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MELISSA RICHARD to Humans

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This is a "connection" page, showing publications MELISSA RICHARD has written about Humans.
MELISSA RICHARD
Connection Strength
0.435
Humans
  1. Sex-Based Differences in Risk of Therapy-Related Myeloid Neoplasms. J Clin Oncol. 2024 Nov; 42(31):3739-3750.
    View in: PubMed
    Score: 0.025
  2. Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. Am J Med Genet A. 2024 06; 194(6):e63569.
    View in: PubMed
    Score: 0.024
  3. Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology Group. J Natl Cancer Inst. 2023 06 08; 115(6):733-741.
    View in: PubMed
    Score: 0.023
  4. Germline Genetic and Treatment-Related Risk Factors for Diabetes Mellitus in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study and St Jude Lifetime Cohorts. JCO Precis Oncol. 2022 12; 6:e2200239.
    View in: PubMed
    Score: 0.022
  5. Differential newborn DNA methylation among individuals with complex congenital heart defects and childhood lymphoma. Birth Defects Res. 2022 12 01; 114(20):1434-1439.
    View in: PubMed
    Score: 0.022
  6. Prevalence and Clustering of Congenital Heart Defects Among Boys With Hypospadias. JAMA Netw Open. 2022 07 01; 5(7):e2224152.
    View in: PubMed
    Score: 0.022
  7. A Role for Genetics in Racial Disparities of Therapy-Related Cardiomyopathy. Cancer Res. 2021 05 01; 81(9):2272-2274.
    View in: PubMed
    Score: 0.020
  8. Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. Cancer. 2021 01 15; 127(2):310-318.
    View in: PubMed
    Score: 0.019
  9. Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias. Sci Rep. 2020 07 29; 10(1):12715.
    View in: PubMed
    Score: 0.019
  10. Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study. PLoS One. 2020; 15(2):e0228887.
    View in: PubMed
    Score: 0.018
  11. The role of genetic variation in DGKK on moderate and severe hypospadias. Birth Defects Res. 2019 08 01; 111(13):932-937.
    View in: PubMed
    Score: 0.017
  12. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. Am J Hum Genet. 2017 Dec 07; 101(6):888-902.
    View in: PubMed
    Score: 0.016
  13. Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids. Transl Psychiatry. 2025 Jun 20; 15(1):207.
    View in: PubMed
    Score: 0.007
  14. Clinical and genetic markers of vascular toxicity in glioblastoma patients: Insights from NRG Oncology RTOG-0825. Neuro Oncol. 2025 Mar 07; 27(3):767-778.
    View in: PubMed
    Score: 0.007
  15. The relationship between physical activity and telomere length in women: A systematic review. Mech Ageing Dev. 2025 Apr; 224:112042.
    View in: PubMed
    Score: 0.007
  16. Evaluation of methotrexate Pharmacogenomic variation to predict acute neurotoxicity in children with acute lymphoblastic leukemia. Pharmacotherapy. 2025 Jan; 45(1):4-11.
    View in: PubMed
    Score: 0.006
  17. Maternal, reproductive and perinatal factors and the risks of birth defects: traditional and emerging factors. Reprod Biomed Online. 2025 Jun; 50(6):104781.
    View in: PubMed
    Score: 0.006
  18. Drug-Resistant Epilepsy in Tuberous Sclerosis Complex Is Associated With TSC2 Genotype: More Findings From the Preventing Epilepsy Using Vigatrin (PREVeNT) Trial. Pediatr Neurol. 2024 Oct; 159:62-71.
    View in: PubMed
    Score: 0.006
  19. Trans-Ancestral Genetic Risk Factors for Treatment-Related Type 2 Diabetes Mellitus in Survivors of Childhood Cancer. J Clin Oncol. 2024 Jul 01; 42(19):2306-2316.
    View in: PubMed
    Score: 0.006
  20. Clonal Hematopoiesis and Therapy-Related Myeloid Neoplasms After Autologous Transplant for Hodgkin Lymphoma. J Clin Oncol. 2024 Jul 10; 42(20):2415-2424.
    View in: PubMed
    Score: 0.006
  21. Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors. Neuro Oncol. 2023 09 05; 25(9):1698-1708.
    View in: PubMed
    Score: 0.006
  22. The risks of birth defects and childhood cancer with conception by assisted reproductive technology. Hum Reprod. 2022 10 31; 37(11):2672-2689.
    View in: PubMed
    Score: 0.006
  23. Epigenetic age acceleration among survivors of pediatric medulloblastoma and primitive neuroectodermal tumor. Pediatr Hematol Oncol. 2023 May; 40(4):407-411.
    View in: PubMed
    Score: 0.005
  24. Short NK- and Na?ve T-Cell Telomere Length Is Associated with Thyroid Cancer in Childhood Cancer Survivors: A Report from the Childhood Cancer Survivor Study. Cancer Epidemiol Biomarkers Prev. 2022 02; 31(2):453-460.
    View in: PubMed
    Score: 0.005
  25. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure. Mol Psychiatry. 2021 11; 26(11):6293-6304.
    View in: PubMed
    Score: 0.005
  26. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat Genet. 2020 12; 52(12):1314-1332.
    View in: PubMed
    Score: 0.005
  27. Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex. Pediatr Neurol. 2020 12; 113:46-50.
    View in: PubMed
    Score: 0.005
  28. Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure. Hypertension. 2020 07; 76(1):195-205.
    View in: PubMed
    Score: 0.005
  29. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels. Circ Genom Precis Med. 2020 08; 13(4):e002772.
    View in: PubMed
    Score: 0.005
  30. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021 Jun; 26(6):2111-2125.
    View in: PubMed
    Score: 0.005
  31. Utilization of archived neonatal dried blood spots for genome-wide genotyping. PLoS One. 2020; 15(2):e0229352.
    View in: PubMed
    Score: 0.005
  32. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Nat Commun. 2019 Nov 12; 10(1):5121.
    View in: PubMed
    Score: 0.005
  33. Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease. Nat Commun. 2019 09 19; 10(1):4267.
    View in: PubMed
    Score: 0.004
  34. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum Mol Genet. 2019 Aug 01; 28(15):2615-2633.
    View in: PubMed
    Score: 0.004
  35. Genetic analyses of diverse populations improves discovery for complex traits. Nature. 2019 06; 570(7762):514-518.
    View in: PubMed
    Score: 0.004
  36. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Am J Epidemiol. 2019 Jun 01; 188(6):1033-1054.
    View in: PubMed
    Score: 0.004
  37. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat Genet. 2019 Apr; 51(4):636-648.
    View in: PubMed
    Score: 0.004
  38. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat Commun. 2019 Jan 22; 10(1):376.
    View in: PubMed
    Score: 0.004
  39. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Hum Mol Genet. 2018 08 15; 27(16):2940-2953.
    View in: PubMed
    Score: 0.004
  40. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLoS One. 2018; 13(6):e0198166.
    View in: PubMed
    Score: 0.004
  41. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet. 2018 Mar 01; 102(3):375-400.
    View in: PubMed
    Score: 0.004
  42. Associations of plasma clusterin and Alzheimer's disease-related MRI markers in adults at mid-life: The CARDIA Brain MRI sub-study. PLoS One. 2018; 13(1):e0190478.
    View in: PubMed
    Score: 0.004
  43. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475?000 Individuals. Circ Cardiovasc Genet. 2017 Oct; 10(5).
    View in: PubMed
    Score: 0.004
  44. Rare coding variants associated with blood pressure variation in 15?914 individuals of African ancestry. J Hypertens. 2017 07; 35(7):1381-1389.
    View in: PubMed
    Score: 0.004
  45. Exosome miR-371b-5p promotes proliferation of lung alveolar progenitor type II cells by using PTEN to orchestrate the PI3K/Akt signaling. Stem Cell Res Ther. 2017 06 08; 8(1):138.
    View in: PubMed
    Score: 0.004
  46. Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. J Lipid Res. 2017 05; 58(5):974-981.
    View in: PubMed
    Score: 0.004
  47. Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations. Heart Rhythm. 2017 04; 14(4):572-580.
    View in: PubMed
    Score: 0.004
  48. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. Am J Hum Genet. 2016 Jul 07; 99(1):8-21.
    View in: PubMed
    Score: 0.004
  49. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. Am J Hum Genet. 2016 Jul 07; 99(1):40-55.
    View in: PubMed
    Score: 0.004
  50. Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases. Am J Hum Genet. 2016 Jul 07; 99(1):22-39.
    View in: PubMed
    Score: 0.004
  51. An Empirical Comparison of Joint and Stratified Frameworks for Studying G ? E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group. Genet Epidemiol. 2016 07; 40(5):404-15.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.