-
1
-
-
66649089490
-
Loci at chromosomes 13, 19 and 20 influence age at natural menopause
-
10.1038/ng.387 19448619
-
Loci at chromosomes 13, 19 and 20 influence age at natural menopause. Stolk L, Zhai G, van Meurs JB, Verbiest MM, Visser JA, Estrada K, Rivadeneira F, Williams FM, Cherkas L, Deloukas P, Soranzo N, de Keyzer JJ, Pop VJ, Lips P, Lebrun CE, van der Schouw YT, Grobbee DE, Witteman J, Hofman A, Pols HA, Laven JS, Spector TD, Uitterlinden AG, Nat Genet 2009 41 645 647 10.1038/ng.387 19448619
-
(2009)
Nat Genet
, vol.41
, pp. 645-647
-
-
Stolk, L.1
Zhai, G.2
Van Meurs, J.B.3
Verbiest, M.M.4
Visser, J.A.5
Estrada, K.6
Rivadeneira, F.7
Williams, F.M.8
Cherkas, L.9
Deloukas, P.10
Soranzo, N.11
De Keyzer, J.J.12
Pop, V.J.13
Lips, P.14
Lebrun, C.E.15
Van Der Schouw, Y.T.16
Grobbee, D.E.17
Witteman, J.18
Hofman, A.19
Pols, H.A.20
Laven, J.S.21
Spector, T.D.22
Uitterlinden, A.G.23
more..
-
2
-
-
84862806974
-
The investigation and analysis of the factors related with the menopausal age of urban women in China
-
The investigation and analysis of the factors related with the menopausal age of urban women in China. Nie GN, Wang XY, Yang HY, Aihua Ou, China maternal and child healthcare (Chinsese) 2011 8 1191 1193
-
(2011)
China Maternal and Child Healthcare (Chinsese)
, vol.8
, pp. 1191-1193
-
-
Nie, G.N.1
Wang, X.Y.2
Yang, H.Y.3
Aihua, O.4
-
3
-
-
34547930676
-
Premenopausal factors influencing premature ovarian failure and early menopause
-
DOI 10.1016/j.maturitas.2007.04.001, PII S0378512207001545
-
Premenopausal factors influencing premature ovarian failure and early menopause. Chang SH, Kim CS, Lee KS, Kim H, Yim SV, Lim YJ, Park SK, Maturitas 2007 58 19 30 10.1016/j.maturitas.2007.04.001 17531410 (Pubitemid 47268703)
-
(2007)
Maturitas
, vol.58
, Issue.1
, pp. 19-30
-
-
Chang, S.H.1
Kim, C.-S.2
Lee, K.-S.3
Kim, H.4
Yim, S.V.5
Lim, Y.J.6
Park, S.K.7
-
4
-
-
77956617098
-
Primary ovarian insufficiency
-
10.1016/S0140-6736(10)60355-8 20708256
-
Primary ovarian insufficiency. De Vos M, Devroey P, Fauser BC, Lancet 2010 376 911 921 10.1016/S0140-6736(10)60355-8 20708256
-
(2010)
Lancet
, vol.376
, pp. 911-921
-
-
De Vos, M.1
Devroey, P.2
Fauser, B.C.3
-
5
-
-
59749096464
-
Clinical practice. Primary ovarian insufficiency
-
10.1056/NEJMcp0808697 19196677
-
Clinical practice. Primary ovarian insufficiency. Nelson LM, N Engl J Med 2009 360 606 614 10.1056/NEJMcp0808697 19196677
-
(2009)
N Engl J Med
, vol.360
, pp. 606-614
-
-
Nelson, L.M.1
-
6
-
-
45549088147
-
Genetic and phenotypic heterogeneity in ovarian failure: Overview of selected candidate genes
-
DOI 10.1196/annals.1429.019, The Menstrual Cycle and Adolescent Health
-
Genetic and phenotypic heterogeneity in ovarian failure: overview of selected candidate genes. Simpson JL, Ann N Y Acad Sci 2008 1135 146 154 10.1196/annals.1429.019 18574220 (Pubitemid 351862133)
-
(2008)
Annals of the New York Academy of Sciences
, vol.1135
, pp. 146-154
-
-
Simpson, J.L.1
-
7
-
-
0029118115
-
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
-
10.1016/0092-8674(95)90275-9 7553856
-
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Aittomaki K, Lucena JL, Pakarinen P, Sistonen P, Tapanainen J, Gromoll J, Kaskikari R, Sankila EM, Lehvaslaiho H, Engel AR, Nieschlag E, Huhtaniemi I, de la Chapelle A, Cell 1995 82 959 968 10.1016/0092-8674(95)90275-9 7553856
-
(1995)
Cell
, vol.82
, pp. 959-968
-
-
Aittomaki, K.1
Lucena, J.L.2
Pakarinen, P.3
Sistonen, P.4
Tapanainen, J.5
Gromoll, J.6
Kaskikari, R.7
Sankila, E.M.8
Lehvaslaiho, H.9
Engel, A.R.10
Nieschlag, E.11
Huhtaniemi, I.12
De La Chapelle, A.13
-
8
-
-
77952744975
-
Genome-wide association study and premature ovarian failure
-
10.1016/j.ando.2010.02.014
-
Genome-wide association study and premature ovarian failure. Christin-Maitre S, Tachdjian G, Ann Endocrinol (Paris) 2010 71 218 221 10.1016/j.ando.2010.02.014
-
(2010)
Ann Endocrinol (Paris)
, vol.71
, pp. 218-221
-
-
Christin-Maitre, S.1
Tachdjian, G.2
-
9
-
-
44449155898
-
Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure
-
DOI 10.1093/humrep/den086
-
Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure. Kang H, Lee SK, Kim MH, Song J, Bae SJ, Kim NK, Lee SH, Kwack K, Hum Reprod 2008 23 1457 1465 10.1093/humrep/den086 18349106 (Pubitemid 351770570)
-
(2008)
Human Reproduction
, vol.23
, Issue.6
, pp. 1457-1465
-
-
Kang, H.1
Lee, S.K.2
Kim, M.-H.3
Song, J.4
Bae, S.J.5
Kim, N.K.6
Lee, S.-H.7
Kwack, K.8
-
10
-
-
68949210498
-
Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene
-
10.1093/humrep/dep197 19508998
-
Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. Knauff EA, Franke L, van Es MA, van den Berg LH, van der Schouw YT, Laven JS, Lambalk CB, Hoek A, Goverde AJ, Christin-Maitre S, Hsueh AJ, Wijmenga C, Fauser BC, Hum Reprod 2009 24 2372 2378 10.1093/humrep/dep197 19508998
-
(2009)
Hum Reprod
, vol.24
, pp. 2372-2378
-
-
Knauff, E.A.1
Franke, L.2
Van Es, M.A.3
Van Den Berg, L.H.4
Van Der Schouw, Y.T.5
Laven, J.S.6
Lambalk, C.B.7
Hoek, A.8
Goverde, A.J.9
Christin-Maitre, S.10
Hsueh, A.J.11
Wijmenga, C.12
Fauser, B.C.13
-
11
-
-
0032708873
-
The idiopathic forms of premature menopause and early menopause show the same genetic pattern
-
DOI 10.1093/humrep/14.11.2731
-
The idiopathic forms of premature menopause and early menopause show the same genetic pattern. Tibiletti MG, Testa G, Vegetti W, Alagna F, Taborelli M, Dalpra L, Bolis PF, Crosignani PG, Hum Reprod 1999 14 2731 2734 10.1093/humrep/14.11.2731 10548611 (Pubitemid 29520682)
-
(1999)
Human Reproduction
, vol.14
, Issue.11
, pp. 2731-2734
-
-
Tibiletti, M.G.1
Testa, G.2
Vegetti, W.3
Alagna, F.4
Taborelli, M.5
Dalpra, L.6
Bolis, P.F.7
Crosignani, P.G.8
-
12
-
-
13244253761
-
Screening for known mutations in EIF2B genes in a large panel of patients with premature ovarian failure
-
DOI 10.1186/1472-6874-4-8
-
Screening for known mutations in EIF2B genes in a large panel of patients with premature ovarian failure. Fogli A, Gauthier-Barichard F, Schiffmann R, Vanderhoof VH, Bakalov VK, Nelson LM, Boespflug-Tanguy O, BMC Womens Health 2004 4 8 10.1186/1472-6874-4-8 15507143 (Pubitemid 40190550)
-
(2004)
BMC Women's Health
, vol.4
, pp. 8
-
-
Fogli, A.1
Gauthier-Barichard, F.2
Schiffmann, R.3
Vanderhoof, V.H.4
Bakalov, V.K.5
Nelson, L.M.6
Boespflug-Tanguy, O.7
-
13
-
-
77952742678
-
Premature ovarian failure and FMR1 gene mutations: An update
-
10.1016/j.ando.2010.02.009
-
Premature ovarian failure and FMR1 gene mutations: an update. Conway GS, Ann Endocrinol (Paris) 2010 71 215 217 10.1016/j.ando.2010.02.009
-
(2010)
Ann Endocrinol (Paris)
, vol.71
, pp. 215-217
-
-
Conway, G.S.1
-
14
-
-
78049415493
-
A large-scale candidate gene association study of age at menarche and age at natural menopause
-
10.1007/s00439-010-0878-4 20734064
-
A large-scale candidate gene association study of age at menarche and age at natural menopause. He C, Kraft P, Chasman DI, Buring JE, Chen C, Hankinson SE, Pare G, Chanock S, Ridker PM, Hunter DJ, Hum Genet 2010 128 515 527 10.1007/s00439-010-0878-4 20734064
-
(2010)
Hum Genet
, vol.128
, pp. 515-527
-
-
He, C.1
Kraft, P.2
Chasman, D.I.3
Buring, J.E.4
Chen, C.5
Hankinson, S.E.6
Pare, G.7
Chanock, S.8
Ridker, P.M.9
Hunter, D.J.10
-
15
-
-
79956323915
-
Common genetic variants are significant risk factors for early menopause: Results from the Breakthrough Generations Study
-
10.1093/hmg/ddq417 20952801
-
Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study. Murray A, Bennett CE, Perry JR, Weedon MN, Jacobs PA, Morris DH, Orr N, Schoemaker MJ, Jones M, Ashworth A, Swerdlow AJ, Hum Mol Genet 2011 20 186 192 10.1093/hmg/ddq417 20952801
-
(2011)
Hum Mol Genet
, vol.20
, pp. 186-192
-
-
Murray, A.1
Bennett, C.E.2
Perry, J.R.3
Weedon, M.N.4
Jacobs, P.A.5
Morris, D.H.6
Orr, N.7
Schoemaker, M.J.8
Jones, M.9
Ashworth, A.10
Swerdlow, A.J.11
-
16
-
-
66649090056
-
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause
-
10.1038/ng.385 19448621
-
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. He C, Kraft P, Chen C, Buring JE, Pare G, Hankinson SE, Chanock SJ, Ridker PM, Hunter DJ, Chasman DI, Nat Genet 2009 41 724 728 10.1038/ng.385 19448621
-
(2009)
Nat Genet
, vol.41
, pp. 724-728
-
-
He, C.1
Kraft, P.2
Chen, C.3
Buring, J.E.4
Pare, G.5
Hankinson, S.E.6
Chanock, S.J.7
Ridker, P.M.8
Hunter, D.J.9
Chasman, D.I.10
-
17
-
-
79959690735
-
Epistasis between FSHR and CYP19A1 polymorphisms is associated with premature ovarian failure
-
Epistasis between FSHR and CYP19A1 polymorphisms is associated with premature ovarian failure. Kim S, Pyun JA, Cha DH, Ko JJ, Kwack K, Fertil Steril 2011
-
(2011)
Fertil Steril
-
-
Kim, S.1
Pyun, J.A.2
Cha, D.H.3
Ko, J.J.4
Kwack, K.5
-
18
-
-
72849148465
-
Estrogen receptor {alpha} gene polymorphisms in patients with idiopathic premature ovarian failure
-
10.1093/humrep/dep375 19861327
-
Estrogen receptor {alpha} gene polymorphisms in patients with idiopathic premature ovarian failure. Yoon SH, Choi YM, Hong MA, Lee GH, Kim JJ, Im HJ, Min EG, Kang BM, Yoon BK, Moon SY, Hum Reprod 2010 25 283 287 10.1093/humrep/dep375 19861327
-
(2010)
Hum Reprod
, vol.25
, pp. 283-287
-
-
Yoon, S.H.1
Choi, Y.M.2
Hong, M.A.3
Lee, G.H.4
Kim, J.J.5
Im, H.J.6
Min, E.G.7
Kang, B.M.8
Yoon, B.K.9
Moon, S.Y.10
-
19
-
-
38949218033
-
Estrogen receptor α gene polymorphisms are associated with idiopathic premature ovarian failure
-
DOI 10.1016/j.fertnstert.2007.03.008, PII S0015028207005432
-
Estrogen receptor alpha gene polymorphisms are associated with idiopathic premature ovarian failure. Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP, Fertil Steril 2008 89 318 324 10.1016/j.fertnstert. 2007.03.008 17706202 (Pubitemid 351215408)
-
(2008)
Fertility and Sterility
, vol.89
, Issue.2
, pp. 318-324
-
-
Bretherick, K.L.1
Hanna, C.W.2
Currie, L.M.3
Fluker, M.R.4
Hammond, G.L.5
Robinson, W.P.6
-
20
-
-
77956554129
-
Estrogen receptor-1 genetic polymorphisms for the risk of premature ovarian failure and early menopause
-
10.1089/jwh.2008.1317
-
Estrogen receptor-1 genetic polymorphisms for the risk of premature ovarian failure and early menopause. Yang JJ, Cho LY, Lim YJ, Ko KP, Lee KS, Kim H, Yim SV, Chang SH, Park SK, J Womens Health (Larchmt) 2010 19 297 304 10.1089/jwh.2008.1317
-
(2010)
J Womens Health (Larchmt)
, vol.19
, pp. 297-304
-
-
Yang, J.J.1
Cho, L.Y.2
Lim, Y.J.3
Ko, K.P.4
Lee, K.S.5
Kim, H.6
Yim, S.V.7
Chang, S.H.8
Park, S.K.9
-
21
-
-
0033304548
-
Estrogen receptor polymorphism predicts the onset of natural and surgical menopause
-
Estrogen receptor polymorphism predicts the onset of natural and surgical menopause. Weel AE, Uitterlinden AG, Westendorp IC, Burger H, Schuit SC, Hofman A, Helmerhorst TJ, van Leeuwen JP, Pols HA, J Clin Endocrinol Metab 1999 84 3146 3150 10.1210/jc.84.9.3146 10487678 (Pubitemid 30646935)
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, Issue.9
, pp. 3146-3150
-
-
Weel, A.E.A.M.1
Uitterlinden, A.G.2
Westendorp, I.C.D.3
Burger, H.4
Schuit, S.C.E.5
Hofman, A.6
Helmerhorst, T.J.M.7
Van Leeuwen, J.P.T.M.8
Pols, H.A.P.9
-
22
-
-
18944381751
-
SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci
-
DOI 10.1038/sj.cr.7290272
-
SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Shi YY, He L, Cell Res 2005 15 97 98 10.1038/sj.cr.7290272 15740637 (Pubitemid 41653949)
-
(2005)
Cell Research
, vol.15
, Issue.2
, pp. 97-98
-
-
Shi, Y.Y.1
He, L.2
-
23
-
-
34247511497
-
LKB1 and SAD Kinases Define a Pathway Required for the Polarization of Cortical Neurons
-
DOI 10.1016/j.cell.2007.03.025, PII S0092867407003911
-
LKB1 and SAD kinases define a pathway required for the polarization of cortical neurons. Barnes AP, Lilley BN, Pan YA, Plummer LJ, Powell AW, Raines AN, Sanes JR, Polleux F, Cell 2007 129 549 563 10.1016/j.cell.2007.03.025 17482548 (Pubitemid 46660970)
-
(2007)
Cell
, vol.129
, Issue.3
, pp. 549-563
-
-
Barnes, A.P.1
Lilley, B.N.2
Pan, Y.A.3
Plummer, L.J.4
Powell, A.W.5
Raines, A.N.6
Sanes, J.R.7
Polleux, F.8
-
24
-
-
84862815139
-
-
GeneAtlas
-
GeneAtlas. http://genatlas.medecine.univ-paris5.fr/
-
-
-
-
25
-
-
3843085169
-
Human SAD1 kinase is involved in UV-induced DNA damage checkpoint function
-
DOI 10.1074/jbc.M404728200
-
Human SAD1 kinase is involved in UV-induced DNA damage checkPOFnt function. Lu R, Niida H, Nakanishi M, J Biol Chem 2004 279 31164 31170 10.1074/jbc.M404728200 15150265 (Pubitemid 39037779)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.30
, pp. 31164-31170
-
-
Lu, R.1
Niida, H.2
Nakanishi, M.3
-
26
-
-
13644267037
-
Mammalian SAD kinases are required for neuronal polarization
-
DOI 10.1126/science.1107403
-
Mammalian SAD kinases are required for neuronal polarization. Kishi M, Pan YA, Crump JG, Sanes JR, Science 2005 307 929 932 10.1126/science.1107403 15705853 (Pubitemid 40229230)
-
(2005)
Science
, vol.307
, Issue.5711
, pp. 929-932
-
-
Kishi, M.1
Pan, Y.A.2
Crump, J.G.3
Sanes, J.R.4
-
27
-
-
38349091986
-
Differential regulation of abundance and deadenylation of maternal transcripts during bovine oocyte maturation in vitro and in vivo
-
10.1186/1471-213X-7-125 17988387
-
Differential regulation of abundance and deadenylation of maternal transcripts during bovine oocyte maturation in vitro and in vivo. Thelie A, Papillier P, Pennetier S, Perreau C, Traverso JM, Uzbekova S, Mermillod P, Joly C, Humblot P, Dalbies-Tran R, BMC Dev Biol 2007 7 125 10.1186/1471-213X-7-125 17988387
-
(2007)
BMC Dev Biol
, vol.7
, pp. 125
-
-
Thelie, A.1
Papillier, P.2
Pennetier, S.3
Perreau, C.4
Traverso, J.M.5
Uzbekova, S.6
Mermillod, P.7
Joly, C.8
Humblot, P.9
Dalbies-Tran, R.10
-
28
-
-
40049109345
-
Spermatogenic cell-specific type 1 hexokinase is the predominant hexokinase in sperm
-
DOI 10.1002/mrd.20791
-
Spermatogenic cell-specific type 1 hexokinase is the predominant hexokinase in sperm. Nakamura N, Shibata H, O'Brien DA, Mori C, Eddy EM, Mol Reprod Dev 2008 75 632 640 10.1002/mrd.20791 17924400 (Pubitemid 351323773)
-
(2008)
Molecular Reproduction and Development
, vol.75
, Issue.4
, pp. 632-640
-
-
Nakamura, N.1
Shibata, H.2
O'Brien, D.A.3
Mori, C.4
Eddy, E.M.5
|