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Browsing Tag

Human Genetics

46 posts
GGenetics
When ganglioside pathways go awry: congenital disorders and experimental insights
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When ganglioside pathways go awry: congenital disorders and experimental insights

  • July 31, 2025
Thudichum JLW. A treatise on the chemical constitution of the brain: Bailliere, Tindall, and Cox, London; 1884. Chiricozzi…
GGenetics
Pangenome analysis provides insights into legume evolution and breeding
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Pangenome analysis provides insights into legume evolution and breeding

  • July 30, 2025
Foyer, C. H. et al. Neglecting legumes has compromised human health and sustainable food production. Nat. Plants 2,…
GGenetics
Methods and applications of in vivo CRISPR screening
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Methods and applications of in vivo CRISPR screening

  • July 29, 2025
Auton, A. et al. A global reference for human genetic variation. Nature 526, 68–74 (2015). Google Scholar  García-García,…
GGenetics
Molecular genetics of J-domain protein-related chaperonopathies in skeletal muscle
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Molecular genetics of J-domain protein-related chaperonopathies in skeletal muscle

  • July 22, 2025
Kampinga HH, Andreasson C, Barducci A, Cheetham ME, Cyr D, Emanuelsson C, et al. Function, evolution, and structure…
GGenetics
Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients
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Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients

  • July 21, 2025
Cohort characteristics and model risk score distribution The study cohort comprised 92,493 patients enrolled in the DT Biobank…
GGenetics
Machine learning reveals complex genetics of fungal resistance in sorghum grain mold
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Machine learning reveals complex genetics of fungal resistance in sorghum grain mold

  • July 19, 2025
Ackerman A, Wenndt A, Boyles R (2021) The sorghum grain mold disease complex: pathogens, host responses, and the…
GGenetics
Decomposition of phenotypic heterogeneity in autism reveals underlying genetic programs
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Decomposition of phenotypic heterogeneity in autism reveals underlying genetic programs

  • July 12, 2025
Ethics We received approval to access and analyze deidentified genetic and phenotypic data from the two cohorts from…
GGenetics
Genetic and oncogenic features of RASGRF fusions
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Genetic and oncogenic features of RASGRF fusions

  • July 5, 2025
Prevalence of RASGRF fusions in solid tumor malignancies We previously reported three RASGRF1 fusions: (1) an OCLN–RASGRF1 fusion…
GGenetics
A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia
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A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia

  • July 4, 2025
Tan W, Lin A, Keppler-Noreuil K. Cranioectodermal Dysplasia. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace…
GGenetics
Pitfalls in the diagnosis of apparent homozygous mutations: two cases of IL10RA deficiency inflammatory bowel disease and a literature review | Orphanet Journal of Rare Diseases
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Pitfalls in the diagnosis of apparent homozygous mutations: two cases of IL10RA deficiency inflammatory bowel disease and a literature review | Orphanet Journal of Rare Diseases

  • July 3, 2025
Clinical phenotypes of two patients with apparent homozygous mutations Patient 1: A 4-month-old boy from a non-consanguineous Chinese…
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