共 25 条
[1]
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
[J].
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
.
NATURE GENETICS,
2000, 26 (01)
:76-80

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Hirschhorn, JN
论文数: 0 引用数: 0
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Klannemark, M
论文数: 0 引用数: 0
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Lindgren, CM
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Vohl, MC
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Nemesh, J
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Lane, CR
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Schaffner, SF
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Bolk, S
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Brewer, C
论文数: 0 引用数: 0
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Tuomi, T
论文数: 0 引用数: 0
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Gaudet, D
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

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Daly, M
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Groop, L
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA

Lander, ES
论文数: 0 引用数: 0
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机构: MIT, Whitehead Inst, Ctr Genome Res, Cambridge, MA 02139 USA
[2]
Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension
[J].
Barroso, I
;
Gurnell, M
;
Crowley, VEF
;
Agostini, M
;
Schwabe, JW
;
Soos, MA
;
Maslen, GL
;
Williams, TDM
;
Lewis, H
;
Schafer, AJ
;
Chatterjee, VKK
;
O'Rahilly, S
.
NATURE,
1999, 402 (6764)
:880-883

Barroso, I
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Gurnell, M
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Crowley, VEF
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Agostini, M
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Schwabe, JW
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Soos, MA
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Maslen, GL
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Williams, TDM
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Lewis, H
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

Schafer, AJ
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机构: Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res, Dept Clin Biochem, Cambridge CB2 2QQ, England

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[3]
Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population
[J].
Chandak, G. R.
;
Janipalli, C. S.
;
Bhaskar, S.
;
Kulkarni, S. R.
;
Mohankrishna, P.
;
Hattersley, A. T.
;
Frayling, T. M.
;
Yajnik, C. S.
.
DIABETOLOGIA,
2007, 50 (01)
:63-67

Chandak, G. R.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Janipalli, C. S.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Bhaskar, S.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Kulkarni, S. R.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Mohankrishna, P.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Hattersley, A. T.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Frayling, T. M.
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机构: King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India

Yajnik, C. S.
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King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India King Edward Mem Hosp & Res Ctr, Kamalnayan Bajaj Diabetol Res Ctr, Pune 410011, Maharashtra, India
[4]
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program
[J].
Florez, Jose C.
;
Jablonski, Kathleen A.
;
Bayley, Nick
;
Pollin, Toni I.
;
de Bakker, Paul I. W.
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Shuldiner, Alan R.
;
Knowler, William C.
;
Nathan, David M.
;
Altshuler, David
.
NEW ENGLAND JOURNAL OF MEDICINE,
2006, 355 (03)
:241-250

Florez, Jose C.
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机构:
George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

Jablonski, Kathleen A.
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

Bayley, Nick
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

Pollin, Toni I.
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

de Bakker, Paul I. W.
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

Shuldiner, Alan R.
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

Knowler, William C.
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George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA George Washington Univ, Diabet Prevent Program Outcomes Study Coordinatin, Rockville, MD USA

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[5]
Type 2 diabetes TCF7L2 risk genotypes alter birth weight:: A study of 24,053 individuals
[J].
Freathy, Rachel M.
;
Weedon, Michael N.
;
Bennett, Amanda
;
Hypponen, Elina
;
Relton, Caroline L.
;
Knight, Beatrice
;
Shields, Beverley
;
Parnell, Kirstie S.
;
Groves, Christopher J.
;
Ring, Susan M.
;
Pembrey, Marcus E.
;
Ben-Shlomo, Yoav
;
Strachan, David P.
;
Power, Chris
;
Jarvelin, Marjo-Riitta
;
McCarthy, Mark I.
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Smith, George Davey
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Hattersley, Andrew T.
;
Frayling, Timothy M.
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AMERICAN JOURNAL OF HUMAN GENETICS,
2007, 80 (06)
:1150-1161

Freathy, Rachel M.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Weedon, Michael N.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Bennett, Amanda
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Hypponen, Elina
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Relton, Caroline L.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Knight, Beatrice
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Shields, Beverley
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Parnell, Kirstie S.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Groves, Christopher J.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Ring, Susan M.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Pembrey, Marcus E.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Ben-Shlomo, Yoav
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Strachan, David P.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Power, Chris
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

Jarvelin, Marjo-Riitta
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

McCarthy, Mark I.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England

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Frayling, Timothy M.
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LU, Devon, England
[6]
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
[J].
Gloyn, AL
;
Pearson, ER
;
Antcliff, JF
;
Proks, P
;
Bruining, GJ
;
Slingerland, AS
;
Howard, N
;
Srinivasan, S
;
Silva, JMCL
;
Molnes, J
;
Edghill, EL
;
Frayling, TM
;
Temple, IK
;
Mackay, D
;
Shield, JPH
;
Sumnik, Z
;
van Rhijn, A
;
Wales, JKH
;
Clark, P
;
Gorman, S
;
Aisenberg, J
;
Ellard, S
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Njolstad, PR
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Ashcroft, FM
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Hattersley, AT
.
NEW ENGLAND JOURNAL OF MEDICINE,
2004, 350 (18)
:1838-1849

Gloyn, AL
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Pearson, ER
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Antcliff, JF
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Proks, P
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Bruining, GJ
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Slingerland, AS
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Howard, N
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Srinivasan, S
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Silva, JMCL
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Molnes, J
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Edghill, EL
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Frayling, TM
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Temple, IK
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Mackay, D
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Shield, JPH
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Sumnik, Z
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

van Rhijn, A
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Wales, JKH
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Clark, P
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Gorman, S
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Aisenberg, J
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Ellard, S
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Njolstad, PR
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Ashcroft, FM
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England

Hattersley, AT
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机构: Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX2 5AX, Devon, England
[7]
Large-scale association studies of variants in genes encoding the pancreatic β-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes
[J].
Gloyn, AL
;
Weedon, MN
;
Owen, KR
;
Turner, MJ
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Knight, BA
;
Hitman, G
;
Walker, M
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Levy, JC
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Sampson, M
;
Halford, S
;
McCarthy, MI
;
Hattersley, AT
;
Frayling, TM
.
DIABETES,
2003, 52 (02)
:568-572

Gloyn, AL
论文数: 0 引用数: 0
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Weedon, MN
论文数: 0 引用数: 0
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Owen, KR
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Turner, MJ
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Knight, BA
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Hitman, G
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Walker, M
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Levy, JC
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

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Halford, S
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

McCarthy, MI
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Hattersley, AT
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England

Frayling, TM
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机构: Peninsula Med Sch, Ctr Mol Genet, Exeter EX2 5AX, Devon, England
[8]
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
[J].
Grant, SFA
;
Thorleifsson, G
;
Reynisdottir, I
;
Benediktsson, R
;
Manolescu, A
;
Sainz, J
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Helgason, A
;
Stefansson, H
;
Emilsson, V
;
Helgadottir, A
;
Styrkarsdottir, U
;
Magnusson, KP
;
Walters, GB
;
Palsdottir, E
;
Jonsdottir, T
;
Gudmundsdottir, T
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Gylfason, A
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Saemundsdottir, J
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Wilensky, RL
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Reilly, MP
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Rader, DJ
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Bagger, Y
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Christiansen, C
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Gudnason, V
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Sigurdsson, G
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Thorsteinsdottir, U
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Gulcher, JR
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Kong, A
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Stefansson, K
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NATURE GENETICS,
2006, 38 (03)
:320-323

Grant, SFA
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Thorleifsson, G
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Reynisdottir, I
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Benediktsson, R
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Manolescu, A
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Sainz, J
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Helgason, A
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Stefansson, H
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Emilsson, V
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Helgadottir, A
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Styrkarsdottir, U
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机构: deCODE Genet, IS-101 Reykjavik, Iceland

Magnusson, KP
论文数: 0 引用数: 0
h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Walters, GB
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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Rader, DJ
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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Bagger, Y
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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Christiansen, C
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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Gudnason, V
论文数: 0 引用数: 0
h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

Kong, A
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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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机构: Inst Phys & Chem Res, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan

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Palsson, Snaebjorn
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h-index: 0
机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Thorleifsson, Gudmar
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Grant, Struan F. A.
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h-index: 0
机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Emilsson, Valur
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h-index: 0
机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Gunnarsdottir, Steinunn
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Adeyemo, Adebowale
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Chen, Yuanxiu
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Chen, Guanjie
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Reynisdottir, Inga
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Benediktsson, Rafn
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Hinney, Anke
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Hansen, Torben
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Andersen, Gitte
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Borch-Johnsen, Knut
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Jorgensen, Torben
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Schaefer, Helmut
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Faruque, Mezbah
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Doumatey, Ayo
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Zhou, Jie
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Wilensky, Robert L.
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Reilly, Muredach P.
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Rader, Daniel J.
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Bagger, Yu
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Christiansen, Claus
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Sigurdsson, Gunnar
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Hebebrand, Johannes
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Pedersen, Oluf
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Thorsteinsdottir, Unnur
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Gulcher, Jeffrey R.
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Kong, Augustine
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Rotimi, Charles
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland

Stefansson, Kari
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机构: DeCODE Genet, IS-101 Reykjavik, Iceland
