Aguilar Salinas C.A.; Orozco L.; Tusie-Luna T.; Minikel E.V.; Karczewski K.J.; Martin H.C.; Cummings B.B.; Whiffin N.; Rhodes D.; Alföldi J.; Trembath R.C.; van Heel D.A.; Daly M.J.; Armean I.M.; Banks E.; Bergelson L.; Cibulskis K.; Collins R.L.; Connolly K.M.; Covarrubias M.; Donnelly S.; Farjoun Y.; Ferriera S.; Francioli L.; Gabriel S.; Gauthier L.D.; Gentry J.; Gupta N.; Jeandet T.; Kaplan D.; Laricchia K.M.; Llanwarne C.; Munshi R.; Neale B.M.; Novod S.; ODonnell-Luria A.H.; Petrillo N.; Poterba T.; Roazen D.; Ruano-Rubio V.; Saltzman A.; Samocha K.E.; Schleicher M.; Seed C.; Solomonson M.; Soto J.; Tiao G.; Tibbetts K.; Tolonen C.; Vittal C.; Wade G.; Wang A.; Wang Q.; Ware J.S.; Watts N.A.; Weisburd B.; Ahmad T.; Albert C.M.; Ardissino D.; Atzmon G.; Barnard J.; Beaugerie L.; Benjamin E.J.; Boehnke M.; Bonnycastle L.L.; Bottinger E.P.; Bowden D.W.; Bown M.J.; Chambers J.C.; Chan J.C.; Chasman D.; Cho J.; Chung M.K.; Cohen B.; Correa A.; Dabelea D.; Darbar D.; Duggirala R.; Dupuis J.; Ellinor P.T.; Elosua R.; Erdmann J.; Esko T.; Färkkilä M.; Florez J.; Franke A.; Getz G.; Glaser B.; Glatt S.J.; Goldstein D.; Gonzalez C.; Groop L.; Haiman C.; Hanis C.; Harms M.; Hiltunen M.; Holi M.M.; Hultman C.M.; Kallela M.; Kaprio J.; Kathiresan S.; Kim B.-J.; Kim Y.J.; Kirov G.; Kooner J.; Koskinen S.; Krumholz H.M.; Kugathasan S.; Kwak S.H.; Laakso M.; Lehtimäki T.; Loos R.J.F.; Lubitz S.A.; Ma R.C.W.; MacArthur D.G.; Marrugat J.; Mattila K.M.; McCarroll S.; McCarthy M.I.; McGovern D.; McPherson R.; Meigs J.B.; Melander O.; Metspalu A.; Nilsson P.M.; ODonovan M.C.; Ongur D.; Owen M.J.; Palmer C.N.A.; Palotie A.; Park K.S.; Pato C.; Pulver A.E.; Rahman N.; Remes A.M.; Rioux J.D.; Ripatti S.; Roden D.M.; Saleheen D.; Salomaa V.; Samani N.J.; Scharf J.; Schunkert H.; Shoemaker M.B.; Sklar P.; Soininen H.; Sokol H.; Spector T.; Sullivan P.F.; Suvisaari J.; Tai E.S.; Teo Y.Y.; Tiinamaija T.; Tsuang M.; Dan Turner T.; Vartiainen E.; Watkins H.; Weersma R.K.; Wessman M.; Wilson J.G.; Xavier R.J.; Schreiber S.L.; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium
Evaluating drug targets through human loss-of-function genetic variation
Nature, Volume 581 Número 7809 Páginas 459 a la 464 DOI: 10.1038/s41586-020-2267-z
2020
Salinas C.A.A.; Orozco L.; Tusie-Luna T.; Collins R.L.; Brand H.; Karczewski K.J.; Zhao X.; Alföldi J.; Francioli L.C.; Khera A.V.; Lowther C.; Gauthier L.D.; Wang H.; Watts N.A.; Solomonson M.; ODonnell-Luria A.; Baumann A.; Munshi R.; Walker M.; Whelan C.W.; Huang Y.; Brookings T.; Sharpe T.; Stone M.R.; Valkanas E.; Fu J.; Tiao G.; Laricchia K.M.; Ruano-Rubio V.; Stevens C.; Gupta N.; Cusick C.; Margolin L.; Armean I.M.; Banks E.; Bergelson L.; Cibulskis K.; Connolly K.M.; Covarrubias M.; Cummings B.; Daly M.J.; Donnelly S.; Farjoun Y.; Ferriera S.; Francioli L.; Gabriel S.; Gentry J.; Jeandet T.; Kaplan D.; Llanwarne C.; Minikel E.V.; Neale B.M.; Novod S.; ODonnell-Luria A.H.; Petrillo N.; Poterba T.; Roazen D.; Saltzman A.; Samocha K.E.; Schleicher M.; Seed C.; Soto J.; Tibbetts K.; Tolonen C.; Vittal C.; Wade G.; Wang A.; Wang Q.; Ware J.S.; Weisburd B.; Whiffin N.; Ahmad T.; Albert C.M.; Ardissino D.; Atzmon G.; Barnard J.; Beaugerie L.; Benjamin E.J.; Boehnke M.; Bonnycastle L.L.; Bottinger E.P.; Bowden D.W.; Bown M.J.; Chambers J.C.; Chan J.C.; Chasman D.; Cho J.; Chung M.K.; Cohen B.; Correa A.; Dabelea D.; Darbar D.; Duggirala R.; Dupuis J.; Ellinor P.T.; Elosua R.; Erdmann J.; Esko T.; Färkkilä M.; Florez J.; Franke A.; Getz G.; Glaser B.; Glatt S.J.; Goldstein D.; Gonzalez C.; Groop L.; Haiman C.; Hanis C.; Harms M.; Hiltunen M.; Holi M.M.; Hultman C.M.; Kallela M.; Kaprio J.; Kathiresan S.; Kim B.-J.; Kim Y.J.; Kirov G.; Kooner J.; Koskinen S.; Krumholz H.M.; Kugathasan S.; Kwak S.H.; Laakso M.; Lehtimäki T.; Loos R.J.F.; Lubitz S.A.; Ma R.C.W.; MacArthur D.G.; Marrugat J.; Mattila K.M.; McCarroll S.; McCarthy M.I.; McGovern D.; McPherson R.; Meigs J.B.; Melander O.; Metspalu A.; Nilsson P.M.; ODonovan M.C.; Ongur D.; Owen M.J.; Palmer C.N.A.; Palotie A.; Park K.S.; Pato C.; Pulver A.E.; Rahman N.; Remes A.M.; Rioux J.D.; Ripatti S.; Roden D.M.; Saleheen D.; Salomaa V.; Samani N.J.; Scharf J.; Schunkert H.; Shoemaker M.B.; Sklar P.; Soininen H.; Sokol H.; Spector T.; Sullivan P.F.; Suvisaari J.; Tai E.S.; Teo Y.Y.; Tiinamaija T.; Tsuang M.; Turner D.; Vartiainen E.; Watkins H.; Weersma R.K.; Wessman M.; Wilson J.G.; Xavier R.J.; Taylor K.D.; Lin H.J.; Rich S.S.; Post W.S.; Chen Y.-D.I.; Rotter J.I.; Nusbaum C.; Philippakis A.; Lander E.; Talkowski M.E.; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium
A structural variation reference for medical and population genetics
Nature, Volume 581 Número 7809 Páginas 444 a la 451 DOI: 10.1038/s41586-020-2287-8
2020
Aguilar Salinas C.A.; Tusie-Luna T.; Wang Q.; Pierce-Hoffman E.; Cummings B.B.; Alföldi J.; Francioli L.C.; Gauthier L.D.; Hill A.J.; ODonnell-Luria A.H.; Armean I.M.; Banks E.; Bergelson L.; Cibulskis K.; Collins R.L.; Connolly K.M.; Covarrubias M.; Daly M.J.; Donnelly S.; Farjoun Y.; Ferriera S.; Gabriel S.; Gentry J.; Gupta N.; Jeandet T.; Kaplan D.; Laricchia K.M.; Llanwarne C.; Minikel E.V.; Munshi R.; Neale B.M.; Novod S.; Petrillo N.; Poterba T.; Roazen D.; Ruano-Rubio V.; Saltzman A.; Samocha K.E.; Schleicher M.; Seed C.; Solomonson M.; Soto J.; Tiao G.; Tibbetts K.; Tolonen C.; Vittal C.; Wade G.; Wang A.; Ware J.S.; Watts N.A.; Weisburd B.; Whiffin N.; Ahmad T.; Albert C.M.; Ardissino D.; Atzmon G.; Barnard J.; Beaugerie L.; Benjamin E.J.; Boehnke M.; Bonnycastle L.L.; Bottinger E.P.; Bowden D.W.; Bown M.J.; Chambers J.C.; Chan J.C.; Chasman D.; Cho J.; Chung M.K.; Cohen B.; Correa A.; Dabelea D.; Darbar D.; Duggirala R.; Dupuis J.; Ellinor P.T.; Elosua R.; Erdmann J.; Esko T.; Färkkilä M.; Florez J.; Franke A.; Getz G.; Glaser B.; Glatt S.J.; Goldstein D.; Gonzalez C.; Groop L.; Haiman C.; Hanis C.; Harms M.; Hiltunen M.; Holi M.M.; Hultman C.M.; Kallela M.; Kaprio J.; Kathiresan S.; Kim B.-J.; Kim Y.J.; Kirov G.; Kooner J.; Koskinen S.; Krumholz H.M.; Kugathasan S.; Kwak S.H.; Laakso M.; Lehtimäki T.; Loos R.J.F.; Lubitz S.A.; Ma R.C.W.; Marrugat J.; Mattila K.M.; McCarroll S.; McCarthy M.I.; McGovern D.; McPherson R.; Meigs J.B.; Melander O.; Metspalu A.; Nilsson P.M.; ODonovan M.C.; Ongur D.; Orozco L.; Owen M.J.; Palmer C.N.A.; Palotie A.; Park K.S.; Pato C.; Pulver A.E.; Rahman N.; Remes A.M.; Rioux J.D.; Ripatti S.; Roden D.M.; Saleheen D.; Salomaa V.; Samani N.J.; Scharf J.; Schunkert H.; Shoemaker M.B.; Sklar P.; Soininen H.; Sokol H.; Spector T.; Sullivan P.F.; Suvisaari J.; Tai E.S.; Teo Y.Y.; Tiinamaija T.; Tsuang M.; Turner D.; Vartiainen E.; Watkins H.; Weersma R.K.; Wessman M.; Wilson J.G.; Xavier R.J.; Karczewski K.J.; MacArthur D.G.; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
Nature Communications, Volume 11 Número 1 DOI: 10.1038/s41467-019-12438-5
2020
Salinas C.A.A.; Tusie-Luna T.; Cummings B.B.; Karczewski K.J.; Kosmicki J.A.; Seaby E.G.; Watts N.A.; Singer-Berk M.; Mudge J.M.; Karjalainen J.; Satterstrom F.K.; ODonnell-Luria A.H.; Poterba T.; Seed C.; Solomonson M.; Alföldi J.; Armean I.M.; Banks E.; Bergelson L.; Cibulskis K.; Collins R.L.; Connolly K.M.; Covarrubias M.; Daly M.J.; Donnelly S.; Farjoun Y.; Ferriera S.; Francioli L.; Gabriel S.; Gauthier L.D.; Gentry J.; Gupta N.; Jeandet T.; Kaplan D.; Laricchia K.M.; Llanwarne C.; Minikel E.V.; Munshi R.; Neale B.M.; Novod S.; Petrillo N.; Roazen D.; Ruano-Rubio V.; Saltzman A.; Samocha K.E.; Schleicher M.; Soto J.; Tiao G.; Tibbetts K.; Tolonen C.; Vittal C.; Wade G.; Wang A.; Wang Q.; Ware J.S.; Weisburd B.; Whiffin N.; Ahmad T.; Albert C.M.; Ardissino D.; Atzmon G.; Barnard J.; Beaugerie L.; Benjamin E.J.; Boehnke M.; Bonnycastle L.L.; Bottinger E.P.; Bowden D.W.; Bown M.J.; Chambers J.C.; Chan J.C.; Chasman D.; Cho J.; Chung M.K.; Cohen B.; Correa A.; Dabelea D.; Darbar D.; Duggirala R.; Dupuis J.; Ellinor P.T.; Elosua R.; Erdmann J.; Esko T.; Färkkilä M.; Florez J.; Franke A.; Getz G.; Glaser B.; Glatt S.J.; Goldstein D.; Gonzalez C.; Groop L.; Haiman C.; Hanis C.; Harms M.; Hiltunen M.; Holi M.M.; Hultman C.M.; Kallela M.; Kaprio J.; Kathiresan S.; Kim B.-J.; Kim Y.J.; Kirov G.; Kooner J.; Koskinen S.; Krumholz H.M.; Kugathasan S.; Kwak S.H.; Laakso M.; Lehtimäki T.; Loos R.J.F.; Lubitz S.A.; Ma R.C.W.; MacArthur D.G.; Marrugat J.; Mattila K.M.; McCarroll S.; McCarthy M.I.; McGovern D.; McPherson R.; Meigs J.B.; Melander O.; Metspalu A.; Nilsson P.M.; ODonovan M.C.; Ongur D.; Orozco L.; Owen M.J.; Palmer C.N.A.; Palotie A.; Park K.S.; Pato C.; Pulver A.E.; Rahman N.; Remes A.M.; Rioux J.D.; Ripatti S.; Roden D.M.; Saleheen D.; Salomaa V.; Samani N.J.; Scharf J.; Schunkert H.; Shoemaker M.B.; Sklar P.; Soininen H.; Sokol H.; Spector T.; Sullivan P.F.; Suvisaari J.; Tai E.S.; Teo Y.Y.; Tiinamaija T.; Tsuang M.; Turner D.; Vartiainen E.; Watkins H.; Weersma R.K.; Wessman M.; Wilson J.G.; Xavier R.J.; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium
Transcript expression-aware annotation improves rare variant interpretation
Nature, Volume 581 Número 7809 Páginas 452 a la 458 DOI: 10.1038/s41586-020-2329-2
2020
Aguilar Salinas C.A.; Tusie-Luna T.; Whiffin N.; Karczewski K.J.; Zhang X.; Chothani S.; Smith M.J.; Evans D.G.; Roberts A.M.; Quaife N.M.; Schafer S.; Rackham O.; Alföldi J.; ODonnell-Luria A.H.; Francioli L.C.; Armean I.M.; Banks E.; Bergelson L.; Cibulskis K.; Collins R.L.; Connolly K.M.; Covarrubias M.; Cummings B.; Daly M.J.; Donnelly S.; Farjoun Y.; Ferriera S.; Gabriel S.; Gauthier L.D.; Gentry J.; Gupta N.; Jeandet T.; Kaplan D.; Laricchia K.M.; Llanwarne C.; Minikel E.V.; Munshi R.; Neale B.M.; Novod S.; Petrillo N.; Poterba T.; Roazen D.; Ruano-Rubio V.; Saltzman A.; Samocha K.E.; Schleicher M.; Seed C.; Solomonson M.; Soto J.; Tiao G.; Tibbetts K.; Tolonen C.; Vittal C.; Wade G.; Wang A.; Wang Q.; Watts N.A.; Weisburd B.; Ahmad T.; Albert C.M.; Ardissino D.; Atzmon G.; Barnard J.; Beaugerie L.; Benjamin E.J.; Boehnke M.; Bonnycastle L.L.; Bottinger E.P.; Bowden D.W.; Bown M.J.; Chambers J.C.; Chan J.C.; Chasman D.; Cho J.; Chung M.K.; Cohen B.; Correa A.; Dabelea D.; Darbar D.; Duggirala R.; Dupuis J.; Ellinor P.T.; Elosua R.; Erdmann J.; Esko T.; Färkkilä M.; Florez J.; Franke A.; Getz G.; Glaser B.; Glatt S.J.; Goldstein D.; Gonzalez C.; Groop L.; Haiman C.; Hanis C.; Harms M.; Hiltunen M.; Holi M.M.; Hultman C.M.; Kallela M.; Kaprio J.; Kathiresan S.; Kim B.-J.; Kim Y.J.; Kirov G.; Kooner J.; Koskinen S.; Krumholz H.M.; Kugathasan S.; Kwak S.H.; Laakso M.; Lehtimäki T.; Loos R.J.F.; Lubitz S.A.; Ma R.C.W.; Marrugat J.; Mattila K.M.; McCarroll S.; McCarthy M.I.; McGovern D.; McPherson R.; Meigs J.B.; Melander O.; Metspalu A.; Nilsson P.M.; ODonovan M.C.; Ongur D.; Orozco L.; Owen M.J.; Palmer C.N.A.; Palotie A.; Park K.S.; Pato C.; Pulver A.E.; Rahman N.; Remes A.M.; Rioux J.D.; Ripatti S.; Roden D.M.; Saleheen D.; Salomaa V.; Samani N.J.; Scharf J.; Schunkert H.; Shoemaker M.B.; Sklar P.; Soininen H.; Sokol H.; Spector T.; Sullivan P.F.; Suvisaari J.; Tai E.S.; Teo Y.Y.; Tiinamaija T.; Tsuang M.; Turner D.; Vartiainen E.; Watkins H.; Weersma R.K.; Wessman M.; Wilson J.G.; Xavier R.J.; Cook S.A.; Barton P.J.R.; MacArthur D.G.; Ware J.S.; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium
Characterising the loss-of-function impact of 5 untranslated region variants in 15,708 individuals
Nature Communications, Volume 11 Número 1 DOI: 10.1038/s41467-019-10717-9
2020
Moreno-Macías H.; Rodríguez-Guillen R.; Vázquez-Cárdenas P.; Aguilar-Salinas C.A.; Tusié-Luna M.T.; Guerra-García M.T.; Ochoa-Guzmán A.; Ordoñez-Sánchez M.L.; Ortíz-Ortega V.M.; Peimbert-Torres M.
The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans
Journal Of Endocrinological Investigation, Volume DOI: 10.1007/s40618-020-01346-x
2020
Perez-Mendez, O.; Zentella-Dehesa, A.; Aguilar-Salinas, C. A.; Tusie-Luna, M. T.; Ochoa-Guzman, A.; Moreno-Macias, H.; Guillen-Quintero, D.; Chavez-Talavera, O.; Ordonez-Sanchez, M. L.; Segura-Kato, Y.; Ortiz, V.; Diaz-Diaz, E.; Munoz-Hernandez, L.; Garcia, A.
R230C but not-565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels
Journal Of Endocrinological Investigation, Volume 43 Número 8 Páginas 1061 a la 1071 DOI: 10.1007/s40618-020-01187-8
2020
Huerta-Chagoya, A; Moreno-Macias, H; Fernandez-Lopez, JC; Ordonez-Sanchez, ML; Rodriguez-Guillen, R; Contreras, A; Hidalgo-Miranda, A; Alfaro-Ruiz, LA; Salazar-Fernandez, EP; Moreno-Estrada, A; Aguilar-Salinas, CA; Tusie-Luna, T
A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos
BMC Genetics 20(1):5 F.I. 2.547
2019
Clark DW, Okada Y, Moore KHS, Mason D, Pirastu N, Gandin I, Mattsson H, Barnes CLK, Lin K, Zhao JH, Deelen P, Rohde R, Schurmann C, Guo X, Giulianini F, Zhang W, Medina-Gomez C, Karlsson R, Bao Y, Bartz TM, Baumbach C, Biino G, Bixley MJ, Brumat M, Chai J, Tusie-Luna, T, et al.
Associations of autozygosity with a broad range of human phenotypes
Nature Communications 10(1):4957 F.I. 11.878
2019
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Development and validation of a predictive model for incident type 2 diabetes in middle-aged Mexican adults: the metabolic syndrome cohort
BMC Endocrine Disorders 19(1):41 F.I. 1.816
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Flannick, J; Mercader, JM; Fuchsberger, C; Udler, MS; Mahajan, A; Wessel, J; Teslovich, TM; Caulkins, L; Koesterer, R; Barajas-Olmos, F; Blackwell, TW; Boerwinkle, E; Brody, JA; Centeno-Cruz, F; Chen, L; Chen, SY; Contreras-Cubas, C; Cordova, E; Correa, A, Tusie-Luna, T, et al.
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Nature 570(7759):71-76 F.I. 43.07
2019
Bello-Chavolla, OY; Antonio-Villa, NE; Vargas-Vzquez, A; Martagn, AJ; Mehta, R; Arellano-Campos, O; Gmez-Velasco, DV; Almeda-Valds, P; Cruz-Bautista, I; Melgarejo-Hernandez, MA; Muoz-Hernandez, L; Guilln, LE; Garduo-Garca, JD; Alvirde, U; Ono-Yoshikawa, Y, Ricardo Choza-Romero, Leobardo Sauque-Reyna, Ma Eugenia Garay-Sevilla, Juan M Malacara-Hernandez, María T Tusié-Luna, Luis M Gutierrez-Robledo, Francisco J Gómez-Pérez, Rosalba Rojas, Carlos A Aguilar-Salinas
Prediction of incident hypertension and arterial stiffness using the non-insulin-based metabolic score for insulin resistance (METS-IR) index
Journal of Clinical Hypertension 21(8):1063-1070 F.I. 2.444
2019
Gallardo-Alvarado, LN; Tusie-Luna, MT; Tussie-Luna, MI; Diaz-Chavez, J; Segura, YX; Bargallo-Rocha, E; Villarreal, C; Herrera-Montalvo, LA; Herrera-Medina, EM; Cantu-de Leon, DF
Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population
BMC Cancer 19(1):118 F.I. 2.933
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Almeda-Valdes, P; Velascol, DVG; Campos, OA; Bello-Chavolla, OY; Sevilla-Gonzalez, MD; Ruiz, TV; Rosado, AJM; Bautista, CJ; Hernandez, LM; Cruz-Bautista, I; Moreno-Maciass, H; Huerta-Chagoya, A; Rodriguez-Alvarez, KG; Watford, GA; Jacobs, SBR; Pineda, LEG, Ma Luisa Ordoñez-Sánchez, Ernesto Roldan-Valadez, Joaquín Azpiroz, Jannette Furuzawa-Carballeda, Patricia Clark, Miguel F Herrera-Hernández, Elena Zambrano, Jose C Florez, María Teresa Tusié Luna, Carlos A Aguilar-Salinas
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes
European Journal of Endocrinology 180(2):99-107 F.I. 5.107
2019
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Frequency of the T307A, N680S, and -29G>A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry.
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Mexican Carriers of the HNF1A p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas.
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Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients.
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Transancestral mapping and genetic load in systemic lupus erythematosus
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SIGMA T2D Genetics Consortium. A loss-of-function splice acceptor variant in IGF2 is protective for type 2 diabetes
Diabetes; 66(11):2903-2914 DOI: 10.2337/db17-0187
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Rusu V, Hoch E, Mercader JM, Tenen DE, Gymrek M, Hartigan CR, DeRan M, von rotthuss M, Fontanillas P, Spooner A, Guzman G, Deik AA, Pierce KA, Dennis C, Clish CB, Carr SA, Wagner BK, Schenone M, Ng MCY, Chen BH; MEDIA Consortium; SIGMA T2D Consortium,Centeno-Cruz F, Zerrweck C, Orozco L, Altshuler DM, Schreiber SL, Florez JC, JacobsSBR,Lander ES. Ng MCY, Shriner D, Chen BH, Li J, Chen WM, Guo X, Liu J, Bielinski SJ, Yanek LR,Nalls MA, Comeau ME, Rasmussen-Torvik LJ, Jensen RA, Evans DS, Sun YV.
Type 2 Diabetes Variants Disrupt Function Of SLC16A11T Through two distinct Mechanism
CELL 170(1):199-212 DOI: 10.1016/j.cell.2017.06.011
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Sánchez E, García de la Torre I, Sacnún M, Goñi M, Berbotto G, Paira S,Musuruana JL, Graf C, Alvarellos A, Messina OD, Babini A, Strusberg I, Marcos JC,Scherbarth H, Spindler A, Quinteros A, Toloza S, Moreno JLC, Catoggio LJ, Tate G, Eimon A, Citera G, Pellet AC, Nasswetter G, Cardiel MH, Miranda P, Ballesteros F, Esquivel-Valerio JA, Maradiaga-Ceceña MA, Acevedo-Vásquez EM, García CG, Tusié-Luna T, Pons-Estel BA, Alarcón-Riquelme ME. GENAR Study
Effects of Amerindian Genetic Ancestry on Clinical Variables and Therapy in Patients with Rheumatoid Arthritis
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Gamboa-Meléndez MA, Huerta-Chagoya A, Moreno-Macías H, Vázquez-Cárdenas P, Ordóñez-Sánchez ML, Rodríguez-Guillén R, Riba L, Rodríguez-Torres M, Guerra-García MT, Guillén-Pineda LE, Choudhry S, Del Bosque-Plata L, Canizales-Quinteros S, Pérez-Ortiz G, Escobedo-Aguirre F, Parra A, Lerman-Garber I, Aguilar-Salinas CA, Tusié-Luna MT.
Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo Population.
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Escamilla-Marquez, MA; Garduno-Garcia, JD; Ordonez-Sanchez, ML; Reza-Albarran, A; Tusie-Luna, MT; Perez, FJG; Aguilar-Salinas, CA
Primary amenorrhea in two sisters: description of a Mexican family with 17 alpha hydroxylase-17 lyase deficiency caused by arginine – stop mutation
Gynecol. Endocrinol., 28(9):733-735, FI.1.581
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Villalobos-Comparan, M; Villamil-Ramirez, H; Villarreal-Molina, T; Larrieta-Carrasco, E; Leon-Mimila, P; Romero-Hidalgo, S; Jacobo-Albavera, L; Liceaga-Fuentes, AE; Campos-Perez, FJ; Lopez-Contreras, BE; Tusie-Luna, T; del Rio-Navarro, BE; Aguilar-Salinas
PCSK1 rs6232 Is Associated with Childhood and Adult Class III Obesity in the Mexican Population
PLoS One, 7(6):e39037, FI.4.092
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Weissglass-Volkov D, Plaisier CL, Huertas-Vázquez A, Cruz-Bautista I, Riaño-Baños D, Herrera-Hernández M, Riba L, Cantor RM, Sinsheimer JS, Aguilar-Salinas CA, Tusié-Luna MT, Pajukanta P.
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.
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Investigation of variants identified in Caucasian genome-wide association studies for plasma HDL cholesterol and triglycerides levels in Mexican dyslipidemic study samples.
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Florez JC, Price AL, Campbell D, Riba L, Parra MV, Yu F, Duque C, Saxena R, Gallego N, Tello- Ruiz M, Franco L, Rodríguez-Torres M, Villegas A, Bedoya G, Aguilar-Salinas CA, Tusié-Luna MT, Ruiz- Linares A and Reich D.
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Galanin is associated with elevated plasma triglycerides.
Atheroeclerosis, Thrombosis and Vascular Biology, 29(1):147-152
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