-
1
-
-
83855165105
-
Repetitive DNA and next-generation sequencing: computational challenges and solutions
-
Treangen TJ, Salzberg SL. Repetitive DNA and next-generation sequencing: computational challenges and solutions. Nat Rev Genet 2011, 13:34-46.
-
(2011)
Nat Rev Genet
, vol.13
, pp. 34-46
-
-
Treangen, T.J.1
Salzberg, S.L.2
-
2
-
-
77952557918
-
Missing heritability and strategies for finding the underlying causes of complex disease
-
10.1038/nrg2809, 2942068, 20479774
-
Eichler EE, Flint J, Gibson G, Kong A, Leal SM, Moore JH, Nadeau JH. Missing heritability and strategies for finding the underlying causes of complex disease. Nat Rev Genet 2010, 11:446-450. 10.1038/nrg2809, 2942068, 20479774.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 446-450
-
-
Eichler, E.E.1
Flint, J.2
Gibson, G.3
Kong, A.4
Leal, S.M.5
Moore, J.H.6
Nadeau, J.H.7
-
3
-
-
84897455649
-
DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism
-
doi:10.1371/journal.pgen.1004241, 10.1371/journal.pgen.1004241, 3961203, 24651471
-
Davis JM, Searles VB, Anderson N, Keeney J, Dumas L, Sikela JM. DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism. PLoS Genet 2014, 10(3):e1004241. doi:10.1371/journal.pgen.1004241, 10.1371/journal.pgen.1004241, 3961203, 24651471.
-
(2014)
PLoS Genet
, vol.10
, Issue.3
-
-
Davis, J.M.1
Searles, V.B.2
Anderson, N.3
Keeney, J.4
Dumas, L.5
Sikela, J.M.6
-
4
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
10.1038/nature09146, 3021798, 20531469
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010, 466:368-372. 10.1038/nature09146, 3021798, 20531469.
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
Regan, R.6
Conroy, J.7
Magalhaes, T.R.8
Correia, C.9
Abrahams, B.S.10
Almeida, J.11
Bacchelli, E.12
Bader, G.D.13
Bailey, A.J.14
Baird, G.15
Battaglia, A.16
Berney, T.17
Bolshakova, N.18
Bölte, S.19
Bolton, P.F.20
Bourgeron, T.21
Brennan, S.22
Brian, J.23
Bryson, S.E.24
Carson, A.R.25
Casallo, G.26
Casey, J.27
Chung, B.H.28
Cochrane, L.29
Corsello, C.30
more..
-
5
-
-
51649107515
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
10.1038/455178a, 18784712, International Schizophrenia Consortium
-
International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008, 455:178-179. 10.1038/455178a, 18784712, International Schizophrenia Consortium.
-
(2008)
Nature
, vol.455
, pp. 178-179
-
-
-
6
-
-
79952710338
-
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
-
10.1176/appi.ajp.2010.10060876, 21285140
-
Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Kendler KS, Freedman R, Dudbridge F, Pe'er I, Hakonarson H, Bergen SE, Fanous AH, Holmans PA, Gejman PV. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry 2011, 168:302-316. 10.1176/appi.ajp.2010.10060876, 21285140.
-
(2011)
Am J Psychiatry
, vol.168
, pp. 302-316
-
-
Levinson, D.F.1
Duan, J.2
Oh, S.3
Wang, K.4
Sanders, A.R.5
Shi, J.6
Zhang, N.7
Mowry, B.J.8
Olincy, A.9
Amin, F.10
Cloninger, C.R.11
Silverman, J.M.12
Buccola, N.G.13
Byerley, W.F.14
Black, D.W.15
Kendler, K.S.16
Freedman, R.17
Dudbridge, F.18
Pe'er, I.19
Hakonarson, H.20
Bergen, S.E.21
Fanous, A.H.22
Holmans, P.A.23
Gejman, P.V.24
more..
-
7
-
-
56749154242
-
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
-
10.1038/ng.279, 2680128, 19029900
-
Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, Lansky-Shafer S, Weaver C, Roeder ER, Grebe TA, Arnold GL, Hutchison T, Reimschisel T, Amato S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, et al. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nat Genet 2008, 40:1466-1471. 10.1038/ng.279, 2680128, 19029900.
-
(2008)
Nat Genet
, vol.40
, pp. 1466-1471
-
-
Brunetti-Pierri, N.1
Berg, J.S.2
Scaglia, F.3
Belmont, J.4
Bacino, C.A.5
Sahoo, T.6
Lalani, S.R.7
Graham, B.8
Lee, B.9
Shinawi, M.10
Shen, J.11
Kang, S.H.12
Pursley, A.13
Lotze, T.14
Kennedy, G.15
Lansky-Shafer, S.16
Weaver, C.17
Roeder, E.R.18
Grebe, T.A.19
Arnold, G.L.20
Hutchison, T.21
Reimschisel, T.22
Amato, S.23
Geragthy, M.T.24
Innis, J.W.25
Obersztyn, E.26
Nowakowska, B.27
Rosengren, S.S.28
Bader, P.I.29
Grange, D.K.30
more..
-
8
-
-
54049094444
-
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
-
10.1056/NEJMoa0805384, 2703742, 18784092
-
Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney VK, Crolla JA, Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, Bongers EM, de Leeuw N, Reardon W, Gimelli S, Bena F, Hennekam RC, Male A, Gaunt L, Clayton-Smith J, Simonic I, Park SM, Mehta SG, Nik-Zainal S, Woods CG, Firth HV, et al. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. N Engl J Med 2008, 359:1685-1699. 10.1056/NEJMoa0805384, 2703742, 18784092.
-
(2008)
N Engl J Med
, vol.359
, pp. 1685-1699
-
-
Mefford, H.C.1
Sharp, A.J.2
Baker, C.3
Itsara, A.4
Jiang, Z.5
Buysse, K.6
Huang, S.7
Maloney, V.K.8
Crolla, J.A.9
Baralle, D.10
Collins, A.11
Mercer, C.12
Norga, K.13
de Ravel, T.14
Devriendt, K.15
Bongers, E.M.16
de Leeuw, N.17
Reardon, W.18
Gimelli, S.19
Bena, F.20
Hennekam, R.C.21
Male, A.22
Gaunt, L.23
Clayton-Smith, J.24
Simonic, I.25
Park, S.M.26
Mehta, S.G.27
Nik-Zainal, S.28
Woods, C.G.29
Firth, H.V.30
more..
-
9
-
-
2942668448
-
Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease
-
10.1161/01.RES.0000133233.38341.17, 15192033
-
Christiansen J, Dyck JD, Elyas BG, Lilley M, Bamforth JS, Hicks M, Sprysak KA, Tomaszewski R, Haase SM, Vicen-Wyhony LM, Somerville MJ. Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease. Circ Res 2004, 94:1401-1402. 10.1161/01.RES.0000133233.38341.17, 15192033.
-
(2004)
Circ Res
, vol.94
, pp. 1401-1402
-
-
Christiansen, J.1
Dyck, J.D.2
Elyas, B.G.3
Lilley, M.4
Bamforth, J.S.5
Hicks, M.6
Sprysak, K.A.7
Tomaszewski, R.8
Haase, S.M.9
Vicen-Wyhony, L.M.10
Somerville, M.J.11
-
10
-
-
68149181705
-
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
-
10.1038/ng.415, 2747103, 19597493
-
Greenway SC, Pereira AC, Lin JC, DePalma SR, Israel SJ, Mesquita SM, Ergul E, Conta JH, Korn JM, McCarroll SA, Gorham JM, Gabriel S, Altshuler DM, Quintanilla-Dieck Mde L, Artunduaga MA, Eavey RD, Plenge RM, Shadick NA, Weinblatt ME, De Jager PL, Hafler DA, Breitbart RE, Seidman JG, Seidman CE. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. Nat Genet 2009, 41:931-935. 10.1038/ng.415, 2747103, 19597493.
-
(2009)
Nat Genet
, vol.41
, pp. 931-935
-
-
Greenway, S.C.1
Pereira, A.C.2
Lin, J.C.3
DePalma, S.R.4
Israel, S.J.5
Mesquita, S.M.6
Ergul, E.7
Conta, J.H.8
Korn, J.M.9
McCarroll, S.A.10
Gorham, J.M.11
Gabriel, S.12
Altshuler, D.M.13
Quintanilla-Dieck Mde, L.14
Artunduaga, M.A.15
Eavey, R.D.16
Plenge, R.M.17
Shadick, N.A.18
Weinblatt, M.E.19
De Jager, P.L.20
Hafler, D.A.21
Breitbart, R.E.22
Seidman, J.G.23
Seidman, C.E.24
more..
-
11
-
-
33846562388
-
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome
-
10.1086/510919, 1785342, 17236129
-
Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. Am J Hum Genet 2007, 80:232-240. 10.1086/510919, 1785342, 17236129.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 232-240
-
-
Klopocki, E.1
Schulze, H.2
Strauss, G.3
Ott, C.E.4
Hall, J.5
Trotier, F.6
Fleischhauer, S.7
Greenhalgh, L.8
Newbury-Ecob, R.A.9
Neumann, L.M.10
Habenicht, R.11
König, R.12
Seemanova, E.13
Megarbane, A.14
Ropers, H.H.15
Ullmann, R.16
Horn, D.17
Mundlos, S.18
-
12
-
-
79952988490
-
Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome
-
10.1016/j.fertnstert.2010.07.1062, 20797712
-
Ledig S, Schippert C, Strick R, Beckmann MW, Oppelt PG, Wieacker P. Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome. Fertil Steril 2011, 95:1589-1594. 10.1016/j.fertnstert.2010.07.1062, 20797712.
-
(2011)
Fertil Steril
, vol.95
, pp. 1589-1594
-
-
Ledig, S.1
Schippert, C.2
Strick, R.3
Beckmann, M.W.4
Oppelt, P.G.5
Wieacker, P.6
-
13
-
-
78650658745
-
Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization
-
10.1093/ndt/gfq400, 20605837
-
Weber S, Landwehr C, Renkert M, Hoischen A, Wühl E, Denecke J, Radlwimmer B, Haffner D, Schaefer F, Weber RG. Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization. Nephrol Dial Transplant 2011, 26:136-143. 10.1093/ndt/gfq400, 20605837.
-
(2011)
Nephrol Dial Transplant
, vol.26
, pp. 136-143
-
-
Weber, S.1
Landwehr, C.2
Renkert, M.3
Hoischen, A.4
Wühl, E.5
Denecke, J.6
Radlwimmer, B.7
Haffner, D.8
Schaefer, F.9
Weber, R.G.10
-
14
-
-
19344366754
-
Lineage-specific gene duplication and loss in human and great ape evolution
-
10.1371/journal.pbio.0020207, 449870, 15252450
-
Fortna A, Kim Y, MacLaren E, Marshall K, Hahn G, Meltesen L, Brenton M, Hink R, Burgers S, Hernandez-Boussard T, Karimpour-Fard A, Glueck D, McGavran L, Berry R, Pollack J, Sikela JM. Lineage-specific gene duplication and loss in human and great ape evolution. PLoS Biol 2004, 2:E207. 10.1371/journal.pbio.0020207, 449870, 15252450.
-
(2004)
PLoS Biol
, vol.2
-
-
Fortna, A.1
Kim, Y.2
MacLaren, E.3
Marshall, K.4
Hahn, G.5
Meltesen, L.6
Brenton, M.7
Hink, R.8
Burgers, S.9
Hernandez-Boussard, T.10
Karimpour-Fard, A.11
Glueck, D.12
McGavran, L.13
Berry, R.14
Pollack, J.15
Sikela, J.M.16
-
15
-
-
33748292822
-
Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains
-
10.1126/science.1127980, 16946073
-
Popesco MC, Maclaren EJ, Hopkins J, Dumas L, Cox M, Meltesen L, McGavran L, Wyckoff GJ, Sikela JM. Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains. Science 2006, 313:1304-1307. 10.1126/science.1127980, 16946073.
-
(2006)
Science
, vol.313
, pp. 1304-1307
-
-
Popesco, M.C.1
Maclaren, E.J.2
Hopkins, J.3
Dumas, L.4
Cox, M.5
Meltesen, L.6
McGavran, L.7
Wyckoff, G.J.8
Sikela, J.M.9
-
16
-
-
77957723599
-
DUF1220 domains, cognitive disease, and human brain evolution
-
10.1101/sqb.2009.74.025, 2902282, 19850849
-
Dumas L, Sikela JM. DUF1220 domains, cognitive disease, and human brain evolution. Cold Spring Harb Symp Quant Biol 2009, 74:375-382. 10.1101/sqb.2009.74.025, 2902282, 19850849.
-
(2009)
Cold Spring Harb Symp Quant Biol
, vol.74
, pp. 375-382
-
-
Dumas, L.1
Sikela, J.M.2
-
17
-
-
84866056199
-
DUF1220-domain copy number implicated in human brain-size pathology and evolution
-
10.1016/j.ajhg.2012.07.016, 3511999, 22901949
-
Dumas LJ, O'Bleness MS, Davis JM, Dickens CM, Anderson N, Keeney JG, Jackson J, Sikela M, Raznahan A, Giedd J, Rapoport J, Nagamani SS, Erez A, Brunetti-Pierri N, Sugalski R, Lupski JR, Fingerlin T, Cheung SW, Sikela JM. DUF1220-domain copy number implicated in human brain-size pathology and evolution. Am J Hum Genet 2012, 91:444-454. 10.1016/j.ajhg.2012.07.016, 3511999, 22901949.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 444-454
-
-
Dumas, L.J.1
O'Bleness, M.S.2
Davis, J.M.3
Dickens, C.M.4
Anderson, N.5
Keeney, J.G.6
Jackson, J.7
Sikela, M.8
Raznahan, A.9
Giedd, J.10
Rapoport, J.11
Nagamani, S.S.12
Erez, A.13
Brunetti-Pierri, N.14
Sugalski, R.15
Lupski, J.R.16
Fingerlin, T.17
Cheung, S.W.18
Sikela, J.M.19
-
19
-
-
33745700416
-
Characterization of the human lineage-specific pericentric inversion that distinguishes human chromosome 1 from the homologous chromosomes of the great apes
-
10.1007/s00439-006-0209-y, 16775709
-
Szamalek J, Goidts V, Cooper D, Hameister H, Kherer-Sawatzki H. Characterization of the human lineage-specific pericentric inversion that distinguishes human chromosome 1 from the homologous chromosomes of the great apes. Hum Genet 2006, 120:126-138. 10.1007/s00439-006-0209-y, 16775709.
-
(2006)
Hum Genet
, vol.120
, pp. 126-138
-
-
Szamalek, J.1
Goidts, V.2
Cooper, D.3
Hameister, H.4
Kherer-Sawatzki, H.5
-
20
-
-
84883169155
-
Evolutionary history and genome organization of DUF1220 protein domains
-
2012, 3429928, 22973535
-
O'Bleness MS, Dickens CM, Dumas LJ, Kehrer-Sawatzki H, Wyckoff GJ, Sikela JM. Evolutionary history and genome organization of DUF1220 protein domains. G3 (Bethesda) 2012, 2:977-986. 2012, 3429928, 22973535.
-
(2012)
G3 (Bethesda)
, vol.2
, pp. 977-986
-
-
O'Bleness, M.S.1
Dickens, C.M.2
Dumas, L.J.3
Kehrer-Sawatzki, H.4
Wyckoff, G.J.5
Sikela, J.M.6
-
21
-
-
84860860685
-
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
-
10.1016/j.cell.2012.03.033, 3365555, 22559943
-
Dennis MY, Nuttle X, Sudmant PH, Antonacci F, Graves TA, Nefedov M, Rosenfeld JA, Sajjadian S, Malig M, Kotkiewicz H, Curry CJ, Shafer S, Shaffer LG, de Jong PJ, Wilson RK, Eichler EE. Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication. Cell 2012, 149(4):912-922. 10.1016/j.cell.2012.03.033, 3365555, 22559943.
-
(2012)
Cell
, vol.149
, Issue.4
, pp. 912-922
-
-
Dennis, M.Y.1
Nuttle, X.2
Sudmant, P.H.3
Antonacci, F.4
Graves, T.A.5
Nefedov, M.6
Rosenfeld, J.A.7
Sajjadian, S.8
Malig, M.9
Kotkiewicz, H.10
Curry, C.J.11
Shafer, S.12
Shaffer, L.G.13
de Jong, P.J.14
Wilson, R.K.15
Eichler, E.E.16
-
22
-
-
0032529138
-
An improved approach for construction of bacterial artificial chromosome libraries
-
10.1006/geno.1998.5423, 9740665
-
Osoegawa K, Woon PY, Zhao B, Frengen E, Tateno M, Catanese JJ, de Jong PJ. An improved approach for construction of bacterial artificial chromosome libraries. Genomics 1998, 52(1):1-8. 10.1006/geno.1998.5423, 9740665.
-
(1998)
Genomics
, vol.52
, Issue.1
, pp. 1-8
-
-
Osoegawa, K.1
Woon, P.Y.2
Zhao, B.3
Frengen, E.4
Tateno, M.5
Catanese, J.J.6
de Jong, P.J.7
-
23
-
-
0141853948
-
PCAP: a whole-genome assembly program
-
10.1101/gr.1390403, 403719, 12952883
-
Huang X, Wang J, Aluru S, Yang SP, Hillier L. PCAP: a whole-genome assembly program. Genome Res 2003, 13(9):2164-2170. 10.1101/gr.1390403, 403719, 12952883.
-
(2003)
Genome Res
, vol.13
, Issue.9
, pp. 2164-2170
-
-
Huang, X.1
Wang, J.2
Aluru, S.3
Yang, S.P.4
Hillier, L.5
-
24
-
-
24044447664
-
Automated generation of heuristics for biological sequence comparison
-
Slater G, Birney E. Automated generation of heuristics for biological sequence comparison. BMC Bioinforma 2005, 6:31.
-
(2005)
BMC Bioinforma
, vol.6
, pp. 31
-
-
Slater, G.1
Birney, E.2
-
25
-
-
69649109364
-
Circos: an information aesthetic for comparative genomics
-
10.1101/gr.092759.109, 2752132, 19541911
-
Krzywinski M, Schein J, Birol I, Connors J, Gascoyne R, Horsman D, Jones SJ, Marra MA. Circos: an information aesthetic for comparative genomics. Genome Res 2009, 19(9):1639-1645. 10.1101/gr.092759.109, 2752132, 19541911.
-
(2009)
Genome Res
, vol.19
, Issue.9
, pp. 1639-1645
-
-
Krzywinski, M.1
Schein, J.2
Birol, I.3
Connors, J.4
Gascoyne, R.5
Horsman, D.6
Jones, S.J.7
Marra, M.A.8
-
26
-
-
23044471766
-
An algorithm for progressive multiple alignment of sequences with insertions
-
10.1073/pnas.0409137102, 1180752, 16000407
-
Löytynoja A, Goldman N. An algorithm for progressive multiple alignment of sequences with insertions. Proc Natl Acad Sci 2005, 102(30):10557-10562. 10.1073/pnas.0409137102, 1180752, 16000407.
-
(2005)
Proc Natl Acad Sci
, vol.102
, Issue.30
, pp. 10557-10562
-
-
Löytynoja, A.1
Goldman, N.2
-
27
-
-
1042304216
-
APE: analyses of phylogenetics and evolution in R language
-
10.1093/bioinformatics/btg412, 14734327
-
Paradis E, Claude J, Strimmer K. APE: analyses of phylogenetics and evolution in R language. Bioinformatics 2004, 20:289-290. 10.1093/bioinformatics/btg412, 14734327.
-
(2004)
Bioinformatics
, vol.20
, pp. 289-290
-
-
Paradis, E.1
Claude, J.2
Strimmer, K.3
-
28
-
-
81255175501
-
High-throughput droplet digital PCR system for absolute quantitation of DNA copy number
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10.1021/ac202028g, 3216358, 22035192
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Hindson BJ, Ness KD, Masquelier DA, Belgrader P, Heredia NJ, Makarewicz AJ, Bright IJ, Lucero MY, Hiddeson AL, Legler TC, Kitano TK, Hodel MR, Petersen JF, Wyatt PW, Steenblock ER, Shah PH, Bousse LJ, Troup CB, Mellen JC, Wittman DK, Erndt NG, Cauley TH, Koehler RT, So AP, Dube S, Rose KA, Montesclaros L, Wang S, Stumbo DP, Hodges SP, et al. High-throughput droplet digital PCR system for absolute quantitation of DNA copy number. Anal Chem 2011, 83(22):8604-8610. 10.1021/ac202028g, 3216358, 22035192.
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(2011)
Anal Chem
, vol.83
, Issue.22
, pp. 8604-8610
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Hindson, B.J.1
Ness, K.D.2
Masquelier, D.A.3
Belgrader, P.4
Heredia, N.J.5
Makarewicz, A.J.6
Bright, I.J.7
Lucero, M.Y.8
Hiddeson, A.L.9
Legler, T.C.10
Kitano, T.K.11
Hodel, M.R.12
Petersen, J.F.13
Wyatt, P.W.14
Steenblock, E.R.15
Shah, P.H.16
Bousse, L.J.17
Troup, C.B.18
Mellen, J.C.19
Wittman, D.K.20
Erndt, N.G.21
Cauley, T.H.22
Koehler, R.T.23
So, A.P.24
Dube, S.25
Rose, K.A.26
Montesclaros, L.27
Wang, S.28
Stumbo, D.P.29
Hodges, S.P.30
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