共 15 条
[1]
Genome-wide association studies provide new insights into type 2 diabetes aetiology
[J].
Frayling, Timothy M.
.
NATURE REVIEWS GENETICS,
2007, 8 (09)
:657-662

Frayling, Timothy M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Exeter, Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LV, Devon, England Univ Exeter, Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter EX1 2LV, Devon, England
[2]
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
;
Helgason, A
;
Stefansson, H
;
Emilsson, V
;
Helgadottir, A
;
Styrkarsdottir, U
;
Magnusson, KP
;
Walters, GB
;
Palsdottir, E
;
Jonsdottir, T
;
Gudmundsdottir, T
;
Gylfason, A
;
Saemundsdottir, J
;
Wilensky, RL
;
Reilly, MP
;
Rader, DJ
;
Bagger, Y
;
Christiansen, C
;
Gudnason, V
;
Sigurdsson, G
;
Thorsteinsdottir, U
;
Gulcher, JR
;
Kong, A
;
Stefansson, K
.
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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h-index: 0
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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h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Christiansen, C
论文数: 0 引用数: 0
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

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

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

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

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

Stefansson, K
论文数: 0 引用数: 0
h-index: 0
机构: deCODE Genet, IS-101 Reykjavik, Iceland
[3]
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
[J].
Lee, MP
;
Hu, RJ
;
Johnson, LA
;
Feinberg, AP
.
NATURE GENETICS,
1997, 15 (02)
:181-185

Lee, MP
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205

Hu, RJ
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205

Johnson, LA
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h-index: 0
机构: JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205

Feinberg, AP
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205
[4]
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
[J].
McCarthy, Mark I.
;
Abecasis, Goncalo R.
;
Cardon, Lon R.
;
Goldstein, David B.
;
Little, Julian
;
Ioannidis, John P. A.
;
Hirschhorn, Joel N.
.
NATURE REVIEWS GENETICS,
2008, 9 (05)
:356-369

McCarthy, Mark I.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Abecasis, Goncalo R.
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h-index: 0
机构:
Univ Michigan, Dept Biostat, Ctr Stat Genet, Ann Arbor, MI 48109 USA Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Cardon, Lon R.
论文数: 0 引用数: 0
h-index: 0
机构:
Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Goldstein, David B.
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Univ, Med Ctr, Ctr Populat Genom & Pharmacogenet, Duke Inst Genom Sci & Policy, Durham, NC 27708 USA Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Little, Julian
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Ioannidis, John P. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Ioannina, Sch Med, Clin & Mol Epidemiol Unit, Dept Hyg & Epidemiol, GR-45110 Ioannina, Greece
Fdn Res & Technol Hellas, Biomed Res Inst, Ioannina 45110, Greece
Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England

Hirschhorn, Joel N.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp, Div Genet & Endocrinol, Boston, MA 02115 USA
Childrens Hosp, Program Genom, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
MIT, Broad Inst, Cambridge, MA 02142 USA
Harvard Univ, Cambridge, MA 02142 USA Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[5]
Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population
[J].
Mori, Shintaro
;
Tanaka, Yasushi
;
Takahashi, Atsushi
;
Hirose, Hiroshi
;
Kashiwagi, Atsunori
;
Kaku, Kohei
;
Kawamori, Ryuzo
;
Nakamura, Yusuke
;
Maeda, Shiro
.
DIABETES,
2008, 57 (03)
:791-795

Mori, Shintaro
论文数: 0 引用数: 0
h-index: 0
机构:
RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Tanaka, Yasushi
论文数: 0 引用数: 0
h-index: 0
机构:
St Marianna Univ, Sch Med, Div Endocrinol & Metab, Dept Internal Med, Kanagawa, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Takahashi, Atsushi
论文数: 0 引用数: 0
h-index: 0
机构:
RIKEN, SNP Res Ctr, Lab Stat Anal, Tokyo, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Hirose, Hiroshi
论文数: 0 引用数: 0
h-index: 0
机构: RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Kashiwagi, Atsunori
论文数: 0 引用数: 0
h-index: 0
机构:
Keio Univ, RIKEN, Sch Med, Ctr Hlth, Tokyo, Japan
Shiga Univ Med Sci, Dept Med, Otsu, Shiga 52021, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Kaku, Kohei
论文数: 0 引用数: 0
h-index: 0
机构:
Kawasaki Med Sch, Dept Internal Med, Div Endocrinol & Metab, Okayama, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Kawamori, Ryuzo
论文数: 0 引用数: 0
h-index: 0
机构:
Juntendo Univ, Sch Med, Dept Med Endocrinol & Metab, Tokyo 113, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Nakamura, Yusuke
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Tokyo, Inst Med Sci, Mol Med Lab, Ctr Human Genome, Tokyo, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan

Maeda, Shiro
论文数: 0 引用数: 0
h-index: 0
机构:
RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan RIKEN, SNP Res Ctr, Lab Diabet Nephropathy, Tsurumi Ku, Kanagawa, Japan
[6]
NEEL JV, 1962, AM J HUM GENET, V14, P353
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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
[J].
Neyroud, N
;
Tesson, F
;
Denjoy, I
;
Leibovici, M
;
Donger, C
;
Barhanin, J
;
Faure, S
;
Gary, F
;
Coumel, P
;
Petit, C
;
Schwartz, K
;
Guicheney, P
.
NATURE GENETICS,
1997, 15 (02)
:186-189

Neyroud, N
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Tesson, F
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Denjoy, I
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h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Leibovici, M
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Donger, C
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Barhanin, J
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Faure, S
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Gary, F
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Coumel, P
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

论文数: 引用数:
h-index:
机构:

Schwartz, K
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE

Guicheney, P
论文数: 0 引用数: 0
h-index: 0
机构: GRP HOSP PITIE SALPETRIERE, INST MYOL, INSERM UR153, F-75013 PARIS, FRANCE
[8]
Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians
[J].
Ng, Maggie C. Y.
;
Park, Kyong Soo
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Oh, Bermseok
;
Tam, Claudia H. T.
;
Cho, Young Min
;
Shin, Hyoung Doo
;
Lam, Vincent K. L.
;
Ma, Ronald C. W.
;
So, Wing Yee
;
Cho, Yoon Shin
;
Kim, Hyung-Lae
;
Lee, Hong Kyu
;
Chan, Juliana C. N.
;
Cho, Nam H.
.
DIABETES,
2008, 57 (08)
:2226-2233

Ng, Maggie C. Y.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Park, Kyong Soo
论文数: 0 引用数: 0
h-index: 0
机构:
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 151, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Oh, Bermseok
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Ctr Genome Sci, Seoul, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Tam, Claudia H. T.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Cho, Young Min
论文数: 0 引用数: 0
h-index: 0
机构:
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 151, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Shin, Hyoung Doo
论文数: 0 引用数: 0
h-index: 0
机构:
Sogang Univ, Dept Life Sci, Lab Genom Divers, Seoul, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Lam, Vincent K. L.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Ma, Ronald C. W.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

So, Wing Yee
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Cho, Yoon Shin
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Ctr Genome Sci, Seoul, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Kim, Hyung-Lae
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Ctr Genome Sci, Seoul, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Lee, Hong Kyu
论文数: 0 引用数: 0
h-index: 0
机构:
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 151, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Chan, Juliana C. N.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
Chinese Univ Hong Kong, Prince Wales Hosp, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China

Cho, Nam H.
论文数: 0 引用数: 0
h-index: 0
机构:
Ajou Univ, Sch Med, Dept Prevent Med, Suwon 441749, South Korea Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
[9]
Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic β-cell function
[J].
Pascoe, Laura
;
Tura, Andrea
;
Patel, Sheila K.
;
Ibrahim, M. Ibrahim
;
Ferrannini, Ele
;
Zeggini, Eleftheria
;
Weedon, Michael N.
;
Mari, Andrea
;
Hattersley, Andrew T.
;
McCarthy, Mark I.
;
Frayling, Timothy M.
;
Walker, Mark
.
DIABETES,
2007, 56 (12)
:3101-3104

Pascoe, Laura
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Tura, Andrea
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Patel, Sheila K.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Ibrahim, M. Ibrahim
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Ferrannini, Ele
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Zeggini, Eleftheria
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Weedon, Michael N.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Mari, Andrea
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Hattersley, Andrew T.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

McCarthy, Mark I.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Frayling, Timothy M.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England

Walker, Mark
论文数: 0 引用数: 0
h-index: 0
机构: Univ Newcastle Upon Tyne, Sch Med, Sch Clin Med Sci, Diabet Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[10]
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs:: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk
[J].
Sanghera, Dharambir K.
;
Ortega, Lyda
;
Han, Shizhong
;
Singh, Jairup
;
Ralhan, Sarju K.
;
Wander, Gurpreet S.
;
Mehra, Narinder K.
;
Mulvihill, John J.
;
Ferrell, Robert E.
;
Nath, Swapan K.
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Kamboh, Mohammed I.
.
BMC MEDICAL GENETICS,
2008, 9

Sanghera, Dharambir K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Ortega, Lyda
论文数: 0 引用数: 0
h-index: 0
机构: Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Han, Shizhong
论文数: 0 引用数: 0
h-index: 0
机构:
Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Singh, Jairup
论文数: 0 引用数: 0
h-index: 0
机构:
Guru Nanak Dev Univ, Amritsar, Punjab, India Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Ralhan, Sarju K.
论文数: 0 引用数: 0
h-index: 0
机构:
Hero DMC Heart Inst, Ludhiana, Punjab, India Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Wander, Gurpreet S.
论文数: 0 引用数: 0
h-index: 0
机构:
Hero DMC Heart Inst, Ludhiana, Punjab, India Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Mehra, Narinder K.
论文数: 0 引用数: 0
h-index: 0
机构:
All India Inst Med Sci, New Delhi, India Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Mulvihill, John J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Ferrell, Robert E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Nath, Swapan K.
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机构:
Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA

Kamboh, Mohammed I.
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h-index: 0
机构:
Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Genet Sect, Oklahoma City, OK 73104 USA