Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and RONIT MAROM.
Connection Strength
0.140
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Biallelic Variants in KMO Cause a Novel Form of Congenital NAD Deficiency. medRxiv. 2026 Aug 27.
Score: 0.062
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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: 0.045
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Identification of novel candidate disease genes from de novo exonic copy number variants. Genome Med. 2017 09 21; 9(1):83.
Score: 0.033