Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and MICHAEL WANGLER.
Connection Strength
0.729
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 Feb 28; 101102.
Score: 0.248
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Digital necrosis in an infant with severe spinal muscular atrophy. Neurol Genet. 2019 Oct; 5(5):e361.
Score: 0.182
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Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. JAMA Pediatr. 2017 12 04; 171(12):e173438.
Score: 0.161
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De novo variants in PLCG1 are associated with hearing impairment, ocular pathology, and cardiac defects. medRxiv. 2024 Jan 09.
Score: 0.061
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Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS Genet. 2017 Jul; 13(7):e1006905.
Score: 0.039
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Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Med. 2017 03 21; 9(1):26.
Score: 0.038