Author details

Full Name

MarÃa Teresa TusiÃ©-Luna

Affiliation

ORCID

Career Start Year

1990

Papers

135

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37530085	The role of SLC16A11 variations in diabetes mellitus.		2023
37821706	Mexican Biobank advances population and medical genomics of diverse ancestries.		2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36941956	A novel nonsense mutation in the insulin receptor gene in a patient with HAIR-AN syndrome and endometrial cancer.		2023
37365052	Implication of myddosome complex genetic variants in outcome severity of COVID-19 patients.		2023
35022935	Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis.	Neurological Sciences	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35354197	ASSOCIATION BETWEEN APOE-Îµ CARRIER STATUS AND QUALITATIVE NEUROIMAGING CHARACTERISTICS IN OLDER ADULTS WITH MILD COGNITIVE IMPAIRMENT.	Revista de Investigacion Clinica	2022
34604815	Genetic discovery and risk characterization in type 2 diabetes across diverse populations.	HGG Adv	2021
33486704	The influence of high-density lipoprotein (HDL) and HDL subfractions on insulin secretion and cholesterol efflux in pancreatic derived Î²-cells.	Journal of Endocrinological Investigation	2021
33588820	Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia.	Lipids in Health and Disease	2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
33574311	Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry.	npj Parkinson's Disease	2021
34256778	LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.	Lipids in Health and Disease	2021
34340684	Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes.	Genome Med	2021
33430178	Association between ApoE Îµ4 Carrier Status and Cardiovascular Risk Factors on Mild Cognitive Impairment among Mexican Older Adults.	Brain Sciences	2021
35046991	Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes.	Frontiers in Genetics	2021
34461981	Correction to: Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes.	Genome Med	2021
34609365	PRECISION MEDICINE FOR METABOLIC DISORDERS IN LOW- AND MIDDLE-INCOME COUNTRIES: AREAS OF OPPORTUNITY AND CHALLENGES FOR THE FUTURE.	Revista de Investigacion Clinica	2021
32925908	The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance.	PLoS Genet	2020
31802109	Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism.	American Journal of Hypertension	2020
31968565	Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study.	Genes	2020
32016916	R230C but not -â¿¿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	2020
32104752	Use of PCSK9 Inhibitor in a Mexican Boy with Compound Heterozygous Familial Hypercholesterolemia: A Case Report.	Journal of the Endocrine Society	2020
30709381	Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population.	BMC Cancer	2019
30475225	The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes.	European Journal of Endocrinology	2019
30621578	A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos.	BMC Genetics	2019
31030672	Development and validation of a predictive model for incident type 2 diabetes in middle-aged Mexican adults: the metabolic syndrome cohort.	BMC Endocrine Disorders	2019
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
31318156	Prediction of incident hypertension and arterial stiffness using the non-insulin-based metabolic score for insulin resistance (METS-IR) index.	Journal of Clinical Hypertension	2019
29844095	Mexican Carriers of the p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas.	Diabetes Care	2018
30340493	Frequency of the T307A, N680S, and -29G>A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry.	Reproductive Biology and Endocrinology	2018
29953444	Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients.	PLoS One	2018
29899519	Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.	Nat Commun	2018
29237696	Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies-Derived Signals? Take a Look in the Native American Populations.	Circulation: Cardiovascular Genetics	2017
28838971	A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes.	Diabetes	2017
28714469	Transancestral mapping and genetic load in systemic lupus erythematosus.	Nat Commun	2017
29093158	Effects of Amerindian Genetic Ancestry on Clinical Variables and Therapy in Patients with Rheumatoid Arthritis.	Journal of Rheumatology	2017
27535533	Analysis of protein-coding genetic variation in 60,706 humans.	Nature	2016
27230431	Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico.	BMC Genetics	2016
26818947	Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.	Nat Commun	2016
27207650	Genome-wide association study of colorectal cancer in Hispanics.	Carcinogenesis	2016
27199446	Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene.	Arterioscler Thromb Vasc Biol	2016
26606652	Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.	Arthritis Rheumatol	2016
27777316	The panorama of familial hypercholesterolemia in Latin America: a systematic review.	Journal of Lipid Research	2016
25973943	Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women.	PLoS ONE	2015
24886709	Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.	Nat Commun	2014
25275849	[Thyroid hormone resistance (THR): a case report].	Gaceta Medica de Mexico	2014
25425215	Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia.	BMC Endocr Disord	2014