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1. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

2. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

3. Phenotype and imaging features associated with APP duplications

4. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

5. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

6. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

7. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

8. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

11. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics

12. Primary brain calcification: an international study reporting novel variants and associated phenotypes.

13. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

14. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

15. Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers

16. Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study

17. Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

19. Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations

20. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

21. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

22. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

23. Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease

24. Biological insights from 108 schizophrenia-associated genetic loci

26. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

27. Genome-wide association analysis identifies 13 new risk loci for schizophrenia.

29. Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use

30. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

31. How local reference panels improve imputation in French populations.

37. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

40. A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

41. A polygenic resilience score moderates the genetic risk for schizophrenia

42. Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders

43. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

44. Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders

45. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

46. Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders

50. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

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