-
3
-
-
21944439953
-
The familial risk of subarachnoid haemorrhage
-
Teasdale GM, Wardlaw JM, White PM, Murray G, Teasdale EM, Easton V: The familial risk of subarachnoid haemorrhage. Brain 2005;128:1677-1685.
-
(2005)
Brain
, vol.128
, pp. 1677-1685
-
-
Teasdale, G.M.1
Wardlaw, J.M.2
White, P.M.3
Murray, G.4
Teasdale, E.M.5
Easton, V.6
-
5
-
-
12344309062
-
Homocysteine and stroke: Evidence on a causal link from Mendelian randomisation
-
Casas JP, Bautista LE, Smeeth L, Sharma P, Hingorani AD: Homocysteine and stroke: evidence on a causal link from Mendelian randomisation. Lancet 2005;365:224-232.
-
(2005)
Lancet
, vol.365
, pp. 224-232
-
-
Casas, J.P.1
Bautista, L.E.2
Smeeth, L.3
Sharma, P.4
Hingorani, A.D.5
-
6
-
-
0041886570
-
Increased risk of the abdominal aortic aneurysm in carriers of the MTHFR 677T allele
-
Strauss E, Waliszewski K, Gabriel M, Zapalski S, Pawlak AL: Increased risk of the abdominal aortic aneurysm in carriers of the MTHFR 677T allele. J Appl Genet 2003;44:85-93.
-
(2003)
J Appl Genet
, vol.44
, pp. 85-93
-
-
Strauss, E.1
Waliszewski, K.2
Gabriel, M.3
Zapalski, S.4
Pawlak, A.L.5
-
7
-
-
34548094049
-
Mild hyperhomocysteinemia and low folate concentrations as risk factors for cervical arterial dissection
-
Arauz A, Hoyos L, Cantu C, Jara A, Martinez L, Garcia I, Fernandez ML, Alonso E: Mild hyperhomocysteinemia and low folate concentrations as risk factors for cervical arterial dissection. Cerebrovasc Dis 2007;24:210-214.
-
(2007)
Cerebrovasc Dis
, vol.24
, pp. 210-214
-
-
Arauz, A.1
Hoyos, L.2
Cantu, C.3
Jara, A.4
Martinez, L.5
Garcia, I.6
Fernandez, M.L.7
Alonso, E.8
-
8
-
-
0035570015
-
Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: A multicenter observational study
-
Yap S, Boers GH, Wilcken B, Wilcken DE, Brenton DP, Lee PJ, Walter JH, Howard PM, Naughten ER: Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study. Arterioscler Thromb Vasc Biol 2001;21:2080-2085.
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 2080-2085
-
-
Yap, S.1
Boers, G.H.2
Wilcken, B.3
Wilcken, D.E.4
Brenton, D.P.5
Lee, P.J.6
Walter, J.H.7
Howard, P.M.8
Naughten, E.R.9
-
9
-
-
33744741661
-
Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system
-
Simon M, Franke D, Ludwig M, Aliashkevich AF, Koster G, Oldenburg J, Bostrom A, Ziegler A, Schramm J: Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system. J Neurosurg 2006;104:945-949.
-
(2006)
J Neurosurg
, vol.104
, pp. 945-949
-
-
Simon, M.1
Franke, D.2
Ludwig, M.3
Aliashkevich, A.F.4
Koster, G.5
Oldenburg, J.6
Bostrom, A.7
Ziegler, A.8
Schramm, J.9
-
10
-
-
11144242572
-
Heritability of carotid artery atherosclerotic lesions: An ultrasound study in 154 families
-
Moskau S, Golla A, Grothe C, Boes M, Pohl C, Klockgether T: Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families. Stroke 2005;36:5-8.
-
(2005)
Stroke
, vol.36
, pp. 5-8
-
-
Moskau, S.1
Golla, A.2
Grothe, C.3
Boes, M.4
Pohl, C.5
Klockgether, T.6
-
11
-
-
33750951720
-
Homocysteine and carotid intimamedia thickness in a German population: Lack of clinical relevance
-
Linnebank M, Moskau S, Farmand S, Fliessbach K, Kolsch H, Bos M, Grothe C, Becker D, Harbrecht U, Pohl C, Wullner U, Klockgether T: Homocysteine and carotid intimamedia thickness in a German population: lack of clinical relevance. Stroke 2006;37:2840-2842.
-
(2006)
Stroke
, vol.37
, pp. 2840-2842
-
-
Linnebank, M.1
Moskau, S.2
Farmand, S.3
Fliessbach, K.4
Kolsch, H.5
Bos, M.6
Grothe, C.7
Becker, D.8
Harbrecht, U.9
Pohl, C.10
Wullner, U.11
Klockgether, T.12
-
13
-
-
4444302308
-
Tests for establishing compatibility of an observed genotype distribution with Hardy-Weinberg equilibrium in the case of a biallelic locus
-
Wellek S: Tests for establishing compatibility of an observed genotype distribution with Hardy-Weinberg equilibrium in the case of a biallelic locus. Biometrics 2004;60:694-703.
-
(2004)
Biometrics
, vol.60
, pp. 694-703
-
-
Wellek, S.1
-
14
-
-
33750196383
-
SNP-based analysis of genetic substructure in the German population
-
Steffens M, Lamina C, Illig T, Bettecken T, Vogler R, Entz P, Suk EK, Toliat MR, Klopp N, Caliebe A, Konig IR, Kohler K, Ludemann J, Diaz LA, Fimmers R, Lichtner P, Ziegler A, Wolf A, Krawczak M, Nurnberg P, Hampe J, Schreiber S, Meitinger T, Wichmann HE, Roeder K, Wienker TF, Baur MP: SNP-based analysis of genetic substructure in the German population. Hum Hered 2006;62:20-29.
-
(2006)
Hum Hered
, vol.62
, pp. 20-29
-
-
Steffens, M.1
Lamina, C.2
Illig, T.3
Bettecken, T.4
Vogler, R.5
Entz, P.6
Suk, E.K.7
Toliat, M.R.8
Klopp, N.9
Caliebe, A.10
Konig, I.R.11
Kohler, K.12
Ludemann, J.13
Diaz, L.A.14
Fimmers, R.15
Lichtner, P.16
Ziegler, A.17
Wolf, A.18
Krawczak, M.19
Nurnberg, P.20
Hampe, J.21
Schreiber, S.22
Meitinger, T.23
Wichmann, H.E.24
Roeder, K.25
Wienker, T.F.26
Baur, M.P.27
more..
-
15
-
-
33846498939
-
-
Guo W, Romano J: A generalized Sidak-Holm procedure and control of generalized error rates under independence. Stat Appl Genet Mol Biol 2007;6:article3.
-
Guo W, Romano J: A generalized Sidak-Holm procedure and control of generalized error rates under independence. Stat Appl Genet Mol Biol 2007;6:article3.
-
-
-
-
16
-
-
0036045429
-
Single nucleotide polymorphisms in the transcobalamin gene: Relationship with transcobalamin concentrations and risk for neural tube defects
-
Afman LA, Lievers KJ, van der Put NM, Trijbels FJ, Blom HJ: Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects. Eur J Hum Genet 2002;10:433-438.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 433-438
-
-
Afman, L.A.1
Lievers, K.J.2
van der Put, N.M.3
Trijbels, F.J.4
Blom, H.J.5
-
17
-
-
0035079052
-
Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defects
-
Afman LA, van der Put NM, Thomas CM, Trijbels JM, Blom HJ: Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defects. QJM 2001;94:159-166.
-
(2001)
QJM
, vol.94
, pp. 159-166
-
-
Afman, L.A.1
van der Put, N.M.2
Thomas, C.M.3
Trijbels, J.M.4
Blom, H.J.5
-
18
-
-
0037100425
-
Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults
-
Miller JW, Ramos MI, Garrod MG, Flynn MA, Green R: Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults. Blood 2002;100:718-720.
-
(2002)
Blood
, vol.100
, pp. 718-720
-
-
Miller, J.W.1
Ramos, M.I.2
Garrod, M.G.3
Flynn, M.A.4
Green, R.5
-
19
-
-
0033594888
-
Novel mechanism for endothelial dysfunction: Dysregulation of dimethylarginine dimethylaminohydrolase
-
Ito A, Tsao PS, Adimoolam S, Kimoto M, Ogawa T, Cooke JP: Novel mechanism for endothelial dysfunction: dysregulation of dimethylarginine dimethylaminohydrolase. Circulation 1999;99:3092-3095.
-
(1999)
Circulation
, vol.99
, pp. 3092-3095
-
-
Ito, A.1
Tsao, P.S.2
Adimoolam, S.3
Kimoto, M.4
Ogawa, T.5
Cooke, J.P.6
-
20
-
-
0035923560
-
Homocysteine impairs the nitric oxide synthase pathway: Role of asymmetric dimethylarginine
-
Stuhlinger MC, Tsao PS, Her JH, Kimoto M, Balint RF, Cooke JP: Homocysteine impairs the nitric oxide synthase pathway: role of asymmetric dimethylarginine. Circulation 2001;104:2569-2575.
-
(2001)
Circulation
, vol.104
, pp. 2569-2575
-
-
Stuhlinger, M.C.1
Tsao, P.S.2
Her, J.H.3
Kimoto, M.4
Balint, R.F.5
Cooke, J.P.6
-
21
-
-
27744511357
-
Asymmetric dimethylarginine and the risk of cardiovascular events and death in patients with coronary artery disease: Results from the AtheroGene Study
-
Schnabel R, Blankenberg S, Lubos E, Lackner KJ, Rupprecht HJ, Espinola-Klein C, Jachmann N, Post F, Peetz D, Bickel C, Cambien F, Tiret L, Munzel T: Asymmetric dimethylarginine and the risk of cardiovascular events and death in patients with coronary artery disease: results from the AtheroGene Study. Circ Res 2005;97:e53-e59.
-
(2005)
Circ Res
, vol.97
-
-
Schnabel, R.1
Blankenberg, S.2
Lubos, E.3
Lackner, K.J.4
Rupprecht, H.J.5
Espinola-Klein, C.6
Jachmann, N.7
Post, F.8
Peetz, D.9
Bickel, C.10
Cambien, F.11
Tiret, L.12
Munzel, T.13
-
22
-
-
1942438521
-
Asymmetrical dimethylarginine: The Uber marker?
-
Cooke JP: Asymmetrical dimethylarginine: the Uber marker? Circulation 2004;109:1813-1818.
-
(2004)
Circulation
, vol.109
, pp. 1813-1818
-
-
Cooke, J.P.1
-
23
-
-
0034738138
-
Prevention of rat cerebral aneurysm formation by inhibition of nitric oxide synthase
-
Fukuda S, Hashimoto N, Naritomi H, Nagata I, Nozaki K, Kondo S, Kurino M, Kikuchi H: Prevention of rat cerebral aneurysm formation by inhibition of nitric oxide synthase. Circulation 2000;101:2532-2538.
-
(2000)
Circulation
, vol.101
, pp. 2532-2538
-
-
Fukuda, S.1
Hashimoto, N.2
Naritomi, H.3
Nagata, I.4
Nozaki, K.5
Kondo, S.6
Kurino, M.7
Kikuchi, H.8
-
24
-
-
0344736983
-
Disruption of gene for inducible nitric oxide synthase reduces progression of cerebral aneurysms
-
Sadamasa N, Nozaki K, Hashimoto N: Disruption of gene for inducible nitric oxide synthase reduces progression of cerebral aneurysms. Stroke 2003;34:2980-2984.
-
(2003)
Stroke
, vol.34
, pp. 2980-2984
-
-
Sadamasa, N.1
Nozaki, K.2
Hashimoto, N.3
-
25
-
-
33746839621
-
The role of endothelial nitric oxide synthase (eNOS) genetic variants in European patients with intracranial aneurysms
-
Krex D, Fortun S, Kuhlisch E, Schackert HK, Schackert G: The role of endothelial nitric oxide synthase (eNOS) genetic variants in European patients with intracranial aneurysms. J Cereb Blood Flow Metab 2006;26:1250-1255.
-
(2006)
J Cereb Blood Flow Metab
, vol.26
, pp. 1250-1255
-
-
Krex, D.1
Fortun, S.2
Kuhlisch, E.3
Schackert, H.K.4
Schackert, G.5
-
26
-
-
33750994630
-
What is the significance of vascular hydrogen sulphide (H2S)?
-
O'Sullivan SE: What is the significance of vascular hydrogen sulphide (H2S)? Br J Pharmacol 2006;149:609-610.
-
(2006)
Br J Pharmacol
, vol.149
, pp. 609-610
-
-
O'Sullivan, S.E.1
-
27
-
-
34147122502
-
A functional 19-base pair deletion polymorphism of dihydrofolate reductase (DHFR) and risk of breast cancer in multivitamin users
-
Xu X, Gammon MD, Wetmur JG, Rao M, Gaudet MM, Teitelbaum SL, Britton JA, Neugut AI, Santella RM, Chen J: A functional 19-base pair deletion polymorphism of dihydrofolate reductase (DHFR) and risk of breast cancer in multivitamin users. Am J Clin Nutr 2007;85:1098-1102.
-
(2007)
Am J Clin Nutr
, vol.85
, pp. 1098-1102
-
-
Xu, X.1
Gammon, M.D.2
Wetmur, J.G.3
Rao, M.4
Gaudet, M.M.5
Teitelbaum, S.L.6
Britton, J.A.7
Neugut, A.I.8
Santella, R.M.9
Chen, J.10
-
28
-
-
0942290719
-
New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?
-
Johnson WG, Stenroos ES, Spychala JR, Chatkupt S, Ming SX, Buyske S: New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): a risk factor for spina bifida acting in mothers during pregnancy? Am J Med Genet A 2004;124:339-345.
-
(2004)
Am J Med Genet A
, vol.124
, pp. 339-345
-
-
Johnson, W.G.1
Stenroos, E.S.2
Spychala, J.R.3
Chatkupt, S.4
Ming, S.X.5
Buyske, S.6
-
29
-
-
15744388471
-
Common dihydrofolate reductase 19-base pair deletion allele: A novel risk factor for preterm delivery
-
Johnson WG, Scholl TO, Spychala JR, Buyske S, Stenroos ES, Chen X: Common dihydrofolate reductase 19-base pair deletion allele: a novel risk factor for preterm delivery. Am J Clin Nutr 2005;81:664-668.
-
(2005)
Am J Clin Nutr
, vol.81
, pp. 664-668
-
-
Johnson, W.G.1
Scholl, T.O.2
Spychala, J.R.3
Buyske, S.4
Stenroos, E.S.5
Chen, X.6
-
30
-
-
0023683407
-
Delivery of folates to the cytoplasm of MA104 cells is mediated by a surface membrane receptor that recycles
-
Kamen BA, Wang MT, Streckfuss AJ, Peryea X, Anderson RG: Delivery of folates to the cytoplasm of MA104 cells is mediated by a surface membrane receptor that recycles. J Biol Chem 1988;263:13602-13609.
-
(1988)
J Biol Chem
, vol.263
, pp. 13602-13609
-
-
Kamen, B.A.1
Wang, M.T.2
Streckfuss, A.J.3
Peryea, X.4
Anderson, R.G.5
-
31
-
-
0033805360
-
A polymorphism (80G→A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia
-
Chango A, Emery-Fillon N, de Courcy GP, Lambert D, Pfister M, Rosenblatt DS, Nicolas JP: A polymorphism (80G→A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia. Mol Genet Metab 2000;70:310-315.
-
(2000)
Mol Genet Metab
, vol.70
, pp. 310-315
-
-
Chango, A.1
Emery-Fillon, N.2
de Courcy, G.P.3
Lambert, D.4
Pfister, M.5
Rosenblatt, D.S.6
Nicolas, J.P.7
|