-
1
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis, G. R., Cardon, L. R., & Cookson, W. O. (2000). A general test of association for quantitative traits in nuclear families. American Journal of Human Genetics, 66, 279-292.
-
(2000)
American Journal of Human Genetics
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
2
-
-
25444482801
-
Speeding disease gene discovery by sequence based candidate prioritization
-
Adie, E. J., Adams, R. R., Evans, K. L., Porteous, D. J. & Pickard, B. S. (2005). Speeding disease gene discovery by sequence based candidate prioritization. BMC Bioinformatics, 6, 55.
-
(2005)
BMC Bioinformatics
, vol.6
, pp. 55
-
-
Adie, E.J.1
Adams, R.R.2
Evans, K.L.3
Porteous, D.J.4
Pickard, B.S.5
-
3
-
-
33646568805
-
Gene prioritization through genomic data fusion
-
Aerts, S., Lambrechts, D., Maity, S., Van Loo, P., Coessens, B., De Smet, F., Tranchevent, L. C., De Moor, B., Marynen, P., Hassan, B., Carmeliet, P., & Moreau, Y. (2006). Gene prioritization through genomic data fusion. Nature Biotechnology, 24, 719.
-
(2006)
Nature Biotechnology
, vol.24
, pp. 719
-
-
Aerts, S.1
Lambrechts, D.2
Maity, S.3
Van Loo, P.4
Coessens, B.5
De Smet, F.6
Tranchevent, L.C.7
De Moor, B.8
Marynen, P.9
Hassan, B.10
Carmeliet, P.11
Moreau, Y.12
-
4
-
-
2442604715
-
The genetic association database
-
Becker, K. G., Barnes, K. C., Bright, T. J., & Wang, S. A. (2004). The genetic association database. Nature Genetics, 36, 431-432.
-
(2004)
Nature Genetics
, vol.36
, pp. 431-432
-
-
Becker, K.G.1
Barnes, K.C.2
Bright, T.J.3
Wang, S.A.4
-
5
-
-
33644873668
-
-
Blake, J. A., Eppig, J. T., Bult, C. J., Kadin, J. A., Richardson, J. E. ; Mouse Genome Database Group. (2006). The Mouse Genome Database (MGD): Updates and enhancements. Nucleic Acids Research, 34(Database issue), D562-567.
-
Blake, J. A., Eppig, J. T., Bult, C. J., Kadin, J. A., Richardson, J. E. ; Mouse Genome Database Group. (2006). The Mouse Genome Database (MGD): Updates and enhancements. Nucleic Acids Research, 34(Database issue), D562-567.
-
-
-
-
6
-
-
0034978141
-
Genetic association studies of schizophrenia using the 8p21-22 genes: Prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1)
-
Blaveri, E., Kalsi, G., Lawrence, J., Quested, D., Moorey, H., Lamb, G., Kohen, D., Shiwach, R., Chowdhury, U., Curtis, D., McQuillin, A., Gramoustianou, E. S., Sc Curling, H. M. (2001). Genetic association studies of schizophrenia using the 8p21-22 genes: Prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1). European Journal of Human Genetics, 9, 469-472.
-
(2001)
European Journal of Human Genetics
, vol.9
, pp. 469-472
-
-
Blaveri, E.1
Kalsi, G.2
Lawrence, J.3
Quested, D.4
Moorey, H.5
Lamb, G.6
Kohen, D.7
Shiwach, R.8
Chowdhury, U.9
Curtis, D.10
McQuillin, A.11
Gramoustianou, E.S.12
Sc Curling, H.M.13
-
7
-
-
0036933302
-
Distribution, markers, and functions of retinal microglia
-
Chen, L., Yang, P., & Kijlstra, A. (2002). Distribution, markers, and functions of retinal microglia. Ocular immunology and inflammation, 10, 27-39.
-
(2002)
Ocular immunology and inflammation
, vol.10
, pp. 27-39
-
-
Chen, L.1
Yang, P.2
Kijlstra, A.3
-
8
-
-
2942722427
-
A novel permutation testing method implicates sixteen nicotinic acetylcholine receptor genes as risk factors for smoking in schizophrenia families
-
Faraone ,S. V., Su, J., Taylor, L., Wilcox, M., Van Eerdewegh, P., Tsuang, M. T. (2004). A novel permutation testing method implicates sixteen nicotinic acetylcholine receptor genes as risk factors for smoking in schizophrenia families. Human Heredity 57, 59-68.
-
(2004)
Human Heredity
, vol.57
, pp. 59-68
-
-
Faraone, S.V.1
Su, J.2
Taylor, L.3
Wilcox, M.4
Van Eerdewegh, P.5
Tsuang, M.T.6
-
9
-
-
33646884801
-
Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. American Journal of Human Genetics, 78, 1011-1025
-
Apr 1025
-
Franke, L., Bakel, H., Fokkens, L., de Jong, E. D., Egmont-Petersen, M., & Wijmenga, C. (2006). Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. American Journal of Human Genetics, 78, 1011-1025. Epub 2006 Apr 1025.
-
(2006)
Epub
, pp. 2006
-
-
Franke, L.1
Bakel, H.2
Fokkens, L.3
de Jong, E.D.4
Egmont-Petersen, M.5
Wijmenga, C.6
-
10
-
-
0037146578
-
Finding genes that underlie complex traits
-
Glazier, A. M., Nadeau, J. H.,& Aitman, T. J .(2002). Finding genes that underlie complex traits. Science, 298, 2345-2349.
-
(2002)
Science
, vol.298
, pp. 2345-2349
-
-
Glazier, A.M.1
Nadeau, J.H.2
Aitman, T.J.3
-
11
-
-
31144432293
-
Literature mining for the biologist: From information retrieval to biological discovery
-
Jensen, L. J., Saric, J., & Bork, P. (2006 ). Literature mining for the biologist: From information retrieval to biological discovery. Nature Review, Genetics, 7, 119-129.
-
(2006)
Nature Review, Genetics
, vol.7
, pp. 119-129
-
-
Jensen, L.J.1
Saric, J.2
Bork, P.3
-
12
-
-
34247599549
-
Regulation of progesterone receptor signaling by BRCA1 in mammary cancer
-
Katiyar, P., Ma,Y., Fan, S., Pestell, R. G., Furth, P. A., & Rosen, E. M. (2006). Regulation of progesterone receptor signaling by BRCA1 in mammary cancer. Nuclear Receptor Signaling, 4, e006.
-
(2006)
Nuclear Receptor Signaling
, vol.4
-
-
Katiyar, P.1
Ma, Y.2
Fan, S.3
Pestell, R.G.4
Furth, P.A.5
Rosen, E.M.6
-
13
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J. Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., Bracken, M. B., Ferris, F. L., Ott, J., Barnstable, C., & Hoh, J. (2005). Complement factor H polymorphism in age-related macular degeneration. Science, 308, 385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.Y.4
Sackler, R.S.5
Haynes, C.6
Henning, A.K.7
SanGiovanni, J.P.8
Mane, S.M.9
Mayne, S.T.10
Bracken, M.B.11
Ferris, F.L.12
Ott, J.13
Barnstable, C.14
Hoh, J.15
-
14
-
-
0032870671
-
Elevated plasma gelatinase A (MMP-2) activity is associated with quiescent Crohn's Disease
-
Kossakowska, A. E., Medlicott, S. A., Edwards, D. R., Guyn, L., Stabbler, A. L., Sutherland, L. R., & Urbanski, S. J. (1999). Elevated plasma gelatinase A (MMP-2) activity is associated with quiescent Crohn's Disease. Annals of the New York Academy of Sciences, 878, 578-580.
-
(1999)
Annals of the New York Academy of Sciences
, vol.878
, pp. 578-580
-
-
Kossakowska, A.E.1
Medlicott, S.A.2
Edwards, D.R.3
Guyn, L.4
Stabbler, A.L.5
Sutherland, L.R.6
Urbanski, S.J.7
-
15
-
-
0038478096
-
Semantic similarity measures as tools for exploring the gene ontology
-
Lord, P. W., Stevens, R. D., Brass, A., & Goble, C. A. (2003). Semantic similarity measures as tools for exploring the gene ontology. Pacific Symposium on Biocomputing. 601-612.
-
(2003)
Pacific Symposium on Biocomputing
, pp. 601-612
-
-
Lord, P.W.1
Stevens, R.D.2
Brass, A.3
Goble, C.A.4
-
16
-
-
37349065439
-
-
McKusick-Nathans Institute for Genetic Medicine, J.H.U.B., MD and National Center for Biotechnology Information. Accessed using PosMed: May 25, 2006 (breast cancer), 12 June 2006 (Crohn's disease), June 14, 2006 (schizophrenia) and July 11, 2006 (macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders above).
-
McKusick-Nathans Institute for Genetic Medicine, J.H.U.B., MD and National Center for Biotechnology Information. Accessed using PosMed: May 25, 2006 (breast cancer), 12 June 2006 (Crohn's disease), June 14, 2006 (schizophrenia) and July 11, 2006 (macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders above).
-
-
-
-
17
-
-
33644873830
-
Clinical value of gene NOD2/CARD15 mutations in Crohn's disease
-
Mendoza, J. L., & Taxonera, C. (2005). Clinical value of gene NOD2/CARD15 mutations in Crohn's disease, Revista Espanola de Enfermades Digestivas, 97, 541-546.
-
(2005)
Revista Espanola de Enfermades Digestivas
, vol.97
, pp. 541-546
-
-
Mendoza, J.L.1
Taxonera, C.2
-
18
-
-
0142216223
-
Genetic epidemiology, genetic maps and positional cloning
-
Morton, N. (2003). Genetic epidemiology, genetic maps and positional cloning, Philosophical Transactions of the Royal Society of London, Series B, Biological Science, 358, 1701-1708.
-
(2003)
Philosophical Transactions of the Royal Society of London, Series B, Biological Science
, vol.358
, pp. 1701-1708
-
-
Morton, N.1
-
19
-
-
0037251964
-
-
Mulder, N. J., Aweiler, R., Attwood, T. K., Bairoch, A., Barrell, D., Bateman, A., Binns, D., Biswas, M., Bradley, P., Bork, P., Bucher, P., Copley, R. R., Courcelle, E., Das, U., Durbin, R., Falquet, L., Fleischmann, W., Griffiths-Jones, S., Haft, D., Harte, N., Hulo, N., Kahn, D., Kanapin, A., Krestyaninova, M., Lopez, R., Letunic, I., Lonsdale, D., Silventoinen, V., Orchard, S. E., Pagni, M., Peyruc, D., Ponting, C. P., Selengut, J. D., Servant, F., Sigrist, C. J., Vaughan, R., & Zdobnov, E. M. (2003). The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Research, 31, 315-318.
-
Mulder, N. J., Aweiler, R., Attwood, T. K., Bairoch, A., Barrell, D., Bateman, A., Binns, D., Biswas, M., Bradley, P., Bork, P., Bucher, P., Copley, R. R., Courcelle, E., Das, U., Durbin, R., Falquet, L., Fleischmann, W., Griffiths-Jones, S., Haft, D., Harte, N., Hulo, N., Kahn, D., Kanapin, A., Krestyaninova, M., Lopez, R., Letunic, I., Lonsdale, D., Silventoinen, V., Orchard, S. E., Pagni, M., Peyruc, D., Ponting, C. P., Selengut, J. D., Servant, F., Sigrist, C. J., Vaughan, R., & Zdobnov, E. M. (2003). The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Research, 31, 315-318.
-
-
-
-
20
-
-
37349097636
-
-
NCBI Entrez Gene Database - PubMed. Accessed using PosMed: May 25, 2006 (breast cancer); June 12, 2006 (Crohn's disease); June 14, 2006 (schizophrenia); July 11, 2006 (Macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders previously listed).
-
NCBI Entrez Gene Database - PubMed. Accessed using PosMed: May 25, 2006 (breast cancer); June 12, 2006 (Crohn's disease); June 14, 2006 (schizophrenia); July 11, 2006 (Macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders previously listed).
-
-
-
-
21
-
-
37349023895
-
-
Online Mendelian Inheritance in Man, OMIM (TM). National Library of Medicine (Bethesda, MD). Accessed using PosMed: May 25, 2006 (breast cancer); June 12, 2006 (Crohn's disease); June 14, 2006 (schizophrenia); July 11, 2006 (macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders previously listed).
-
Online Mendelian Inheritance in Man, OMIM (TM). National Library of Medicine (Bethesda, MD). Accessed using PosMed: May 25, 2006 (breast cancer); June 12, 2006 (Crohn's disease); June 14, 2006 (schizophrenia); July 11, 2006 (macular degeneration). GeneSniffer accessed the database August 20, 2006 (all of the disorders previously listed).
-
-
-
-
22
-
-
0033967692
-
Introducing RefSeq and LocusLink: Curated human genome resources at the NCBI
-
Pruitt, K. D., Katz, K. S., Sicotte, H., & Maglott, D. R. (2000). Introducing RefSeq and LocusLink: Curated human genome resources at the NCBI. Trends in Genetics, 16, 44-47.
-
(2000)
Trends in Genetics
, vol.16
, pp. 44-47
-
-
Pruitt, K.D.1
Katz, K.S.2
Sicotte, H.3
Maglott, D.R.4
-
23
-
-
0031008841
-
Microsatellite instability and loss of heterozygosity in primary breast tumours
-
Sourvinos, G., Kiaris, H., Tsikkinis, A., Vassilaros, S., & Spandidos, D. A. (1997). Microsatellite instability and loss of heterozygosity in primary breast tumours. Tumour Biology, 18, 157-166.
-
(1997)
Tumour Biology
, vol.18
, pp. 157-166
-
-
Sourvinos, G.1
Kiaris, H.2
Tsikkinis, A.3
Vassilaros, S.4
Spandidos, D.A.5
-
24
-
-
0013375948
-
-
Stefansson, H., Sigurdsson, E., Steinthorsdottir, V., Bjornsdottir, S., Sigmundsson, T., Ghosh, S., Brynjolfsson, J., Gunnarsdottir, S., Ivarsson, O., Chou, T. T., Hjaltason, O., Birgisdottir, B., Jonsson, H., Gudnadottir, V. G., Gudmundsdottir, E., Bjornsson, A., Ingvarsson, B., Ingason, A., Sigfusson, S., Hardardottir, H., Harvey, R. P., Lai, D., Zhou, M., Brunner, D., Mutel, V., Gonzalo, A., Lemke, G., Sainz, J., Johannesson, G., Andresson, T., Gudbjartsson, D., Manolescu, A., Frigge, M. L., Gurney, M. E., Kong, A., Gulcher, J. R., Petursson, H., & Stefansson, K. (2002). Neuregulin 1 and susceptibility to schizophrenia. American Journal of Human Genetics, 71, 877-892. Epub 2002, July 23.
-
Stefansson, H., Sigurdsson, E., Steinthorsdottir, V., Bjornsdottir, S., Sigmundsson, T., Ghosh, S., Brynjolfsson, J., Gunnarsdottir, S., Ivarsson, O., Chou, T. T., Hjaltason, O., Birgisdottir, B., Jonsson, H., Gudnadottir, V. G., Gudmundsdottir, E., Bjornsson, A., Ingvarsson, B., Ingason, A., Sigfusson, S., Hardardottir, H., Harvey, R. P., Lai, D., Zhou, M., Brunner, D., Mutel, V., Gonzalo, A., Lemke, G., Sainz, J., Johannesson, G., Andresson, T., Gudbjartsson, D., Manolescu, A., Frigge, M. L., Gurney, M. E., Kong, A., Gulcher, J. R., Petursson, H., & Stefansson, K. (2002). Neuregulin 1 and susceptibility to schizophrenia. American Journal of Human Genetics, 71, 877-892. Epub 2002, July 23.
-
-
-
-
25
-
-
0037903275
-
Human Gene Mutation Database (HGMD): 2003 update
-
Stenson, P. D., Ball, E. V., Mort, M., Phillips, A. D., Shiel, J. A., Thomas, N. S., Abeysinghe, S., Krawczak, M., Sc Cooper, D. N. (2003). Human Gene Mutation Database (HGMD): 2003 update. Human Mutation, 21, 577-581.
-
(2003)
Human Mutation
, vol.21
, pp. 577-581
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shiel, J.A.5
Thomas, N.S.6
Abeysinghe, S.7
Krawczak, M.8
Sc Cooper, D.N.9
-
26
-
-
33745154860
-
Computational disease gene identification: A concert of methods prioritizes type 2 diabetes and obesity candidate genes
-
Tiffin, N., Adie, E., Turner, F., Brunner, H. G., van Driel, M. A., Od, M., Lopez-Bigas, N., Ouzounis, C., Perez-Iratxeta, C., Andrade-Navarro, M. A., Adeyemo, A., Patti, M. E., Semple, C. A., & Hide, W. (2006). Computational disease gene identification: A concert of methods prioritizes type 2 diabetes and obesity candidate genes. Nucleic Acids Research, 34, 3067-3081.
-
(2006)
Nucleic Acids Research
, vol.34
, pp. 3067-3081
-
-
Tiffin, N.1
Adie, E.2
Turner, F.3
Brunner, H.G.4
van Driel, M.A.5
Od, M.6
Lopez-Bigas, N.7
Ouzounis, C.8
Perez-Iratxeta, C.9
Andrade-Navarro, M.A.10
Adeyemo, A.11
Patti, M.E.12
Semple, C.A.13
Hide, W.14
-
27
-
-
15044341082
-
Integration of text- and data-mining using ontologies successfully selects disease gene candidates
-
Tiffin, N., Kelso, J. F., Powell, A. R., Pan, H., Bajic, V. B., & Hide, W. A. (2005). Integration of text- and data-mining using ontologies successfully selects disease gene candidates. Nucleic Acids Research, 33, 1544-1552.
-
(2005)
Nucleic Acids Research
, vol.33
, pp. 1544-1552
-
-
Tiffin, N.1
Kelso, J.F.2
Powell, A.R.3
Pan, H.4
Bajic, V.B.5
Hide, W.A.6
-
28
-
-
24344433989
-
Association between the neuregulin 1 gene and schizophrenia: A systematic review
-
Tosato, S., Dazzan, P., & Collier, D. (2005). Association between the neuregulin 1 gene and schizophrenia: A systematic review. Schizophrenia Bulletin, 31, 613-617.
-
(2005)
Schizophrenia Bulletin
, vol.31
, pp. 613-617
-
-
Tosato, S.1
Dazzan, P.2
Collier, D.3
-
29
-
-
3142742711
-
Prediction of the confidence interval of QTL location
-
Visscher, P. M., & Goddard, M. E. (2004). Prediction of the confidence interval of QTL location. Behavior Genetics, 34, 477-482.
-
(2004)
Behavior Genetics
, vol.34
, pp. 477-482
-
-
Visscher, P.M.1
Goddard, M.E.2
-
30
-
-
3543130803
-
Lack of a genetic association between the frizzled-3 gene and schizophrenia in a British population
-
Wei, J. & Hemmings, G. P. (2004). Lack of a genetic association between the frizzled-3 gene and schizophrenia in a British population. Neuroscience Letter, 366, 336-338.
-
(2004)
Neuroscience Letter
, vol.366
, pp. 336-338
-
-
Wei, J.1
Hemmings, G.P.2
-
31
-
-
3342964099
-
Positive association of the human frizzled 3 (FZD3) gene haplotype with schizophrenia in Chinese Han population
-
Zhang, Y., Yu, X., Yuan, Y., Ling, Y., Ruan, Y., Si, T., Lu, T., Wu, S., Gong, X., Zhu, Z., Yang, J., Wang, F., & Zhang, D. (2004). Positive association of the human frizzled 3 (FZD3) gene haplotype with schizophrenia in Chinese Han population. American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics. 129, 16-19.
-
(2004)
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
, vol.129
, pp. 16-19
-
-
Zhang, Y.1
Yu, X.2
Yuan, Y.3
Ling, Y.4
Ruan, Y.5
Si, T.6
Lu, T.7
Wu, S.8
Gong, X.9
Zhu, Z.10
Yang, J.11
Wang, F.12
Zhang, D.13
|