-
1
-
-
59749096464
-
Clinical practice. Primary ovarian insufficiency
-
L.M. Nelson Clinical practice. Primary ovarian insufficiency N Engl J Med 360 2009 606 614
-
(2009)
N Engl J Med
, vol.360
, pp. 606-614
-
-
Nelson, L.M.1
-
2
-
-
0021032662
-
Evidence for a genetic factor in the etiology of premature ovarian failure
-
C.B. Coulam, S. Stringfellow, and D. Hoefnagel Evidence for a genetic factor in the etiology of premature ovarian failure Fertil Steril 40 1983 693 695
-
(1983)
Fertil Steril
, vol.40
, pp. 693-695
-
-
Coulam, C.B.1
Stringfellow, S.2
Hoefnagel, D.3
-
3
-
-
2342635196
-
The fragile-X premutation: A maturing perspective
-
P.J. Hagerman, and R.J. Hagerman The fragile-X premutation: a maturing perspective Am J Hum Genet 74 2004 805 816
-
(2004)
Am J Hum Genet
, vol.74
, pp. 805-816
-
-
Hagerman, P.J.1
Hagerman, R.J.2
-
4
-
-
0025833298
-
Absence of expression of the FMR-1 gene in fragile X syndrome
-
M. Pieretti, F.P. Zhang, Y.H. Fu, S.T. Warren, B.A. Oostra, and C.T. Caskey Absence of expression of the FMR-1 gene in fragile X syndrome Cell 66 1991 817 822
-
(1991)
Cell
, vol.66
, pp. 817-822
-
-
Pieretti, M.1
Zhang, F.P.2
Fu, Y.H.3
Warren, S.T.4
Oostra, B.A.5
Caskey, C.T.6
-
5
-
-
0029097960
-
Fragile X premutations in familial premature ovarian failure
-
G.S. Conway, S. Hettiarachchi, A. Murray, and P.A. Jacobs Fragile X premutations in familial premature ovarian failure Lancet 346 1995 309 310
-
(1995)
Lancet
, vol.346
, pp. 309-310
-
-
Conway, G.S.1
Hettiarachchi, S.2
Murray, A.3
Jacobs, P.A.4
-
6
-
-
0033515496
-
Fragile X premutation is a significant risk factor for premature ovarian failure: The International Collaborative POF in Fragile X study - Preliminary data
-
D.J. Allingham-Hawkins, R. Babul-Hirji, D. Chitayat, J.J. Holden, K.T. Yang, and C. Lee Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study - preliminary data Am J Med Genet 83 1999 322 325
-
(1999)
Am J Med Genet
, vol.83
, pp. 322-325
-
-
Allingham-Hawkins, D.J.1
Babul-Hirji, R.2
Chitayat, D.3
Holden, J.J.4
Yang, K.T.5
Lee, C.6
-
7
-
-
0034522229
-
Premature ovarian failure in the fragile X syndrome
-
S.L. Sherman Premature ovarian failure in the fragile X syndrome Am J Med Genet 97 2000 189 194
-
(2000)
Am J Med Genet
, vol.97
, pp. 189-194
-
-
Sherman, S.L.1
-
8
-
-
14044268841
-
Association of FMR1 repeat size with ovarian dysfunction
-
A.K. Sullivan, M. Marcus, M.P. Epstein, E.G. Allen, A.E. Anido, and J.J. Paquin Association of FMR1 repeat size with ovarian dysfunction Hum Reprod 20 2005 402 412
-
(2005)
Hum Reprod
, vol.20
, pp. 402-412
-
-
Sullivan, A.K.1
Marcus, M.2
Epstein, M.P.3
Allen, E.G.4
Anido, A.E.5
Paquin, J.J.6
-
9
-
-
0030610425
-
The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians
-
S.H. Chen, J.M. Schoof, N.E. Buroker, and C.R. Scott The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians Hum Genet 99 1997 793 795
-
(1997)
Hum Genet
, vol.99
, pp. 793-795
-
-
Chen, S.H.1
Schoof, J.M.2
Buroker, N.E.3
Scott, C.R.4
-
10
-
-
0038025990
-
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; Implications for the cerebellar tremor/ataxia syndrome
-
R. Willemsen, M. Hoogeveen-Westerveld, S. Reis, J. Holstege, L.A. Severijnen, and I.M. Nieuwenhuizen The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome Hum Mol Genet 12 2003 949 959
-
(2003)
Hum Mol Genet
, vol.12
, pp. 949-959
-
-
Willemsen, R.1
Hoogeveen-Westerveld, M.2
Reis, S.3
Holstege, J.4
Severijnen, L.A.5
Nieuwenhuizen, I.M.6
-
11
-
-
0034128910
-
Reproductive and menstrual history of females with fragile X expansions
-
A. Murray, S. Ennis, F. MacSwiney, J. Webb, and N.E. Morton Reproductive and menstrual history of females with fragile X expansions Eur J Hum Genet 8 2000 247 252
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 247-252
-
-
Murray, A.1
Ennis, S.2
MacSwiney, F.3
Webb, J.4
Morton, N.E.5
-
12
-
-
77957220436
-
ACOG Committee Opinion no. 469: Carrier screening for fragile X syndrome
-
ACOG Committee Opinion no. 469: carrier screening for fragile X syndrome Obstet Gynecol 116 2010 1008 1010
-
(2010)
Obstet Gynecol
, vol.116
, pp. 1008-1010
-
-
-
13
-
-
0037320928
-
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
-
S.L. Nolin, W.T. Brown, A. Glicksman, G.E. Houck Jr., A.D. Gargano, and A. Sullivan Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles Am J Hum Genet 72 2003 454 464
-
(2003)
Am J Hum Genet
, vol.72
, pp. 454-464
-
-
Nolin, S.L.1
Brown, W.T.2
Glicksman, A.3
Houck, Jr.G.E.4
Gargano, A.D.5
Sullivan, A.6
-
14
-
-
78049407994
-
The FMR1 gene as regulator of ovarian recruitment and ovarian reserve
-
N. Gleicher, and D.H. Barad The FMR1 gene as regulator of ovarian recruitment and ovarian reserve Obstet Gynecol Surv 65 2010 523 530
-
(2010)
Obstet Gynecol Surv
, vol.65
, pp. 523-530
-
-
Gleicher, N.1
Barad, D.H.2
-
15
-
-
23944493381
-
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure
-
K.L. Bretherick, M.R. Fluker, and W.P. Robinson FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure Hum Genet 117 2005 376 382
-
(2005)
Hum Genet
, vol.117
, pp. 376-382
-
-
Bretherick, K.L.1
Fluker, M.R.2
Robinson, W.P.3
-
16
-
-
33645314905
-
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation
-
B. Bodega, S. Bione, L. Dalpra, D. Toniolo, F. Ornaghi, and W. Vegetti Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation Hum Reprod 21 2006 952 957
-
(2006)
Hum Reprod
, vol.21
, pp. 952-957
-
-
Bodega, B.1
Bione, S.2
Dalpra, L.3
Toniolo, D.4
Ornaghi, F.5
Vegetti, W.6
-
17
-
-
77649278097
-
Relevance of triple CGG repeats in the FMR1 gene to ovarian reserve
-
N. Gleicher, A. Weghofer, K. Oktay, and D. Barad Relevance of triple CGG repeats in the FMR1 gene to ovarian reserve Reprod Biomed Online 19 2009 385 390
-
(2009)
Reprod Biomed Online
, vol.19
, pp. 385-390
-
-
Gleicher, N.1
Weghofer, A.2
Oktay, K.3
Barad, D.4
-
18
-
-
77954309591
-
Ovarian reserve determinations suggest new function of FMR1 (fragile X gene) in regulating ovarian ageing
-
N. Gleicher, A. Weghofer, and D.H. Barad Ovarian reserve determinations suggest new function of FMR1 (fragile X gene) in regulating ovarian ageing Reprod Biomed Online 20 2010 768 775
-
(2010)
Reprod Biomed Online
, vol.20
, pp. 768-775
-
-
Gleicher, N.1
Weghofer, A.2
Barad, D.H.3
-
19
-
-
67349105624
-
A pilot study of premature ovarian senescence: I. Correlation of triple CGG repeats on the FMR1 gene to ovarian reserve parameters FSH and anti-Mullerian hormone
-
N. Gleicher, A. Weghofer, and D.H. Barad A pilot study of premature ovarian senescence: I. Correlation of triple CGG repeats on the FMR1 gene to ovarian reserve parameters FSH and anti-Mullerian hormone Fertil Steril 91 2009 1700 1706
-
(2009)
Fertil Steril
, vol.91
, pp. 1700-1706
-
-
Gleicher, N.1
Weghofer, A.2
Barad, D.H.3
-
20
-
-
77951652465
-
Effects of race/ethnicity on triple CGG counts in the FMR1 gene in infertile women and egg donors
-
N. Gleicher, A. Weghofer, and D.H. Barad Effects of race/ethnicity on triple CGG counts in the FMR1 gene in infertile women and egg donors Reprod Biomed Online 20 2010 485 491
-
(2010)
Reprod Biomed Online
, vol.20
, pp. 485-491
-
-
Gleicher, N.1
Weghofer, A.2
Barad, D.H.3
-
21
-
-
0344668735
-
The (CGG)n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter
-
L.S. Chen, F. Tassone, P. Sahota, and P.J. Hagerman The (CGG)n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter Hum Mol Genet 12 2003 3067 3074
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3067-3074
-
-
Chen, L.S.1
Tassone, F.2
Sahota, P.3
Hagerman, P.J.4
-
22
-
-
33947168860
-
The FMR1 premutation and reproduction
-
M.D. Wittenberger, R.J. Hagerman, S.L. Sherman, A. McConkie-Rosell, C.K. Welt, and R.W. Rebar The FMR1 premutation and reproduction Fertil Steril 87 2007 456 465
-
(2007)
Fertil Steril
, vol.87
, pp. 456-465
-
-
Wittenberger, M.D.1
Hagerman, R.J.2
Sherman, S.L.3
McConkie-Rosell, A.4
Welt, C.K.5
Rebar, R.W.6
-
23
-
-
57049092347
-
Testing for fragile X gene mutations throughout the life span
-
R.J. Hagerman, and P.J. Hagerman Testing for fragile X gene mutations throughout the life span JAMA 300 2008 2419 2421
-
(2008)
JAMA
, vol.300
, pp. 2419-2421
-
-
Hagerman, R.J.1
Hagerman, P.J.2
-
24
-
-
0027500851
-
Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate
-
T. Arinami, M. Asano, K. Kobayashi, H. Yanagi, and H. Hamaguchi Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate Hum Genet 92 1993 431 436
-
(1993)
Hum Genet
, vol.92
, pp. 431-436
-
-
Arinami, T.1
Asano, M.2
Kobayashi, K.3
Yanagi, H.4
Hamaguchi, H.5
-
25
-
-
73749084776
-
Fragile X carrier screening and FMR1 allele distribution in the Japanese population
-
S. Otsuka, Y. Sakamoto, H. Siomi, M. Itakura, K. Yamamoto, and H. Matumoto Fragile X carrier screening and FMR1 allele distribution in the Japanese population Brain Dev 32 2010 110 114
-
(2010)
Brain Dev
, vol.32
, pp. 110-114
-
-
Otsuka, S.1
Sakamoto, Y.2
Siomi, H.3
Itakura, M.4
Yamamoto, K.5
Matumoto, H.6
-
26
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Y.H. Fu, D.P. Kuhl, A. Pizzuti, M. Pieretti, J.S. Sutcliffe, and S. Richards Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox Cell 67 1991 1047 1058
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.2
Pizzuti, A.3
Pieretti, M.4
Sutcliffe, J.S.5
Richards, S.6
-
27
-
-
0031857007
-
Studies of FRAXA and FRAXE in women with premature ovarian failure
-
A. Murray, J. Webb, S. Grimley, G. Conway, and P. Jacobs Studies of FRAXA and FRAXE in women with premature ovarian failure J Med Genet 35 1998 637 640
-
(1998)
J Med Genet
, vol.35
, pp. 637-640
-
-
Murray, A.1
Webb, J.2
Grimley, S.3
Conway, G.4
Jacobs, P.5
-
28
-
-
0031471187
-
Fragile X premutations are not a major cause of early menopause
-
A. Kenneson, D.W. Cramer, and S.T. Warren Fragile X premutations are not a major cause of early menopause Am J Hum Genet 61 1997 1362 1369
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1362-1369
-
-
Kenneson, A.1
Cramer, D.W.2
Warren, S.T.3
-
29
-
-
0031809893
-
Fragile X premutation screening in women with premature ovarian failure
-
G.S. Conway, N.N. Payne, J. Webb, A. Murray, and P.A. Jacobs Fragile X premutation screening in women with premature ovarian failure Hum Reprod 13 1998 1184 1187
-
(1998)
Hum Reprod
, vol.13
, pp. 1184-1187
-
-
Conway, G.S.1
Payne, N.N.2
Webb, J.3
Murray, A.4
Jacobs, P.A.5
-
30
-
-
0033612244
-
Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data
-
M.L. Uzielli, S. Guarducci, E. Lapi, A. Cecconi, U. Ricci, and G. Ricotti Premature ovarian failure (POF) and fragile X premutation females: from POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data Am J Med Genet 84 1999 300 303
-
(1999)
Am J Med Genet
, vol.84
, pp. 300-303
-
-
Uzielli, M.L.1
Guarducci, S.2
Lapi, E.3
Cecconi, A.4
Ricci, U.5
Ricotti, G.6
-
31
-
-
0033982829
-
Association between idiopathic premature ovarian failure and fragile X premutation
-
A. Marozzi, W. Vegetti, E. Manfredini, M.G. Tibiletti, G. Testa, and P.G. Crosignani Association between idiopathic premature ovarian failure and fragile X premutation Hum Reprod 15 2000 197 202
-
(2000)
Hum Reprod
, vol.15
, pp. 197-202
-
-
Marozzi, A.1
Vegetti, W.2
Manfredini, E.3
Tibiletti, M.G.4
Testa, G.5
Crosignani, P.G.6
-
32
-
-
0041622691
-
Fragile X premutation in women with sporadic premature ovarian failure in Slovenia
-
K. Gersak, H. Meden-Vrtovec, and B. Peterlin Fragile X premutation in women with sporadic premature ovarian failure in Slovenia Hum Reprod 18 2003 1637 1640
-
(2003)
Hum Reprod
, vol.18
, pp. 1637-1640
-
-
Gersak, K.1
Meden-Vrtovec, H.2
Peterlin, B.3
-
33
-
-
69249122535
-
CGG repeat sizing in the FMR1 gene in Indian women with premature ovarian failure
-
S. Chatterjee, A. Maitra, S. Kadam, Z. Patel, J. Gokral, and P. Meherji CGG repeat sizing in the FMR1 gene in Indian women with premature ovarian failure Reprod Biomed Online 19 2009 281 286
-
(2009)
Reprod Biomed Online
, vol.19
, pp. 281-286
-
-
Chatterjee, S.1
Maitra, A.2
Kadam, S.3
Patel, Z.4
Gokral, J.5
Meherji, P.6
-
34
-
-
78650719629
-
FMR1 genotype with autoimmunity-associated polycystic ovary-like phenotype and decreased pregnancy chance
-
N. Gleicher, A. Weghofer, I.H. Lee, and D.H. Barad FMR1 genotype with autoimmunity-associated polycystic ovary-like phenotype and decreased pregnancy chance PLoS One 5 2010 e15303
-
(2010)
PLoS One
, vol.5
, pp. 15303
-
-
Gleicher, N.1
Weghofer, A.2
Lee, I.H.3
Barad, D.H.4
|