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1. A first update on mapping the human genetic architecture of COVID-19

2. Genomic diagnosis of rare pediatric disease in the United Kingdom and Ireland

3. MC3R links nutritional state to childhood growth and the timing of puberty

4. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals

5. Mapping the human genetic architecture of COVID-19

6. Evaluating drug targets through human loss-of-function genetic variation (vol 581, pg 459, 2020)

7. Evaluating potential drug targets through human loss-of-function genetic variation

8. Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice

9. Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

10. Imperfect centered miRNA binding sites are common and can mediate repression of target mRNAs

11. Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

12. Cisplatin-induzierte Hörstörungen in Abhängigkeit von der Pigmentierung

13. MicroRNAs and their isomiRs function cooperatively to target common biological pathways

14. Genetic architecture of routinely acquired blood tests in a British South Asian cohort.

15. The importance of family-based sampling for biobanks.

16. Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

17. Noncoding variants are a rare cause of recessive developmental disorders in trans with coding variants.

18. Genetic links between ovarian ageing, cancer risk and de novo mutation rates.

19. An axis of genetic heterogeneity in autism is indexed by age at diagnosis and is associated with varying developmental and mental health profiles.

20. Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders.

21. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference.

22. Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty.

23. Discovering genes that affect cognitive ability.

24. Influence of autozygosity on common disease risk across the phenotypic spectrum.

25. Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes.

26. Author Correction: The power of genetic diversity in genome-wide association studies of lipids.

27. Polygenic prediction of preeclampsia and gestational hypertension.

28. Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.

29. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.

30. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.

31. Genetic correlates of phenotypic heterogeneity in autism.

32. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals.

33. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

34. Recommendations for clinical interpretation of variants found in non-coding regions of the genome.

35. Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study.

36. Reduced reproductive success is associated with selective constraint on human genes.

37. Fine-scale population structure and demographic history of British Pakistanis.

38. The power of genetic diversity in genome-wide association studies of lipids.

39. Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders.

40. MC3R links nutritional state to childhood growth and the timing of puberty.

41. The immunologic response to severe acute respiratory syndrome coronavirus 2.

42. The genomic history of the Middle East.

45. The contribution of X-linked coding variation to severe developmental disorders.

46. Evidence for 28 genetic disorders discovered by combining healthcare and research data.

47. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.

48. Evaluating drug targets through human loss-of-function genetic variation.

49. Nature via Nurture, the Martin Way.

50. Cohort Profile: East London Genes & Health (ELGH), a community-based population genomics and health study in British Bangladeshi and British Pakistani people.

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