Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and KIM WORLEY.
Connection Strength
0.627
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Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. Am J Med Genet A. 2022 11; 188(11):3184-3190.
Score: 0.201
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LMOD2-related dilated cardiomyopathy presenting in late infancy. Am J Med Genet A. 2022 06; 188(6):1858-1862.
Score: 0.194
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Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. Elife. 2025 Aug 27; 13.
Score: 0.062
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Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. medRxiv. 2025 May 29.
Score: 0.061
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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: 0.056
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Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay. J Med Genet. 2023 11; 60(11):1092-1104.
Score: 0.053