-
1
-
-
77949769087
-
Epigenetic signatures of Silver–Russell syndrome
-
COI: 1:CAS:528:DC%2BC3cXlt1yjt74%3D, PID: 20305090
-
Abu-Amero S, Wakeling EL, Preece M, Whittaker J, Stanier P, Moore GE (2010) Epigenetic signatures of Silver–Russell syndrome. J Med Genet 47(3):150–154. doi:10.1136/jmg.2009.071316
-
(2010)
J Med Genet
, vol.47
, Issue.3
, pp. 150-154
-
-
Abu-Amero, S.1
Wakeling, E.L.2
Preece, M.3
Whittaker, J.4
Stanier, P.5
Moore, G.E.6
-
2
-
-
84908566266
-
Comprehensive analysis of DNA methylation data with RnBeads
-
Assenov Y, Müller F, Lutsik P, Walter J, Lengauer T, Bock C (2014) Comprehensive analysis of DNA methylation data with RnBeads. Nat Methods 11(11):1138–1140. doi:10.1038/nmeth.3115
-
(2014)
Nat Methods
, vol.11
, Issue.11
, pp. 1138-1140
-
-
Assenov, Y.1
Müller, F.2
Lutsik, P.3
Walter, J.4
Lengauer, T.5
Bock, C.6
-
3
-
-
70450162112
-
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
-
COI: 1:CAS:528:DC%2BD1MXhsVGltbvO, PID: 19755383
-
Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I (2009) Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet 18(24):4724–4733. doi:10.1093/hmg/ddp435
-
(2009)
Hum Mol Genet
, vol.18
, Issue.24
, pp. 4724-4733
-
-
Azzi, S.1
Rossignol, S.2
Steunou, V.3
Sas, T.4
Thibaud, N.5
Danton, F.6
Le Jule, M.7
Heinrichs, C.8
Cabrol, S.9
Gicquel, C.10
Le Bouc, Y.11
Netchine, I.12
-
4
-
-
0001677717
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Roy Stat Soc Ser B 57(1):289–300
-
(1995)
J Roy Stat Soc Ser B
, vol.57
, Issue.1
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
5
-
-
80053304450
-
High density DNA methylation array with single CpG site resolution
-
COI: 1:CAS:528:DC%2BC3MXht1ClsbfK, PID: 21839163
-
Bibikova M, Barnes B, Tsan C, Ho V, Klotzle B, Le JM, Delano D, Zhang L, Schroth GP, Gunderson KL, Fan JB, Shen R (2011) High density DNA methylation array with single CpG site resolution. Genomics 98(4):288–295. doi:10.1016/j.ygeno.2011.07.007
-
(2011)
Genomics
, vol.98
, Issue.4
, pp. 288-295
-
-
Bibikova, M.1
Barnes, B.2
Tsan, C.3
Ho, V.4
Klotzle, B.5
Le, J.M.6
Delano, D.7
Zhang, L.8
Schroth, G.P.9
Gunderson, K.L.10
Fan, J.B.11
Shen, R.12
-
6
-
-
33645463808
-
Hypomethylation of the H19 gene causes not only Silver–Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
-
COI: 1:CAS:528:DC%2BD28Xjt1Glsb4%3D, PID: 16532391
-
Bliek J, Terhal P, van den Bogaard MJ, Maas S, Hamel B, Salieb-Beugelaar G, Simon M, Letteboer T, van der Smagt J, Kroes H, Mannens M (2006) Hypomethylation of the H19 gene causes not only Silver–Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. Am J Hum Genet 78(4):604–614. doi:10.1086/502981
-
(2006)
Am J Hum Genet
, vol.78
, Issue.4
, pp. 604-614
-
-
Bliek, J.1
Terhal, P.2
van den Bogaard, M.J.3
Maas, S.4
Hamel, B.5
Salieb-Beugelaar, G.6
Simon, M.7
Letteboer, T.8
van der Smagt, J.9
Kroes, H.10
Mannens, M.11
-
7
-
-
84871688621
-
Analysing and interpreting DNA methylation data
-
COI: 1:CAS:528:DC%2BC38XhtlGntrrF, PID: 22986265
-
Bock C (2012) Analysing and interpreting DNA methylation data. Nat Rev Genet 13(10):705–719. doi:10.1038/nrg3273
-
(2012)
Nat Rev Genet
, vol.13
, Issue.10
, pp. 705-719
-
-
Bock, C.1
-
8
-
-
77955403504
-
Imprinting of RB1 (the new kid on the block)
-
COI: 1:CAS:528:DC%2BC3cXpsFKgsr8%3D, PID: 20551090
-
Buiting K, Kanber D, Horsthemke B, Lohmann D (2010) Imprinting of RB1 (the new kid on the block). Brief Funct Genomics 9(4):347–353. doi:10.1093/bfgp/elq014
-
(2010)
Brief Funct Genomics
, vol.9
, Issue.4
, pp. 347-353
-
-
Buiting, K.1
Kanber, D.2
Horsthemke, B.3
Lohmann, D.4
-
9
-
-
84880309035
-
Intrauterine calorie restriction affects placental DNA methylation and gene expression
-
COI: 1:CAS:528:DC%2BC3sXht1OmtLjL, PID: 23695884
-
Chen PY, Ganguly A, Rubbi L, Orozco LD, Morselli M, Ashraf D, Jaroszewicz A, Feng S, Jacobsen SE, Nakano A, Devaskar SU, Pellegrini M (2013) Intrauterine calorie restriction affects placental DNA methylation and gene expression. Physiol Genomics 45(14):565–576. doi:10.1152/physiolgenomics.00034.2013
-
(2013)
Physiol Genomics
, vol.45
, Issue.14
, pp. 565-576
-
-
Chen, P.Y.1
Ganguly, A.2
Rubbi, L.3
Orozco, L.D.4
Morselli, M.5
Ashraf, D.6
Jaroszewicz, A.7
Feng, S.8
Jacobsen, S.E.9
Nakano, A.10
Devaskar, S.U.11
Pellegrini, M.12
-
10
-
-
84861894813
-
Prevention of age-related changes in hippocampal levels of 5-methylcytidine by caloric restriction
-
COI: 1:CAS:528:DC%2BC38XotFaksLY%3D, PID: 21764481
-
Chouliaras L, van den Hove DL, Kenis G, Keitel S, Hof PR, van Os J, Steinbusch HW, Schmitz C, Rutten BP (2012) Prevention of age-related changes in hippocampal levels of 5-methylcytidine by caloric restriction. Neurobiol Aging 33(8):1672–1681. doi:10.1016/j.neurobiolaging.2011.06.003
-
(2012)
Neurobiol Aging
, vol.33
, Issue.8
, pp. 1672-1681
-
-
Chouliaras, L.1
van den Hove, D.L.2
Kenis, G.3
Keitel, S.4
Hof, P.R.5
van Os, J.6
Steinbusch, H.W.7
Schmitz, C.8
Rutten, B.P.9
-
11
-
-
27244436752
-
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome
-
COI: 1:CAS:528:DC%2BD2MXovVOiurc%3D, PID: 15999116
-
Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER (2005) Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome. Eur J Hum Genet 13(9):1025–1032. doi:10.1038/sj.ejhg.5201463
-
(2005)
Eur J Hum Genet
, vol.13
, Issue.9
, pp. 1025-1032
-
-
Cooper, W.N.1
Luharia, A.2
Evans, G.A.3
Raza, H.4
Haire, A.C.5
Grundy, R.6
Bowdin, S.C.7
Riccio, A.8
Sebastio, G.9
Bliek, J.10
Schofield, P.N.11
Reik, W.12
Macdonald, F.13
Maher, E.R.14
-
12
-
-
84875549355
-
Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes
-
COI: 1:CAS:528:DC%2BC3sXksFKkurs%3D, PID: 23335487
-
Court F, Martin-Trujillo A, Romanelli V, Garin I, Iglesias-Platas I, Salafsky I, Guitart M, Perez de Nanclares G, Lapunzina P, Monk D (2013) Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes. Hum Mutat 34(4):595–602. doi:10.1002/humu.22276
-
(2013)
Hum Mutat
, vol.34
, Issue.4
, pp. 595-602
-
-
Court, F.1
Martin-Trujillo, A.2
Romanelli, V.3
Garin, I.4
Iglesias-Platas, I.5
Salafsky, I.6
Guitart, M.7
Perez de Nanclares, G.8
Lapunzina, P.9
Monk, D.10
-
13
-
-
79956330964
-
CpG islands and the regulation of transcription
-
COI: 1:CAS:528:DC%2BC3MXmslOgsLY%3D, PID: 21576262
-
Deaton AM, Bird A (2011) CpG islands and the regulation of transcription. Genes Dev 25(10):1010–1022. doi:10.1101/gad.2037511
-
(2011)
Genes Dev
, vol.25
, Issue.10
, pp. 1010-1022
-
-
Deaton, A.M.1
Bird, A.2
-
14
-
-
84868613969
-
Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in Silver–Russell syndrome
-
COI: 1:CAS:528:DC%2BC38Xhs12ku7vL, PID: 22942387
-
Dias RP, Bogdarina I, Cazier JB, Buchanan C, Donaldson MC, Johnston LB, Hokken-Koelega AC, Clark AJ (2012) Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in Silver–Russell syndrome. J Clin Endocrinol Metab 97(11):E2188–E2193. doi:10.1210/jc.2012-1980
-
(2012)
J Clin Endocrinol Metab
, vol.97
, Issue.11
, pp. E2188-E2193
-
-
Dias, R.P.1
Bogdarina, I.2
Cazier, J.B.3
Buchanan, C.4
Donaldson, M.C.5
Johnston, L.B.6
Hokken-Koelega, A.C.7
Clark, A.J.8
-
15
-
-
34447313147
-
Assessment and disease comparisons of hybrid developmental defects
-
COI: 1:CAS:528:DC%2BD2sXmsVWntr8%3D, PID: 17339267
-
Duselis AR, Vrana PB (2007) Assessment and disease comparisons of hybrid developmental defects. Hum Mol Genet 16(7):808–819. doi:10.1093/hmg/ddm025
-
(2007)
Hum Mol Genet
, vol.16
, Issue.7
, pp. 808-819
-
-
Duselis, A.R.1
Vrana, P.B.2
-
16
-
-
38349179230
-
Of lineage and legacy: the development of mammalian hematopoietic stem cells
-
COI: 1:CAS:528:DC%2BD1cXovV2msw%3D%3D, PID: 18204427
-
Dzierzak E, Speck NA (2008) Of lineage and legacy: the development of mammalian hematopoietic stem cells. Nat Immunol 9(2):129–136. doi:10.1038/ni1560
-
(2008)
Nat Immunol
, vol.9
, Issue.2
, pp. 129-136
-
-
Dzierzak, E.1
Speck, N.A.2
-
17
-
-
33745903915
-
Epigenetic mutations in 11p15 in Silver–Russell syndrome are restricted to the telomeric imprinting domain
-
COI: 1:CAS:528:DC%2BD28XotFarurs%3D, PID: 16236811
-
Eggermann T, Schonherr N, Meyer E, Obermann C, Mavany M, Eggermann K, Ranke MB, Wollmann HA (2006) Epigenetic mutations in 11p15 in Silver–Russell syndrome are restricted to the telomeric imprinting domain. J Med Genet 43(7):615–616. doi:10.1136/jmg.2005.038687
-
(2006)
J Med Genet
, vol.43
, Issue.7
, pp. 615-616
-
-
Eggermann, T.1
Schonherr, N.2
Meyer, E.3
Obermann, C.4
Mavany, M.5
Eggermann, K.6
Ranke, M.B.7
Wollmann, H.A.8
-
18
-
-
80054769799
-
Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders
-
COI: 1:CAS:528:DC%2BC3MXhtlWjtbzN, PID: 22126250
-
Eggermann T, Leisten I, Binder G, Begemann M, Spengler S (2011) Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders. Epigenomics 3(5):625–637. doi:10.2217/epi.11.84
-
(2011)
Epigenomics
, vol.3
, Issue.5
, pp. 625-637
-
-
Eggermann, T.1
Leisten, I.2
Binder, G.3
Begemann, M.4
Spengler, S.5
-
19
-
-
84903300881
-
Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing
-
PID: 24658748
-
Eggermann T, Heilsberg AK, Bens S, Siebert R, Beygo J, Buiting K, Begemann M, Soellner L (2014) Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing. J Mol Med. doi:10.1007/s00109-014-1141-6
-
(2014)
J Mol Med
-
-
Eggermann, T.1
Heilsberg, A.K.2
Bens, S.3
Siebert, R.4
Beygo, J.5
Buiting, K.6
Begemann, M.7
Soellner, L.8
-
20
-
-
33846689706
-
Using GOstats to test gene lists for GO term association
-
COI: 1:CAS:528:DC%2BD2sXotFGntA%3D%3D, PID: 17098774
-
Falcon S, Gentleman R (2007) Using GOstats to test gene lists for GO term association. Bioinformatics 23(2):257–258. doi:10.1093/bioinformatics/btl567
-
(2007)
Bioinformatics
, vol.23
, Issue.2
, pp. 257-258
-
-
Falcon, S.1
Gentleman, R.2
-
21
-
-
25844449770
-
Galaxy: a platform for interactive large-scale genome analysis
-
COI: 1:CAS:528:DC%2BD2MXhtFajurnE, PID: 16169926
-
Giardine B, Riemer C, Hardison RC, Burhans R, Elnitski L, Shah P, Zhang Y, Blankenberg D, Albert I, Taylor J, Miller W, Kent WJ, Nekrutenko A (2005) Galaxy: a platform for interactive large-scale genome analysis. Genome Res 15(10):1451–1455. doi:10.1101/gr.4086505
-
(2005)
Genome Res
, vol.15
, Issue.10
, pp. 1451-1455
-
-
Giardine, B.1
Riemer, C.2
Hardison, R.C.3
Burhans, R.4
Elnitski, L.5
Shah, P.6
Zhang, Y.7
Blankenberg, D.8
Albert, I.9
Taylor, J.10
Miller, W.11
Kent, W.J.12
Nekrutenko, A.13
-
22
-
-
25144454048
-
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver–Russell syndrome
-
COI: 1:CAS:528:DC%2BD2MXpsFWisbg%3D, PID: 16086014
-
Gicquel C, Rossignol S, Cabrol S, Houang M, Steunou V, Barbu V, Danton F, Thibaud N, LeMerrer M, Burglen L, Bertrand AM, Netchine I, Le Bouc Y (2005) Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver–Russell syndrome. Nat Genet 37(9):1003–1007
-
(2005)
Nat Genet
, vol.37
, Issue.9
, pp. 1003-1007
-
-
Gicquel, C.1
Rossignol, S.2
Cabrol, S.3
Houang, M.4
Steunou, V.5
Barbu, V.6
Danton, F.7
Thibaud, N.8
LeMerrer, M.9
Burglen, L.10
Bertrand, A.M.11
Netchine, I.12
Le Bouc, Y.13
-
23
-
-
84889654038
-
Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications
-
COI: 1:CAS:528:DC%2BC3sXhvVGrsbjJ, PID: 24283884
-
Girardot M, Feil R, Lleres D (2013) Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications. Epigenomics 5(6):715–728. doi:10.2217/epi.13.66
-
(2013)
Epigenomics
, vol.5
, Issue.6
, pp. 715-728
-
-
Girardot, M.1
Feil, R.2
Lleres, D.3
-
24
-
-
84871420316
-
Age-related changes in the global DNA methylation profile of leukocytes are linked to nutrition but are not associated with the MTHFR C677T genotype or to functional capacities
-
COI: 1:CAS:528:DC%2BC3sXlsVKhsA%3D%3D, PID: 23285094
-
Gomes MV, Toffoli LV, Arruda DW, Soldera LM, Pelosi GG, Neves-Souza RD, Freitas ER, Castro DT, Marquez AS (2012) Age-related changes in the global DNA methylation profile of leukocytes are linked to nutrition but are not associated with the MTHFR C677T genotype or to functional capacities. PLoS One 7(12):e52570. doi:10.1371/journal.pone.0052570
-
(2012)
PLoS One
, vol.7
, Issue.12
, pp. e52570
-
-
Gomes, M.V.1
Toffoli, L.V.2
Arruda, D.W.3
Soldera, L.M.4
Pelosi, G.G.5
Neves-Souza, R.D.6
Freitas, E.R.7
Castro, D.T.8
Marquez, A.S.9
-
25
-
-
57449095858
-
Impaired bone development and increased mesenchymal progenitor cells in calvaria of RB1−/− mice
-
COI: 1:CAS:528:DC%2BD1cXhsVyhsrvL, PID: 19020086
-
Gutierrez GM, Kong E, Sabbagh Y, Brown NE, Lee JS, Demay MB, Thomas DM, Hinds PW (2008) Impaired bone development and increased mesenchymal progenitor cells in calvaria of RB1−/− mice. Proc Natl Acad Sci 105(47):18402–18407. doi:10.1073/pnas.0805925105
-
(2008)
Proc Natl Acad Sci
, vol.105
, Issue.47
, pp. 18402-18407
-
-
Gutierrez, G.M.1
Kong, E.2
Sabbagh, Y.3
Brown, N.E.4
Lee, J.S.5
Demay, M.B.6
Thomas, D.M.7
Hinds, P.W.8
-
26
-
-
84892610407
-
Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7
-
Hannula-Jouppi K, Muurinen M, Lipsanen-Nyman M, Reinius LE, Ezer S, Greco D, Kere J (2013) Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7. Epigenetics 9(3):351–365. doi:10.4161/epi.27160
-
(2013)
Epigenetics
, vol.9
, Issue.3
, pp. 351-365
-
-
Hannula-Jouppi, K.1
Muurinen, M.2
Lipsanen-Nyman, M.3
Reinius, L.E.4
Ezer, S.5
Greco, D.6
Kere, J.7
-
27
-
-
0023686773
-
Abnormalities in structure and expression of the human retinoblastoma gene in SCLC
-
COI: 1:CAS:528:DyaL1cXlt1emsbo%3D, PID: 2838909
-
Harbour JW, Lai SL, Whang-Peng J, Gazdar AF, Minna JD, Kaye FJ (1988) Abnormalities in structure and expression of the human retinoblastoma gene in SCLC. Science 241(4863):353–357
-
(1988)
Science
, vol.241
, Issue.4863
, pp. 353-357
-
-
Harbour, J.W.1
Lai, S.L.2
Whang-Peng, J.3
Gazdar, A.F.4
Minna, J.D.5
Kaye, F.J.6
-
28
-
-
0028111681
-
Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea
-
COI: 1:STN:280:DyaK2M%2FivFektw%3D%3D, PID: 7942853
-
Hoglund P, Holmberg C, de la Chapelle A, Kere J (1994) Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. Am J Hum Genet 55(4):747–752
-
(1994)
Am J Hum Genet
, vol.55
, Issue.4
, pp. 747-752
-
-
Hoglund, P.1
Holmberg, C.2
de la Chapelle, A.3
Kere, J.4
-
29
-
-
0025304297
-
Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells
-
COI: 1:CAS:528:DyaK3cXitleitLw%3D, PID: 2181449
-
Horowitz JM, Park SH, Bogenmann E, Cheng JC, Yandell DW, Kaye FJ, Minna JD, Dryja TP, Weinberg RA (1990) Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells. Proc Natl Acad Sci 87(7):2775–2779
-
(1990)
Proc Natl Acad Sci
, vol.87
, Issue.7
, pp. 2775-2779
-
-
Horowitz, J.M.1
Park, S.H.2
Bogenmann, E.3
Cheng, J.C.4
Yandell, D.W.5
Kaye, F.J.6
Minna, J.D.7
Dryja, T.P.8
Weinberg, R.A.9
-
30
-
-
84878107771
-
The role of imprinted genes in humans
-
COI: 1:CAS:528:DC%2BC3sXnvVGksbY%3D, PID: 22771538
-
Ishida M, Moore GE (2013) The role of imprinted genes in humans. Mol Aspects Med 34(4):826–840. doi:10.1016/j.mam.2012.06.009
-
(2013)
Mol Aspects Med
, vol.34
, Issue.4
, pp. 826-840
-
-
Ishida, M.1
Moore, G.E.2
-
31
-
-
84863986133
-
Functions of DNA methylation: islands, start sites, gene bodies and beyond
-
COI: 1:CAS:528:DC%2BC38Xns1SqtLw%3D, PID: 22641018
-
Jones PA (2012) Functions of DNA methylation: islands, start sites, gene bodies and beyond. Nat Rev Genet 13(7):484–492. doi:10.1038/nrg3230
-
(2012)
Nat Rev Genet
, vol.13
, Issue.7
, pp. 484-492
-
-
Jones, P.A.1
-
32
-
-
74249112469
-
The human retinoblastoma gene is imprinted
-
PID: 20041224
-
Kanber D, Berulava T, Ammerpohl O, Mitter D, Richter J, Siebert R, Horsthemke B, Lohmann D, Buiting K (2009) The human retinoblastoma gene is imprinted. PLoS Genet 5(12):e1000790. doi:10.1371/journal.pgen.1000790
-
(2009)
PLoS Genet
, vol.5
, Issue.12
, pp. e1000790
-
-
Kanber, D.1
Berulava, T.2
Ammerpohl, O.3
Mitter, D.4
Richter, J.5
Siebert, R.6
Horsthemke, B.7
Lohmann, D.8
Buiting, K.9
-
33
-
-
84858283030
-
Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver–Russell syndrome
-
COI: 1:CAS:528:DC%2BC38XnsVCmsL8%3D, PID: 22248018
-
Kannenberg K, Urban C, Binder G (2012) Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver–Russell syndrome. Clin Genet 81(4):366–377. doi:10.1111/j.1399-0004.2012.01844.x
-
(2012)
Clin Genet
, vol.81
, Issue.4
, pp. 366-377
-
-
Kannenberg, K.1
Urban, C.2
Binder, G.3
-
34
-
-
36448973787
-
Idiographica: a general-purpose web application to build idiograms on-demand for human, mouse and rat
-
COI: 1:CAS:528:DC%2BD2sXhtlaqsL3K, PID: 17893084
-
Kin T, Ono Y (2007) Idiographica: a general-purpose web application to build idiograms on-demand for human, mouse and rat. Bioinformatics 23(21):2945–2946. doi:10.1093/bioinformatics/btm455
-
(2007)
Bioinformatics
, vol.23
, Issue.21
, pp. 2945-2946
-
-
Kin, T.1
Ono, Y.2
-
35
-
-
84884826911
-
The next-generation sequencing revolution and its impact on genomics
-
COI: 1:CAS:528:DC%2BC3sXhsFentr7F, PID: 24074859
-
Koboldt DC, Steinberg KM, Larson DE, Wilson RK, Mardis ER (2013) The next-generation sequencing revolution and its impact on genomics. Cell 155(1):27–38. doi:10.1016/j.cell.2013.09.006
-
(2013)
Cell
, vol.155
, Issue.1
, pp. 27-38
-
-
Koboldt, D.C.1
Steinberg, K.M.2
Larson, D.E.3
Wilson, R.K.4
Mardis, E.R.5
-
36
-
-
77958592153
-
Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality
-
PID: 20838620
-
Lee DH, Singh P, Tsark WM, Szabo PE (2010) Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality. PLoS One 5(9):e12630. doi:10.1371/journal.pone.0012630
-
(2010)
PLoS One
, vol.5
, Issue.9
, pp. e12630
-
-
Lee, D.H.1
Singh, P.2
Tsark, W.M.3
Szabo, P.E.4
-
37
-
-
84862173149
-
SWAN: subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips
-
PID: 22703947
-
Maksimovic J, Gordon L, Oshlack A (2012) SWAN: subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips. Genome Biol 13(6):R44. doi:10.1186/gb-2012-13-6-r44
-
(2012)
Genome Biol
, vol.13
, Issue.6
, pp. R44
-
-
Maksimovic, J.1
Gordon, L.2
Oshlack, A.3
-
38
-
-
84858794353
-
Next generation sequencing in epigenetics: insights and challenges
-
COI: 1:CAS:528:DC%2BC38XksFWru70%3D, PID: 22027613
-
Meaburn E, Schulz R (2012) Next generation sequencing in epigenetics: insights and challenges. Semin Cell Dev Biol 23(2):192–199. doi:10.1016/j.semcdb.2011.10.010
-
(2012)
Semin Cell Dev Biol
, vol.23
, Issue.2
, pp. 192-199
-
-
Meaburn, E.1
Schulz, R.2
-
39
-
-
0025958320
-
Genomic imprinting in mammalian development: a parental tug-of-war
-
COI: 1:STN:280:DyaK3M3ktVGmug%3D%3D, PID: 2035190
-
Moore T, Haig D (1991) Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet 7(2):45–49. doi:10.1016/0168-9525(91)90230-N
-
(1991)
Trends Genet
, vol.7
, Issue.2
, pp. 45-49
-
-
Moore, T.1
Haig, D.2
-
40
-
-
0031778075
-
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia
-
COI: 1:CAS:528:DyaK1cXlslChs74%3D, PID: 9585585
-
Pan Y, McCaskill CD, Thompson KH, Hicks J, Casey B, Shaffer LG, Craigen WJ (1998) Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia. Am J Hum Genet 62(6):1551–1555. doi:10.1086/301857
-
(1998)
Am J Hum Genet
, vol.62
, Issue.6
, pp. 1551-1555
-
-
Pan, Y.1
McCaskill, C.D.2
Thompson, K.H.3
Hicks, J.4
Casey, B.5
Shaffer, L.G.6
Craigen, W.J.7
-
41
-
-
75449110360
-
Methylation profiling in individuals with Russell–Silver syndrome
-
COI: 1:CAS:528:DC%2BC3cXis1Wksbw%3D, PID: 20082469
-
Penaherrera MS, Weindler S, Van Allen MI, Yong SL, Metzger DL, McGillivray B, Boerkoel C, Langlois S, Robinson WP (2010) Methylation profiling in individuals with Russell–Silver syndrome. Am J Med Genet A 152A(2):347–355. doi:10.1002/ajmg.a.33204
-
(2010)
Am J Med Genet A
, vol.152A
, Issue.2
, pp. 347-355
-
-
Penaherrera, M.S.1
Weindler, S.2
Van Allen, M.I.3
Yong, S.L.4
Metzger, D.L.5
McGillivray, B.6
Boerkoel, C.7
Langlois, S.8
Robinson, W.P.9
-
42
-
-
84877929407
-
Beyond transposons: the epigenetic and somatic functions of the Piwi-piRNA mechanism
-
COI: 1:CAS:528:DC%2BC3sXjsFCgsrw%3D, PID: 23465540
-
Peng JC, Lin H (2013) Beyond transposons: the epigenetic and somatic functions of the Piwi-piRNA mechanism. Curr Opin Cell Biol 25(2):190–194. doi:10.1016/j.ceb.2013.01.010
-
(2013)
Curr Opin Cell Biol
, vol.25
, Issue.2
, pp. 190-194
-
-
Peng, J.C.1
Lin, H.2
-
43
-
-
0031036341
-
Maternal uniparental disomy 7 in Silver–Russell syndrome
-
COI: 1:STN:280:DyaK2s7osVyksA%3D%3D, PID: 9032641
-
Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE (1997) Maternal uniparental disomy 7 in Silver–Russell syndrome. J Med Genet 34(1):6–9
-
(1997)
J Med Genet
, vol.34
, Issue.1
, pp. 6-9
-
-
Preece, M.A.1
Price, S.M.2
Davies, V.3
Clough, L.4
Stanier, P.5
Trembath, R.C.6
Moore, G.E.7
-
44
-
-
0033042181
-
An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver–Russell syndrome probands
-
COI: 1:CAS:528:DyaK1MXktF2js7s%3D, PID: 10874633
-
Preece MA, Abu-Amero SN, Ali Z, Abu-Amero KK, Wakeling EL, Stanier P, Moore GE (1999) An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver–Russell syndrome probands. J Med Genet 36(6):457–460
-
(1999)
J Med Genet
, vol.36
, Issue.6
, pp. 457-460
-
-
Preece, M.A.1
Abu-Amero, S.N.2
Ali, Z.3
Abu-Amero, K.K.4
Wakeling, E.L.5
Stanier, P.6
Moore, G.E.7
-
45
-
-
0032758850
-
The spectrum of Silver–Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria
-
COI: 1:STN:280:DC%2BD3c%2FhtlSmtg%3D%3D, PID: 10544228
-
Price S, Stanhope R, Garrett C, Preece MA, Trembath RC (1999) The spectrum of Silver–Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 36:837–842
-
(1999)
J Med Genet
, vol.36
, pp. 837-842
-
-
Price, S.1
Stanhope, R.2
Garrett, C.3
Preece, M.A.4
Trembath, R.C.5
-
46
-
-
84866862172
-
Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes
-
COI: 1:CAS:528:DC%2BC38Xht1aktbvJ, PID: 22902559
-
Proudhon C, Duffie R, Ajjan S, Cowley M, Iranzo J, Carbajosa G, Saadeh H, Holland ML, Oakey RJ, Rakyan VK, Schulz R, Bourc’his D (2012) Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes. Mol Cell 47(6):909–920. doi:10.1016/j.molcel.2012.07.010
-
(2012)
Mol Cell
, vol.47
, Issue.6
, pp. 909-920
-
-
Proudhon, C.1
Duffie, R.2
Ajjan, S.3
Cowley, M.4
Iranzo, J.5
Carbajosa, G.6
Saadeh, H.7
Holland, M.L.8
Oakey, R.J.9
Rakyan, V.K.10
Schulz, R.11
Bourc’his, D.12
-
47
-
-
84880235349
-
The epigenetic regulator PLZF represses L1 retrotransposition in germ and progenitor cells
-
COI: 1:CAS:528:DC%2BC3sXosFWrtb0%3D, PID: 23727884
-
Puszyk W, Down T, Grimwade D, Chomienne C, Oakey RJ, Solomon E, Guidez F (2013) The epigenetic regulator PLZF represses L1 retrotransposition in germ and progenitor cells. EMBO J 32(13):1941–1952. doi:10.1038/emboj.2013.118
-
(2013)
EMBO J
, vol.32
, Issue.13
, pp. 1941-1952
-
-
Puszyk, W.1
Down, T.2
Grimwade, D.3
Chomienne, C.4
Oakey, R.J.5
Solomon, E.6
Guidez, F.7
-
48
-
-
84926113028
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
-
PID: 24923327
-
Rademacher K, Schroder C, Kanber D, Klein-Hitpass L, Wallner S, Zeschnigk M, Horsthemke B (2014) Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse. Genome Biol Evol. doi:10.1093/gbe/evu125
-
(2014)
Genome Biol Evol
-
-
Rademacher, K.1
Schroder, C.2
Kanber, D.3
Klein-Hitpass, L.4
Wallner, S.5
Zeschnigk, M.6
Horsthemke, B.7
-
49
-
-
84864359044
-
Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility
-
COI: 1:CAS:528:DC%2BC38XhtFamsr%2FO, PID: 22848472
-
Reinius LE, Acevedo N, Joerink M, Pershagen G, Dahlen SE, Greco D, Soderhall C, Scheynius A, Kere J (2012) Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility. PLoS One 7(7):e41361. doi:10.1371/journal.pone.0041361
-
(2012)
PLoS One
, vol.7
, Issue.7
, pp. e41361
-
-
Reinius, L.E.1
Acevedo, N.2
Joerink, M.3
Pershagen, G.4
Dahlen, S.E.5
Greco, D.6
Soderhall, C.7
Scheynius, A.8
Kere, J.9
-
50
-
-
0038668852
-
Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors
-
COI: 1:CAS:528:DC%2BD3sXls1Ogsbs%3D, PID: 12885459
-
Sandberg AA, Bridge JA (2003) Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors. Cancer Genet Cytogenet 145(1):1–30
-
(2003)
Cancer Genet Cytogenet
, vol.145
, Issue.1
, pp. 1-30
-
-
Sandberg, A.A.1
Bridge, J.A.2
-
51
-
-
47149114764
-
WAMIDEX: a web atlas of murine genomic imprinting and differential expression
-
PID: 18398312
-
Schulz R, Woodfine K, Menheniott TR, Bourc’his D, Bestor T, Oakey RJ (2008) WAMIDEX: a web atlas of murine genomic imprinting and differential expression. Epigenetics 3(2):89–96
-
(2008)
Epigenetics
, vol.3
, Issue.2
, pp. 89-96
-
-
Schulz, R.1
Woodfine, K.2
Menheniott, T.R.3
Bourc’his, D.4
Bestor, T.5
Oakey, R.J.6
-
52
-
-
80051664488
-
Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia
-
COI: 1:CAS:528:DC%2BC3MXhtVajt7bE, PID: 21782149
-
Sirmaci A, Spiliopoulos M, Brancati F, Powell E, Duman D, Abrams A, Bademci G, Agolini E, Guo S, Konuk B, Kavaz A, Blanton S, Digilio MC, Dallapiccola B, Young J, Zuchner S, Tekin M (2011) Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia. Am J Hum Genet 89(2):289–294. doi:10.1016/j.ajhg.2011.06.007
-
(2011)
Am J Hum Genet
, vol.89
, Issue.2
, pp. 289-294
-
-
Sirmaci, A.1
Spiliopoulos, M.2
Brancati, F.3
Powell, E.4
Duman, D.5
Abrams, A.6
Bademci, G.7
Agolini, E.8
Guo, S.9
Konuk, B.10
Kavaz, A.11
Blanton, S.12
Digilio, M.C.13
Dallapiccola, B.14
Young, J.15
Zuchner, S.16
Tekin, M.17
-
54
-
-
84880029998
-
Haploinsufficiency of ANKRD11 (16q24.3) is not obligatorily associated with cognitive impairment but shows a clinical overlap with Silver–Russell syndrome
-
COI: 1:CAS:528:DC%2BC3sXhtVylu7%2FF, PID: 23885231
-
Spengler S, Oehl-Jaschkowitz B, Begemann M, Hennes P, Zerres K, Eggermann T (2013) Haploinsufficiency of ANKRD11 (16q24.3) is not obligatorily associated with cognitive impairment but shows a clinical overlap with Silver–Russell syndrome. Mol Syndromol 4(5):246–249. doi:10.1159/000351765
-
(2013)
Mol Syndromol
, vol.4
, Issue.5
, pp. 246-249
-
-
Spengler, S.1
Oehl-Jaschkowitz, B.2
Begemann, M.3
Hennes, P.4
Zerres, K.5
Eggermann, T.6
-
55
-
-
54949156063
-
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios
-
PID: 18831757
-
Staaf J, Vallon-Christersson J, Lindgren D, Juliusson G, Rosenquist R, Hoglund M, Borg A, Ringner M (2008) Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios. BMC Bioinformatics 9:409. doi:10.1186/1471-2105-9-409
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 409
-
-
Staaf, J.1
Vallon-Christersson, J.2
Lindgren, D.3
Juliusson, G.4
Rosenquist, R.5
Hoglund, M.6
Borg, A.7
Ringner, M.8
-
56
-
-
84872564830
-
A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450k DNA methylation data
-
COI: 1:CAS:528:DC%2BC3sXhtFygsro%3D, PID: 23175756
-
Teschendorff AE, Marabita F, Lechner M, Bartlett T, Tegner J, Gomez-Cabrero D, Beck S (2013) A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450k DNA methylation data. Bioinformatics 29(2):189–196. doi:10.1093/bioinformatics/bts680
-
(2013)
Bioinformatics
, vol.29
, Issue.2
, pp. 189-196
-
-
Teschendorff, A.E.1
Marabita, F.2
Lechner, M.3
Bartlett, T.4
Tegner, J.5
Gomez-Cabrero, D.6
Beck, S.7
-
57
-
-
84862266444
-
Complete pipeline for Infinium((R)) Human Methylation 450K BeadChip data processing using subset quantile normalization for accurate DNA methylation estimation
-
COI: 1:CAS:528:DC%2BC38XosVahs7s%3D, PID: 22690668
-
Touleimat N, Tost J (2012) Complete pipeline for Infinium((R)) Human Methylation 450K BeadChip data processing using subset quantile normalization for accurate DNA methylation estimation. Epigenomics 4(3):325–341. doi:10.2217/epi.12.21
-
(2012)
Epigenomics
, vol.4
, Issue.3
, pp. 325-341
-
-
Touleimat, N.1
Tost, J.2
-
58
-
-
77952671659
-
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci
-
COI: 1:CAS:528:DC%2BC3cXmt1OjsL4%3D, PID: 20104244
-
Turner CL, Mackay DM, Callaway JL, Docherty LE, Poole RL, Bullman H, Lever M, Castle BM, Kivuva EC, Turnpenny PD, Mehta SG, Mansour S, Wakeling EL, Mathew V, Madden J, Davies JH, Temple IK (2010) Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. Eur J Hum Genet 18(6):648–655. doi:10.1038/ejhg.2009.246
-
(2010)
Eur J Hum Genet
, vol.18
, Issue.6
, pp. 648-655
-
-
Turner, C.L.1
Mackay, D.M.2
Callaway, J.L.3
Docherty, L.E.4
Poole, R.L.5
Bullman, H.6
Lever, M.7
Castle, B.M.8
Kivuva, E.C.9
Turnpenny, P.D.10
Mehta, S.G.11
Mansour, S.12
Wakeling, E.L.13
Mathew, V.14
Madden, J.15
Davies, J.H.16
Temple, I.K.17
-
59
-
-
78149339689
-
Epigenotype-phenotype correlations in Silver–Russell syndrome
-
COI: 1:STN:280:DC%2BC3cbhtFWmsg%3D%3D, PID: 20685669
-
Wakeling EL, Amero SA, Alders M, Bliek J, Forsythe E, Kumar S, Lim DH, MacDonald F, Mackay DJ, Maher ER, Moore GE, Poole RL, Price SM, Tangeraas T, Turner CL, Van Haelst MM, Willoughby C, Temple IK, Cobben JM (2010) Epigenotype-phenotype correlations in Silver–Russell syndrome. J Med Genet 47(11):760–768. doi:10.1136/jmg.2010.079111
-
(2010)
J Med Genet
, vol.47
, Issue.11
, pp. 760-768
-
-
Wakeling, E.L.1
Amero, S.A.2
Alders, M.3
Bliek, J.4
Forsythe, E.5
Kumar, S.6
Lim, D.H.7
MacDonald, F.8
Mackay, D.J.9
Maher, E.R.10
Moore, G.E.11
Poole, R.L.12
Price, S.M.13
Tangeraas, T.14
Turner, C.L.15
Van Haelst, M.M.16
Willoughby, C.17
Temple, I.K.18
Cobben, J.M.19
-
60
-
-
79956052873
-
Role for piRNAs and noncoding RNA in de novo DNA methylation of the imprinted mouse Rasgrf1 locus
-
COI: 1:CAS:528:DC%2BC3MXlslylsL4%3D, PID: 21566194
-
Watanabe T, Tomizawa S, Mitsuya K, Totoki Y, Yamamoto Y, Kuramochi-Miyagawa S, Iida N, Hoki Y, Murphy PJ, Toyoda A, Gotoh K, Hiura H, Arima T, Fujiyama A, Sado T, Shibata T, Nakano T, Lin H, Ichiyanagi K, Soloway PD, Sasaki H (2011) Role for piRNAs and noncoding RNA in de novo DNA methylation of the imprinted mouse Rasgrf1 locus. Science 332(6031):848–852. doi:10.1126/science.1203919
-
(2011)
Science
, vol.332
, Issue.6031
, pp. 848-852
-
-
Watanabe, T.1
Tomizawa, S.2
Mitsuya, K.3
Totoki, Y.4
Yamamoto, Y.5
Kuramochi-Miyagawa, S.6
Iida, N.7
Hoki, Y.8
Murphy, P.J.9
Toyoda, A.10
Gotoh, K.11
Hiura, H.12
Arima, T.13
Fujiyama, A.14
Sado, T.15
Shibata, T.16
Nakano, T.17
Lin, H.18
Ichiyanagi, K.19
Soloway, P.D.20
Sasaki, H.21
more..
-
61
-
-
0029033861
-
The retinoblastoma protein and cell cycle control
-
COI: 1:CAS:528:DyaK2MXlsFSrs7k%3D, PID: 7736585
-
Weinberg RA (1995) The retinoblastoma protein and cell cycle control. Cell 81(3):323–330
-
(1995)
Cell
, vol.81
, Issue.3
, pp. 323-330
-
-
Weinberg, R.A.1
-
62
-
-
77949659390
-
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome
-
COI: 1:CAS:528:DC%2BC3cXjsFCrsrg%3D, PID: 19920853
-
Willemsen MH, Fernandez BA, Bacino CA, Gerkes E, de Brouwer AP, Pfundt R, Sikkema-Raddatz B, Scherer SW, Marshall CR, Potocki L, van Bokhoven H, Kleefstra T (2010) Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. Eur J Hum Genet 18(4):429–435. doi:10.1038/ejhg.2009.192
-
(2010)
Eur J Hum Genet
, vol.18
, Issue.4
, pp. 429-435
-
-
Willemsen, M.H.1
Fernandez, B.A.2
Bacino, C.A.3
Gerkes, E.4
de Brouwer, A.P.5
Pfundt, R.6
Sikkema-Raddatz, B.7
Scherer, S.W.8
Marshall, C.R.9
Potocki, L.10
van Bokhoven, H.11
Kleefstra, T.12
-
63
-
-
79251579948
-
Quantitative analysis of DNA methylation at all human imprinted regions reveals preservation of epigenetic stability in adult somatic tissue
-
COI: 1:CAS:528:DC%2BC3MXjtFymtb8%3D, PID: 21281512
-
Woodfine K, Huddleston JE, Murrell A (2011) Quantitative analysis of DNA methylation at all human imprinted regions reveals preservation of epigenetic stability in adult somatic tissue. Epigenetics Chromatin 4(1):1. doi:10.1186/1756-8935-4-1
-
(2011)
Epigenetics Chromatin
, vol.4
, Issue.1
, pp. 1
-
-
Woodfine, K.1
Huddleston, J.E.2
Murrell, A.3
-
64
-
-
0024835010
-
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling
-
COI: 1:STN:280:DyaK3c%2FotFOmtQ%3D%3D, PID: 2594029
-
Yandell DW, Campbell TA, Dayton SH, Petersen R, Walton D, Little JB, McConkie-Rosell A, Buckley EG, Dryja TP (1989) Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling. N Engl J Med 321(25):1689–1695. doi:10.1056/NEJM198912213212501
-
(1989)
N Engl J Med
, vol.321
, Issue.25
, pp. 1689-1695
-
-
Yandell, D.W.1
Campbell, T.A.2
Dayton, S.H.3
Petersen, R.4
Walton, D.5
Little, J.B.6
McConkie-Rosell, A.7
Buckley, E.G.8
Dryja, T.P.9
-
65
-
-
84887454672
-
Expression of cilium-associated genes defines novel molecular subtypes of idiopathic pulmonary fibrosis
-
PID: 23783374
-
Yang IV, Coldren CD, Leach SM, Seibold MA, Murphy E, Lin J, Rosen R, Neidermyer AJ, McKean DF, Groshong SD, Cool C, Cosgrove GP, Lynch DA, Brown KK, Schwarz MI, Fingerlin TE, Schwartz DA (2013) Expression of cilium-associated genes defines novel molecular subtypes of idiopathic pulmonary fibrosis. Thorax 68(12):1114–1121. doi:10.1136/thoraxjnl-2012-202943
-
(2013)
Thorax
, vol.68
, Issue.12
, pp. 1114-1121
-
-
Yang, I.V.1
Coldren, C.D.2
Leach, S.M.3
Seibold, M.A.4
Murphy, E.5
Lin, J.6
Rosen, R.7
Neidermyer, A.J.8
McKean, D.F.9
Groshong, S.D.10
Cool, C.11
Cosgrove, G.P.12
Lynch, D.A.13
Brown, K.K.14
Schwarz, M.I.15
Fingerlin, T.E.16
Schwartz, D.A.17
|