-
1
-
-
0037038230
-
Getting ready for gene-based medicine
-
DOI 10.1056/NEJMe020119
-
Varmus, H. (2002) Getting ready for gene-based medicine. N. Engl. J. Med., 347, 1526-1527. (Pubitemid 35257595)
-
(2002)
New England Journal of Medicine
, vol.347
, Issue.19
, pp. 1526-1527
-
-
Varmus, H.1
-
2
-
-
0037464588
-
A vision for the future of genomics research
-
DOI 10.1038/nature01626
-
Collins, F.S., Green, E.D., Guttmacher, A.E. et al. (2003) A vision for the future of genomics research. Nature, 422, 835-847. (Pubitemid 36520032)
-
(2003)
Nature
, vol.422
, Issue.6934
, pp. 835-847
-
-
Collins, F.S.1
Green, E.D.2
Guttmacher, A.E.3
Guyer, M.S.4
-
3
-
-
77952786822
-
Genomic medicine- an updated primer
-
Feero, W.G., Guttmacher, A.E. and Collins, F.S. (2010) Genomic medicine- an updated primer. N. Engl. J. Med., 362, 2001-2011.
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 2001-2011
-
-
Feero, W.G.1
Guttmacher, A.E.2
Collins, F.S.3
-
4
-
-
34547618083
-
Drinking from the fire hose - Statistical issues in genomewide association studies
-
DOI 10.1056/NEJMp078120
-
Hunter, D.J. and Kraft, P. (2007) Drinking from the fire hose-statistical issues in genomewide association studies. N. Engl. J. Med., 357, 436-439. (Pubitemid 47204871)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.5
, pp. 436-439
-
-
Hunter, D.J.1
Kraft, P.2
-
5
-
-
65949099120
-
Genetic risk prediction-are we there yet?
-
Kraft, P. and Hunter, D.J. (2009) Genetic risk prediction-are we there yet? N. Engl. J. Med., 360, 1701-1703.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1701-1703
-
-
Kraft, P.1
Hunter, D.J.2
-
6
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein, D.B. (2009) Common genetic variation and human traits. N. Engl. J. Med., 360, 1696-1698.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
7
-
-
65949124249
-
Genomewide association studies-illuminating biologic pathways
-
Hirschhorn, J.N. (2009) Genomewide association studies-illuminating biologic pathways. N. Engl. J. Med., 360, 1699-1701.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1699-1701
-
-
Hirschhorn, J.N.1
-
8
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli, E.T. and Goldstein, D.B. (2010) Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat. Rev. Genet., 11, 415-425.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
9
-
-
77951702343
-
Genetic heterogeneity in human disease
-
McClellan, J. and King, M.C. (2010) Genetic heterogeneity in human disease. Cell, 141, 210-217.
-
(2010)
Cell
, vol.141
, pp. 210-217
-
-
McClellan, J.1
King, M.C.2
-
10
-
-
33751011889
-
HTRA1 promoter polymorphism in wet age-related macular degeneration
-
DOI 10.1126/science.1133807
-
Dewan, A., Liu, M., Hartman, S. et al. (2006) HTRA1 promoter polymorphism in wet age-related macular degeneration. Science, 314, 989-992. (Pubitemid 44749943)
-
(2006)
Science
, vol.314
, Issue.5801
, pp. 989-992
-
-
DeWan, A.1
Liu, M.2
Hartman, S.3
Zhang, S.S.-M.4
Liu, D.T.L.5
Zhao, C.6
Tam, P.O.S.7
Chan, W.M.8
Lam, D.S.C.9
Snyder, M.10
Barnstable, C.11
Pang, C.P.12
Hoh, J.13
-
11
-
-
37249006192
-
New links to the pathogenesis of Crohn disease provided by genome-wide association scans
-
DOI 10.1038/nrg2203, PII NRG2203
-
Mathew, C.G. (2008) New links to the pathogenesis of Crohn disease provided by genome-wide association scans. Nat. Rev. Genet., 9, 9-14. (Pubitemid 350277296)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.1
, pp. 9-14
-
-
Mathew, C.G.1
-
12
-
-
78249239776
-
A genome-wide study reveals copy number variants exclusive to childhood obesity cases
-
Glessner, J.T., Bradfield, J.P., Wang, K. et al. (2010) A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am. J. Hum. Genet., 87, 661-666.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 661-666
-
-
Glessner, J.T.1
Bradfield, J.P.2
Wang, K.3
-
13
-
-
78650115977
-
A robust multifactor dimensionality reduction method for detecting gene-gene interactions with application to the genetic analysis of bladder cancer susceptibility
-
Gui, J., Andrew, A.S., Andrews, P. et al. (2010) A robust multifactor dimensionality reduction method for detecting gene-gene interactions with application to the genetic analysis of bladder cancer susceptibility. Ann. Hum. Genet, 75, 20-8.
-
(2010)
Ann. Hum. Genet
, vol.75
, pp. 20-8
-
-
Gui, J.1
Andrew, A.S.2
Andrews, P.3
-
14
-
-
67349166946
-
Detecting gene-gene interactions that underlie human diseases
-
Cordell, H.J. (2009) Detecting gene-gene interactions that underlie human diseases. Nat. Rev. Genet., 10, 392-404.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 392-404
-
-
Cordell, H.J.1
-
15
-
-
77958469463
-
Detecting, characterizing, and interpreting nonlinear gene-gene interactions using multifactor dimensionality reduction
-
Moore, J.H. (2010) Detecting, characterizing, and interpreting nonlinear gene-gene interactions using multifactor dimensionality reduction. Adv. Genet., 72, 101-116.
-
(2010)
Adv. Genet.
, vol.72
, pp. 101-116
-
-
Moore, J.H.1
-
16
-
-
78549251736
-
Analysing biological pathways in genome-wide association studies
-
Wang, K., Li, M. and Hakonarson, H. (2010) Analysing biological pathways in genome-wide association studies. Nat. Rev. Genet., 11, 843-854.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 843-854
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
17
-
-
78650136869
-
Using biological knowledge to uncover the mystery in the search for epistasis in genome-wide association studies
-
Ritchie, M.D. (2011) Using biological knowledge to uncover the mystery in the search for epistasis in genome-wide association studies. Ann. Hum. Genet., 75, 172-182.
-
(2011)
Ann. Hum. Genet.
, vol.75
, pp. 172-182
-
-
Ritchie, M.D.1
-
18
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry, S.T., Ward, M.H., Kholodov, M. et al. (2001) dbSNP: The NCBI database of genetic variation. Nucleic Acids Res., 29, 308-311. (Pubitemid 32054478)
-
(2001)
Nucleic Acids Research
, vol.29
, Issue.1
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.-H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
Sirotkin, K.7
-
19
-
-
13444272087
-
Entrez Gene: Gene-centered information at NCBI
-
DOI 10.1093/nar/gki031
-
Maglott, D., Ostell, J., Pruitt, K.D. et al. (2005) Entrez Gene: Gene-centered information at NCBI. Nucleic Acids Res., 33, D54-D58. (Pubitemid 40207830)
-
(2005)
Nucleic Acids Research
, vol.33
, Issue.DATABASE ISS.
-
-
Maglott, D.1
Ostell, J.2
Pruitt, K.D.3
Tatusova, T.4
-
20
-
-
38549117309
-
The HGNC database in 2008: A resource for the human genome
-
DOI 10.1093/nar/gkm881
-
Bruford, E.A., Lush, M.J., Wright, M.W. et al. (2008) The HGNC Database in 2008: A resource for the human genome. Nucleic Acids Res., 36, D445-D448. (Pubitemid 351149764)
-
(2008)
Nucleic Acids Research
, vol.36
, Issue.SUPPL. 1
-
-
Bruford, E.1
Lush, M.J.2
Wright, M.W.3
Sneddon, T.P.4
Povey, S.5
Birney, E.6
-
21
-
-
62549104880
-
SciMiner: Web-based literature mining tool for target identification and functional enrichment analysis
-
Hur, J., Schuyler, A.D., States, D.J. et al. (2009) SciMiner: Web-based literature mining tool for target identification and functional enrichment analysis. Bioinformatics, 25, 838-840.
-
(2009)
Bioinformatics
, vol.25
, pp. 838-840
-
-
Hur, J.1
Schuyler, A.D.2
States, D.J.3
-
22
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium et al
-
International HapMap Consortium et al. (2005) A haplotype map of the human genome. Nature, 437, 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
23
-
-
0030246854
-
The statistical analysis of kappa statistics in multiple samples
-
DOI 10.1016/0895-4356(96)00057-1
-
Donner, A. and Klar, N. (1996) The statistical analysis of kappa statistics in multiple samples. J. Clin. Epidemiol., 49, 1053-1058. (Pubitemid 26319041)
-
(1996)
Journal of Clinical Epidemiology
, vol.49
, Issue.9
, pp. 1053-1058
-
-
Donner, A.1
Klar, N.2
-
24
-
-
0034254199
-
Homogeneity of kappa statistics in multiple samples
-
DOI 10.1016/S0169-2607(00)00074-2, PII S0169260700000742
-
Reed, J.F. III (2000) Homogeneity of kappa statistics in multiple samples. Comput. Methods Programs Biomed., 63, 43-46. (Pubitemid 30601740)
-
(2000)
Computer Methods and Programs in Biomedicine
, vol.63
, Issue.1
, pp. 43-46
-
-
Reed III, J.F.1
-
25
-
-
74049140006
-
Early pregnancy peripheral blood gene expression and risk of preterm delivery: A nested case control study
-
Enquobahrie, D.A., Williams, M.A., Qiu, C. et al. (2009) Early pregnancy peripheral blood gene expression and risk of preterm delivery: A nested case control study. BMC Pregnancy Childbirth, 9, 56.
-
(2009)
BMC Pregnancy Childbirth
, vol.9
, pp. 56
-
-
Enquobahrie, D.A.1
Williams, M.A.2
Qiu, C.3
-
26
-
-
77951856382
-
Human effector/initiator gene sets that regulate myometrial contractility during term and preterm labor
-
Weiner, C.P., Mason, C.W., Dong, Y. et al. (2010) Human effector/initiator gene sets that regulate myometrial contractility during term and preterm labor. Am. J. Obstet. Gynecol., 202, 474 e1-e20.
-
(2010)
Am. J. Obstet. Gynecol.
, vol.202
, Issue.474
-
-
Weiner, C.P.1
Mason, C.W.2
Dong, Y.3
-
27
-
-
57449100878
-
Fetal inflammatory response in women with proteomic biomarkers characteristic of intra-amniotic inflammation and preterm birth
-
Buhimschi, C.S., Dulay, A.T., Abdel-Razeq, S. et al. (2009) Fetal inflammatory response in women with proteomic biomarkers characteristic of intra-amniotic inflammation and preterm birth. BJOG, 116, 257-267.
-
(2009)
BJOG
, vol.116
, pp. 257-267
-
-
Buhimschi, C.S.1
Dulay, A.T.2
Abdel-Razeq, S.3
-
28
-
-
0036081062
-
The KEGG databases at GenomeNet
-
Kanehisa, M., Goto, S., Kawashima, S. et al. (2002) The KEGG databases at GenomeNet. Nucleic Acids Res., 30, 42-46.
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 42-46
-
-
Kanehisa, M.1
Goto, S.2
Kawashima, S.3
-
29
-
-
77951731266
-
The pursuit of genome-wide association studies: Where are we now?
-
Ku, C.S., Loy, E.Y., Pawitan, Y. et al. (2010) The pursuit of genome-wide association studies: Where are we now? J. Hum. Genet., 55, 195-206.
-
(2010)
J. Hum. Genet.
, vol.55
, pp. 195-206
-
-
Ku, C.S.1
Loy, E.Y.2
Pawitan, Y.3
-
30
-
-
72849144434
-
Sequencing technologies - The next generation
-
Metzker, M.L. (2010) Sequencing technologies - The next generation. Nat. Rev. Genet., 11, 31-46.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
31
-
-
55549147191
-
Personal genomes: The case of the missing heritability
-
Maher, B. (2008) Personal genomes: The case of the missing heritability. Nature, 456, 18-21.
-
(2008)
Nature
, vol.456
, pp. 18-21
-
-
Maher, B.1
-
32
-
-
77952557918
-
Missing heritability and strategies for finding the underlying causes of complex disease
-
Eichler, E.E., Flint, J., Gibson, G. et al. (2010) Missing heritability and strategies for finding the underlying causes of complex disease. Nat. Rev. Genet., 11, 446-450.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 446-450
-
-
Eichler, E.E.1
Flint, J.2
Gibson, G.3
-
33
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T.A., Collins, F.S., Cox, N.J. et al. (2009) Finding the missing heritability of complex diseases. Nature, 461, 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
34
-
-
77954136357
-
Hints of hidden heritability in GWAS
-
Gibson, G. (2010) Hints of hidden heritability in GWAS. Nat. Genet., 42, 558-560.
-
(2010)
Nat. Genet.
, vol.42
, pp. 558-560
-
-
Gibson, G.1
-
35
-
-
58849112975
-
Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission
-
Askland, K., Read, C. and Moore, J. (2008) Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission. Hum. Genet., 125, 63-79.
-
(2008)
Hum. Genet.
, vol.125
, pp. 63-79
-
-
Askland, K.1
Read, C.2
Moore, J.3
-
36
-
-
78549252909
-
Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility
-
O'Dushlaine, C., Kenny, E., Heron, E. et al. (2010) Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Mol. Psychiatry, 16, 286-92.
-
(2010)
Mol. Psychiatry
, vol.16
, pp. 286-92
-
-
O'Dushlaine, C.1
Kenny, E.2
Heron, E.3
-
37
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
Wang, K., Zhang, H., Ma, D. et al. (2009) Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature, 459, 528-533.
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
-
38
-
-
20344369286
-
The genetic contribution towards preterm delivery
-
DOI 10.1016/j.siny.2004.04.001
-
Adams, K.M. and Eschenbach, D.A. (2004) The genetic contribution towards preterm delivery. Semin. Fetal Neonatal. Med., 9, 445-452. (Pubitemid 41123651)
-
(2004)
Seminars in Fetal and Neonatal Medicine
, vol.9
, Issue.6
, pp. 445-452
-
-
Adams, K.M.1
Eschenbach, D.A.2
-
39
-
-
28644438349
-
Genetic variation associated with preterm birth: A HuGE review
-
DOI 10.1097/01.gim.0000187223.69947.db
-
Crider, K.S., Whitehead, N. and Buus, R.M. (2005) Genetic variation associated with preterm birth: A HuGE review. Genet. Med., 7, 593-604. (Pubitemid 41753010)
-
(2005)
Genetics in Medicine
, vol.7
, Issue.9
, pp. 593-604
-
-
Crider, K.S.1
Whitehead, N.2
Buus, R.M.3
-
40
-
-
33845451012
-
Genetic associations in preterm birth: A primer of marker selection, study design, and data analysis
-
DOI 10.1016/j.jsgi.2006.09.006, PII S1071557606014997
-
Menon, R., Fortunato, S.J., Thorsen, P. et al. (2006) Genetic associations in preterm birth: A primer of marker selection, study design, and data analysis. J. Soc. Gynecol. Investig., 13, 531-541. (Pubitemid 44908989)
-
(2006)
Journal of the Society for Gynecologic Investigation
, vol.13
, Issue.8
, pp. 531-541
-
-
Menon, R.1
Fortunato, S.J.2
Thorsen, P.3
Williams, S.4
-
41
-
-
33846940547
-
Genetic epidemiologic studies of preterm birth: Guidelines for research
-
DOI 10.1016/j.ajog.2006.03.109, PII S0002937806024756
-
Pennell, C.E., Jacobsson, B., Williams, S.M. et al. (2007) Genetic epidemiologic studies of preterm birth: Guidelines for research. Am. J. Obstet. Gynecol., 196, 107-118. (Pubitemid 46239999)
-
(2007)
American Journal of Obstetrics and Gynecology
, vol.196
, Issue.2
, pp. 107-118
-
-
Pennell, C.E.1
Jacobsson, B.2
Williams, S.M.3
Buus, R.M.4
Muglia, L.J.5
Dolan, S.M.6
Morken, N.-H.7
Ozcelik, H.8
Lye, S.J.9
Relton, C.10
-
42
-
-
41649105451
-
Genetic contributions to preterm birth: Implications from epidemiological and genetic association studies
-
Plunkett, J. and Muglia, L.J. (2008) Genetic contributions to preterm birth: Implications from epidemiological and genetic association studies. Ann. Med., 40, 167-195.
-
(2008)
Ann. Med.
, vol.40
, pp. 167-195
-
-
Plunkett, J.1
Muglia, L.J.2
-
43
-
-
33845567710
-
The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome
-
DOI 10.1111/j.1471-0528.2006.01150.x
-
Romero, R., Espinoza, J., Gotsch, F. et al. (2006) The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome. BJOG, 113 (Suppl. 3), 118-135. (Pubitemid 44934682)
-
(2006)
BJOG: An International Journal of Obstetrics and Gynaecology
, vol.113
, Issue.SUPPL. 3
, pp. 118-135
-
-
Romero, R.1
Espinoza, J.2
Gotsch, F.3
Kusanovic, J.P.4
Friel, L.A.5
Erez, O.6
Mazaki-Tovi, S.7
Than, N.G.8
Hassan, S.9
Tromp, G.10
-
44
-
-
70849100075
-
The genetics of preterm birth: Using what we know to design better association studies
-
Weinberg, C.R. and Shi, M. (2009) The genetics of preterm birth: Using what we know to design better association studies. Am. J. Epidemiol., 170, 1373-1381.
-
(2009)
Am. J. Epidemiol.
, vol.170
, pp. 1373-1381
-
-
Weinberg, C.R.1
Shi, M.2
-
45
-
-
0034763963
-
Tumor necrosis factor-α promoter variant 2 (TNF2) is associated with pre-term delivery, infant mortality, and malaria morbidity in western Kenya: Asembo bay cohort project IX
-
DOI 10.1002/gepi.1029
-
Aidoo, M., McElroy, P.D., Kolczak, M.S. et al. (2001) Tumor necrosis factor-alpha promoter variant 2 (TNF2) is associated with pre-term delivery, infant mortality, and malaria morbidity in western Kenya: Asembo Bay Cohort Project IX. Genet. Epidemiol., 21, 201-211. (Pubitemid 33021274)
-
(2001)
Genetic Epidemiology
, vol.21
, Issue.3
, pp. 201-211
-
-
Aidoo, M.1
McElroy, P.D.2
Kolczak, M.S.3
Terlouw, D.J.4
Ter Kuile, F.O.5
Nahlen, B.6
Lal, A.A.7
Udhayakumar, V.8
-
46
-
-
0037155249
-
A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes
-
DOI 10.1074/jbc.M107865200
-
Fujimoto, T., Parry, S., Urbanek, M. et al. (2002) A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes. J. Biol. Chem., 277, 6296-6302. (Pubitemid 34968421)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.8
, pp. 6296-6302
-
-
Fujimoto, T.1
Parry, S.2
Urbanek, M.3
Sammel, M.4
Macones, G.5
Kuivaniemi, H.6
Romero, R.7
Strauss, J.F.8
-
47
-
-
0036077629
-
Polymorphism in the interleukin-1 gene complex and spontaneous preterm delivery
-
DOI 10.1067/mob.2002.122407
-
Genc, M.R., Gerber, S., Nesin, M. et al. (2002) Polymorphism in the interleukin-1 gene complex and spontaneous preterm delivery. Am. J. Obstet. Gynecol., 187, 157-163. (Pubitemid 34800315)
-
(2002)
American Journal of Obstetrics and Gynecology
, vol.187
, Issue.1
, pp. 157-163
-
-
Genc, M.R.1
Gerber, S.2
Nesin, M.3
Witkin, S.S.4
-
48
-
-
1642423714
-
Interleukin-4 and -10 gene polymorphisms and spontaneous preterm birth in multifetal gestations
-
DOI 10.1016/j.ajog.2003.09.066
-
Kalish, R.B., Vardhana, S., Gupta, M. et al. (2004) Interleukin-4 and - 10 gene polymorphisms and spontaneous preterm birth in multifetal gestations. Am. J. Obstet. Gynecol., 190, 702-706. (Pubitemid 38406781)
-
(2004)
American Journal of Obstetrics and Gynecology
, vol.190
, Issue.3
, pp. 702-706
-
-
Kalish, R.B.1
Vardhana, S.2
Gupta, M.3
Perni, S.C.4
Witkin, S.S.5
-
49
-
-
0036832451
-
Beta2-Adrenergic receptor genotype and preterm delivery
-
DOI 10.1067/mob.2002.128524
-
Landau, R., Xie, H.G., Dishy, V. et al. (2002) beta2-Adrenergic receptor genotype and preterm delivery. Am. J. Obstet. Gynecol., 187, 1294-1298. (Pubitemid 35397478)
-
(2002)
American Journal of Obstetrics and Gynecology
, vol.187
, Issue.5
, pp. 1294-1298
-
-
Landau, R.1
Xie, H.G.2
Dishy, V.3
Stein, C.M.4
Wood, A.J.J.5
Moore, J.H.6
Emala, C.W.7
Smiley, R.M.8
-
50
-
-
85047684648
-
Association between the Asp299Gly polymorphisms in the toll-like receptor 4 and premature births in the Finnish population
-
DOI 10.1203/01.PDR.0000025342.83436.53
-
Lorenz, E., Hallman, M., Marttila, R. et al. (2002) Association between the Asp299Gly polymorphisms in the Toll-like receptor 4 and premature births in the Finnish population. Pediatr. Res., 52, 373-376. (Pubitemid 34920267)
-
(2002)
Pediatric Research
, vol.52
, Issue.3
, pp. 373-376
-
-
Lorenz, E.1
Hallman, M.2
Marttila, R.3
Haataja, R.4
Schwartz, D.A.5
-
51
-
-
0036284406
-
Association of the Gln27Glu polymorphism of the beta-2-adrenergic receptor with preterm labor
-
DOI 10.1016/S0020-7292(02)00035-8, PII S0020729202000358
-
Ozkur, M., Dogulu, F., Ozkur, A. et al. (2002) Association of the Gln27Glu polymorphism of the beta-2-adrenergic receptor with preterm labor. Int. J. Gynaecol. Obstet., 77, 209-215. (Pubitemid 34628519)
-
(2002)
International Journal of Gynecology and Obstetrics
, vol.77
, Issue.3
, pp. 209-215
-
-
Ozkur, M.1
Dogulu, F.2
Ozkur, A.3
Gokmen, B.4
Inaloz, S.S.5
Aynacioglu, A.S.6
-
52
-
-
2042447785
-
Association of -634G/C and 936C/T polymorphisms of the vascular endothelial growth factor with spontaneous preterm delivery
-
DOI 10.1111/j.0001-6349.2004.00403.x
-
Papazoglou, D., Galazios, G., Koukourakis, M.I. et al. (2004) Association of -634G/C and 936C/T polymorphisms of the vascular endothelial growth factor with spontaneous preterm delivery. Acta Obstet. Gynecol. Scand., 83, 461-465. (Pubitemid 38534765)
-
(2004)
Acta Obstetricia et Gynecologica Scandinavica
, vol.83
, Issue.5
, pp. 461-465
-
-
Papazoglou, D.1
Galazios, G.2
Koukourakis, M.I.3
Kontomanolis, E.N.4
Maltezos, E.5
-
53
-
-
0010243393
-
Association of polymorphism within the promoter of the tumor necrosis factor α gene with increased risk of preterm premature rupture of the fetal membranes
-
DOI 10.1016/S0002-9378(99)70632-0
-
Roberts, A.K., Monzon-Bordonaba, F., Van Deerlin, P.G. et al. (1999) Association of polymorphism within the promoter of the tumor necrosis factor alpha gene with increased risk of preterm premature rupture of the fetal membranes. Am. J. Obstet. Gynecol., 180, 1297-1302. (Pubitemid 29259032)
-
(1999)
American Journal of Obstetrics and Gynecology
, vol.180
, Issue.5
, pp. 1297-1302
-
-
Roberts, A.K.1
Monzon-Bordonaba, F.2
Van Deerlin, P.G.3
Holder, J.4
Macones, G.A.5
Morgan, M.A.6
Strauss III, J.F.7
Parry, S.8
-
54
-
-
0242677635
-
Interleukin-6 promoter - 174 polymorphism and spontaneous preterm birth
-
DOI 10.1067/S0002-9378(03)00843-3
-
Simhan, H.N., Krohn, M.A., Roberts, J.M. et al. (2003) Interleukin-6 promoter -174 polymorphism and spontaneous preterm birth. Am. J. Obstet. Gynecol., 189, 915-918. (Pubitemid 37373868)
-
(2003)
American Journal of Obstetrics and Gynecology
, vol.189
, Issue.4
, pp. 915-918
-
-
Simhan, H.N.1
Krohn, M.A.2
Roberts, J.M.3
Zeevi, A.4
Caritis, S.N.5
-
55
-
-
0346120406
-
Polymorphism in intron 2 of the fetal interleukin-1 receptor antagonist genotype influences midtrimester amniotic fluid concentrations of interleukin-1β and interleukin-1 receptor antagonist and pregnancy outcome
-
DOI 10.1067/S0002-9378(03)00630-6
-
Witkin, S.S., Vardhana, S., Yih, M. et al. (2003) Polymorphism in intron 2 of the fetal interleukin-1 receptor antagonist genotype influences midtrimester amniotic fluid concentrations of interleukin-1beta and interleukin-1 receptor antagonist and pregnancy outcome. Am. J. Obstet. Gynecol., 189, 1413-1417. (Pubitemid 37542183)
-
(2003)
American Journal of Obstetrics and Gynecology
, vol.189
, Issue.5
, pp. 1413-1417
-
-
Witkin, S.S.1
Vardhana, S.2
Yih, M.3
Doh, K.4
Bongiovanni, A.M.5
Gerber, S.6
-
56
-
-
0034018471
-
Genetic influence on birthweight and gestational length determined by studies in offspring of twins
-
Clausson, B., Lichtenstein, P. and Cnattingius, S. (2000) Genetic influence on birthweight and gestational length determined by studies in offspring of twins. BJOG, 107, 375-381. (Pubitemid 30145380)
-
(2000)
British Journal of Obstetrics and Gynaecology
, vol.107
, Issue.3
, pp. 375-381
-
-
Clausson, B.1
Lichtenstein, P.2
Cnattingius, S.3
-
57
-
-
0033916562
-
Genetic influences on premature parturition in an australian twin sample
-
Treloar, S.A., Macones, G.A., Mitchell, L.E. et al. (2000) Genetic influences on premature parturition in an Australian twin sample. Twin Res., 3, 80-82. (Pubitemid 30431149)
-
(2000)
Twin Research
, vol.3
, Issue.2
, pp. 80-82
-
-
Treloar, S.A.1
Macones, G.A.2
Mitchell, L.E.3
Martin, N.G.4
-
58
-
-
0016282720
-
Familial trends in low birth weight
-
Johnstone, F. and Inglis, L. (1974) Familial trends in low birth weight. Br. Med. J., 3, 659-661.
-
(1974)
Br. Med. J.
, vol.3
, pp. 659-661
-
-
Johnstone, F.1
Inglis, L.2
-
59
-
-
27944453555
-
The heritability of preterm delivery
-
Ward, K., Argyle, V., Meade, M. et al. (2005) The heritability of preterm delivery. Obstet. Gynecol., 106, 1235-1239. (Pubitemid 41668940)
-
(2005)
Obstetrics and Gynecology
, vol.106
, Issue.6
, pp. 1235-1239
-
-
Ward, K.1
Argyle, V.2
Meade, M.3
Nelson, L.4
-
61
-
-
0033568824
-
Recurrence risk of congenital anomalies - The impact of paternal, social, and environmental factors: A population-based study in Denmark
-
Basso, O., Olsen, J. and Christensen, K. (1999) Recurrence risk of congenital anomalies-the impact of paternal, social, and environmental factors: A population-based study in Denmark. Am. J. Epidemiol., 150, 598-604. (Pubitemid 29426904)
-
(1999)
American Journal of Epidemiology
, vol.150
, Issue.6
, pp. 598-604
-
-
Basso, O.1
Olsen, J.2
Christensen, K.3
-
62
-
-
0032797106
-
Low birthweight and prematurity in relation to paternal factors: A study of recurrence
-
DOI 10.1093/ije/28.4.695
-
Basso, O., Olsen, J. and Christensen, K. (1999) Low birthweight and prematurity in relation to paternal factors: A study of recurrence. Int. J. Epidemiol., 28, 695-700. (Pubitemid 29401329)
-
(1999)
International Journal of Epidemiology
, vol.28
, Issue.4
, pp. 695-700
-
-
Basso, O.1
Olsen, J.2
Christensen, K.3
-
63
-
-
70849096100
-
Maternal contributions to preterm delivery
-
Boyd, H.A., Poulsen, G., Wohlfahrt, J. 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
-
64
-
-
70849102601
-
Maternal effects for preterm birth: A genetic epidemiologic study of 630, 000 families
-
Svensson, A.C., Sandin, S., Cnattingius, S. 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
-
65
-
-
70849089830
-
Invited commentary: Maternal effects in preterm birth-effects of maternal genotype, mitochondrial DNA, imprinting, or environment? Am
-
Little, J. (2009) Invited commentary: Maternal effects in preterm birth-effects of maternal genotype, mitochondrial DNA, imprinting, or environment? Am. J. Epidemiol., 170, 1382-1385.
-
(2009)
J. Epidemiol.
, vol.170
, pp. 1382-1385
-
-
Little, J.1
-
66
-
-
70849100075
-
The genetics of preterm birth: Using what we know to design better association studies
-
Weinberg, C.R. and Shi, M. (2009) The genetics of preterm birth: Using what we know to design better association studies. Am. J. Epidemiol., 170, 1373-1381.
-
(2009)
Am. J. Epidemiol.
, vol.170
, pp. 1373-1381
-
-
Weinberg, C.R.1
Shi, M.2
-
67
-
-
79952272417
-
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis
-
Haataja, R., Karjalainen, M.K., Luukkonen, A. et al. (2011) Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. PLoS Genet., 7, e1001293.
-
(2011)
PLoS Genet.
, vol.7
-
-
Haataja, R.1
Karjalainen, M.K.2
Luukkonen, A.3
-
68
-
-
33847681021
-
Ehlers-Danlos syndrome: Insights on obstetric aspects
-
DOI 10.1097/01.ogx.0000251027.32142.63, PII 0000625420070100000023
-
Volkov, N., Nisenblat, V., Ohel, G. et al. (2007) Ehlers-Danlos syndrome: Insights on obstetric aspects. Obstet. Gynecol. Surv., 62, 51-57. (Pubitemid 46360534)
-
(2007)
Obstetrical and Gynecological Survey
, vol.62
, Issue.1
, pp. 51-57
-
-
Volkov, N.1
Nisenblat, V.2
Ohel, G.3
Gonen, R.4
-
69
-
-
76649105134
-
The enigma of spontaneous preterm birth
-
Muglia, L.J. and Katz, M. (2010) The enigma of spontaneous preterm birth. N. Engl. J. Med., 362, 529-535.
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 529-535
-
-
Muglia, L.J.1
Katz, M.2
|