Co-Authors
This is a "connection" page, showing publications co-authored by KEREN MACHOL and LINDSAY BURRAGE.
Connection Strength
0.959
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Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies. Am J Med Genet A. 2017 Mar; 173(3):733-739.
Score: 0.513
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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: 0.248
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Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma. Neurol Genet. 2018 Aug; 4(4):e248.
Score: 0.144
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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