244 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. April, again
18. Genes=disease (?)
19. The value of exomes across the ages
20. Investigation and management of Wilson's disease: a practical guide from the British Association for the Study of the Liver
21. New year, new genes
22. The utility of population level genomic research
23. Genome sequencing—do you know what you are getting into?
24. Happy 30th birthday to the European Journal of Human Genetics!
25. Guidelines, guidelines everywhere—and still I’m not sure what to do
26. Clinical genomics testing: mainstreaming and globalising
27. What’s new in genetics in June 2022?
28. Predictive genetic testing for Motor neuron disease: time for a guideline?
29. No gene to predict the future?
30. Exome sequencing—one test to rule them all?
31. No April fools in clinical genomics
32. A new system for variant classification?
33. A report of resources used by clinicians in the UK to support motor neuron disease genomic testing.
34. Correction: 2021 at European Journal of Human Genetics: the year in review
35. New year, new issue
36. 2021 at European Journal of Human Genetics: the year in review
37. Genomics elucidates both common and rare disease aetiology
38. Genotyping arrays, population genetic studies and clinical implications
39. Good genotype-phenotype relationships in rare disease are hard to find
40. Comment on: Bi-allelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2
41. Fond farewell to clinical utility gene cards
42. Multimodal assessment of mitochondrial function in Parkinson's disease.
43. Clinical genomics—but faster
44. What’s new in EJHG in April
45. A new impact factor for European Journal of Human Genetics
46. Short report: Behavioural characterisation of SOX11 syndrome
47. A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease.
48. Clinical genetics—it’s polygenic
49. Out now in May’s EJHG
50. No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs
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