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Publications

A general and efficient representation of ancestral recombination graphs.

Wong Y, Ignatieva A, Koskela J, Gorjanc G, Wohns AW, Kelleher J. A general and efficient representation of ancestral recombination graphs. Genetics. 2024. doi:10.1093/genetics/iyae100

A general and efficient representation of ancestral recombination graphs.

Wong Y, Ignatieva A, Koskela J, Gorjanc G, Wohns AW, Kelleher J. A general and efficient representation of ancestral recombination graphs. Genetics. 2024. doi:10.1093/genetics/iyae100

A general and efficient representation of ancestral recombination graphs.

Wong Y, Ignatieva A, Koskela J, Gorjanc G, Wohns AW, Kelleher J. A general and efficient representation of ancestral recombination graphs. Genetics. 2024. doi:10.1093/genetics/iyae100

A general and efficient representation of ancestral recombination graphs.

Wong Y, Ignatieva A, Koskela J, Gorjanc G, Wohns AW, Kelleher J. A general and efficient representation of ancestral recombination graphs. Genetics. 2024. doi:10.1093/genetics/iyae100

Using Mendelian Randomisation to search for modifiable risk factors influencing the development of clonal haematopoiesis.

Hislop JM, Went M, Mills C, Sud A, Law PJ, Houlston RS. Using Mendelian Randomisation to search for modifiable risk factors influencing the development of clonal haematopoiesis. Blood cancer journal. 2024;14(1):114. doi:10.1038/s41408-024-01101-y

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Rots D, Choufani S, Faundes V, et al. Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.06.009

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Rots D, Choufani S, Faundes V, et al. Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.06.009

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Rots D, Choufani S, Faundes V, et al. Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.06.009

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Rots D, Choufani S, Faundes V, et al. Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.06.009

Using Mendelian Randomisation to search for modifiable risk factors influencing the development of clonal haematopoiesis.

Hislop JM, Went M, Mills C, Sud A, Law PJ, Houlston RS. Using Mendelian Randomisation to search for modifiable risk factors influencing the development of clonal haematopoiesis. Blood cancer journal. 2024;14(1):114. doi:10.1038/s41408-024-01101-y