FRITZ SEDLAZECK to Phenotype
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Phenotype.
Connection Strength
0.383
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Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
Score: 0.122
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Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 Dec 18; 16(1):146.
Score: 0.121
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Beyond the exome: What's next in diagnostic testing for Mendelian conditions. Am J Hum Genet. 2023 08 03; 110(8):1229-1248.
Score: 0.028
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The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models. Cell. 2023 03 30; 186(7):1493-1511.e40.
Score: 0.027
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Towards accurate and reliable resolution of structural variants for clinical diagnosis. Genome Biol. 2022 03 03; 23(1):68.
Score: 0.025
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Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato. Cell. 2020 07 09; 182(1):145-161.e23.
Score: 0.022
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A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet. 2019 11 07; 105(5):974-986.
Score: 0.021
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The genomic basis of circadian and circalunar timing adaptations in a midge. Nature. 2016 12 01; 540(7631):69-73.
Score: 0.017