-
1
-
-
84861956278
-
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
-
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
-
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
-
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
-
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
-
6
-
-
45649084541
-
Heritability of parturition timing: an extended twin design analysis
-
e41-45
-
Kistka ZA, DeFranco EA, Ligthart L, Willemsen G, Plunkett J,et al. (2008) Heritability of parturition timing: an extended twin design analysis. Am J Obstet Gynecol 199: 43 e41-45.
-
(2008)
Am J Obstet Gynecol
, vol.199
, pp. 43
-
-
Kistka, Z.A.1
DeFranco, E.A.2
Ligthart, L.3
Willemsen, G.4
Plunkett, J.5
-
7
-
-
70849096100
-
Maternal contributions to preterm delivery
-
Boyd HA, Poulsen G, Wohlfahrt J, Murray JC, Feenstra B, et al. (2009) Maternal contributions to preterm delivery. Am J Epidemiol 170: 1358-1364.
-
(2009)
Am J Epidemiol
, vol.170
, pp. 1358-1364
-
-
Boyd, H.A.1
Poulsen, G.2
Wohlfahrt, J.3
Murray, J.C.4
Feenstra, B.5
-
8
-
-
70849102601
-
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
-
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
-
10
-
-
0036796213
-
Fetal sex and preterm birth: are males at greater risk?
-
Zeitlin J, Saurel-Cubizolles MJ, De Mouzon J, Rivera L, Ancel PY, et al. (2002) Fetal sex and preterm birth: are males at greater risk? Hum Reprod 17: 2762-2768.
-
(2002)
Hum Reprod
, vol.17
, pp. 2762-2768
-
-
Zeitlin, J.1
Saurel-Cubizolles, M.J.2
De Mouzon, J.3
Rivera, L.4
Ancel, P.Y.5
-
11
-
-
0026599788
-
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
-
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
-
13
-
-
0028897851
-
Interleukin-1 receptor antagonist in the fetomaternal compartment
-
Bry K, Teramo K, Lappalainen U, Waffarn F, Hallman M, (1995) Interleukin-1 receptor antagonist in the fetomaternal compartment. Acta Paediatr 84: 233-236.
-
(1995)
Acta Paediatr
, vol.84
, pp. 233-236
-
-
Bry, K.1
Teramo, K.2
Lappalainen, U.3
Waffarn, F.4
Hallman, M.5
-
14
-
-
39749159112
-
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
-
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
-
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
-
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
-
18
-
-
78651229757
-
Common variants in DGKK are strongly associated with risk of hypospadias
-
van der Zanden LFM, van Rooij IALM, Feitz WFJ, Knight J, Donders ART, et al. (2011) Common variants in DGKK are strongly associated with risk of hypospadias. Nat Genet 43: 48-50.
-
(2011)
Nat Genet
, vol.43
, pp. 48-50
-
-
van der Zanden, L.F.M.1
van Rooij, I.A.L.M.2
Feitz, W.F.J.3
Knight, J.4
Donders, A.R.T.5
-
19
-
-
82455162436
-
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
-
20
-
-
0036284834
-
Risk Factors for Spontaneous Preterm Birth: A Northern Italian Multicenter Case-Control Study
-
Carlini L, Somigliana E, Rossi G, Veglia F, Busacca M, et al. (2002) Risk Factors for Spontaneous Preterm Birth: A Northern Italian Multicenter Case-Control Study. Gynecologic and Obstetric Investigation 53: 174-180.
-
(2002)
Gynecologic and Obstetric Investigation
, vol.53
, pp. 174-180
-
-
Carlini, L.1
Somigliana, E.2
Rossi, G.3
Veglia, F.4
Busacca, M.5
-
22
-
-
84862573335
-
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
-
24
-
-
0033927905
-
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
-
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
-
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
-
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
-
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
-
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
-
30
-
-
17144466340
-
The Danish National Birth Cohort - its background, structure and aim
-
Olsen J, Melbye M, Olsen SF, Sørensen TIA, Aaby P, et al. (2001) The Danish National Birth Cohort- its background, structure and aim. Scandinavian Journal of Public Health 29: 300-307.
-
(2001)
Scandinavian Journal of Public Health
, vol.29
, pp. 300-307
-
-
Olsen, J.1
Melbye, M.2
Olsen, S.F.3
Sørensen, T.I.A.4
Aaby, P.5
-
31
-
-
33750216250
-
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
-
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
-
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
-
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
-
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
-
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
-
39
-
-
33847230623
-
No Gene Is an Island: The Flip-Flop Phenomenon
-
Lin P-I, Vance JM, Pericak-Vance MA, Martin ER, (2007) No Gene Is an Island: The Flip-Flop Phenomenon. The American Journal of Human Genetics 80: 531-538.
-
(2007)
The American Journal of Human Genetics
, vol.80
, pp. 531-538
-
-
Lin, P.-I.1
Vance, J.M.2
Pericak-Vance, M.A.3
Martin, E.R.4
-
40
-
-
0347444723
-
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
-
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
-
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
-
43
-
-
57049170205
-
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
-
Piton A, Michaud JL, Peng H, Aradhya S, Gauthier J, et al. (2008) Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Human Molecular Genetics 17: 3965-3974.
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 3965-3974
-
-
Piton, A.1
Michaud, J.L.2
Peng, H.3
Aradhya, S.4
Gauthier, J.5
-
44
-
-
0027258802
-
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
|