430 results on '"Mcneill, Alisdair"'
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2. Hitting the heights with CiteScore
3. What’s new in EJHG in June 2024?
4. Novel insights into cancer predisposition genes
5. Artificial intelligence – the next generation of sequencing?
6. Using exomes better
7. Managing genetic information sharing at family and population level
8. Deep phenotyping and population-level data can help resolve genomic variants
9. Ambivalence and regret in genome sequencing
10. Expanding what we know about rare genetic diseases
11. Why don’t we all use genomic testing?
12. A new impact factor for EJHG in 2022
13. 2022: the year that was in the European Journal of Human Genetics
14. Unusual genomic variants require unusual analyses
15. ENROLL-HD for MND?
16. Molecular explanations for variability of clinical phenotypes
17. Solving medical mysteries with genomics
18. April, again
19. Genes=disease (?)
20. The value of exomes across the ages
21. Investigation and management of Wilson's disease: a practical guide from the British Association for the Study of the Liver
22. New year, new genes
23. The utility of population level genomic research
24. Genome sequencing—do you know what you are getting into?
25. Variability of Multiple Sclerosis Walking Scale and Multiple Sclerosis Impact Scale Scores in People Without Multiple Sclerosis
26. A report of resources used by clinicians in the UK to support motor neuron disease genomic testing
27. Multimodal assessment of mitochondrial function in Parkinson's disease
28. Happy 30th birthday to the European Journal of Human Genetics!
29. Guidelines, guidelines everywhere—and still I’m not sure what to do
30. Clinical genomics testing: mainstreaming and globalising
31. What’s new in genetics in June 2022?
32. Predictive genetic testing for Motor neuron disease: time for a guideline?
33. No gene to predict the future?
34. Exome sequencing—one test to rule them all?
35. No April fools in clinical genomics
36. A new system for variant classification?
37. Correction: 2021 at European Journal of Human Genetics: the year in review
38. New year, new issue
39. 2021 at European Journal of Human Genetics: the year in review
40. Genomics elucidates both common and rare disease aetiology
41. Genotyping arrays, population genetic studies and clinical implications
42. Good genotype-phenotype relationships in rare disease are hard to find
43. Comment on: Bi-allelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2
44. Fond farewell to clinical utility gene cards
45. Multimodal assessment of mitochondrial function in Parkinson's disease.
46. A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease
47. Diagnosis of Neurogenetic Disorders : Contribution of Next Generation Sequencing and Deep Phenotyping
48. Clinical genomics—but faster
49. A Double-Blind, Randomized, Placebo-Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease
50. What’s new in EJHG in April
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