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1. Phenotype and imaging features associated with APP duplications

2. Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

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

4. Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

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

6. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease

7. Generation of 17q21.31 duplication iPSC-derived neurons as a model for primary tauopathies

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

9. Identification of TCERG1 as a new genetic modulator of TDP-43 production in Drosophila

10. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila

11. Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons

12. Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds

13. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.

14. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease.

15. Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies

16. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

17. Association study of the GAB2 gene with the risk of developing Alzheimer's disease

18. Correction: Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes.

19. ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease

20. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.

21. Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes.

22. Manic Depressive Illness and Tyrosine Hydroxylase Gene: Linkage Heterogeneity and Association

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

24. New insights into the genetic etiology of Alzheimer's disease and related dementias

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

26. Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

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

28. Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation

29. Haploinsufficiency of the Primary Familial Brain Calcification Gene <scp> SLC20A2 </scp> Mediated by Disruption of a Regulatory Element

30. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease

31. Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

32. Generation of 17q21.31 duplication iPSC-derived neurons as a model for primary tauopathies

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

34. Penetrance estimation of SORL1 loss-of-function variants using a family-based strategy adjusted on APOE genotypes suggest a non-monogenic inheritance

35. SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data

36. Validation de la version française de l’échelle autoévaluation des symptômes négatifs (SNS)

37. Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing

38. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

39. Assessment of SORL1 rare variants segregation in Alzheimer disease families and in vitro models suggests diverse penetrance and oligogenic inheritance

40. Phenotypes associated with MAPT duplications

41. Moderate Overexpression of Tau in Drosophila Exacerbates Amyloid-β-Induced Neuronal Phenotypes and Correlates with Tau Oligomerization

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

43. Exome sequencing identifies novel AD-associated genes

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

45. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

46. Detection of copy number variations from NGS data using read depth information: a diagnostic performance evaluation

47. De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype

48. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in

49. Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer’s Disease Patient

50. Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification

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