-
1
-
-
0015029234
-
Congenital heart disease in 56,109 births. Incidence and natural history
-
5102136
-
Congenital heart disease in 56,109 births. Incidence and natural history. SC Mitchell SB Korones HW Berendes, Circulation 1971 43 3 323 332 5102136
-
(1971)
Circulation
, vol.43
, Issue.3
, pp. 323-332
-
-
Mitchell, S.C.1
Korones, S.B.2
Berendes, H.W.3
-
2
-
-
39749191367
-
The developmental genetics of congenital heart disease
-
10.1038/nature06801. 18288184
-
The developmental genetics of congenital heart disease. BG Bruneau, Nature 2008 451 7181 943 948 10.1038/nature06801 18288184
-
(2008)
Nature
, vol.451
, Issue.7181
, pp. 943-948
-
-
Bruneau, B.G.1
-
3
-
-
41149125478
-
Genetic mechanisms controlling cardiovascular development
-
10.1196/annals.1420.003. 18375573
-
Genetic mechanisms controlling cardiovascular development. J Bentham S Bhattacharya, Ann N Y Acad Sci 2008 1123 10 19 10.1196/annals.1420.003 18375573
-
(2008)
Ann N y Acad Sci
, vol.1123
, pp. 10-19
-
-
Bentham, J.1
Bhattacharya, S.2
-
5
-
-
0032583944
-
Recurrence risks in offspring of adults with major heart defects: Results from first cohort of British collaborative study
-
10.1016/S0140-6736(97)06486-6. 9652610
-
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study. J Burn P Brennan J Little S Holloway R Coffey J Somerville NR Dennis L Allan R Arnold JE Deanfield M Godman A Houston B Keeton C Oakley O Scott E Silove J Wilkinson M Pembrey AS Hunter, Lancet 1998 351 9099 311 316 10.1016/S0140-6736(97)06486-6 9652610
-
(1998)
Lancet
, vol.351
, Issue.9099
, pp. 311-316
-
-
Burn, J.1
Brennan, P.2
Little, J.3
Holloway, S.4
Coffey, R.5
Somerville, J.6
Dennis, N.R.7
Allan, L.8
Arnold, R.9
Deanfield, J.E.10
Godman, M.11
Houston, A.12
Keeton, B.13
Oakley, C.14
Scott, O.15
Silove, E.16
Wilkinson, J.17
Pembrey, M.18
Hunter, A.S.19
-
6
-
-
0025124318
-
Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogy
-
10.1016/0002-9149(90)90825-L. 2305694
-
Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogy. TM Zellers DJ Driscoll VV Michels, Am J Cardiol 1990 65 7 523 526 10.1016/0002-9149(90)90825-L 2305694
-
(1990)
Am J Cardiol
, vol.65
, Issue.7
, pp. 523-526
-
-
Zellers, T.M.1
Driscoll, D.J.2
Michels, V.V.3
-
7
-
-
0043097670
-
Congenital heart disease
-
London: Churchill Livingstone Ringmoin DL, Conner JM, Pyeritz RE
-
Congenital heart disease. J Burn J Goodship, Principles and Practice of Medical Genetics London: Churchill Livingstone, Ringmoin DL, Conner JM, Pyeritz RE, 2002
-
(2002)
Principles and Practice of Medical Genetics
-
-
Burn, J.1
Goodship, J.2
-
8
-
-
0242636701
-
NKX2.5 mutations in patients with congenital heart disease
-
10.1016/j.jacc.2003.05.004. 14607454
-
NKX2.5 mutations in patients with congenital heart disease. DB McElhinney E Geiger J Blinder DW Benson E Goldmuntz, J Am Coll Cardiol 2003 42 9 1650 1655 10.1016/j.jacc.2003.05.004 14607454
-
(2003)
J Am Coll Cardiol
, vol.42
, Issue.9
, pp. 1650-1655
-
-
McElhinney, D.B.1
Geiger, E.2
Blinder, J.3
Benson, D.W.4
Goldmuntz, E.5
-
9
-
-
0035830860
-
Principles for the buffering of genetic variation
-
10.1126/science.291.5506.1001. 11232561
-
Principles for the buffering of genetic variation. JLt Hartman B Garvik L Hartwell, Science 2001 291 5506 1001 1004 10.1126/science.291.5506.1001 11232561
-
(2001)
Science
, vol.291
, Issue.5506
, pp. 1001-1004
-
-
Jlt, H.1
Garvik, B.2
Hartwell, L.3
-
10
-
-
0037226648
-
Quantitative epigenetics
-
10.1038/ng0103-6. 12509772
-
Quantitative epigenetics. SL Rutherford S Henikoff, Nat Genet 2003 33 1 6 8 10.1038/ng0103-6 12509772
-
(2003)
Nat Genet
, vol.33
, Issue.1
, pp. 6-8
-
-
Rutherford, S.L.1
Henikoff, S.2
-
11
-
-
0742287679
-
Waddington's widget: Hsp90 and the inheritance of acquired characters
-
10.1016/j.semcdb.2003.09.024. 14986860
-
Waddington's widget: Hsp90 and the inheritance of acquired characters. DM Ruden MD Garfinkel VE Sollars X Lu, Semin Cell Dev Biol 2003 14 5 301 310 10.1016/j.semcdb.2003.09.024 14986860
-
(2003)
Semin Cell Dev Biol
, vol.14
, Issue.5
, pp. 301-310
-
-
Ruden, D.M.1
Garfinkel, M.D.2
Sollars, V.E.3
Lu, X.4
-
12
-
-
0037228526
-
Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution
-
10.1038/ng1067. 12483213
-
Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution. V Sollars X Lu L Xiao X Wang MD Garfinkel DM Ruden, Nat Genet 2003 33 1 70 74 10.1038/ng1067 12483213
-
(2003)
Nat Genet
, vol.33
, Issue.1
, pp. 70-74
-
-
Sollars, V.1
Lu, X.2
Xiao, L.3
Wang, X.4
Garfinkel, M.D.5
Ruden, D.M.6
-
13
-
-
4544235083
-
Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits
-
10.1038/nature02885. 15311209
-
Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits. HL True I Berlin SL Lindquist, Nature 2004 431 7005 184 187 10.1038/nature02885 15311209
-
(2004)
Nature
, vol.431
, Issue.7005
, pp. 184-187
-
-
True, H.L.1
Berlin, I.2
Lindquist, S.L.3
-
14
-
-
0037504378
-
Genome-wide array analysis of normal and malformed human hearts
-
10.1161/01.CIR.0000066694.21510.E2. 12742993
-
Genome-wide array analysis of normal and malformed human hearts. B Kaynak A von Heydebreck S Mebus D Seelow S Hennig J Vogel HP Sperling R Pregla V Alexi-Meskishvili R Hetzer PE Lange M Vingron H Lehrach S Sperling, Circulation 2003 107 19 2467 2474 10.1161/01.CIR.0000066694.21510.E2 12742993
-
(2003)
Circulation
, vol.107
, Issue.19
, pp. 2467-2474
-
-
Kaynak, B.1
Von Heydebreck, A.2
Mebus, S.3
Seelow, D.4
Hennig, S.5
Vogel, J.6
Sperling, H.P.7
Pregla, R.8
Alexi-Meskishvili, V.9
Hetzer, R.10
Lange, P.E.11
Vingron, M.12
Lehrach, H.13
Sperling, S.14
-
16
-
-
77949458939
-
Identification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum
-
10.1371/journal.pone.0009198. 20169146
-
Identification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum. S Koirala G Corfas, PLoS One 2010 5 2 9198 10.1371/journal.pone.0009198 20169146
-
(2010)
PLoS One
, vol.5
, Issue.2
, pp. 59198
-
-
Koirala, S.1
Corfas, G.2
-
17
-
-
33846331967
-
Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana
-
10.1073/pnas.0609063103. 17197417
-
Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana. C Laloi M Stachowiak E Pers-Kamczyc E Warzych I Murgia K Apel, Proc Natl Acad Sci USA 2007 104 2 672 677 10.1073/pnas.0609063103 17197417
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, Issue.2
, pp. 672-677
-
-
Laloi, C.1
Stachowiak, M.2
Pers-Kamczyc, E.3
Warzych, E.4
Murgia, I.5
Apel, K.6
-
18
-
-
33847417017
-
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome
-
17036336
-
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. DC Bittel N Kibiryeva SG McNulty DJ Driscoll MG Butler RA White, Am J Med Genet A 2007 143 5 422 429 17036336
-
(2007)
Am J Med Genet A
, vol.143
, Issue.5
, pp. 422-429
-
-
Bittel, D.C.1
Kibiryeva, N.2
McNulty, S.G.3
Driscoll, D.J.4
Butler, M.G.5
White, R.A.6
-
19
-
-
33847386635
-
Whole genome microarray analysis of gene expression in Prader-Willi syndrome
-
DOI 10.1002/ajmg.a.31606
-
Whole genome microarray analysis of gene expression in Prader-Willi syndrome. DC Bittel N Kibiryeva SM Sell TV Strong MG Butler, Am J Med Genet A 2007 143 5 430 442 17236194 (Pubitemid 46348914)
-
(2007)
American Journal of Medical Genetics, Part A
, vol.143
, Issue.5
, pp. 430-442
-
-
Bittel, D.C.1
Kibiryeva, N.2
Sell, S.M.3
Strong, T.V.4
Butler, M.G.5
-
20
-
-
34547662012
-
Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
-
DOI 10.1097/GIM.0b013e3180ca9a9a, PII 0012581720070700000008
-
Whole genome microarray analysis of gene expression in subjects with fragile X syndrome. DC Bittel N Kibiryeva MG Butler, Genet Med 2007 9 7 464 472 10.1097/GIM.0b013e3180ca9a9a 17666893 (Pubitemid 47222139)
-
(2007)
Genetics in Medicine
, vol.9
, Issue.7
, pp. 464-472
-
-
Bittel, D.C.1
Kibiryeva, N.2
Butler, M.G.3
-
21
-
-
10644257888
-
Microarray analysis of gene/transcript expression in Angelman syndrome: Deletion versus UPD
-
10.1016/j.ygeno.2004.10.010. 15607424
-
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. DC Bittel N Kibiryeva Z Talebizadeh DJ Driscoll MG Butler, Genomics 2005 85 1 85 91 10.1016/j.ygeno.2004.10.010 15607424
-
(2005)
Genomics
, vol.85
, Issue.1
, pp. 85-91
-
-
Bittel, D.C.1
Kibiryeva, N.2
Talebizadeh, Z.3
Driscoll, D.J.4
Butler, M.G.5
-
22
-
-
0036801060
-
Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse
-
12361961
-
Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse. T Fujiwara DB Dehart KK Sulik BL Hogan, Development 2002 129 20 4685 4696 12361961
-
(2002)
Development
, vol.129
, Issue.20
, pp. 4685-4696
-
-
Fujiwara, T.1
Dehart, D.B.2
Sulik, K.K.3
Hogan, B.L.4
-
23
-
-
0034119237
-
The hypoplastic heart in congenital diaphragmatic hernia: Reduced expression of basic fibroblast growth factor and platelet-derived growth factor
-
10.1007/s003830050737. 10898222
-
The hypoplastic heart in congenital diaphragmatic hernia: reduced expression of basic fibroblast growth factor and platelet-derived growth factor. N Guarino H Shima P Puri, Pediatr Surg Int 2000 16 4 243 246 10.1007/s003830050737 10898222
-
(2000)
Pediatr Surg Int
, vol.16
, Issue.4
, pp. 243-246
-
-
Guarino, N.1
Shima, H.2
Puri, P.3
-
24
-
-
0032764442
-
Advances in the molecular genetics of congenital structural heart disease
-
10464664
-
Advances in the molecular genetics of congenital structural heart disease. CS Mah CJ Vaughan CT Basson, Genet Test 1999 3 2 157 172 10464664
-
(1999)
Genet Test
, vol.3
, Issue.2
, pp. 157-172
-
-
Mah, C.S.1
Vaughan, C.J.2
Basson, C.T.3
|