Co-Authors
This is a "connection" page, showing publications co-authored by LORRAINE POTOCKI and KEREN MACHOL.
Connection Strength
0.379
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Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder. Am J Hum Genet. 2026 Jul 02; 113(7):1558-1569.
Score: 0.245
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The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing. Am J Hum Genet. 2024 05 02; 111(5):841-862.
Score: 0.053
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Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans. Am J Med Genet A. 2021 03; 185(3):836-840.
Score: 0.042
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Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer. Sci Adv. 2020 01; 6(4):eaax0021.
Score: 0.039