Agatha Schlüter

Instituto de Investigación Marqués de Valdecilla

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 11 papers. Top paper: “Inborn errors of type I IFN immunity in patients with life-threatening COVID-19”.

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Science(2020)10.1126/science.abd4570

N/A

5.6DataRank · unranked

2400 citations

Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada‐Vélez, Jie Chen +95 more

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

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

0.907DataRank · unranked

422 citations

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

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

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

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

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

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

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