| 1 | Multiomics reveal key inflammatory drivers of severe obesity: IL4R, LILRA5, and OSM | Coautor: Tusié-Luna M.T., Chen H.-H., Highland H.M., Frankel E.G., et al. | 2025 | Cell Genomics | WoS-id: 001447566400001
Scopus-id: 2-s2.0-86000482483
| 1 | 1 |
| 2 | Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits | Coautor: Tusie-Luna, T, Petty, LE, Chen, HH, Frankel, EG, et al. | 2025 | NATURE COMMUNICATIONS | WoS-id: 001465426800011
Scopus-id: 2-s2.0-105003323438
| 0 | 0 |
| 3 | Inferring compound heterozygosity from large-scale exome sequencing data | Coautor: Tusie-Luna T., Guo M.H., Francioli L.C., Stenton S.L., et al. | 2024 | NATURE GENETICS | WoS-id: 001114668000001
Scopus-id: 2-s2.0-85181415190
| 8 | 9 |
| 4 | A genomic mutational constraint map using variation in 76,156 human genomes | Coautor: Tusie-Luna T., Chen S., Francioli L.C., Goodrich J.K., et al. | 2024 | Nature | WoS-id: 001136836700004
Scopus-id: 2-s2.0-85180828283
| 429 | 446 |
| 5 | Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort | Coautor: Tusié-Luna T., Solomon O., Lanata C.M., Adams C., et al. | 2024 | ARTHRITIS & RHEUMATOLOGY | WoS-id: 001151758500001
Scopus-id: 2-s2.0-85183934518
| 0 | 0 |
| 6 | Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes (Nature, (2024), 625, 7993, (92-100), 10.1038/s41586-023-06045-0) | Coautor: Tusie-Luna T., Chen S., Francioli L.C., Goodrich J.K., et al. | 2024 | Nature | WoS-id: 001179126600001
Scopus-id: 2-s2.0-85182477492
| 7 | 8 |
| 7 | The fatal contribution of serine protease-related genetic variants to COVID-19 outcomes | Coautor: Tusie-Luna T., Martínez-Gómez L.E., Martinez-Armenta C., Vázquez-Cárdenas P., et al. | 2024 | FRONTIERS IN IMMUNOLOGY | WoS-id: 001198836300001
Scopus-id: 2-s2.0-85189882791
| 2 | 2 |
| 8 | Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation | Coautor: Tusie-Luna T., Wilson-Verdugo M., Bustos-García B., Adame-Guerrero O., et al. | 2024 | Life Science Alliance | WoS-id: 001229208400001
Scopus-id: 2-s2.0-85193464078
| 1 | 1 |
| 9 | Identification and Properties of TRPV4 Mutant Channels Present in Polycystic Kidney Disease Patients | Coautor: Tusié-Luna, T, Hernández-Vega, AM, Llorente, I, Sánchez-Hernández, R, et al. | 2024 | Function | WoS-id: 001309542500005
Scopus-id: 2-s2.0-85203857568
| 1 | 1 |
| 10 | Metabolomic Profile Alterations Associated with the SLC16A11 Risk Haplotype Following a Lifestyle Intervention in People With Prediabetes | Coautor: Tusie-Luna T., Sevilla-González M., Garibay-Gutiérrez M.F., Vargas-Vázquez A., et al. | 2024 | Current Developments in Nutrition | WoS-id: 001312344900001
Scopus-id: 2-s2.0-85203405416
| 1 | 0 |
| 11 | Combined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer | Coautor: Tusié M.T., São José C., Ferreira M., Arrieta O., et al. | 2023 | Gastric Cancer | WoS-id: 000999645000001
Scopus-id: 2-s2.0-85160585792
| 4 | 6 |
| 12 | The role of SLC16A11 variations in diabetes mellitus | 2ᵒ autor y autor de correspondencia: Tusie Luna M.T., Aguilar-Salinas, Carlos A. | 2023 | CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION | WoS-id: 001041450700009
Scopus-id: 2-s2.0-85166065609
| 3 | 2 |
| 13 | Implication of myddosome complex genetic variants in outcome severity of COVID-19 patients | Coautor: Tusie-Luna T., Martínez-Gómez L.E., Martinez-Armenta C., Medina-Luna D., et al. | 2023 | JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION | WoS-id: 001124460700001
Scopus-id: 2-s2.0-85162877417
| 7 | 7 |
| 14 | Mexican Biobank advances population and medical genomics of diverse ancestries | Coautor: Tusié-Luna M.T., Sohail M., Palma-Martínez M.J., Chong A.Y., et al. | 2023 | Nature | WoS-id: 001169105200014
Scopus-id: 2-s2.0-85173865392
| 46 | 45 |
| 15 | Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis | Coautor: Tusié-Luna M.T., García-Grimshaw M., Chirino-Pérez A., Flores-Silva F.D., et al. | 2022 | NEUROLOGICAL SCIENCES | WoS-id: 000741878300003
Scopus-id: 2-s2.0-85122832625
| 16 | 16 |
| 16 | Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes | Coautor: Tusie-Luna, Teresa, Jimenez-Kaufmann, Andres, Chong, Amanda Y., Cortes, Adrian, et al. | 2022 | Frontiers in Genetics | WoS-id: 000745703100001
Scopus-id: 2-s2.0-85123123221
| 7 | 8 |
| 17 | Rare coding variants in 35 genes associate with circulating lipid levels?A multi-ancestry analysis of 170,000 exomes | Coautor: Tusié-Luna T., Hindy G., Dornbos P., Chaffin M.D., et al. | 2022 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000748493200007
Scopus-id: 2-s2.0-85122004213
| 22 | 23 |
| 18 | Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium | Coautor: Tusie-Luna, Teresa, Fernandez-Rhodes, Lindsay, Graff, Mariaelisa, Buchanan, Victoria L., et al. | 2022 | Human Genetics And Genomics Advances | WoS-id: 000787647900014
Scopus-id: 2-s2.0-85127345671
| 16 | 16 |
| 19 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation | Coautor: Tusie-Luna, Teresa, Mahajan, Anubha, Spracklen, Cassandra N., Zhang, Weihua, et al. | 2022 | NATURE GENETICS | WoS-id: 000794118000004
Scopus-id: 2-s2.0-85130637871
| 351 | 352 |
| 20 | ASSOCIATION BETWEEN APOE-e4 CARRIER STATUS AND QUALITATIVE NEUROIMAGING CHARACTERISTICS IN OLDER ADULTS WITH MILD COGNITIVE IMPAIRMENT | Coautor: Tusie-Luna T., Mimenza-Alvarado A.J., Suing-Ortega M.J., Juárez-Cedillo T., et al. | 2022 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000822434300007
Scopus-id: 2-s2.0-85127262137
| 0 | 0 |
| 21 | A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids | Coautor: Tusié-Luna T., Ramdas S., Judd J., Graham S.E., et al. | 2022 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000850681500003
Scopus-id: 2-s2.0-85135598739
| 21 | 22 |
| 22 | A saturated map of common genetic variants associated with human height | Coautor: Tusie-Luna, Maria-Teresa, Yengo, Loic, Vedantam, Sailaja, Marouli, Eirini, et al. | 2022 | Nature | WoS-id: 000866362700001
Scopus-id: 2-s2.0-85139748621
| 308 | 333 |
| 23 | Metabolic Reprogramming in SARS-CoV-2 Infection Impacts the Outcome of COVID-19 Patients | Coautor: Tusie, Teresa, Martinez-Gomez, Laura E., Ibarra-Gonzalez, Isabel, Fernandez-Lainez, Cynthia, et al. | 2022 | FRONTIERS IN IMMUNOLOGY | WoS-id: 000880077100001
Scopus-id: 2-s2.0-85141374972
| 21 | 24 |
| 24 | Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis | Coautor: Tusié-Luna T., Kanoni S., Graham S.E., Wang Y., et al. | 2022 | GENOME BIOLOGY | WoS-id: 000927879600003
Scopus-id: 2-s2.0-85144774123
| 27 | 29 |
| 25 | The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans | Coautor: Tusié-Luna M.T., Guerra-García M.T., Moreno-Macías H., Ochoa-Guzmán A., et al. | 2021 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | WoS-id: 000545040800001
Scopus-id: 2-s2.0-85087490959
| 10 | 10 |
| 26 | Association between ApoE epsilon 4 Carrier Status and Cardiovascular Risk Factors on Mild Cognitive Impairment among Mexican Older Adults | Coautor: Tusie-Luna, Teresa, Aguilar-Navarro, Sara G., Gonzalez-Aparicio, Itzel I., Avila-Funes, Jose Alberto, et al. | 2021 | Brain Sciences | WoS-id: 000609862100001
Scopus-id: 2-s2.0-85099412311
| 4 | 2 |
| 27 | The influence of high-density lipoprotein (HDL) and HDL subfractions on insulin secretion and cholesterol efflux in pancreatic derived beta-cells | Coautor: Tusie-Luna, M. T., Ochoa-Guzman, A., Guillen-Quintero, D., Munoz-Hernandez, L., et al. | 2021 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | WoS-id: 000610850300001
Scopus-id: 2-s2.0-85099804865
| 8 | 8 |
| 28 | Author Correction: Evaluating drug targets through human loss-of-function genetic variation (Nature, (2020), 581, 7809, (459-464), 10.1038/s41586-020-2267-z) | Coautor: Tusie-Luna T., Martin H.C., Rhodes D., Trembath R.C., et al. | 2021 | Nature | WoS-id: 000614414900006
Scopus-id: 2-s2.0-85100458973
| 1 | 2 |
| 29 | Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (Nature, (2020), 581, 7809, (434-443), 10.1038/s41586-020-2308-7) | Coautor: Tusie-Luna T., Karczewski K.J., Francioli L.C., Tiao G., et al. | 2021 | Nature | WoS-id: 000614414900012
Scopus-id: 2-s2.0-85100468298
| 96 | 52 |
| 30 | Author Correction: A structural variation reference for medical and population genetics (Nature, (2020), 581, 7809, (444-451), 10.1038/s41586-020-2287-8) | Coautor: Tusie-Luna T., Brand H., Zhao X., Francioli L.C., et al. | 2021 | Nature | WoS-id: 000614414900013
Scopus-id: 2-s2.0-85100482354
| 4 | 4 |
| 31 | Author Correction: Transcript expression-aware annotation improves rare variant interpretation (Nature, (2020), 581, 7809, (452-458), 10.1038/s41586-020-2329-2) | Coautor: Tusie-Luna T., Kosmicki J.A., Seaby E.G., Singer-Berk M., et al. | 2021 | Nature | WoS-id: 000614414900014
Scopus-id: 2-s2.0-85100514194
| 0 | 0 |
| 32 | Author Correction: Characterising the loss-of-function impact of 5? untranslated region variants in 15,708 individuals (Nature Communications, (2020), 11, 1, (2523), 10.1038/s41467-019-10717-9) | Coautor: Tusie-Luna T., Whiffin N., Karczewski K.J., Zhang X., et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000617063200001
Scopus-id: 2-s2.0-85100257530
| 1 | 0 |
| 33 | Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (Nature Communications, (2020), 11, 1, (2539), 10.1038/s41467-019-12438-5) | Coautor: Tusie-Luna T., Wang Q., Pierce-Hoffman E., Cummings B.B., et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000617063700001
Scopus-id: 2-s2.0-85100273346
| 2 | 1 |
| 34 | Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry | Coautor: Tusie-Luna, Teresa, Romero-Gutierrez, Elizabeth, Vazquez-Cardenas, Paola, Moreno-Macias, Hortensia, et al. | 2021 | Npj Parkinsons Disease | WoS-id: 000617190000001
Scopus-id: 2-s2.0-85101061471
| 5 | 7 |
| 35 | Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia | Coautor: Tusie-Luna, Maria Teresa, Cruz-Bautista, Ivette, Huerta-Chagoya, Alicia, Moreno-Macias, Hortensia, et al. | 2021 | LIPIDS IN HEALTH AND DISEASE | WoS-id: 000620219200002
Scopus-id: 2-s2.0-85101485953
| 7 | 9 |
| 36 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes | Coautor: Tusie-Luna, Teresa, Goodrich, Julia K., Singer-Berk, Moriel, Son, Rachel, et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000664874700036
Scopus-id: 2-s2.0-85107774343
| 50 | 52 |
| 37 | Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes | Coautor: Tusié-Luna M.T., Pan D.Z., Miao Z., Comenho C., et al. | 2021 | GENOME MEDICINE | WoS-id: 000680537000001
Scopus-id: 2-s2.0-85111720948
| 24 | 26 |
| 38 | Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes (vol 13, 123, 2021) | Coautor: Teresa Tusie-Luna, Maria, Pan, David Z., Miao, Zong, Comenho, Caroline, et al. | 2021 | GENOME MEDICINE | WoS-id: 000692394500001
Scopus-id: 2-s2.0-85113868985
| 1 | 1 |
| 39 | The power of genetic diversity in genome-wide association studies of lipids | Coautor: Tusie-Luna, Teresa, Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., et al. | 2021 | Nature | WoS-id: 000728504500001
Scopus-id: 2-s2.0-85121605114
| 462 | 462 |
| 40 | PRECISION MEDICINE FOR METABOLIC DISORDERS IN LOW- AND MIDDLE-INCOME COUNTRIES: AREAS OF OPPORTUNITY AND CHALLENGES FOR THE FUTURE | 1ᵉʳ autor: Tusié-Luna M.T., Aguilar-Salinas, Carlos A. | 2021 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000755113000011
Scopus-id: 2-s2.0-85118096580
| 3 | 4 |
| 41 | Genetic discovery and risk characterization in type 2 diabetes across diverse populations | Coautor: Tusie-Luna, Teresa, Polfus, Linda M., Darst, Burcu F., Highland, Heather, et al. | 2021 | Human Genetics And Genomics Advances | WoS-id: 000787671400008
Scopus-id: 2-s2.0-85111311121
| 31 | 33 |
| 42 | Factores de riesgo en pacientes con fisura de labio y paladar en México. Estudio en 209 pacientes | Coautor: Tusie-Luna M.T., Pérez-González A., Lavielle-Sotomayor P., Clark P., et al. | 2021 | Cirugia Plastica Ibero-Latinoamericana | Scopus-id: 2-s2.0-85130160386
| 0 | 3 |
| 43 | Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study | Coautor: Tusie-Luna, Teresa, Huerta-Chagoya, Alicia, Moreno-Macias, Hortensia, Sevilla-Gonzalez, Magdalena, et al. | 2020 | GENES | WoS-id: 000514898000041
Scopus-id: 2-s2.0-85078260878
| 8 | 8 |
| 44 | 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 | Coautor: Tusie-Luna, M. T., Ochoa-Guzman, A., Moreno-Macias, H., Guillen-Quintero, D., et al. | 2020 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | WoS-id: 000515838400001
Scopus-id: 2-s2.0-85079463418
| 9 | 7 |
| 45 | Use of PCSK9 inhibitor in a Mexican boy with compound heterozygous familial hypercholesterolemia: A case report | Coautor: Tusié-Luna M.T., Ceballos-Macías J.J., Madriz-Prado R., Vázquez Cárdenas N.A., et al. | 2020 | Journal Of The Endocrine Society | WoS-id: 000518167600015
Scopus-id: 2-s2.0-85083050984
| 3 | 3 |
| 46 | Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism | Coautor: Tusie-Luna, Teresa, Ostrosky-Frid, Mauricio, Chavez-Canales, Maria, Romo, Miriam, et al. | 2020 | AMERICAN JOURNAL OF HYPERTENSION | WoS-id: 000522656000011
Scopus-id: 2-s2.0-85081944968
| 5 | 5 |
| 47 | Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes | Coautor: Tusie-Luna T., Wang Q., Pierce-Hoffman E., Cummings B.B., et al. | 2020 | NATURE COMMUNICATIONS | WoS-id: 000538031600001
Scopus-id: 2-s2.0-85085576031
| 83 | 101 |
| 48 | Characterising the loss-of-function impact of 5? untranslated region variants in 15,708 individuals | Coautor: Tusie-Luna T., Whiffin N., Karczewski K.J., Zhang X., et al. | 2020 | NATURE COMMUNICATIONS | WoS-id: 000538032800001
Scopus-id: 2-s2.0-85085581111
| 99 | 101 |
| 49 | The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance | Coautor: Tusie-Luna, Teresa, Miao, Zong, Alvarez, Marcus, Ko, Arthur, et al. | 2020 | PLOS GENETICS | WoS-id: 000573373800002
Scopus-id: 2-s2.0-85091627918
| 42 | 46 |
| 50 | The mutational constraint spectrum quantified from variation in 141,456 humans | Coautor: Tusie-Luna T., Karczewski K.J., Francioli L.C., Tiao G., et al. | 2020 | Nature | WoS-id: 000576060200003
Scopus-id: 2-s2.0-85085542423
| 5113 | 6124 |
| 51 | A structural variation reference for medical and population genetics | Coautor: Tusie-Luna T., Brand H., Zhao X., Francioli L.C., et al. | 2020 | Nature | WoS-id: 000576060200004
Scopus-id: 2-s2.0-85085567000
| 565 | 585 |
| 52 | Transcript expression-aware annotation improves rare variant interpretation | Coautor: Tusie-Luna T., Kosmicki J.A., Seaby E.G., Singer-Berk M., et al. | 2020 | Nature | WoS-id: 000576060200005
Scopus-id: 2-s2.0-85085576216
| 117 | 123 |
| 53 | Evaluating drug targets through human loss-of-function genetic variation | Coautor: Tusie-Luna T., Martin H.C., Rhodes D., Trembath R.C., et al. | 2020 | Nature | WoS-id: 000576060200006
Scopus-id: 2-s2.0-85085564434
| 104 | 113 |
| 54 | Local Genetic Ancestry Associations with Clinical Features of Systemic Lupus Erythematosus | Coautor: Tusie-Luna, Teresa, Solomon, Olivia, Lanata, Cristina, Adams, Cameron, et al. | 2020 | ARTHRITIS & RHEUMATOLOGY | WoS-id: 000587568500299
| 0 | 0 |
| 55 | A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos 06 Biological Sciences 0604 Genetics | Coautor: Tusié-Luna T., Huerta-Chagoya A., Moreno-Macías H., Carlos Fernandez-Lopez, Juan, et al. | 2019 | BMC GENETICS | WoS-id: 000455208900002
Scopus-id: 2-s2.0-85059768837
| 9 | 10 |
| 56 | The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes | Coautor: Luna M.T.T., Almeda-Valdes P., Velasco D.V.G., Campos O.A., et al. | 2019 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | WoS-id: 000457062800008
Scopus-id: 2-s2.0-85058857855
| 19 | 16 |
| 57 | Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population | 2ᵒ autor: Tusié-Luna M.T., Gallardo-Alvarado L.N., Tussié-Luna M.I., Díaz-Chávez J., et al. | 2019 | Bmc Cancer | WoS-id: 000457454100001
Scopus-id: 2-s2.0-85060907017
| 14 | 15 |
| 58 | Development and validation of a predictive model for incident type 2 diabetes in middle-aged Mexican adults: The metabolic syndrome cohort | Coautor: Tusie-Luna M.T., Arellano-Campos, Olimpia, Gomez-Velasco, Donaji V., Bello-Chavolla, Omar Yaxmehen, et al. | 2019 | BMC ENDOCRINE DISORDERS | WoS-id: 000466884400001
Scopus-id: 2-s2.0-85065253215
| 31 | 34 |
| 59 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls | Coautor: Tusie-Luna, Teresa, Flannick, Jason, Mercader, Josep M., Fuchsberger, Christian, et al. | 2019 | Nature | WoS-id: 000470149000041
Scopus-id: 2-s2.0-85066251977
| 218 | 217 |
| 60 | Associations of autozygosity with a broad range of human phenotypes | Coautor: Tusie-Luna, Teresa, Clark, David W., Okada, Yukinori, Moore K.H.S., et al. | 2019 | NATURE COMMUNICATIONS | WoS-id: 000493438700005
Scopus-id: 2-s2.0-85074297784
| 77 | 82 |
| 61 | Identification of population-stratified coding variants for low and high serum triglycerides in Mexicans | Coautor: Tusie-Luna, Teresa, Ko, Arthur, Nikkola, Elina, Garske, Kristina, et al. | 2018 | HUMAN GENOMICS | WoS-id: 000427728400061
| 0 | 0 |
| 62 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes | Coautor: Tusie-Luna, Teresa, Gusarova, Viktoria, O'Dushlaine, Colm, Teslovich, Tanya M., et al. | 2018 | NATURE COMMUNICATIONS | WoS-id: 000435079300001
Scopus-id: 2-s2.0-85048556517
| 106 | 114 |
| 63 | Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients | Coautor: Tusie-Luna, Teresa, Lanata, Cristina M., Nititham, Joanne, Taylor, Kimberly E., et al. | 2018 | PLOS ONE | WoS-id: 000436645400012
Scopus-id: 2-s2.0-85049139823
| 54 | 52 |
| 64 | Mexican carriers of the HNF1A p. E508K variant do not experiencean enhanced response to sulfonylureas | Coautor: Teresa Tusie-Luna, Maria, Martagon, Alexandro J., Yaxmehen Bello-Chavolla, Omar, Arellano-Campos, Olimpia, et al. | 2018 | Diabetes Care | WoS-id: 000439288600024
Scopus-id: 2-s2.0-85050948618
| 17 | 20 |
| 65 | Frequency of the T307A, N680S, and-29G > A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry | Coautor: Tusié-Luna T., García-Jiménez G., Zariñán T., Rodríguez-Valentín R., et al. | 2018 | REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY | WoS-id: 000447769900002
Scopus-id: 2-s2.0-85055071762
| 15 | 15 |
| 66 | Transancestral mapping and genetic load in systemic lupus erythematosus | Coautor: Tusié-Luna T., Langefeld C.D., Ainsworth H.C., Graham D.S.C., et al. | 2017 | NATURE COMMUNICATIONS | WoS-id: 000405680100001
Scopus-id: 2-s2.0-85024906085
| 288 | 313 |
| 67 | Genome-Wide DNA Methylation Study in Lupus in an Admixed Mexican Population | Coautor: Tusie-Luna, Maria Teresa, Teruel, Maria, Coit, Patrick, Dozmorov, Mikhail, et al. | 2017 | ARTHRITIS & RHEUMATOLOGY | WoS-id: 000411824100178
| 0 | 0 |
| 68 | A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes | Coautor: Tusie-Luna, Teresa, Mercader, Josep M., Liao, Rachel G., Bell, Avery D., et al. | 2017 | Diabetes | WoS-id: 000413559100019
Scopus-id: 2-s2.0-85037582424
| 44 | 45 |
| 69 | Effects of amerindian genetic ancestry on clinical variables and therapy in patients with rheumatoid arthritis | Coautor: Tusié-Luna T., Sánchez E., De La Torre I.G., Sacnún M., et al. | 2017 | JOURNAL OF RHEUMATOLOGY | WoS-id: 000416883500007
Scopus-id: 2-s2.0-85037131683
| 1 | 1 |
| 70 | Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes | Coautor: Tusie-Luna, Teresa, Imamura, Minako, Takahashi, Atsushi, Yamauchi, Toshimasa, et al. | 2016 | NATURE COMMUNICATIONS | WoS-id: 000369024700002
Scopus-id: 2-s2.0-84956612031
| 127 | 131 |
| 71 | Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture | Coautor: Tusie-Luna, Teresa, Alarcon-Riquelme, Marta E., Ziegler, Julie T., Molineros, Julio, et al. | 2016 | ARTHRITIS & RHEUMATOLOGY | WoS-id: 000373130300019
Scopus-id: 2-s2.0-84962045963
| 131 | 135 |
| 72 | Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico | Coautor: Tusie-Luna, Teresa, Luis Acosta, Jose, Cristal Hernandez-Mondragon, Alma, Carolina Correa-Acosta, Laura, et al. | 2016 | BMC GENETICS | WoS-id: 000376650100001
Scopus-id: 2-s2.0-84969961807
| 3 | 4 |
| 73 | Genome-wide association study of colorectal cancer in Hispanics | Coautor: Tusie-Luna, Teresa, Schmit, Stephanie L., Schumacher, Fredrick R., Edlund, Christopher K., et al. | 2016 | Carcinogenesis | WoS-id: 000377915800003
Scopus-id: 2-s2.0-84973597762
| 30 | 30 |
| 74 | Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene | Coautor: Tusie-Luna, Teresa, Rodriguez, Alejandra, Gonzalez, Luis, Ko, Arthur, et al. | 2016 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000378497000009
Scopus-id: 2-s2.0-84969674393
| 10 | 9 |
| 75 | Analysis of protein-coding genetic variation in 60,706 humans | Coautor: Tusie-Luna M.T., Lek M., Karczewski K.J., Minikel E.V., et al. | 2016 | Nature | WoS-id: 000381804900026
Scopus-id: 2-s2.0-84982253941
| 7490 | 7549 |
| 76 | The panorama of familial hypercholesterolemia in Latin America: a systematic review | Coautor: Tusie-Luna, Maria Teresa, Mehta, Roopa, Zubiran, Rafael, Martagon, Alexandro J., et al. | 2016 | JOURNAL OF LIPID RESEARCH | WoS-id: 000389473000003
Scopus-id: 2-s2.0-85002744802
| 25 | 28 |
| 77 | TP53 germline mutations in young females with early onset breast cancer in a Mexican population. | 2ᵒ autor: Tusie-Luna, Teresa, Gallardo, Lenny Nadia, Tusie-Luna, Maria Isabel, Diaz-Chavez, Jose, et al. | 2016 | JOURNAL OF CLINICAL ONCOLOGY | WoS-id: 000404665402166
| 1 | 0 |
| 78 | Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women | Coautor: Tusié-Luna T., Huerta-Chagoya A., Vázquez-Cárdenas P., Moreno-Macías H., et al. | 2015 | PLOS ONE | WoS-id: 000354545600050
Scopus-id: 2-s2.0-84929346819
| 65 | 66 |
| 79 | Association of a low-frequency variant in HNF1A with type 2 diabetes in a latino population the SIGMA Type 2 Diabetes Consortium | Coautor: Tusie-Luna, T, Estrada, K, Aukrust, I, Bjorkhaug, L, et al. | 2014 | JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | WoS-id: 000336972600022
Scopus-id: 2-s2.0-84902185032
| 199 | 198 |
| 80 | Genetic and environmental determinants of the susceptibility of Amerindian derived populations for having hypertriglyceridemia | 2ᵒ autor: Tusie-Luna T., Aguilar-Salinas C.A., Pajukanta P. | 2014 | METABOLISM-CLINICAL AND EXPERIMENTAL | WoS-id: 000337715000002
Scopus-id: 2-s2.0-84902551930
| 32 | 36 |
| 81 | Amerindian-specific regions under positive selection harbour new lipid variants in Latinos | Coautor: Tusie-Luna T., Ko A., Cantor R.M., Weissglas-Volkov D., et al. | 2014 | NATURE COMMUNICATIONS | WoS-id: 000338835400001
Scopus-id: 2-s2.0-84901949893
| 73 | 74 |
| 82 | Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes | Coautor: Tusié-Luna T., Majithia A.R., Flannick J., Shahinian P., et al. | 2014 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: 000341625600043
Scopus-id: 2-s2.0-84907013152
| 139 | 145 |
| 83 | Factors associated with postprandial lipemia and apolipoprotein a-v levels in individuals with familial combined hyperlipidemia | Coautor: Tusie-Luna M.T., Almeda-Valdes P., Cuevas-Ramos D., Mehta R., et al. | 2014 | BMC ENDOCRINE DISORDERS | WoS-id: 000345709600001
Scopus-id: 2-s2.0-84924336747
| 9 | 11 |
| 84 | Resistencia a hormonas tiroideas (RTH). reporte de caso | Coautor: Teresa Tusié-Luna M., Almeda-Valdés P., Pérez-Enríquez B., Cuevas-Ramos D., et al. | 2014 | GACETA MEDICA DE MEXICO | WoS-id: 000348592700010
Scopus-id: 2-s2.0-84908110315
| 0 | 0 |
| 85 | Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci | Coautor: Tusie-Luna, T, Weissglas-Volkov, D, Aguilar-Salinas, CA, Nikkola, E, et al. | 2013 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000317563800004
Scopus-id: 2-s2.0-84878849984
| 100 | 99 |
| 86 | The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus | Coautor: Tusie-Luna M.T., Aguilar-Salinas C.A., Munoz-Hernandez, LL, Cobos-Bonilla M., et al. | 2013 | METABOLISM-CLINICAL AND EXPERIMENTAL | WoS-id: 000318260500004
Scopus-id: 2-s2.0-84876694184
| 12 | 11 |
| 87 | Rheumatoid arthritis in latin americans enriched for amerindian ancestry is associated with loci in chromosomes 1, 12, and 13, and the HLA Class II region | Coautor: Tusie-Luna, T, Herraez, DL, Martinez-Bueno, M, Riba, L, et al. | 2013 | ARTHRITIS AND RHEUMATISM | WoS-id: 000319740600007
Scopus-id: 2-s2.0-84878560466
| 32 | 36 |
| 88 | GWAS In Hispanic and Latin American Individuals Enriched For Amerindian Ancestry Identifies a New Locus Associated With Systemic Lupus Erythematosus | Coautor: Tusie-Luna, T, Riquelme, MEA, Ziegler, JT, Comeau, ME, et al. | 2013 | ARTHRITIS AND RHEUMATISM | WoS-id: 000325359204103
| 0 | 0 |
| 89 | PCSK1 rs6232 Is Associated with Childhood and Adult Class III Obesity in the Mexican Population | Coautor: Tusié-Luna T., Villalobos-Comparán M., Villamil-Ramírez H., Villarreal-Molina T., et al. | 2012 | PLOS ONE | WoS-id: 000305695100025
Scopus-id: 2-s2.0-84862653589
| 23 | 26 |
| 90 | Reconstructing Native American population history | Coautor: Tusié-Luna T., Reich D., Patterson N., Campbell D., et al. | 2012 | Nature | WoS-id: 000307501000040
Scopus-id: 2-s2.0-84865120805
| 542 | 576 |
| 91 | Primary amenorrhea in two sisters: description of a Mexican family with 17 alpha hydroxylase-17 lyase deficiency caused by arginine - stop mutation | Coautor: Tusie-Luna M.T., Escamilla-Márquez M.A., Garduno-Garcia, JD, Ordonez-Sanchez, ML, et al. | 2012 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000307672900013
Scopus-id: 2-s2.0-84865327013
| 2 | 2 |
| 92 | Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations | Coautor: Tusié-Luna T., Sánchez E., Rasmussen A., Riba L., et al. | 2012 | ARTHRITIS AND RHEUMATISM | WoS-id: 000310544500022
Scopus-id: 2-s2.0-84868092719
| 65 | 68 |
| 93 | Erratum: Reconstructing Native American population history (Nature (2012) 488 (370-374) DOI:10.1038/nature11258) | Coautor: Tusié-Luna T., Reich D., Patterson N., Campbell D., et al. | 2012 | Nature | WoS-id: 000310774300052
Scopus-id: 2-s2.0-84868618389
| 0 | 1 |
| 94 | Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo Population | Coautor: Tusié-Luna M.T., Gamboa-Meléndez M.A., Huerta-Chagoya A., Moreno-Macías H., et al. | 2012 | Diabetes | WoS-id: 000312041700039
Scopus-id: 2-s2.0-84870311448
| 82 | 92 |
| 95 | Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes | Coautor: Tusie-Luna T., Haas B.E., Horvath S., Pietilainen, KH, et al. | 2012 | BMC MEDICAL GENOMICS | WoS-id: 000313566500001
Scopus-id: 2-s2.0-84870461579
| 31 | 32 |
| 96 | Evidence of How rs7575840 Influences Apolipoprotein B-Containing Lipid Particles | Coautor: Tusie-Luna T., Haas B.E., Weissglas-Volkov D., Aguilar-Salinas C.A., et al. | 2011 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000289720800037
Scopus-id: 2-s2.0-79955624738
| 12 | 14 |
| 97 | The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: A population bas | Coautor: Tusié-Luna M.T., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martínez R., et al. | 2011 | Atherosclerosis | WoS-id: 000290205800023
Scopus-id: 2-s2.0-79955528671
| 23 | 23 |
| 98 | Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease | Coautor: Tusié-Luna M.T., Gutiérrez-Cirlos C., Ordonez-Sanchez, ML, Patterson B.W., et al. | 2011 | Annals Of Hepatology | WoS-id: 000290636300006
Scopus-id: 2-s2.0-79956016360
| 14 | 17 |
| 99 | Early onset type 2 diabetes in Jamaica and in Mexico. Opportunities derived from an interethnic study | 2ᵒ autor: Tusie-Luna, MT, Irving R., Mills J., Wright-Pascoe R., et al. | 2011 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000292220400012
Scopus-id: 2-s2.0-79960015312
| 14 | 14 |
| 100 | The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans | Coautor: Tusie-Luna T., Weissglas-Volkov D., Calkin A.C., Sinsheimer J.S., et al. | 2011 | JOURNAL OF CLINICAL INVESTIGATION | WoS-id: 000293495500017
Scopus-id: 2-s2.0-79960985140
| 51 | 57 |
| 101 | Familial homozygous hypercholesterolemia due to the c2271delT mutation in the LDL receptor gene, detected exclusively in mexicans | Coautor: Tusié-Luna M.T., Martínez L., Sanchez, MLO, Letona R., et al. | 2011 | GACETA MEDICA DE MEXICO | WoS-id: 000300817700003
Scopus-id: 2-s2.0-83655192548
| 5 | 7 |
| 102 | Identification of Two Common Variants Contributing to Serum Apolipoprotein B Levels in Mexicans | Coautor: Tusie-Luna T., Weissglas-Volkov D., Plaisier C.L., Huertas-Vazquez A., et al. | 2010 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000273799900036
Scopus-id: 2-s2.0-75149145515
| 13 | 13 |
| 103 | Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican Dyslipidemi | Coautor: Tusie-Luna T., Weissglas-Volkov D., Aguilar-Salinas C.A., Sinsheimer J.S., et al. | 2010 | CIRCULATION-CARDIOVASCULAR GENETICS | WoS-id: 000275979700006
Scopus-id: 2-s2.0-77952533413
| 44 | 43 |
| 104 | A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans | Coautor: Tusié-Luna T., Acuna-Alonzo, V, Flores-Dorantes T., Kruit J.K., et al. | 2010 | HUMAN MOLECULAR GENETICS | WoS-id: 000279469100012
Scopus-id: 2-s2.0-77954145711
| 113 | 119 |
| 105 | Fifty years studying hiperlipidemias: The case of familial combined hyperlipidemia | Coautor y autor de correspondencia: Tusié-Luna M.T., Aguilar-Salinas C.A., Gómez-Díaz R. | 2010 | INVESTIGACION CLINICA | WoS-id: 000279719900002
Scopus-id: 2-s2.0-78149235611
| 3 | 4 |
| 106 | Association of R230C ABCA1 gene variant with low HDL-C levels and abnormal HDL subclass distribution in Mexican school-aged children | Coautor: Tusié-Luna T., Flores-Dorantes T., Arellano-Campos O., Posadas-Sánchez R., et al. | 2010 | CLINICA CHIMICA ACTA | WoS-id: 000280033400008
Scopus-id: 2-s2.0-77954144155
| 17 | 17 |
| 107 | PRSS1, SPINK1 and CFTR Mutations in Families and Unrelated Subjects With Idiopathic Early Onset Chronic (CP) or Recurrent Acute Pancreatitis (RAP) in Mexico City | Coautor: Tusie-Luna, MT, Pelaez-Luna, M, Robles-Diaz, G, Canizales, S | 2010 | Pancreas | WoS-id: 000282946600179
| 0 | 0 |
| 108 | Genetically Determined Amerindian Ancestry Correlates With Increased Frequency of Risk Alleles for Systemic Lupus Erythematosus | Coautor: Tusié-Luna T., Sanchez E., Webb R.D., Rasmussen A., et al. | 2010 | ARTHRITIS AND RHEUMATISM | WoS-id: 000285210200025
Scopus-id: 2-s2.0-78650065026
| 63 | 70 |
| 109 | Galanin Preproprotein Is Associated With Elevated Plasma Triglycerides | Coautor: Tusié-Luna T., Plaisier C.L., Kyttala, M, Weissglas-Volkov D., et al. | 2009 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000261797200024
Scopus-id: 2-s2.0-58849095360
| 26 | 24 |
| 110 | Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment | Coautor: Tusié-Luna M.T., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martfnez R., et al. | 2009 | CURRENT OPINION IN LIPIDOLOGY | WoS-id: 000264956600002
Scopus-id: 2-s2.0-64549120714
| 29 | 33 |
| 111 | Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes | Coautor: Tusié-Luna M.T., Florez J.C., Price A.L., Campbell D., et al. | 2009 | Diabetologia | WoS-id: 000268006200010
Scopus-id: 2-s2.0-67650663161
| 71 | 75 |
| 112 | Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A | Coautor: Tusie-Luna, T, Medeiros-Domingo, A, Tan, BH, Iturralde-Torres, P, et al. | 2009 | Heart Rhythm | WoS-id: 000268867700011
Scopus-id: 2-s2.0-67650741355
| 19 | 18 |
| 113 | Obesity and metabolic syndrome. A challenge for the Mexican Institutes of Health [La obesidad y el síndrome metabólico. Un reto para los Institutos Nationales de Salud] | Coautor: Tusié-Luna M.T., García-García E., De La Llata-Romero M., Kaufer-Horwitz M., et al. | 2009 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000270791200011
Scopus-id: 2-s2.0-70350170312
| 4 | 4 |
| 114 | A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia | Coautor: Tusie-Luna T., Plaisier C.L., Horvath S., Huertas-Vazquez A., et al. | 2009 | PLOS GENETICS | WoS-id: 000270817800026
Scopus-id: 2-s2.0-70349656509
| 134 | 136 |
| 115 | TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia | Coautor: Tusie-Luna T., Huertas-Vazquez A., Plaisier C., Weissglas-Volkov D., et al. | 2008 | Diabetologia | WoS-id: 000251320900010
Scopus-id: 2-s2.0-36649027501
| 47 | 50 |
| 116 | High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes | Coautor: Tusié-Luna M.T., Menjívar M., Granados-Silvestre M.A., Montúfar-Robles I., et al. | 2008 | CLINICAL GENETICS | WoS-id: 000252319900012
Scopus-id: 2-s2.0-38349194536
| 13 | 11 |
| 117 | Association of the ATP-binding cassette transporter a1 R230C variant with early-onset type 2 diabetes in a Mexican population | Coautor: Tusie-Luna, MT, Villarreal-Molina, MT, Flores-Dorantes, MT, Arellano-Campos, O, et al. | 2008 | Diabetes | WoS-id: 000252914400029
Scopus-id: 2-s2.0-40749127658
| 87 | 87 |
| 118 | Estimating ethnic admixture from pedigree data | Coautor: Tusie-Luna T., Sinsheimer J.S., Plaisier C.L., Huertas-Vazquez A., et al. | 2008 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000254067800019
Scopus-id: 2-s2.0-41149113412
| 6 | 6 |
| 119 | WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels | Coautor: Tusie-Luna T., Lee J.C., Weissglas-Volkov D., Kyttala, M, et al. | 2008 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000258418200003
Scopus-id: 2-s2.0-48349120779
| 43 | 50 |
| 120 | The FTO gene is associated with adulthood obesity in the Mexican population | Coautor: Tusie-Luna, MT, Villalobos-Comparán M., Flores-Dorantes, T, Villarreal-Molina, T, et al. | 2008 | Obesity | WoS-id: 000259649400016
Scopus-id: 2-s2.0-53849111547
| 152 | 159 |
| 121 | High adiponectin concentrations are associated with the metabolically healthy obese phenotype | Coautor: Luna, MTT, Aguilar-Salinas C.A., García E., Robles L., et al. | 2008 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | WoS-id: 000259903700060
Scopus-id: 2-s2.0-53249149870
| 231 | 246 |
| 122 | Obesity and metabolic syndrome as public health problem. A reflection [La obesidad y el síndrome metabólico como problema de salud pública. Una reflexión] | Coautor: Tusié-Luna M.T., García-García E., De La Llata-Romero M., Kaufer-Horwitz M., et al. | 2008 | SALUD PUBLICA DE MEXICO | WoS-id: 000261057400015
Scopus-id: 2-s2.0-57349115686
| 31 | 35 |
| 123 | Obesity and metabolic syndrome as public health problem. A reflection [La obesidad y el síndrome metabólico como problema de salud pública. Una reflexión] | Coautor: Tusié-Luna M.T., García-García E., De La Llata-Romero M., Kaufer-Horwitz M., et al. | 2008 | ARCHIVOS DE CARDIOLOGIA DE MEXICO | Scopus-id: 2-s2.0-53649089321
| 0 | 6 |
| 124 | Recurrent DNA inversion rearrangements in the human genome | Coautor: Tusie-Luna T., Flores M., Morales L., Gonzaga-Jauregui C., et al. | 2007 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: 000245737500004
Scopus-id: 2-s2.0-34547531150
| 74 | 78 |
| 125 | A genomewide admixture map for latino populations | Coautor: Tusie-Luna T., Price A.L., Patterson N., Yu F., et al. | 2007 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000246553800003
Scopus-id: 2-s2.0-34250894969
| 225 | 236 |
| 126 | The ATP-binding cassette transporter A1 R230C variant affects HDL cholesterol levels and BMI in the Mexican population: Association with obesity and obesity-related comorbidities | Coautor: Tusie-Luna M.T., Villarreal-Molina M.T., Aguilar-Salinas C.A., Rodríguez-Cruz M., et al. | 2007 | Diabetes | WoS-id: 000247768000016
Scopus-id: 2-s2.0-34347382714
| 96 | 98 |
| 127 | SCN4B-encoded sodium channel ß4 subunit in congenital long-QT syndrome | Coautor: Tusié-Luna M.T., Medeiros-Domingo A., Kaku T., Tester D.J., et al. | 2007 | Circulation | WoS-id: 000247902600003
Scopus-id: 2-s2.0-34447307435
| 266 | 305 |
| 128 | Association of PPARG2 Pro12Ala variant with larger body mass index in Mestizo and Amerindian populations of Mexico | Coautor: Tusié-Luna M.T., Canizales-Quinteros S., Aguilar-Salinas C.A., Ortiz-López M.G., et al. | 2007 | HUMAN BIOLOGY | WoS-id: 000250770700008
Scopus-id: 2-s2.0-35548988953
| 26 | 26 |
| 129 | A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia | Coautor: Tusié-Luna T., Tan B.-H., Iturralde-Torres P., Medeiros-Domingo A., et al. | 2007 | CARDIOVASCULAR RESEARCH | WoS-id: 000251478400007
Scopus-id: 2-s2.0-35548941783
| 35 | 37 |
| 130 | Successful collaborations between three Mexican institutions in the study of dyslipidemia, obesity and diabetes [Colaboraciones exitosas entre tres instituciones mexicanas en el estudio de las dislipidemias, la obesidad y la diabetes] | Coautor: Tusié-Luna M.T., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martínez R., et al. | 2007 | GACETA MEDICA DE MEXICO | WoS-id: 000254327800001
Scopus-id: 2-s2.0-42949164155
| 2 | 4 |
| 131 | Genetic markers for the understanding of the pathophysiology of diseases [Marcadores genéticos para el entendimiento de la fisiopatología de las enfermedades] | 1ᵉʳ autor y autor de correspondencia: Tusié-Luna M.T. | 2007 | SALUD PUBLICA DE MEXICO | Scopus-id: 2-s2.0-34250875808
| 0 | 0 |
| 132 | Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma | Coautor: Tusié-Luna M.T., Rasmussen A., Nava-Salazar S., Yescas P., et al. | 2006 | JOURNAL OF NEUROSURGERY | WoS-id: 000236188500009
Scopus-id: 2-s2.0-33644661728
| 21 | 21 |
| 133 | Common hepatic nuclear factor-4a variants are associated with high serum lipid levels and the metabolic syndrome | Coautor: Tusie-Luna T., Weissglas-Volkov D., Huertas-Vazquez A., Suviolahti E., et al. | 2006 | Diabetes | WoS-id: 000238764600009
Scopus-id: 2-s2.0-33747039577
| 51 | 53 |
| 134 | Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families | Coautor: Tusié-Luna M.T., Yescas P., Huertas-Vazquez A., Villarreal-Molina M.T., et al. | 2006 | Neurogenetics | WoS-id: 000239043000008
Scopus-id: 2-s2.0-33746103277
| 44 | 46 |
| 135 | HNF-1a G574S is a functional variant with decreased transactivation activity | Coautor: Tusié-Luna M.T., Navalón-García K., Mendoza-Alcantar L., Díaz-Vargas M.E., et al. | 2006 | DIABETIC MEDICINE | WoS-id: 000243135700004
Scopus-id: 2-s2.0-33751253099
| 4 | 5 |
| 136 | GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus | Coautor: Tusié-Luna M.T., Romero-Hidalgo S., Rodrigues E.R., Gutiérrez-Peña E., et al. | 2005 | Genetica | WoS-id: 000228542300004
Scopus-id: 2-s2.0-18144378086
| 2 | 3 |
| 137 | Genes and type 2 diabetes mellitus | 1ᵉʳ autor y autor de correspondencia: Tusié Luna M.T. | 2005 | Archives Of Medical Research | WoS-id: 000230038000004
Scopus-id: 2-s2.0-19944363176
| 28 | 35 |
| 138 | Familial combined hyperlipidemia in mexicans: Association with upstream transcription factor 1 and linkage on chromosome 16q24.1 | Coautor: Tusie-Luna T., Huertas-Vazquez A., Aguilar-Salinas C., Lusis A.J., et al. | 2005 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000231502500035
Scopus-id: 2-s2.0-24144435303
| 62 | 65 |
| 139 | Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families | Coautor: Tusié-Luna M.T., Domínguez-López A., Miliar-García Á., Segura-Kato Y.X., et al. | 2005 | Journal of the Pancreas | Scopus-id: 2-s2.0-27644491272
| 0 | 22 |
| 140 | Identifying different susceptibility loci associated with early onset diabetes and cardiovascular disease in Mexican families [Identificación de distintos loci de susceptibilidad relacionados al desarrollo de diabetes de inicio temprano y e | Coautor: Tusié-Luna M.T., Canizales-Quinteros S., Huertas-Vázquez A., Riba-Ramírez L., et al. | 2005 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-20944438524
| 0 | 2 |
| 141 | Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population | Coautor: Tusié-Luna M.T., Del Bosque-Plata L., Aguilar-Salinas C.A., Ramírez-Jiménez S., et al. | 2004 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000188718400007
Scopus-id: 2-s2.0-0347931740
| 39 | 45 |
| 142 | Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia | Coautor: Tusié-Luna M.T., Canizales-Quinteros S., Aguilar-Salinas C.A., Reyes-Rodríguez E., et al. | 2003 | CIRCULATION RESEARCH | WoS-id: 000181711300015
Scopus-id: 2-s2.0-0037459359
| 29 | 32 |
| 143 | Towards a molecular understanding of disease [El camino hacia la comprensión molecular de las enfermedades] | 1ᵉʳ autor y autor de correspondencia: Tusié Luna Ma.T. | 2003 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0038386013
| 0 | 2 |
| 144 | With the finished human genome in hand, what next? | Coautor y autor de correspondencia: Tusié-Luna M.T., Collado-Vides J., Medrano-Soto A. | 2003 | GENOME BIOLOGY | Scopus-id: 2-s2.0-0042810681
| 0 | 1 |
| 145 | Early-onset type 2 diabetes in Mexico | Coautor: Tusié-Luna T., García-García E., Aguilar-Salinas C.A., Rull-Rodrigo J.A. | 2002 | ISRAEL MEDICAL ASSOCIATION JOURNAL | WoS-id: 000182574300012
Scopus-id: 2-s2.0-0036283396
| 12 | 13 |
| 146 | The human genetic variability map, single nucleotide polymorphisms (SNP's) and some of their applications to medicine [El mapa de la variabilidad genética del humano, los polimorfismos de un solo nucleótido (SNP's) y algunas de sus aplicac | 1ᵉʳ autor y autor de correspondencia: Tusié Luna M.T. | 2001 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000171274800004
Scopus-id: 2-s2.0-0035403753
| 2 | 2 |
| 147 | The genetics of type 2 diabetes: Genes involved in early-onset diabetes [La genética de la diabetes mellitus tipo 2: Genes implicados en la diabetes de aparición temprana] | 1ᵉʳ autor y autor de correspondencia: Luna Ma.T.T. | 2000 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0034181417
| 0 | 2 |
| 148 | Mutation analysis in patients with congenital adrenal hyperplasia in the Spanish population: Identification of putative novel steroid 21-hydroxylase deficiency alleles associated with the classic form of the disease | Coautor: Tusié-Luna M.T., Lobato M.N., Ordóñez-Sánchez M.L., Meseguer A. | 1999 | HUMAN HEREDITY | WoS-id: 000080792600009
Scopus-id: 2-s2.0-0345279922
| 21 | 22 |
| 149 | Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: Identification of possible new mutations and high prevalence of apparent germ-line mutations | Coautor: Tusié-Luna M.T., Ordoñez-Sánchez M.L., Ramírez-Jiménez S., López-Gutierrez A.U., et al. | 1998 | HUMAN GENETICS | WoS-id: 000072457500008
Scopus-id: 2-s2.0-2642651108
| 52 | 59 |
| 150 | Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: Evidence of different genetic mechanisms involved in the production of the disease | Coautor: Tusié-Luna M.T., López-Gutiérrez A.U., Riba L., Ordoñez-Sánchez M.L., et al. | 1998 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000077266400010
Scopus-id: 2-s2.0-0031759339
| 23 | 28 |
| 151 | Analysis of the glucokinase gene in Mexican families displaying early- onset non-insulin-dependent diabetes mellitus including MODY families | Coautor: Tusie-Luna M.T., Del Bosque-Plata L., Garcia-Garcia E., Ramirez-Jimenez S., et al. | 1997 | AM J MED GENET | WoS-id: A1997YD48100003
Scopus-id: 2-s2.0-0030735219
| 6 | 7 |
| 152 | Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms | 1ᵉʳ autor: Tusie-Luna M.-T., White P.C. | 1995 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: A1995TD89000072
Scopus-id: 2-s2.0-0028786666
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| 153 | Mutations in steroid 21-hydroxylase (CYP21) | 2ᵒ autor: Tusie-Luna M.-T., White P.C., New M.I., Speiser P.W. | 1994 | HUMAN MUTATION | WoS-id: A1994NT13300007
Scopus-id: 2-s2.0-0028179432
| 102 | 115 |
| 154 | R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions | 2ᵒ autor: Tusie-Luna M.-T., Helmberg A., Tabarelli M., Kofler R., et al. | 1992 | MOL ENDOCRINOL | WoS-id: A1992JL96300017
Scopus-id: 2-s2.0-0026673224
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| 155 | Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Coautor: Tusie-Luna M.-T., Speiser P.W., Dupont J., Zhu D., et al. | 1992 | JOURNAL OF CLINICAL INVESTIGATION | WoS-id: A1992JH80100036
Scopus-id: 2-s2.0-0026641101
| 467 | 537 |
| 156 | The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex | 2ᵒ autor: Tusie-Lunaf M.-T., Curnow K.M., Pascoe L., Natarajan R., et al. | 1991 | MOL ENDOCRINOL | WoS-id: A1991GL38900018
Scopus-id: 2-s2.0-0025999564
| 315 | 331 |
| 157 | A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele | 1ᵉʳ autor: Tusie-Luna M.-T., Speiser P.W., Dumic M., New M.I., et al. | 1991 | MOL ENDOCRINOL | WoS-id: A1991FM56700010
Scopus-id: 2-s2.0-0025773734
| 163 | 175 |
| 158 | Expression of 11ß-hydroxysteroid dehydrogenase using recombinant vaccinia virus | 2ᵒ autor: Tusie-Luna M.-T., Agarwal A.K., Monder C., White P.C. | 1990 | MOL ENDOCRINOL | WoS-id: A1990EQ42800008
Scopus-id: 2-s2.0-0025611952
| 171 | 172 |
| 159 | Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus | 1ᵉʳ autor: Tusie-Luna M.-T., Traktman P., White P.C. | 1990 | JOURNAL OF BIOLOGICAL CHEMISTRY | WoS-id: A1990EL02000033
Scopus-id: 2-s2.0-0025696003
| 224 | 242 |
| 160 | The effect of LRRK2 loss-of-function variants in humans | Coautor: Tusie-Luna T., Kleinman A., Marshall J.L., Goodrich J.K., et al. | | NATURE MEDICINE | WoS-id: 000535873800002
Scopus-id: 2-s2.0-85085479654
| 81 | 83 |
| 161 | Author Correction: The effect of LRRK2 loss-of-function variants in humans (Nature Medicine, (2020), 26, 6, (869-877), 10.1038/s41591-020-0893-5) | Coautor: Tusie-Luna T., Whiffin N., Kleinman A., Marshall J.L., et al. | | NATURE MEDICINE | WoS-id: 000609952600001
Scopus-id: 2-s2.0-85099834831
| 0 | 0 |
ID's SCOPUS 