-
1
-
-
0034096320
-
Velo-cardio-facial syndrome: A distinctive behavioral phenotype
-
R.J. Shprintzen Velo-cardio-facial syndrome: A distinctive behavioral phenotype Ment Retard Dev Disabil Res Rev 6 2000 142 147
-
(2000)
Ment Retard Dev Disabil Res Rev
, vol.6
, pp. 142-147
-
-
Shprintzen, R.J.1
-
2
-
-
71149112408
-
Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome
-
T. Green, D. Gothelf, B. Glaser, M. Debbane, A. Frisch, and M. Kotler et al. Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome J Am Acad Child Adolesc Psychiatry 48 2009 1060 1068
-
(2009)
J Am Acad Child Adolesc Psychiatry
, vol.48
, pp. 1060-1068
-
-
Green, T.1
Gothelf, D.2
Glaser, B.3
Debbane, M.4
Frisch, A.5
Kotler, M.6
-
3
-
-
84871434625
-
Deficits in mental state attributions in individuals with 22q11. 2 deletion syndrome (veloâcardioâfacial syndrome)
-
J.S. Ho, P.D. Radoeva, M. Jalbrzikowski, C. Chow, J. Hopkins, and W.C. Tran et al. Deficits in mental state attributions in individuals with 22q11. 2 deletion syndrome (veloâcardioâfacial syndrome) Autism Res 5 2012 407 418
-
(2012)
Autism Res
, vol.5
, pp. 407-418
-
-
Ho, J.S.1
Radoeva, P.D.2
Jalbrzikowski, M.3
Chow, C.4
Hopkins, J.5
Tran, W.C.6
-
4
-
-
77949656899
-
Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: A 3-year follow-up study
-
K.M. Antshel, R. Shprintzen, W. Fremont, A.M. Higgins, S.V. Faraone, and W.R. Kates Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: A 3-year follow-up study J Am Acad Child Adolesc Psychiatry 49 2010 333 344
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 333-344
-
-
Antshel, K.M.1
Shprintzen, R.2
Fremont, W.3
Higgins, A.M.4
Faraone, S.V.5
Kates, W.R.6
-
5
-
-
0031009068
-
Intelligence and psychosocial adjustment in velocardiofacial syndrome: A study of 37 children and adolescents with VCFS
-
A. Swillen, K. Devriendt, E. Legius, B. Eyskens, M. Dumoulin, and M. Gewillig et al. Intelligence and psychosocial adjustment in velocardiofacial syndrome: A study of 37 children and adolescents with VCFS J Med Genet 34 1997 453 458
-
(1997)
J Med Genet
, vol.34
, pp. 453-458
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
Eyskens, B.4
Dumoulin, M.5
Gewillig, M.6
-
6
-
-
27644524899
-
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
-
D. Gothelf, S. Eliez, T. Thompson, C. Hinard, L. Penniman, and C. Feinstein et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Nat Neurosci 8 2005 1500 1502
-
(2005)
Nat Neurosci
, vol.8
, pp. 1500-1502
-
-
Gothelf, D.1
Eliez, S.2
Thompson, T.3
Hinard, C.4
Penniman, L.5
Feinstein, C.6
-
7
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
K.C. Murphy, L.A. Jones, and M.J. Owen High rates of schizophrenia in adults with velo-cardio-facial syndrome Arch Gen Psychiatry 56 1999 940 945
-
(1999)
Arch Gen Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
8
-
-
84855926937
-
The genetic architecture of schizophrenia: New mutations and emerging paradigms
-
L. Rodriguez-Murillo, J.A. Gogos, and M. Karayiorgou The genetic architecture of schizophrenia: New mutations and emerging paradigms Annu Rev Med 63 2012 63 80
-
(2012)
Annu Rev Med
, vol.63
, pp. 63-80
-
-
Rodriguez-Murillo, L.1
Gogos, J.A.2
Karayiorgou, M.3
-
9
-
-
77952738956
-
22q11. 2 microdeletions: Linking DNA structural variation to brain dysfunction and schizophrenia
-
M. Karayiorgou, T.J. Simon, and J.A. Gogos 22q11. 2 microdeletions: Linking DNA structural variation to brain dysfunction and schizophrenia Nat Rev Neurosci 11 2010 402 416
-
(2010)
Nat Rev Neurosci
, vol.11
, pp. 402-416
-
-
Karayiorgou, M.1
Simon, T.J.2
Gogos, J.A.3
-
10
-
-
0035810850
-
Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
M.F. Egan, T.E. Goldberg, B.S. Kolachana, J.H. Callicott, C.M. Mazzanti, and R.E. Straub et al. Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia Proc Natl Acad Sci U S A 98 2001 6917 6922
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
Callicott, J.H.4
Mazzanti, C.M.5
Straub, R.E.6
-
11
-
-
0036913209
-
A highly significant association between a COMT haplotype and schizophrenia
-
S. Shifman, M. Bronstein, M. Sternfeld, A. Pisante-Shalom, E. Lev-Lehman, and A. Weizman et al. A highly significant association between a COMT haplotype and schizophrenia Am J Hum Genet 71 2002 1296 1302
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisante-Shalom, A.4
Lev-Lehman, E.5
Weizman, A.6
-
12
-
-
0042322750
-
Aggressive behavior in schizophrenia is associated with the low enzyme activity COMT polymorphism: A replication study
-
R.D. Strous, K.A. Nolan, R. Lapidus, L. Diaz, T. Saito, and H.M. Lachman Aggressive behavior in schizophrenia is associated with the low enzyme activity COMT polymorphism: A replication study Am J Med Genet B Neuropsychiatr Genet 120B 2003 29 34
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.120 B
, pp. 29-34
-
-
Strous, R.D.1
Nolan, K.A.2
Lapidus, R.3
Diaz, L.4
Saito, T.5
Lachman, H.M.6
-
13
-
-
33745703902
-
Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond
-
E.M Tunbridge, P.J Harrison, and D.R. Weinberger Catechol-o- methyltransferase, cognition, and psychosis: Val158Met and beyond Biol Psychiatry 60 2006 141 151
-
(2006)
Biol Psychiatry
, vol.60
, pp. 141-151
-
-
Tunbridge, E.M.1
Harrison, P.J.2
Weinberger, D.R.3
-
14
-
-
6344265879
-
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): Effects on mRNA, protein, and enzyme activity in postmortem human brain
-
J. Chen, B.K. Lipska, N. Halim, Q.D. Ma, M. Matsumoto, and S. Melhem et al. Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): Effects on mRNA, protein, and enzyme activity in postmortem human brain Am J Hum Genet 75 2004 807 821
-
(2004)
Am J Hum Genet
, vol.75
, pp. 807-821
-
-
Chen, J.1
Lipska, B.K.2
Halim, N.3
Ma, Q.D.4
Matsumoto, M.5
Melhem, S.6
-
15
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
-
H.M. Lachman, D.F. Papolos, T. Saito, Y.M. Yu, C.L. Szumlanski, and R.M. Weinshilboum Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders Pharmacogenetics 6 1996 243
-
(1996)
Pharmacogenetics
, vol.6
, pp. 243
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
Yu, Y.M.4
Szumlanski, C.L.5
Weinshilboum, R.M.6
-
16
-
-
0028918413
-
Kinetics of human soluble and membrane-bound catechol O-methyltransferase: A revised mechanism and description of the thermolabile variant of the enzyme
-
T. Lotta, J. Vidgren, C. Tilgmann, I. Ulmanen, K. Melen, and I. Julkunen et al. Kinetics of human soluble and membrane-bound catechol O-methyltransferase: A revised mechanism and description of the thermolabile variant of the enzyme Biochemistry 34 1995 4202 4210
-
(1995)
Biochemistry
, vol.34
, pp. 4202-4210
-
-
Lotta, T.1
Vidgren, J.2
Tilgmann, C.3
Ulmanen, I.4
Melen, K.5
Julkunen, I.6
-
17
-
-
33845330255
-
Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation
-
E.M. Drabant, A.R. Hariri, A. Meyer-Lindenberg, K.E. Munoz, V.S. Mattay, and B.S. Kolachana et al. Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation Arch Gen Psychiatry 63 2006 1396
-
(2006)
Arch Gen Psychiatry
, vol.63
, pp. 1396
-
-
Drabant, E.M.1
Hariri, A.R.2
Meyer-Lindenberg, A.3
Munoz, K.E.4
Mattay, V.S.5
Kolachana, B.S.6
-
18
-
-
33746053450
-
The effects of catechol O-methyltransferase genotype on brain activation elicited by affective stimuli and cognitive tasks
-
A. Heinz, and M.N. Smolka The effects of catechol O-methyltransferase genotype on brain activation elicited by affective stimuli and cognitive tasks Rev Neurosci 17 2006 359
-
(2006)
Rev Neurosci
, vol.17
, pp. 359
-
-
Heinz, A.1
Smolka, M.N.2
-
19
-
-
33748944189
-
Prefrontal-hippocampal coupling during memory processing is modulated by COMT val158met genotype
-
A. Bertolino, V. Rubino, F. Sambataro, G. Blasi, V. Latorre, and L. Fazio et al. Prefrontal-hippocampal coupling during memory processing is modulated by COMT val158met genotype Biol Psychiatry 60 2006 1250 1258
-
(2006)
Biol Psychiatry
, vol.60
, pp. 1250-1258
-
-
Bertolino, A.1
Rubino, V.2
Sambataro, F.3
Blasi, G.4
Latorre, V.5
Fazio, L.6
-
20
-
-
77956327951
-
Quantitative role of COMT in dopamine clearance in the prefrontal cortex of freely moving mice
-
M. Käenmäki, A. Tammimäki, T. Myöhänen, K. Pakarinen, C. Amberg, and M. Karayiorgou et al. Quantitative role of COMT in dopamine clearance in the prefrontal cortex of freely moving mice J Neurochem 114 2010 1745 1755
-
(2010)
J Neurochem
, vol.114
, pp. 1745-1755
-
-
Käenmäki, M.1
Tammimäki, A.2
Myöhänen, T.3
Pakarinen, K.4
Amberg, C.5
Karayiorgou, M.6
-
21
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: The SzGene database
-
N.C. Allen, S. Bagade, M.B. McQueen, J.P.A. Ioannidis, F.K. Kavvoura, and M.J. Khoury et al. Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: The SzGene database Nat Genet 40 2008 827 834
-
(2008)
Nat Genet
, vol.40
, pp. 827-834
-
-
Allen, N.C.1
Bagade, S.2
McQueen, M.B.3
Ioannidis, J.P.A.4
Kavvoura, F.K.5
Khoury, M.J.6
-
22
-
-
0038389841
-
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain
-
N.J. Bray, P.R. Buckland, N.M. Williams, H.J. Williams, N. Norton, and M.J. Owen et al. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain Am J Hum Genet 73 2003 152 161
-
(2003)
Am J Hum Genet
, vol.73
, pp. 152-161
-
-
Bray, N.J.1
Buckland, P.R.2
Williams, N.M.3
Williams, H.J.4
Norton, N.5
Owen, M.J.6
-
23
-
-
84884288739
-
Polymorphisms in microRNA target sites influence susceptibility to schizophrenia by altering the binding of miRNAs to their targets [published online ahead of print January 15]
-
Y. Gong, C.N. Wu, J. Xu, G. Feng, Q. Xing, and W. Fu et al. Polymorphisms in microRNA target sites influence susceptibility to schizophrenia by altering the binding of miRNAs to their targets [published online ahead of print January 15] Eur Neuropsychopharmacol 2013
-
(2013)
Eur Neuropsychopharmacol
-
-
Gong, Y.1
Wu, C.N.2
Xu, J.3
Feng, G.4
Xing, Q.5
Fu, W.6
-
24
-
-
41649100270
-
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS
-
E. Michaelovsky, D. Gothelf, M. Korostishevsky, A. Frisch, M. Burg, and M. Carmel et al. Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS Int J Neuropsychopharmacol 11 2008 351 363
-
(2008)
Int J Neuropsychopharmacol
, vol.11
, pp. 351-363
-
-
Michaelovsky, E.1
Gothelf, D.2
Korostishevsky, M.3
Frisch, A.4
Burg, M.5
Carmel, M.6
-
25
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
A. Nackley, S. Shabalina, I. Tchivileva, K. Satterfield, O. Korchynskyi, and S. Makarov et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure Science 314 2006 1930 1933
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.1
Shabalina, S.2
Tchivileva, I.3
Satterfield, K.4
Korchynskyi, O.5
Makarov, S.6
-
26
-
-
12944249385
-
Siteâspecific cytosine methylation in SâCOMT promoter in 31 brain regions with implications for studies involving schizophrenia
-
B.C. Murphy, R.L. O'Reilly, and S.M. Singh Siteâspecific cytosine methylation in SâCOMT promoter in 31 brain regions with implications for studies involving schizophrenia Am J Med Genet B Neuropsychiatr Genet 133 2005 37 42
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.133
, pp. 37-42
-
-
Murphy, B.C.1
O'Reilly, R.L.2
Singh, S.M.3
-
27
-
-
79955782889
-
Stress-related methylation of the catechol-O-methyltransferase Val158 allele predicts human prefrontal cognition and activity
-
G. Ursini, V. Bollati, L. Fazio, A. Porcelli, L. Iacovelli, and A. Catalani et al. Stress-related methylation of the catechol-O-methyltransferase Val158 allele predicts human prefrontal cognition and activity J Neurosci 31 2011 6692 6698
-
(2011)
J Neurosci
, vol.31
, pp. 6692-6698
-
-
Ursini, G.1
Bollati, V.2
Fazio, L.3
Porcelli, A.4
Iacovelli, L.5
Catalani, A.6
-
28
-
-
33645922451
-
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome
-
B. Glaser, M. Debbane, C. Hinard, M.A. Morris, S.P. Dahoun, and S.E. Antonarakis et al. No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome Am J Psychiatry 163 2006 537 539
-
(2006)
Am J Psychiatry
, vol.163
, pp. 537-539
-
-
Glaser, B.1
Debbane, M.2
Hinard, C.3
Morris, M.A.4
Dahoun, S.P.5
Antonarakis, S.E.6
-
29
-
-
34249795781
-
Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome
-
D. Gothelf, F. Hoeft, C. Hinard, J.F. Hallmayer, J.V. Stoecker, and S.E. Antonarakis et al. Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome Hum Brain Mapp 28 2007 533 542
-
(2007)
Hum Brain Mapp
, vol.28
, pp. 533-542
-
-
Gothelf, D.1
Hoeft, F.2
Hinard, C.3
Hallmayer, J.F.4
Stoecker, J.V.5
Antonarakis, S.E.6
-
30
-
-
34247842799
-
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome
-
D. Gothelf, E. Michaelovsky, A. Frisch, A.H. Zohar, G. Presburger, and M. Burg et al. Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome Int J Neuropsychopharmacol 10 2007 301 308
-
(2007)
Int J Neuropsychopharmacol
, vol.10
, pp. 301-308
-
-
Gothelf, D.1
Michaelovsky, E.2
Frisch, A.3
Zohar, A.H.4
Presburger, G.5
Burg, M.6
-
31
-
-
63849198530
-
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome
-
Y. Takarae, L. Schmidt, F. Tassone, and T.J. Simon Catechol-O- methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome Cogn Affect Behav Neurosci 9 2009 83 90
-
(2009)
Cogn Affect Behav Neurosci
, vol.9
, pp. 83-90
-
-
Takarae, Y.1
Schmidt, L.2
Tassone, F.3
Simon, T.J.4
-
32
-
-
21344471660
-
COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome
-
K. Baker, T. Baldeweg, S. Sivagnanasundaram, P. Scambler, and D. Skuse COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome Biol Psychiatry 58 2005 23 31
-
(2005)
Biol Psychiatry
, vol.58
, pp. 23-31
-
-
Baker, K.1
Baldeweg, T.2
Sivagnanasundaram, S.3
Scambler, P.4
Skuse, D.5
-
33
-
-
27644524899
-
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
-
D. Gothelf, S. Eliez, T. Thompson, C. Hinard, L. Penniman, and C. Feinstein et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Nat Neurosci 8 2005 1500 1502
-
(2005)
Nat Neurosci
, vol.8
, pp. 1500-1502
-
-
Gothelf, D.1
Eliez, S.2
Thompson, T.3
Hinard, C.4
Penniman, L.5
Feinstein, C.6
-
34
-
-
34247636739
-
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome
-
A.S. Bassett, O. Caluseriu, R. Weksberg, D.A. Young, and E.W. Chow Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome Biol Psychiatry 61 2007 1135 1140
-
(2007)
Biol Psychiatry
, vol.61
, pp. 1135-1140
-
-
Bassett, A.S.1
Caluseriu, O.2
Weksberg, R.3
Young, D.A.4
Chow, E.W.5
-
35
-
-
0033966919
-
Family-based linkage disequilibrium mapping using SNP marker haplotypes: Application to a potential locus for schizophrenia at chromosome 22q11
-
T. Li, D. Ball, J. Zhao, R. Murray, X. Liu, and P. Sham et al. Family-based linkage disequilibrium mapping using SNP marker haplotypes: Application to a potential locus for schizophrenia at chromosome 22q11 Mol Psychiatry 5 2000 77
-
(2000)
Mol Psychiatry
, vol.5
, pp. 77
-
-
Li, T.1
Ball, D.2
Zhao, J.3
Murray, R.4
Liu, X.5
Sham, P.6
-
36
-
-
33748055408
-
Impact of complex genetic variation in COMT on human brain function
-
A. Meyer-Lindenberg, T. Nichols, J.H. Callicott, J. Ding, B. Kolachana, and J. Buckholtz et al. Impact of complex genetic variation in COMT on human brain function Mol Psychiatry 11 2006 867 877
-
(2006)
Mol Psychiatry
, vol.11
, pp. 867-877
-
-
Meyer-Lindenberg, A.1
Nichols, T.2
Callicott, J.H.3
Ding, J.4
Kolachana, B.5
Buckholtz, J.6
-
37
-
-
0020040983
-
Rapid and sensitive singleâstep radiochemical assay for catecholâoâmethyltransferase
-
G. Zürcher, and M. Prada Rapid and sensitive singleâstep radiochemical assay for catecholâoâmethyltransferase J Neurochem 38 1982 191 195
-
(1982)
J Neurochem
, vol.38
, pp. 191-195
-
-
Zürcher, G.1
Prada, M.2
-
38
-
-
70349492911
-
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
-
D.W. Meechan, E.S. Tucker, T.M. Maynard, and A.S. LaMantia Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome Proc Natl Acad Sci U S A 106 2009 16434 16445
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 16434-16445
-
-
Meechan, D.W.1
Tucker, E.S.2
Maynard, T.M.3
Lamantia, A.S.4
-
39
-
-
33847283299
-
Differential gene expression in the hippocampus of the Df1/+ mice: A model for 22q11. 2 deletion syndrome and schizophrenia
-
S. Sivagnanasundaram, D. Fletcher, M. Hubank, E. Illingworth, D. Skuse, and P. Scambler Differential gene expression in the hippocampus of the Df1/+ mice: A model for 22q11. 2 deletion syndrome and schizophrenia Brain Res 1139 2007 48 59
-
(2007)
Brain Res
, vol.1139
, pp. 48-59
-
-
Sivagnanasundaram, S.1
Fletcher, D.2
Hubank, M.3
Illingworth, E.4
Skuse, D.5
Scambler, P.6
-
40
-
-
34247175696
-
Catechol-o-methyltransferase enzyme activity and protein expression in human prefrontal cortex across the postnatal lifespan
-
E.M. Tunbridge, C.S. Weickert, J.E. Kleinman, M.M. Herman, J. Chen, and B.S. Kolachana et al. Catechol-o-methyltransferase enzyme activity and protein expression in human prefrontal cortex across the postnatal lifespan Cereb Cortex 17 2007 1206 1212
-
(2007)
Cereb Cortex
, vol.17
, pp. 1206-1212
-
-
Tunbridge, E.M.1
Weickert, C.S.2
Kleinman, J.E.3
Herman, M.M.4
Chen, J.5
Kolachana, B.S.6
-
41
-
-
84878798054
-
Epigenetic determinants of healthy and diseased brain aging and cognitiondeterminants of healthy and diseased brain aging
-
S. Akbarian, M.S. Beeri, and V. Haroutunian Epigenetic determinants of healthy and diseased brain aging and cognitiondeterminants of healthy and diseased brain aging JAMA Neurol 70 2013 711 718
-
(2013)
JAMA Neurol
, vol.70
, pp. 711-718
-
-
Akbarian, S.1
Beeri, M.S.2
Haroutunian, V.3
|