-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
2
-
-
66249112837
-
Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium
-
Albrechtsen A, Sand KT, Moltke I, van Overseem HT, Nielsen FC, Nielsen R. Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genet Epidemiol 2009;33:266-274.
-
(2009)
Genet Epidemiol
, vol.33
, pp. 266-274
-
-
Albrechtsen, A.1
Sand, K.T.2
Moltke, I.3
van Overseem, H.T.4
Nielsen, F.C.5
Nielsen, R.6
-
3
-
-
0034957328
-
Cytokine promoter gene polymorphisms and idiopathic recurrent pregnancy loss
-
Babbage SJ, Arkwright PD, Vince GS, Perrey C, Pravica V, Quenby S, Bates M, Hutchinson IV. Cytokine promoter gene polymorphisms and idiopathic recurrent pregnancy loss. J Reprod Immunol 2001;51:21-27.
-
(2001)
J Reprod Immunol
, vol.51
, pp. 21-27
-
-
Babbage, S.J.1
Arkwright, P.D.2
Vince, G.S.3
Perrey, C.4
Pravica, V.5
Quenby, S.6
Bates, M.7
Hutchinson, I.V.8
-
4
-
-
34347326198
-
Recurrent pregnancy loss: the key potential mechanisms
-
Baek KH, Lee EJ, Kim YS. Recurrent pregnancy loss: the key potential mechanisms. Trends Mol Med 2007;13:310-317.
-
(2007)
Trends Mol Med
, vol.13
, pp. 310-317
-
-
Baek, K.H.1
Lee, E.J.2
Kim, Y.S.3
-
5
-
-
70449556517
-
Expression profiles of schizophrenia susceptibility genes during human prefrontal cortical development
-
Choi KH, Zepp ME, Higgs BW, Weickert CS, Webster MJ. Expression profiles of schizophrenia susceptibility genes during human prefrontal cortical development. J. Psychiatry Neurosci 2009;34:450-458.
-
(2009)
J. Psychiatry Neurosci
, vol.34
, pp. 450-458
-
-
Choi, K.H.1
Zepp, M.E.2
Higgs, B.W.3
Weickert, C.S.4
Webster, M.J.5
-
6
-
-
0024433838
-
Association of maternal HLA haplotypes with recurrent spontaneous abortions
-
Christiansen OB, Riisom K, Lauritsen JG, Grunnet N, Jersild C. Association of maternal HLA haplotypes with recurrent spontaneous abortions. Tissue Antigens 1989;34:190-199.
-
(1989)
Tissue Antigens
, vol.34
, pp. 190-199
-
-
Christiansen, O.B.1
Riisom, K.2
Lauritsen, J.G.3
Grunnet, N.4
Jersild, C.5
-
8
-
-
0028131324
-
HLA class II alleles confer susceptibility to recurrent fetal losses in Danish women
-
Christiansen OB, Rasmussen KL, Jersild C, Grunnet N. HLA class II alleles confer susceptibility to recurrent fetal losses in Danish women. Tissue Antigens 1994;44:225-233.
-
(1994)
Tissue Antigens
, vol.44
, pp. 225-233
-
-
Christiansen, O.B.1
Rasmussen, K.L.2
Jersild, C.3
Grunnet, N.4
-
9
-
-
48449103651
-
Multifactorial etiology of recurrent miscarriage and its scientific and clinical implications
-
Christiansen OB, Steffensen R, Nielsen HS, Varming K. Multifactorial etiology of recurrent miscarriage and its scientific and clinical implications. Gynecol Obstet Invest 2008;66:257-267.
-
(2008)
Gynecol Obstet Invest
, vol.66
, pp. 257-267
-
-
Christiansen, O.B.1
Steffensen, R.2
Nielsen, H.S.3
Varming, K.4
-
10
-
-
70449657762
-
IGF2 mRNA-binding protein 2 biological function and putative role in type 2 diabetes
-
Christiansen J, Kolte AM, Hansen TO, Nielsen FC. IGF2 mRNA-binding protein 2: biological function and putative role in type 2 diabetes. J Mol Endocrinol 2009a;43:187-195.
-
(2009)
J Mol Endocrinol
, vol.43
, pp. 187-195
-
-
Christiansen, J.1
Kolte, A.M.2
Hansen, T.O.3
Nielsen, F.C.4
-
11
-
-
58449109509
-
Mannose-binding lectin-2 genotypes and recurrent late pregnancy losses
-
Christiansen OB, Nielsen HS, Lund M, Steffensen R, Varming K. Mannose-binding lectin-2 genotypes and recurrent late pregnancy losses. Hum Reprod 2009b;24:291-299.
-
(2009)
Hum Reprod
, vol.24
, pp. 291-299
-
-
Christiansen, O.B.1
Nielsen, H.S.2
Lund, M.3
Steffensen, R.4
Varming, K.5
-
12
-
-
0036488829
-
Associations between cytokine gene polymorphisms and recurrent pregnancy loss
-
Daher S, Shulzhenko N, Morgun A, Mattar R, Rampim GF, Camano L, DeLima MG. Associations between cytokine gene polymorphisms and recurrent pregnancy loss. J Reprod Immunol 2003;58:69-77.
-
(2003)
J Reprod Immunol
, vol.58
, pp. 69-77
-
-
Daher, S.1
Shulzhenko, N.2
Morgun, A.3
Mattar, R.4
Rampim, G.F.5
Camano, L.6
DeLima, M.G.7
-
13
-
-
77449141738
-
Fragile histidine triad protein: structure, function, and its association with tumorogenesis
-
Hassan MI, Naiyer A, Ahmad F. Fragile histidine triad protein: structure, function, and its association with tumorogenesis. J. Cancer Res Clin Oncol 2010;136:333-350.
-
(2010)
J. Cancer Res Clin Oncol
, vol.136
, pp. 333-350
-
-
Hassan, M.I.1
Naiyer, A.2
Ahmad, F.3
-
14
-
-
3042698491
-
Association between human leukocyte antigen-G genotype and success of in vitro fertilization and pregnancy outcome
-
Hviid TV, Hylenius S, Lindhard A, Christiansen OB. Association between human leukocyte antigen-G genotype and success of in vitro fertilization and pregnancy outcome. Tissue Antigens 2004;64:66-69.
-
(2004)
Tissue Antigens
, vol.64
, pp. 66-69
-
-
Hviid, T.V.1
Hylenius, S.2
Lindhard, A.3
Christiansen, O.B.4
-
15
-
-
85047695028
-
Linkage and association of the glutamate receptor 6 gene with autism
-
Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T. Linkage and association of the glutamate receptor 6 gene with autism. Mol. Psychiatry 2002;7:302-310.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 302-310
-
-
Jamain, S.1
Betancur, C.2
Quach, H.3
Philippe, A.4
Fellous, M.5
Giros, B.6
Gillberg, C.7
Leboyer, M.8
Bourgeron, T.9
-
16
-
-
0028789983
-
Association between mannan binding protein deficiency and recurrent miscarriage
-
Kilpatrick DC, Bevan BH, Liston WA. Association between mannan binding protein deficiency and recurrent miscarriage. Hum Reprod 1995;10:2501-2505.
-
(1995)
Hum Reprod
, vol.10
, pp. 2501-2505
-
-
Kilpatrick, D.C.1
Bevan, B.H.2
Liston, W.A.3
-
17
-
-
77951939524
-
Study of the structure and impact of human leukocyte antigen (HLA)-G-A, HLA-G-B, and HLA-G-DRB1 haplotypes in families with recurrent miscarriage
-
Kolte AM, Steffensen R, Nielsen HS, Hviid TV, Christiansen OB. Study of the structure and impact of human leukocyte antigen (HLA)-G-A, HLA-G-B, and HLA-G-DRB1 haplotypes in families with recurrent miscarriage. Hum Immunol 2010;71:482-488.
-
(2010)
Hum Immunol
, vol.71
, pp. 482-488
-
-
Kolte, A.M.1
Steffensen, R.2
Nielsen, H.S.3
Hviid, T.V.4
Christiansen, O.B.5
-
18
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, Richardsson B, Sigurdardottir S, Barnard J, Hallbeck B, Masson G. et al. A high-resolution recombination map of the human genome. Nat Genet 2002;31:241-247.
-
(2002)
Nat Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
-
19
-
-
0036856196
-
Low serum level of mannan-binding lectin is a determinant for pregnancy outcome in women with recurrent spontaneous abortion
-
Kruse C, Rosgaard A, Steffensen R, Varming K, Jensenius JC, Christiansen OB. Low serum level of mannan-binding lectin is a determinant for pregnancy outcome in women with recurrent spontaneous abortion. Am J Obstet Gynecol 2002;187:1313-1320.
-
(2002)
Am J Obstet Gynecol
, vol.187
, pp. 1313-1320
-
-
Kruse, C.1
Rosgaard, A.2
Steffensen, R.3
Varming, K.4
Jensenius, J.C.5
Christiansen, O.B.6
-
20
-
-
2442503690
-
A study of HLA-DR and -DQ alleles in 588 patients and 562 controls confirms that HLA-DRB1*03 is associated with recurrent miscarriage
-
Kruse C, Steffensen R, Varming K, Christiansen OB. A study of HLA-DR and -DQ alleles in 588 patients and 562 controls confirms that HLA-DRB1*03 is associated with recurrent miscarriage. Hum Reprod 2004;19:1215-1221.
-
(2004)
Hum Reprod
, vol.19
, pp. 1215-1221
-
-
Kruse, C.1
Steffensen, R.2
Varming, K.3
Christiansen, O.B.4
-
21
-
-
77952357708
-
Genome-wide screening for risk loci of idiopathic recurrent miscarriage in a Han Chinese population: a pilot study
-
LiW, Zeng CW, Cui X, Xiao FL, Mao SY. Genome-wide screening for risk loci of idiopathic recurrent miscarriage in a Han Chinese population: a pilot study. Reprod Sci 2010;17:578-584.
-
(2010)
Reprod Sci
, vol.17
, pp. 578-584
-
-
Li, W.1
Zeng, C.W.2
Cui, X.3
Xiao, F.L.4
Mao, S.Y.5
-
22
-
-
0032867615
-
Evidence for the GluR6 gene associated with younger onset age of Huntington's disease
-
MacDonald ME, Vonsattel JP, Shrinidhi J, Couropmitree NN, Cupples LA, Bird ED, Gusella JF, Myers RH. Evidence for the GluR6 gene associated with younger onset age of Huntington's disease. Neurology 1999; 53:1330-1332.
-
(1999)
Neurology
, vol.53
, pp. 1330-1332
-
-
MacDonald, M.E.1
Vonsattel, J.P.2
Shrinidhi, J.3
Couropmitree, N.N.4
Cupples, L.A.5
Bird, E.D.6
Gusella, J.F.7
Myers, R.H.8
-
23
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
24
-
-
34547784323
-
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation
-
Motazacker MM, Rost BR, Hucho T, Garshasbi M, Kahrizi K, Ullmann R, Abedini SS, Nieh SE, Amini SH, Goswami C. et al. A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation. Am J Hum Genet 2007; 81:792-798.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 792-798
-
-
Motazacker, M.M.1
Rost, B.R.2
Hucho, T.3
Garshasbi, M.4
Kahrizi, K.5
Ullmann, R.6
Abedini, S.S.7
Nieh, S.E.8
Amini, S.H.9
Goswami, C.10
-
25
-
-
64549147053
-
Association of HY-restricting HLA class II alleles with pregnancy outcome in patients with recurrent miscarriage subsequent to a firstborn boy
-
Nielsen HS, Steffensen R, Varming K, Van Halteren AG, Spierings E, Ryder LP, Goulmy E, Christiansen OB. Association of HY-restricting HLA class II alleles with pregnancy outcome in patients with recurrent miscarriage subsequent to a firstborn boy. Hum Mol Genet 2009; 18:1684-1691.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1684-1691
-
-
Nielsen, H.S.1
Steffensen, R.2
Varming, K.3
Van Halteren, A.G.4
Spierings, E.5
Ryder, L.P.6
Goulmy, E.7
Christiansen, O.B.8
-
26
-
-
0034709737
-
Maternal age and fetal loss: population based register linkage study
-
Nybo Andersen AM, Wohlfahrt J, Christens P, Olsen J, Melbye M. Maternal age and fetal loss: population based register linkage study. BMJ 2000;320:1708-1712.
-
(2000)
BMJ
, vol.320
, pp. 1708-1712
-
-
Nybo Andersen, A.M.1
Wohlfahrt, J.2
Christens, P.3
Olsen, J.4
Melbye, M.5
-
27
-
-
0037443934
-
Thrombophilic disorders and fetal loss: a meta-analysis
-
Rey E, Kahn SR, David M, Shrier I. Thrombophilic disorders and fetal loss: a meta-analysis. Lancet 2003;361:901-908.
-
(2003)
Lancet
, vol.361
, pp. 901-908
-
-
Rey, E.1
Kahn, S.R.2
David, M.3
Shrier, I.4
-
28
-
-
0025008677
-
Linkage strategies for genetically complex traits II. The power of affected relative pairs
-
Risch N. Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am J Hum Genet 1990;46:229-241.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
29
-
-
42349098697
-
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13 1 and 14q12
-
Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C. et al. Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12. Mol Psychiatry 2008;13:522-530.
-
(2008)
Mol Psychiatry
, vol.13
, pp. 522-530
-
-
Romanos, M.1
Freitag, C.2
Jacob, C.3
Craig, D.W.4
Dempfle, A.5
Nguyen, T.T.6
Halperin, R.7
Walitza, S.8
Renner, T.J.9
Seitz, C.10
-
30
-
-
0029951573
-
Frequency of factors associated with habitual abortion in 197 couples
-
Stephenson MD. Frequency of factors associated with habitual abortion in 197 couples. Fertil Steril 1996;66:24-29.
-
(1996)
Fertil Steril
, vol.66
, pp. 24-29
-
-
Stephenson, M.D.1
-
31
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Welcome Trust Case Control Consortium
-
Welcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007;447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
32
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J. A class of tests for linkage using affected pedigree members. Biometrics 1994;50:118-127.
-
(1994)
Biometrics
, vol.50
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
33
-
-
33751362126
-
Association of -592C/A -819C/T and -1082A/G interleukin-10 promoter polymorphisms with idiopathic recurrent spontaneous abortion
-
Zammiti W, Mtiraoui N, Cochery-Nouvellon E, Mahjoub T, Almawi WY, Gris JC. Association of -592C/A, -819C/T and -1082A/G interleukin-10 promoter polymorphisms with idiopathic recurrent spontaneous abortion. Mol Hum Reprod 2006;12:771-776.
-
(2006)
Mol Hum Reprod
, vol.12
, pp. 771-776
-
-
Zammiti, W.1
Mtiraoui, N.2
Cochery-Nouvellon, E.3
Mahjoub, T.4
Almawi, W.Y.5
Gris, J.C.6
|