Year |
Citation |
Score |
2013 |
Chun S, Plunkett J, Teramo K, Muglia LJ, Fay JC. Fine-mapping an association of FSHR with preterm birth in a Finnish population. Plos One. 8: e78032. PMID 24205076 DOI: 10.1371/Journal.Pone.0078032 |
0.692 |
|
2013 |
Kim J, Stirling KJ, Cooper ME, Ascoli M, Momany AM, McDonald EL, Ryckman KK, Rhea L, Schaa KL, Cosentino V, Gadow E, Saleme C, Shi M, Hallman M, Plunkett J, et al. Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study. Bmc Medical Genetics. 14: 77. PMID 23889750 DOI: 10.1186/1471-2350-14-77 |
0.689 |
|
2012 |
Karjalainen MK, Huusko JM, Ulvila J, Sotkasiira J, Luukkonen A, Teramo K, Plunkett J, Anttila V, Palotie A, Haataja R, Muglia LJ, Hallman M. A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. Plos One. 7: e51378. PMID 23227263 DOI: 10.1371/Journal.Pone.0051378 |
0.688 |
|
2011 |
Plunkett J, Doniger S, Orabona G, Morgan T, Haataja R, Hallman M, Puttonen H, Menon R, Kuczynski E, Norwitz E, Snegovskikh V, Palotie A, Peltonen L, Fellman V, DeFranco EA, et al. An evolutionary genomic approach to identify genes involved in human birth timing. Plos Genetics. 7: e1001365. PMID 21533219 DOI: 10.1371/Journal.Pgen.1001365 |
0.726 |
|
2011 |
Defranco EA, Jacobs TS, Plunkett J, Chaudhari BP, Huettner PC, Muglia LJ. Placental pathologic aberrations in cases of familial idiopathic spontaneous preterm birth. Placenta. 32: 386-90. PMID 21440297 DOI: 10.1016/J.Placenta.2011.02.010 |
0.574 |
|
2011 |
Haataja R, Karjalainen MK, Luukkonen A, Teramo K, Puttonen H, Ojaniemi M, Varilo T, Chaudhari BP, Plunkett J, Murray JC, McCarroll SA, Peltonen L, Muglia LJ, Palotie A, Hallman M. Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. Plos Genetics. 7: e1001293. PMID 21304894 DOI: 10.1371/Journal.Pgen.1001293 |
0.64 |
|
2010 |
Plunkett J, Doniger S, Morgan T, Haataja R, Hallman M, Puttonen H, Menon R, Kuczynski E, Norwitz E, Snegovskikh V, Palotie A, Peltonen L, Fellman V, DeFranco EA, Chaudhari BP, et al. Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth. Bmc Medical Genomics. 3: 62. PMID 21184677 DOI: 10.1186/1755-8794-3-62 |
0.719 |
|
2009 |
Daw EW, Plunkett J, Feitosa M, Gao X, Van Brunt A, Ma D, Czajkowski J, Province MA, Borecki I. A framework for analyzing both linkage and association: an analysis of Genetic Analysis Workshop 16 simulated data. Bmc Proceedings. 3: S98. PMID 20018095 DOI: 10.1186/1753-6561-3-S7-S98 |
0.365 |
|
2009 |
Plunkett J, Feitosa MF, Trusgnich M, Wangler MF, Palomar L, Kistka ZA, DeFranco EA, Shen TT, Stormo AE, Puttonen H, Hallman M, Haataja R, Luukkonen A, Fellman V, Peltonen L, et al. Mother's genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth. Human Heredity. 68: 209-19. PMID 19521103 DOI: 10.1159/000224641 |
0.68 |
|
2009 |
Flaquer A, Fischer C, Wienker TF, Plunkett J, Feitosa MF, Trusgnich M, Wangler MF, Palomar L, Kistka ZA-, DeFranco EA, Shen TT, Stormo AED, Puttonen H, Hallman M, Haataja R, et al. Dr. Richard Spielman Human Heredity. 68: 221-221. DOI: 10.1159/000225931 |
0.434 |
|
2008 |
Chaudhari BP, Plunkett J, Ratajczak CK, Shen TT, DeFranco EA, Muglia LJ. The genetics of birth timing: insights into a fundamental component of human development. Clinical Genetics. 74: 493-501. PMID 19037974 DOI: 10.1111/J.1399-0004.2008.01124.X |
0.733 |
|
2008 |
Plunkett J, Borecki I, Morgan T, Stamilio D, Muglia LJ. Population-based estimate of sibling risk for preterm birth, preterm premature rupture of membranes, placental abruption and pre-eclampsia. Bmc Genetics. 9: 44. PMID 18611258 DOI: 10.1186/1471-2156-9-44 |
0.654 |
|
2008 |
Plunkett J, Muglia LJ. Genetic contributions to preterm birth: implications from epidemiological and genetic association studies. Annals of Medicine. 40: 167-95. PMID 18382883 DOI: 10.1080/07853890701806181 |
0.654 |
|
2008 |
Kistka ZA, DeFranco EA, Ligthart L, Willemsen G, Plunkett J, Muglia LJ, Boomsma DI. Heritability of parturition timing: an extended twin design analysis. American Journal of Obstetrics and Gynecology. 199: 43.e1-5. PMID 18295169 DOI: 10.1016/J.Ajog.2007.12.014 |
0.605 |
|
2007 |
Dick DM, Wang JC, Plunkett J, Aliev F, Hinrichs A, Bertelsen S, Budde JP, Goldstein EL, Kaplan D, Edenberg HJ, Nurnberger J, Hesselbrock V, Schuckit M, Kuperman S, Tischfield J, et al. Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1. Alcoholism, Clinical and Experimental Research. 31: 1645-53. PMID 17850642 DOI: 10.1111/J.1530-0277.2007.00470.X |
0.358 |
|
2007 |
Dick DM, Plunkett J, Hamlin D, Nurnberger J, Kuperman S, Schuckit M, Hesselbrock V, Edenberg H, Bierut L. Association analyses of the serotonin transporter gene with lifetime depression and alcohol dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample. Psychiatric Genetics. 17: 35-8. PMID 17167343 DOI: 10.1097/Ypg.0B013E328011188B |
0.321 |
|
2007 |
Plunkett J, Muglia L. 648: Sibling risk for adverse pregnancy outcomes American Journal of Obstetrics and Gynecology. 197: S186. DOI: 10.1016/J.Ajog.2007.10.675 |
0.536 |
|
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