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1. Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

2. Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

3. Using Organoids to Model Sex Differences in the Human Brain

4. Neutrophil-inflicted vasculature damage suppresses immune-mediated optic nerve regeneration

5. Transcriptional cartography integrates multiscale biology of the human cortex

6. Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

7. P300 promotes tumor recurrence by regulating radiation-induced conversion of glioma stem cells to vascular-like cells

8. Clinically relevant small-molecule promotes nerve repair and visual function recovery

9. Transcriptomic architecture of nuclei in the marmoset CNS

10. Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

11. Transcription factor network analysis identifies REST/NRSF as an intrinsic regulator of CNS regeneration in mice

12. Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder

13. MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size

14. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

15. The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank

16. Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors

17. The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regeneration

18. Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sex

19. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

20. Abnormal sleep physiology in children with 15q11.2-13.1 duplication (Dup15q) syndrome

21. Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytes

22. Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

23. Case Report: Novel CSF1R Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching Behavior

24. Gene co-expression network analysis in human spinal cord highlights mechanisms underlying amyotrophic lateral sclerosis susceptibility

25. Evolutionary conservation and divergence of the human brain transcriptome

26. Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

27. Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

28. Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

29. Human in vitro models for understanding mechanisms of autism spectrum disorder

30. Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants

32. Increased Striatal Presynaptic Dopamine in a Nonhuman Primate Model of Maternal Immune Activation: A Longitudinal Neurodevelopmental Positron Emission Tomography Study With Implications for Schizophrenia

33. Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility

34. CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes

35. Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors

36. Analysis of the immune response to sciatic nerve injury identifies efferocytosis as a key mechanism of nerve debridement

37. Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression

38. Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

39. Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex

40. Mechanistic Differences in Neuropathic Pain Modalities Revealed by Correlating Behavior with Global Expression Profiling

41. NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism

42. Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection

43. Pathway-based Approach Reveals Differential Sensitivity to E2F1 Inhibition in Glioblastoma

44. A neural stem cell paradigm of pediatric hydrocephalus

48. Data from Pathway-based Approach Reveals Differential Sensitivity to E2F1 Inhibition in Glioblastoma

49. Genetic architecture of epigenetic and neuronal ageing rates in human brain regions

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

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