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Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
114 auth.
Amy L. Williams,
S. Jacobs,
H. Moreno-Macías,
A. Huerta-Chagoya,
C. Churchhouse,
Carla Márquez-Luna,
H. García-Ortiz,
María José Gómez-Vázquez,
N. Burtt,
C. Aguilar-Salinas,
C. González‐Villalpando,
J. Florez,
L. Orozco,
C. Haiman,
Teresa Tusié-Luna,
...
D. Altshuler,
S. Ripke,
A. Manning,
B. Neale,
D. Reich,
D. Stram,
J. Fernández-López,
S. Romero-Hidalgo,
N. Patterson,
I. Aguilar-Delfín,
A. Martinez-Hernandez,
Federico Centeno-Cruz,
E. Mendoza-Caamal,
C. Revilla-Monsalve,
S. Islas-Andrade,
E. Córdova,
Eunice Rodríguez-Arellano,
X. Soberón,
Clicerio María Elena González-Villalpando González-Villalpando,
M. González-Villalpando,
B. Henderson,
K. Monroe,
L. Wilkens,
L. Kolonel,
L. Le Marchand,
L. Riba,
M. Ordoñez-Sánchez,
R. Rodríguez-Guillén,
I. Cruz-Bautista,
M. Rodríguez-Torres,
L. L. Muñóz-Hernández,
Tamara Sáenz,
D. Gómez,
Ulices Alvirde,
R. Onofrio,
W. Brodeur,
D. Gage,
Jacquelyn Murphy,
J. Franklin,
Scott Mahan,
K. Ardlie,
A. Crenshaw,
W. Winckler,
Kay Prüfer,
M. Shunkov,
S. Sawyer,
U. Stenzel,
J. Kelso,
M. Lek,
S. Sankararaman,
D. MacArthur,
A. Derevianko,
S. Pääbo,
Shuba Gopal,
James A. Grammatikos,
Ian C. Smith,
Kevin Bullock,
A. Deik,
Amanda L. Souza,
K. Pierce,
C. Clish,
Timothy Yossi Broad Stacey Fennell Farjoun Genomics Platform* Gabriel,
T. Fennell,
Y. Farjoun,
Broad Genomics Platform*,
S. Gabriel,
Daniel O. Myron D. Mark A. Mark Woon-Puay E-Shyong Stram Gross Pereira Seielstad Koh Tai,
M. Gross,
Mark A Pereira,
Mark Seielstad,
W. Koh,
E. Tai,
J. Flannick,
P. Fontanillas,
Andrew P Morris,
Tanya M. Teslovich,
G. Atzmon,
J. Blangero,
D. Bowden,
J. Chambers,
Yoon Shin Cho,
R. Duggirala,
Benjamin Glaser,
Craig Hanis,
J. Kooner,
M. Laakso,
Jong-Young Lee,
Yik Ying Teo,
James G. Wilson,
S. Puppala,
V. Farook,
F. Thameem,
H. Abboud,
R. DeFronzo,
C. Jenkinson,
D. Lehman,
J. Curran,
Noël P. Maria L. Burtt Cortes,
M. Cortés
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2013 |
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