Co-Authors
This is a "connection" page, showing publications co-authored by LINDSAY BURRAGE and SHAMIKA KETKAR.
Connection Strength
0.952
-
Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk. Ann Rheum Dis. 2025 Aug; 84(8):1363-1374.
Score: 0.236
-
RNA Sequencing as a Diagnostic Tool. JAMA. 2023 01 03; 329(1):85-86.
Score: 0.199
-
A novel, de novo intronic variant in POGZ causes White-Sutton syndrome. Am J Med Genet A. 2022 07; 188(7):2198-2203.
Score: 0.189
-
The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. Am J Hum Genet. 2025 Nov 06; 112(11):2578-2590.
Score: 0.060
-
The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics. medRxiv. 2025 Jan 29.
Score: 0.058
-
Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 09 19; 33(19):1643-1647.
Score: 0.056
-
Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 Jan; 197(1):e63845.
Score: 0.056
-
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: 0.054
-
Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. J Clin Invest. 2021 01 04; 131(1).
Score: 0.043