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1. An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports KAT6B as a novel neuroblastoma susceptibility gene

2. Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

3. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

4. Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

5. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

6. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.

7. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

8. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

9. Accounting for population structure in genetic studies of cystic fibrosis

10. Genome Sequencing in the Parkinson Disease Clinic

11. Human whole-exome genotype data for Alzheimer’s disease

12. Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma

13. A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

14. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

15. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

16. Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality.

17. Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants.

18. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

19. Genome sequencing in the Parkinson disease clinic

20. Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children’s Oncology Group

21. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

22. Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group.

23. Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children: Novel Obesity Loci in Hispanic Children

25. A genetic-association study of circulating coagulation factor VIII and von Willebrand factor levels

26. A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay

27. Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia

28. A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay.

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