1 | Estudio cromosómico de 303 pérdidas gestacionales en México | Coautor: Torres L., Garduño-Zarazúa L.M., Mayén D.G., Meléndez-Hernández R., et al. | 2024 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-85191736508
| 0 | 0 |
2 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Torres, Leda, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001 Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
3 | Fanconi anemia, Part 2. Methodological strategy for molecular diagnosis in patients with Fanconi anemia | 1ᵉʳ autor: Torres, Leda, Juarez, Ulises, Reyes, Pedro, Frias, Sara | 2023 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000951351000005 Scopus-id: 2-s2.0-85150722120
| 0 | 0 |
4 | A Boolean network model of the double-strand break repair pathway choice | Coautor: Torres, Leda, Ayala-Zambrano, Cecilia, Yuste, Mariana, Frias, Sara, et al. | 2023 | JOURNAL OF THEORETICAL BIOLOGY | WoS-id: 001068786200001 Scopus-id: 2-s2.0-85169622136
| 2 | 2 |
5 | Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG | Coautor: Torres L., Reyes P., García-De Teresa B., Juárez U., et al. | 2022 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000971202400001 Scopus-id: 2-s2.0-85124879348
| 7 | 7 |
6 | MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia | Coautor: Torres L., Rodríguez A., Zhang K., Färkkilä A., et al. | 2021 | Cell Stem Cell | WoS-id: 000606536600009 Scopus-id: 2-s2.0-85092635441
| 35 | 37 |
7 | Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes | Coautor: Torres, Leda, Barrientos-Rios, Rehotbevely, Frias, Sara, Velazquez-Aragon, Jose A., et al. | 2019 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000461972100001 Scopus-id: 2-s2.0-85063099458
| 4 | 5 |
8 | WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways | Coautor: Torres L., Rodríguez A., Jesús Naveja J., De Teresa B.G., et al. | 2019 | Frontiers in Genetics | WoS-id: 000467461500003 Scopus-id: 2-s2.0-85067855840
| 5 | 5 |
9 | FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México | Coautor: Torres L., García-de Teresa B., Frias S., Molina B., et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000476745400049 Scopus-id: 2-s2.0-85067281483
| 6 | 6 |
10 | Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics | Coautor: Torres L., Yokoyama E., Del Castillo V., Sánchez S., et al. | 2018 | MOLECULAR CYTOGENETICS | WoS-id: 000431897500002 Scopus-id: 2-s2.0-85046671603
| 5 | 6 |
11 | ROLE OF KLOTHO RS9536282 GENE POLYMORPHISM ON BMD IN MEXICAN CHILDREN AND ADOLESCENT WITH TURNER SYNDROME | 2ᵒ autor: Torres-Maldonado, L. T. M., Altamirano-Bustamante, N. A. B., Banrrientos-Rios, R. B. R., Altamirano-Bustamante, M. A. B., et al. | 2018 | OSTEOPOROSIS INTERNATIONAL | WoS-id: 000440102404174
| 0 | 0 |
12 | In Search of Candidate Genes Genotype Phenotype Correlation: Role of Klotho Polymorphisms and Vitamin D Receptor in Bone Mineral Density in Mexican Children and Adolescents with Turner Syndrome | Coautor: Torres, Leda, Leon, Adareli, Rios, Rehotbevely, Vazquez, Sara, et al. | 2018 | HORMONE RESEARCH IN PAEDIATRICS | WoS-id: 000453593700002
| 0 | 0 |
13 | Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells | Coautor: Torres L., Molina B., Marchetti F., Gómez L., et al. | 2015 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000356426200004 Scopus-id: 2-s2.0-84931043203
| 6 | 6 |
14 | Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process | 2ᵒ autor: Torres L., Rodríguez A., Juárez U., Sosa D., et al. | 2015 | THEORETICAL BIOLOGY AND MEDICAL MODELLING | WoS-id: 000361668200001 Scopus-id: 2-s2.0-84941771494
| 13 | 14 |
15 | A Boolean network model of human gonadal sex determination | Coautor: Torres L., Ríos O., Frias S., Rodríguez A., et al. | 2015 | THEORETICAL BIOLOGY AND MEDICAL MODELLING | WoS-id: 000364754700001 Scopus-id: 2-s2.0-84960333621
| 33 | 34 |
16 | External ear microRNA expression profiles during mouse development | 1ᵉʳ autor: Torres L., Juárez U., García L., Miranda-Ríos J., et al. | 2015 | INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY | WoS-id: 000372858700011 Scopus-id: 2-s2.0-84961298567
| 12 | 12 |
17 | Interstitial Deletion of 2q24.2: Further Delineation of an Emerging Syndrome Associated With Intellectual Disability, Severe Hypotonia and Moderate Intrauterine Growth Restriction | Coautor: Torres L., Yokoyama E., Villarroel C.E., Del Castillo V., et al. | 2014 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000331978700038 Scopus-id: 2-s2.0-84894226111
| 1 | 1 |
18 | A Boolean network model of the FA/BRCA pathway | Coautor: Torres, L, Rodriguez, A, Sosa, D, Molina, B, et al. | 2012 | Bioinformatics | WoS-id: 000301972900015 Scopus-id: 2-s2.0-84859054645
| 34 | 37 |
19 | Disturbed Expression of Sox9 in Pre-Sertoli Cells Underlies Sex-Reversal in Mice B6.Ytir1 | 2ᵒ autor: Torres-Maldonado L., Moreno-Mendoza N., Chimal-Monroy J., Harley V., et al. | 2004 | BIOLOGY OF REPRODUCTION | WoS-id: 000187572500016 Scopus-id: 2-s2.0-0346093954
| 12 | 13 |
20 | Expression profiles of Dax1, Dmrt1, and Sox9 during temperature sex determination in gonads of the sea turtle Lepidochelys olivacea | 1ᵉʳ autor: Torres Maldonado L.C., Landa Piedra A., Moreno Mendoza N., Marmolejo Valencia A., et al. | 2003 | GENERAL AND COMPARATIVE ENDOCRINOLOGY | WoS-id: 000179284400003 Scopus-id: 2-s2.0-0037210301
| 88 | 91 |
21 | Timing of SOX9 downregulation and female sex determination in gonads of the sea turtle Lepidochelys olivacea | 1ᵉʳ autor: Torres-Maldonado L., Moreno-Mendoza N., Landa A., Merchant-Larios H. | 2001 | J EXP ZOOL | WoS-id: 000170899500008 Scopus-id: 2-s2.0-0035883835
| 19 | 22 |
22 | An atypical contiguous gene syndrome: Molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis | 2ᵒ autor: Torres L., Maya-Nuñez G., Ulloa-Aguirre A., Zenteno J.C., et al. | 1999 | CLINICAL ENDOCRINOLOGY | WoS-id: 000078992700004 Scopus-id: 2-s2.0-0033017287
| 13 | 19 |
23 | Scant XYqh- testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh- patient | Coautor: Torres L., Méndez J.P., Canto P., López M., et al. | 1999 | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY | WoS-id: 000083662300013 Scopus-id: 2-s2.0-0345061676
| 4 | 4 |
24 | Frequency of Y chromosomal material in Mexican patients with Ullrich- Turner syndrome | Coautor: Torres L., Lopez M., Canto P., Aguinaga M., et al. | 1998 | AM J MED GENET | WoS-id: 000072258700003 Scopus-id: 2-s2.0-0032485202
| 36 | 39 |
25 | Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes | 1ᵉʳ autor: Torres L., López M., Méndez J.P., Canto P., et al. | 1996 | AM J MED GENET | WoS-id: A1996UP71300006 Scopus-id: 2-s2.0-0029937146
| 19 | 20 |
26 | SRY alone can induce normal male sexual differentiation | 2ᵒ autor: Torres L., Lopez M., Mendez J.P., Cervantes A., et al. | 1995 | AM J MED GENET | WoS-id: A1995QH88300020 Scopus-id: 2-s2.0-0028876671
| 12 | 15 |
27 | Clinical traits and molecular findings in 46,XX males | 2ᵒ autor: Torres L., López M., Méndez J.P., Cervantes A., et al. | 1995 | CLINICAL GENETICS | WoS-id: A1995RK65800006 Scopus-id: 2-s2.0-0029038901
| 28 | 32 |
28 | Molecular detection of chromosome Y DNA sequences in patients with Turner's syndrome [Detección molecular de secuencias de ADN derivadas del cromosoma Y en pacientes con síndrome de Turner.] | 2ᵒ autor: Torres Maldonado L.C., López López M., Pablo Méndez J., Cervantes Peredo A., et al. | 1993 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1993LR58600004 Scopus-id: 2-s2.0-0027600993
| 2 | 2 |
29 | An update of molecular genetics in medicine [Actualidades de la genética molecular en medicina.] | Coautor: Torres Maldonado L.C., Salamanca Gómez F., Carnevale A., Kofman-Alfaro S., et al. | 1993 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0027628766
| 0 | 1 |