Co-Authors
This is a "connection" page, showing publications co-authored by PAWEL STANKIEWICZ and JENNIFER POSEY.
Connection Strength
0.488
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Clinical genomics and contextualizing genome variation in the diagnostic laboratory. Expert Rev Mol Diagn. 2020 10; 20(10):995-1002.
Score: 0.168
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Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions. Genet Med. 2020 11; 22(11):1768-1776.
Score: 0.165
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Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes. Genome Med. 2025 10 24; 17(1):129.
Score: 0.060
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Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes. medRxiv. 2025 Mar 30.
Score: 0.057
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Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases. Genome Med. 2019 05 17; 11(1):30.
Score: 0.038