Co-Authors
This is a "connection" page, showing publications co-authored by PILAR MAGOULAS and RONIT MAROM.
Connection Strength
0.189
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Barriers to a successful healthcare transition for individuals with urea cycle disorders. Mol Genet Metab. 2023 07; 139(3):107609.
Score: 0.055
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Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies. Genet Med. 2022 02; 24(2):364-373.
Score: 0.050
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Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Hum Mutat. 2020 03; 41(3):641-654.
Score: 0.044
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De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features. Am J Hum Genet. 2018 07 05; 103(1):154-162.
Score: 0.040