Standout Papers

Prevalence of the Congenital Long-QT Syndrome 2009 2026 2014 2020 667
  1. Prevalence of the Congenital Long-QT Syndrome (2009)
    Peter J. Schwartz, Marco Stramba‐Badiale et al. Circulation

Immediate Impact

1 by Nobel laureates 5 from Science/Nature 70 standout
Sub-graph 1 of 20

Citing Papers

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
2024 Standout
Alanyl-tRNA synthetase, AARS1, is a lactate sensor and lactyltransferase that lactylates p53 and contributes to tumorigenesis
2024 Standout
2 intermediate papers

Works of Roberto Insolia being referenced

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome
2009
Novel human pathological mutations
2006

Author Peers

Author Last Decade Papers Cites
Roberto Insolia 2119 1490 185 208 26 2.4k
Chiara Ferrandi 1108 1219 169 116 26 2.3k
Argelia Medeiros‐Domingo 2464 1480 134 247 87 2.8k
Giuliano Bosi 1487 951 181 126 12 1.8k
Melissa L. Will 3542 2284 69 256 40 3.8k
Carmen R. Valdivia 2547 2648 94 603 62 3.3k
Nynke Hofman 1941 1129 36 158 42 2.2k
Carla Spazzolini 3460 1967 37 195 33 3.7k
Raymond K. Kudej 935 830 80 119 51 1.8k
Anna Iglesias 1552 843 42 159 73 1.9k
Alexander N. Katchman 1078 1084 72 519 40 1.8k

All Works

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2026