| Year |
Citation |
Score |
| 2018 |
Del Gobbo GF, Price EM, Hanna CW, Robinson WP. No evidence for association of677C>T and 1298A>C variants with placental DNA methylation. Clinical Epigenetics. 10: 34. PMID 29564022 DOI: 10.1186/S13148-018-0468-1 |
0.598 |
|
| 2017 |
Barha CK, Salvante KG, Hanna CW, Wilson SL, Robinson WP, Altman RM, Nepomnaschy PA. Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers. Plos One. 12: e0177869. PMID 28542264 DOI: 10.1371/Journal.Pone.0177869 |
0.69 |
|
| 2016 |
Hanna CW, Peñaherrera MS, Saadeh H, Andrews S, McFadden DE, Kelsey G, Robinson WP. Pervasive polymorphic imprinted methylation in the human placenta. Genome Research. PMID 26769960 DOI: 10.1101/Gr.196139.115 |
0.732 |
|
| 2016 |
Barha CK, Hanna CW, Salvante KG, Wilson SL, Robinson WP, Altman RM, Nepomnaschy PA. Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation. Plos One. 11: e0146424. PMID 26731744 DOI: 10.1371/Journal.Pone.0146424 |
0.693 |
|
| 2016 |
Del Gobbo G, Price EM, Hanna C, Robinson W. Placental MTHFR 677C>T genotypes in pregnancy pathologies Placenta. 45: 112. DOI: 10.1016/J.Placenta.2016.06.177 |
0.598 |
|
| 2015 |
Wen J, Hanna CW, Martell S, Leung PC, Lewis SM, Robinson WP, Stephenson MD, Rajcan-Separovic E. Functional consequences of copy number variants in miscarriage. Molecular Cytogenetics. 8: 6. PMID 25674159 DOI: 10.1186/s13039-015-0109-8 |
0.496 |
|
| 2015 |
Bagheri H, Wen J, Hanna CW, Tang F, Martell S, Qiao Y, Leung P, Robinson W, Stephenson M, Rajcan-Separovic E. MG-123 Genomics of early pregnancy loss Journal of Medical Genetics. 52: A6.1-A6. DOI: 10.1136/Jmedgenet-2015-103577.15 |
0.499 |
|
| 2015 |
Hanna C, Penaherrera M, Saadeh H, McFadden D, Kelsey G, Robinson W. Transient and placenta-specific imprinting in human development Placenta. 36: A39. DOI: 10.1016/J.Placenta.2015.07.303 |
0.713 |
|
| 2013 |
Hanna CW, McFadden DE, Robinson WP. DNA methylation profiling of placental villi from karyotypically normal miscarriage and recurrent miscarriage. The American Journal of Pathology. 182: 2276-84. PMID 23583422 DOI: 10.1016/j.ajpath.2013.02.021 |
0.499 |
|
| 2013 |
Manokhina I, Hanna CW, Stephenson MD, McFadden DE, Robinson WP. Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage. Molecular Human Reproduction. 19: 539-44. PMID 23515668 DOI: 10.1093/molehr/gat019 |
0.534 |
|
| 2012 |
Hogg K, Price EM, Hanna CW, Robinson WP. Prenatal and perinatal environmental influences on the human fetal and placental epigenome. Clinical Pharmacology and Therapeutics. 92: 716-26. PMID 23047650 DOI: 10.1038/clpt.2012.141 |
0.587 |
|
| 2012 |
Hanna CW, Bloom MS, Robinson WP, Kim D, Parsons PJ, vom Saal FS, Taylor JA, Steuerwald AJ, Fujimoto VY. DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF. Human Reproduction (Oxford, England). 27: 1401-10. PMID 22381621 DOI: 10.1093/Humrep/Des038 |
0.498 |
|
| 2012 |
Hanna CW, Blair JD, Stephenson MD, Robinson WP. Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage. Reproductive Biomedicine Online. 24: 251-3. PMID 22197129 DOI: 10.1016/j.rbmo.2011.10.013 |
0.452 |
|
| 2010 |
Hanna CW, Bretherick KL, Liu CC, Stephenson MD, Robinson WP. Genetic variation within the hypothalamus-pituitary-ovarian axis in women with recurrent miscarriage. Human Reproduction (Oxford, England). 25: 2664-71. PMID 20716560 DOI: 10.1093/humrep/deq211 |
0.744 |
|
| 2010 |
Fujii R, Fujita S, Waseda T, Oka Y, Takagi H, Tomizawa H, Sasagawa T, Makinoda S, Cavagna M, Braga DPAF, Figueira RCS, Aoki T, Maldonado LGL, Iaconelli A, Borges E, ... ... Hanna CW, et al. Posters * Reproductive Endocrinology (i.e. PCOS, Menarche, Menopause etc.) Human Reproduction. 25: i285-i321. DOI: 10.1093/humrep/de.25.s1.438 |
0.693 |
|
| 2009 |
Hanna CW, Bretherick KL, Gair JL, Fluker MR, Stephenson MD, Robinson WP. Telomere length and reproductive aging. Human Reproduction (Oxford, England). 24: 1206-11. PMID 19202142 DOI: 10.1093/humrep/dep007 |
0.64 |
|
| 2008 |
Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP. Estrogen receptor alpha gene polymorphisms are associated with idiopathic premature ovarian failure. Fertility and Sterility. 89: 318-24. PMID 17706202 DOI: 10.1016/j.fertnstert.2007.03.008 |
0.738 |
|
| 2008 |
Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP. Estrogen receptor α gene polymorphisms are associated with idiopathic premature ovarian failure Obstetrical and Gynecological Survey. 63: 435-436. DOI: 10.1097/01.ogx.0000318078.78865.25 |
0.735 |
|
| 2008 |
Ghahremani M, Hanna C, Bretherick K, Penaherrera M, Fluker M, Robinson W. Epigenetic alterations associated with premature ovarian failure Fertility and Sterility. 90: S122-S123. DOI: 10.1016/j.fertnstert.2008.07.125 |
0.735 |
|
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