Phillip E. Melton, Ph.D. - Publications

Affiliations: 
2008 Anthropology University of Kansas, Lawrence, KS, United States 
Area:
Physical Anthropology, Genetics

54 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Keshawarz A, Joehanes R, Ma J, Lee GY, Costeira R, Tsai PC, Masachs OM, Bell JT, Wilson R, Thorand B, Winkelmann J, Peters A, Linseisen J, Waldenberger M, Lehtimäki T, ... ... Melton PE, et al. Dietary and supplemental intake of vitamins C and E is associated with altered DNA methylation in an epigenome-wide association study meta-analysis. Epigenetics. 18: 2211361. PMID 37233989 DOI: 10.1080/15592294.2023.2211361  0.473
2021 Min JL, Hemani G, Hannon E, Dekkers KF, Castillo-Fernandez J, Luijk R, Carnero-Montoro E, Lawson DJ, Burrows K, Suderman M, Bretherick AD, Richardson TG, Klughammer J, Iotchkova V, Sharp G, ... ... Melton P, et al. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics. 53: 1311-1321. PMID 34493871 DOI: 10.1038/s41588-021-00923-x  0.361
2020 Justice AE, Chittoor G, Gondalia R, Melton PE, Lim E, Grove ML, Whitsel EA, Liu CT, Cupples LA, Fernandez-Rhodes L, Guan W, Bressler J, Fornage M, Boerwinkle E, Li Y, et al. Methylome-wide association study of central adiposity implicates genes involved in immune and endocrine systems. Epigenomics. PMID 32901515 DOI: 10.2217/Epi-2019-0276  0.612
2020 Alghamdi MA, Wallace HJ, Melton PE, Moses EK, Stevenson A, Al-Eitan LN, Rea S, Duke JM, Danielsen PL, Prêle CM, Wood FM, Fear MW. Identification of Differentially Methylated CpG Sites in Fibroblasts from Keloid Scars. Biomedicines. 8. PMID 32605309 DOI: 10.3390/Biomedicines8070181  0.309
2020 Merid SK, Novoloaca A, Sharp GC, Küpers LK, Kho AT, Roy R, Gao L, Annesi-Maesano I, Jain P, Plusquin M, Kogevinas M, Allard C, Vehmeijer FO, Kazmi N, Salas LA, ... ... Melton PE, et al. Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age. Genome Medicine. 12: 25. PMID 32114984 DOI: 10.1186/S13073-020-0716-9  0.317
2020 Cadby G, Melton PE, McCarthy NS, Giles C, Mellett NA, Huynh K, Hung J, Beilby J, Dubé MP, Watts GF, Blangero J, Meikle PJ, Moses EK. Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study. Journal of Lipid Research. PMID 32060071 DOI: 10.1194/Jlr.Ra119000594  0.341
2019 Barton SJ, Melton PE, Titcombe P, Murray R, Rauschert S, Lillycrop KA, Huang RC, Holbrook JD, Godfrey KM. In Epigenomic Studies, Including Cell-Type Adjustments in Regression Models Can Introduce Multicollinearity, Resulting in Apparent Reversal of Direction of Association. Frontiers in Genetics. 10: 816. PMID 31552104 DOI: 10.3389/Fgene.2019.00816  0.329
2019 Küpers LK, Monnereau C, Sharp GC, Yousefi P, Salas LA, Ghantous A, Page CM, Reese SE, Wilcox AJ, Czamara D, Starling AP, Novoloaca A, Lent S, Roy R, Hoyo C, ... ... Melton PE, et al. Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight. Nature Communications. 10: 1893. PMID 31015461 DOI: 10.1038/S41467-019-09671-3  0.331
2019 Ariff A, Melton PE, Brennecke SP, Moses EK. Analysis of the Epigenome in Multiplex Pre-eclampsia Families Identifies , , and as Novel Candidate Risk Genes. Frontiers in Genetics. 10: 227. PMID 30941163 DOI: 10.3389/Fgene.2019.00227  0.38
2019 Melton PE, Johnson MP, Gokhale-Agashe D, Rea AJ, Ariff A, Cadby G, Peralta JM, Mcnab TJ, Allcock RJ, Abraham LJ, Blangero J, Brennecke SP, Moses EK. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes. Journal of Hypertension. PMID 30633125 DOI: 10.1097/Hjh.0000000000002023  0.328
2018 Wallace HJ, Cadby G, Melton PE, Wood FM, Falder S, Crowe MM, Martin LJ, Marlow K, Ward SV, Fear MW. Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study. Burns : Journal of the International Society For Burn Injuries. PMID 30595539 DOI: 10.1016/J.Burns.2018.10.027  0.399
2018 Nustad HE, Almeida M, Canty AJ, LeBlanc M, Page CM, Melton PE. Epigenetics, heritability and longitudinal analysis. Bmc Genetics. 19: 77. PMID 30255778 DOI: 10.1186/S12863-018-0648-1  0.339
2017 Cadby G, Melton PE, McCarthy NS, Almeida M, Williams-Blangero S, Curran JE, VandeBerg JL, Hui J, Beilby J, Musk AW, James AL, Hung J, Blangero J, Moses EK. Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study. Human Genetics. PMID 29181734 DOI: 10.1007/S00439-017-1856-X  0.368
2017 McCarthy NS, Badcock JC, Clark ML, Knowles EEM, Cadby G, Melton PE, Morgan VA, Blangero J, Moses EK, Glahn DC, Jablensky A. Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia. Schizophrenia Bulletin. PMID 29040798 DOI: 10.1093/Schbul/Sbx141  0.342
2017 Sharp GC, Salas LA, Monnereau C, Allard C, Yousefi P, Everson TM, Bohlin J, Xu Z, Huang RC, Reese SE, Xu CJ, Baïz N, Hoyo C, Agha G, Roy R, ... ... Melton PE, et al. Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium. Human Molecular Genetics. 26: 4067-4085. PMID 29016858 DOI: 10.1093/Hmg/Ddx290  0.345
2017 Lillycrop K, Murray R, Cheong C, Teh AL, Clarke-Harris R, Barton S, Costello P, Garratt E, Cook E, Titcombe P, Shunmuganathan B, Liew SJ, Chua YC, Lin X, Wu Y, ... ... Melton PE, et al. ANRIL Promoter DNA Methylation: A Perinatal Marker for Later Adiposity. Ebiomedicine. PMID 28473239 DOI: 10.1016/J.Ebiom.2017.03.037  0.339
2017 McCarthy N, Clark M, Cadby G, Blangero J, Dragovic M, Melton P, Moses E, Badcock J, Jablensky A. Association Between Polygenic Risk Score for Schizophrenia and Neurocognitive Measures in the Western Australian Family Study of Schizophrenia (Wafss) European Neuropsychopharmacology. 27: S505-S506. DOI: 10.1016/J.Euroneuro.2016.09.611  0.337
2016 Beaty KG, Mosher MJ, Crawford MH, Melton P. Paternal Genetic Structure in Contemporary Mennonite Communities from the American Midwest. Human Biology. 88: 95-108. PMID 28161998 DOI: 10.13110/Humanbiology.88.2.0095  0.769
2016 Mosher MJ, Melton PE, Stapleton P, Schanfield MS, Crawford MH. Patterns of DNA Methylation Across the Leptin Core Promoter in Four Diverse Asian and North American Populations. Human Biology. 88: 121-135. PMID 28161997 DOI: 10.13110/Humanbiology.88.2.0121  0.716
2016 Melton PE, Peralta JM, Almasy L. Constrained multivariate association with longitudinal phenotypes. Bmc Proceedings. 10: 329-332. PMID 27980657 DOI: 10.1186/S12919-016-0051-8  0.396
2016 Engelman CD, Greenwood CM, Bailey JN, Cantor RM, Kent JW, König IR, Bermejo JL, Melton PE, Santorico SA, Schillert A, Wijsman EM, MacCluer JW, Almasy L. Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals. Bmc Proceedings. 10: 67-70. PMID 27980613 DOI: 10.1186/S12919-016-0007-Z  0.366
2016 McCarthy NS, Melton PE, Ward SV, Allan SM, Dragovic M, Clark ML, Morar B, Rubio JP, Blangero J, Badcock JC, Morgan VA, Moses EK, Jablensky A. Exome array analysis suggests an increased variant burden in families with schizophrenia. Schizophrenia Research. PMID 27939555 DOI: 10.1016/J.Schres.2016.12.007  0.339
2016 Chiu YF, Justice AE, Melton PE. Longitudinal analytical approaches to genetic data. Bmc Genetics. 17: 4. PMID 26866891 DOI: 10.1186/S12863-015-0312-Y  0.652
2015 Yong HE, Melton PE, Johnson MP, Freed KA, Kalionis B, Murthi P, Brennecke SP, Keogh RJ, Moses EK. Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes. Plos One. 10: e0128230. PMID 26010865 DOI: 10.1371/Journal.Pone.0128230  0.343
2015 Thomsen LC, McCarthy N, Melton PE, Tollaksen K, Lyslo I, Solberg P, Roten LT, Nygård OK, Cadby G, Austgulen R, Moses EK, Iversen AC, Bjørge L. [278-POS]: A genetic connection between preeclampsia and chronic hypertension in Norwegian families. Pregnancy Hypertension. 5: 138-9. PMID 25787627 DOI: 10.1016/J.Preghy.2014.10.284  0.365
2015 Yong HE, Melton PE, Johnson MP, Freed KA, Kalionis B, Murthi P, Brennecke SP, Keogh RJ, Moses EK. [81-OR]: Genome-wide transcriptome directed pathway analysis of maternal preeclampsia susceptibility genes. Pregnancy Hypertension. 5: 43-4. PMID 25787431 DOI: 10.1016/J.Preghy.2014.10.085  0.318
2015 Thomsen LC, McCarthy N, Melton P, Cadby G, Austgulen R, Moses E, Bjørge L, Iversen A. P36. Identifying a novel link between preeclampsia and chronic hypertension in the MTHFR-gene using the population based Norwegian HUNT Study Pregnancy Hypertension: An International Journal of Women's Cardiovascular Health. 5: 243-244. DOI: 10.1016/J.Preghy.2015.07.089  0.345
2015 Moses E, Melton P, Johnson M, Gokhale-Agashe D, Rea A, Allcock R, Blangero J, Brennecke S. O4. Genome wide sequencing approaches to identify missing heritability of preeclampsia Pregnancy Hypertension: An International Journal of Women's Cardiovascular Health. 5: 209-210. DOI: 10.1016/J.Preghy.2015.07.005  0.369
2014 Melton PE, Almasy LA. Bivariate association analysis of longitudinal phenotypes in families. Bmc Proceedings. 8: S90. PMID 25519346 DOI: 10.1186/1753-6561-8-S1-S90  0.386
2014 Bickeböller H, Bailey JN, Beyene J, Cantor RM, Cordell HJ, Culverhouse RC, Engelman CD, Fardo DW, Ghosh S, König IR, Lorenzo Bermejo J, Melton PE, Santorico SA, Satten GA, Sun L, et al. Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees. Bmc Proceedings. 8: S1. PMID 25519310 DOI: 10.1186/1753-6561-8-S1-S1  0.386
2014 McCarthy NS, Melton PE, Cadby G, Yazar S, Franchina M, Moses EK, Mackey DA, Hewitt AW. Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns. Bmc Genomics. 15: 981. PMID 25406947 DOI: 10.1186/1471-2164-15-981  0.314
2014 Baldi NF, Melton PE, Crawford MH. Effect of recent historical events on migration and isonymic stratification among the Rama Amerindians from Nicaragua. Human Biology. 86: 37-50. PMID 25401985 DOI: 10.3378/027.086.0105  0.59
2014 Seyerle AA, Young AM, Jeff JM, Melton PE, Jorgensen NW, Lin Y, Carty CL, Deelman E, Heckbert SR, Hindorff LA, Jackson RD, Martin LW, Okin PM, Perez MV, Psaty BM, et al. Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval. Epidemiology (Cambridge, Mass.). 25: 790-8. PMID 25166880 DOI: 10.1097/Ede.0000000000000168  0.46
2014 Wu Z, Hu Y, Melton PE. Longitudinal data analysis for genetic studies in the whole-genome sequencing era. Genetic Epidemiology. 38: S74-80. PMID 25112193 DOI: 10.1002/Gepi.21829  0.402
2013 Løset M, Johnson MP, Melton PE, Ang W, Marsh J, Huang RC, Mori T, Beilin L, Pennell C, Roten LT, Iversen AC, Austgulen R, East CE, Blangero J, Brennecke SP, et al. OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits. Pregnancy Hypertension. 3: 63. PMID 26105849 DOI: 10.1016/J.Preghy.2013.04.020  0.379
2013 Jones RM, Cadby G, Melton PE, Abraham LJ, Whitehouse AJ, Moses EK. Genome-wide association study of autistic-like traits in a general population study of young adults. Frontiers in Human Neuroscience. 7: 658. PMID 24133439 DOI: 10.3389/Fnhum.2013.00658  0.379
2013 Cadby G, Mukherjee S, Musk AW, Reid A, Garlepp M, Dick I, Robinson C, Hui J, Fiorito G, Guarrera S, Beilby J, Melton PE, Moses EK, Ugolini D, Mirabelli D, et al. A genome-wide association study for malignant mesothelioma risk. Lung Cancer (Amsterdam, Netherlands). 82: 1-8. PMID 23827383 DOI: 10.1016/J.Lungcan.2013.04.018  0.354
2013 Melton PE, Baldi NF, Barrantes R, Crawford MH. Microevolution, migration, and the population structure of five Amerindian populations from Nicaragua and Costa Rica. American Journal of Human Biology : the Official Journal of the Human Biology Council. 25: 480-90. PMID 23559443 DOI: 10.1002/Ajhb.22382  0.626
2013 Melton PE, Carless MA, Curran JE, Dyer TD, Göring HH, Kent JW, Drigalenko E, Johnson MP, Maccluer JW, Moses EK, Comuzzie AG, Mahaney MC, O'Leary DH, Blangero J, Almasy L. Genetic architecture of carotid artery intima-media thickness in Mexican Americans. Circulation. Cardiovascular Genetics. 6: 211-21. PMID 23487405 DOI: 10.1161/Circgenetics.113.000079  0.341
2013 Johnson MP, Brennecke SP, East CE, Dyer TD, Roten LT, Proffitt JM, Melton PE, Fenstad MH, Aalto-Viljakainen T, Mäkikallio K, Heinonen S, Kajantie E, Kere J, Laivuori H, et al. Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. Molecular Human Reproduction. 19: 423-37. PMID 23420841 DOI: 10.1093/Molehr/Gat011  0.362
2013 Rubicz R, Yolken R, Drigalenko E, Carless MA, Dyer TD, Bauman L, Melton PE, Kent JW, Harley JB, Curran JE, Johnson MP, Cole SA, Almasy L, Moses EK, Dhurandhar NV, et al. A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). Plos Genetics. 9: e1003147. PMID 23326239 DOI: 10.1371/Journal.Pgen.1003147  0.696
2012 Løset M, Johnson MP, Pennell C, Huang RC, Mori T, Beilin L, Melton P, Roten LT, Iversen AC, Austgulen R, East C, Blangero J, Brennecke SP, Moses EK. OS070. Shared genetic risk factors for preeclampsia and cardiovascular disease. Pregnancy Hypertension. 2: 214-5. PMID 26105283 DOI: 10.1016/J.Preghy.2012.04.071  0.408
2012 Melton PE. Serum bilirubin and the genetic epidemiology of complex disease Bilirubin: Chemistry, Regulation and Disorder. 185-212.  0.341
2011 Melton PE, Kent JW, Dyer TD, Almasy L, Blangero J. Genetic signal maximization using environmental regression. Bmc Proceedings. 5: S72. PMID 22373104 DOI: 10.1186/1753-6561-5-S9-S72  0.378
2011 Melton PE, Pankratz N. Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data. Genetic Epidemiology. 35: S67-73. PMID 22128062 DOI: 10.1002/Gepi.20653  0.357
2011 Kumar S, Bellis C, Zlojutro M, Melton PE, Blangero J, Curran JE. Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins. Bmc Evolutionary Biology. 11: 293. PMID 21978175 DOI: 10.1186/1471-2148-11-293  0.735
2011 Melton PE, Haack K, Göring HH, Laston S, Umans JG, Lee ET, Fabsitz RR, Devereux RB, Best LG, Maccluer JW, Almasy L, Cole SA. Genetic influences on serum bilirubin in American Indians: The Strong Heart Family Study. American Journal of Human Biology : the Official Journal of the Human Biology Council. 23: 118-25. PMID 21080475 DOI: 10.1002/Ajhb.21114  0.429
2010 Melton PE, Mosher MJ, Rubicz R, Zlojutro M, Crawford MH. Mitochondrial DNA diversity in Mennonite communities from the midwestern United States. Human Biology. 82: 267-89. PMID 20649384 DOI: 10.3378/027.082.0302  0.699
2010 Melton PE, Rutherford S, Voruganti VS, Göring HH, Laston S, Haack K, Comuzzie AG, Dyer TD, Johnson MP, Kent JW, Curran JE, Moses EK, Blangero J, Barac A, Lee ET, et al. Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. Human Molecular Genetics. 19: 3662-71. PMID 20601674 DOI: 10.1093/Hmg/Ddq274  0.379
2010 Rubicz R, Melton PE, Spitsyn V, Sun G, Deka R, Crawford MH. Genetic structure of native circumpolar populations based on autosomal, mitochondrial, and Y chromosome DNA markers. American Journal of Physical Anthropology. 143: 62-74. PMID 20333712 DOI: 10.1002/Ajpa.21290  0.77
2007 Melton PE, Briceño I, Gómez A, Devor EJ, Bernal JE, Crawford MH. Biological relationship between Central and South American Chibchan speaking populations: evidence from mtDNA. American Journal of Physical Anthropology. 133: 753-70. PMID 17340631 DOI: 10.1002/Ajpa.20581  0.586
2006 Melton PE, Zlojutro M, Kimminau K, Crawford MH. Biological aging and Cox hazard analysis of mortality trends in a Mennonite community from south-central Kansas. American Journal of Human Biology : the Official Journal of the Human Biology Council. 18: 387-401. PMID 16634024 DOI: 10.1002/Ajhb.20514  0.745
2006 Tarskaia LA, Melton P. Comparative analysis of mitochondrial DNA of Yakuts and other Asian populations Russian Journal of Genetics. 42: 1439-1446. DOI: 10.1134/S102279540612012X  0.414
2006 Rubicz RC, Melton PE, Crawford MH. Molecular markers in anthropological genetic studies Anthropological Genetics: Theory, Methods and Applications. 141-186. DOI: 10.1017/CBO9781139167222.007  0.725
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