-
1
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database
-
Allen NC, Bagade S, McQueen MB, Ioannidis JPA, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L. 2008. Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database. Nat Genet 40:827-834.
-
(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
Tanzi, R.E.7
Bertram, L.8
-
2
-
-
33845892752
-
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database
-
Bertram L, McQueen MB, Mullin K, Blacker D, Tanzi RE. 2007. Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. Nat Genet 39:17-23.
-
(2007)
Nat Genet
, vol.39
, pp. 17-23
-
-
Bertram, L.1
McQueen, M.B.2
Mullin, K.3
Blacker, D.4
Tanzi, R.E.5
-
3
-
-
80051959840
-
Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma
-
Chatzinasiou F, Lill CM, Kypreou K, Stefanaki I, Nicolaou V, Spyrou G, Evangelou E, Roehr JT, Kodela E, Katsambas A, Tsao H, Ioannidis JPA, et al. 2011. Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. J Natl Cancer Inst 103:1227-1235.
-
(2011)
J Natl Cancer Inst
, vol.103
, pp. 1227-1235
-
-
Chatzinasiou, F.1
Lill, C.M.2
Kypreou, K.3
Stefanaki, I.4
Nicolaou, V.5
Spyrou, G.6
Evangelou, E.7
Roehr, J.T.8
Kodela, E.9
Katsambas, A.10
Tsao, H.11
Ioannidis, J.P.A.12
-
4
-
-
77950440741
-
Has the revolution arrived?
-
Collins F. 2010. Has the revolution arrived? Nature 464:674-675.
-
(2010)
Nature
, vol.464
, pp. 674-675
-
-
Collins, F.1
-
5
-
-
34047165392
-
Recommendations of the 2006 Human Variome Project meeting
-
Cotton RGH, Appelbe W, Auerbach AD, Becker K, Bodmer W, Boone DJ, Boulyjenkov V, Brahmachari S, Brody L, Brookes A, Brown AF, Byers P, et al. 2007. Recommendations of the 2006 Human Variome Project meeting. Nat Genet 39:433-436.
-
(2007)
Nat Genet
, vol.39
, pp. 433-436
-
-
Cotton, R.G.H.1
Appelbe, W.2
Auerbach, A.D.3
Becker, K.4
Bodmer, W.5
Boone, D.J.6
Boulyjenkov, V.7
Brahmachari, S.8
Brody, L.9
Brookes, A.10
Brown, A.F.11
Byers, P.12
-
6
-
-
80052999290
-
Assessing and managing risk when sharing aggregate genetic variant data
-
Craig DW, Goor RM, Wang Z, Paschall J, Ostell J, Feolo M, Sherry ST, Manolio TA. 2011. Assessing and managing risk when sharing aggregate genetic variant data. Nat Rev Genet 12:730-736.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 730-736
-
-
Craig, D.W.1
Goor, R.M.2
Wang, Z.3
Paschall, J.4
Ostell, J.5
Feolo, M.6
Sherry, S.T.7
Manolio, T.A.8
-
7
-
-
0032408458
-
Molecular genetics of Alzheimer's disease
-
Cruts M, Van Broeckhoven C. 1998. Molecular genetics of Alzheimer's disease. Ann Med 30:560-565.
-
(1998)
Ann Med
, vol.30
, pp. 560-565
-
-
Cruts, M.1
Van Broeckhoven, C.2
-
8
-
-
56749171877
-
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update
-
Gijselinck I, Van Broeckhoven C, Cruts M. 2008. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update. Hum Mutat 29:1373-1386.
-
(2008)
Hum Mutat
, vol.29
, pp. 1373-1386
-
-
Gijselinck, I.1
Van Broeckhoven, C.2
Cruts, M.3
-
9
-
-
79951472909
-
Charting a course for genomic medicine from base pairs to bedside
-
Green ED, Guyer MS. 2011. Charting a course for genomic medicine from base pairs to bedside. Nature 470:204-213.
-
(2011)
Nature
, vol.470
, pp. 204-213
-
-
Green, E.D.1
Guyer, M.S.2
-
10
-
-
84555204803
-
Call for participation in the neurogenetics consortium within the Human Variome Project
-
Haworth A, Bertram L, Carrera P, Elson JL, Braastad CD, Cox DW, Cruts M, den Dunnen JT, Farrer MJ, Fink JK, Hamed SA, Houlden H, et al. 2011. Call for participation in the neurogenetics consortium within the Human Variome Project. Neurogenetics 12:169-173.
-
(2011)
Neurogenetics
, vol.12
, pp. 169-173
-
-
Haworth, A.1
Bertram, L.2
Carrera, P.3
Elson, J.L.4
Braastad, C.D.5
Cox, D.W.6
Cruts, M.7
den Dunnen, J.T.8
Farrer, M.J.9
Fink, J.K.10
Hamed, S.A.11
Houlden, H.12
-
11
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362-9367.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
12
-
-
50849101381
-
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
-
Homer N, Szelinger S, Redman M, Duggan D, Tembe W, Muehling J, Pearson JV, Stephan DA, Nelson SF, Craig DW. 2008. Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays. PLoS Genet 4:e1000167.
-
(2008)
PLoS Genet
, vol.4
-
-
Homer, N.1
Szelinger, S.2
Redman, M.3
Duggan, D.4
Tembe, W.5
Muehling, J.6
Pearson, J.V.7
Stephan, D.A.8
Nelson, S.F.9
Craig, D.W.10
-
13
-
-
70350632730
-
A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies
-
Jacobs KB, Yeager M, Wacholder S, Craig D, Kraft P, Hunter DJ, Paschal J, Manolio TA, Tucker M, Hoover RN, Thomas GD, Chanock SJ, Chatterjee N. 2009. A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies. Nat Genet 41:1253-1257.
-
(2009)
Nat Genet
, vol.41
, pp. 1253-1257
-
-
Jacobs, K.B.1
Yeager, M.2
Wacholder, S.3
Craig, D.4
Kraft, P.5
Hunter, D.J.6
Paschal, J.7
Manolio, T.A.8
Tucker, M.9
Hoover, R.N.10
Thomas, G.D.11
Chanock, S.J.12
Chatterjee, N.13
-
14
-
-
77955895425
-
BigWig and BigBed: enabling browsing of large distributed datasets
-
Kent WJ, Zweig AS, Barber G, Hinrichs AS, Karolchik D. 2010. BigWig and BigBed: enabling browsing of large distributed datasets. Bioinformatics 26:2204-2207.
-
(2010)
Bioinformatics
, vol.26
, pp. 2204-2207
-
-
Kent, W.J.1
Zweig, A.S.2
Barber, G.3
Hinrichs, A.S.4
Karolchik, D.5
-
15
-
-
79959763071
-
Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases
-
Lill CM, Abel O, Bertram L, Al-Chalabi A. 2011. Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases. Amyotroph Lateral Scler 12:238-249.
-
(2011)
Amyotroph Lateral Scler
, vol.12
, pp. 238-249
-
-
Lill, C.M.1
Abel, O.2
Bertram, L.3
Al-Chalabi, A.4
-
16
-
-
77954865034
-
Online-Datenbanken und systematische Metaanalysen komplex-genetischer Erkrankungen
-
Lill CM, Bertram L. 2010. Online-Datenbanken und systematische Metaanalysen komplex-genetischer Erkrankungen. Medizinische Genetik 22: 235-41.
-
(2010)
Medizinische Genetik
, vol.22
, pp. 235-241
-
-
Lill, C.M.1
Bertram, L.2
-
17
-
-
84856200093
-
Towards unveiling the genetics of neurodegenerative diseases
-
Lill CM, Bertram L. 2011. Towards unveiling the genetics of neurodegenerative diseases. Semin Neurol 31:531-541.
-
(2011)
Semin Neurol
, vol.31
, pp. 531-541
-
-
Lill, C.M.1
Bertram, L.2
-
18
-
-
84859339977
-
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database
-
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide B-MM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, et al. 2012. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database. PLoS Genet 8:e1002548.
-
(2012)
PLoS Genet
, vol.8
-
-
Lill, C.M.1
Roehr, J.T.2
McQueen, M.B.3
Kavvoura, F.K.4
Bagade, S.5
Schjeide, B.-M.6
Schjeide, L.M.7
Meissner, E.8
Zauft, U.9
Allen, N.C.10
Liu, T.11
Schilling, M.12
-
19
-
-
77949462739
-
Correspondence to Sand "Critical reappraisal of a catechol-o-methyltransferase transversion variant in schizophrenia."
-
Lill CM, Schjeide B-MM, Roehr JT, Zauft U, Allen NC, Zipp F, McQueen MB, Kavvoura FK, Ioannidis JPA, Khoury MJ, Tanzi RE, Bertram L. 2010. Correspondence to Sand et al. "Critical reappraisal of a catechol-o-methyltransferase transversion variant in schizophrenia." Biol Psychiatry 67:e45-e48.
-
(2010)
Biol Psychiatry
, vol.67
-
-
Lill, C.M.1
Schjeide, B.-M.2
Roehr, J.T.3
Zauft, U.4
Allen, N.C.5
Zipp, F.6
McQueen, M.B.7
Kavvoura, F.K.8
Ioannidis, J.P.A.9
Khoury, M.J.10
Tanzi, R.E.11
Bertram, L.12
-
20
-
-
61449255938
-
Strengthening the reporting of genetic association studies
-
Little J, Higgins JP, Ioannidis JP, Moher D, Gagnon F, von Elm E, Khoury MJ, Cohen B, Davey-Smith G, Grimshaw J, Scheet P, Gwinn M, et al. 2009. Strengthening the reporting of genetic association studies. PLoS Med 6:e22.
-
(2009)
PLoS Med
, vol.6
-
-
Little, J.1
Higgins, J.P.2
Ioannidis, J.P.3
Moher, D.4
Gagnon, F.5
von Elm, E.6
Khoury, M.J.7
Cohen, B.8
Davey-Smith, G.9
Grimshaw, J.10
Scheet, P.11
Gwinn, M.12
-
21
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P. 2007. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39:906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
22
-
-
77954104112
-
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
-
Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C. 2010. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. Hum Mutat 31:763-780.
-
(2010)
Hum Mutat
, vol.31
, pp. 763-780
-
-
Nuytemans, K.1
Theuns, J.2
Cruts, M.3
Van Broeckhoven, C.4
-
24
-
-
84865196862
-
Large-scale replication and heterogeneity in Parkinson disease genetic loci
-
Sharma M, Ioannidis JPA, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, et al. 2012. Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 79:1-9.
-
(2012)
Neurology
, vol.79
, pp. 1-9
-
-
Sharma, M.1
Ioannidis, J.P.A.2
Aasly, J.O.3
Annesi, G.4
Brice, A.5
Van Broeckhoven, C.6
Bertram, L.7
Bozi, M.8
Crosiers, D.9
Clarke, C.10
Facheris, M.11
Farrer, M.12
-
25
-
-
77953774727
-
Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies
-
Siontis KCM, Patsopoulos NA, Ioannidis JPA. 2010. Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies. Eur J Hum Genet 18:832-837.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 832-837
-
-
Siontis, K.C.M.1
Patsopoulos, N.A.2
Ioannidis, J.P.A.3
-
26
-
-
84863686275
-
Towards modernizing the systematic review pipeline in genetics: efficient updating via data mining
-
doi: 10.1038/gim.2012.7.
-
Wallace BC, Small K, Brodley CE, Lau J, Schmid CH, Bertram L, Lill CM, Cohen JT, Trikalinos TA. 2012. Towards modernizing the systematic review pipeline in genetics: efficient updating via data mining. Genet Med doi: 10.1038/gim.2012.7.
-
(2012)
Genet Med
-
-
Wallace, B.C.1
Small, K.2
Brodley, C.E.3
Lau, J.4
Schmid, C.H.5
Bertram, L.6
Lill, C.M.7
Cohen, J.T.8
Trikalinos, T.A.9
-
27
-
-
48249151156
-
ALSOD: the amyotrophic lateral sclerosis online database
-
Wroe R, Wai-Ling Butler A, Andersen PM, Powell JF, Al-Chalabi A. 2008. ALSOD: the amyotrophic lateral sclerosis online database. Amyotroph Lateral Scler 9:249-250.
-
(2008)
Amyotroph Lateral Scler
, vol.9
, pp. 249-250
-
-
Wroe, R.1
Wai-Ling Butler, A.2
Andersen, P.M.3
Powell, J.F.4
Al-Chalabi, A.5
|