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

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

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

5. Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

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

7. Common and rare variant associations with clonal haematopoiesis phenotypes

8. Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

11. “PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black Patients”

12. Biallelic BRCA Loss and Homologous Recombination Deficiency in Nonbreast/Ovarian Tumors in Germline BRCA1/2 Carriers

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

14. Multi-ethnic heterozygote frequencies of cancer susceptibility genes to inform counseling of reproductive risk

16. Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial

17. PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients

18. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions

22. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

24. The Wilms tumor suppressor WT1 (ital) encodes a transcriptional activator of amphiregulin (ital)

25. UGT1A1genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab

28. Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

31. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

32. Antagonism of mGluR5 in Fragile X: A Randomized, Placebo-Controlled, Proof-of-Concept Study of AFQ056, a Novel, Sub-Type Selective mGluR5 Antagonist

34. Abstract 13322: Patients With a High Genetic Risk Score for Coronary Artery Disease May Receive Greater Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial

35. Epigenetic Modification of the FMR1Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

36. ANO2 Genetic Variants and Anti-VEGF Treatment Response in Neovascular AMD: A Pharmacogenetic Substudy of VIEW 1 and VIEW 2.

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