| 1 | Viral Hepatitis in Pregnant Mexican Women: Its Impact in Mother?Child Binomial Health and the Strategies for Its Eradication | Coautor: Cervantes A., García-Romero C.S., Guzmán C., Martínez-Ibarra A., et al. | 2024 | Pathogens | WoS-id: 001304704100001
Scopus-id: 2-s2.0-85202475517
| 1 | 1 |
| 2 | Which side of the coin are you on regarding possible postnatal oogenesis? | Coautor: Cervantes A., Morales-Sánchez E., Campuzano-Caballero J.C., Martínez-Ibarra A., et al. | 2024 | Archives Of Medical Research | WoS-id: 001308806700001
Scopus-id: 2-s2.0-85202912374
| 0 | 0 |
| 3 | Body mass index implications in intrahepatic cholestasis of pregnancy and placental histopathological alterations | Coautor: Cervantes-Peredo, Alicia, Valdovinos-Bello, Violeta, Garcia-Romero, Carmen Selene, Garcia-Gomez, Elizabeth, et al. | 2023 | Annals Of Hepatology | WoS-id: 000899935000002
Scopus-id: 2-s2.0-85143530726
| 8 | 9 |
| 4 | Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event | 2ᵒ autor: Cervantes, Alicia, Fabiola Moran-Barroso, Veronica, del Refugio Rivera-Vega, Maria, del Castillo-Moreno, Adriana, et al. | 2021 | Molecular Genetics & Genomic Medicine | WoS-id: 000674868400001
Scopus-id: 2-s2.0-85110692137
| 2 | 2 |
| 5 | X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient | Coautor: Cervantes, Alicia, Noriega-Juarez, Miguel A., Garcia-Delgado, Constanza, Villasenor-Dominguez, America, et al. | 2020 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | WoS-id: 000551909000008
Scopus-id: 2-s2.0-85066485106
| 1 | 1 |
| 6 | High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia | Coautor: Cervantes A., García-Delgado C., Noriega-Juárez M., Abad-Flores J., et al. | 2020 | DERMATOLOGICA SINICA | WoS-id: 000601214900006
Scopus-id: 2-s2.0-85091512458
| 0 | 0 |
| 7 | Displasia ectodérmica hipohidrótica ligada al cromosoma X de novo por variante recurrente en un paciente mexicano | Coautor: Cervantes A., Noriega-Juárez M.A., García-Delgado C., Villaseñor-Domínguez A., et al. | 2020 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | WoS-id: 000551909000008
Scopus-id: 2-s2.0-85088622686
| 2 | 3 |
| 8 | Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature | Coautor: Cervantes A., Gómez-Laguna L., Martínez-Herrera A., Reyes-de la Rosa A.D.P., et al. | 2018 | OPHTHALMIC GENETICS | WoS-id: 000428520500011
Scopus-id: 2-s2.0-85029587680
| 6 | 7 |
| 9 | Monosomy 9p24 in two non-related patients as result of a translocation (2;9) | Coautor: Cervantes, C. Alicia, Leon-Carlos, Nayla Y., Garcia-Delgado, Constanza, Morales-Jimenez, Ariadna B., et al. | 2018 | ARCHIVOS ARGENTINOS DE PEDIATRIA | WoS-id: 000439814600026
Scopus-id: 2-s2.0-85051330739
| 1 | 2 |
| 10 | Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia | Coautor: Cervantes, A., Monroy-Jaramillo, N., Abad-Flores, J. D., Garcia-Delgado, C., et al. | 2017 | JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY | WoS-id: 000406075900010
Scopus-id: 2-s2.0-85013498119
| 8 | 8 |
| 11 | Congenital hypertrichosis universalis in Mexican female twins | 1ᵉʳ autor: Cervantes, Alicia, Garcia-Delgado, Constanza, Fernandez-Ramirez, Fernando, Valencia-Herrera, Adriana, et al. | 2016 | INTERNATIONAL JOURNAL OF DERMATOLOGY | WoS-id: 000368089600007
Scopus-id: 2-s2.0-84953835011
| 2 | 2 |
| 12 | Cytogenetic Profile in 1,921 Cases of Trisomy 21 Syndrome | Coautor: Cervantes A., Flores-Ramírez F., Palacios-Guerrero C., García-Delgado C., et al. | 2015 | Archives Of Medical Research | WoS-id: 000361782700007
Scopus-id: 2-s2.0-84941278041
| 21 | 29 |
| 13 | Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): Further delineation of the syndromes | 1ᵉʳ autor: Cervantes A., García-Delgado C., Fernández-Ramírez F., Galaz-Montoya C., et al. | 2014 | BMC MEDICAL GENOMICS | WoS-id: 000342094500001
Scopus-id: 2-s2.0-84908160780
| 3 | 4 |
| 14 | 19q13.11 microdeletion concomitant with ins (2;19)(p25.3;q13.1q13.4)dn in a boy: Potential role of UBA2 in the associated phenotype | Coautor: Cervantes A., Venegas-Vega C., Nieto-Martínez K., Martínez-Herrera A., et al. | 2014 | MOLECULAR CYTOGENETICS | WoS-id: 000347350100001
Scopus-id: 2-s2.0-84989311431
| 15 | 15 |
| 15 | Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012 | Coautor: Cervantes-Peredo A., Galaz-Montoya C.I., García-Delgado C., García-Morales L., et al. | 2014 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84934755757
| 0 | 1 |
| 16 | Prevalence of mosaicism for trisomy 21 and cytogenetic variant analysis in patients with clinical diagnosis of down syndrome: A 24-year review (1986-2010) at the servicio de genética, hospital general de México "Dr. Eduardo Liceaga" | Coautor: Peredo A.B.C., Garduño-Zarazúa L.M., Giammatteo Alois L., Kofman-Epstein S. | 2013 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84877098273
| 0 | 6 |
| 17 | Importance of the diagnosis of protein connexin 26 mutations in the integral management of non-syndromic congenital deafness | Coautor: Cervantes-Peredo A., Mendelsberg-Fishbein P., Márquez-Ávila C.S., García-Delgado C., et al. | 2013 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84877148716
| 0 | 3 |
| 18 | Clinical profile of a patient cohort with Beckwith-Wiedemann syndrome treated at the hospital Infantil de México Federico Gómez (2007 to 2012) | Coautor: Cervantes-Peredo A., Moreno-Salgado R., García-Delgado C., García-Morales L., et al. | 2013 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84877156230
| 0 | 4 |
| 19 | Persistence of decidual NK cells and KIR genotypes in healthy pregnant and preeclamptic women: A case-control study in the third trimester of gestation | Coautor: Cervantes-Peredo A., Sánchez-Rodríguez E.N., Nava-Salazar S., Mendoza-Rodríguez C.A., et al. | 2011 | REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY | WoS-id: 000287155400001
Scopus-id: 2-s2.0-78651482474
| 23 | 27 |
| 20 | A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient | Coautor: Cervantes-Peredo, A, Garcia-Delgado, C, Bahena-Martinez, E, Aparicio-Onofre, A, et al. | 2010 | GENET COUNSEL | WoS-id: 000282665700006
Scopus-id: 2-s2.0-77957745560
| 4 | 3 |
| 21 | CLINICAL DELINEATION OF A PATIENT WITH TRISOMY 1q32-qter AND MONOSOMY 5p RESULTING FROM A FAMILIAL TRANSLOCATION 1;5 | Coautor: Peredo, ABC, Ramirez, FF, Gonzalez, MA, Delgado, CG, et al. | 2010 | GENET COUNSEL | WoS-id: 000285490900002
Scopus-id: 2-s2.0-78650753994
| 1 | 0 |
| 22 | Mix Gonadal Dysgenesis Associated with Ring Y Chromosome Mosaics in a Phenotypic Male | Coautor: Cervantes, A, Lopez-Valdes, JA, Nieto, K, Najera, N, et al. | 2009 | SEXUAL DEVELOPMENT | WoS-id: 000269789400001
Scopus-id: 2-s2.0-70349272265
| 4 | 7 |
| 23 | Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype | Coautor: Cervantes A., Zafra De La Rosa G., Venegas-Vega C.A., Monroy N., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230288400006
Scopus-id: 2-s2.0-22044437226
| 9 | 9 |
| 24 | DNA methylation: An epigenetic process of medical importance [Metilación del ADN: Un fenómeno epigenético de importancia Médica] | Coautor: Cervantes A., Rodríguez-Dorantes M., Téllez-Ascencio N., Cerbón M.A., et al. | 2004 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000221071600010
Scopus-id: 2-s2.0-2342621426
| 22 | 23 |
| 25 | Sensitivity and specificity of endoscopy for the detection of velocardiofacial syndrome [Sensibilidad y especificidad de la endoscopia para la detección del síndrome velocardiofacial] | Coautor: Cervantes A., Ysunza A., Pamplona M., Silva-Rojas A., et al. | 2004 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000224764000006
Scopus-id: 2-s2.0-7444246844
| 5 | 5 |
| 26 | Microsatellite analysis in Turner syndrome: Parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes | Coautor: Cervantes A., Monroy N., López M., García-Cruz D., et al. | 2002 | AM J MED GENET | WoS-id: 000173116600001
Scopus-id: 2-s2.0-0037154032
| 16 | 22 |
| 27 | ¿What do you know about... The human genome project? [¿Qué sabe usted acerca... del Proyecto del genoma humano?] | 2ᵒ autor y autor de correspondencia: Cervantes Peredo Q.F.B.A., López López M. | 2002 | Revista Mexicana de Ciencias Farmaceuticas | Scopus-id: 2-s2.0-0036817394
| 0 | 0 |
| 28 | PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype | 1ᵉʳ autor: Cervantes A., Guevara-Yáñez R., López M., Monroy N., et al. | 2001 | CLINICAL GENETICS | WoS-id: 000172475000014
Scopus-id: 2-s2.0-0035184239
| 6 | 10 |
| 29 | Pharmacy, pharmacogenetics, pharmacogenomics? [¿Farmacia, farmacogenética, farmacogenómica?] | 1ᵉʳ autor: Cervantes Peredo A., López López M., Sandoval H., Del Muro R. | 2001 | Revista Mexicana de Ciencias Farmaceuticas | Scopus-id: 2-s2.0-0035670502
| 0 | 0 |
| 30 | A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism | Coautor: Cervantes A., Canto P., De La Chesnaye E., López M., et al. | 2000 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | WoS-id: 000088387300030
Scopus-id: 2-s2.0-0034351406
| 37 | 46 |
| 31 | What do you know about...Hereditary monogenic diseases? [Que sabe usted acerca de...Las enfermedades hereditarias monogenicas?] | 2ᵒ autor y autor de correspondencia: Cervantes Peredo Q.F.B.A., Lopez Lopez M.C.M. | 1999 | Revista Mexicana de Ciencias Farmaceuticas | Scopus-id: 2-s2.0-0032770672
| 0 | 0 |
| 32 | Frequency of Y chromosomal material in Mexican patients with Ullrich- Turner syndrome | Coautor: Cervantes A., Lopez M., Canto P., Aguinaga M., et al. | 1998 | AM J MED GENET | WoS-id: 000072258700003
Scopus-id: 2-s2.0-0032485202
| 36 | 39 |
| 33 | Cytogenetic findings in 303 Mexican patients with de novo acute myeloblastic leukemia | Coautor: Cervantes-Peredo A., Arana-Trejo R.M., Gomez-Morales E., Rubio-Borja Ma.E., et al. | 1997 | Archives Of Medical Research | WoS-id: A1997XE08000009
Scopus-id: 2-s2.0-0030977435
| 6 | 6 |
| 34 | Interferon in the suppression of Philadelphia chromosome of chronic myeloid leukemia [El interferón en la erradicación del cromosoma Filadelfia de la leucemia mieloide crónica] | Coautor: Cervantes-Peredo A., Arana-Trejo R.M., Ovilla-Martínez R., Gómez-Morales E., et al. | 1997 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1997XT74000007
Scopus-id: 2-s2.0-3242842358
| 0 | 0 |
| 35 | Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes | Coautor: Cervantes A., Torres L., López M., Méndez J.P., et al. | 1996 | AM J MED GENET | WoS-id: A1996UP71300006
Scopus-id: 2-s2.0-0029937146
| 19 | 20 |
| 36 | Genetic disorders of the adult age [Padecimientos genéticos de la edad adulta.] | Coautor: Cervantes A., Salamanca-Gómez F., Armendares S., Alonso-Vilatela M.E., et al. | 1996 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0030185771
| 0 | 0 |
| 37 | Advances in the genetic process of human sex differentiation [Avances en el conocimiento del proceso genético en la diferenciación sexual del humano] | 2ᵒ autor: Cervantes-Peredo A., López-López M., Kofman-Alfaro S. | 1996 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1996UX37600007
Scopus-id: 2-s2.0-3743111616
| 1 | 1 |
| 38 | Chromosomic alterations induced by domestic dust in the city of Mexicali, Baja California [ALTERACIONES CROMOSOMICAS INDUCIDAS POR POLVO CASERO DE LA CIUDAD DE MEXICALI, BAJA CALIFORNIA] | Coautor: Cervantes Peredo A., Alfaro Moreno E., Arenas Huertero F., Taja Chayeb L.G., et al. | 1995 | Revista Del Instituto Nacional De Cancerología | Scopus-id: 2-s2.0-0029550290
| 0 | 0 |
| 39 | Cytogenetic study of 22 adults and 3 children with acute lymphoblastic leukemia [Estudio citogenético en 22 adultos y tres niños con leucemia linfoblástica aguda.] | 2ᵒ autor: Cervantes-Peredo A., Arana-Trejo R.M., Rozen E., Kassack J.J., et al. | 1993 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1993KT53800005
Scopus-id: 2-s2.0-0002447913
| 6 | 6 |
| 40 | 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.] | Coautor: Cervantes Peredo A., López López M., Torres Maldonado L.C., Pablo Méndez J., et al. | 1993 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1993LR58600004
Scopus-id: 2-s2.0-0027600993
| 2 | 2 |
| 41 | Familial Yqs chromosome in 4 generations [Yqs familiar en cuatro generaciones.] | 1ᵉʳ autor: Cervantes-Peredo A., Kofman-Alfaro S. | 1989 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0024839093
| 0 | 1 |
ID's SCOPUS 