, Walid Haouari +12 more

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

medRxiv(2022)10.1101/2022.10.22.22281221

N/A

0DataRank · unranked

10 citations

Estelle Talouarn, Astrid Marchal, Jérémy Manry, Yoann Seeleuthner, Yu Zhang +95 more

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Nature(2023)10.1038/s41586-023-06717-x

N/A

0DataRank · unranked

107 citations

Audrey V. Parent, Xian Liu, Axel Cederholm, Adrian Gervais, Jérémie Rosain +95 more

Biomarker-based risk prediction for the onset of neuroinflammation in X-linked adrenoleukodystrophy

EBioMedicine(2023)10.1016/j.ebiom.2023.104781

N/A

0DataRank · unranked

33 citations

Paulus Rommer, Andreas Gleiß, Markus Ponleitner, Bettina Zierfuss, Petra Waidhofer‐Söllner +21 more

RINT1 deficiency disrupts lipid metabolism and underlies a complex hereditary spastic paraplegia

Journal of Clinical Investigation(2023)10.1172/jci162836

N/A

0DataRank · unranked

15 citations

Montserrat Ruíz, Laura Planas‐Serra, Edgard Verdura, Agustí Rodríguez‐Palmero, Agatha Schlüter +13 more

Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2023.02.003

N/A

0DataRank · unranked

16 citations

Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Fahd Al‐Mulla, Evangelos Andreakos +70 more

Biallelic variants in RINT1 present as early-onset pure hereditary spastic paraplegia

Journal of Clinical Investigation(2024)10.1172/jci178919

N/A

0DataRank · unranked

3 citations

Laura Planas‐Serra, Abigail Sveden, Amy Tam, Hyo‐Min Kim, Umar Zubair +10 more

The seven enigmas of SARS-CoV-2: From the past to the future

Journal of Human Immunity(2025)10.70962/jhi.20250149

N/A

0DataRank · unranked

3 citations

Lisa M. Arkin, Paul Bastard, Alexandre Bolze, A. Borghesi, Petter Brodin +64 more

Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2

Nature Communications(2025)10.1038/s41467-025-65308-8

N/A

0DataRank · unranked

3 citations

Renée M. van der Sluis, Kennith Brian Castelino, Bao‐cun Zhang, Andreas Ronit, Thomas Zillinger +95 more

OAS1 and OAS3 genetic variants enhance inflammatory responses to SARS-CoV-2

iScience(2025)10.1016/j.isci.2025.113966

N/A

0DataRank · unranked

1 citations

Raúl López-Fernández-Sobrino, Jordi Pedragosa, Darío López-García, Aitor Nogales, Jordi Durbán +49 more

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.015

N/A

0DataRank · unranked

0 citations

María E. Rodríguez-Ruiz, Eric N. Anderson, Agustí Rodríguez‐Palmero, Valentina Vélez-Santamaría, Agatha Schlüter +41 more

A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

Cell(2020)10.1016/j.cell.2020.05.016

N/A

0DataRank · unranked

235 citations

Helen C. Su, Laurent Abel, Alessandro Aiuti, Saleh Al‐Muhsen, Andrés A. Arias +59 more

Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome

Acta Neuropathologica(2020)10.1007/s00401-020-02223-w

N/A

0DataRank · unranked

46 citations

Edgard Verdura, Natalia Juliá‐Palacios, Eric N. Anderson, Leire Goicoechea, Laura Planas‐Serra +33 more