-
1
-
-
70149115051
-
Understanding abdominal aortic aneurysm
-
doi:10.1056/NEJMcibr0905244
-
Weintraub, N. L. (2009). Understanding abdominal aortic aneurysm. The New England Journal of Medicine, 361(11), 1114-1116. doi:10.1056/NEJMcibr0905244.
-
(2009)
The New England Journal of Medicine
, vol.361
, Issue.11
, pp. 1114-1116
-
-
Weintraub, N.L.1
-
2
-
-
0022518005
-
Familial tendency for abdominal aortic aneurysms
-
DOI 10.1001/jama.256.14.1934
-
Johansen, K., & Koepsell, T. (1986). Familial tendency for abdominal aortic aneurysms. Journal of the American Medical Association, 256(14), 1934-1936. (Pubitemid 16033398)
-
(1986)
Journal of the American Medical Association
, vol.256
, Issue.14
, pp. 1934-1936
-
-
Johansen, K.1
Koepsell, T.2
-
3
-
-
0037368507
-
Abdominal aortic aneurysm: An illustrated narrative review
-
DOI 10.1016/S0161-4754(02)54111-7
-
Crawford, C. M., Hurtgen-Grace, K., Talarico, E., & Marley, J. (2003). Abdominal aortic aneurysm: an illustrated narrative review. Journal of Manipulative and Physiological Therapeutics, 26(3), 184-195. doi:10.1016/S0161-4754 (02) 54111-7. (Pubitemid 36506197)
-
(2003)
Journal of Manipulative and Physiological Therapeutics
, vol.26
, Issue.3
, pp. 184-195
-
-
Crawford, C.M.1
Hurtgen-Grace, K.2
Talarico, E.3
Marley, J.4
-
4
-
-
13244259140
-
Risk factors for asymptomatic abdominal aortic aneurysm: Sytematic review and meta-analysis of population-based screening studies
-
DOI 10.1093/eurpub/14.4.343
-
Cornuz, J., Sidoti Pinto, C., Tevaearai, H., & Egger, M. (2004). Risk factors for asymptomatic abdominal aortic aneurysm: systematic review and meta-analysis of population-based screening studies. European Journal of Public Health, 14(4), 343-349. doi:10.1093/eurpub/14.4.343. (Pubitemid 40186442)
-
(2004)
European Journal of Public Health
, vol.14
, Issue.4
, pp. 343-349
-
-
Cornuz, J.1
Pinto, C.S.2
Tevaearai, H.3
Egger, M.4
-
5
-
-
0031254213
-
Diagnosis and treatment of diseases of the aorta
-
Lindsay, J., Jr. (1997). Diagnosis and treatment of diseases of the aorta. Current Problems in Cardiology, 22(10), 485-542. doi:S0146-2806 (97) 80004-7. (Pubitemid 127703807)
-
(1997)
Current Problems in Cardiology
, vol.22
, Issue.10
, pp. 485-542
-
-
Lindsay Jr., J.1
-
6
-
-
72549087148
-
Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population
-
doi:10.1016/j. jvs.2009.08.036. discussion 7
-
Wahlgren, C. M., Larsson, E., Magnusson, P. K., Hultgren, R., & Swedenborg, J. (2010). Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population. Journal of Vascular Surgery, 51(1), 3-7. doi:10.1016/j. jvs.2009.08.036. discussion 7.
-
(2010)
Journal of Vascular Surgery
, vol.51
, Issue.1
, pp. 3-7
-
-
Wahlgren, C.M.1
Larsson, E.2
Magnusson, P.K.3
Hultgren, R.4
Swedenborg, J.5
-
7
-
-
27644586450
-
The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: An analysis of 187 aneurysm families in Nova Scotia, Canada
-
DOI 10.1016/j.jvs.2005.08.002, PII S0741521405012516
-
Ogata, T., MacKean, G. L., Cole, C. W., Arthur, C., Andreou, P., Tromp, G., et al. (2005). The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: an analysis of 187 aneurysm families in Nova Scotia, Canada. Journal of Vascular Surgery, 42(5), 891-897. doi:10.1016/j.jvs.2005.08.002. (Pubitemid 41571954)
-
(2005)
Journal of Vascular Surgery
, vol.42
, Issue.5
, pp. 891-897
-
-
Ogata, T.1
MacKean, G.L.2
Cole, C.W.3
Arthur, C.4
Andreou, P.5
Tromp, G.6
Kuivaniemi, H.7
-
8
-
-
2442493147
-
Genome Scan for Familial Abdominal Aortic Aneurysm Using Sex and Family History as Covariates Suggests Genetic Heterogeneity and Identifies Linkage to Chromosome 19q13
-
DOI 10.1161/01.CIR.0000127857.77161.A1
-
Shibamura, H., Olson, J. M., van Vlijmen-Van, K. C., Buxbaum, S. G., Dudek, D. M., Tromp, G., et al. (2004). Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation, 109(17), 2103-2108. doi:10.1161/01. CIR.0000127857.77161. A1. (Pubitemid 38620219)
-
(2004)
Circulation
, vol.109
, Issue.17
, pp. 2103-2108
-
-
Shibamura, H.1
Olson, J.M.2
Van Vlijmen-Van Keulen, C.3
Buxbaum, S.G.4
Dudek, D.M.5
Tromp, G.6
Ogata, T.7
Skunca, M.8
Sakalihasan, N.9
Pals, G.10
Limet, R.11
MacKean, G.L.12
Defawe, O.13
Verloes, A.14
Arthur, C.15
Lossing, A.G.16
Burnett, M.17
Sueda, T.18
Kuivaniemi, H.19
-
9
-
-
20144381543
-
Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3
-
DOI 10.1016/j.ejvs.2004.12.029, PII S1078588404006045
-
Van Vlijmen-Van Keulen, C. J., Rauwerda, J. A., & Pals, G. (2005). Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3. European Journal of Vascular and Endovascular Surgery, 30(1), 29-35. doi:10.1016/j.ejvs.2004.12.029. (Pubitemid 40775129)
-
(2005)
European Journal of Vascular and Endovascular Surgery
, vol.30
, Issue.1
, pp. 29-35
-
-
Van Vlijmen-Van Keulen, C.J.1
Rauwerda, J.A.2
Pals, G.3
-
10
-
-
77949897640
-
Association study of single nucleotide polymorphisms on chromosome 19q13 with abdominal aortic aneurysm
-
doi:10.1177/0003319709354752
-
Baas, A. F., Medic, J., van't Slot, R., de Vries, J. P., van Sambeek, M. R., Geelkerken, B. H., et al. (2010). Association study of single nucleotide polymorphisms on chromosome 19q13 with abdominal aortic aneurysm. Angiology, 61(3), 243-247. doi:10.1177/0003319709354752.
-
(2010)
Angiology
, vol.61
, Issue.3
, pp. 243-247
-
-
Baas, A.F.1
Medic, J.2
Van't Slot, R.3
De Vries, J.P.4
Van Sambeek, M.R.5
Geelkerken, B.H.6
-
11
-
-
38649091662
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
-
DOI 10.1038/ng.72, PII NG72
-
Helgadottir, A., Thorleifsson, G., Magnusson, K. P., Gretarsdottir, S., Steinthorsdottir, V., Manolescu, A., et al. (2008). The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nature Genetics, 40(2), 217-224. doi:10.1038/ng.72. (Pubitemid 351171400)
-
(2008)
Nature Genetics
, vol.40
, Issue.2
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
Gretarsdottir, S.4
Steinthorsdottir, V.5
Manolescu, A.6
Jones, G.T.7
Rinkel, G.J.E.8
Blankensteijn, J.D.9
Ronkainen, A.10
Jaaskelainen, J.E.11
Kyo, Y.12
Lenk, G.M.13
Sakalihasan, N.14
Kostulas, K.15
Gottsater, A.16
Flex, A.17
Stefansson, H.18
Hansen, T.19
Andersen, G.20
Weinsheimer, S.21
Borch-Johnsen, K.22
Jorgensen, T.23
Shah, S.H.24
Quyyumi, A.A.25
Granger, C.B.26
Reilly, M.P.27
Austin, H.28
Levey, A.I.29
Vaccarino, V.30
Palsdottir, E.31
Walters, G.B.32
Jonsdottir, T.33
Snorradottir, S.34
Magnusdottir, D.35
Gudmundsson, G.36
Ferrell, R.E.37
Sveinbjornsdottir, S.38
Hernesniemi, J.39
Niemela, M.40
Limet, R.41
Andersen, K.42
Sigurdsson, G.43
Benediktsson, R.44
Verhoeven, E.L.G.45
Teijink, J.A.W.46
Grobbee, D.E.47
Rader, D.J.48
Collier, D.A.49
Pedersen, O.50
Pola, R.51
Hillert, J.52
Lindblad, B.53
Valdimarsson, E.M.54
Magnadottir, H.B.55
Wijmenga, C.56
Tromp, G.57
Baas, A.F.58
Ruigrok, Y.M.59
Van Rij, A.M.60
Kuivaniemi, H.61
Powell, J.T.62
Matthiasson, S.E.63
Gulcher, J.R.64
Thorgeirsson, G.65
Kong, A.66
Thorsteinsdottir, U.67
Stefansson, K.68
more..
-
12
-
-
66149112940
-
Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association
-
doi:10.1016/j.jvs.2009.01.041
-
Elmore, J. R., Obmann, M. A., Kuivaniemi, H., Tromp, G., Gerhard, G. S., Franklin, D. P., et al. (2009). Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association. Journal of Vascular Surgery, 49(6), 1525-1531. doi:10.1016/j.jvs.2009.01.041.
-
(2009)
Journal of Vascular Surgery
, vol.49
, Issue.6
, pp. 1525-1531
-
-
Elmore, J.R.1
Obmann, M.A.2
Kuivaniemi, H.3
Tromp, G.4
Gerhard, G.S.5
Franklin, D.P.6
-
13
-
-
84947899513
-
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
-
doi:10.1038/ng.622
-
Gretarsdottir, S., Baas, A. F., Thorleifsson, G., Holm, H., den Heijer, M., de Vries, J. P., et al. (2010). Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nature Genetics, 42(8), 692-697. doi:10.1038/ng.622.
-
(2010)
Nature Genetics
, vol.42
, Issue.8
, pp. 692-697
-
-
Gretarsdottir, S.1
Baas, A.F.2
Thorleifsson, G.3
Holm, H.4
Heijer, D.M.5
De Vries, J.P.6
-
14
-
-
78650226181
-
Abdominal aortic aneurysm: A review of the genetic basis
-
doi:10.1177/0003319710373092
-
Saratzis, A., Abbas, A., Kiskinis, D., Melas, N., Saratzis, N., & Kitas, G. D. (2010). Abdominal aortic aneurysm: a review of the genetic basis. Angiology. doi:10.1177/0003319710373092.
-
(2010)
Angiology
-
-
Saratzis, A.1
Abbas, A.2
Kiskinis, D.3
Melas, N.4
Saratzis, N.5
Kitas, G.D.6
-
15
-
-
74449083978
-
Association of the TGF-beta receptor genes with abdominal aortic aneurysm
-
doi:10.1038/ejhg.2009.141
-
Baas, A. F., Medic, J., van't Slot, R., de Kovel, C. G., Zhernakova, A., Geelkerken, R. H., et al. (2010). Association of the TGF-beta receptor genes with abdominal aortic aneurysm. European Journal of Human Genetics, 18(2), 240-244. doi:10.1038/ejhg.2009.141.
-
(2010)
European Journal of Human Genetics
, vol.18
, Issue.2
, pp. 240-244
-
-
Baas, A.F.1
Medic, J.2
Van't Slot, R.3
De Kovel, C.G.4
Zhernakova, A.5
Geelkerken, R.H.6
-
16
-
-
78650084232
-
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
-
International HIV Controllers Study
-
International HIV Controllers Study, Pereyra, F., Jia, X., McLaren, P. J., et al. (2010). The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science, 330(6010), 1551-1557.
-
(2010)
Science
, vol.330
, Issue.6010
, pp. 1551-1557
-
-
Pereyra, F.1
Jia, X.2
McLaren, P.J.3
-
17
-
-
44349132708
-
Common and rare variants in multifactorial susceptibility to common diseases
-
DOI 10.1038/ng.f.136, PII NGF136
-
Bodmer, W., & Bonilla, C. (2008). Common and rare variants in multifactorial susceptibility to common diseases. Nature Genetics, 40(6), 695-701. doi:10.1038/ng.f.136. (Pubitemid 351748875)
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 695-701
-
-
Bodmer, W.1
Bonilla, C.2
-
18
-
-
78649484216
-
A de novo paradigm for mental retardation
-
doi:10.1038/ng.712
-
Vissers, L. E., de Ligt, J., Gilissen, C., Janssen, I., Steehouwer, M., de Vries, P., et al. (2010). A de novo paradigm for mental retardation. Nature Genetics, 42(12), 1109-1112. doi:10.1038/ng.712.
-
(2010)
Nature Genetics
, vol.42
, Issue.12
, pp. 1109-1112
-
-
Vissers, L.E.1
De Ligt, J.2
Gilissen, C.3
Janssen, I.4
Steehouwer, M.5
De Vries, P.6
-
19
-
-
77954091424
-
Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries
-
doi:10.1093/nar/gkq072
-
Mokry, M., Feitsma, H., Nijman, I. J., de Bruijn, E., van der Zaag, P. J., Guryev, V., et al. (2010). Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries. Nucleic Acids Research, 38(10), e116. doi:10.1093/nar/gkq072.
-
(2010)
Nucleic Acids Research
, vol.38
, Issue.10
-
-
Mokry, M.1
Feitsma, H.2
Nijman, I.J.3
De Bruijn, E.4
Van Der Zaag, P.J.5
Guryev, V.6
-
20
-
-
78049321160
-
Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples
-
doi:10.1038/nmeth.1516
-
Nijman, I. J., Mokry, M., van Boxtel, R., Toonen, P., de Bruijn, E., & Cuppen, E. (2010). Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples. Nature Methods, 7(11), 913-915. doi:10.1038/nmeth.1516.
-
(2010)
Nature Methods
, vol.7
, Issue.11
, pp. 913-915
-
-
Nijman, I.J.1
Mokry, M.2
Van Boxtel, R.3
Toonen, P.4
De Bruijn, E.5
Cuppen, E.6
-
21
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
doi:10.1093/bioinformatics/btp324
-
Li, H., & Durbin, R. (2009). Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25(14), 1754-1760. doi:10.1093/bioinformatics/btp324.
-
(2009)
Bioinformatics
, vol.25
, Issue.14
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
22
-
-
78651392567
-
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome
-
doi:10.1038/ejhg.2010.144
-
Krumbiegel, M., Pasutto, F., Schlotzer-Schrehardt, U., Uebe, S., Zenkel, M., Mardin, C. Y., et al. (2010). Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics. doi:10.1038/ejhg.2010.144.
-
(2010)
European Journal of Human Genetics
-
-
Krumbiegel, M.1
Pasutto, F.2
Schlotzer-Schrehardt, U.3
Uebe, S.4
Zenkel, M.5
Mardin, C.Y.6
-
23
-
-
67651180973
-
A genome-wide association study in 574 schizophrenia trios using DNA pooling
-
doi:10.1038/mp. 2008.33
-
Kirov, G., Zaharieva, I., Georgieva, L., Moskvina, V., Nikolov, I., Cichon, S., et al. (2009). A genome-wide association study in 574 schizophrenia trios using DNA pooling. Molecular Psychiatry, 14(8), 796-803. doi:10.1038/mp. 2008.33.
-
(2009)
Molecular Psychiatry
, vol.14
, Issue.8
, pp. 796-803
-
-
Kirov, G.1
Zaharieva, I.2
Georgieva, L.3
Moskvina, V.4
Nikolov, I.5
Cichon, S.6
-
24
-
-
68049148052
-
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
-
doi:10.1186/1755-8794-1-44
-
Abraham, R., Moskvina, V., Sims, R., Hollingworth, P., Morgan, A., Georgieva, L., et al. (2008). A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Medical Genomics, 1, 44. doi:10.1186/1755-8794-1-44.
-
(2008)
BMC Medical Genomics
, vol.1
, pp. 44
-
-
Abraham, R.1
Moskvina, V.2
Sims, R.3
Hollingworth, P.4
Morgan, A.5
Georgieva, L.6
-
25
-
-
77954202495
-
A statistical method for the detection of variants from next-generation resequencing of DNA pools
-
doi:10.1093/bioinformatics/btq214
-
Bansal, V. (2010). A statistical method for the detection of variants from next-generation resequencing of DNA pools. Bioinformatics, 26(12), i318-324. doi:10.1093/bioinformatics/btq214.
-
(2010)
Bioinformatics
, vol.26
, Issue.12
-
-
Bansal, V.1
-
26
-
-
77957606541
-
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
-
doi:10.1038/ng.659
-
Calvo, S. E., Tucker, E. J., Compton, A. G., Kirby, D. M., Crawford, G., Burtt, N. P., et al. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nature Genetics, 42(10), 851-858. doi:10.1038/ng.659.
-
(2010)
Nature Genetics
, vol.42
, Issue.10
, pp. 851-858
-
-
Calvo, S.E.1
Tucker, E.J.2
Compton, A.G.3
Kirby, D.M.4
Crawford, G.5
Burtt, N.P.6
-
27
-
-
78651255163
-
Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals
-
doi:10.1007/s00439-010-0902-8
-
Janssen, S., Ramaswami, G., Davis, E. E., Hurd, T., Airik, R., Kasanuki, J. M., et al. (2010). Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals. Human Genetics. doi:10.1007/s00439-010-0902-8.
-
(2010)
Human Genetics
-
-
Janssen, S.1
Ramaswami, G.2
Davis, E.E.3
Hurd, T.4
Airik, R.5
Kasanuki, J.M.6
-
28
-
-
79551634466
-
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
-
doi:10.1136/jmg.2010.082552
-
Otto, E. A., Ramaswami, G., Janssen, S., Chaki, M., Allen, S. J., Zhou, W., et al. (2010). Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy. Journal of Medical Genetics. doi:10.1136/jmg.2010.082552.
-
(2010)
Journal of Medical Genetics
-
-
Otto, E.A.1
Ramaswami, G.2
Janssen, S.3
Chaki, M.4
Allen, S.J.5
Zhou, W.6
|