-
1
-
-
0035880416
-
Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite
-
Albanese V, Biguet NF, Kiefer H, Bayard E, Mallet J, Meloni R. Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite. 2001. Hum Mol Genet 10:1785-1792.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1785-1792
-
-
Albanese, V.1
Biguet, N.F.2
Kiefer, H.3
Bayard, E.4
Mallet, J.5
Meloni, R.6
-
2
-
-
0042958577
-
Breakthrough of the year: Peering into 2000
-
Anonymous. 1999. Breakthrough of the year: peering into 2000. Science 286:2240.
-
(1999)
Science
, vol.286
, pp. 2240
-
-
-
3
-
-
0029587022
-
Gametic imprinting in mammals
-
Barlow DP. 1995. Gametic imprinting in mammals. Science 270:1610-1613.
-
(1995)
Science
, vol.270
, pp. 1610-1613
-
-
Barlow, D.P.1
-
4
-
-
0017640298
-
Linkage between an X-chromosome marker (deutan color blindness) and bipolar affective illness. Occurrence in the family of a lithium carbonate-responsive schizo-affective proband
-
Baron M. 1977. Linkage between an X-chromosome marker (deutan color blindness) and bipolar affective illness. Occurrence in the family of a lithium carbonate-responsive schizo-affective proband. Arch Gen Psychiatry 34:721-725.
-
(1977)
Arch Gen Psychiatry
, vol.34
, pp. 721-725
-
-
Baron, M.1
-
5
-
-
0023146964
-
Genetic linkage between X-chromosome markers and bipolar affective illness
-
Baron M, Risch N, Hamburger R, Mandel B, Kushner S, Newman M, Drumer D, Belmaker RH. 1987. Genetic linkage between X-chromosome markers and bipolar affective illness. Nature 326:289-292.
-
(1987)
Nature
, vol.326
, pp. 289-292
-
-
Baron, M.1
Risch, N.2
Hamburger, R.3
Mandel, B.4
Kushner, S.5
Newman, M.6
Drumer, D.7
Belmaker, R.H.8
-
6
-
-
0027509066
-
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees
-
Baron M, Freimer NF, Risch N, Lerer B, Alexander JR, Straub RE, Asokan S, Das K, Peterson A, Amos J, Endicott J, Oh J, Gilliam TC. 1993. Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Nat Genet 3:49-55.
-
(1993)
Nat Genet
, vol.3
, pp. 49-55
-
-
Baron, M.1
Freimer, N.F.2
Risch, N.3
Lerer, B.4
Alexander, J.R.5
Straub, R.E.6
Asokan, S.7
Das, K.8
Peterson, A.9
Amos, J.10
Endicott, J.11
Oh, J.12
Gilliam, T.C.13
-
7
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell AC, Felsenfeld G. 2000. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405:482-485.
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
8
-
-
0020080870
-
The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences
-
Bell GI, Selby MJ, Rutter WJ. 1982. The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences. Nature 295:31-35.
-
(1982)
Nature
, vol.295
, pp. 31-35
-
-
Bell, G.I.1
Selby, M.J.2
Rutter, W.J.3
-
9
-
-
0021343570
-
A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus
-
Bell GI, Horita S, Karam JH. 1984. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes 33:176-183.
-
(1984)
Diabetes
, vol.33
, pp. 176-183
-
-
Bell, G.I.1
Horita, S.2
Karam, J.H.3
-
10
-
-
0029885015
-
Genetic control of X inactivation and processes leading to X-inactivation skewing
-
Belmont JW. 1996. Genetic control of X inactivation and processes leading to X-inactivation skewing. Am J Hum Genet 58:1101-1108.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1101-1108
-
-
Belmont, J.W.1
-
11
-
-
0028871202
-
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
-
Bennett ST, Lucassen AM, Gough SC, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F, et al. 1995. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nat Genet 9:284-292.
-
(1995)
Nat Genet
, vol.9
, pp. 284-292
-
-
Bennett, S.T.1
Lucassen, A.M.2
Gough, S.C.3
Powell, E.E.4
Undlien, D.E.5
Pritchard, L.E.6
Merriman, M.E.7
Kawaguchi, Y.8
Dronsfield, M.J.9
Pociot, F.10
-
12
-
-
0001017310
-
IDDM2-VNTR-encoded susceptibility to type 1 diabetes: Dominant protection and parental transmission of alleles of the insulin gene-linked minisatellite locus
-
Bennett ST, Wilson AJ, Cucca F, Nerup J, Pociot F, McKinney PA, Barnett AH, Bain SC, Todd JA. 1996. IDDM2-VNTR-encoded susceptibility to type 1 diabetes: dominant protection and parental transmission of alleles of the insulin gene-linked minisatellite locus. J Autoimmun 9:415-421.
-
(1996)
J Autoimmun
, vol.9
, pp. 415-421
-
-
Bennett, S.T.1
Wilson, A.J.2
Cucca, F.3
Nerup, J.4
Pociot, F.5
McKinney, P.A.6
Barnett, A.H.7
Bain, S.C.8
Todd, J.A.9
-
13
-
-
16944366697
-
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele
-
The IMDIAB Group
-
Bennett ST, Wilson AJ, Esposito L, Bouzekri N, Undlien DE, Cucca F, Nistico L, Buzzetti R, Bosi E, Pociot F, Nerup J, Cambon-Thomsen A, Pugliese A, Shield JP, McKinney PA, Bain SC, Polychronakos C, Todd JA. 1997. Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group. Nat Genet 17:350-352.
-
(1997)
Nat Genet
, vol.17
, pp. 350-352
-
-
Bennett, S.T.1
Wilson, A.J.2
Esposito, L.3
Bouzekri, N.4
Undlien, D.E.5
Cucca, F.6
Nistico, L.7
Buzzetti, R.8
Bosi, E.9
Pociot, F.10
Nerup, J.11
Cambon-Thomsen, A.12
Pugliese, A.13
Shield, J.P.14
McKinney, P.A.15
Bain, S.C.16
Polychronakos, C.17
Todd, J.A.18
-
14
-
-
0035688515
-
Molecular linkage studies of bipolar disorders
-
Berrettini WH. 2001. Molecular linkage studies of bipolar disorders. Bipolar Disord 3:276-283.
-
(2001)
Bipolar Disord
, vol.3
, pp. 276-283
-
-
Berrettini, W.H.1
-
15
-
-
0017355226
-
A Danish twin study of manic-depressive disorders
-
Bertelsen A, Harvald B, Hauge M. 1977. A Danish twin study of manic-depressive disorders. Br J Psychiatry 130:330-351.
-
(1977)
Br J Psychiatry
, vol.130
, pp. 330-351
-
-
Bertelsen, A.1
Harvald, B.2
Hauge, M.3
-
16
-
-
0033753779
-
The DNA methyltransferases of mammals
-
Bestor TH. 2000. The DNA methyltransferases of mammals. Hum Mol Genet 9:2395-2402.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2395-2402
-
-
Bestor, T.H.1
-
17
-
-
0033569899
-
Family-based association study between bipolar disorder and DRD2, DRD4, DAT, and SERT in Sardinia
-
Bocchetta A, Piccardi MP, Palmas MA, Chillotti C, Oi A, Del Zompo M. 1999. Family-based association study between bipolar disorder and DRD2, DRD4, DAT, and SERT in Sardinia. Am J Med Genet 88:522-526.
-
(1999)
Am J Med Genet
, vol.88
, pp. 522-526
-
-
Bocchetta, A.1
Piccardi, M.P.2
Palmas, M.A.3
Chillotti, C.4
Oi, A.5
Del Zompo, M.6
-
18
-
-
0036641071
-
X-chromosome inactivation: Closing in on proteins that bind Xist RNA
-
Brockdorff N. 2002. X-chromosome inactivation: closing in on proteins that bind Xist RNA. Trends Genet 18:352-358.
-
(2002)
Trends Genet
, vol.18
, pp. 352-358
-
-
Brockdorff, N.1
-
19
-
-
0033577029
-
Skewed X-chromosome inactivation: Cause or consequence?
-
Brown CJ. 1999. Skewed X-chromosome inactivation: cause or consequence? J Natl Cancer Inst 91:304-305.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 304-305
-
-
Brown, C.J.1
-
20
-
-
0033594960
-
Heterogeneous gene expression from the inactive X chromosome: An X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others
-
Carrel L, Willard HF. 1999. Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. Proc Natl Acad Sci USA 96:7364-7369.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 7364-7369
-
-
Carrel, L.1
Willard, H.F.2
-
22
-
-
0036640628
-
On the epigenetic regulation of the human reelin promoter
-
Chen Y, Sharma RP, Costa RH, Costa E, Grayson DR. 2002. On the epigenetic regulation of the human reelin promoter. Nucleic Acids Res 30:2930-2939.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 2930-2939
-
-
Chen, Y.1
Sharma, R.P.2
Costa, R.H.3
Costa, E.4
Grayson, D.R.5
-
25
-
-
0028044550
-
Non-linkage of bipolar illness to tyrosine hydroxylase, tyrosinase, and D2 and D4 dopamine receptor genes on chromosome 11
-
De bruyn A, Mendelbaum K, Sandkuijl LA, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C. 1994a. Non-linkage of bipolar illness to tyrosine hydroxylase, tyrosinase, and D2 and D4 dopamine receptor genes on chromosome 11. Am J Psychiatry 151:102-106.
-
(1994)
Am J Psychiatry
, vol.151
, pp. 102-106
-
-
De Bruyn, A.1
Mendelbaum, K.2
Sandkuijl, L.A.3
Delvenne, V.4
Hirsch, D.5
Staner, L.6
Mendlewicz, J.7
Van Broeckhoven, C.8
-
26
-
-
0028673724
-
Linkage analysis of bipolar illness with X-chromosome DNA markers: A susceptibility gene in Xq27-q28 cannot be excluded
-
De bruyn A, Raeymaekers P, Mendelbaum K, Sandkuijl LA, Raes G, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C. 1994b. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded. Am J Med Genet 54:411-419.
-
(1994)
Am J Med Genet
, vol.54
, pp. 411-419
-
-
De Bruyn, A.1
Raeymaekers, P.2
Mendelbaum, K.3
Sandkuijl, L.A.4
Raes, G.5
Delvenne, V.6
Hirsch, D.7
Staner, L.8
Mendlewicz, J.9
Van Broeckhoven, C.10
-
27
-
-
0028128380
-
Genetic linkage mapping for a susceptibility locus to bipolar illness: Chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter
-
Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D, et al. 1994. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter. Am J Med Genet 54:206-218.
-
(1994)
Am J Med Genet
, vol.54
, pp. 206-218
-
-
Detera-Wadleigh, S.D.1
Hsieh, W.T.2
Berrettini, W.H.3
Goldin, L.R.4
Rollins, D.Y.5
Muniec, D.6
Grewal, R.7
Guroff, J.J.8
Turner, G.9
Coffman, D.10
-
28
-
-
0023091644
-
Bipolar affective disorders linked to DNA markers on chromosome 11
-
Egeland JA, Gerhard DS, Pauls DL, Sussex JN, Kidd KK, Allen CR, Hostetter AM, Housman DE. 1987. Bipolar affective disorders linked to DNA markers on chromosome 11. Nature 325:783-787.
-
(1987)
Nature
, vol.325
, pp. 783-787
-
-
Egeland, J.A.1
Gerhard, D.S.2
Pauls, D.L.3
Sussex, J.N.4
Kidd, K.K.5
Allen, C.R.6
Hostetter, A.M.7
Housman, D.E.8
-
29
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer M, McDonald LE, Millar DS, Collis CM, Watt F, Grigg GW, Molloy PL, Paul CL. 1992. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci USA 89:1827-1831.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
Collis, C.M.4
Watt, F.5
Grigg, G.W.6
Molloy, P.L.7
Paul, C.L.8
-
30
-
-
0033525030
-
Analysis and meta-analysis of two polymorphisms within the tyrosine hydroxylase gene in bipolar and unipolar affective disorders
-
Furlong RA, Rubinsztein JS, Ho L, Walsh C, Coleman TA, Muir WJ, Paykel ES, Blackwood DH, Rubinsztein DC. 1999. Analysis and meta-analysis of two polymorphisms within the tyrosine hydroxylase gene in bipolar and unipolar affective disorders. Am J Med Genet 88:88-94.
-
(1999)
Am J Med Genet
, vol.88
, pp. 88-94
-
-
Furlong, R.A.1
Rubinsztein, J.S.2
Ho, L.3
Walsh, C.4
Coleman, T.A.5
Muir, W.J.6
Paykel, E.S.7
Blackwood, D.H.8
Rubinsztein, D.C.9
-
31
-
-
0018576999
-
Color blindness not closely linked to bipolar illness. Report of a new pedigree series
-
Gershon ES, Targum SD, Matthysse S, Bunney WE Jr. 1979. Color blindness not closely linked to bipolar illness. Report of a new pedigree series. Arch Gen Psychiatry 36:1423-1430.
-
(1979)
Arch Gen Psychiatry
, vol.36
, pp. 1423-1430
-
-
Gershon, E.S.1
Targum, S.D.2
Matthysse, S.3
Bunney W.E., Jr.4
-
32
-
-
0018888604
-
A collaborative study of genetic linkage of bipolar manic-depressive illness and red/green colorblindness. A project of the biological psychiatry collaborative program of the World Health Organization
-
Gershon ES, Mendlewicz J, Gastpar M, Bech P, Goldin LR, Kielholz P, Refaelsen OJ, Vartanian F, Bunney WE Jr. 1980. A collaborative study of genetic linkage of bipolar manic-depressive illness and red/green colorblindness. A project of the biological psychiatry collaborative program of the World Health Organization. Acta Psychiatr Scand 61:319-338.
-
(1980)
Acta Psychiatr Scand
, vol.61
, pp. 319-338
-
-
Gershon, E.S.1
Mendlewicz, J.2
Gastpar, M.3
Bech, P.4
Goldin, L.R.5
Kielholz, P.6
Refaelsen, O.J.7
Vartanian, F.8
Bunney W.E., Jr.9
-
34
-
-
0039886479
-
Developmental genetics and ontogenetic psychology: Overdue detente' and propositions from a matchmaker
-
Pick AD, editor. Minneapolis: University of Minnesota Press
-
Gottesman II. 1974. Developmental genetics and ontogenetic psychology: overdue detente' and propositions from a matchmaker. In: Pick AD, editor. Minnesota Symposia on Child Psychology. Minneapolis: University of Minnesota Press. p 55-80.
-
(1974)
Minnesota Symposia on Child Psychology
, pp. 55-80
-
-
Gottesman, I.I.1
-
37
-
-
0028871874
-
Clinical evidence for genomic imprinting in bipolar I disorder
-
Grigoroiu-Serbanescu M, Nothen M, Propping P, Poustka F, Magureanu S, Vasilescu R, Marinescu E, Ardelean V. 1995. Clinical evidence for genomic imprinting in bipolar I disorder. Acta Psychiatr Scand 92:365-370.
-
(1995)
Acta Psychiatr Scand
, vol.92
, pp. 365-370
-
-
Grigoroiu-Serbanescu, M.1
Nothen, M.2
Propping, P.3
Poustka, F.4
Magureanu, S.5
Vasilescu, R.6
Marinescu, E.7
Ardelean, V.8
-
38
-
-
0025360106
-
Genomic imprinting: Review and relevance to human diseases
-
Hall JG. 1990. Genomic imprinting: review and relevance to human diseases. Am J Hum Genet 46:857-873.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 857-873
-
-
Hall, J.G.1
-
39
-
-
0000748749
-
Mood disorders: Clinical features
-
Kaplan HI, Sadock BJ, editors. Baltimore: Williams and Wilkins. Chapter 17.3
-
Hamilton M. 1989. Mood disorders: clinical features. In: Kaplan HI, Sadock BJ, editors. Comprehensive textbook of psychiatry, 5th edition. Baltimore: Williams and Wilkins. Chapter 17.3.
-
(1989)
Comprehensive Textbook of Psychiatry, 5th Edition
-
-
Hamilton, M.1
-
40
-
-
0031201685
-
Exploring and explaining epigenetic effects
-
Henikoff S, Matzke MA. 1997. Exploring and explaining epigenetic effects. Trends Genet 13:293-295.
-
(1997)
Trends Genet
, vol.13
, pp. 293-295
-
-
Henikoff, S.1
Matzke, M.A.2
-
42
-
-
0002671050
-
DNA methylation in eukaryotes: 20 Years on
-
Russo V, Martienssen R, Riggs A, editors. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Holliday R. 1996. DNA methylation in eukaryotes: 20 years on. In: Russo V, Martienssen R, Riggs A, editors. Epigenetic mechanisms of gene regulation. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press. p 5-27.
-
(1996)
Epigenetic Mechanisms of Gene Regulation
, pp. 5-27
-
-
Holliday, R.1
-
43
-
-
0002671050
-
Gene silencing in mammalian cells
-
Russo V. Martienssen R, Riggs A, editors. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Holliday R, Ho T, Paulin R. 1996. Gene silencing in mammalian cells. In: Russo V. Martienssen R, Riggs A, editors. Epigenetic mechanisms of gene regulation. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press. p 47-59.
-
(1996)
Epigenetic Mechanisms of Gene Regulation
, pp. 47-59
-
-
Holliday, R.1
Ho, T.2
Paulin, R.3
-
45
-
-
0033959416
-
Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles
-
Huxtable SJ, Saker PJ, Haddad L, Walker M, Frayling TM, Levy JC, Hitman GA, O'Rahilly S, Hattersley AT, McCarthy MI. 2000. Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles. Diabetes 49:126-130.
-
(2000)
Diabetes
, vol.49
, pp. 126-130
-
-
Huxtable, S.J.1
Saker, P.J.2
Haddad, L.3
Walker, M.4
Frayling, T.M.5
Levy, J.C.6
Hitman, G.A.7
O'Rahilly, S.8
Hattersley, A.T.9
McCarthy, M.I.10
-
46
-
-
0035839136
-
Translating the histone code
-
Jenuwein T, Allis CD. 2001. Translating the histone code. Science 293:1074-1080.
-
(2001)
Science
, vol.293
, pp. 1074-1080
-
-
Jenuwein, T.1
Allis, C.D.2
-
47
-
-
0028342915
-
Mosaic and polymorphic imprinting of the WT1 gene in humans
-
Jinno Y, Yun K, Nishiwaki K, Kubota T, Ogawa O, Reeve AE, Niikawa N. 1994. Mosaic and polymorphic imprinting of the WT1 gene in humans. Nat Genet 6:305-309.
-
(1994)
Nat Genet
, vol.6
, pp. 305-309
-
-
Jinno, Y.1
Yun, K.2
Nishiwaki, K.3
Kubota, T.4
Ogawa, O.5
Reeve, A.E.6
Niikawa, N.7
-
48
-
-
0031837109
-
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
-
Jones PL, Veenstra GJ, Wade PA, Vermaak D, Kass SU, Landsberger N, Strouboulis J, Wolffe AP. 1998. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat Genet 19:187-191.
-
(1998)
Nat Genet
, vol.19
, pp. 187-191
-
-
Jones, P.L.1
Veenstra, G.J.2
Wade, P.A.3
Vermaak, D.4
Kass, S.U.5
Landsberger, N.6
Strouboulis, J.7
Wolffe, A.P.8
-
49
-
-
0012114353
-
Genetics of affective disorder
-
McGuffin P, Owen MJ, Gottesman II, editors. Oxford: Oxford University Press
-
Jones I, Kent L, Craddock N. 2002. Genetics of affective disorder. In: McGuffin P, Owen MJ, Gottesman II, editors. Psychiatric genetics and genomics. Oxford: Oxford University Press. p 211-245.
-
(2002)
Psychiatric Genetics and Genomics
, pp. 211-245
-
-
Jones, I.1
Kent, L.2
Craddock, N.3
-
50
-
-
0025995836
-
Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility
-
Julier C, Hyer RN, Davies J, Merlin F, Soularue P, Briant L, Cathelineau G, Deschamps I, Rotter JI, Froguel P, et al. 1991. Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility. Nature 354:155-159.
-
(1991)
Nature
, vol.354
, pp. 155-159
-
-
Julier, C.1
Hyer, R.N.2
Davies, J.3
Merlin, F.4
Soularue, P.5
Briant, L.6
Cathelineau, G.7
Deschamps, I.8
Rotter, J.I.9
Froguel, P.10
-
51
-
-
0034644120
-
Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive
-
Kanduri C, Pant V, Loukinov D, Pugacheva E, Qi CF, Wolffe A, Ohlsson R, Lobanenkov VV. 2000. Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive. Curr Biol 10:853-856.
-
(2000)
Curr Biol
, vol.10
, pp. 853-856
-
-
Kanduri, C.1
Pant, V.2
Loukinov, D.3
Pugacheva, E.4
Qi, C.F.5
Wolffe, A.6
Ohlsson, R.7
Lobanenkov, V.V.8
-
52
-
-
0024437794
-
Reevaluation of the linkage relationship between chromosome 11 p loci and the gene for bipolar affective disorder in the Old Order Amish
-
Kelsoe JR, Ginns EI, Egeland JA, Gerhard DS, Goldstein AM, Bale SJ, Pauls DL, Long RT, Kidd KK, Conte G, et al. 1989. Reevaluation of the linkage relationship between chromosome 11 p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature 342:238-243.
-
(1989)
Nature
, vol.342
, pp. 238-243
-
-
Kelsoe, J.R.1
Ginns, E.I.2
Egeland, J.A.3
Gerhard, D.S.4
Goldstein, A.M.5
Bale, S.J.6
Pauls, D.L.7
Long, R.T.8
Kidd, K.K.9
Conte, G.10
-
53
-
-
0025340339
-
Tyrosine hydroxylase polymorphisms associated with manic-depressive illness
-
Leboyer M, Malafosse A, Boularand S, Campion D, Gheysen F, Samolyk D, Henriksson B, Denise E, des Lauriers A, Lepine JP. 1990. Tyrosine hydroxylase polymorphisms associated with manic-depressive illness. Lancet 335:1219.
-
(1990)
Lancet
, vol.335
, pp. 1219
-
-
Leboyer, M.1
Malafosse, A.2
Boularand, S.3
Campion, D.4
Gheysen, F.5
Samolyk, D.6
Henriksson, B.7
Denise, E.8
Des Lauriers, A.9
Lepine, J.P.10
-
54
-
-
0011131318
-
The meaning of epigenetics
-
Lederberg J. 2001. The meaning of epigenetics. Scientist 15:6.
-
(2001)
Scientist
, vol.15
, pp. 6
-
-
Lederberg, J.1
-
55
-
-
0030026007
-
Women with bipolar illness: Clinical and research issues
-
Leibenluft E. 1996. Women with bipolar illness: clinical and research issues. Am J Psychiatry 153:163-173.
-
(1996)
Am J Psychiatry
, vol.153
, pp. 163-173
-
-
Leibenluft, E.1
-
56
-
-
0036733675
-
Chromatin modification and epigenetic reprogramming in mammalian development
-
Li E. 2002. Chromatin modification and epigenetic reprogramming in mammalian development. Nat Rev Genet 3:662-673.
-
(2002)
Nat Rev Genet
, vol.3
, pp. 662-673
-
-
Li, E.1
-
57
-
-
0032783522
-
Association analysis between dopamine receptor genes and bipolar affective disorder
-
Li T, Liu X, Sham PC, Aitchison KJ, Cai G, Arranz MJ, Deng H, Liu J, Kirov G, Murray RM. Collier DA. 1999. Association analysis between dopamine receptor genes and bipolar affective disorder. Psychiatry Res 86:193-201.
-
(1999)
Psychiatry Res
, vol.86
, pp. 193-201
-
-
Li, T.1
Liu, X.2
Sham, P.C.3
Aitchison, K.J.4
Cai, G.5
Arranz, M.J.6
Deng, H.7
Liu, J.8
Kirov, G.9
Murray, R.M.10
Collier, D.A.11
-
58
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
-
Maher ER, Reik W. 2000. Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J Clin Invest 105:247-252.
-
(2000)
J Clin Invest
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
59
-
-
0030662348
-
A twin-pronged attack on complex traits
-
Martin N, Boomsma D, Machin G. 1997. A twin-pronged attack on complex traits. Nat Genet 17:387-392.
-
(1997)
Nat Genet
, vol.17
, pp. 387-392
-
-
Martin, N.1
Boomsma, D.2
Machin, G.3
-
60
-
-
0034598784
-
Demethylation of the zygotic paternal genome
-
Mayer W, Niveleau A, Walter J, Fundele R, Haaf T. 2000. Demethylation of the zygotic paternal genome. Nature 403:501-502.
-
(2000)
Nature
, vol.403
, pp. 501-502
-
-
Mayer, W.1
Niveleau, A.2
Walter, J.3
Fundele, R.4
Haaf, T.5
-
61
-
-
0025255080
-
Models of a dual inheritance system
-
Maynard Smith J. 1990. Models of a dual inheritance system. J Theor Biol 143:41-53.
-
(1990)
J Theor Biol
, vol.143
, pp. 41-53
-
-
Maynard Smith, J.1
-
62
-
-
0034748350
-
A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: A linkage study in 13 target chromosomes
-
Maziade M, Roy MA, Rouillard E, Bissonnette L, Fournier JP, Roy A, Garneau Y, Montgrain N, Potvin A, Cliche D, Dion C, Wallot H, Fournier A, Nicole L, Lavallee JC, Merette C. 2001. A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes. Mol Psychiatry 6:684-693.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 684-693
-
-
Maziade, M.1
Roy, M.A.2
Rouillard, E.3
Bissonnette, L.4
Fournier, J.P.5
Roy, A.6
Garneau, Y.7
Montgrain, N.8
Potvin, A.9
Cliche, D.10
Dion, C.11
Wallot, H.12
Fournier, A.13
Nicole, L.14
Lavallee, J.C.15
Merette, C.16
-
63
-
-
10544220423
-
A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees
-
McInnes LA, Escamilla MA, Service SK, Reus VI, Leon P, Silva S, Rojas E, Spesny M, Baharloo S, Blankenship K, Peterson A, Tyler D, Shimayoshi N, Tobey C, Batki S, Vinogradov S, Meza L, Gallegos A, Fournier E, Smith LB, Barondes SH, Sandkuijl LA, Freimer NB. 1996. A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees. Proc Natl Acad Sci USA 93:13060-13065.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13060-13065
-
-
McInnes, L.A.1
Escamilla, M.A.2
Service, S.K.3
Reus, V.I.4
Leon, P.5
Silva, S.6
Rojas, E.7
Spesny, M.8
Baharloo, S.9
Blankenship, K.10
Peterson, A.11
Tyler, D.12
Shimayoshi, N.13
Tobey, C.14
Batki, S.15
Vinogradov, S.16
Meza, L.17
Gallegos, A.18
Fournier, E.19
Smith, L.B.20
Barondes, S.H.21
Sandkuijl, L.A.22
Freimer, N.B.23
more..
-
64
-
-
0029021719
-
Patterns of maternal transmission in bipolar affective disorder
-
McMahon FJ, Stine OC, Meyers DA, Simpson SG, DePaulo JR. 1995. Patterns of maternal transmission in bipolar affective disorder. Am J Hum Genet 56:1277-1286.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1277-1286
-
-
McMahon, F.J.1
Stine, O.C.2
Meyers, D.A.3
Simpson, S.G.4
DePaulo, J.R.5
-
65
-
-
0031886282
-
A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro
-
Meloni R, Albanese V, Ravassard P, Treilhov F, Mallet J. 1998. A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro. Hum Mol Genet 7:423-428.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 423-428
-
-
Meloni, R.1
Albanese, V.2
Ravassard, P.3
Treilhov, F.4
Mallet, J.5
-
67
-
-
0019142381
-
Linkage between glucose-6-phosphate dehydrogenase deficiency and manic-depressive psychosis
-
Mendlewicz J, Linkowski P, Wilmotte J. 1980. Linkage between glucose-6-phosphate dehydrogenase deficiency and manic-depressive psychosis. Br J Psychiatry 137:337-342.
-
(1980)
Br J Psychiatry
, vol.137
, pp. 337-342
-
-
Mendlewicz, J.1
Linkowski, P.2
Wilmotte, J.3
-
68
-
-
0023119242
-
Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development
-
Monk M, Boubelik M, Lehnert S. 1987. Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development. Development 99:371-382.
-
(1987)
Development
, vol.99
, pp. 371-382
-
-
Monk, M.1
Boubelik, M.2
Lehnert, S.3
-
69
-
-
0035153058
-
Evidence that insulin is imprinted in the human yolk sac
-
Moore GE, Abu-Amero SN, Bell G, Wakeling EL, Kingsnorth A, Stanier P, Jauniaux E, Bennett ST. 2001. Evidence that insulin is imprinted in the human yolk sac. Diabetes 50:199-203.
-
(2001)
Diabetes
, vol.50
, pp. 199-203
-
-
Moore, G.E.1
Abu-Amero, S.N.2
Bell, G.3
Wakeling, E.L.4
Kingsnorth, A.5
Stanier, P.6
Jauniaux, E.7
Bennett, S.T.8
-
70
-
-
0036382921
-
Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: Evidence for a role of DRD4
-
Muglia P, Petronis A, Mundo E, Lander S, Cate T, Kennedy JL. 2002. Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4. Mol Psychiatry 7:860-866.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 860-866
-
-
Muglia, P.1
Petronis, A.2
Mundo, E.3
Lander, S.4
Cate, T.5
Kennedy, J.L.6
-
71
-
-
0342437491
-
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
-
Nan X, Campoy FJ, Bird A. 1997. MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell 88:471-481.
-
(1997)
Cell
, vol.88
, pp. 471-481
-
-
Nan, X.1
Campoy, F.J.2
Bird, A.3
-
72
-
-
0030009776
-
Heritability of X chromosome-inactivation phenotype in a large family
-
Naumova AK, Plenge RM, Bird LM, Leppert M, Morgan K, Willard HF, Sapienza C. 1996. Heritability of X chromosome-inactivation phenotype in a large family. Am J Hum Genet 58:1111-1119.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1111-1119
-
-
Naumova, A.K.1
Plenge, R.M.2
Bird, L.M.3
Leppert, M.4
Morgan, K.5
Willard, H.F.6
Sapienza, C.7
-
73
-
-
0025331383
-
Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52
-
Neiswanger K, Slaugenhaupt SA, Hughes HB, Frank E, Frankel DR, McCarty MJ, Chakravarti A, Zubenko GS, Kupfer DJ, Kaplan BB. 1990. Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52. Biol Psychiatry 28:63-72.
-
(1990)
Biol Psychiatry
, vol.28
, pp. 63-72
-
-
Neiswanger, K.1
Slaugenhaupt, S.A.2
Hughes, H.B.3
Frank, E.4
Frankel, D.R.5
McCarty, M.J.6
Chakravarti, A.7
Zubenko, G.S.8
Kupfer, D.J.9
Kaplan, B.B.10
-
74
-
-
0033047220
-
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
-
Nothen MM, Cichon S, Rohleder H, Hemmer S, Franzek E, Fritze J, Albus M, Borrmann-Hassenbach M, Kreiner R, Weigelt B, Minges J, Lichtermann D, Maier W, Craddock N, Fimmers R, Holler T, Baur MP, Rietschel M, Propping P. 1999. Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families. Mol Psychiatry 4:76-84.
-
(1999)
Mol Psychiatry
, vol.4
, pp. 76-84
-
-
Nothen, M.M.1
Cichon, S.2
Rohleder, H.3
Hemmer, S.4
Franzek, E.5
Fritze, J.6
Albus, M.7
Borrmann-Hassenbach, M.8
Kreiner, R.9
Weigelt, B.10
Minges, J.11
Lichtermann, D.12
Maier, W.13
Craddock, N.14
Fimmers, R.15
Holler, T.16
Baur, M.P.17
Rietschel, M.18
Propping, P.19
-
75
-
-
0034565915
-
Natural selection and the function of genome imprinting: Beyond the silenced minority
-
Pardo-Manuel de Villena F, de la Casa-Esperon E, Sapienza C. 2000. Natural selection and the function of genome imprinting: beyond the silenced minority. Trends Genet 16:573-579.
-
(2000)
Trends Genet
, vol.16
, pp. 573-579
-
-
Pardo-Manuel de Villena, F.1
De la Casa-Esperon, E.2
Sapienza, C.3
-
76
-
-
0027490840
-
Paramutation, an allelic interaction, is associated with a stable and heritable reduction of transcription of the maize b regulatory gene
-
Patterson GI, Thorpe CJ, Chandler VL. 1993. Paramutation, an allelic interaction, is associated with a stable and heritable reduction of transcription of the maize b regulatory gene. Genetics 135:881-894.
-
(1993)
Genetics
, vol.135
, pp. 881-894
-
-
Patterson, G.I.1
Thorpe, C.J.2
Chandler, V.L.3
-
77
-
-
0028866539
-
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree
-
Pekkarinen P, Terwilliger J, Bredbacka PE, Lonnqvist J, Peltonen L. 1995. Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree. Genome Res 5:105-115.
-
(1995)
Genome Res
, vol.5
, pp. 105-115
-
-
Pekkarinen, P.1
Terwilliger, J.2
Bredbacka, P.E.3
Lonnqvist, J.4
Peltonen, L.5
-
78
-
-
0032816455
-
Alzheimer's disease and down syndrome: From meiosis to dementia
-
Petronis A. 1999. Alzheimer's disease and down syndrome: from meiosis to dementia. Exp Neurol 158:403-413.
-
(1999)
Exp Neurol
, vol.158
, pp. 403-413
-
-
Petronis, A.1
-
79
-
-
0034125860
-
The genes for major psychosis: Aberrant sequence or regulation?
-
Petronis A. 2000. The genes for major psychosis: aberrant sequence or regulation? Neuropsychopharmacology 23:1-12.
-
(2000)
Neuropsychopharmacology
, vol.23
, pp. 1-12
-
-
Petronis, A.1
-
80
-
-
0035283058
-
Human morbid genetics revisited: Relevance of epigenetics
-
Petronis A. 2001. Human morbid genetics revisited: relevance of epigenetics. Trends Genet 17:142-146.
-
(2001)
Trends Genet
, vol.17
, pp. 142-146
-
-
Petronis, A.1
-
81
-
-
0038825296
-
Monozygotic twins exhibit numerous epigenetic differences: Clues to twin discordance?
-
Petronis A, Gottesman II, Kan PX, Kennedy JL, Basile VS, Paterson AD, Popendikyte V. 2003. Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance? Schizophrenia Bull 29:169-178.
-
(2003)
Schizophrenia Bull
, vol.29
, pp. 169-178
-
-
Petronis, A.1
Gottesman, I.I.2
Kan, P.X.3
Kennedy, J.L.4
Basile, V.S.5
Paterson, A.D.6
Popendikyte, V.7
-
82
-
-
0025119812
-
Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: Methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability
-
Pfeifer GP, Steigerwald SD, Hansen RS, Gartler SM, Riggs AD. 1990. Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability. Proc Natl Acad Sci USA 87:8252-8256.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 8252-8256
-
-
Pfeifer, G.P.1
Steigerwald, S.D.2
Hansen, R.S.3
Gartler, S.M.4
Riggs, A.D.5
-
83
-
-
0030723262
-
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
-
Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF. 1997. A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. Nat Genet 17:353-356.
-
(1997)
Nat Genet
, vol.17
, pp. 353-356
-
-
Plenge, R.M.1
Hendrich, B.D.2
Schwartz, C.3
Arena, J.F.4
Naumova, A.5
Sapienza, C.6
Winter, R.M.7
Willard, H.F.8
-
84
-
-
0036306870
-
Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders
-
Plenge RM, Stevenson RA, Lubs HA, Schwartz CE, Willard HF. 2002. Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. Am J Hum Genet 71:168-173.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 168-173
-
-
Plenge, R.M.1
Stevenson, R.A.2
Lubs, H.A.3
Schwartz, C.E.4
Willard, H.F.5
-
86
-
-
0033606062
-
DNA methylation at the putative promoter region of the human dopamine D2 receptor gene
-
Popendikyte V, Laurinavicius A, Paterson AD, Macciardi F, Kennedy JL, Petronis A. 1999. DNA methylation at the putative promoter region of the human dopamine D2 receptor gene. Neuroreport 10:1249-1255.
-
(1999)
Neuroreport
, vol.10
, pp. 1249-1255
-
-
Popendikyte, V.1
Laurinavicius, A.2
Paterson, A.D.3
Macciardi, F.4
Kennedy, J.L.5
Petronis, A.6
-
87
-
-
0032576744
-
X inactivation in females with X-linked disease
-
Puck JM, Willard HF. 1998. X inactivation in females with X-linked disease. N Engl J Med 338:325-328.
-
(1998)
N Engl J Med
, vol.338
, pp. 325-328
-
-
Puck, J.M.1
Willard, H.F.2
-
88
-
-
18244421874
-
The insulin gene is transcribed in the hundan thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes
-
Pugliese A, Zeller M, Fernandez A Jr, Zalcberg LJ, Bartlett RJ, Ricordi C, Pietropaolo M, Eisenbarth GS, Bennett ST, Patel DD. 1997. The insulin gene is transcribed in the hundan thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes. Nat Genet 15:293-297.
-
(1997)
Nat Genet
, vol.15
, pp. 293-297
-
-
Pugliese, A.1
Zeller, M.2
Fernandez A., Jr.3
Zalcberg, L.J.4
Bartlett, R.J.5
Ricordi, C.6
Pietropaolo, M.7
Eisenbarth, G.S.8
Bennett, S.T.9
Patel, D.D.10
-
89
-
-
0026769338
-
The aggregation of the 5′ insulin gene polymorphism in insulin dependent (type 1) diabetes mellitus families
-
Raffel LJ, Hitman GA, Toyoda H, Karam JH, Bell GI, Rotter JI. 1992. The aggregation of the 5′ insulin gene polymorphism in insulin dependent (type 1) diabetes mellitus families. J Med Genet 29:447-450.
-
(1992)
J Med Genet
, vol.29
, pp. 447-450
-
-
Raffel, L.J.1
Hitman, G.A.2
Toyoda, H.3
Karam, J.H.4
Bell, G.I.5
Rotter, J.I.6
-
90
-
-
0035874481
-
The marks, mechanisms and memory of epigenetic states in mammals
-
Rakyan VK, Preis J, Morgan HD, Whitelaw E. 2001. The marks, mechanisms and memory of epigenetic states in mammals. Biochem J 356:1-10.
-
(2001)
Biochem J
, vol.356
, pp. 1-10
-
-
Rakyan, V.K.1
Preis, J.2
Morgan, H.D.3
Whitelaw, E.4
-
92
-
-
0002021183
-
Overview of epigenetic mechanisms
-
Russo V, Martienssen R, Riggs A, editors. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Riggs A, Porter T. 1996. Overview of epigenetic mechanisms. In: Russo V, Martienssen R, Riggs A, editors. Epigenetic mechanisms of gene regulation. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press. p 29-45.
-
(1996)
Epigenetic Mechanisms of Gene Regulation
, pp. 29-45
-
-
Riggs, A.1
Porter, T.2
-
93
-
-
0031617319
-
Methylation dynamics, epigenetic fidelity and X chromosome structure
-
Wolffe A, editor. Chichester: John Wiley & Sons
-
Riggs A, Xiong Z, Wang L, LeBon JM. 1998. Methylation dynamics, epigenetic fidelity and X chromosome structure. In: Wolffe A, editor. Epigenetics. Chichester: John Wiley & Sons. p 214-227.
-
(1998)
Epigenetics
, pp. 214-227
-
-
Riggs, A.1
Xiong, Z.2
Wang, L.3
LeBon, J.M.4
-
94
-
-
0034305821
-
DNA methylation in health and disease
-
Robertson KD, Wolffe AP. 2000. DNA methylation in health and disease. Nat Rev Genet 1:11-19.
-
(2000)
Nat Rev Genet
, vol.1
, pp. 11-19
-
-
Robertson, K.D.1
Wolffe, A.P.2
-
95
-
-
0037306505
-
Additional, physically ordered markers increase linkage signal for bipolar disorder on chromosome 18q22
-
Schulze TG, Chen YS, Badner JA, McInnis MG, DePaulo JR, McMahon FJ. 2003. Additional, physically ordered markers increase linkage signal for bipolar disorder on chromosome 18q22. Biol Psychiatry 53:239-243.
-
(2003)
Biol Psychiatry
, vol.53
, pp. 239-243
-
-
Schulze, T.G.1
Chen, Y.S.2
Badner, J.A.3
McInnis, M.G.4
DePaulo, J.R.5
McMahon, F.J.6
-
96
-
-
0030721742
-
Psychopathology in women and men: Focus on female hormones
-
Seeman MV. 1997. Psychopathology in women and men: focus on female hormones. Am J Psychiatry 154:1641-1647.
-
(1997)
Am J Psychiatry
, vol.154
, pp. 1641-1647
-
-
Seeman, M.V.1
-
97
-
-
0031919877
-
Tyrosine hydroxylase gene in linkage disequilibrium with mood disorders
-
Serretti A, Macciardi F, Cusin C, Verga M, Pedrini S, Smeraldi E. 1998. Tyrosine hydroxylase gene in linkage disequilibrium with mood disorders. Mol Psychiatry 3:169-174.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 169-174
-
-
Serretti, A.1
Macciardi, F.2
Cusin, C.3
Verga, M.4
Pedrini, S.5
Smeraldi, E.6
-
98
-
-
0035826476
-
DRD4 exon 3 variants associated with delusional symptomatology in major psychoses: A study on 2,011 affected subjects
-
Serretti A, Lilli R, Lorenzi C, Lattuada E, Smeraldi E. 2001. DRD4 exon 3 variants associated with delusional symptomatology in major psychoses: a study on 2,011 affected subjects. Am J Med Genet 105:283-290.
-
(2001)
Am J Med Genet
, vol.105
, pp. 283-290
-
-
Serretti, A.1
Lilli, R.2
Lorenzi, C.3
Lattuada, E.4
Smeraldi, E.5
-
99
-
-
76549178298
-
Thought disorder and family relations of schizophrenics: IV. Results and implications
-
Singer MT, Wynne LC. 1965. Thought disorder and family relations of schizophrenics: IV. Results and implications. Arch Gen Psychiatry. 12:201-212.
-
(1965)
Arch Gen Psychiatry
, vol.12
, pp. 201-212
-
-
Singer, M.T.1
Wynne, L.C.2
-
100
-
-
0031081694
-
Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
-
Smyth C, Kalsi G, Curtis D, Brynjolfsson J, O'Neill J, Rifkin L, Moloney E, Murphy P, Petursson H, Gurling H. 1997. Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22. Genomics 39:271-278.
-
(1997)
Genomics
, vol.39
, pp. 271-278
-
-
Smyth, C.1
Kalsi, G.2
Curtis, D.3
Brynjolfsson, J.4
O'Neill, J.5
Rifkin, L.6
Moloney, E.7
Murphy, P.8
Petursson, H.9
Gurling, H.10
-
101
-
-
0033569889
-
Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: A multicenter association study
-
Souery D, Lipp O, Rivelli SK, Massat I, Serretti A, Cavallini C, Ackenheil M, Adolfsson R, Aschauer H, Blackwood D, Dam H, Dikeos D, Fuchshuber S, Heiden M, Jakovljevic M, Kaneva R, Kessing L, Lerer B, Lonnqvist J, Mellerup T, Milanova V, Muir W, Nylander PO, Oruc L, Mendlewicz J, et al. 1999. Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: a multicenter association study. Am J Med Genet 88:527-532.
-
(1999)
Am J Med Genet
, vol.88
, pp. 527-532
-
-
Souery, D.1
Lipp, O.2
Rivelli, S.K.3
Massat, I.4
Serretti, A.5
Cavallini, C.6
Ackenheil, M.7
Adolfsson, R.8
Aschauer, H.9
Blackwood, D.10
Dam, H.11
Dikeos, D.12
Fuchshuber, S.13
Heiden, M.14
Jakovljevic, M.15
Kaneva, R.16
Kessing, L.17
Lerer, B.18
Lonnqvist, J.19
Mellerup, T.20
Milanova, V.21
Muir, W.22
Nylander, P.O.23
Oruc, L.24
Mendlewicz, J.25
more..
-
102
-
-
17544402946
-
Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: Chromosomes 2, 11, 13, 14, and X
-
Stine OC, McMahon FJ, Chen L, Xu J, Meyers DA, MacKinnon DF, Simpson S, McInnis MG, Rice JP, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI Jr, Detera-Wadleigh SD, Goldin LR, Guroff J, Gershon ES, Blehar MC, DePaulo JR. 1997. Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X. Am J Med Genet 74:263-269.
-
(1997)
Am J Med Genet
, vol.74
, pp. 263-269
-
-
Stine, O.C.1
McMahon, F.J.2
Chen, L.3
Xu, J.4
Meyers, D.A.5
MacKinnon, D.F.6
Simpson, S.7
McInnis, M.G.8
Rice, J.P.9
Goate, A.10
Reich, T.11
Edenberg, H.J.12
Foroud, T.13
Nurnberger J.I., Jr.14
Detera-Wadleigh, S.D.15
Goldin, L.R.16
Guroff, J.17
Gershon, E.S.18
Blehar, M.C.19
DePaulo, J.R.20
more..
-
103
-
-
0037168650
-
An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability
-
Tremolizzo L, Carboni G, Ruzicka WB, Mitchell CP, Sugaya I, Tueting P, Sharma R, Grayson DR, Costa E, Guidotti A. 2002. An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability. Proc Natl Acad Sci USA 99:17095-17100.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 17095-17100
-
-
Tremolizzo, L.1
Carboni, G.2
Ruzicka, W.B.3
Mitchell, C.P.4
Sugaya, I.5
Tueting, P.6
Sharma, R.7
Grayson, D.R.8
Costa, E.9
Guidotti, A.10
-
104
-
-
0030175721
-
Imprinted and genotype-specific expression of genes at the IDDM2 locus in pancreas and leucocytes
-
Vafiadis P, Bennett ST, Colle E, Grabs R, Goodyer CG, Polychronakos C. 1996. Imprinted and genotype-specific expression of genes at the IDDM2 locus in pancreas and leucocytes. J Autoimmun 9:397-403.
-
(1996)
J Autoimmun
, vol.9
, pp. 397-403
-
-
Vafiadis, P.1
Bennett, S.T.2
Colle, E.3
Grabs, R.4
Goodyer, C.G.5
Polychronakos, C.6
-
105
-
-
0031018819
-
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
-
Vafiadis P, Bennett ST, Todd JA, Nadeau J, Grabs R, Goodyer CG, Wickramasinghe S, Colle E, Polychronakos C. 1997. Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. Nat Genet 15:289-292.
-
(1997)
Nat Genet
, vol.15
, pp. 289-292
-
-
Vafiadis, P.1
Bennett, S.T.2
Todd, J.A.3
Nadeau, J.4
Grabs, R.5
Goodyer, C.G.6
Wickramasinghe, S.7
Colle, E.8
Polychronakos, C.9
-
106
-
-
0034891347
-
Class III alleles of the variable number of tandem repeat insulin polymorphism associated with silencing of thymic insulin predispose to type 1 diabetes
-
Vafiadis P, Ounissi-Benkalha H, Palumbo M, Grabs R, Rousseau M, Goodyer CG, Polychronakos C. 2001. Class III alleles of the variable number of tandem repeat insulin polymorphism associated with silencing of thymic insulin predispose to type 1 diabetes. J Clin Endocrinol Metab 86:3705-3710.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 3705-3710
-
-
Vafiadis, P.1
Ounissi-Benkalha, H.2
Palumbo, M.3
Grabs, R.4
Rousseau, M.5
Goodyer, C.G.6
Polychronakos, C.7
-
107
-
-
0034842939
-
Skewed X inactivation in X-linked disorders
-
Van den Veyver IB. 2001. Skewed X inactivation in X-linked disorders. Semin Reprod Med 19:183-191.
-
(2001)
Semin Reprod Med
, vol.19
, pp. 183-191
-
-
Van den Veyver, I.B.1
-
109
-
-
0002403834
-
The sex chromosomes and X chromosome inactivation
-
Scriver CR, et al., editors. New York: McGraw-Hill
-
Willard HF. 2000. The sex chromosomes and X chromosome inactivation. In: Scriver CR, et al., editors. The metabolic and molecular basis of inherited disease, 8th edition. New York: McGraw-Hill. p 1191-1211.
-
(2000)
The Metabolic and Molecular Basis of Inherited Disease, 8th Edition
, pp. 1191-1211
-
-
Willard, H.F.1
-
110
-
-
0033569641
-
Epigenetics: Regulation through repression
-
Wolffe AP, Matzke MA. 1999. Epigenetics: regulation through repression. Science 286:481-486.
-
(1999)
Science
, vol.286
, pp. 481-486
-
-
Wolffe, A.P.1
Matzke, M.A.2
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