Co-Authors
This is a "connection" page, showing publications co-authored by CHAYA MURALI and HALEY STREFF.
Connection Strength
0.569
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A familial deletion of 10p12.1 associated with thrombocytopenia. Am J Med Genet A. 2024 01; 194(1):77-81.
Score: 0.229
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A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome. Am J Med Genet A. 2023 06; 191(6):1576-1580.
Score: 0.220
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Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes. Eur J Hum Genet. 2024 Nov; 32(11):1378-1386.
Score: 0.061
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
Score: 0.059