-
1
-
-
33745302079
-
Familial and genetic susceptibility to major neonatal morbidities in preterm twins
-
Bhandari V, Bizzarro MJ, Shetty A, Zhong X, Page GP, Zhang H, Ment LR, Gruen JR. 2006. Familial and genetic susceptibility to major neonatal morbidities in preterm twins. Pediatrics 117:1901-1906.
-
(2006)
Pediatrics
, vol.117
, pp. 1901-1906
-
-
Bhandari, V.1
Bizzarro, M.J.2
Shetty, A.3
Zhong, X.4
Page, G.P.5
Zhang, H.6
Ment, L.R.7
Gruen, J.R.8
-
2
-
-
80051781709
-
Copy number variations and primary open-angle glaucoma
-
Davis LK, Meyer KJ, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, Scheetz TE, Braun TA, Fingert JH, Alward WLM, Kwon YH, Folk JC, Russell SR, Wassink TH, Sheffield VC, Stone EM. 2011. Copy number variations and primary open-angle glaucoma. Invest Ophthalmol Vis Sci 52:7122-7133.
-
(2011)
Invest Ophthalmol Vis Sci
, vol.52
, pp. 7122-7133
-
-
Davis, L.K.1
Meyer, K.J.2
Schindler, E.I.3
Beck, J.S.4
Rudd, D.S.5
Grundstad, A.J.6
Scheetz, T.E.7
Braun, T.A.8
Fingert, J.H.9
Alward, W.L.M.10
Kwon, Y.H.11
Folk, J.C.12
Russell, S.R.13
Wassink, T.H.14
Sheffield, V.C.15
Stone, E.M.16
-
3
-
-
67349182343
-
Autism genomewide copy number variation reveals ubiquitin and neuronal genes
-
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PMA, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SFA, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H. 2009. Autism genomewide copy number variation reveals ubiquitin and neuronal genes. Nature 459:569-573.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
Zhang, H.7
Estes, A.8
Brune, C.W.9
Bradfield, J.P.10
Imielinski, M.11
Frackelton, E.C.12
Reichert, J.13
Crawford, E.L.14
Munson, J.15
Sleiman, P.M.A.16
Chiavacci, R.17
Annaiah, K.18
Thomas, K.19
Hou, C.20
Glaberson, W.21
Flory, J.22
Otieno, F.23
Garris, M.24
Soorya, L.25
Klei, L.26
Piven, J.27
Meyer, K.J.28
Anagnostou, E.29
Sakurai, T.30
Game, R.M.31
Rudd, D.S.32
Zurawiecki, D.33
McDougle, C.J.34
Davis, L.K.35
Miller, J.36
Posey, D.J.37
Michaels, S.38
Kolevzon, A.39
Silverman, J.M.40
Bernier, R.41
Levy, S.E.42
Schultz, R.T.43
Dawson, G.44
Owley, T.45
McMahon, W.M.46
Wassink, T.H.47
Sweeney, J.A.48
Nurnberger, J.I.49
Coon, H.50
Sutcliffe, J.S.51
Minshew, N.J.52
Grant, S.F.A.53
Bucan, M.54
Cook, E.H.55
Buxbaum, J.D.56
Devlin, B.57
Schellenberg, G.D.58
Hakonarson, H.59
more..
-
4
-
-
77953776675
-
Strong synaptic transmission impact by copy number variations in schizophrenia
-
Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PMA, Flory JH, Imielinski M, Frackelton EC, Chiavacci R, Thomas KA, Garris M, Otieno FG, Davidson M, Weiser M, Reichenberg A, Davis KL, Friedman JI, Cappola TP, Margulies KB, Rader DJ, Grant SFA, Buxbaum JD, Gur RE, Hakonarson H. 2010. Strong synaptic transmission impact by copy number variations in schizophrenia. Proc Natl Acad Sci USA 107:10584-10589.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 10584-10589
-
-
Glessner, J.T.1
Reilly, M.P.2
Kim, C.E.3
Takahashi, N.4
Albano, A.5
Hou, C.6
Bradfield, J.P.7
Zhang, H.8
Sleiman, P.M.A.9
Flory, J.H.10
Imielinski, M.11
Frackelton, E.C.12
Chiavacci, R.13
Thomas, K.A.14
Garris, M.15
Otieno, F.G.16
Davidson, M.17
Weiser, M.18
Reichenberg, A.19
Davis, K.L.20
Friedman, J.I.21
Cappola, T.P.22
Margulies, K.B.23
Rader, D.J.24
Grant, S.F.A.25
Buxbaum, J.D.26
Gur, R.E.27
Hakonarson, H.28
more..
-
5
-
-
84876372476
-
Parse CNV integrative copy number variation association software with quality tracking
-
Glessner JT, Li J, Hakonarson H. 2013. Parse CNV integrative copy number variation association software with quality tracking. Nucleic Acids Res 41: e64-e64.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. e64-e64
-
-
Glessner, J.T.1
Li, J.2
Hakonarson, H.3
-
6
-
-
77950940258
-
The role of regional collaboratives: The California Perinatal Quality Care Collaborative Model
-
Gould JB. 2010. The role of regional collaboratives: The California Perinatal Quality Care Collaborative Model. Clin Perinatol 37:71-86.
-
(2010)
Clin Perinatol
, vol.37
, pp. 71-86
-
-
Gould, J.B.1
-
7
-
-
85007069160
-
Genome Studio Data Analysis Software [Whitepaper]
-
Illumina. 2011. Genome Studio Data Analysis Software [Whitepaper]. Retrieved from http://res.illumina.com/documents/products/datasheets/datasheet_genomestudio_software.pdf.
-
(2011)
-
-
-
9
-
-
51649115601
-
Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health
-
Lavoie PM, Pham C, Jang KL. 2008. Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health. Pediatrics 122:479-485.
-
(2008)
Pediatrics
, vol.122
, pp. 479-485
-
-
Lavoie, P.M.1
Pham, C.2
Jang, K.L.3
-
10
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
Need AC, Ge D, Weale ME, Maia J, Feng S, Heinzen EL, Shianna KV, Yoon W, Kasperavičiüte˙ D, Gennarelli M, Strittmatter WJ, Bonvicini C, Rossi G, Jayathilake K, Cola PA, McEvoy JP, Keefe RSE, Fisher EMC, St Jean PL, Giegling I, Hartmann AM, Möller H-J, Ruppert A, Fraser G, Crombie C, Middleton LT, St Clair D, Roses AD, Muglia P, Francks C, Rujescu D, Meltzer HY, Goldstein DB. 2009. A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet 5:e1000373.
-
(2009)
PLoS Genet
, vol.5
, pp. e1000373
-
-
Need, A.C.1
Ge, D.2
Weale, M.E.3
Maia, J.4
Feng, S.5
Heinzen, E.L.6
Shianna, K.V.7
Yoon, W.8
Kasperavičiüte, D.9
Gennarelli, M.10
Strittmatter, W.J.11
Bonvicini, C.12
Rossi, G.13
Jayathilake, K.14
Cola, P.A.15
McEvoy, J.P.16
Keefe, R.S.E.17
Fisher, E.M.C.18
St Jean, P.L.19
Giegling, I.20
Hartmann, A.M.21
Möller, H.-J.22
Ruppert, A.23
Fraser, G.24
Crombie, C.25
Middleton, L.T.26
St Clair, D.27
Roses, A.D.28
Muglia, P.29
Francks, C.30
Rujescu, D.31
Meltzer, H.Y.32
Goldstein, D.B.33
more..
-
11
-
-
84878495450
-
High quality genome-wide genotyping from archived dried blood spots without DNA amplification
-
St Julien KR, Jelliffe-Pawlowski LL, Shaw GM, Stevenson DK, O'Brodovich HM, Krasnow MA, the Stanford BPD Study Group. 2013. High quality genome-wide genotyping from archived dried blood spots without DNA amplification. PLoS ONE 8:e64710.
-
(2013)
PLoS ONE
, vol.8
, pp. e64710
-
-
St Julien, K.R.1
Jelliffe-Pawlowski, L.L.2
Shaw, G.M.3
Stevenson, D.K.4
O'Brodovich, H.M.5
Krasnow, M.A.6
-
12
-
-
16644364184
-
Impact of a physiologic definition on bronchopulmonary dysplasia rates
-
Walsh MC, Yao Q, Gettner P, Hale E, Collins M, Hensman A, Everette R, Peters N, Miller N, Muran G, Auten K, Newman N, Rowan G, Grisby C, Arnell K, Miller L, Ball B, McDavid G. 2004. Impact of a physiologic definition on bronchopulmonary dysplasia rates. Pediatrics 114:1305-1311.
-
(2004)
Pediatrics
, vol.114
, pp. 1305-1311
-
-
Walsh, M.C.1
Yao, Q.2
Gettner, P.3
Hale, E.4
Collins, M.5
Hensman, A.6
Everette, R.7
Peters, N.8
Miller, N.9
Muran, G.10
Auten, K.11
Newman, N.12
Rowan, G.13
Grisby, C.14
Arnell, K.15
Miller, L.16
Ball, B.17
McDavid, G.18
-
13
-
-
35948984173
-
Penn CNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, Hakonarson H, Bucan M. 2007. Penn CNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 17:1665-1674.
-
(2007)
Genome Res
, vol.17
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.A.6
Hakonarson, H.7
Bucan, M.8
-
14
-
-
84882257642
-
A genome-wide association study (GWAS) for bronchopulmonary dysplasia
-
Wang H, St Julien KR, Stevenson DK, Hoffmann TJ, Witte JS, Lazzeroni LC, Krasnow MA, Quaintance CC, Oehlert JW, Jelliffe-Pawlowski LL, Gould JB, Shaw GM, O'Brodovich HM. 2013. A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Pediatrics 132:290-297.
-
(2013)
Pediatrics
, vol.132
, pp. 290-297
-
-
Wang, H.1
St Julien, K.R.2
Stevenson, D.K.3
Hoffmann, T.J.4
Witte, J.S.5
Lazzeroni, L.C.6
Krasnow, M.A.7
Quaintance, C.C.8
Oehlert, J.W.9
Jelliffe-Pawlowski, L.L.10
Gould, J.B.11
Shaw, G.M.12
O'Brodovich, H.M.13
|