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110 results on '"Alhusaini, S"'

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1. Reproducibility in the absence of selective reporting: An illustration from large-scale brain asymmetry research

2. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

3. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

4. A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies

5. Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression

6. Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study

7. The genetic architecture of the human cerebral cortex

8. The genetic architecture of the human cerebral cortex

9. Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study

10. Genetic architecture of subcortical brain structures in 38,854 individuals worldwide

12. Genetic architecture of subcortical brain structures in 38,851 individuals

13. Genetic architecture of subcortical brain structures in 38,851 individuals

14. Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium

15. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study

16. Novel genetic loci associated with hippocampal volume

17. Novel genetic loci underlying human intracranial volume identified through genome-wide association

20. Novel genetic loci associated with hippocampal volume

21. Novel genetic loci associated with hippocampal volume

22. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

23. Novel genetic loci underlying human intracranial volume identified through genome-wide association

24. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

25. The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data

27. Common genetic variants influence human subcortical brain structures

28. Common genetic variants influence human subcortical brain structures

29. Common genetic variants influence human subcortical brain structures

30. The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data

31. The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data

32. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

33. Identification of common variants associated with human hippocampal and intracranial volumes.

34. Identification of common variants associated with human hippocampal and intracranial volumes

35. Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

36. The role of endoplasmic reticulum in human adipose tissue

37. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

38. Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

39. HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.

40. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries.

41. Experience from a Fast-Track Multidisciplinary Clinic Integrating Movement Disorders Neurologists in Normal Pressure Hydrocephalus Evaluation.

43. Autopsy-Proven "Pure" Parkinson's Disease with Rapidly Progressive Dementia and Cognitive Fluctuations in a Patient with GBA Mutation.

44. A WORLDWIDE ENIGMA STUDY ON EPILEPSY-RELATED GRAY AND WHITE MATTER COMPROMISE ACROSS THE ADULT LIFESPAN.

47. Real-world risk of brain metastases in stage III non-small cell lung cancer in the era of PET and MRI staging.

48. Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data.

49. Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.

50. SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.

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