-
1
-
-
0038049458
-
Genetic epidemiology of type 1 diabetes.
-
Hirschhorn JN 2003 Genetic epidemiology of type 1 diabetes. Pediatr Diabetes 4:87-100
-
(2003)
Pediatr Diabetes
, vol.4
, pp. 87-100
-
-
Hirschhorn, J.N.1
-
3
-
-
0019226693
-
Gene dosage and susceptibility to insulin-dependent diabetes.
-
Spielman RS, Baker L, Zmijewski CM 1980 Gene dosage and susceptibility to insulin-dependent diabetes. Ann Hum Genet 44:135-150
-
(1980)
Ann Hum Genet
, vol.44
, pp. 135-150
-
-
Spielman, R.S.1
Baker, L.2
Zmijewski, C.M.3
-
4
-
-
0025019555
-
Linkage strategies for genetically complex traits. I. Multilocus models.
-
Risch N 1990 Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet 46:222-228
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
5
-
-
0242524453
-
The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits.
-
Florez JC, Hirschhorn J, Altshuler D 2003 The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits. Annu Rev Genomics Hum Genet 4:257-291
-
(2003)
Annu Rev Genomics Hum Genet
, vol.4
, pp. 257-291
-
-
Florez, J.C.1
Hirschhorn, J.2
Altshuler, D.3
-
6
-
-
0036844002
-
Genomewide linkage analysis of body mass index across 28 years of the Framingham Heart Study.
-
Atwood LD, Heard-Costa NL, Cupples LA, Jaquish CE, Wilson PW, D’Agostino RB 2002 Genomewide linkage analysis of body mass index across 28 years of the Framingham Heart Study. Am J Hum Genet 71:1044-1050
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1044-1050
-
-
Atwood, L.D.1
Heard-Costa, N.L.2
Cupples, L.A.3
Jaquish, C.E.4
Wilson, P.W.5
D’Agostino, R.B.6
-
7
-
-
0033770421
-
Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study.
-
Levy D, DeStefano AL, Larson MG, O’Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH 2000 Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study. Hypertension 36:477-483
-
(2000)
Hypertension
, vol.36
, pp. 477-483
-
-
Levy, D.1
DeStefano, A.L.2
Larson, M.G.3
O’Donnell, C.J.4
Lifton, R.P.5
Gavras, H.6
Cupples, L.A.7
Myers, R.H.8
-
8
-
-
0028090414
-
Genetic dissection of complex traits.
-
Lander ES, Schork NJ 1994 Genetic dissection of complex traits. Science 265:2037-2048
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
9
-
-
84984932946
-
Population genetics—making sense out of sequence.
-
Chakravarti A 1999 Population genetics—making sense out of sequence. Nat Genet 21:56-60
-
(1999)
Nat Genet
, vol.21
, pp. 56-60
-
-
Chakravarti, A.1
-
10
-
-
0035451780
-
On the allelic spectrum of human disease.
-
Reich DE, Lander ES 2001 On the allelic spectrum of human disease. Trends Genet 17:502-510
-
(2001)
Trends Genet
, vol.17
, pp. 502-510
-
-
Reich, D.E.1
Lander, E.S.2
-
11
-
-
18444369013
-
The structure of haplotype blocks in the human genome.
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D 2002 The structure of haplotype blocks in the human genome. Science 296:2225-2229
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
12
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.
-
Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, Rogers J, Bentley DR, Kwok PY, Mardis ER, Yeh RT, Schultz B, Cook L, Davenport R, Dante M, Fulton L, Hillier L, Waterston RH, McPherson JD, Gilman B, Schaffner S, Van Etten WJ, Reich D, Higgins J, Daly MJ, Blumenstiel B, Baldwin J, Stange-Thomann N, Zody MC, Linton L, Lander ES, Altshuler D; International SNP Map Working Group 2001 A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409:928-933
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
Mullikin, J.C.8
Mortimore, B.J.9
Willey, D.L.10
Hunt, S.E.11
Cole, C.G.12
Coggill, P.C.13
Rice, C.M.14
Ning, Z.15
Rogers, J.16
Bentley, D.R.17
Kwok, P.Y.18
Mardis, E.R.19
Yeh, R.T.20
Schultz, B.21
Cook, L.22
Davenport, R.23
Dante, M.24
Fulton, L.25
Hillier, L.26
Waterston, R.H.27
McPherson, J.D.28
Gilman, B.29
Schaffner, S.30
Van Etten, W.J.31
Reich, D.32
Higgins, J.33
Daly, M.J.34
Blumenstiel, B.35
Baldwin, J.36
Stange-Thomann, N.37
Zody, M.C.38
Linton, L.39
Lander, E.S.40
Altshuler, D.41
more..
-
13
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard JK 2001 Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124-137
-
(2001)
Am J Hum Genet
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
14
-
-
0016682938
-
The first arrival time and mean age of a deleterious mutant gene in a finite population.
-
Li WH 1975 The first arrival time and mean age of a deleterious mutant gene in a finite population. Am J Hum Genet 27:274-286
-
(1975)
Am J Hum Genet
, vol.27
, pp. 274-286
-
-
Li, W.H.1
-
15
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease.
-
Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN 2003 Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet 33:177-182
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
16
-
-
0034758045
-
Genomewide scans of complex human diseases: true linkage is hard to find.
-
Altmuller J, Palmer LJ, Fischer G, Scherb H, Wjst M 2001 Genomewide scans of complex human diseases: true linkage is hard to find. Am J Hum Genet 69:936-950
-
(2001)
Am J Hum Genet
, vol.69
, pp. 936-950
-
-
Altmuller, J.1
Palmer, L.J.2
Fischer, G.3
Scherb, H.4
Wjst, M.5
-
17
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits.
-
Hirschhorn JN, Daly MJ 2005 Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 6:95-108
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
18
-
-
0029741063
-
The future of genetic studies of complex human diseases.
-
Risch N, Merikangas K 1996 The future of genetic studies of complex human diseases. Science 273:1516-1517
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
19
-
-
0033624575
-
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.
-
Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J, Lane CR, Schaffner SF, Bolk S, Brewer C, Tuomi T, Gaudet D, Hudson TJ, Daly M, Groop L, Lander ES 2000 The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26:76-80
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
Tuomi, T.11
Gaudet, D.12
Hudson, T.J.13
Daly, M.14
Groop, L.15
Lander, E.S.16
-
20
-
-
3042698329
-
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
-
Barratt BJ, Payne F, Lowe CE, Hermann R, Healy BC, Harold D, Concannon P, Gharani N, McCarthy MI, Olavesen MG, McCormack R, Guja C, Ionescu-Tirgoviste C, Undlien DE, Ronningen KS, Gillespie KM, Tuomilehto-Wolf E, Tuomilehto J, Bennett ST, Clayton DG, Cordell HJ, Todd JA 2004 Remapping the insulin gene/IDDM2 locus in type 1 diabetes. Diabetes 53:1884-1889
-
(2004)
Diabetes
, vol.53
, pp. 1884-1889
-
-
Barratt, B.J.1
Payne, F.2
Lowe, C.E.3
Hermann, R.4
Healy, B.C.5
Harold, D.6
Concannon, P.7
Gharani, N.8
McCarthy, M.I.9
Olavesen, M.G.10
McCormack, R.11
Guja, C.12
Ionescu-Tirgoviste, C.13
Undlien, D.E.14
Ronningen, K.S.15
Gillespie, K.M.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Bennett, S.T.19
Clayton, D.G.20
Cordell, H.J.21
Todd, J.A.22
more..
-
21
-
-
0034821661
-
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
-
Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, Concannon P 2001 Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families. Am J Hum Genet 69:820-830
-
(2001)
Am J Hum Genet
, vol.69
, pp. 820-830
-
-
Cox, N.J.1
Wapelhorst, B.2
Morrison, V.A.3
Johnson, L.4
Pinchuk, L.5
Spielman, R.S.6
Todd, J.A.7
Concannon, P.8
-
22
-
-
2642583283
-
Mapping complex disease loci in whole-genome association studies.
-
Carlson CS, Eberle MA, Kruglyak L, Nickerson DA 2004 Mapping complex disease loci in whole-genome association studies. Nature 429:446-452
-
(2004)
Nature
, vol.429
, pp. 446-452
-
-
Carlson, C.S.1
Eberle, M.A.2
Kruglyak, L.3
Nickerson, D.A.4
-
25
-
-
0345164399
-
Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation.
-
Yen CJ, Beamer BA, Negri C, Silver K, Brown KA, Yarnall DP, Burns DK, Roth J, Shuldiner AR 1997 Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation. Biochem Biophys Res Commun 241:270-274
-
(1997)
Biochem Biophys Res Commun
, vol.241
, pp. 270-274
-
-
Yen, C.J.1
Beamer, B.A.2
Negri, C.3
Silver, K.4
Brown, K.A.5
Yarnall, D.P.6
Burns, D.K.7
Roth, J.8
Shuldiner, A.R.9
-
26
-
-
0031595923
-
A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity.
-
Deeb SS, Fajas L, Nemoto M, Pihlajamaki J, Mykkanen L, Kuusisto J, Laakso M, Fujimoto W, Auwerx J 1998 A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nat Genet 20:284-287
-
(1998)
Nat Genet
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
Fajas, L.2
Nemoto, M.3
Pihlajamaki, J.4
Mykkanen, L.5
Kuusisto, J.6
Laakso, M.7
Fujimoto, W.8
Auwerx, J.9
-
27
-
-
0034728762
-
The Pro12Ala polymorphism in PPAR gamma2 may confer resistance to type 2 diabetes.
-
Hara K, Okada T, Tobe K, Yasuda K, Mori Y, Kadowaki H, Hagura R, Akanuma Y, Kimura S, Ito C, Kadowaki T 2000 The Pro12Ala polymorphism in PPAR gamma2 may confer resistance to type 2 diabetes. Biochem Biophys Res Commun 271:212-216
-
(2000)
Biochem Biophys Res Commun
, vol.271
, pp. 212-216
-
-
Hara, K.1
Okada, T.2
Tobe, K.3
Yasuda, K.4
Mori, Y.5
Kadowaki, H.6
Hagura, R.7
Akanuma, Y.8
Kimura, S.9
Ito, C.10
Kadowaki, T.11
-
28
-
-
0033060302
-
Pro12Ala substitution in the peroxisome proliferator-activated receptor- gamma2 is not associated with type 2 diabetes.
-
Mancini FP, Vaccaro O, Sabatino L, Tufano A, Rivellese AA, Riccardi G, Colantuoni V 1999 Pro12Ala substitution in the peroxisome proliferator-activated receptor- gamma2 is not associated with type 2 diabetes. Diabetes 48:1466-1468
-
(1999)
Diabetes
, vol.48
, pp. 1466-1468
-
-
Mancini, F.P.1
Vaccaro, O.2
Sabatino, L.3
Tufano, A.4
Rivellese, A.A.5
Riccardi, G.6
Colantuoni, V.7
-
29
-
-
0033582258
-
Pro12Ala missense mutation of the peroxisome proliferator activated receptor gamma and diabetes mellitus.
-
Ringel J, Engeli S, Distler A, Sharma AM 1999 Pro12Ala missense mutation of the peroxisome proliferator activated receptor gamma and diabetes mellitus. Biochem Biophys Res Commun 254:450-453
-
(1999)
Biochem Biophys Res Commun
, vol.254
, pp. 450-453
-
-
Ringel, J.1
Engeli, S.2
Distler, A.3
Sharma, A.M.4
-
30
-
-
0004509649
-
The Pro115Gln and Pro12Ala PPAR gamma gene mutations in obesity and type 2 diabetes.
-
Clement K, Hercberg S, Passinge B, Galan P, Varroud-Vial M, Shuldiner AR, Beamer BA, Charpentier G, Guy-Grand B, Froguel P, Vaisse C 2000 The Pro115Gln and Pro12Ala PPAR gamma gene mutations in obesity and type 2 diabetes. Int J Obes Relat Metab Disord 24:391-393
-
(2000)
Int J Obes Relat Metab Disord
, vol.24
, pp. 391-393
-
-
Clement, K.1
Hercberg, S.2
Passinge, B.3
Galan, P.4
Varroud-Vial, M.5
Shuldiner, A.R.6
Beamer, B.A.7
Charpentier, G.8
Guy-Grand, B.9
Froguel, P.10
Vaisse, C.11
-
31
-
-
0001491179
-
Impact of the peroxisome proliferator activated receptor gamma2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus.
-
Meirhaeghe A, Fajas L, Helbecque N, Cottel D, Auwerx J, Deeb SS, Amouyel P 2000 Impact of the peroxisome proliferator activated receptor gamma2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus. Int J Obes Relat Metab Disord 24:195-199
-
(2000)
Int J Obes Relat Metab Disord
, vol.24
, pp. 195-199
-
-
Meirhaeghe, A.1
Fajas, L.2
Helbecque, N.3
Cottel, D.4
Auwerx, J.5
Deeb, S.S.6
Amouyel, P.7
-
32
-
-
0034745184
-
The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences.
-
Douglas JA, Erdos MR, Watanabe RM, Braun A, Johnston CL, Oeth P, Mohlke KL, Valle TT, Ehnholm C, Buchanan TA, Bergman RN, Collins FS, Boehnke M, Tuomilehto J 2001 The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences. Diabetes 50:886-890
-
(2001)
Diabetes
, vol.50
, pp. 886-890
-
-
Douglas, J.A.1
Erdos, M.R.2
Watanabe, R.M.3
Braun, A.4
Johnston, C.L.5
Oeth, P.6
Mohlke, K.L.7
Valle, T.T.8
Ehnholm, C.9
Buchanan, T.A.10
Bergman, R.N.11
Collins, F.S.12
Boehnke, M.13
Tuomilehto, J.14
-
33
-
-
0034745185
-
The Pro12 ->Ala substitution in PPAR-gamma is associated with resistance to development of diabetes in the general population: possible involvement in impairment of insulin secretion in individuals with type 2 diabetes.
-
Mori H, Ikegami H, Kawaguchi Y, Seino S, Yokoi N, Takeda J, Inoue I, Seino Y, Yasuda K, Hanafusa T, Yamagata K, Awata T, Kadowaki T, Hara K, Yamada N, Gotoda T, Iwasaki N, Iwamoto Y, Sanke T, Nanjo K, Oka Y, Matsutani A, Maeda E, Kasuga M 2001 The Pro12 ->Ala substitution in PPAR-gamma is associated with resistance to development of diabetes in the general population: possible involvement in impairment of insulin secretion in individuals with type 2 diabetes. Diabetes 50:891-894
-
(2001)
Diabetes
, vol.50
, pp. 891-894
-
-
Mori, H.1
Ikegami, H.2
Kawaguchi, Y.3
Seino, S.4
Yokoi, N.5
Takeda, J.6
Inoue, I.7
Seino, Y.8
Yasuda, K.9
Hanafusa, T.10
Yamagata, K.11
Awata, T.12
Kadowaki, T.13
Hara, K.14
Yamada, N.15
Gotoda, T.16
Iwasaki, N.17
Iwamoto, Y.18
Sanke, T.19
Nanjo, K.20
Oka, Y.21
Matsutani, A.22
Maeda, E.23
Kasuga, M.24
more..
-
34
-
-
0036071296
-
Testing for population subdivision and association in four case-control studies.
-
Ardlie KG, Lunetta KL, Seielstad M 2002 Testing for population subdivision and association in four case-control studies. Am J Hum Genet 71:304-311
-
(2002)
Am J Hum Genet
, vol.71
, pp. 304-311
-
-
Ardlie, K.G.1
Lunetta, K.L.2
Seielstad, M.3
-
35
-
-
0034972487
-
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.
-
Hirschhorn JN, Lindgren CM, Daly MJ, Kirby A, Schaffner SF, Burtt NP, Altshuler D, Parker A, Rioux JD, Platko J, Gaudet D, Hudson TJ, Groop LC, Lander ES 2001 Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet 69:106-116
-
(2001)
Am J Hum Genet
, vol.69
, pp. 106-116
-
-
Hirschhorn, J.N.1
Lindgren, C.M.2
Daly, M.J.3
Kirby, A.4
Schaffner, S.F.5
Burtt, N.P.6
Altshuler, D.7
Parker, A.8
Rioux, J.D.9
Platko, J.10
Gaudet, D.11
Hudson, T.J.12
Groop, L.C.13
Lander, E.S.14
-
36
-
-
0034969436
-
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.
-
Perola M, Ohman M, Hiekkalinna T, Leppavuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L 2001 Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. Am J Hum Genet 69:117-123
-
(2001)
Am J Hum Genet
, vol.69
, pp. 117-123
-
-
Perola, M.1
Ohman, M.2
Hiekkalinna, T.3
Leppavuori, J.4
Pajukanta, P.5
Wessman, M.6
Koskenvuo, M.7
Palotie, A.8
Lange, K.9
Kaprio, J.10
Peltonen, L.11
-
37
-
-
0036724841
-
Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.
-
Xu J, Bleecker ER, Jongepier H, Howard TD, Koppelman GH, Postma DS, Meyers DA 2002 Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12. Am J Hum Genet 71:646-650
-
(2002)
Am J Hum Genet
, vol.71
, pp. 646-650
-
-
Xu, J.1
Bleecker, E.R.2
Jongepier, H.3
Howard, T.D.4
Koppelman, G.H.5
Postma, D.S.6
Meyers, D.A.7
-
38
-
-
0037368905
-
Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program.
-
Wu X, Cooper RS, Boerwinkle E, Turner ST, Hunt S, Myers R, Olshen RA, Curb D, Zhu X, Kan D, Luke A 2003 Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program. Eur J Hum Genet 11:271-274
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 271-274
-
-
Wu, X.1
Cooper, R.S.2
Boerwinkle, E.3
Turner, S.T.4
Hunt, S.5
Myers, R.6
Olshen, R.A.7
Curb, D.8
Zhu, X.9
Kan, D.10
Luke, A.11
-
39
-
-
0035261381
-
Genomic strategies to identify mammalian regulatory sequences.
-
Pennacchio LA, Rubin EM 2001 Genomic strategies to identify mammalian regulatory sequences. Nat Rev Genet 2:100-109
-
(2001)
Nat Rev Genet
, vol.2
, pp. 100-109
-
-
Pennacchio, L.A.1
Rubin, E.M.2
-
40
-
-
0014632032
-
Primary adult lactose intolerance and the milking habit: a problem in biologic and cultural interrelations. I. Review of the medical research.
-
Simoons FJ 1969 Primary adult lactose intolerance and the milking habit: a problem in biologic and cultural interrelations. I. Review of the medical research. Am J Dig Dis 14:819-836
-
(1969)
Am J Dig Dis
, vol.14
, pp. 819-836
-
-
Simoons, F.J.1
-
41
-
-
0014832106
-
Primary adult lactose intolerance and the milking habit: a problem in biologic and cultural interrelations. II. A culture historical hypothesis.
-
Simoons FJ 1970 Primary adult lactose intolerance and the milking habit: a problem in biologic and cultural interrelations. II. A culture historical hypothesis. Am J Dig Dis 15:695-710
-
(1970)
Am J Dig Dis
, vol.15
, pp. 695-710
-
-
Simoons, F.J.1
-
42
-
-
0036479030
-
Identification of a variant associated with adult-type hypolactasia.
-
Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Jarvela I 2002 Identification of a variant associated with adult-type hypolactasia. Nat Genet 30:233-237
-
(2002)
Nat Genet
, vol.30
, pp. 233-237
-
-
Enattah, N.S.1
Sahi, T.2
Savilahti, E.3
Terwilliger, J.D.4
Peltonen, L.5
Jarvela, I.6
|