-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. 2002. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
2
-
-
0041386344
-
Quantitative risk factors as indices of alcoholism susceptibility
-
Almasy L. 2003. Quantitative risk factors as indices of alcoholism susceptibility. Ann Med 35:337-343.
-
(2003)
Ann Med
, vol.35
, pp. 337-343
-
-
Almasy, L.1
-
3
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L, Blangero J. 1998. Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 62:1198-1211.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
4
-
-
0031439473
-
Bivariate quantitative trait linkage analysis: Pleiotropy versus co-incident linkages
-
Almasy L, Dyer TD, Blangero J. 1997. Bivariate quantitative trait linkage analysis: Pleiotropy versus co-incident linkages. Genet Epidemol 14:953-958.
-
(1997)
Genet Epidemol
, vol.14
, pp. 953-958
-
-
Almasy, L.1
Dyer, T.D.2
Blangero, J.3
-
5
-
-
79851512361
-
Double-blind, randomized, placebo-controlled 6-week study on the efficacy and safety of the tamoxifen adjunctive to lithium in acute bipolar mania
-
Amrollahi Z, Rezaei F, Salehi B, Modabbernia AH, Maroufi A, Esfandiari GR, Naderi M, Ghebleh F, Ahmadi-Abhari SA, Sadeghi M, Tabrizi M, Akhondzadeh S. 2011. Double-blind, randomized, placebo-controlled 6-week study on the efficacy and safety of the tamoxifen adjunctive to lithium in acute bipolar mania. J Affect Disord 129:327-331.
-
(2011)
J Affect Disord
, vol.129
, pp. 327-331
-
-
Amrollahi, Z.1
Rezaei, F.2
Salehi, B.3
Modabbernia, A.H.4
Maroufi, A.5
Esfandiari, G.R.6
Naderi, M.7
Ghebleh, F.8
Ahmadi-Abhari, S.A.9
Sadeghi, M.10
Tabrizi, M.11
Akhondzadeh, S.12
-
6
-
-
77649237272
-
Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities
-
Ballif BC, Theisen A, Rosenfeld JA, Traylor RN, Gastier-Foster J, Thrush DL, Astbury C, Bartholomew D, McBride KL, Pyatt RE, Shane K, Smith WE, Banks V, Gallentine WB, Brock P, Rudd MK, Adam MP, Keene JA, Phillips JA III, Pfotenhauer JP, Gowans GC, Stankiewicz P, Bejjani BA, Shaffer LG. 2010. Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities. Am J Hum Genet 86:454-461.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 454-461
-
-
Ballif, B.C.1
Theisen, A.2
Rosenfeld, J.A.3
Traylor, R.N.4
Gastier-Foster, J.5
Thrush, D.L.6
Astbury, C.7
Bartholomew, D.8
McBride, K.L.9
Pyatt, R.E.10
Shane, K.11
Smith, W.E.12
Banks, V.13
Gallentine, W.B.14
Brock, P.15
Rudd, M.K.16
Adam, M.P.17
Keene, J.A.18
Phillips III, J.A.19
Pfotenhauer, J.P.20
Gowans, G.C.21
Stankiewicz, P.22
Bejjani, B.A.23
Shaffer, L.G.24
more..
-
7
-
-
0036883717
-
Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer
-
Barlund M, Monni O, Weaver JD, Kauraniemi P, Sauter G, Heiskanen M, Kallioniemi OP, Kallioniemi A. 2002. Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer. Genes Chromosomes Cancer 35:311-317.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 311-317
-
-
Barlund, M.1
Monni, O.2
Weaver, J.D.3
Kauraniemi, P.4
Sauter, G.5
Heiskanen, M.6
Kallioniemi, O.P.7
Kallioniemi, A.8
-
8
-
-
33646934703
-
Endophenotypes for psychiatric disorders: Ready for primetime
-
Bearden CE, Freimer NB. 2006. Endophenotypes for psychiatric disorders: Ready for primetime? Trends Genet 22:306-313.
-
(2006)
Trends Genet
, vol.22
, pp. 306-313
-
-
Bearden, C.E.1
Freimer, N.B.2
-
9
-
-
0027720035
-
Statistical genetic, approaches to, human adaptability
-
Blangero J, 1993. Statistical genetic, approaches to, human adaptability. Hum Biol 65(6):941-966.
-
(1993)
Hum Biol
, vol.65
, Issue.6
, pp. 941-966
-
-
Blangero, J.1
-
10
-
-
0025964920
-
Allele frequency estimation from data on relatives
-
Boehnke M. 1991. Allele frequency estimation from data on relatives. Am J Hum Genet 48:22-25.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 22-25
-
-
Boehnke, M.1
-
11
-
-
58149178891
-
Cognitive endophenotypes of bipolar disorder: A meta-analysis of neuropsychological deficits in euthymic patients and their first-degree relatives
-
Bora E, Yucel M, Pantelis C. 2009. Cognitive endophenotypes of bipolar disorder: A meta-analysis of neuropsychological deficits in euthymic patients and their first-degree relatives. J Affect Disord 113:1-20.
-
(2009)
J Affect Disord
, vol.113
, pp. 1-20
-
-
Bora, E.1
Yucel, M.2
Pantelis, C.3
-
12
-
-
77956309916
-
Notch targets and their regulation
-
Bray S, Bernard F. 2010. Notch targets and their regulation. Curr Top Dev Biol 92:253-275.
-
(2010)
Curr Top Dev Biol
, vol.92
, pp. 253-275
-
-
Bray, S.1
Bernard, F.2
-
13
-
-
16544371717
-
Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22
-
Cai G, Cole SA, Bastarrachea RA, Maccluer JW, Blangero J, Comuzzie AG. 2004. Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22. Am J Clin Nutr 80:1410-1414.
-
(2004)
Am J Clin Nutr
, vol.80
, pp. 1410-1414
-
-
Cai, G.1
Cole, S.A.2
Bastarrachea, R.A.3
Maccluer, J.W.4
Blangero, J.5
Comuzzie, A.G.6
-
15
-
-
0034781050
-
A simple correction for multiple comparisons in interval mapping genome scans
-
Cheverud JM. 2001. A simple correction for multiple comparisons in interval mapping genome scans. Heredity (Edinb) 87:52-58.
-
(2001)
Heredity (Edinb)
, vol.87
, pp. 52-58
-
-
Cheverud, J.M.1
-
16
-
-
67349188883
-
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
-
Cho YS, Go MJ, Kim YJ, Heo JY, Oh JH, Ban HJ, Yoon D, Lee MH, Kim DJ, Park M, Cha SH, Kim JW, Han BG, Min H, Ahn Y, Park MS, Han HR, Jang HY, Cho EY, Lee JE, Cho NH, Shin C, Park T, Park JW, Lee JK, Cardon L, Clarke G, McCarthy MI, Lee JY, Lee JK, Oh B, Kim HL. 2009. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet 41:527-534.
-
(2009)
Nat Genet
, vol.41
, pp. 527-534
-
-
Cho, Y.S.1
Go, M.J.2
Kim, Y.J.3
Heo, J.Y.4
Oh, J.H.5
Ban, H.J.6
Yoon, D.7
Lee, M.H.8
Kim, D.J.9
Park, M.10
Cha, S.H.11
Kim, J.W.12
Han, B.G.13
Min, H.14
Ahn, Y.15
Park, M.S.16
Han, H.R.17
Jang, H.Y.18
Cho, E.Y.19
Lee, J.E.20
Cho, N.H.21
Shin, C.22
Park, T.23
Park, J.W.24
Lee, J.K.25
Cardon, L.26
Clarke, G.27
McCarthy, M.I.28
Lee, J.Y.29
Lee, J.K.30
Oh, B.31
Kim, H.L.32
more..
-
17
-
-
0041700113
-
Learning and memory deficits in notch mutant mice
-
Costa RM, Honjo T, Silva AJ. 2003. Learning and memory deficits in notch mutant mice. Curr Biol 13:1348-1354.
-
(2003)
Curr Biol
, vol.13
, pp. 1348-1354
-
-
Costa, R.M.1
Honjo, T.2
Silva, A.J.3
-
20
-
-
0033535504
-
A presenilin-1-dependent gamma-secretase-like protease mediates release of notch intracellular domain
-
De Strooper B, Annaert W, Cupers P, Saftig P, Craessaerts K, Mumm JS, Schroeter EH, Schrijvers V, Wolfe MS, Ray WJ, Goate A, Kopan R. 1999. A presenilin-1-dependent gamma-secretase-like protease mediates release of notch intracellular domain. Nature 398:518-522.
-
(1999)
Nature
, vol.398
, pp. 518-522
-
-
De Strooper, B.1
Annaert, W.2
Cupers, P.3
Saftig, P.4
Craessaerts, K.5
Mumm, J.S.6
Schroeter, E.H.7
Schrijvers, V.8
Wolfe, M.S.9
Ray, W.J.10
Goate, A.11
Kopan, R.12
-
21
-
-
82955169673
-
Intelligence
-
Deary IJ. 2012. Intelligence. Annu Rev Psychol 63:453-482.
-
(2012)
Annu Rev Psychol
, vol.63
, pp. 453-482
-
-
Deary, I.J.1
-
22
-
-
67651095887
-
Genetic foundations of human intelligence
-
Deary IJ, Johnson W, Houlihan LM. 2009. Genetic foundations of human intelligence. Hum Genet 126:215-232.
-
(2009)
Hum Genet
, vol.126
, pp. 215-232
-
-
Deary, I.J.1
Johnson, W.2
Houlihan, L.M.3
-
23
-
-
77949647891
-
Suggestive linkage of the child behavior checklist juvenile bipolar disorder phenotype to 1p21, 6p21, and 8q21
-
Doyle AE, Biederman J, Ferreira MA, Wong P, Smoller JW, Faraone SV. 2010. Suggestive linkage of the child behavior checklist juvenile bipolar disorder phenotype to 1p21, 6p21, and 8q21. J Am Acad Child Adolesc Psychiatry 49:378-387.
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 378-387
-
-
Doyle, A.E.1
Biederman, J.2
Ferreira, M.A.3
Wong, P.4
Smoller, J.W.5
Faraone, S.V.6
-
24
-
-
0035801604
-
Differential regulation of basic helix-loop-helix mRNAs in the dentate gyrus following status epilepticus
-
Elliott RC, Khademi S, Pleasure SJ, Parent JM, Lowenstein DH. 2001. Differential regulation of basic helix-loop-helix mRNAs in the dentate gyrus following status epilepticus. Neuroscience 106:79-88.
-
(2001)
Neuroscience
, vol.106
, pp. 79-88
-
-
Elliott, R.C.1
Khademi, S.2
Pleasure, S.J.3
Parent, J.M.4
Lowenstein, D.H.5
-
25
-
-
0027487931
-
Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent
-
Feingold E, Brown PO, Siegmund D. 1993. Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent. Am J Hum Genet 53:234-251.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 234-251
-
-
Feingold, E.1
Brown, P.O.2
Siegmund, D.3
-
26
-
-
34547922380
-
Delta-notch-and then? protein interactions and proposed modes of repression by hes and hey bHLH factors
-
Fischer A, Gessler M. 2007. Delta-notch-and then? protein interactions and proposed modes of repression by hes and hey bHLH factors. Nucleic Acids Res 35:4583-4596.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 4583-4596
-
-
Fischer, A.1
Gessler, M.2
-
27
-
-
17044423443
-
Identification and characterization of the Hesr1/Hey1 as a candidate trans-acting factor on gene expression through the 3' non-coding polymorphic region of the human dopamine transporter (DAT1) gene
-
Fuke S, Sasagawa N, Ishiura S. 2005. Identification and characterization of the Hesr1/Hey1 as a candidate trans-acting factor on gene expression through the 3' non-coding polymorphic region of the human dopamine transporter (DAT1) gene. J Biochem 137:205-216.
-
(2005)
J Biochem
, vol.137
, pp. 205-216
-
-
Fuke, S.1
Sasagawa, N.2
Ishiura, S.3
-
28
-
-
3042796016
-
Notch signaling in drosophila long-term memory formation
-
Ge X, Hannan F, Xie Z, Feng C, Tully T, Zhou H, Xie Z, Zhong Y. 2004. Notch signaling in drosophila long-term memory formation. Proc Natl Acad Sci U S A 101:10172-10176.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 10172-10176
-
-
Ge, X.1
Hannan, F.2
Xie, Z.3
Feng, C.4
Tully, T.5
Zhou, H.6
Xie, Z.7
Zhong, Y.8
-
29
-
-
84870529525
-
Diverse types of genetic variation converge on functional gene networks involved in schizophrenia
-
Gilman SR, Chang J, Xu B, Bawa TS, Gogos JA, Karayiorgou M, Vitkup D. 2012. Diverse types of genetic variation converge on functional gene networks involved in schizophrenia. Nat Neurosci 15:1723-1728.
-
(2012)
Nat Neurosci
, vol.15
, pp. 1723-1728
-
-
Gilman, S.R.1
Chang, J.2
Xu, B.3
Bawa, T.S.4
Gogos, J.A.5
Karayiorgou, M.6
Vitkup, D.7
-
30
-
-
12244266463
-
Spatial working memory as an endophenotype for schizophrenia
-
Glahn DC, Therman S, Manninen M, Huttunen M, Kaprio J, Lonnqvist J, Cannon TD. 2003. Spatial working memory as an endophenotype for schizophrenia. Biol Psychiatry 53:624-626.
-
(2003)
Biol Psychiatry
, vol.53
, pp. 624-626
-
-
Glahn, D.C.1
Therman, S.2
Manninen, M.3
Huttunen, M.4
Kaprio, J.5
Lonnqvist, J.6
Cannon, T.D.7
-
31
-
-
33745843694
-
Differential working memory impairment in bipolar disorder and schizophrenia: Effects of lifetime history of psychosis
-
Glahn DC, Bearden CE, Cakir S, Barrett JA, Najt P, Serap Monkul E, Maples N, Velligan DI, Soares JC. 2006. Differential working memory impairment in bipolar disorder and schizophrenia: Effects of lifetime history of psychosis. Bipolar Disord 8:117-123.
-
(2006)
Bipolar Disord
, vol.8
, pp. 117-123
-
-
Glahn, D.C.1
Bearden, C.E.2
Cakir, S.3
Barrett, J.A.4
Najt, P.5
Serap Monkul, E.6
Maples, N.7
Velligan, D.I.8
Soares, J.C.9
-
32
-
-
34047244699
-
Adjudicating neurocognitive endophenotypes for schizophrenia
-
Glahn DC, Almasy L, Blangero J, Burk GM, Estrada J, Peralta JM, Meyenberg N, Castro MP, Barrett J, Nicolini H, Raventos H, Escamilla MA. 2007a. Adjudicating neurocognitive endophenotypes for schizophrenia. Am J Med Genet Part B Neuropsychiatr Genet 144B:242-249.
-
(2007)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.144
, pp. 242-249
-
-
Glahn, D.C.1
Almasy, L.2
Blangero, J.3
Burk, G.M.4
Estrada, J.5
Peralta, J.M.6
Meyenberg, N.7
Castro, M.P.8
Barrett, J.9
Nicolini, H.10
Raventos, H.11
Escamilla, M.A.12
-
33
-
-
34047244699
-
Adjudicating neurocognitive endophenotypes for schizophrenia
-
Glahn DC, Almasy L, Blangero J, Burk GM, Estrada J, Peralta JM, Meyenberg N, Castro MP, Barrett J, Nicolini H, Raventos H, Escamilla MA. 2007b. Adjudicating neurocognitive endophenotypes for schizophrenia. Am J Med Genet Part B Neuropsychiatr Genet 144B:242-249.
-
(2007)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.144
, pp. 242-249
-
-
Glahn, D.C.1
Almasy, L.2
Blangero, J.3
Burk, G.M.4
Estrada, J.5
Peralta, J.M.6
Meyenberg, N.7
Castro, M.P.8
Barrett, J.9
Nicolini, H.10
Raventos, H.11
Escamilla, M.A.12
-
34
-
-
76149085872
-
Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families
-
Glahn DC, Almasy L, Barguil M, Hare E, Peralta JM, Kent JW Jr, Dassori A, Contreras J, Pacheco A, Lanzagorta N, Nicolini H, Raventos H, Escamilla MA. 2010. Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families. Arch Gen Psychiatry 67:168-177.
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 168-177
-
-
Glahn, D.C.1
Almasy, L.2
Barguil, M.3
Hare, E.4
Peralta, J.M.5
Kent Jr, J.W.6
Dassori, A.7
Contreras, J.8
Pacheco, A.9
Lanzagorta, N.10
Nicolini, H.11
Raventos, H.12
Escamilla, M.A.13
-
35
-
-
82755192975
-
High dimensional endophenotype ranking in the search for major depression risk genes
-
Glahn DC, Curran JE, Winkler AM, Carless MA, Kent JW Jr, Charlesworth JC, Johnson MP, Goring HH, Cole SA, Dyer TD, Moses EK, Olvera RL, Kochunov P, Duggirala R, Fox PT, Almasy L, Blangero J. 2012. High dimensional endophenotype ranking in the search for major depression risk genes. Biol Psychiatry 71:6-14.
-
(2012)
Biol Psychiatry
, vol.71
, pp. 6-14
-
-
Glahn, D.C.1
Curran, J.E.2
Winkler, A.M.3
Carless, M.A.4
Kent Jr, J.W.5
Charlesworth, J.C.6
Johnson, M.P.7
Goring, H.H.8
Cole, S.A.9
Dyer, T.D.10
Moses, E.K.11
Olvera, R.L.12
Kochunov, P.13
Duggirala, R.14
Fox, P.T.15
Almasy, L.16
Blangero, J.17
-
36
-
-
0038823525
-
The endophenotype concept in psychiatry: Etymology and strategic intentions
-
Gottesman II, Gould TD. 2003. The endophenotype concept in psychiatry: Etymology and strategic intentions. Am J Psychiatry 160:636-645.
-
(2003)
Am J Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
37
-
-
33646238716
-
MTA1, a transcriptional activator of breast cancer amplified sequence 3
-
Gururaj AE, Singh RR, Rayala SK, Holm C, den Hollander P, Zhang H, Balasenthil S, Talukder AH, Landberg G, Kumar R. 2006. MTA1, a transcriptional activator of breast cancer amplified sequence 3. Proc Natl Acad Sci U S A 103:6670-6675.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 6670-6675
-
-
Gururaj, A.E.1
Singh, R.R.2
Rayala, S.K.3
Holm, C.4
den Hollander, P.5
Zhang, H.6
Balasenthil, S.7
Talukder, A.H.8
Landberg, G.9
Kumar, R.10
-
38
-
-
0030833349
-
Markov chain Monte Carlo segregation and linkage analysis for oligogenic models
-
Heath SC. 1997. Markov chain Monte Carlo segregation and linkage analysis for oligogenic models. Am J Hum Genet 61:748-760.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 748-760
-
-
Heath, S.C.1
-
39
-
-
0031903740
-
Neurocognitive deficit in schizophrenia: A quantitative review of the evidence
-
Heinrichs RW, Zakzanis KK. 1998. Neurocognitive deficit in schizophrenia: A quantitative review of the evidence. Neuropsychology 12:426-445.
-
(1998)
Neuropsychology
, vol.12
, pp. 426-445
-
-
Heinrichs, R.W.1
Zakzanis, K.K.2
-
40
-
-
12944312691
-
Familial cognitive deficits in schizophrenia
-
Hoff AL, Svetina C, Maurizio AM, Crow TJ, Spokes K, DeLisi LE. 2005. Familial cognitive deficits in schizophrenia. Am J Med Genet Part B Neuropsychiatr Genet 133B:43-49.
-
(2005)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.133
, pp. 43-49
-
-
Hoff, A.L.1
Svetina, C.2
Maurizio, A.M.3
Crow, T.J.4
Spokes, K.5
DeLisi, L.E.6
-
42
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta KL, Dupuis J, de Bakker PI, O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J, Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M, Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA. 2009. Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 41:56-65.
-
(2009)
Nat Genet
, vol.41
, pp. 56-65
-
-
Kathiresan, S.1
Willer, C.J.2
Peloso, G.M.3
Demissie, S.4
Musunuru, K.5
Schadt, E.E.6
Kaplan, L.7
Bennett, D.8
Li, Y.9
Tanaka, T.10
Voight, B.F.11
Bonnycastle, L.L.12
Jackson, A.U.13
Crawford, G.14
Surti, A.15
Guiducci, C.16
Burtt, N.P.17
Parish, S.18
Clarke, R.19
Zelenika, D.20
Kubalanza, K.A.21
Morken, M.A.22
Scott, L.J.23
Stringham, H.M.24
Galan, P.25
Swift, A.J.26
Kuusisto, J.27
Bergman, R.N.28
Sundvall, J.29
Laakso, M.30
Ferrucci, L.31
Scheet, P.32
Sanna, S.33
Uda, M.34
Yang, Q.35
Lunetta, K.L.36
Dupuis, J.37
de Bakker, P.I.38
O'Donnell, C.J.39
Chambers, J.C.40
Kooner, J.S.41
Hercberg, S.42
Meneton, P.43
Lakatta, E.G.44
Scuteri, A.45
Schlessinger, D.46
Tuomilehto, J.47
Collins, F.S.48
Groop, L.49
Altshuler, D.50
Collins, R.51
Lathrop, G.M.52
Melander, O.53
Salomaa, V.54
Peltonen, L.55
Orho-Melander, M.56
Ordovas, J.M.57
Boehnke, M.58
Abecasis, G.R.59
Mohlke, K.L.60
Cupples, L.A.61
more..
-
43
-
-
33846311393
-
Evidence of linkage to psychosis on chromosome 5q33-34 in pedigrees ascertained for bipolar disorder
-
Kerner B, Brugman DL, Freimer NB. 2007. Evidence of linkage to psychosis on chromosome 5q33-34 in pedigrees ascertained for bipolar disorder. Am J Med Genet Part B Neuropsychiatr Genet 144B:74-78.
-
(2007)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.144
, pp. 74-78
-
-
Kerner, B.1
Brugman, D.L.2
Freimer, N.B.3
-
44
-
-
35748963239
-
Genome-wide association with bone mass and geometry in the framingham heart study
-
Kiel DP, Demissie S, Dupuis J, Lunetta KL, Murabito JM, Karasik D. 2007. Genome-wide association with bone mass and geometry in the framingham heart study. BMC Med Genet 8(Suppl 1):S14.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL 1
-
-
Kiel, D.P.1
Demissie, S.2
Dupuis, J.3
Lunetta, K.L.4
Murabito, J.M.5
Karasik, D.6
-
46
-
-
0033526856
-
Identification and expression of a novel family of bHLH cDNAs related to drosophila hairy and enhancer of split
-
Kokubo H, Lun Y, Johnson RL. 1999. Identification and expression of a novel family of bHLH cDNAs related to drosophila hairy and enhancer of split. Biochem Biophys Res Commun 260:459-465.
-
(1999)
Biochem Biophys Res Commun
, vol.260
, pp. 459-465
-
-
Kokubo, H.1
Lun, Y.2
Johnson, R.L.3
-
47
-
-
33644872106
-
A pilot study of hormone modulation as a new treatment for mania in women with bipolar affective disorder
-
Kulkarni J, Garland KA, Scaffidi A, Headey B, Anderson R, de Castella A, Fitzgerald P, Davis SR. 2006. A pilot study of hormone modulation as a new treatment for mania in women with bipolar affective disorder. Psychoneuroendocrinology 31:543-547.
-
(2006)
Psychoneuroendocrinology
, vol.31
, pp. 543-547
-
-
Kulkarni, J.1
Garland, K.A.2
Scaffidi, A.3
Headey, B.4
Anderson, R.5
de Castella, A.6
Fitzgerald, P.7
Davis, S.R.8
-
48
-
-
84855774121
-
Notch signaling proteins HES-1 and hey-1 bind to insulin degrading enzyme (IDE) proximal promoter and repress its transcription and activity: Implications for cellular abeta metabolism
-
Leal MC, Surace EI, Holgado MP, Ferrari CC, Tarelli R, Pitossi F, Wisniewski T, Castano EM, Morelli L. 2012. Notch signaling proteins HES-1 and hey-1 bind to insulin degrading enzyme (IDE) proximal promoter and repress its transcription and activity: Implications for cellular abeta metabolism. Biochim Biophys Acta 1823:227-235.
-
(2012)
Biochim Biophys Acta
, vol.1823
, pp. 227-235
-
-
Leal, M.C.1
Surace, E.I.2
Holgado, M.P.3
Ferrari, C.C.4
Tarelli, R.5
Pitossi, F.6
Wisniewski, T.7
Castano, E.M.8
Morelli, L.9
-
49
-
-
28544436939
-
Working memory impairments in schizophrenia: A meta-analysis
-
Lee J, Park S. 2005. Working memory impairments in schizophrenia: A meta-analysis. J Abnorm Psychol 114:599-611.
-
(2005)
J Abnorm Psychol
, vol.114
, pp. 599-611
-
-
Lee, J.1
Park, S.2
-
50
-
-
0033166951
-
Hey genes: A novel subfamily of hairy- and enhancer of split related genes specifically expressed during mouse embryogenesis
-
Leimeister C, Externbrink A, Klamt B, Gessler M. 1999. Hey genes: A novel subfamily of hairy- and enhancer of split related genes specifically expressed during mouse embryogenesis. Mech Dev 85:173-177.
-
(1999)
Mech Dev
, vol.85
, pp. 173-177
-
-
Leimeister, C.1
Externbrink, A.2
Klamt, B.3
Gessler, M.4
-
52
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW. 2008. Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 82:477-488.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
Skaug, J.6
Shago, M.7
Moessner, R.8
Pinto, D.9
Ren, Y.10
Thiruvahindrapduram, B.11
Fiebig, A.12
Schreiber, S.13
Friedman, J.14
Ketelaars, C.E.15
Vos, Y.J.16
Ficicioglu, C.17
Kirkpatrick, S.18
Nicolson, R.19
Sloman, L.20
Summers, A.21
Gibbons, C.A.22
Teebi, A.23
Chitayat, D.24
Weksberg, R.25
Thompson, A.26
Vardy, C.27
Crosbie, V.28
Luscombe, S.29
Baatjes, R.30
Zwaigenbaum, L.31
Roberts, W.32
Fernandez, B.33
Szatmari, P.34
Scherer, S.W.35
more..
-
53
-
-
0037629099
-
The heritability of bipolar affective disorder and the genetic relationship to unipolar depression
-
McGuffin P, Rijsdijk F, Andrew M, Sham P, Katz R, Cardno A. 2003. The heritability of bipolar affective disorder and the genetic relationship to unipolar depression. Arch Gen Psychiatry 60:497-502.
-
(2003)
Arch Gen Psychiatry
, vol.60
, pp. 497-502
-
-
McGuffin, P.1
Rijsdijk, F.2
Andrew, M.3
Sham, P.4
Katz, R.5
Cardno, A.6
-
54
-
-
2342635193
-
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22
-
Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisener AF, Brown A, Petryshen TL, Kirby AN, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Azevedo MH, Kennedy JL, Daly MJ, Sklar P, Pato CN. 2004. Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am J Hum Genet 74:886-897.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 886-897
-
-
Middleton, F.A.1
Pato, M.T.2
Gentile, K.L.3
Morley, C.P.4
Zhao, X.5
Eisener, A.F.6
Brown, A.7
Petryshen, T.L.8
Kirby, A.N.9
Medeiros, H.10
Carvalho, C.11
Macedo, A.12
Dourado, A.13
Coelho, I.14
Valente, J.15
Soares, M.J.16
Ferreira, C.P.17
Lei, M.18
Azevedo, M.H.19
Kennedy, J.L.20
Daly, M.J.21
Sklar, P.22
Pato, C.N.23
more..
-
55
-
-
41149140859
-
Epigenomic profiling reveals DNA-methylation changes associated with major psychosis
-
Mill J, Tang T, Kaminsky Z, Khare T, Yazdanpanah S, Bouchard L, Jia P, Assadzadeh A, Flanagan J, Schumacher A, Wang SC, Petronis A. 2008. Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet 82:696-711.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 696-711
-
-
Mill, J.1
Tang, T.2
Kaminsky, Z.3
Khare, T.4
Yazdanpanah, S.5
Bouchard, L.6
Jia, P.7
Assadzadeh, A.8
Flanagan, J.9
Schumacher, A.10
Wang, S.C.11
Petronis, A.12
-
56
-
-
50249187303
-
On multiple-testing correction in genome-wide association studies
-
Moskvina V, Schmidt KM. 2008. On multiple-testing correction in genome-wide association studies. Genet Epidemiol 32(6):567-573.
-
(2008)
Genet Epidemiol
, vol.32
, Issue.6
, pp. 567-573
-
-
Moskvina, V.1
Schmidt, K.M.2
-
58
-
-
0030608273
-
Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain
-
341-354.
-
Nagase T, Seki N, Ishikawa K, Ohira M, Kawarabayasi Y, Ohara O, Tanaka A, Kotani H, Miyajima N, Nomura N. 1996. Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain. DNA Res 3:321-329 341-354.
-
(1996)
DNA Res
, vol.3
, pp. 321-329
-
-
Nagase, T.1
Seki, N.2
Ishikawa, K.3
Ohira, M.4
Kawarabayasi, Y.5
Ohara, O.6
Tanaka, A.7
Kotani, H.8
Miyajima, N.9
Nomura, N.10
-
59
-
-
79251524212
-
Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension
-
Nimmakayalu M, Major H, Sheffield V, Solomon DH, Smith RJ, Patil SR, Shchelochkov OA. 2011. Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension. Am J Med Genet Part A 155A:418-423.
-
(2011)
Am J Med Genet Part A
, vol.155
, pp. 418-423
-
-
Nimmakayalu, M.1
Major, H.2
Sheffield, V.3
Solomon, D.H.4
Smith, R.J.5
Patil, S.R.6
Shchelochkov, O.A.7
-
60
-
-
79958701495
-
Common genetic influences on depression, alcohol, and substance use disorders in mexican-american families
-
Olvera RL, Bearden CE, Velligan DI, Almasy L, Carless MA, Curran JE, Williamson DE, Duggirala R, Blangero J, Glahn DC. 2011. Common genetic influences on depression, alcohol, and substance use disorders in mexican-american families. Am J Med Genet Part B Neuropsychiatr Genet 156B:561-568.
-
(2011)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.156
, pp. 561-568
-
-
Olvera, R.L.1
Bearden, C.E.2
Velligan, D.I.3
Almasy, L.4
Carless, M.A.5
Curran, J.E.6
Williamson, D.E.7
Duggirala, R.8
Blangero, J.9
Glahn, D.C.10
-
61
-
-
79952315009
-
Genetic overlap between episodic memory deficits and schizophrenia: Results from the Maudsley twin study
-
Owens SF, Picchioni MM, Rijsdijk FV, Stahl D, Vassos E, Rodger AK, Collier DA, Murray RM, Toulopoulou T. 2011. Genetic overlap between episodic memory deficits and schizophrenia: Results from the Maudsley twin study. Psychol Med 41:521-532.
-
(2011)
Psychol Med
, vol.41
, pp. 521-532
-
-
Owens, S.F.1
Picchioni, M.M.2
Rijsdijk, F.V.3
Stahl, D.4
Vassos, E.5
Rodger, A.K.6
Collier, D.A.7
Murray, R.M.8
Toulopoulou, T.9
-
62
-
-
0026485577
-
Schizophrenics show spatial working memory deficits
-
Park S, Holzman PS. 1992. Schizophrenics show spatial working memory deficits. Arch Gen Psychiatry 49:975-982.
-
(1992)
Arch Gen Psychiatry
, vol.49
, pp. 975-982
-
-
Park, S.1
Holzman, P.S.2
-
63
-
-
0036532578
-
Genetics and general cognitive ability (g)
-
Plomin R, Spinath FM. 2002. Genetics and general cognitive ability (g). Trends Cogn Sci 6:169-176.
-
(2002)
Trends Cogn Sci
, vol.6
, pp. 169-176
-
-
Plomin, R.1
Spinath, F.M.2
-
64
-
-
79961135005
-
-
R Development Core Team. Vienna, Austria: R Foundation for Statistical Computing.
-
R Development Core Team. 2011. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.
-
(2011)
R: A language and environment for statistical computing
-
-
-
65
-
-
34548819017
-
Neuropsychological impairments in schizophrenia: Integration of performance-based and brain imaging findings
-
Reichenberg A, Harvey PD. 2007. Neuropsychological impairments in schizophrenia: Integration of performance-based and brain imaging findings. Psychol Bull 133:833-858.
-
(2007)
Psychol Bull
, vol.133
, pp. 833-858
-
-
Reichenberg, A.1
Harvey, P.D.2
-
67
-
-
0242582168
-
The basic helix-loop-helix genes Hesr1/Hey1 and Hesr2/Hey2 regulate maintenance of neural precursor cells in the brain
-
Sakamoto M, Hirata H, Ohtsuka T, Bessho Y, Kageyama R. 2003. The basic helix-loop-helix genes Hesr1/Hey1 and Hesr2/Hey2 regulate maintenance of neural precursor cells in the brain. J Biol Chem 278:44808-44815.
-
(2003)
J Biol Chem
, vol.278
, pp. 44808-44815
-
-
Sakamoto, M.1
Hirata, H.2
Ohtsuka, T.3
Bessho, Y.4
Kageyama, R.5
-
68
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium.
-
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium. 2011. Genome-wide association study identifies five new schizophrenia loci. Nat Genet 43:969-976.
-
(2011)
Nat Genet
, vol.43
, pp. 969-976
-
-
-
69
-
-
84907319426
-
Asymptotic properties of maximum likelihood estimators and likelihood ratio tests under nonstandard conditions
-
Self SG, Liang KY. 1987. Asymptotic properties of maximum likelihood estimators and likelihood ratio tests under nonstandard conditions. J Am Stat Assoc 82(398):605-610.
-
(1987)
J Am Stat Assoc
, vol.82
, Issue.398
, pp. 605-610
-
-
Self, S.G.1
Liang, K.Y.2
-
70
-
-
0035081475
-
Alzheimer's disease results from the cerebral accumulation and cytotoxicity of amyloid beta-protein
-
Selkoe DJ. 2001. Alzheimer's disease results from the cerebral accumulation and cytotoxicity of amyloid beta-protein. J Alzheimers Dis 3:75-80.
-
(2001)
J Alzheimers Dis
, vol.3
, pp. 75-80
-
-
Selkoe, D.J.1
-
71
-
-
4644226078
-
Cognitive deficits in relatives of patients with schizophrenia: A meta-analysis
-
Sitskoorn MM, Aleman A, Ebisch SJ, Appels MC, Kahn RS. 2004. Cognitive deficits in relatives of patients with schizophrenia: A meta-analysis. Schizophr Res 71:285-295.
-
(2004)
Schizophr Res
, vol.71
, pp. 285-295
-
-
Sitskoorn, M.M.1
Aleman, A.2
Ebisch, S.J.3
Appels, M.C.4
Kahn, R.S.5
-
72
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. 1996. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
73
-
-
0036011255
-
Notch1 and its ligands delta-like and jagged are expressed and active in distinct cell populations in the postnatal mouse brain
-
Stump G, Durrer A, Klein AL, Lutolf S, Suter U, Taylor V. 2002. Notch1 and its ligands delta-like and jagged are expressed and active in distinct cell populations in the postnatal mouse brain. Mech Dev 114:153-159.
-
(2002)
Mech Dev
, vol.114
, pp. 153-159
-
-
Stump, G.1
Durrer, A.2
Klein, A.L.3
Lutolf, S.4
Suter, U.5
Taylor, V.6
-
74
-
-
33846642542
-
The genetics of schizophrenia
-
Sullivan PF. 2005. The genetics of schizophrenia. PLoS Med 2:e212.
-
(2005)
PLoS Med
, vol.2
-
-
Sullivan, P.F.1
-
75
-
-
0344305525
-
Schizophrenia as a complex trait: Evidence from a meta-analysis of twin studies
-
Sullivan PF, Kendler KS, Neale MC. 2003. Schizophrenia as a complex trait: Evidence from a meta-analysis of twin studies. Arch Gen Psychiatry 60:1187-1192.
-
(2003)
Arch Gen Psychiatry
, vol.60
, pp. 1187-1192
-
-
Sullivan, P.F.1
Kendler, K.S.2
Neale, M.C.3
-
76
-
-
36849056624
-
Substantial genetic overlap between neurocognition and schizophrenia: Genetic modeling in twin samples
-
Toulopoulou T, Picchioni M, Rijsdijk F, Hua-Hall M, Ettinger U, Sham P, Murray R. 2007. Substantial genetic overlap between neurocognition and schizophrenia: Genetic modeling in twin samples. Arch Gen Psychiatry 64:1348-1355.
-
(2007)
Arch Gen Psychiatry
, vol.64
, pp. 1348-1355
-
-
Toulopoulou, T.1
Picchioni, M.2
Rijsdijk, F.3
Hua-Hall, M.4
Ettinger, U.5
Sham, P.6
Murray, R.7
-
77
-
-
77956355318
-
Impaired intellect and memory: A missing link between genetic risk and schizophrenia
-
Toulopoulou T, Goldberg TE, Mesa IR, Picchioni M, Rijsdijk F, Stahl D, Cherny SS, Sham P, Faraone SV, Tsuang M, Weinberger DR, Seidman LJ, Murray RM. 2010. Impaired intellect and memory: A missing link between genetic risk and schizophrenia? Arch Gen Psychiatry 67:905-913.
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 905-913
-
-
Toulopoulou, T.1
Goldberg, T.E.2
Mesa, I.R.3
Picchioni, M.4
Rijsdijk, F.5
Stahl, D.6
Cherny, S.S.7
Sham, P.8
Faraone, S.V.9
Tsuang, M.10
Weinberger, D.R.11
Seidman, L.J.12
Murray, R.M.13
-
78
-
-
78649746026
-
Phenotypic complexity, measurement bias, and poor phenotypic resolution contribute to the missing heritability problem in genetic association studies
-
van der Sluis S, Verhage M, Posthuma D, Dolan CV. 2010. Phenotypic complexity, measurement bias, and poor phenotypic resolution contribute to the missing heritability problem in genetic association studies. PLoS ONE 5:e13929.
-
(2010)
PLoS ONE
, vol.5
-
-
van der Sluis, S.1
Verhage, M.2
Posthuma, D.3
Dolan, C.V.4
-
79
-
-
58149163142
-
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
-
Wellcome Trust Case Control Consortium., Genetic Investigation of ANthropometric Traits Consortium.
-
Willer CJ, Speliotes EK, Loos RJ, Li S, Lindgren CM, Heid IM, Berndt SI, Elliott AL, Jackson AU, Lamina C, Lettre G, Lim N, Lyon HN, McCarroll SA, Papadakis K, Qi L, Randall JC, Roccasecca RM, Sanna S, Scheet P, Weedon MN, Wheeler E, Zhao JH, Jacobs LC, Prokopenko I, Soranzo N, Tanaka T, Timpson NJ, Almgren P, Bennett A, Bergman RN, Bingham SA, Bonnycastle LL, Brown M, Burtt NP, Chines P, Coin L, Collins FS, Connell JM, Cooper C, Smith GD, Dennison EM, Deodhar P, Elliott P, Erdos MR, Estrada K, Evans DM, Gianniny L, Gieger C, Gillson CJ, Guiducci C, Hackett R, Hadley D, Hall AS, Havulinna AS, Hebebrand J, Hofman A, Isomaa B, Jacobs KB, Johnson T, Jousilahti P, Jovanovic Z, Khaw KT, Kraft P, Kuokkanen M, Kuusisto J, Laitinen J, Lakatta EG, Luan J, Luben RN, Mangino M, McArdle WL, Meitinger T, Mulas A, Munroe PB, Narisu N, Ness AR, Northstone K, O'Rahilly S, Purmann C, Rees MG, Ridderstrale M, Ring SM, Rivadeneira F, Ruokonen A, Sandhu MS, Saramies J, Scott LJ, Scuteri A, Silander K, Sims MA, Song K, Stephens J, Stevens S, Stringham HM, Tung YC, Valle TT, Van Duijn CM, Vimaleswaran KS, Vollenweider P, Waeber G, Wallace C, Watanabe RM, Waterworth DM, Watkins N. Wellcome Trust Case Control Consortium. Witteman JC, Zeggini E, Zhai G, Zillikens MC, Altshuler D, Caulfield MJ, Chanock SJ, Farooqi IS, Ferrucci L, Guralnik JM, Hattersley AT, Hu FB, Jarvelin MR, Laakso M, Mooser V, Ong KK, Ouwehand WH, Salomaa V, Samani NJ, Spector TD, Tuomi T, Tuomilehto J, Uda M, Uitterlinden AG, Wareham NJ, Deloukas P, Frayling TM, Groop LC, Hayes RB, Hunter DJ, Mohlke KL, Peltonen L, Schlessinger D, Strachan DP, Wichmann HE, McCarthy MI, Boehnke M, Barroso I, Abecasis GR, Hirschhorn JN, Genetic Investigation of ANthropometric Traits Consortium. 2009. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 41:25-34.
-
(2009)
Nat Genet
, vol.41
, pp. 25-34
-
-
Willer, C.J.1
Speliotes, E.K.2
Loos, R.J.3
Li, S.4
Lindgren, C.M.5
Heid, I.M.6
Berndt, S.I.7
Elliott, A.L.8
Jackson, A.U.9
Lamina, C.10
Lettre, G.11
Lim, N.12
Lyon, H.N.13
McCarroll, S.A.14
Papadakis, K.15
Qi, L.16
Randall, J.C.17
Roccasecca, R.M.18
Sanna, S.19
Scheet, P.20
Weedon, M.N.21
Wheeler, E.22
Zhao, J.H.23
Jacobs, L.C.24
Prokopenko, I.25
Soranzo, N.26
Tanaka, T.27
Timpson, N.J.28
Almgren, P.29
Bennett, A.30
Bergman, R.N.31
Bingham, S.A.32
Bonnycastle, L.L.33
Brown, M.34
Burtt, N.P.35
Chines, P.36
Coin, L.37
Collins, F.S.38
Connell, J.M.39
Cooper, C.40
Smith, G.D.41
Dennison, E.M.42
Deodhar, P.43
Elliott, P.44
Erdos, M.R.45
Estrada, K.46
Evans, D.M.47
Gianniny, L.48
Gieger, C.49
Gillson, C.J.50
Guiducci, C.51
Hackett, R.52
Hadley, D.53
Hall, A.S.54
Havulinna, A.S.55
Hebebrand, J.56
Hofman, A.57
Isomaa, B.58
Jacobs, K.B.59
Johnson, T.60
Jousilahti, P.61
Jovanovic, Z.62
Khaw, K.T.63
Kraft, P.64
Kuokkanen, M.65
Kuusisto, J.66
Laitinen, J.67
Lakatta, E.G.68
Luan, J.69
Luben, R.N.70
Mangino, M.71
McArdle, W.L.72
Meitinger, T.73
Mulas, A.74
Munroe, P.B.75
Narisu, N.76
Ness, A.R.77
Northstone, K.78
O'Rahilly, S.79
Purmann, C.80
Rees, M.G.81
Ridderstrale, M.82
Ring, S.M.83
Rivadeneira, F.84
Ruokonen, A.85
Sandhu, M.S.86
Saramies, J.87
Scott, L.J.88
Scuteri, A.89
Silander, K.90
Sims, M.A.91
Song, K.92
Stephens, J.93
Stevens, S.94
Stringham, H.M.95
Tung, Y.C.96
Valle, T.T.97
Van Duijn, C.M.98
Vimaleswaran, K.S.99
Vollenweider, P.100
Waeber, G.101
Wallace, C.102
Watanabe, R.M.103
Waterworth, D.M.104
Watkins, N.105
Witteman, J.C.106
Zeggini, E.107
Zhai, G.108
Zillikens, M.C.109
Altshuler, D.110
Caulfield, M.J.111
Chanock, S.J.112
Farooqi, I.S.113
Ferrucci, L.114
Guralnik, J.M.115
Hattersley, A.T.116
Hu, F.B.117
Jarvelin, M.R.118
Laakso, M.119
Mooser, V.120
Ong, K.K.121
Ouwehand, W.H.122
Salomaa, V.123
Samani, N.J.124
Spector, T.D.125
Tuomi, T.126
Tuomilehto, J.127
Uda, M.128
Uitterlinden, A.G.129
Wareham, N.J.130
Deloukas, P.131
Frayling, T.M.132
Groop, L.C.133
Hayes, R.B.134
Hunter, D.J.135
Mohlke, K.L.136
Peltonen, L.137
Schlessinger, D.138
Strachan, D.P.139
Wichmann, H.E.140
McCarthy, M.I.141
Boehnke, M.142
Barroso, I.143
Abecasis, G.R.144
Hirschhorn, J.N.145
more..
|