-
1
-
-
0031778072
-
Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins
-
Carmelli D, DeCarli C, Swan GE, Jack LM, Reed T, Wolf PA, Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins. Stroke 1998 29 1177 1181
-
(1998)
Stroke
, vol.29
, pp. 1177-1181
-
-
Carmelli, D.1
DeCarli, C.2
Swan, G.E.3
Jack, L.M.4
Reed, T.5
Wolf, P.A.6
-
2
-
-
3042555253
-
Genetic variation in white matter hyperintensity volume in the Framingham Study
-
Atwood LD, Wolf PA, Heard-Costa NL, Massaro JM, Beiser A, D'Agostino RB, Genetic variation in white matter hyperintensity volume in the Framingham Study. Stroke 2004 35 1609 1613. doi: 10.1161/01.STR.0000129643.77045.10
-
(2004)
Stroke
, vol.35
, pp. 1609-1613
-
-
Atwood, L.D.1
Wolf, P.A.2
Heard-Costa, N.L.3
Massaro, J.M.4
Beiser, A.5
D'Agostino, R.B.6
-
3
-
-
0842289489
-
Heritability of leukoaraiosis in hypertensive sibships
-
Turner ST, Jack CR, Fornage M, Mosley TH, Boerwinkle E, de Andrade M, Heritability of leukoaraiosis in hypertensive sibships. Hypertension 2004 43 483 487. doi: 10.1161/01.HYP.0000112303.26158.92
-
(2004)
Hypertension
, vol.43
, pp. 483-487
-
-
Turner, S.T.1
Jack, C.R.2
Fornage, M.3
Mosley, T.H.4
Boerwinkle, E.5
De Andrade, M.6
-
4
-
-
0038049262
-
Vascular cognitive impairment
-
O'Brien JT, Erkinjuntti T, Reisberg B, Roman G, Sawada T, Pantoni L, Vascular cognitive impairment. Lancet Neurol 2003 2 89 98
-
(2003)
Lancet Neurol
, vol.2
, pp. 89-98
-
-
O'Brien, J.T.1
Erkinjuntti, T.2
Reisberg, B.3
Roman, G.4
Sawada, T.5
Pantoni, L.6
-
5
-
-
66849141259
-
Genetic determinants of white matter hyperintensities on brain scans: A systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19,000 subjects
-
Paternoster L, Chen W, Sudlow CL, Genetic determinants of white matter hyperintensities on brain scans: a systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19,000 subjects. Stroke 2009 40 2020 2026. doi: 10.1161/STROKEAHA.108.542050
-
(2009)
Stroke
, vol.40
, pp. 2020-2026
-
-
Paternoster, L.1
Chen, W.2
Sudlow, C.L.3
-
6
-
-
84867579225
-
Genetics of age-related white matter lesions from linkage to genome wide association studies
-
Freudenberger P, Schmidt R, Schmidt H, Genetics of age-related white matter lesions from linkage to genome wide association studies. J Neurol Sci 2012 322 82 86. doi: 10.1016/j.jns.2012.06.016
-
(2012)
J Neurol Sci
, vol.322
, pp. 82-86
-
-
Freudenberger, P.1
Schmidt, R.2
Schmidt, H.3
-
7
-
-
81055147238
-
Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease
-
Schmidt H, Zeginigg M, Wiltgen M, Freudenberger P, Petrovic K, Cavalieri M, CHARGE consortium Neurology working group Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. Brain 2011 134 pt 11 3384 3397. doi: 10.1093/brain/awr252
-
(2011)
Brain
, vol.134
, pp. 3384-3397
-
-
Schmidt, H.1
Zeginigg, M.2
Wiltgen, M.3
Freudenberger, P.4
Petrovic, K.5
Cavalieri, M.6
-
8
-
-
63449100039
-
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
-
Psaty BM, O'Donnell CJ, Gudnason V, Lunetta KL, Folsom AR, Rotter JI, CHARGE Consortium Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ Cardiovasc Genet 2009 2 73 80. doi: 10.1161/CIRCGENETICS.108.829747
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 73-80
-
-
Psaty, B.M.1
O'Donnell, C.J.2
Gudnason, V.3
Lunetta, K.L.4
Folsom, A.R.5
Rotter, J.I.6
-
9
-
-
79959397958
-
Genome-wide association studies of cerebral white matter lesion burden: The CHARGE consortium
-
Fornage M, Debette S, Bis JC, Schmidt H, Ikram MA, Dufouil C, Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. Ann Neurol 2011 69 928 939. doi: 10.1002/ana.22403
-
(2011)
Ann Neurol
, vol.69
, pp. 928-939
-
-
Fornage, M.1
Debette, S.2
Bis, J.C.3
Schmidt, H.4
Ikram, M.A.5
Dufouil, C.6
-
10
-
-
80054979530
-
Replication study of chr17q25 with cerebral white matter lesion volume
-
Verhaaren BF, de Boer R, Vernooij MW, Rivadeneira F, Uitterlinden AG, Hofman A, Replication study of chr17q25 with cerebral white matter lesion volume. Stroke 2011 42 3297 3299. doi: 10.1161/STROKEAHA.111.623090
-
(2011)
Stroke
, vol.42
, pp. 3297-3299
-
-
Verhaaren, B.F.1
De Boer, R.2
Vernooij, M.W.3
Rivadeneira, F.4
Uitterlinden, A.G.5
Hofman, A.6
-
11
-
-
84880180775
-
17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status
-
Adib-Samii P, Rost N, Traylor M, Devan W, Biffi A, Lanfranconi S, Australian Stroke Genetics Collaborative; Wellcome Trust Case-Control Consortium-2 (WTCCC2); METASTROKE; International Stroke Genetics Consortium 17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status. Stroke 2013 44 1609 1615. doi: 10.1161/STROKEAHA.113.679936
-
(2013)
Stroke
, vol.44
, pp. 1609-1615
-
-
Adib-Samii, P.1
Rost, N.2
Traylor, M.3
Devan, W.4
Biffi, A.5
Lanfranconi, S.6
-
12
-
-
84876325430
-
Association of Chr17q25 with cerebral white matter hyperintensities and cognitive impairment: The J-SHIPP study
-
Tabara Y, Igase M, Okada Y, Nagai T, Uetani E, Kido T, Association of Chr17q25 with cerebral white matter hyperintensities and cognitive impairment: the J-SHIPP study. Eur J Neurol 2013 20 860 862. doi: 10.1111/j.1468-1331.2012.03879.x
-
(2013)
Eur J Neurol
, vol.20
, pp. 860-862
-
-
Tabara, Y.1
Igase, M.2
Okada, Y.3
Nagai, T.4
Uetani, E.5
Kido, T.6
-
13
-
-
34247126863
-
Age, Gene/Environment Susceptibility-Reykjavik Study: Multidisciplinary applied phenomics
-
Harris TB, Launer LJ, Eiriksdottir G, Kjartansson O, Jonsson PV, Sigurdsson G, Age, Gene/Environment Susceptibility-Reykjavik Study: multidisciplinary applied phenomics. Am J Epidemiol 2007 165 1076 1087. doi: 10.1093/aje/kwk115
-
(2007)
Am J Epidemiol
, vol.165
, pp. 1076-1087
-
-
Harris, T.B.1
Launer, L.J.2
Eiriksdottir, G.3
Kjartansson, O.4
Jonsson, P.V.5
Sigurdsson, G.6
-
14
-
-
0024591825
-
The atherosclerosis risk in communities (ARIC) study: Design and objectives
-
Investigators TA
-
Investigators TA, The atherosclerosis risk in communities (ARIC) study: design and objectives. Am J Epidemiol 1989 129 687 702
-
(1989)
Am J Epidemiol
, vol.129
, pp. 687-702
-
-
-
15
-
-
0027965004
-
Assessment of cerebrovascular risk profiles in healthy persons: Definition of research goals and the Austrian Stroke Prevention Study (ASPS)
-
Schmidt R, Lechner H, Fazekas F, Niederkorn K, Reinhart B, Grieshofer P, Assessment of cerebrovascular risk profiles in healthy persons: definition of research goals and the Austrian Stroke Prevention Study (ASPS). Neuroepidemiology 1994 13 308 313
-
(1994)
Neuroepidemiology
, vol.13
, pp. 308-313
-
-
Schmidt, R.1
Lechner, H.2
Fazekas, F.3
Niederkorn, K.4
Reinhart, B.5
Grieshofer, P.6
-
16
-
-
33845506466
-
C-reactive protein, carotid atherosclerosis, and cerebral small-vessel disease: Results of the Austrian Stroke Prevention Study
-
Schmidt R, Schmidt H, Pichler M, Enzinger C, Petrovic K, Niederkorn K, C-reactive protein, carotid atherosclerosis, and cerebral small-vessel disease: results of the Austrian Stroke Prevention Study. Stroke 2006 37 2910 2916. doi: 10.1161/01.STR.0000248768.40043.f9
-
(2006)
Stroke
, vol.37
, pp. 2910-2916
-
-
Schmidt, R.1
Schmidt, H.2
Pichler, M.3
Enzinger, C.4
Petrovic, K.5
Niederkorn, K.6
-
17
-
-
0025913116
-
The Cardiovascular Health Study: Design and rationale
-
Fried LP, Borhani NO, Enright P, Furberg CD, Gardin JM, Kronmal RA, The Cardiovascular Health Study: design and rationale. Ann Epidemiol 1991 1 263 276
-
(1991)
Ann Epidemiol
, vol.1
, pp. 263-276
-
-
Fried, L.P.1
Borhani, N.O.2
Enright, P.3
Furberg, C.D.4
Gardin, J.M.5
Kronmal, R.A.6
-
18
-
-
0013955116
-
The Framingham study. An epidemiological approach to coronary heart disease
-
Dawber TR, Kannel WB, The Framingham study. An epidemiological approach to coronary heart disease. Circulation 1966 34 553 555
-
(1966)
Circulation
, vol.34
, pp. 553-555
-
-
Dawber, T.R.1
Kannel, W.B.2
-
19
-
-
84886623285
-
The Framingham Offspring Study. Design and preliminary data
-
Feinleib M, Kannel WB, Garrison RJ, McNamara PM, Castelli WP, The Framingham Offspring Study. Design and preliminary data. Prev Med 1975 4 518 525
-
(1975)
Prev Med
, vol.4
, pp. 518-525
-
-
Feinleib, M.1
Kannel, W.B.2
Garrison, R.J.3
McNamara, P.M.4
Castelli, W.P.5
-
20
-
-
0032707276
-
The design of a prospective study of Pravastatin in the Elderly at Risk (PROSPER). PROSPER Study Group. PROspective Study of Pravastatin in the Elderly at Risk
-
Shepherd J, Blauw GJ, Murphy MB, Cobbe SM, Bollen EL, Buckley BM, The design of a prospective study of Pravastatin in the Elderly at Risk (PROSPER). PROSPER Study Group. PROspective Study of Pravastatin in the Elderly at Risk. Am J Cardiol 1999 84 1192 1197
-
(1999)
Am J Cardiol
, vol.84
, pp. 1192-1197
-
-
Shepherd, J.1
Blauw, G.J.2
Murphy, M.B.3
Cobbe, S.M.4
Bollen, E.L.5
Buckley, B.M.6
-
21
-
-
0037164314
-
PROspective Study of Pravastatin in the Elderly at Risk Pravastatin in elderly individuals at risk of vascular disease (PROSPER): A randomised controlled trial
-
Shepherd J, Blauw GJ, Murphy MB, Bollen EL, Buckley BM, Cobbe SM, PROSPER study group. PROspective Study of Pravastatin in the Elderly at Risk Pravastatin in elderly individuals at risk of vascular disease (PROSPER): a randomised controlled trial. Lancet 2002 360 1623 1630
-
(2002)
Lancet
, vol.360
, pp. 1623-1630
-
-
Shepherd, J.1
Blauw, G.J.2
Murphy, M.B.3
Bollen, E.L.4
Buckley, B.M.5
Cobbe, S.M.6
-
22
-
-
70349236841
-
The Rotterdam Study: 2010 objectives and design update
-
Hofman A, Breteler MM, van Duijn CM, Janssen HL, Krestin GP, Kuipers EJ, The Rotterdam Study: 2010 objectives and design update. Eur J Epidemiol 2009 24 553 572. doi: 10.1007/s10654-009-9386-z
-
(2009)
Eur J Epidemiol
, vol.24
, pp. 553-572
-
-
Hofman, A.1
Breteler, M.M.2
Van Duijn, C.M.3
Janssen, H.L.4
Krestin, G.P.5
Kuipers, E.J.6
-
23
-
-
60549112211
-
Cerebral white matter lesions, gait, and the risk of incident falls: A prospective population-based study
-
Srikanth V, Beare R, Blizzard L, Phan T, Stapleton J, Chen J, Cerebral white matter lesions, gait, and the risk of incident falls: a prospective population-based study. Stroke 2009 40 175 180. doi: 10.1161/STROKEAHA.108.524355
-
(2009)
Stroke
, vol.40
, pp. 175-180
-
-
Srikanth, V.1
Beare, R.2
Blizzard, L.3
Phan, T.4
Stapleton, J.5
Chen, J.6
-
24
-
-
0142025392
-
Vascular factors and risk of dementia: Design of the three-city study and baseline characteristics of the study population
-
Group CS
-
Group CS, Vascular factors and risk of dementia: design of the three-city study and baseline characteristics of the study population. Neuroepidemiology 2003 22 316 325
-
(2003)
Neuroepidemiology
, vol.22
, pp. 316-325
-
-
-
25
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L, Blangero J, Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 1998 62 1198 1211. doi: 10.1086/301844
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
26
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR, METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 2010 26 2190 2191. doi: 10.1093/bioinformatics/btq340
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
27
-
-
84864454040
-
SNPnexus: A web server for functional annotation of novel and publicly known genetic variants (2012 update)
-
Web Server Issue
-
Dayem Ullah AZ, Lemoine NR, Chelala C, SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update). Nucleic Acids Res 2012 40 Web Server issue W65 W70. doi: 10.1093/nar/gks364
-
(2012)
Nucleic Acids Res
, vol.40
, pp. W65-W70
-
-
Dayem Ullah, A.Z.1
Lemoine, N.R.2
Chelala, C.3
-
28
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Hakonarson H, ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 2010 38 e164. doi: 10.1093/nar/gkq603
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
29
-
-
57249114505
-
SNAP: A web-based tool for identification and annotation of proxy SNPs using HapMap
-
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, de Bakker PI, SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 2008 24 2938 2939. doi: 10.1093/bioinformatics/btn564
-
(2008)
Bioinformatics
, vol.24
, pp. 2938-2939
-
-
Johnson, A.D.1
Handsaker, R.E.2
Pulit, S.L.3
Nizzari, M.M.4
O'Donnell, C.J.5
De Bakker, P.I.6
-
30
-
-
77956586071
-
LocusZoom: Regional visualization of genome-wide association scan results
-
Pruim RJ, Welch RP, Sanna S, Teslovich TM, Chines PS, Gliedt TP, LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 2010 26 2336 2337. doi: 10.1093/bioinformatics/btq419
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
Gliedt, T.P.6
-
32
-
-
0031711978
-
Are genetic factors important in the aetiology of leukoaraiosis? Results from a memory clinic population
-
Amar K, MacGowan S, Wilcock G, Lewis T, Scott M, Are genetic factors important in the aetiology of leukoaraiosis? Results from a memory clinic population. Int J Geriatr Psychiatry 1998 13 585 590
-
(1998)
Int J Geriatr Psychiatry
, vol.13
, pp. 585-590
-
-
Amar, K.1
MacGowan, S.2
Wilcock, G.3
Lewis, T.4
Scott, M.5
-
33
-
-
0036188197
-
Angiotensin converting enzyme insertion/deletion genotype is associated with leukoaraiosis in lacunar syndromes
-
Hassan A, Lansbury A, Catto AJ, Guthrie A, Spencer J, Craven C, Angiotensin converting enzyme insertion/deletion genotype is associated with leukoaraiosis in lacunar syndromes. J Neurol Neurosurg Psychiatry 2002 72 343 346
-
(2002)
J Neurol Neurosurg Psychiatry
, vol.72
, pp. 343-346
-
-
Hassan, A.1
Lansbury, A.2
Catto, A.J.3
Guthrie, A.4
Spencer, J.5
Craven, C.6
-
34
-
-
0036182440
-
Renin-angiotensin system genetic polymorphisms and cerebral white matter lesions in essential hypertension
-
Sierra C, Coca A, Gómez-Angelats E, Poch E, Sobrino J, de la Sierra A, Renin-angiotensin system genetic polymorphisms and cerebral white matter lesions in essential hypertension. Hypertension 2002 39 2 pt 2 343 347
-
(2002)
Hypertension
, vol.39
, Issue.2
, pp. 343-347
-
-
Sierra, C.1
Coca, A.2
Gómez-Angelats, E.3
Poch, E.4
Sobrino, J.5
De La Sierra, A.6
-
35
-
-
0037967343
-
MTHFR gene polymorphism as a risk factor for silent brain infarcts and white matter lesions in the Japanese general population: The NILS-LSA Study
-
Kohara K, Fujisawa M, Ando F, Tabara Y, Niino N, Miki T, NILS-LSA Study MTHFR gene polymorphism as a risk factor for silent brain infarcts and white matter lesions in the Japanese general population: The NILS-LSA Study. Stroke 2003 34 1130 1135. doi: 10.1161/01.STR.0000069163.02611.B0
-
(2003)
Stroke
, vol.34
, pp. 1130-1135
-
-
Kohara, K.1
Fujisawa, M.2
Ando, F.3
Tabara, Y.4
Niino, N.5
Miki, T.6
-
36
-
-
0346097879
-
Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunction
-
Hassan A, Hunt BJ, O'Sullivan M, Bell R, D'Souza R, Jeffery S, Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunction. Brain 2004 127 pt 1 212 219. doi: 10.1093/brain/awh023
-
(2004)
Brain
, vol.127
, pp. 212-219
-
-
Hassan, A.1
Hunt, B.J.2
O'Sullivan, M.3
Bell, R.4
D'Souza, R.5
Jeffery, S.6
-
37
-
-
33846898749
-
Polymorphisms in genes of the renin-angiotensin system and cerebral small vessel disease
-
Gormley K, Bevan S, Markus HS, Polymorphisms in genes of the renin-angiotensin system and cerebral small vessel disease. Cerebrovasc Dis 2007 23 148 155. doi: 10.1159/000097052
-
(2007)
Cerebrovasc Dis
, vol.23
, pp. 148-155
-
-
Gormley, K.1
Bevan, S.2
Markus, H.S.3
-
38
-
-
0035571556
-
Angiotensinogen polymorphism M235T, carotid atherosclerosis, and small-vessel disease-related cerebral abnormalities
-
Schmidt R, Schmidt H, Fazekas F, Launer LJ, Niederkorn K, Kapeller P, Angiotensinogen polymorphism M235T, carotid atherosclerosis, and small-vessel disease-related cerebral abnormalities. Hypertension 2001 38 110 115
-
(2001)
Hypertension
, vol.38
, pp. 110-115
-
-
Schmidt, R.1
Schmidt, H.2
Fazekas, F.3
Launer, L.J.4
Niederkorn, K.5
Kapeller, P.6
-
39
-
-
34848862776
-
Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology
-
van Rijn MJ, Bos MJ, Isaacs A, Yazdanpanah M, Arias-Vásquez A, Stricker BH, Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology. J Neurol Neurosurg Psychiatry 2007 78 1083 1087. doi: 10.1136/jnnp.2006.109819
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 1083-1087
-
-
Van Rijn, M.J.1
Bos, M.J.2
Isaacs, A.3
Yazdanpanah, M.4
Arias-Vásquez, A.5
Stricker, B.H.6
-
40
-
-
0033060127
-
White matter lesions in Alzheimer patients are influenced by apolipoprotein e genotype
-
Bronge L, Fernaeus SE, Blomberg M, Ingelson M, Lannfelt L, Isberg B, White matter lesions in Alzheimer patients are influenced by apolipoprotein E genotype. Dement Geriatr Cogn Disord 1999 10 89 96
-
(1999)
Dement Geriatr Cogn Disord
, vol.10
, pp. 89-96
-
-
Bronge, L.1
Fernaeus, S.E.2
Blomberg, M.3
Ingelson, M.4
Lannfelt, L.5
Isberg, B.6
-
41
-
-
2142769752
-
Interaction between hypertension, apoE, and cerebral white matter lesions
-
de Leeuw FE, Richard F, de Groot JC, van Duijn CM, Hofman A, Van Gijn J, Interaction between hypertension, apoE, and cerebral white matter lesions. Stroke 2004 35 1057 1060. doi: 10.1161/01.STR.0000125859.71051.83
-
(2004)
Stroke
, vol.35
, pp. 1057-1060
-
-
De Leeuw, F.E.1
Richard, F.2
De Groot, J.C.3
Van Duijn, C.M.4
Hofman, A.5
Van Gijn, J.6
-
42
-
-
34249938433
-
Heritability of magnetic resonance imaging (MRI) traits in Alzheimer disease cases and their siblings in the MIRAGE study
-
Lunetta KL, Erlich PM, Cuenco KT, Cupples LA, Green RC, Farrer LA, MIRAGE Study Group Heritability of magnetic resonance imaging (MRI) traits in Alzheimer disease cases and their siblings in the MIRAGE study. Alzheimer Dis Assoc Disord 2007 21 85 91. doi: 10.1097/WAD.0b013e3180653bf7
-
(2007)
Alzheimer Dis Assoc Disord
, vol.21
, pp. 85-91
-
-
Lunetta, K.L.1
Erlich, P.M.2
Cuenco, K.T.3
Cupples, L.A.4
Green, R.C.5
Farrer, L.A.6
-
43
-
-
33947431508
-
The apolipoprotein e epsilon4-allele and antihypertensive treatment are associated with increased risk of cerebral MRI white matter hyperintensities
-
Høgh P, Garde E, Mortensen EL, Jørgensen OS, Krabbe K, Waldemar G, The apolipoprotein E epsilon4-allele and antihypertensive treatment are associated with increased risk of cerebral MRI white matter hyperintensities. Acta Neurol Scand 2007 115 248 253. doi: 10.1111/j.1600-0404.2006.00779.x
-
(2007)
Acta Neurol Scand
, vol.115
, pp. 248-253
-
-
Høgh, P.1
Garde, E.2
Mortensen, E.L.3
Jørgensen, O.S.4
Krabbe, K.5
Waldemar, G.6
-
44
-
-
73849094087
-
Assessing the performance of prediction models: A framework for traditional and novel measures
-
Steyerberg EW, Vickers AJ, Cook NR, Gerds T, Gonen M, Obuchowski N, Assessing the performance of prediction models: a framework for traditional and novel measures. Epidemiology 2010 21 128 138. doi: 10.1097/EDE.0b013e3181c30fb2
-
(2010)
Epidemiology
, vol.21
, pp. 128-138
-
-
Steyerberg, E.W.1
Vickers, A.J.2
Cook, N.R.3
Gerds, T.4
Gonen, M.5
Obuchowski, N.6
-
45
-
-
77956887506
-
A note on a general definition of the coefficient of determination
-
Nagelkerke NJD, A note on a general definition of the coefficient of determination. Biometrika 1991 78 691 692
-
(1991)
Biometrika
, vol.78
, pp. 691-692
-
-
Nagelkerke, N.J.D.1
-
46
-
-
84878659130
-
A comprehensive family-based replication study of schizophrenia genes
-
Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, A comprehensive family-based replication study of schizophrenia genes. JAMA Psychiatry 2013 70 573 581. doi: 10.1001/jamapsychiatry.2013.288
-
(2013)
JAMA Psychiatry
, vol.70
, pp. 573-581
-
-
Aberg, K.A.1
Liu, Y.2
Bukszár, J.3
McClay, J.L.4
Khachane, A.N.5
Andreassen, O.A.6
-
47
-
-
84876296688
-
Identification of risk loci with shared effects on five major psychiatric disorders: A genome-wide analysis
-
Cross-Disorder Group of the Psychiatric Genomics C Identification of risk loci with shared effects on five major psychiatric disorders: A genome-wide analysis. Lancet 2013 381 1371 1379
-
(2013)
Lancet
, vol.381
, pp. 1371-1379
-
-
-
48
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Schizophrenia Psychiatric Genome-Wide Association Study C Genome-wide association study identifies five new schizophrenia loci. Nat Genet 2011 43 969 976
-
(2011)
Nat Genet
, vol.43
, pp. 969-976
-
-
-
49
-
-
84856950582
-
Longitudinal genetic analysis of brain volumes in normal elderly male twins
-
Lessov-Schlaggar CN, Hardin J, DeCarli C, Krasnow RE, Reed T, Wolf PA, Longitudinal genetic analysis of brain volumes in normal elderly male twins. Neurobiol Aging 2012 33 636 644. doi: 10.1016/j.neurobiolaging.2010.06.002
-
(2012)
Neurobiol Aging
, vol.33
, pp. 636-644
-
-
Lessov-Schlaggar, C.N.1
Hardin, J.2
DeCarli, C.3
Krasnow, R.E.4
Reed, T.5
Wolf, P.A.6
-
50
-
-
0036790395
-
The heritability of level and rate-of-change in cognitive functioning in Danish twins aged 70 years and older
-
McGue M, Christensen K, The heritability of level and rate-of-change in cognitive functioning in Danish twins aged 70 years and older. Exp Aging Res 2002 28 435 451. doi: 10.1080/03610730290080416
-
(2002)
Exp Aging Res
, vol.28
, pp. 435-451
-
-
McGue, M.1
Christensen, K.2
-
51
-
-
12444266764
-
Quantitative genetic analysis of latent growth curve models of cognitive abilities in adulthood
-
Reynolds CA, Finkel D, McArdle JJ, Gatz M, Berg S, Pedersen NL, Quantitative genetic analysis of latent growth curve models of cognitive abilities in adulthood. Dev Psychol 2005 41 3 16. doi: 10.1037/0012-1649.41.1.3
-
(2005)
Dev Psychol
, vol.41
, pp. 3-16
-
-
Reynolds, C.A.1
Finkel, D.2
McArdle, J.J.3
Gatz, M.4
Berg, S.5
Pedersen, N.L.6
-
52
-
-
84885020424
-
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
-
Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Multicenter Genetic Studies of Schizophrenia Consortium; Psychosis Endophenotypes International Consortium; Wellcome Trust Case Control Consortium 2 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 45 1150 1159. doi: 10.1038/ng.2742
-
(2013)
Nat Genet
, vol.45
, pp. 1150-1159
-
-
Ripke, S.1
O'Dushlaine, C.2
Chambert, K.3
Moran, J.L.4
Kähler, A.K.5
Akterin, S.6
-
53
-
-
84866358306
-
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder
-
Bergen SE, O'Dushlaine CT, Ripke S, Lee PH, Ruderfer DM, Akterin S, Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. Mol Psychiatry 2012 17 880 886. doi: 10.1038/mp.2012.73
-
(2012)
Mol Psychiatry
, vol.17
, pp. 880-886
-
-
Bergen, S.E.1
O'Dushlaine, C.T.2
Ripke, S.3
Lee, P.H.4
Ruderfer, D.M.5
Akterin, S.6
-
54
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L, Wellcome Trust Case Control Consortium Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009 41 666 676. doi: 10.1038/ng.361
-
(2009)
Nat Genet
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
Tobin, M.D.4
Bochud, M.5
Coin, L.6
-
55
-
-
78650802616
-
Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study
-
Ho JE, Levy D, Rose L, Johnson AD, Ridker PM, Chasman DI, Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study. J Hypertens 2011 29 62 69. doi: 10.1097/HJH.0b013e3283406927
-
(2011)
J Hypertens
, vol.29
, pp. 62-69
-
-
Ho, J.E.1
Levy, D.2
Rose, L.3
Johnson, A.D.4
Ridker, P.M.5
Chasman, D.I.6
-
56
-
-
80053907554
-
International Consortium for Blood Pressure Genome-Wide Association Studies. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, International Consortium for Blood Pressure Genome-Wide Association Studies. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011 478 103 109
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
Bochud, M.4
Johnson, A.D.5
-
57
-
-
84886434475
-
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci
-
Kelly TN, Takeuchi F, Tabara Y, Edwards TL, Kim YJ, Chen P, Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci. Hypertension 2013 62 853 859. doi: 10.1161/HYPERTENSIONAHA.113.01148
-
(2013)
Hypertension
, vol.62
, pp. 853-859
-
-
Kelly, T.N.1
Takeuchi, F.2
Tabara, Y.3
Edwards, T.L.4
Kim, Y.J.5
Chen, P.6
-
58
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Cardiogenics; CARDIoGRAM Consortium Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 43 333 338. doi: 10.1038/ng.784
-
(2011)
Nat Genet
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
König, I.R.2
Kathiresan, S.3
Reilly, M.P.4
Assimes, T.L.5
Holm, H.6
-
59
-
-
77951768060
-
Genome-wide association study of intracranial aneurysm identifies three new risk loci
-
Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010 42 420 425. doi: 10.1038/ng.563
-
(2010)
Nat Genet
, vol.42
, pp. 420-425
-
-
Yasuno, K.1
Bilguvar, K.2
Bijlenga, P.3
Low, S.K.4
Krischek, B.5
Auburger, G.6
-
60
-
-
84926481920
-
Arsenic exposure, AS3MT polymorphism, and neuropsychological functioning among rural dwelling adults and elders: A cross-sectional study
-
Edwards M, Hall J, Gong G, O'Bryant SE, Arsenic exposure, AS3MT polymorphism, and neuropsychological functioning among rural dwelling adults and elders: a cross-sectional study. Environ Health 2014 13 15. doi: 10.1186/1476-069X-13-15
-
(2014)
Environ Health
, vol.13
, pp. 15
-
-
Edwards, M.1
Hall, J.2
Gong, G.3
O'Bryant, S.E.4
-
61
-
-
0036270006
-
Na+:HCO3-cotransporters (NBC): Expression and regulation in the kidney
-
Soleimani M, Na+:HCO3-cotransporters (NBC): expression and regulation in the kidney. J Nephrol 2002 15 suppl 5 S32 S40
-
(2002)
J Nephrol
, vol.15
, pp. S32-S40
-
-
Soleimani, M.1
-
62
-
-
0033002224
-
Characterization of Na+/HCO-3 cotransporter isoform NBC-3
-
Amlal H, Burnham CE, Soleimani M, Characterization of Na+/HCO-3 cotransporter isoform NBC-3. Am J Physiol 1999 276 6 pt 2 F903 F913
-
(1999)
Am J Physiol
, vol.276
, Issue.6
, pp. F903-F913
-
-
Amlal, H.1
Burnham, C.E.2
Soleimani, M.3
-
63
-
-
0035896555
-
Cloning, characterization, and chromosomal mapping of a human electroneutral Na(+)-driven Cl-HCO3 exchanger
-
Grichtchenko II, Choi I, Zhong X, Bray-Ward P, Russell JM, Boron WF, Cloning, characterization, and chromosomal mapping of a human electroneutral Na(+)-driven Cl-HCO3 exchanger. J Biol Chem 2001 276 8358 8363. doi: 10.1074/jbc.C000716200
-
(2001)
J Biol Chem
, vol.276
, pp. 8358-8363
-
-
Grichtchenko, I.I.1
Choi, I.2
Zhong, X.3
Bray-Ward, P.4
Russell, J.M.5
Boron, W.F.6
-
64
-
-
77449149991
-
Genome-wide association studies of MRI-defined brain infarcts: Meta-analysis from the CHARGE Consortium
-
Debette S, Bis JC, Fornage M, Schmidt H, Ikram MA, Sigurdsson S, Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium. Stroke 2010 41 210 217. doi: 10.1161/STROKEAHA.109.569194
-
(2010)
Stroke
, vol.41
, pp. 210-217
-
-
Debette, S.1
Bis, J.C.2
Fornage, M.3
Schmidt, H.4
Ikram, M.A.5
Sigurdsson, S.6
-
65
-
-
84883333125
-
Incident lacunes preferentially localize to the edge of white matter hyperintensities: Insights into the pathophysiology of cerebral small vessel disease
-
Duering M, Csanadi E, Gesierich B, Jouvent E, Hervé D, Seiler S, Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease. Brain 2013 136 pt 9 2717 2726. doi: 10.1093/brain/awt184
-
(2013)
Brain
, vol.136
, pp. 2717-2726
-
-
Duering, M.1
Csanadi, E.2
Gesierich, B.3
Jouvent, E.4
Hervé, D.5
Seiler, S.6
-
66
-
-
84923920708
-
MACROD2 gene associated with autistic-like traits in a general population sample
-
Jones RM, Cadby G, Blangero J, Abraham LJ, Whitehouse AJ, Moses EK, MACROD2 gene associated with autistic-like traits in a general population sample. Psychiatr Genet 2014 24 241 248. doi: 10.1097/YPG.0000000000000052
-
(2014)
Psychiatr Genet
, vol.24
, pp. 241-248
-
-
Jones, R.M.1
Cadby, G.2
Blangero, J.3
Abraham, L.J.4
Whitehouse, A.J.5
Moses, E.K.6
-
67
-
-
0022870759
-
Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. I. Correlation with age and cerebrovascular risk factors
-
Awad IA, Spetzler RF, Hodak JA, Awad CA, Carey R, Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. I. Correlation with age and cerebrovascular risk factors. Stroke 1986 17 1084 1089
-
(1986)
Stroke
, vol.17
, pp. 1084-1089
-
-
Awad, I.A.1
Spetzler, R.F.2
Hodak, J.A.3
Awad, C.A.4
Carey, R.5
-
68
-
-
0023813073
-
White matter signal abnormalities in normal individuals: Correlation with carotid ultrasonography, cerebral blood flow measurements, and cerebrovascular risk factors
-
Fazekas F, Niederkorn K, Schmidt R, Offenbacher H, Horner S, Bertha G, White matter signal abnormalities in normal individuals: correlation with carotid ultrasonography, cerebral blood flow measurements, and cerebrovascular risk factors. Stroke 1988 19 1285 1288
-
(1988)
Stroke
, vol.19
, pp. 1285-1288
-
-
Fazekas, F.1
Niederkorn, K.2
Schmidt, R.3
Offenbacher, H.4
Horner, S.5
Bertha, G.6
|