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214 results on '"Machado, Rajiv"'

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1. Defining the clinical validity of genes reported to cause pulmonary arterial hypertension

2. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

3. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.

4. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

6. The molecular cloning and characterisation of the gene mutated in primary pulmonary hypertension

7. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

8. Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality

9. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

10. Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension

11. Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

12. Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

13. Whole-genome sequencing of patients with rare diseases in a national health system

15. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

16. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

19. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

20. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia

21. Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension

22. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

25. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

26. Reduced transfer coefficient of carbon monoxide in pulmonary arterial hypertension implicates rare protein-truncating variants in KDR

29. Genetic Association of the Serotonin Transporter in Pulmonary Arterial Hypertension

30. Mutations of the TGF-β Type II Receptor BMPR2 in Pulmonary Arterial Hypertension

33. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

35. Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-β family

36. Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension

37. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018)

38. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

39. Genetic determinants of risk and survival in pulmonary arterial hypertension

41. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

42. Biallelic variants of ATP13A3cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality

43. BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

44. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

45. Erratum to: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (Scientific Reports, (2018), 8, 1, (1300), 10.1038/s41598-017-14403-y)

46. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

48. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

49. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

50. Identification of novel rare sequence variation underlying heritable pulmonary arterial hypertension

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