-
1
-
-
22144432283
-
A systematic review of the prevalence of schizophrenia
-
Saha S, Chant D, Welham J, et al. A systematic review of the prevalence of schizophrenia. PLoS Med. 2005;2:e141.
-
(2005)
PLoS Med.
, vol.2
, pp. e141
-
-
Saha, S.1
Chant, D.2
Welham, J.3
-
2
-
-
0344305525
-
Schizophrenia as a complex trait: Evidence from a meta-analysis of twin studies
-
Sullivan PF, Kendler KS, Neale MC. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch Gen Psychiatry. 2003;60:1187-1192.
-
(2003)
Arch Gen Psychiatry.
, vol.60
, pp. 1187-1192
-
-
Sullivan, P.F.1
Kendler, K.S.2
Neale, M.C.3
-
4
-
-
77954513019
-
Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia
-
Owen MJ, Craddock N, O'Donovan MC. Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. Arch Gen Psychiatry. 2010;67:667-673.
-
(2010)
Arch Gen Psychiatry.
, vol.67
, pp. 667-673
-
-
Owen, M.J.1
Craddock, N.2
O'Donovan, M.C.3
-
5
-
-
84863980709
-
Genetic architectures of psychiatric disorders: The emerging picture and its implications
-
Sullivan PF, Daly MJ, O'Donovan M. Genetic architectures of psychiatric disorders: The emerging picture and its implications. Nat Rev Genet. 2012;13:537-551.
-
(2012)
Nat Rev Genet.
, vol.13
, pp. 537-551
-
-
Sullivan, P.F.1
Daly, M.J.2
O'Donovan, M.3
-
6
-
-
84863115845
-
Allelic differences between Han Chinese and Europeans for functional variants in ZNF804A and their association with schizophrenia
-
Li M, Luo XJ, Xiao X, et al. Allelic differences between Han Chinese and Europeans for functional variants in ZNF804A and their association with schizophrenia. Am J Psychiatry. 2011;168:1318-1325.
-
(2011)
Am J Psychiatry.
, vol.168
, pp. 1318-1325
-
-
Li, M.1
Luo, X.J.2
Xiao, X.3
-
7
-
-
40149105889
-
Genomewide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women
-
Shifman S, Johannesson M, Bronstein M, et al. Genomewide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genet. 2008;4:e28.
-
(2008)
PLoS Genet.
, vol.4
, pp. e28
-
-
Shifman, S.1
Johannesson, M.2
Bronstein, M.3
-
8
-
-
84874899732
-
Analysis of common genetic variants identifies RELN as a risk gene for schizophrenia in Chinese population
-
Li M, Luo XJ, Xiao X, et al. Analysis of common genetic variants identifies RELN as a risk gene for schizophrenia in Chinese population. World J Biol Psychiatry. 2013;14:91-99.
-
(2013)
World J Biol Psychiatry.
, vol.14
, pp. 91-99
-
-
Li, M.1
Luo, X.J.2
Xiao, X.3
-
9
-
-
50449100461
-
Identification of loci associated with schizophrenia by genome-wide association and follow-up
-
O'Donovan MC, Craddock N, Norton N, et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet. 2008;40:1053-1055.
-
(2008)
Nat Genet.
, vol.40
, pp. 1053-1055
-
-
O'Donovan, M.C.1
Craddock, N.2
Norton, N.3
-
10
-
-
84898054241
-
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility
-
Li M, Luo XJ, Rietschel M, et al. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Mol Psychiatry. 2014;19:452-461.
-
(2014)
Mol Psychiatry.
, vol.19
, pp. 452-461
-
-
Li, M.1
Luo, X.J.2
Rietschel, M.3
-
12
-
-
0029886621
-
Familial risks and reproductive fitness in schizophrenia
-
Battaglia M, Bellodi L. Familial risks and reproductive fitness in schizophrenia. Schizophr Bull. 1996;22:191-195.
-
(1996)
Schizophr Bull.
, vol.22
, pp. 191-195
-
-
Battaglia, M.1
Bellodi, L.2
-
13
-
-
84871964302
-
Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings
-
Power RA, Kyaga S, Uher R, et al. Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings. JAMA Psychiatry. 2013;70:22-30.
-
(2013)
JAMA Psychiatry.
, vol.70
, pp. 22-30
-
-
Power, R.A.1
Kyaga, S.2
Uher, R.3
-
14
-
-
82255175590
-
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
-
Shi Y, Li Z, Xu Q, et al. Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Nat Genet. 2011;43:1224-1227.
-
(2011)
Nat Genet.
, vol.43
, pp. 1224-1227
-
-
Shi, Y.1
Li, Z.2
Xu, Q.3
-
15
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, et al. Common variants conferring risk of schizophrenia. Nature. 2009;460:744-747.
-
(2009)
Nature.
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
-
16
-
-
1242298646
-
Schizophrenia-an evolutionary enigma?
-
Brüne M. Schizophrenia-an evolutionary enigma? Neurosci Biobehav Rev. 2004;28:41-53.
-
(2004)
Neurosci Biobehav Rev.
, vol.28
, pp. 41-53
-
-
Brüne, M.1
-
17
-
-
46249105511
-
The 'big bang' theory of the origin of psychosis and the faculty of language
-
Crow TJ. The 'big bang' theory of the origin of psychosis and the faculty of language. Schizophr Res. 2008;102:31-52.
-
(2008)
Schizophr Res.
, vol.102
, pp. 31-52
-
-
Crow, T.J.1
-
18
-
-
49649084779
-
Metabolic changes in schizophrenia and human brain evolution
-
Khaitovich P, Lockstone HE, Wayland MT, et al. Metabolic changes in schizophrenia and human brain evolution. Genome Biol. 2008;9:R124.
-
(2008)
Genome Biol.
, vol.9
, pp. R124
-
-
Khaitovich, P.1
Lockstone, H.E.2
Wayland, M.T.3
-
19
-
-
79951640772
-
The emergence of human-evolutionary medical genomics
-
Crespi BJ. The emergence of human-evolutionary medical genomics. Evol Appl. 2011;4:292-314.
-
(2011)
Evol Appl.
, vol.4
, pp. 292-314
-
-
Crespi, B.J.1
-
20
-
-
84897068638
-
Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes
-
Andreassen OA, McEvoy LK, Thompson WK, et al. Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes. Hypertension. 2014;63:819-826.
-
(2014)
Hypertension.
, vol.63
, pp. 819-826
-
-
Andreassen, O.A.1
McEvoy, L.K.2
Thompson, W.K.3
-
21
-
-
84926348812
-
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: Differential involvement of immune-related gene loci
-
Andreassen OA, Harbo HF, Wang Y, et al. Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Mol Psychiatry. 2015;20:207-214.
-
(2015)
Mol Psychiatry.
, vol.20
, pp. 207-214
-
-
Andreassen, O.A.1
Harbo, H.F.2
Wang, Y.3
-
22
-
-
84876834541
-
Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate
-
Andreassen OA, Thompson WK, Schork AJ, et al. Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate. PLoS Genet. 2013;9:e1003455.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003455
-
-
Andreassen, O.A.1
Thompson, W.K.2
Schork, A.J.3
-
23
-
-
84873701087
-
Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors
-
Andreassen OA, Djurovic S, Thompson WK, et al. Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. Am J Human Genet. 2013;92:197-209.
-
(2013)
Am J Human Genet.
, vol.92
, pp. 197-209
-
-
Andreassen, O.A.1
Djurovic, S.2
Thompson, W.K.3
-
24
-
-
84871281959
-
TCF4 (e2-2; ITF2): A schizophrenia-associated gene with pleiotropic effects on human disease
-
Navarrete K, Pedroso I, De Jong S, et al. TCF4 (e2-2; ITF2): A schizophrenia-associated gene with pleiotropic effects on human disease. Am J Med Genet B Neuropsychiatr Genet. 2013;162B:1-16.
-
(2013)
Am J Med Genet B Neuropsychiatr Genet.
, vol.162 B
, pp. 1-16
-
-
Navarrete, K.1
Pedroso, I.2
De Jong, S.3
-
25
-
-
84938775282
-
Systematic integration of brain eQTL and GWAS identifies ZNF323 as a novel schizophrenia risk gene and suggests recent positive selection based on compensatory advantage on pulmonary function
-
Luo XJ, Mattheisen M, Li M, et al. Systematic integration of brain eQTL and GWAS identifies ZNF323 as a novel schizophrenia risk gene and suggests recent positive selection based on compensatory advantage on pulmonary function. Schizophr Bull. 2015; doi:10.1093/schbul/sbv017.
-
(2015)
Schizophr Bull.
-
-
Luo, X.J.1
Mattheisen, M.2
Li, M.3
-
26
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Altshuler DM, Lander ES, Ambrogio L, et al. A map of human genome variation from population-scale sequencing. Nature. 2010;467:1061-1073.
-
(2010)
Nature.
, vol.467
, pp. 1061-1073
-
-
Altshuler, D.M.1
Lander, E.S.2
Ambrogio, L.3
-
27
-
-
66049157487
-
Signals of recent positive selection in a worldwide sample of human populations
-
Pickrell JK, Coop G, Novembre J, et al. Signals of recent positive selection in a worldwide sample of human populations. Genome Res. 2009;19:826-837.
-
(2009)
Genome Res.
, vol.19
, pp. 826-837
-
-
Pickrell, J.K.1
Coop, G.2
Novembre, J.3
-
28
-
-
39749181521
-
Worldwide human relationships inferred from genome-wide patterns of variation
-
Li JZ, Absher DM, Tang H, et al. Worldwide human relationships inferred from genome-wide patterns of variation. Science. 2008;319:1100-1104.
-
(2008)
Science.
, vol.319
, pp. 1100-1104
-
-
Li, J.Z.1
Absher, D.M.2
Tang, H.3
-
29
-
-
0037167852
-
Detecting recent positive selection in the human genome from haplotype structure
-
Sabeti PC, Reich DE, Higgins JM, et al. Detecting recent positive selection in the human genome from haplotype structure. Nature. 2002;419:832-837.
-
(2002)
Nature.
, vol.419
, pp. 832-837
-
-
Sabeti, P.C.1
Reich, D.E.2
Higgins, J.M.3
-
30
-
-
84921569624
-
Selscan: An efficient multithreaded program to perform EHH-based scans for positive selection
-
Szpiech ZA, Hernandez RD. selscan: an efficient multithreaded program to perform EHH-based scans for positive selection. Mol Biol Evol. 2014;31:2824-2827.
-
(2014)
Mol Biol Evol.
, vol.31
, pp. 2824-2827
-
-
Szpiech, Z.A.1
Hernandez, R.D.2
-
31
-
-
35349012592
-
Genome-wide detection and characterization of positive selection in human populations
-
Sabeti PC, Varilly P, Fry B, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 2007;449:913-918.
-
(2007)
Nature.
, vol.449
, pp. 913-918
-
-
Sabeti, P.C.1
Varilly, P.2
Fry, B.3
-
32
-
-
33644981509
-
A map of recent positive selection in the human genome
-
Voight BF, Kudaravalli S, Wen X, et al. A map of recent positive selection in the human genome. PLoS Biol 2006;4:e72.
-
(2006)
PLoS Biol
, vol.4
, pp. e72
-
-
Voight, B.F.1
Kudaravalli, S.2
Wen, X.3
-
33
-
-
65649117685
-
DnaSP v5: A software for comprehensive analysis of DNA polymorphism data
-
Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25:1451-1452.
-
(2009)
Bioinformatics.
, vol.25
, pp. 1451-1452
-
-
Librado, P.1
Rozas, J.2
-
34
-
-
0032900678
-
Median-joining networks for inferring intraspecific phylogenies
-
Bandelt HJ, Forster P, Röhl A. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol. 1999;16:37-48.
-
(1999)
Mol Biol Evol.
, vol.16
, pp. 37-48
-
-
Bandelt, H.J.1
Forster, P.2
Röhl, A.3
-
35
-
-
83555168307
-
Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia
-
Carrera N, Arrojo M, Sanjuán J, et al. Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia. Biol Psychiatry. 2012;71:169-177.
-
(2012)
Biol Psychiatry.
, vol.71
, pp. 169-177
-
-
Carrera, N.1
Arrojo, M.2
Sanjuán, J.3
-
36
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, et al. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007;81:559-575.
-
(2007)
Am J Hum Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
37
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7:248-249.
-
(2010)
Nat Methods.
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
-
38
-
-
78651320424
-
The UCSC Genome Browser database: Update 2011
-
Fujita PA, Rhead B, Zweig AS, et al. The UCSC Genome Browser database: update 2011. Nucleic Acids Res. 2011;39:D876-D882.
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. D876-D882
-
-
Fujita, P.A.1
Rhead, B.2
Zweig, A.S.3
-
39
-
-
0033578684
-
Protein secondary structure prediction based on position-specific scoring matrices
-
Jones DT. Protein secondary structure prediction based on position-specific scoring matrices. J Mol Biol. 1999;292:195-202.
-
(1999)
J Mol Biol.
, vol.292
, pp. 195-202
-
-
Jones, D.T.1
-
40
-
-
84883591545
-
Scalable web services for the PSIPRED Protein Analysis Workbench
-
Buchan DW, Minneci F, Nugent TC, et al. Scalable web services for the PSIPRED Protein Analysis Workbench. Nucleic Acids Res. 2013;41:W349-W357.
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. W349-W357
-
-
Buchan, D.W.1
Minneci, F.2
Nugent, T.C.3
-
41
-
-
63849246525
-
Protein structure prediction on the Web: A case study using the Phyre server
-
Kelley LA, Sternberg MJ. Protein structure prediction on the Web: A case study using the Phyre server. Nat Protoc. 2009;4:363-371.
-
(2009)
Nat Protoc.
, vol.4
, pp. 363-371
-
-
Kelley, L.A.1
Sternberg, M.J.2
-
43
-
-
80053383403
-
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
-
Wain LV, Verwoert GC, O'Reilly PF, et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet. 2011;43:1005-1011.
-
(2011)
Nat Genet.
, vol.43
, pp. 1005-1011
-
-
Wain, L.V.1
Verwoert, G.C.2
O'Reilly, P.F.3
-
44
-
-
0004095905
-
Independent prognostic information provided by sphygmomanometrically determined pulse pressure and mean arterial pressure in patients with left ventricular dysfunction
-
Domanski MJ, Mitchell GF, Norman JE, et al. Independent prognostic information provided by sphygmomanometrically determined pulse pressure and mean arterial pressure in patients with left ventricular dysfunction. J Am Coll Cardiol. 1999;33:951-958.
-
(1999)
J Am Coll Cardiol.
, vol.33
, pp. 951-958
-
-
Domanski, M.J.1
Mitchell, G.F.2
Norman, J.E.3
-
45
-
-
59849087350
-
Single versus combined blood pressure components and risk for cardiovascular disease: The Framingham Heart Study
-
Franklin SS, Lopez VA, Wong ND, et al. Single versus combined blood pressure components and risk for cardiovascular disease: The Framingham Heart Study. Circulation. 2009;119:243-250.
-
(2009)
Circulation.
, vol.119
, pp. 243-250
-
-
Franklin, S.S.1
Lopez, V.A.2
Wong, N.D.3
-
47
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
Speliotes EK, Willer CJ, Berndt SI, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010;42:937-948.
-
(2010)
Nat Genet.
, vol.42
, pp. 937-948
-
-
Speliotes, E.K.1
Willer, C.J.2
Berndt, S.I.3
-
48
-
-
84940871436
-
-
New York, NY: Oxford University Press
-
Willett W. Nutritional epidemiology, Vol 40. New York, NY: Oxford University Press; 2013.
-
(2013)
Nutritional Epidemiology
, vol.40
-
-
Willett, W.1
-
49
-
-
84875914619
-
Novel locus including FGF21 is associated with dietary macronutrient intake
-
Chu AY, Workalemahu T, Paynter NP, et al. Novel locus including FGF21 is associated with dietary macronutrient intake. Hum Mol Genet. 2013;22:1895-1902.
-
(2013)
Hum Mol Genet.
, vol.22
, pp. 1895-1902
-
-
Chu, A.Y.1
Workalemahu, T.2
Paynter, N.P.3
-
50
-
-
84875922294
-
Genome-wide metaanalysis of observational studies shows common genetic variants associated with macronutrient intake
-
Tanaka T, Ngwa JS, van Rooij FJ, et al. Genome-wide metaanalysis of observational studies shows common genetic variants associated with macronutrient intake. Am J Clin Nutr. 2013;97:1395-1402.
-
(2013)
Am J Clin Nutr.
, vol.97
, pp. 1395-1402
-
-
Tanaka, T.1
Ngwa, J.S.2
Van Rooij, F.J.3
-
51
-
-
35748938784
-
A genomewide association study for blood lipid phenotypes in the Framingham Heart Study
-
Kathiresan S, Manning AK, Demissie S, et al. A genomewide association study for blood lipid phenotypes in the Framingham Heart Study. BMC Med Genet. 2007;8(suppl 1):S17.
-
(2007)
BMC Med Genet.
, vol.8
, pp. S17
-
-
Kathiresan, S.1
Manning, A.K.2
Demissie, S.3
-
52
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010;466:707-713.
-
(2010)
Nature.
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
-
54
-
-
43049180910
-
Use of y chromosome and mitochondrial DNA population structure in tracing human migrations
-
Underhill PA, Kivisild T. Use of y chromosome and mitochondrial DNA population structure in tracing human migrations. Annu Rev Genet. 2007;41:539-564.
-
(2007)
Annu Rev Genet.
, vol.41
, pp. 539-564
-
-
Underhill, P.A.1
Kivisild, T.2
-
55
-
-
33745121154
-
Positive natural selection in the human lineage
-
Sabeti PC, Schaffner SF, Fry B, et al. Positive natural selection in the human lineage. Science. 2006;312:1614-1620.
-
(2006)
Science.
, vol.312
, pp. 1614-1620
-
-
Sabeti, P.C.1
Schaffner, S.F.2
Fry, B.3
-
56
-
-
79953221100
-
A genomewide association study in Europeans and South Asians identifies five new loci for coronary artery disease
-
Coronary Artery Disease Genetics Consortium. A genomewide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet. 2011;43:339-344.
-
(2011)
Nat Genet.
, vol.43
, pp. 339-344
-
-
Coronary Artery Disease Genetics Consortium1
-
57
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert H, Konig IR, Kathiresan S, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011;43:333-338.
-
(2011)
Nat Genet.
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
Konig, I.R.2
Kathiresan, S.3
-
58
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight BF, Scott LJ, Steinthorsdottir V, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet. 2010;42:579-589.
-
(2010)
Nat Genet.
, vol.42
, pp. 579-589
-
-
Voight, B.F.1
Scott, L.J.2
Steinthorsdottir, V.3
-
59
-
-
1342344814
-
The SLC39 family of metal ion transporters
-
Eide DJ. The SLC39 family of metal ion transporters. Pflugers Arch. 2004;447:796-800.
-
(2004)
Pflugers Arch.
, vol.447
, pp. 796-800
-
-
Eide, D.J.1
-
61
-
-
84860743865
-
Towards an encyclopaedia of mammalian gene function: The International Mouse Phenotyping Consortium
-
Brown SD, Moore MW. Towards an encyclopaedia of mammalian gene function: The International Mouse Phenotyping Consortium. Dis Model Mech. 2012;5:289-292.
-
(2012)
Dis Model Mech.
, vol.5
, pp. 289-292
-
-
Brown, S.D.1
Moore, M.W.2
-
62
-
-
48949119323
-
The human zinc transporter SLC39A8 (Zip8) is critical in zinc-mediated cytoprotection in lung epithelia
-
Besecker B, Bao S, Bohacova B, et al. The human zinc transporter SLC39A8 (Zip8) is critical in zinc-mediated cytoprotection in lung epithelia. Am J Physiol Lung Cell Mol Physiol. 2008;294:L1127-L1136.
-
(2008)
Am J Physiol Lung Cell Mol Physiol.
, vol.294
, pp. L1127-L1136
-
-
Besecker, B.1
Bao, S.2
Bohacova, B.3
-
63
-
-
14744280164
-
Identification of mouse SLC39A8 as the transporter responsible for cadmiuminduced toxicity in the testis
-
Dalton TP, He L, Wang B, et al. Identification of mouse SLC39A8 as the transporter responsible for cadmiuminduced toxicity in the testis. Proc Natl Acad Sci USA. 2005;102:3401-3406.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 3401-3406
-
-
Dalton, T.P.1
He, L.2
Wang, B.3
-
64
-
-
34247398618
-
Enhanced cadmium-induced testicular necrosis and renal proximal tubule damage caused by gene-dose increase in a Slc39a8-transgenic mouse line
-
Wang B, Schneider SN, Dragin N, et al. Enhanced cadmium-induced testicular necrosis and renal proximal tubule damage caused by gene-dose increase in a Slc39a8-transgenic mouse line. Am J Physiol Cell Physiol. 2007;292:C1523-C1535.
-
(2007)
Am J Physiol Cell Physiol.
, vol.292
, pp. C1523-C1535
-
-
Wang, B.1
Schneider, S.N.2
Dragin, N.3
-
65
-
-
33846418747
-
Evolution and hypertension
-
Weder AB. Evolution and hypertension. Hypertension. 2007;49:260-265.
-
(2007)
Hypertension.
, vol.49
, pp. 260-265
-
-
Weder, A.B.1
-
66
-
-
40149096254
-
Adaptations to climate in candidate genes for common metabolic disorders
-
Hancock AM, Witonsky DB, Gordon AS, et al. Adaptations to climate in candidate genes for common metabolic disorders. PLoS Genet. 2008;4:e32.
-
(2008)
PLoS Genet.
, vol.4
, pp. e32
-
-
Hancock, A.M.1
Witonsky, D.B.2
Gordon, A.S.3
-
67
-
-
0015816179
-
Blood pressure and dietary salt in human populations
-
Gleibermann L. Blood pressure and dietary salt in human populations. Ecol Food Nutr. 1973;2:143-156.
-
(1973)
Ecol Food Nutr.
, vol.2
, pp. 143-156
-
-
Gleibermann, L.1
-
68
-
-
2342459066
-
Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world
-
Nakajima T, Wooding S, Sakagami T, et al. Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. Am J Hum Genet. 2004;74:898-916.
-
(2004)
Am J Hum Genet.
, vol.74
, pp. 898-916
-
-
Nakajima, T.1
Wooding, S.2
Sakagami, T.3
-
69
-
-
8844271778
-
CYP3A variation and the evolution of salt-sensitivity variants
-
Thompson EE, Kuttab-Boulos H, Witonsky D, et al. CYP3A variation and the evolution of salt-sensitivity variants. Am J Hum Genet. 2004;75:1059-1069.
-
(2004)
Am J Hum Genet.
, vol.75
, pp. 1059-1069
-
-
Thompson, E.E.1
Kuttab-Boulos, H.2
Witonsky, D.3
-
70
-
-
84998080646
-
The prevalence and mechanisms of metabolic syndrome in schizophrenia: A review
-
Papanastasiou E. The prevalence and mechanisms of metabolic syndrome in schizophrenia: A review. Ther Adv Psychopharmacol. 2013;3:33-51.
-
(2013)
Ther Adv Psychopharmacol.
, vol.3
, pp. 33-51
-
-
Papanastasiou, E.1
|