-
2
-
-
33645574663
-
Searching for genetic clues to the causes of pre-eclampsia
-
Chappell S, Morgan L. Searching for genetic clues to the causes of pre-eclampsia. Clin Sci 2006; 110: 443-58.
-
(2006)
Clin Sci
, vol.110
, pp. 443-458
-
-
Chappell, S.1
Morgan, L.2
-
3
-
-
0034018471
-
Genetic influence on birthweight and gestational length determined by studies in offspring of twins
-
Clausson B, Lichtenstein P, Cnattingius S. Genetic influence on birthweight and gestational length determined by studies in offspring of twins. Br J Obstet Gynaecol 2000; 107: 375-81.
-
(2000)
Br J Obstet Gynaecol
, vol.107
, pp. 375-381
-
-
Clausson, B.1
Lichtenstein, P.2
Cnattingius, S.3
-
4
-
-
0032474219
-
Fetal and maternal contributions to risk of pre-eclampsia: Population based study
-
Lie RT, Rasmussen S, Brunborg H et al. Fetal and maternal contributions to risk of pre-eclampsia: population based study. Brit Med J 1998; 316: 1343-7.
-
(1998)
Brit Med J
, vol.316
, pp. 1343-1347
-
-
Lie, R.T.1
Rasmussen, S.2
Brunborg, H.3
-
6
-
-
0031983660
-
Family history of preeclampsia as a predictor for pre-eclampsia in primigravidas
-
Cincotta RB, Brennecke S P. Family history of preeclampsia as a predictor for pre-eclampsia in primigravidas. Int J Gynaecol Obstet 1998; 60: 23-7.
-
(1998)
Int J Gynaecol Obstet
, vol.60
, pp. 23-27
-
-
Cincotta, R.B.1
Brennecke, S.P.2
-
7
-
-
0032988092
-
Twin mothers, pregnancy hypertension and pre-eclampsia
-
Thornton J G, Macdonald A M. Twin mothers, pregnancy hypertension and pre-eclampsia. Br J Obstet Gynaecol 1999; 106: 570-5.
-
(1999)
Br J Obstet Gynaecol
, vol.106
, pp. 570-575
-
-
Thornton, J.G.1
Macdonald, A.M.2
-
8
-
-
0034709264
-
Genetic effects on the liability of developing preeclampsia and gestational hypertension
-
Salonen Ros H, Lichtenstein P, Lipworth L, Cnattingius S. Genetic effects on the liability of developing preeclampsia and gestational hypertension. AmJMed Genet 2000; 91: 256-60.
-
(2000)
Amjmed Genet
, vol.91
, pp. 256-260
-
-
Salonen Ros, H.1
Lichtenstein, P.2
Lipworth, L.3
Cnattingius, S.4
-
9
-
-
7444238608
-
Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population- based swedish cohort study
-
Cnattingius S, Reilly M, Pawitan Y, Lichtenstein P. Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: a population- based Swedish cohort study. Am J Med Genet 2004; A130: 365-71.
-
(2004)
Am J Med Genet
, vol.A130
, pp. 365-371
-
-
Cnattingius, S.1
Reilly, M.2
Pawitan, Y.3
Lichtenstein, P.4
-
10
-
-
0037110878
-
Searching for preeclampsia genes: The current position
-
Lachmeijer A M A, Dekker G A, Pals G et al. Searching for preeclampsia genes: the current position. Eur J Obstet GynRB 2002; 105: 94-113.
-
(2002)
Eur J Obstet Gynrb
, vol.105
, pp. 94-113
-
-
Lachmeijer, A.M.A.1
Dekker, G.A.2
Pals, G.3
-
12
-
-
13244271259
-
Genetic thrombophilias and preeclampsia: A meta-analysis
-
Lin J, August P. Genetic thrombophilias and preeclampsia: a meta-analysis. Obstet Gynecol 2005; 105: 182-92.
-
(2005)
Obstet Gynecol
, vol.105
, pp. 182-192
-
-
Lin, J.1
August, P.2
-
13
-
-
1842637313
-
The association between adverse pregnancy outcomes and maternal factor v leiden genotype: A meta-analysis
-
Dudding T E, Attia J. The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis. Thromb Haemost 2004; 91: 700-11.
-
(2004)
Thromb Haemost
, vol.91
, pp. 700-711
-
-
Dudding, T.E.1
Attia, J.2
-
14
-
-
0041767403
-
Association of leiden mutation in factor v gene with hypertension in pregnancy and pre-eclampsia: A meta-analysis
-
Kosmas I P, Tatsioni A, Ioannidis J P A. Association of Leiden mutation in Factor V gene with hypertension in pregnancy and pre-eclampsia: a meta-analysis. J Hypertens 2003; 21: 1221-8.
-
(2003)
J Hypertens
, vol.21
, pp. 1221-1228
-
-
Kosmas, I.P.1
Tatsioni, A.2
Ioannidis, J.P.A.3
-
15
-
-
54249125584
-
Factor v leiden is associated with pre-eclampsia but not with fetal growth restriction: A genetic association study and meta-analysis
-
Dudding T, Heron J, Thakkinstian A et al. Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis. J Thromb Haemost 2008; 6: 1868-75.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1868-1875
-
-
Dudding, T.1
Heron, J.2
Thakkinstian, A.3
-
16
-
-
0016746677
-
Evidence for hl-a- linked genes in “juvenile” diabetes mellitus
-
Cudworth A G, Woodrow J C. Evidence for HL-A- linked genes in “juvenile” diabetes mellitus. Br Med J 1975; 3(5976): 133-5.
-
(1975)
Br Med J
, vol.3
, Issue.5976
, pp. 133-135
-
-
Cudworth, A.G.1
Woodrow, J.C.2
-
17
-
-
23444438235
-
The apolipoprotein e/ci/cii gene cluster and late-onset alzheimer disease
-
Yu C-E, Payami H, Olson JM et al. The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease. Am J Hum Genet 1994; 54: 631-42.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 631-642
-
-
Yu, C.-E.1
Payami, H.2
Olson, J.M.3
-
18
-
-
0344132050
-
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13
-
Arngrimsson R, Sigurardottir S, Frigge ML et al. A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. Hum Mol Genet 1999; 8: 1799-805.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1799-1805
-
-
Arngrimsson, R.1
Sigurardottir, S.2
Frigge, M.L.3
-
19
-
-
0033659638
-
A genome scan in families from australia and new zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2
-
Moses E K, Lade J A, Guo G et al. A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2. Am JHum Genet 2000; 67:1581-5.
-
(2000)
Am Jhum Genet
, vol.67
, pp. 1581-1585
-
-
Moses, E.K.1
Lade, J.A.2
Guo, G.3
-
21
-
-
0037219649
-
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in finnish families
-
Laivuori H, Lahermo P, Ollikainen V et al. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families. Am J Hum Gene 2003; 72: 168-77.
-
(2003)
Am J Hum Gene
, vol.72
, pp. 168-177
-
-
Laivuori, H.1
Lahermo, P.2
Ollikainen, V.3
-
22
-
-
20444395829
-
Genetics of type 2 diabetes mellitus
-
Malecki M T. Genetics of type 2 diabetes mellitus. Diabetes Res Clin Pract 2005; 68 (Suppl 1): S10-21.
-
(2005)
Diabetes Res Clin Pract
, vol.68
, pp. S10-S21
-
-
Malecki, M.T.1
-
23
-
-
42149107502
-
Genetic aspects of alzheimer disease
-
Bird T D. Genetic aspects of Alzheimer disease. Genet Med 2008; 10: 231-9.
-
(2008)
Genet Med
, vol.10
, pp. 231-239
-
-
Bird, T.D.1
-
24
-
-
33747889710
-
Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22
-
Moses EK, Fitzpatrick E, Freed K A et al. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22. Mol Hum Reprod 2006; 12: 505-12.
-
(2006)
Mol Hum Reprod
, vol.12
, pp. 505-512
-
-
Moses, E.K.1
Fitzpatrick, E.2
Freed, K.A.3
-
25
-
-
58349118696
-
Association between the candidate susceptibility gene acvr2a on chromosome 2q22 and pre-eclampsia in a large norwegian population-based study (the hunt study)
-
Roten LT, Johnson M, Forsmo S et al. Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study). Eur JHum Genet 2009; 17(2): 250-7.
-
(2009)
Eur Jhum Genet
, vol.17
, Issue.2
, pp. 250-257
-
-
Roten, L.T.1
Johnson, M.2
Forsmo, S.3
-
26
-
-
4344708984
-
The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
-
Oudejans CB, Mulders J, Lachmeijer AM et al. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas. Mol Hum Reprod 2004; 10: 589-98.
-
(2004)
Mol Hum Reprod
, vol.10
, pp. 589-598
-
-
Oudejans, C.B.1
Mulders, J.2
Lachmeijer, A.M.3
-
27
-
-
0345451625
-
Genomic imprinting, development and disease - is pre-eclampsia caused by a maternally imprinted gene?
-
Graves J A M. Genomic imprinting, development and disease - is pre-eclampsia caused by a maternally imprinted gene? Reprod Fert Develop 1998; 10: 23-9.
-
(1998)
Reprod Fert Develop
, vol.10
, pp. 23-29
-
-
Graves, J.A.M.1
-
28
-
-
18144377731
-
Maternal segregation of the dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family
-
van Dijk M, Mulders J, Poutsma A et al. Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family. Nat Genet 2005; 37: 514-9.
-
(2005)
Nat Genet
, vol.37
, pp. 514-519
-
-
Van Dijk, M.1
Mulders, J.2
Poutsma, A.3
-
29
-
-
33847295115
-
Stox1 is not imprinted and is not likely to be involved in pre-eclampsia
-
Iglesias-Platas I, Monk D, Jebbink J et al. STOX1 is not imprinted and is not likely to be involved in pre-eclampsia. Nat Genet 2007; 39: 279-80.
-
(2007)
Nat Genet
, vol.39
, pp. 279-280
-
-
Iglesias-Platas, I.1
Monk, D.2
Jebbink, J.3
-
30
-
-
84969213492
-
Genome-wide association study of seven common diseases and 3000 shared controls
-
The Wellcome Trust Case Control Consortium
-
The Wellcome Trust Case Control Consortium. Genome-wide association study of seven common diseases and 3000 shared controls. Nature 2007; 447: 661-78.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
31
-
-
34249895023
-
Replication of genome-wide association signals in uk samples reveals risk loci for type 2 diabetes
-
Zeggini E, Weedon M N, Lindgren CM et al. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 2007; 316: 1336-41.
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
-
32
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science 1996; 273: 1516-7. http://www.ncbi.nlm.nih.gov/projects/SNP
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
33
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. A haplotype map of the human genome. Nature 2005; 437:1299-319.
-
(2005)
Nature
, vol.437
, pp. 1299-1319
-
-
-
34
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million snps
-
The International HapMap Consortium
-
The International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007; 449: 851-62. http://www.hapmap.org
-
(2007)
Nature
, vol.449
, pp. 851-862
-
-
-
35
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E, Scott L J, Saxena R, Voight B F. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008; 40: 638-45.
-
(2008)
Nat Genet
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
Voight, B.F.4
-
36
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (iddm)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993; 52: 506-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
37
-
-
20544448502
-
Disentangling fetal and maternal susceptibility for pre-eclampsia: A british multicenter candidate-gene study
-
The GOPEC Consortium
-
The GOPEC Consortium. Disentangling fetal and maternal susceptibility for pre-eclampsia: a British multicenter candidate-gene study. Am J Hum Genet 2005; 77: 127-31.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 127-131
-
-
-
38
-
-
33750216250
-
Cohort profile: The norwegian mother and child cohort study (moba)
-
Magnus P, Irgens L, Haug K et al. Cohort profile: the Norwegian Mother and Child Cohort Study (MoBa). Int J Epidemiol 2006; 35: 1146-50.
-
(2006)
Int J Epidemiol
, vol.35
, pp. 1146-1150
-
-
Magnus, P.1
Irgens, L.2
Haug, K.3
-
39
-
-
7244234068
-
Combinations of maternal kir and fetal hla-c genes influence the risk of preeclampsia and reproductive success
-
Hiby S, Walker J, O’shaughnessy K et al. Combinations of maternal KIR and fetal HLA-C genes influence the risk of preeclampsia and reproductive success. J Exp Med 2004; 200: 957-65.
-
(2004)
J Exp Med
, vol.200
, pp. 957-965
-
-
Hiby, S.1
Walker, J.2
O’shaughnessy, K.3
-
40
-
-
0037373006
-
Excess placental soluble fms-like tyrosine kinase 1 (sflt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia
-
Maynard S E, Min J Y, Merchan J et al. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia. J Clin Invest 2003; 111: 649-58.
-
(2003)
J Clin Invest
, vol.111
, pp. 649-658
-
-
Maynard, S.E.1
Min, J.Y.2
Merchan, J.3
-
41
-
-
0023180369
-
Pre-eclampsia and trisomy 13: A possible association
-
Boyd P A, Lindenbaum R H, Redman C. Pre-eclampsia and trisomy 13: a possible association. Lancet 1987; 2 (8556): 425-7.
-
(1987)
Lancet
, vol.2
, Issue.8556
, pp. 425-427
-
-
Boyd, P.A.1
Lindenbaum, R.H.2
Redman, C.3
-
43
-
-
55649105963
-
Clinical risk factors, dna variants, and the development of type 2 diabetes
-
Lyssenko V, Jonsson A, Almgren P et al. Clinical risk factors, DNA variants, and the development of type 2 diabetes. N Engl J Med 2008; 359: 2220-32.
-
(2008)
N Engl J Med
, vol.359
, pp. 2220-2232
-
-
Lyssenko, V.1
Jonsson, A.2
Almgren, P.3
|