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2. DNA Methylation Signatures Identify Biologically Distinct Subtypes in Acute Myeloid Leukemia

3. Genome-wide epigenetic analysis delineates a biologically distinct immature acute leukemia with myeloid/T-lymphoid features

4. Genetic disease risks of under-represented founder populations in New York City.

5. Prenatal vitamin D deficiency exposure leads to long-term changes in immune cell proportions.

6. Single-cell analysis identifies distinct CD4+ T cells associated with the pathobiology of pediatric obesity-related asthma.

7. MYH11 rare variant augments aortic growth and induces cardiac hypertrophy and heart failure with pressure overload.

8. Response to Widen et al.

9. Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population.

10. Physician and informal care use explained by the Pediatric Quality of Life Inventory (PedsQL) in children with suspected genetic disorders.

11. Prenatal vitamin D deficiency alters immune cell proportions of young adult offspring through alteration of long-term stem cell fates.

12. Regulatory landscape enrichment analysis (RLEA): a computational toolkit for non-coding variant enrichment and cell type prioritization.

13. Acute Lymphoblastic Leukemia with Myeloid Mutations Is a High-Risk Disease Associated with Clonal Hematopoiesis.

14. Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).

15. Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.

16. Egr1 is a sex-specific regulator of neuronal chromatin, synaptic plasticity, and behaviour.

17. The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families.

18. Urine Proteomics Link Complement Activation with Interstitial Fibrosis/Tubular Atrophy in Lupus Nephritis Patients.

19. Early-life stress and ovarian hormones alter transcriptional regulation in the nucleus accumbens resulting in sex-specific responses to cocaine.

20. Regulatory Landscape Enrichment Analysis (RLEA) using gaiaAssociation.

21. Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.

22. Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.

23. The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.

24. An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies.

25. The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.

26. Detection of mosaic variants using genome sequencing in a large pediatric cohort.

27. Using epigenomics to understand cellular responses to environmental influences in diseases.

28. Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders.

29. Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.

30. Umbilical cord blood: an undervalued and underutilized resource in allogeneic hematopoietic stem cell transplant and novel cell therapy applications.

31. Genomic insights into host and parasite interactions during intracellular infection by Toxoplasma gondii.

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

33. Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function.

34. The Genomics of Colorectal Cancer in Populations with African and European Ancestry.

35. Cell type-specific chromatin accessibility analysis in the mouse and human brain.

36. Master Transcription Regulators and Transcription Factors Regulate Immune-Associated Differences Between Patients of African and European Ancestry With Colorectal Cancer.

37. Author Correction: The SEQC2 epigenomics quality control (EpiQC) study.

38. The SEQC2 epigenomics quality control (EpiQC) study.

39. GenomeDiver: a platform for phenotype-guided medical genomic diagnosis.

40. Disproportionate Vitamin A Deficiency in Women of Specific Ethnicities Linked to Differences in Allele Frequencies of Vitamin A-Related Polymorphisms.

41. GUÍA: a digital platform to facilitate result disclosure in genetic counseling.

42. Preleukemic and leukemic evolution at the stem cell level.

43. Correction to: The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.

44. The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.

45. The shape of gene expression distributions matter: how incorporating distribution shape improves the interpretation of cancer transcriptomic data.

46. Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.

47. Identification of a novel subgroup of endometrial cancer patients with loss of thyroid hormone receptor beta expression and improved survival.

48. Quantitative Kinetic Analyses of Histone Turnover Using Imaging and Flow Cytometry.

49. Functional Genomics of the Pediatric Obese Asthma Phenotype Reveal Enrichment of Rho-GTPase Pathways.

50. A Cellular Stress Response Induced by the CRISPR-dCas9 Activation System Is Not Heritable Through Cell Divisions.

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