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Your search keyword '"Salerno W."' showing total 32 results

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32 results on '"Salerno W."'

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1. A deep catalogue of protein-coding variation in 983,578 individuals.

2. Common and rare variant associations with clonal haematopoiesis phenotypes

3. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))

4. The Alzheimerʼs Disease Sequencing Project: Study design and sample selection

5. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))

6. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

7. Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

8. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

9. Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

10. Clinical/Scientific Notes: The Alzheimer's disease sequencing project: Study design and sample selection

11. Human genome meeting 2016

13. Human genome meeting 2016

14. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

15. Development of a core outcome set for recurrent acute and chronic pancreatitis: Results of a Delphi poll.

16. A deep catalogue of protein-coding variation in 983,578 individuals.

17. Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

18. A deep catalog of protein-coding variation in 985,830 individuals.

19. Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

20. Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.

21. xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments.

22. Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.

23. Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.

24. A catalog of associations between rare coding variants and COVID-19 outcomes.

25. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.

26. Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.

27. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.

28. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.

29. The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences.

30. Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.

31. Comparative genomics of the social amoebae Dictyostelium discoideum and Dictyostelium purpureum.

32. Scale-invariant structure of strongly conserved sequence in genomic intersections and alignments.

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