| 1 | Environmental and Genetic Risk Factors in Developmental Dysplasia of the Hip for Early Detection of the Affected Population | Coautor: Valdes-Flores M., Ramírez-Rosete J.A., Hurtado-Vazquez A., Miranda-Duarte A., et al. | 2024 | Diagnostics | WoS-id: 001219785500001
Scopus-id: 2-s2.0-85192738881
| 0 | 0 |
| 2 | Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease | Coautor: Valdés-Flores M., PerezGrovas-Saltijeral A., Ochoa-Morales A., Jara-Prado A., et al. | 2023 | EUROPEAN JOURNAL OF NEUROLOGY | WoS-id: 000895575900001
Scopus-id: 2-s2.0-85144034133
| 1 | 2 |
| 3 | Administration of Tamoxifen Can Regulate Changes in Gene Expression during the Acute Phase of Traumatic Spinal Cord Injury | Coautor: Valdés-Flores M., Cabrera-Aldana E.E., Balderas-Martínez Y.I., Velázquez-Cruz R., et al. | 2023 | Current Issues in Molecular Biology | WoS-id: 001073309500001
Scopus-id: 2-s2.0-85172155977
| 1 | 0 |
| 4 | Association of MTHFR rs1801133 and homocysteine with Legg?Calvé?Perthes disease in Mexican patients | Coautor: Valdés-Flores M., Buendía-Pazarán J.G., Hernández-Zamora E., Rodríguez-Olivas A.O., et al. | 2022 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000766563800001
Scopus-id: 2-s2.0-85126080971
| 4 | 5 |
| 5 | Association of Polymorphisms in Estrogen Receptor Genes (ESR1 and ESR2) with Osteoporosis and Fracture-Involvement of Comorbidities and Epistasis | Coautor: Valdés-Flores M., García-Rojas M.D., Palma-Cordero G., Martínez-Ramírez C.O., et al. | 2022 | DNA AND CELL BIOLOGY | WoS-id: 000771039200001
Scopus-id: 2-s2.0-85129632106
| 6 | 6 |
| 6 | A novel model to culture cells from giant cell tumor of bone using three-dimensional (3D) polycaprolactone scaffold | 2ᵒ autor: Valdes-Flores, Margarita, Estrada-Villasenor, Erendira, Meneses-Garcia, Abelardo, Silva-Bermudez, Phaedra, et al. | 2021 | ENGINEERING IN LIFE SCIENCES | WoS-id: 000667742700001
Scopus-id: 2-s2.0-85108806271
| 2 | 2 |
| 7 | circRNA Regulates Dopaminergic Synapse, MAPK, and Long-term Depression Pathways in Huntington Disease | Coautor: Valdes-Flores M., Marfil-Marin E., Santamaría-Olmedo M., PerezGrovas-Saltijeral A., et al. | 2021 | MOLECULAR NEUROBIOLOGY | WoS-id: 000692085400001
Scopus-id: 2-s2.0-85114100099
| 7 | 9 |
| 8 | Evidence of possible SARS-CoV-2 vertical transmission according to World Health Organization criteria in asymptomatic pregnant women | Coautor: Valdes-Flores M., Sevilla-Montoya R., Hidalgo-Bravo A., Estrada-Gutiérrez G., et al. | 2021 | ULTRASOUND IN OBSTETRICS & GYNECOLOGY | WoS-id: 000724388000012
Scopus-id: 2-s2.0-85122490161
| 15 | 14 |
| 9 | Single-nucleotide polymorphism rs10036727 in the SLIT3 gene is associated with osteoporosis at the femoral neck in older Mexican postmenopausal women | Coautor: Valdés-Flores M., Hidalgo-Bravo A., Hernández-Medrano C., Sevilla-Montoya R., et al. | 2020 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000556518900001
Scopus-id: 2-s2.0-85089178803
| 5 | 5 |
| 10 | COL1A1, CCDC170, and ESR1 single nucleotide polymorphisms associated with distal radius fracture in postmenopausal Mexican women | Coautor: Valdés-Flores M., Farias-Cisneros E., Hidalgo-Bravo A., Miranda-Duarte A., et al. | 2020 | Climacteric | Scopus-id: 2-s2.0-85068218094
| 0 | 6 |
| 11 | MicroRNA expression in relation with clinical evolution of osteosarcoma | Coautor: Valdés-Flores M., Monterde-Cruz L., Ramírez-Salazar E.G., Rico-Martínez G., et al. | 2020 | PATHOLOGY RESEARCH AND PRACTICE | Scopus-id: 2-s2.0-85086594410
| 0 | 7 |
| 12 | Association of RMND1/CCDC170?ESR1 single nucleotide polymorphisms with hip fracture and osteoporosis in postmenopausal women | Coautor: Valdés-Flores M., Hidalgo-Bravo A., Parra-Torres A.Y., Casas-Avila L., et al. | 2019 | Climacteric | WoS-id: 000458564000018
Scopus-id: 2-s2.0-85059684505
| 11 | 12 |
| 13 | Association of the Promoter Methylation and the rs12917 Polymorphism of MGMT with Formation of DNA Bulky Adducts and the Risk of Lung Cancer in Mexican Mestizo Population | Coautor: Valdes-Flores, Margarita, Martinez-Ramirez, Ollin Celeste, Perez-Morales, Rebeca, Castro-Hernandez, Clementina, et al. | 2019 | DNA AND CELL BIOLOGY | WoS-id: 000463614100004
Scopus-id: 2-s2.0-85063946553
| 7 | 7 |
| 14 | High risk of lumbar spine osteoporosis with the RANK rs3018362 polymorphism | Coautor: Valdés-Flores M., Casas-Avila L., Cruz-Arenas E., Ponce-de-León-Suárez V., et al. | 2019 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000469643700001
Scopus-id: 2-s2.0-85066901673
| 1 | 1 |
| 15 | Serum proteomic analysis reveals vitamin d-binding protein (Vdbp) as a potential biomarker for low bone mineral density in mexican postmenopausal women | Coautor: Valdes-Flores, Margarita, Martinez-Aguilar, Mayeli M., Aparicio-Bautista, Diana I., Ramirez-Salazar, Eric G., et al. | 2019 | Nutrients | WoS-id: 000506917800015
Scopus-id: 2-s2.0-85075361437
| 22 | 23 |
| 16 | Estimación del riesgo absoluto para fractura por fragilidad en mujeres mexicanas con menopausia temprana y menopausia natural | Coautor: Valdés-Flores M., Ramírez-Pérez E., Clark P., Barredo-Prieto B., et al. | 2019 | CIRUGIA Y CIRUJANOS | WoS-id: 000510022500003
Scopus-id: 2-s2.0-85066959430
| 2 | 2 |
| 17 | Association of the IL6 rs1800796, but not of the IL6 rs1800795, IL6R rs4845617 and rs2228145 polymorphisms with hip fracture in elderly Mexican women | 2ᵒ autor: Valdés-Flores M., Ponce de León-Suárez V., Miranda-Duarte A., Ramírez-Pérez E., et al. | 2018 | AGING CLINICAL AND EXPERIMENTAL RESEARCH | WoS-id: 000428851500015
Scopus-id: 2-s2.0-85020288994
| 4 | 4 |
| 18 | Two novel mutations in the GAN gene causing giant axonal neuropathy | Coautor: Valdes-Flores M., Normendez-Martínez M.I., Monterde-Cruz L., Martínez R., et al. | 2018 | WORLD JOURNAL OF PEDIATRICS | WoS-id: 000435711200014
Scopus-id: 2-s2.0-85048060768
| 13 | 13 |
| 19 | Serum miRNAs miR-140-3p and miR-23b-3p as potential biomarkers for osteoporosis and osteoporotic fracture in postmenopausal Mexican-Mestizo women | Coautor: Valdés-Flores M., Ramírez-Salazar E.G., Carrillo-Patiño S., Hidalgo-Bravo A., et al. | 2018 | Gene | WoS-id: 000448096300003
Scopus-id: 2-s2.0-85052662047
| 54 | 56 |
| 20 | Identification of drugs as regulators on the activity of Egr-1 promoter in human fibroblasts transduced with Ad Delta egr-1-Luc7 | Coautor: Valdes-Flores, Margarita, Martinez-Flores, Francisco, Sandoval, Hugo, Arce de la Vega, Elizabeth, et al. | 2018 | CIRUGIA Y CIRUJANOS | WoS-id: 000510017200004
| 0 | 0 |
| 21 | Circulating miR-215-5p and miR-642a-5p as potential biomarker for diagnosis of osteosarcoma in Mexican population | Coautor: Valdés-Flores M., Monterde-Cruz L., Ramírez-Salazar E.G., Rico-Martínez G., et al. | 2018 | HUMAN CELL | Scopus-id: 2-s2.0-85048543944
| 0 | 36 |
| 22 | identificación de fármacos reguladores de la actividad del promotor Egr-1 en fibroblastos humanos transducidos con Ad egr-1-Luc7 | Coautor: Valdes-Flores M., Martínez-Flores F., Sandoval H., Arce de la Vega E., et al. | 2018 | CIRUGIA Y CIRUJANOS | Scopus-id: 2-s2.0-85054052015
| 0 | 0 |
| 23 | Dermochondrocorneal dystrophy (Francois syndrome) in a Mexican patient and literature review | Coautor: Valdes-Flores M., Hidalgo-Bravo A., Acosta-Nieto M.L., Normendez-Martinez M.I., et al. | 2016 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000368811500021
Scopus-id: 2-s2.0-84956962313
| 1 | 3 |
| 24 | Association of the COL1A1 gene polymorphisms in Mexican postmenopausal women with fracture or with low bone mineral density at the hip | Coautor: Valdés-Flores M., Falcón-Ramírez E., Hidalgo-Bravo A., Barredo-Prieto B.A., et al. | 2016 | AGING CLINICAL AND EXPERIMENTAL RESEARCH | WoS-id: 000376683700027
Scopus-id: 2-s2.0-84944691491
| 4 | 5 |
| 25 | Clinical and molecular analysis in a series of Mexican patients with clinical diagnosis of Fibrodysplasia Ossificans Progressiva (FOP) | Coautor: Valdes-Flores M., Flores-Gallegos L., Hidalgo-Bravo A., Casas-Avila L., et al. | 2016 | INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | Scopus-id: 2-s2.0-84957541515
| 0 | 1 |
| 26 | WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: Findings of a pathway-based high-density single nucleotide screening | Coautor: Valdés-Flores M., Velázquez-Cruz R., García-Ortiz H., Castillejos-López M., et al. | 2014 | AGE | WoS-id: 000342142300039
Scopus-id: 2-s2.0-84905378784
| 29 | 30 |
| 27 | Aspectos genet´icos de la osteoporosis | 1ᵉʳ autor: Valdés-Flores M., Casas-Ávila L., Falcón-Ramírez E., Ponce-de-León-Suárez V. | 2012 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000309196300011
Scopus-id: 2-s2.0-84867144612
| 0 | 0 |
| 28 | Association of interleukin-6 gene Polymorphisms with bone mineral density in Mexican women | Coautor: Valdés-Flores M., Magana, JJ, Gómez R., Cisneros B., et al. | 2008 | Archives Of Medical Research | WoS-id: 000258282100011
Scopus-id: 2-s2.0-47749104489
| 19 | 21 |
| 29 | Molecular analysis of CAG repeat in Mexican patients with spinocerebellar ataxia type 2 [Análisis molecular de los repetidos CAG en pacientes mexicanos con ataxia espinocerebelosa tipo 2] | Coautor: Valdés-Flores M., Magaña J.J., Vergara M.D., Sierra-Martínez M., et al. | 2008 | GACETA MEDICA DE MEXICO | WoS-id: 000261051000006
Scopus-id: 2-s2.0-60749129312
| 6 | 7 |
| 30 | Molecular study of a family with gene PMP22 duplication and large phenotypic variability [Estudio molecular de una familia con duplicación del gen PMP22 y gran variabilidad fenotípica] | Coautor: Valdés-Flores M., De La Luz Arenas-Sordo M., Hernández-Zamora E., Gómez-Ortega R., et al. | 2008 | CIRUGIA Y CIRUJANOS | Scopus-id: 2-s2.0-77956277675
| 0 | 0 |
| 31 | Association of the estrogen receptor a gene polymorphisms with osteoporosis in the Mexican population | Coautor: Valdés-Flores M., Gómez A.B., Magaña J.J., Cisneros B., et al. | 2007 | CLINICAL GENETICS | WoS-id: 000250915800015
Scopus-id: 2-s2.0-36248940799
| 22 | 25 |
| 32 | p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly | Coautor: Valdés-Flores M., Berdón-Zapata V., Granillo-Álvarez M., García-Ortiz J.E., et al. | 2004 | J ORTHOP RES | WoS-id: 000187884300001
Scopus-id: 2-s2.0-17144447237
| 15 | 19 |
| 33 | A novel association in a family with oculo-auriculo-vertebral spectrum and X-linked ichthyosis [3] | Coautor: Valdes-Flores M., Rivera-Vega M.R., Dueñas E., Jimenez-Vaca A.L., et al. | 2003 | PEDIATRIC DERMATOLOGY | Scopus-id: 2-s2.0-0037361367
| 0 | 3 |
| 34 | Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier | Coautor: Valdes-Flores M., Cuevas-Covarrubias S.A., Jiménez-Vaca A.L., González-Huerta L.M., et al. | 2002 | JOURNAL OF INVESTIGATIVE DERMATOLOGY | WoS-id: 000179072800030
Scopus-id: 2-s2.0-0036431398
| 8 | 14 |
| 35 | Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis | 1ᵉʳ autor: Valdes-Flores M., Kofman-Alfaro S.H., Jimenez Vaca A.L., Cuevas-Covarrubias S.A. | 2001 | JOURNAL OF INVESTIGATIVE DERMATOLOGY | WoS-id: 000167222200015
Scopus-id: 2-s2.0-0035092927
| 15 | 18 |
| 36 | Characterization of a novel point mutation (Arg432His) in X-linked ichthyosis [1] | 1ᵉʳ autor: Valdes-Flores M., Jimenez Vaca A.L., Kofman-Alfaro S.H., Cuevas-Covarrubias S.A. | 2001 | ACTA DERM-VENEREOL | WoS-id: 000168891600015
Scopus-id: 2-s2.0-0035010669
| 5 | 5 |
| 37 | Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis | 1ᵉʳ autor: Valdes-Flores M., Kofman-Alfaro S.H., Jimenez-Vaca A.L., Cuevas-Covarrubias S.A. | 2001 | AM J MED GENET | WoS-id: 000170001400005
Scopus-id: 2-s2.0-0035425950
| 16 | 21 |
| 38 | Maternal transmission of the 3 bp deletion within exon 7 of the STS gene in steroid sulfatase deficiency [5] | 1ᵉʳ autor: Valdes-Flores M., Jimenez Vaca A.L., Rivera-Vega M.R., Kofman-Alfaro S.H., et al. | 2001 | JOURNAL OF INVESTIGATIVE DERMATOLOGY | WoS-id: 000171847500031
Scopus-id: 2-s2.0-0034778477
| 3 | 3 |
| 39 | Unusual clinical presentation in two cases of multiple sulfatase deficiency | Coautor: Valdes-Flores M., Blanco-Aguirre M.E., Kofman-Alfaro S.H., Rivera-Vega M.R., et al. | 2001 | PEDIATRIC DERMATOLOGY | WoS-id: 000172198200005
Scopus-id: 2-s2.0-0035171732
| 19 | 20 |
| 40 | Deletion pattern of the STS gene in X-linked ichthyosis in a Mexican population | 2ᵒ autor: Valdes-Flores M., Jimenez Vaca A.L., Rivera-Vega M.D.R., González-Huerta L.M., et al. | 2001 | MOLECULAR MEDICINE | Scopus-id: 2-s2.0-0035717589
| 0 | 28 |
| 41 | A novel partial deletion of exons 2-10 of the STS gene in recessive X- linked ichthyosis | 1ᵉʳ autor: Valdes-Flores M., Kofman-Alfaro S.H., Jimenez Vaca A.L., Cuevas-Covarrubias S.A. | 2000 | JOURNAL OF INVESTIGATIVE DERMATOLOGY | WoS-id: 000086187800028
Scopus-id: 2-s2.0-0034146404
| 21 | 21 |
| 42 | Steroid sulfatase activity in leukocytes: A comparative study in 45,X;46,Xi(Xq) and carriers of steroid sulfatase deficiency | 2ᵒ autor: Valdés-Flores M., Miranda-Duarte A., Miranda-Zamora R., Díaz-Zagoya J.C., et al. | 1999 | BIOCHEM MOL BIOL INT | WoS-id: 000079024100014
Scopus-id: 2-s2.0-0344177609
| 5 | 5 |
| 43 | Most 'sporadic' cases of X-linked ichthyosis are not de novo mutations | 2ᵒ autor: Valdes-Flores M., Cuevas-Covarrubias S.A., Orozco E.O., Díaz-Zagoya J.C., et al. | 1999 | ACTA DERM-VENEREOL | WoS-id: 000079702800012
Scopus-id: 2-s2.0-0032968580
| 6 | 9 |
| 44 | Oral-facial-digital (OFD) syndrome with associated features: A new syndrome or genetic heterogeneity and variability? | 2ᵒ autor: Valdés Flores M., Morân-Barroso V., Garcia-Cavazos R., Kofman-Alfaro S., et al. | 1998 | CLINICAL DYSMORPHOLOGY | WoS-id: 000071513300010
Scopus-id: 2-s2.0-15644367437
| 14 | 17 |
| 45 | Are atopy and palm-sole hyperlinearity clinical tools in the differential diagnosis between ichthyosis vulgaris and X-linked ichthyosis? [1] | 2ᵒ autor: Valdés-Flores M., Cuevas-Covarrubias S.A., Orozco E.O., Díaz-Zagoya J.C., et al. | 1998 | JOURNAL OF DERMATOLOGY | Scopus-id: 2-s2.0-0031688594
| 0 | 3 |
ID's SCOPUS 