메뉴 건너뛰기




Volumn 8, Issue 4, 2013, Pages

X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARTICLE; CASE MOTHER DYAD; CASE PARENT TRIAD; CONTROLLED STUDY; DENMARK; FEMALE; FERM DOMAIN CONTAINING 7 GENE; FETUS; GENE; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; GESTATIONAL AGE; HEREDITY; HUMAN; NORWAY; PREMATURE LABOR; REPLICATION STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; STUDY DESIGN; X CHROMOSOME;

EID: 84876187162     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0061781     Document Type: Article
Times cited : (25)

References (44)
  • 1
    • 84861956278 scopus 로고    scopus 로고
    • National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications
    • Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, et al. (2012) National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet 379: 2162-2172.
    • (2012) Lancet , vol.379 , pp. 2162-2172
    • Blencowe, H.1    Cousens, S.2    Oestergaard, M.Z.3    Chou, D.4    Moller, A.B.5
  • 2
    • 47549088161 scopus 로고    scopus 로고
    • Long-term medical and social consequences of preterm birth
    • Moster D, Lie RT, Markestad T, (2008) Long-term medical and social consequences of preterm birth. N Engl J Med 359: 262-273.
    • (2008) N Engl J Med , vol.359 , pp. 262-273
    • Moster, D.1    Lie, R.T.2    Markestad, T.3
  • 3
    • 54049147321 scopus 로고    scopus 로고
    • Reference population for international comparisons and time trend surveillance of preterm delivery proportions in three countries
    • Morken NH, Vogel I, Kallen K, Skjaerven R, Langhoff-Roos J, et al. (2008) Reference population for international comparisons and time trend surveillance of preterm delivery proportions in three countries. BMC Womens Health 8: 16.
    • (2008) BMC Womens Health , vol.8 , pp. 16
    • Morken, N.H.1    Vogel, I.2    Kallen, K.3    Skjaerven, R.4    Langhoff-Roos, J.5
  • 4
    • 0033916562 scopus 로고    scopus 로고
    • Genetic influences on premature parturition in an Australian twin sample
    • Treloar SA, Macones GA, Mitchell LE, Martin NG, (2000) Genetic influences on premature parturition in an Australian twin sample. Twin Res 3: 80-82.
    • (2000) Twin Res , vol.3 , pp. 80-82
    • Treloar, S.A.1    Macones, G.A.2    Mitchell, L.E.3    Martin, N.G.4
  • 5
    • 0034018471 scopus 로고    scopus 로고
    • Genetic influence on birthweight and gestational length determined by studies in offspring of twins
    • Clausson B, Lichtenstein P, Cnattingius S, (2000) Genetic influence on birthweight and gestational length determined by studies in offspring of twins. Bjog 107: 375-381.
    • (2000) Bjog , vol.107 , pp. 375-381
    • Clausson, B.1    Lichtenstein, P.2    Cnattingius, S.3
  • 8
    • 70849102601 scopus 로고    scopus 로고
    • Maternal effects for preterm birth: a genetic epidemiologic study of 630,000 families
    • Svensson AC, Sandin S, Cnattingius S, Reilly M, Pawitan Y, et al. (2009) Maternal effects for preterm birth: a genetic epidemiologic study of 630,000 families. Am J Epidemiol 170: 1365-1372.
    • (2009) Am J Epidemiol , vol.170 , pp. 1365-1372
    • Svensson, A.C.1    Sandin, S.2    Cnattingius, S.3    Reilly, M.4    Pawitan, Y.5
  • 9
    • 33947210381 scopus 로고    scopus 로고
    • Genetic and environmental influences on birth weight, birth length, head circumference, and gestational age by use of population-based parent-offspring data
    • Lunde A, Melve KK, Gjessing HK, Skjaerven R, Irgens LM, (2007) Genetic and environmental influences on birth weight, birth length, head circumference, and gestational age by use of population-based parent-offspring data. Am J Epidemiol 165: 734-741.
    • (2007) Am J Epidemiol , vol.165 , pp. 734-741
    • Lunde, A.1    Melve, K.K.2    Gjessing, H.K.3    Skjaerven, R.4    Irgens, L.M.5
  • 11
    • 0026599788 scopus 로고
    • Fetal Gender Differences in Preterm Birth: Findings in a North American Cohort
    • 48
    • McGregor JA, Leff M, Orleans M, Baron A (1992) Fetal Gender Differences in Preterm Birth: Findings in a North American Cohort. Amer J Perinatol 9: 43,48.
    • (1992) Amer J Perinatol , vol.9 , pp. 43
    • McGregor, J.A.1    Leff, M.2    Orleans, M.3    Baron, A.4
  • 12
    • 0030221627 scopus 로고    scopus 로고
    • Excess males in preterm birth: interactions with gestational age, race, and multiple birth
    • Cooperstock M, Campbell J, (1996) Excess males in preterm birth: interactions with gestational age, race, and multiple birth. Obstetrics & Gynecology 88: 189-193.
    • (1996) Obstetrics & Gynecology , vol.88 , pp. 189-193
    • Cooperstock, M.1    Campbell, J.2
  • 14
    • 39749159112 scopus 로고    scopus 로고
    • Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
    • Gudmundsson J, Sulem P, Rafnar T, Bergthorsson JT, Manolescu A, et al. (2008) Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Nat Genet 40: 281-283.
    • (2008) Nat Genet , vol.40 , pp. 281-283
    • Gudmundsson, J.1    Sulem, P.2    Rafnar, T.3    Bergthorsson, J.T.4    Manolescu, A.5
  • 15
    • 77954143522 scopus 로고    scopus 로고
    • Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
    • Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, et al. (2010) Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet 42: 579-589.
    • (2010) Nat Genet , vol.42 , pp. 579-589
    • Voight, B.F.1    Scott, L.J.2    Steinthorsdottir, V.3    Morris, A.P.4    Dina, C.5
  • 16
    • 0042487762 scopus 로고    scopus 로고
    • Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia-Parkinsonism (DYT3)
    • Németh AH, Nolte D, Dunne E, Niemann S, Kostrzewa M, et al. (1999) Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia-Parkinsonism (DYT3). Genomics 60: 320-329.
    • (1999) Genomics , vol.60 , pp. 320-329
    • Németh, A.H.1    Nolte, D.2    Dunne, E.3    Niemann, S.4    Kostrzewa, M.5
  • 17
    • 79960837617 scopus 로고    scopus 로고
    • Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
    • Piton A, Gauthier J, Hamdan FF, Lafreniere RG, Yang Y, et al. (2011) Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia. Mol Psychiatry 16: 867-880.
    • (2011) Mol Psychiatry , vol.16 , pp. 867-880
    • Piton, A.1    Gauthier, J.2    Hamdan, F.F.3    Lafreniere, R.G.4    Yang, Y.5
  • 19
    • 82455162436 scopus 로고    scopus 로고
    • Association of sex hormone receptor gene polymorphisms with recurrent pregnancy loss: a systematic review and meta-analysis
    • e1431
    • Su MT, Lin SH, Chen YC (2011) Association of sex hormone receptor gene polymorphisms with recurrent pregnancy loss: a systematic review and meta-analysis. Fertil Steril 96: 1435-1444 e1431.
    • (2011) Fertil Steril , vol.96 , pp. 1435-1444
    • Su, M.T.1    Lin, S.H.2    Chen, Y.C.3
  • 22
    • 84862573335 scopus 로고    scopus 로고
    • X-linked genes and risk of orofacial clefts: evidence from two population-based studies in scandinavia
    • Jugessur A, Skare O, Lie RT, Wilcox AJ, Christensen K, et al. (2012) X-linked genes and risk of orofacial clefts: evidence from two population-based studies in scandinavia. PLoS One 7: e39240.
    • (2012) PLoS One , vol.7
    • Jugessur, A.1    Skare, O.2    Lie, R.T.3    Wilcox, A.J.4    Christensen, K.5
  • 23
  • 24
    • 0033927905 scopus 로고    scopus 로고
    • The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers
    • Horvath S, Laird NM, Knapp M, (2000) The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers. Am J Hum Genet 66: 1161-1167.
    • (2000) Am J Hum Genet , vol.66 , pp. 1161-1167
    • Horvath, S.1    Laird, N.M.2    Knapp, M.3
  • 25
    • 33846007739 scopus 로고    scopus 로고
    • X-APL: an improved family-based test of association in the presence of linkage for the X chromosome
    • Chung RH, Morris RW, Zhang L, Li YJ, Martin ER, (2007) X-APL: an improved family-based test of association in the presence of linkage for the X chromosome. Am J Hum Genet 80: 59-68.
    • (2007) Am J Hum Genet , vol.80 , pp. 59-68
    • Chung, R.H.1    Morris, R.W.2    Zhang, L.3    Li, Y.J.4    Martin, E.R.5
  • 26
    • 63749091904 scopus 로고    scopus 로고
    • Association test for X-linked QTL in family-based designs
    • Zhang L, Martin ER, Morris RW, Li YJ, (2009) Association test for X-linked QTL in family-based designs. Am J Hum Genet 84: 431-444.
    • (2009) Am J Hum Genet , vol.84 , pp. 431-444
    • Zhang, L.1    Martin, E.R.2    Morris, R.W.3    Li, Y.J.4
  • 27
    • 33748653394 scopus 로고    scopus 로고
    • Monte Carlo pedigree disequilibrium test for markers on the X chromosome
    • Ding J, Lin S, Liu Y, (2006) Monte Carlo pedigree disequilibrium test for markers on the X chromosome. Am J Hum Genet 79: 567-573.
    • (2006) Am J Hum Genet , vol.79 , pp. 567-573
    • Ding, J.1    Lin, S.2    Liu, Y.3
  • 28
    • 43249130654 scopus 로고    scopus 로고
    • X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design
    • Zhang L, Martin ER, Chung RH, Li YJ, Morris RW, (2008) X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design. Genet Epidemiol 32: 370-380.
    • (2008) Genet Epidemiol , vol.32 , pp. 370-380
    • Zhang, L.1    Martin, E.R.2    Chung, R.H.3    Li, Y.J.4    Morris, R.W.5
  • 29
    • 0035528919 scopus 로고    scopus 로고
    • Reconstructing Parental Genotypes When Testing for Linkage in the Presence of Association
    • Knapp M, (2001) Reconstructing Parental Genotypes When Testing for Linkage in the Presence of Association. Theoretical Population Biology 60: 141-148.
    • (2001) Theoretical Population Biology , vol.60 , pp. 141-148
    • Knapp, M.1
  • 31
    • 33750216250 scopus 로고    scopus 로고
    • Cohort profile: the Norwegian Mother and Child Cohort Study (MoBa)
    • Magnus P, Irgens LM, Haug K, Nystad W, Skjaerven R, et al. (2006) Cohort profile: the Norwegian Mother and Child Cohort Study (MoBa). Int J Epidemiol 35: 1146-1150.
    • (2006) Int J Epidemiol , vol.35 , pp. 1146-1150
    • Magnus, P.1    Irgens, L.M.2    Haug, K.3    Nystad, W.4    Skjaerven, R.5
  • 32
    • 33749621790 scopus 로고    scopus 로고
    • The biobank of the Norwegian Mother and Child Cohort Study: a resource for the next 100 years
    • Ronningen KS, Paltiel L, Meltzer HM, Nordhagen R, Lie KK, et al. (2006) The biobank of the Norwegian Mother and Child Cohort Study: a resource for the next 100 years. Eur J Epidemiol 21: 619-625.
    • (2006) Eur J Epidemiol , vol.21 , pp. 619-625
    • Ronningen, K.S.1    Paltiel, L.2    Meltzer, H.M.3    Nordhagen, R.4    Lie, K.K.5
  • 34
    • 33645727811 scopus 로고    scopus 로고
    • Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes
    • Gjessing HK, Lie RT, (2006) Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes. Ann Hum Genet 70: 382-396.
    • (2006) Ann Hum Genet , vol.70 , pp. 382-396
    • Gjessing, H.K.1    Lie, R.T.2
  • 36
    • 33750466907 scopus 로고    scopus 로고
    • Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
    • Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, et al. (2006) Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Nat Genet 38: 1242-1244.
    • (2006) Nat Genet , vol.38 , pp. 1242-1244
    • Tarpey, P.1    Thomas, S.2    Sarvananthan, N.3    Mallya, U.4    Lisgo, S.5
  • 37
    • 77949471924 scopus 로고    scopus 로고
    • The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development
    • Betts-Henderson J, Bartesaghi S, Crosier M, Lindsay S, Chen HL, et al. (2010) The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development. Hum Mol Genet 19: 342-351.
    • (2010) Hum Mol Genet , vol.19 , pp. 342-351
    • Betts-Henderson, J.1    Bartesaghi, S.2    Crosier, M.3    Lindsay, S.4    Chen, H.L.5
  • 38
    • 0142084743 scopus 로고    scopus 로고
    • Scanning Human Gene Deserts for Long-Range Enhancers
    • Nobrega MA, Ovcharenko I, Afzal V, Rubin EM, (2003) Scanning Human Gene Deserts for Long-Range Enhancers. Science 302: 413-413.
    • (2003) Science , vol.302 , pp. 413
    • Nobrega, M.A.1    Ovcharenko, I.2    Afzal, V.3    Rubin, E.M.4
  • 40
    • 0347444723 scopus 로고    scopus 로고
    • MicroRNAs: genomics, biogenesis, mechanism, and function
    • Bartel DP, (2004) MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116: 281-297.
    • (2004) Cell , vol.116 , pp. 281-297
    • Bartel, D.P.1
  • 41
    • 0035913720 scopus 로고    scopus 로고
    • IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system
    • Ferrante MI, Ghiani M, Bulfone A, Franco B, (2001) IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system. Gene 275: 217-221.
    • (2001) Gene , vol.275 , pp. 217-221
    • Ferrante, M.I.1    Ghiani, M.2    Bulfone, A.3    Franco, B.4
  • 42
    • 0034730618 scopus 로고    scopus 로고
    • Identification and characterization of two members of a novel class of the interleukin-1 receptor (IL-1R) family. Delineation Of a new class of IL-1R-related proteins based on signaling
    • Born TL, Smith DE, Garka KE, Renshaw BR, Bertles JS, et al. (2000) Identification and characterization of two members of a novel class of the interleukin-1 receptor (IL-1R) family. Delineation Of a new class of IL-1R-related proteins based on signaling. J Biol Chem 275: 41528.
    • (2000) J Biol Chem , vol.275 , pp. 41528
    • Born, T.L.1    Smith, D.E.2    Garka, K.E.3    Renshaw, B.R.4    Bertles, J.S.5
  • 44
    • 0027258802 scopus 로고
    • Preterm birth and cerebral palsy: is tumor necrosis factor the missing link?
    • Leviton A, (1993) Preterm birth and cerebral palsy: is tumor necrosis factor the missing link? Dev Med Child Neurol 35: 553-558.
    • (1993) Dev Med Child Neurol , vol.35 , pp. 553-558
    • Leviton, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.