-
1
-
-
0026669336
-
Molecular basis of human hypertension: Role of angiotensinogen
-
Jeunemaitre X, Soubrier F, Kotelevtsev YV, Liftou RP, Williams CS, Charru A, Hunt SC, Hopkins PN, Williams RR, Lalouel JM. Molecular basis of human hypertension: role of angiotensinogen. Cell. 1992;71:169-180.
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
Soubrier, F.2
Kotelevtsev, Y.V.3
Liftou, R.P.4
Williams, C.S.5
Charru, A.6
Hunt, S.C.7
Hopkins, P.N.8
Williams, R.R.9
Lalouel, J.M.10
-
2
-
-
0028331270
-
Angiotensinogen as a risk factor for essential hypertension in Japan
-
Hata A, Namikawa C, Sasaki M, Sato K, Nakamura T, Tamura K, Lalouel JM. Angiotensinogen as a risk factor for essential hypertension in Japan. J Clin Invest. 1994;93:1285-1287.
-
(1994)
J Clin Invest
, vol.93
, pp. 1285-1287
-
-
Hata, A.1
Namikawa, C.2
Sasaki, M.3
Sato, K.4
Nakamura, T.5
Tamura, K.6
Lalouel, J.M.7
-
3
-
-
0030893575
-
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro
-
Inoue I, Nakajima T, Williams CS, Quackenbush J, Puryear R, Powers M, Cheng T, Ludwig EH, Sharma AM, Hata A, Jeunemaitre X, Lalouel JM. A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro. J Clin Invest. 1997;99:1786-1797.
-
(1997)
J Clin Invest
, vol.99
, pp. 1786-1797
-
-
Inoue, I.1
Nakajima, T.2
Williams, C.S.3
Quackenbush, J.4
Puryear, R.5
Powers, M.6
Cheng, T.7
Ludwig, E.H.8
Sharma, A.M.9
Hata, A.10
Jeunemaitre, X.11
Lalouel, J.M.12
-
4
-
-
0028046423
-
Angiotensinogen gene in human hypertension: Lack of an association of the 235T allele among African Americans
-
Rotimi C, Morrison L, Cooper R, Oyejide C, Effiong E, Ladipo M, Osotemihen B, Ward R. Angiotensinogen gene in human hypertension: lack of an association of the 235T allele among African Americans. Hypertension. 1994;24:591-594.
-
(1994)
Hypertension
, vol.24
, pp. 591-594
-
-
Rotimi, C.1
Morrison, L.2
Cooper, R.3
Oyejide, C.4
Effiong, E.5
Ladipo, M.6
Osotemihen, B.7
Ward, R.8
-
5
-
-
0023831020
-
Frequency in hypertensives of alleles for a RFLP associated with the renin gene
-
Morris BJ, Griffiths LR. Frequency in hypertensives of alleles for a RFLP associated with the renin gene. Biochem Biophys Res Commun. 1988; 150:219-224.
-
(1988)
Biochem Biophys Res Commun
, vol.150
, pp. 219-224
-
-
Morris, B.J.1
Griffiths, L.R.2
-
6
-
-
0024828162
-
A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension
-
Naftilan AJ, Williams R, Burt D, Paul M, Pratt RE, Hobart P, Chirgwin J, Dzau VJ. A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension. Hypertension. 1989;14:614-618.
-
(1989)
Hypertension
, vol.14
, pp. 614-618
-
-
Naftilan, A.J.1
Williams, R.2
Burt, D.3
Paul, M.4
Pratt, R.E.5
Hobart, P.6
Chirgwin, J.7
Dzau, V.J.8
-
7
-
-
0026501994
-
Sib pair linkage analysis of renin gene haplotypes in human essential hypertension
-
Jeunemaitre X, Rigat B, Charru A, Houot AM, Soubrier F, Corvol P. Sib pair linkage analysis of renin gene haplotypes in human essential hypertension. Hum Genet. 1992;88:301-306.
-
(1992)
Hum Genet
, vol.88
, pp. 301-306
-
-
Jeunemaitre, X.1
Rigat, B.2
Charru, A.3
Houot, A.M.4
Soubrier, F.5
Corvol, P.6
-
8
-
-
0033404255
-
Human renin gene BglI dimorphism associated with hypertension in two independent populations
-
Frossard PM, Lestringant GG, Malloy MJ, Kane JP. Human renin gene BglI dimorphism associated with hypertension in two independent populations. Clin Genet. 1999;56:428-433.
-
(1999)
Clin Genet
, vol.56
, pp. 428-433
-
-
Frossard, P.M.1
Lestringant, G.G.2
Malloy, M.J.3
Kane, J.P.4
-
9
-
-
0028367403
-
The angiotensin I-converting enzyme gene polymorphism: Implication in hypertension and myocardial infarction
-
Soubrier F, Cambien F. The angiotensin I-converting enzyme gene polymorphism: implication in hypertension and myocardial infarction. Curr Opin Nephrol Hypertens. 1994;3:25-29.
-
(1994)
Curr Opin Nephrol Hypertens
, vol.3
, pp. 25-29
-
-
Soubrier, F.1
Cambien, F.2
-
10
-
-
18744411518
-
Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides
-
Cox R, Bouzekri N, Martin S, Southam L, Hugill A, Golamaully M, Cooper R, Adeyemo A, Soubrier F, Ward R, Lathrop GM, Matsuda F, Farrall M. Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Hum Mol Genet. 2002;11:2969-2977.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2969-2977
-
-
Cox, R.1
Bouzekri, N.2
Martin, S.3
Southam, L.4
Hugill, A.5
Golamaully, M.6
Cooper, R.7
Adeyemo, A.8
Soubrier, F.9
Ward, R.10
Lathrop, G.M.11
Matsuda, F.12
Farrall, M.13
-
11
-
-
0030021814
-
Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoples
-
Barley J, Blackwood A, Miller M, Markandu ND, Carter ND, Jeffery S, Cappuccio FP, MacGregor GA, Sagnella GA. Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoples. J Hum Hypertens. 1996;10:31-35.
-
(1996)
J Hum Hypertens
, vol.10
, pp. 31-35
-
-
Barley, J.1
Blackwood, A.2
Miller, M.3
Markandu, N.D.4
Carter, N.D.5
Jeffery, S.6
Cappuccio, F.P.7
MacGregor, G.A.8
Sagnella, G.A.9
-
12
-
-
0031026596
-
Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI Family Heart Study
-
Borecki IB, Province MA, Ludwig EH, Ellison RC, Folsom AR, Heiss G, Lalouel JM, Higgins M, Rao DC. Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: the NHLBI Family Heart Study. Ann Epidemiol. 1997;7:13-21.
-
(1997)
Ann Epidemiol
, vol.7
, pp. 13-21
-
-
Borecki, I.B.1
Province, M.A.2
Ludwig, E.H.3
Ellison, R.C.4
Folsom, A.R.5
Heiss, G.6
Lalouel, J.M.7
Higgins, M.8
Rao, D.C.9
-
13
-
-
0028118849
-
Angiotensin-converting enzyme polymorphism and essential hypertension
-
Morise T, Takeuchi Y, Takeda R. Angiotensin-converting enzyme polymorphism and essential hypertension. Lancet. 1994;343:125.
-
(1994)
Lancet
, vol.343
, pp. 125
-
-
Morise, T.1
Takeuchi, Y.2
Takeda, R.3
-
14
-
-
0027232658
-
Polymorphism of the angiotensin I converting enzyme gene is apparently not related to high blood pressure: Dutch Hypertension and Offspring Study
-
Schmidt S, van Hooft IM, Grobbee DE, Ganten D, Ritz E. Polymorphism of the angiotensin I converting enzyme gene is apparently not related to high blood pressure: Dutch Hypertension and Offspring Study. J Hypertens. 1993;11:345-348.
-
(1993)
J Hypertens
, vol.11
, pp. 345-348
-
-
Schmidt, S.1
Van Hooft, I.M.2
Grobbee, D.E.3
Ganten, D.4
Ritz, E.5
-
15
-
-
0030198577
-
Angiotensin converting enzyme gene polymorphism is not related to essential hypertension in a Greek population
-
Vassilikioti S, Doumas M, Douma S, Petidis K, Karagiannis A, Balaska K, Vyzantiadis A, Zamboulis C. Angiotensin converting enzyme gene polymorphism is not related to essential hypertension in a Greek population. Am J Hypertens. 1996;9:700-702.
-
(1996)
Am J Hypertens
, vol.9
, pp. 700-702
-
-
Vassilikioti, S.1
Doumas, M.2
Douma, S.3
Petidis, K.4
Karagiannis, A.5
Balaska, K.6
Vyzantiadis, A.7
Zamboulis, C.8
-
16
-
-
0035006837
-
Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure
-
Zhu X, Bouzekri N, Southam L, Cooper RS, Adeyemo A, McKenzie CA, Luke A, Chen G, Elston RC, Ward R. Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure. Am J Hum Genet. 2001;68:1139-1148.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1139-1148
-
-
Zhu, X.1
Bouzekri, N.2
Southam, L.3
Cooper, R.S.4
Adeyemo, A.5
McKenzie, C.A.6
Luke, A.7
Chen, G.8
Elston, R.C.9
Ward, R.10
-
17
-
-
0344193095
-
Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males
-
Fornage M, Amos CI, Kardia S, Sing CF, Turner ST, Boerwinkle E. Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males. Circulation. 1998;97:1773-1779.
-
(1998)
Circulation
, vol.97
, pp. 1773-1779
-
-
Fornage, M.1
Amos, C.I.2
Kardia, S.3
Sing, C.F.4
Turner, S.T.5
Boerwinkle, E.6
-
18
-
-
0345486977
-
Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study
-
O'Donnell CJ, Lindpaintner K, Larson MG, Rao VS, Ordovas JM, Schaefer EJ, Myers RH, Levy D. Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study. Circulation. 1998;97:1766-1772.
-
(1998)
Circulation
, vol.97
, pp. 1766-1772
-
-
O'Donnell, C.J.1
Lindpaintner, K.2
Larson, M.G.3
Rao, V.S.4
Ordovas, J.M.5
Schaefer, E.J.6
Myers, R.H.7
Levy, D.8
-
19
-
-
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. 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. 2000;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
-
20
-
-
0033037576
-
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension
-
Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvanen AC, Vartiainen E, Peltonen L, Kontula K. Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension. Hypertension. 1999;33:844-849.
-
(1999)
Hypertension
, vol.33
, pp. 844-849
-
-
Kainulainen, K.1
Perola, M.2
Terwilliger, J.3
Kaprio, J.4
Koskenvuo, M.5
Syvanen, A.C.6
Vartiainen, E.7
Peltonen, L.8
Kontula, K.9
-
21
-
-
0028290165
-
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension
-
Bonnardeaux A, Davies E, Jeunemaitre X, Fery I, Charru A, Clauser E, Tiret L, Cambien F, Corvol P, Soubrier F. Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension. Hypertension. 1994;24:63-69.
-
(1994)
Hypertension
, vol.24
, pp. 63-69
-
-
Bonnardeaux, A.1
Davies, E.2
Jeunemaitre, X.3
Fery, I.4
Charru, A.5
Clauser, E.6
Tiret, L.7
Cambien, F.8
Corvol, P.9
Soubrier, F.10
-
22
-
-
0031394825
-
Angiotensin II type I receptor polymorphism in African Americans: Lower frequency of the C1166 variant
-
Gainer JV, Hunley TE, Kon V, Nadeau JH, Muldowney JA 3rd, Brown NJ. Angiotensin II type I receptor polymorphism in African Americans: lower frequency of the C1166 variant. Biochem Mol Biol Int. 1997;43:227-231.
-
(1997)
Biochem Mol Biol Int
, vol.43
, pp. 227-231
-
-
Gainer, J.V.1
Hunley, T.E.2
Kon, V.3
Nadeau, J.H.4
Muldowney J.A. III5
Brown, N.J.6
-
23
-
-
0033941303
-
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program
-
Province MA, Boerwinkle E, Chakravarti A, Cooper R, Fornage M, Leppert M, Risch N, Ranade K. Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. J Hypertens. 2000;18:867-876.
-
(2000)
J Hypertens
, vol.18
, pp. 867-876
-
-
Province, M.A.1
Boerwinkle, E.2
Chakravarti, A.3
Cooper, R.4
Fornage, M.5
Leppert, M.6
Risch, N.7
Ranade, K.8
-
24
-
-
12244297741
-
A genome wide linkage analysis investigating the determinants of blood pressure in Caucasians and African Americans
-
Thiel B, Chakravarti A, Cooper R, Luke A, Lewis S, Lynn A, Tiwari H, Schork N, Weder A. A genome wide linkage analysis investigating the determinants of blood pressure in Caucasians and African Americans. Am J Hypertens. 2003;16:151-153.
-
(2003)
Am J Hypertens
, vol.16
, pp. 151-153
-
-
Thiel, B.1
Chakravarti, A.2
Cooper, R.3
Luke, A.4
Lewis, S.5
Lynn, A.6
Tiwari, H.7
Schork, N.8
Weder, A.9
-
25
-
-
0037313361
-
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: Findings from the Family Blood Pressure Program
-
Zhu X, Yan D, Cooper R, Luke A, Ikeda MA, Chang YPC, Weder A, Chakravarti A. Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the Family Blood Pressure Program. Genome Res. 2003;13:173-181.
-
(2003)
Genome Res
, vol.13
, pp. 173-181
-
-
Zhu, X.1
Yan, D.2
Cooper, R.3
Luke, A.4
Ikeda, M.A.5
Chang, Y.P.C.6
Weder, A.7
Chakravarti, A.8
-
26
-
-
0003752712
-
-
Sunderland, Mass: Sinauer Associates
-
Weir B. Genetic Data Analysis II. Sunderland, Mass: Sinauer Associates; 1996.
-
(1996)
Genetic Data Analysis Ii
-
-
Weir, B.1
-
27
-
-
0029130796
-
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
-
Excoffier L, Slatkin M. Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol. 1995;12:921-927.
-
(1995)
Mol Biol Evol
, vol.12
, pp. 921-927
-
-
Excoffier, L.1
Slatkin, M.2
-
28
-
-
0029372419
-
HAPLO: A program using the EM algorithm to estimate the frequencies of multi-site haplotypes
-
Hawley ME, Kidd KK. HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered. 1995;86:409-411.
-
(1995)
J Hered
, vol.86
, pp. 409-411
-
-
Hawley, M.E.1
Kidd, K.K.2
-
29
-
-
0028913523
-
An E-M algorithm and testing strategy for multiple-locus haplotypes
-
Long JC, Williams RC, Urbanek M. An E-M algorithm and testing strategy for multiple-locus haplotypes. Am J Hum Genet. 1995;56:799-810.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 799-810
-
-
Long, J.C.1
Williams, R.C.2
Urbanek, M.3
-
30
-
-
0033794938
-
Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data
-
Fallin D, Schork NJ. Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data. Am J Hum Genet. 2000;67:947-959.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 947-959
-
-
Fallin, D.1
Schork, N.J.2
-
31
-
-
0033990339
-
Model-free analysis and permutation tests for allelic associations
-
Zhao JH, Curtis D, Sham PC. Model-free analysis and permutation tests for allelic associations. Hum Hered. 2000;50:133-139.
-
(2000)
Hum Hered
, vol.50
, pp. 133-139
-
-
Zhao, J.H.1
Curtis, D.2
Sham, P.C.3
-
32
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D. A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet. 1999;65:1170-1177.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
33
-
-
0033910721
-
Comparison of tests for association and linkage in incomplete families
-
Cervino AC, Hill AV. Comparison of tests for association and linkage in incomplete families. Am J Hum Genet. 2000;67:120-132.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 120-132
-
-
Cervino, A.C.1
Hill, A.V.2
-
34
-
-
0031912715
-
A sibship test for linkage in the presence of association: The sib transmission/disequilibrium test
-
Spielman RS, Ewens WJ. A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test. Am J Hum Genet. 1998;62:450-458.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 450-458
-
-
Spielman, R.S.1
Ewens, W.J.2
-
35
-
-
0033364961
-
The transmission/disequilibrium test and parental-genotype reconstruction: The reconstruction-combined transmission/disequilibrium test
-
Knapp M. The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/disequilibrium test. Am J Hum Genet. 1999;64:861-870.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 861-870
-
-
Knapp, M.1
-
36
-
-
0034791035
-
Highresolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES. Highresolution haplotype structure in the human genome. Nat Genet. 2001; 29:229-232.
-
(2001)
Nat Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
37
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science. 2001;294:1719-1723.
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
Nguyen, B.T.11
Norris, M.C.12
Sheehan, J.B.13
Shen, N.14
Stern, D.15
Stokowski, R.P.16
Thomas, D.J.17
Trulson, M.O.18
Vyas, K.R.19
Frazer, K.A.20
Fodor, S.P.21
Cox, D.R.22
more..
-
38
-
-
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. The structure of haplotype blocks in the human genome. Science. 2002; 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
-
39
-
-
0035257236
-
Association study designs for complex diseases
-
Cardon LR, Bell JI. Association study designs for complex diseases. Nat Rev Genet. 2001;2:91-99.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
40
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science. 1996;273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
41
-
-
0029805706
-
The new genomics: Global views of biology
-
Lander ES. The new genomics: global views of biology. Science. 1996; 274:536-539.
-
(1996)
Science
, vol.274
, pp. 536-539
-
-
Lander, E.S.1
-
42
-
-
0032231375
-
Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus
-
Nielsen DM, Ehm MG, Weir BS. Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus. Am J Hum Genet. 1998;63:1531-1540.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1531-1540
-
-
Nielsen, D.M.1
Ehm, M.G.2
Weir, B.S.3
-
43
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Wolff RK, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996;13:399-408.
-
(1996)
Nat Genet
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
Tsuchihashi, Z.4
Ruddy, D.A.5
Basava, A.6
Dormishian, F.7
Domingo R., Jr.8
Ellis, M.C.9
Fullan, A.10
Hinton, L.M.11
Jones, N.L.12
Kimmel, B.E.13
Kronmal, G.S.14
Lauer, P.15
Lee, V.K.16
Loeb, D.B.17
Mapa, F.A.18
McClelland, E.19
Meyer, N.C.20
Mintier, G.A.21
Moeller, N.22
Moore, T.23
Morikang, E.24
Wolff, R.K.25
more..
-
44
-
-
17344380534
-
An SNP map of human chromosome 22
-
Mullikin JC, Hunt SE, Cole CG, Mortimore BJ, Rice CM, Burton J, Matthews LH, Pavitt R, Plumb RW, Sims SK, Ainscough RM, Attwood J, Bailey JM, Barlow K, Bruskiewich RM, Butcher PN, Carter NP, Chen Y, Clee CM, Coggill PC, Davies J, Davies RM, Dawson E, Francis MD, Joy AA, Lamble RG, Langford CF, Macarthy J, Mall V, Moreland A, Overton-Larty EK, Ross MT, Smith LC, Steward CA, Sulston JE, Tinsley EJ, Turney KJ, Willey DL, Wilson GD, McMurray AA, Dunham I, Rogers J, Bentley DR. An SNP map of human chromosome 22. Nature. 2000;407:516-520.
-
(2000)
Nature
, vol.407
, pp. 516-520
-
-
Mullikin, J.C.1
Hunt, S.E.2
Cole, C.G.3
Mortimore, B.J.4
Rice, C.M.5
Burton, J.6
Matthews, L.H.7
Pavitt, R.8
Plumb, R.W.9
Sims, S.K.10
Ainscough, R.M.11
Attwood, J.12
Bailey, J.M.13
Barlow, K.14
Bruskiewich, R.M.15
Butcher, P.N.16
Carter, N.P.17
Chen, Y.18
Clee, C.M.19
Coggill, P.C.20
Davies, J.21
Davies, R.M.22
Dawson, E.23
Francis, M.D.24
Joy, A.A.25
Lamble, R.G.26
Langford, C.F.27
Macarthy, J.28
Mall, V.29
Moreland, A.30
Overton-Larty, E.K.31
Ross, M.T.32
Smith, L.C.33
Steward, C.A.34
Sulston, J.E.35
Tinsley, E.J.36
Turney, K.J.37
Willey, D.L.38
Wilson, G.D.39
McMurray, A.A.40
Dunham, I.41
Rogers, J.42
Bentley, D.R.43
more..
-
45
-
-
0034727107
-
An SNP map of the human genome generated by reduced representation shotgun sequencing
-
Altshuler D, Pollara VJ, Cowles CR, Van Etten WJ, Baldwin J, Linton L, Lander ES. An SNP map of the human genome generated by reduced representation shotgun sequencing. Nature. 2000;407:513-516.
-
(2000)
Nature
, vol.407
, pp. 513-516
-
-
Altshuler, D.1
Pollara, V.J.2
Cowles, C.R.3
Van Etten, W.J.4
Baldwin, J.5
Linton, L.6
Lander, E.S.7
-
46
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R, Lander ES. Linkage disequilibrium in the human genome. Nature. 2001;411:199-204.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
|