Source: ISSN: 2666-979X ; Cell Genomics ; https://u-paris.hal.science/hal-04096029 ; Cell Genomics, 2023, 3 (2), pp.100248. ⟨10.1016/j.xgen.2022.100248⟩.

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Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

Authors : Kerner, Gaspard; Neehus, Anna-Lena; Philippot, Quentin ...

Subjects: ancient DNA; immunity; host defense

Source: ISSN: 2666-979X ; Cell Genomics ; https://u-paris.hal.science/hal-04096029 ; Cell Genomics, 2023, 3 (2), pp.100248. ⟨10.1016/j.xgen.2022.100248⟩.

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High level of heterozygous haplotype of hemoglobin in Abidjan population with mild malaria

Authors : Koui, Tossea Armand Stephane; Gnondjui, Alloh Albert; Gbessi, Adji Eric ...

Subjects: Sickle cell anemia; Haplotype; Ivory coast

Source: ISSN: 1755-8794 ; BMC Medical Genomics ; https://hal.science/hal-04217533 ; BMC Medical Genomics, 2023, 15 (1), pp.120. ⟨10.1186/s12920-022-01263-3⟩.

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New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome

Authors : Masingue, Marion; Cattaneo, Olivia; Wolff, Nicolas ...

Subjects: [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics; [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

Source: ISSN: 2045-2322.

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Automatic landmarking identifies new loci associated with face morphology and implicates Neanderthal introgression in human nasal shape.

Authors : Li, Qing; Chen, Jieyi; Faux, Pierre ...

Subjects: Genome-wide association studies; Quantitative trait; MESH: Humans

Source: ISSN: 2399-3642 ; Communications Biology ; https://u-bourgogne.hal.science/hal-04115851 ; Communications Biology, 2023, 6 (1), pp.481. ⟨10.1038/s42003-023-04838-7⟩ ;

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Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome

Authors : Crochemore, Clément; Chica, Claudia; Garagnani, Paolo ...

Subjects: [SDV]Life Sciences [q-bio]; [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

Source: ISSN: 1474-9718.

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Genetic heterogeneity shapes brain connectivity in psychiatry

Authors : Moreau, Clara; Harvey, Annabelle; Kumar, Kuldeep ...

Subjects: Genetic heterogeneity; Copy number variant; Functional connectivity

Source: ISSN: 0006-3223 ; Biological Psychiatry ; https://pasteur.hal.science/pasteur-03819076 ; Biological Psychiatry, 2023, 93 (1), pp.54-58. ⟨10.1016/j.biopsych.2022.08.024⟩.

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نتائج البحث

فلترة النتائج

Multi-trait GWAS for diverse ancestries: Mapping the knowledge gap

Linking the genetic structure of neuroanatomical phenotypes with psychiatric disorders

Polygenic risk score prediction accuracy convergence

Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

High level of heterozygous haplotype of hemoglobin in Abidjan population with mild malaria

New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome

Automatic landmarking identifies new loci associated with face morphology and implicates Neanderthal introgression in human nasal shape.

Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome

Genetic heterogeneity shapes brain connectivity in psychiatry

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