CHRISTOPHER GROCHOWSKI to Whole Genome Sequencing
This is a "connection" page, showing publications CHRISTOPHER GROCHOWSKI has written about Whole Genome Sequencing.
Connection Strength
0.486
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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: 0.199
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Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes. Hum Mutat. 2018 07; 39(7):939-946.
Score: 0.119
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Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencing. Genome Res. 2026 04 07; 36(4):661-670.
Score: 0.051
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Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps. Genome Res. 2024 11 20; 34(11):1785-1797.
Score: 0.047
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Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3593-3600.
Score: 0.035
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Cytogenetically visible inversions are formed by multiple molecular mechanisms. Hum Mutat. 2020 11; 41(11):1979-1998.
Score: 0.035