| 1 | CFTR pathogenic variants spectrum in a cohort of Mexican patients with cystic fibrosis | 1ᵉʳ autor: Martínez-Hernández A., Mendoza-Caamal E.C., Mendiola-Vidal N.G., Barajas-Olmos F., et al. | 2024 | Heliyon | WoS-id: 001226662900001
Scopus-id: 2-s2.0-85189700727
| 1 | 1 |
| 2 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Martinez-Hernandez, Angelica, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 3 | The role of single nucleotide variant rs3819817 of the Histidine Ammonia-Lyase gene and 25-Hydroxyvitamin D on bone mineral density, adiposity markers, and skin pigmentation, in Mexican population | Coautor: Martinez-Hernandez, A., Rivera-Paredez, B., Hidalgo-Bravo, A., Leon-Reyes, G., et al. | 2023 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | WoS-id: 000942967100002
Scopus-id: 2-s2.0-85149126451
| 2 | 2 |
| 4 | DNA Methylation Remodeling after Bariatric Surgery Correlates with Clinical Parameters | Coautor: Martínez-Hernández A., Sánchez E.C., Barajas-Olmos F., Baca P., et al. | 2023 | ADVANCED BIOLOGY | WoS-id: 000981518100001
Scopus-id: 2-s2.0-85158145511
| 0 | 1 |
| 5 | Augmented reality simulation as training model of ventricular puncture: Evidence in the improvement of the quality of punctures | Coautor: Martinez-Hernandez, Adriana, Dominguez-Velasco, Cesar F., Tello-Mata, Isaac E., Guinto-Nishimura, Gerardo, et al. | 2023 | INTERNATIONAL JOURNAL OF MEDICAL ROBOTICS AND COMPUTER ASSISTED SURGERY | WoS-id: 001000166100001
Scopus-id: 2-s2.0-85161411030
| 5 | 4 |
| 6 | Rare coding variants in 35 genes associate with circulating lipid levels?A multi-ancestry analysis of 170,000 exomes | Coautor: Martínez-Hernández A., 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 |
| 7 | Exome Sequencing Data Analysis and a Case-Control Study in Mexican Population Reveals Lipid Trait Associations of New and Known Genetic Variants in Dyslipidemia-Associated Loci | Coautor: Martinez-Hernandez, Angelica, Jurado-Camacho, Pedro A., Cid-Soto, Miguel A., Barajas-Olmos, Francisco, et al. | 2022 | Frontiers in Genetics | WoS-id: 000806612000001
Scopus-id: 2-s2.0-85131733069
| 3 | 3 |
| 8 | Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review | 1ᵉʳ autor: Martinez-Hernandez, A., Martinez-Anaya, D., Duran-McKinster, C., Del Castillo-Ruiz, V, et al. | 2022 | BMC MEDICAL GENOMICS | WoS-id: 000877014900002
Scopus-id: 2-s2.0-85140943693
| 0 | 1 |
| 9 | Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico | Coautor: Martínez-Hernández A., García-Ortiz H., Barajas-Olmos F., Contreras-Cubas C., et al. | 2022 | GENES | Scopus-id: 2-s2.0-85144535810
| 0 | 4 |
| 10 | Reconstruction of ancient microbial genomes from the human gut | Coautor: Martínez-Hernández A., Wibowo M.C., Yang Z., Borry M., et al. | 2021 | Nature | WoS-id: 000650200300003
Scopus-id: 2-s2.0-85105780311
| 141 | 154 |
| 11 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes | Coautor: Martinez-Hernandez, Angelica, Goodrich, Julia K., Singer-Berk, Moriel, Son, Rachel, et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000664874700036
Scopus-id: 2-s2.0-85107774343
| 52 | 54 |
| 12 | Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum | Coautor: Martínez-Hernández A., Mendoza-Caamal E.C., Barajas-Olmos F., Mirzaeicheshmeh E., et al. | 2021 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000671281100001
Scopus-id: 2-s2.0-85108990517
| 9 | 9 |
| 13 | Alterations of DNA methylation during adipogenesis differentiation of mesenchymal stem cells isolated from adipose tissue of patients with obesity is associated with type 2 diabetes | Coautor: Martinez-Hernandez, Angelica, Mirzaeicheshmeh, Elaheh, ZERRWECK, CARLOS, Centeno-Cruz, Federico, et al. | 2021 | Adipocyte | WoS-id: 000711201500001
Scopus-id: 2-s2.0-85118329024
| 6 | 7 |
| 14 | Metabolic syndrome in indigenous communities in Mexico: A descriptive and cross-sectional study | Coautor: Martínez-Hernández A., Mendoza-Caamal E.C., Barajas-Olmos F., Garciá-Ortiz H., et al. | 2020 | Bmc Public Health | WoS-id: 000521311600003
Scopus-id: 2-s2.0-85082025059
| 35 | 34 |
| 15 | A homozygous CEP57 c.915_925dupCAATGTTCAGC mutation in a patient with mosaic variegated aneuploidy syndrome with rhizomelic shortening in the upper and lower limbs and a narrow thorax | Coautor: Martínez-Hernández A., De la Torre-García O., Mar-Aldama R., Salgado-Sangri R., et al. | 2019 | EUROPEAN JOURNAL OF MEDICAL GENETICS | WoS-id: 000457638200008
Scopus-id: 2-s2.0-85049879950
| 8 | 7 |
| 16 | Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report | 1ᵉʳ autor: Martínez-Hernández A., Larrosa J., Barajas-Olmos F., García-Ortíz H., et al. | 2019 | BMC MEDICAL GENOMICS | WoS-id: 000468792300002
Scopus-id: 2-s2.0-85066442854
| 4 | 4 |
| 17 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls | Coautor: Martinez-Hernandez, Angelica, Flannick, Jason, Mercader, Josep M., Fuchsberger, Christian, et al. | 2019 | Nature | WoS-id: 000470149000041
Scopus-id: 2-s2.0-85066251977
| 221 | 220 |
| 18 | Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans | Coautor: Martínez-Hernández A., Contreras-Cubas C., García-Ortiz H., Velázquez-Cruz R., et al. | 2019 | SCIENTIFIC REPORTS | WoS-id: 000481999500019
Scopus-id: 2-s2.0-85071008674
| 12 | 15 |
| 19 | Association between APOE polymorphisms and lipid profile in Mexican Amerindian population | Coautor: Martinez-Hernandez A.G., Martínez-Magaña J.J., Genis-Mendoza A.D., Tovilla-Zarate C.A., et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000494745700020
Scopus-id: 2-s2.0-85073922350
| 14 | 19 |
| 20 | Variation in actionable pharmacogenetic markers in natives and mestizos from Mexico | Coautor: Martínez-Hernández A., Gonzalez-Covarrubias V., Morales-Franco M., Cruz-Correa O.F., et al. | 2019 | FRONTIERS IN PHARMACOLOGY | WoS-id: 000497523700001
Scopus-id: 2-s2.0-85074210789
| 16 | 16 |
| 21 | Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population | Coautor: Martínez-Hernández A., Salas-Martínez M.G., Saldaña-Alvarez Y., Cordova E.J., et al. | 2019 | PLOS ONE | WoS-id: 000533930800022
Scopus-id: 2-s2.0-85075803215
| 5 | 6 |
| 22 | Altered DNA methylation in liver and adipose tissues derived from individuals with obesity and type 2 diabetes | Coautor: Martínez-Hernández A., Barajas-Olmos F., Centeno-Cruz F., Zerrweck C., et al. | 2018 | BMC MEDICAL GENETICS | WoS-id: 000426095300001
Scopus-id: 2-s2.0-85042417139
| 34 | 36 |
| 23 | Deep multi-OMICs and multi-tissue characterization in a pre-and postprandial state in human volunteers: The GEMM family study research design | Coautor: Martínez-Hernández A., Bastarrachea R.A., Laviada-Molina H.A., Nava-Gonzalez E.J., et al. | 2018 | GENES | WoS-id: 000451636700017
Scopus-id: 2-s2.0-85056579145
| 8 | 10 |
| 24 | GSTT1 and GSTM1 null variants in mestizo and amerindian populations from Northwestern Mexico and a literature review | Coautor: Martínez-Hernández A., Palma-Cano L.E., Córdova E.J., Orozco L., et al. | 2017 | Genetics And Molecular Biology | WoS-id: 000416364000001
Scopus-id: 2-s2.0-85035749703
| 14 | 17 |
| 25 | Association of HMOX1 and NQO1 polymorphisms with metabolic syndrome components | 1ᵉʳ autor: Martínez-Hernández A., Córdova E.J., Rosillo-Salazar O., García-Ortíz H., et al. | 2015 | PLOS ONE | WoS-id: 000353887100019
Scopus-id: 2-s2.0-84929121316
| 23 | 30 |
| 26 | The NRF2-KEAP1 pathway is an early responsive gene network in arsenic exposed lymphoblastoid cells | 2ᵒ autor: Martínez-Hernández A., Córdova E.J., Uribe-Figueroa L., Centeno F., et al. | 2014 | PLOS ONE | WoS-id: 000330834400027
Scopus-id: 2-s2.0-84895739598
| 21 | 20 |
| 27 | HMOX1 promoter (GT)n polymorphism is associated with childhood-onset systemic lupus erythematosus but not with juvenile rheumatoid arthritis in a Mexican population | 2ᵒ autor: Martínez-Hernández A., Córdova E.J., Ramírez-Bello J., Velázquez-Cruz R., et al. | 2012 | CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | WoS-id: 000303905800026
Scopus-id: 2-s2.0-84863732055
| 11 | 11 |
ORCID's 