| 1 | Establishment of induced pluripotent stem cell lines derived from Parkinson's disease Mexican patients: A sporadic (UNAMi002-A) and a familial (UNAMi003-A) case carrying a mutation in PINK1 | Coautor: Monroy-Jaramillo N., Flores-Ponce X., López-Ornelas A., Escobedo-Avila I., et al. | 2024 | STEM CELL RESEARCH | WoS-id: 001186923700001
Scopus-id: 2-s2.0-85185275101
| 0 | 0 |
| 2 | Longitudinal Changes in Mitochondrial DNA Copy Number and Telomere Length in Patients with Parkinson?s Disease | Coautor: Monroy-Jaramillo N., Ortega-Vázquez A., Sánchez-Badajos S., Ramírez-García M.Á., et al. | 2023 | GENES | WoS-id: 001099286300001
Scopus-id: 2-s2.0-85175279429
| 2 | 4 |
| 3 | Relationship between APOE, PER2, PER3 and OX2R Genetic Variants and Neuropsychiatric Symptoms in Patients with Alzheimer?s Disease | Coautor: Monroy-Jaramillo N., Lozano-Tovar S., Rodríguez-Agudelo Y., Dávila-Ortiz de Montellano D.J., et al. | 2023 | INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH | Scopus-id: 2-s2.0-85149793827
| 0 | 4 |
| 4 | The role of alcohol intake in the pharmacogenetics of treatment with clozapine | 1ᵉʳ autor: Monroy-Jaramillo N., Martínez-Magaña J.J., Pérez-Aldana B.E., Ortega-Vázquez A., et al. | 2022 | Pharmacogenomics | WoS-id: 000771718100001
Scopus-id: 2-s2.0-85128396262
| 3 | 3 |
| 5 | Clozapine Long-Term Treatment Might Reduce Epigenetic Age Through Hypomethylation of Longevity Regulatory Pathways Genes | Coautor: Monroy-Jaramillo N., Pérez-Aldana B.E., Martínez-Magaña J.J., Mayén-Lobo Y.G., et al. | 2022 | Frontiers in Psychiatry | WoS-id: 000806123100001
Scopus-id: 2-s2.0-85131601297
| 2 | 2 |
| 6 | Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia | Coautor: Monroy-Jaramillo N., Fricke-Galindo I., Pérez-Aldana B.E., Macías-Kauffer L.R., et al. | 2022 | Archives Of Medical Research | WoS-id: 000880002700006
Scopus-id: 2-s2.0-85127327227
| 2 | 2 |
| 7 | Generation of a human induced pluripotent stem cell line (UNAMi001-A) from a Mexican patient with sporadic Parkinson's disease | Coautor: Monroy-Jaramillo, Nancy, Flores-Ponce, Xochitl, Lopez-Ornelas, Adolfo, Escobedo-Avila, Itzel, et al. | 2022 | STEM CELL RESEARCH | WoS-id: 000933957000007
Scopus-id: 2-s2.0-85143645518
| 0 | 0 |
| 8 | Alcohol intake potentiates clozapine adverse effects associated to CYP1A2*1C in patients with refractory psychosis | Coautor: Monroy-Jaramillo N., Ortega-Vázquez A., Mayen-Lobo Y.G., Dávila-Ortiz de Montellano D.J., et al. | 2021 | DRUG DEVELOPMENT RESEARCH | WoS-id: 000599520400001
Scopus-id: 2-s2.0-85097666570
| 5 | 5 |
| 9 | Candidate pharmacological treatments for substance use disorder and suicide identified by gene co-expression network-based drug repositioning | Coautor: Monroy-Jaramillo, Nancy, Cabrera-Mendoza, Brenda, Jaime Martinez-Magana, Jose, Delia Genis-Mendoza, Alma, et al. | 2021 | AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | WoS-id: 000604970900001
Scopus-id: 2-s2.0-85099037015
| 5 | 5 |
| 10 | Working Memory Impairment as an Endophenotypic Marker in Patients with Schizophrenia: Failures in Encoding or Maintenance? | 2ᵒ autor: Monroy-Jaramillo, Nancy, Elisa Rodriguez-Martinez, Ana, Rodriguez-Agudelo, Yaneth, Solis-Vivanco, Rodolfo | 2021 | Neuropsychobiology | WoS-id: 000619098700001
Scopus-id: 2-s2.0-85100901461
| 2 | 1 |
| 11 | Relevance of NR1I2 variants on carbamazepine therapy in Mexican Mestizos with epilepsy at a tertiary-care hospital | Coautor: Monroy-Jaramillo, Nancy, Fricke-Galindo, Ingrid, Jung-Cook, Helgi, Martinez-Juarez, Iris E., et al. | 2021 | Pharmacogenomics | WoS-id: 000703916100001
Scopus-id: 2-s2.0-85117349986
| 1 | 1 |
| 12 | Linking the Triad of Telomere Length, Inflammation, and Gut Dysbiosis in the Manifestation of Depression | Coautor: Monroy-Jaramillo N., Bazaz M.R., Balasubramanian R., Dandekar M.P. | 2021 | ACS CHEMICAL NEUROSCIENCE | WoS-id: 000706182800002
Scopus-id: 2-s2.0-85116710482
| 12 | 13 |
| 13 | Integrative DNA Methylation and Gene Expression Analysis in the Prefrontal Cortex of Mexicans Who Died by Suicide | Coautor: Monroy-Jaramillo N., Romero-Pimentel A.L., Almeida D., Munõz-Montero S., et al. | 2021 | INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY | WoS-id: 000733379100001
Scopus-id: 2-s2.0-85118343004
| 12 | 12 |
| 14 | Integrative genomic?epigenomic analysis of clozapine-treated patients with refractory psychosis | Coautor: Monroy-Jaramillo N., Mayén-Lobo Y.G., Martínez-Magaña J.J., Pérez-Aldana B.E., et al. | 2021 | Pharmaceuticals | Scopus-id: 2-s2.0-85100802082
| 0 | 9 |
| 15 | Sex differences in brain gene expression among suicide completers | Coautor: Monroy-Jaramillo, Nancy, Cabrera-Mendoza, Brenda, Fresno, Cristobal, Fries, Gabriel Rodrigo, et al. | 2020 | JOURNAL OF AFFECTIVE DISORDERS | WoS-id: 000519542100010
Scopus-id: 2-s2.0-85079553043
| 13 | 12 |
| 16 | Influence of genetic variants and antiepileptic drug co-treatment on lamotrigine plasma concentration in Mexican Mestizo patients with epilepsy | Coautor: Monroy-Jaramillo N., Ortega-Vázquez A., Fricke-Galindo I., Dorado P., et al. | 2020 | PHARMACOGENOMICS JOURNAL | WoS-id: 000537022300001
Scopus-id: 2-s2.0-85085899958
| 10 | 10 |
| 17 | BRAIN GENE EXPRESSION PROFILING OF INDIVIDUALS WITH DUAL DIAGNOSIS WHO DIED BY SUICIDE | Coautor: Monroy-Jaramillo, Nancy, Cabrera, Brenda, Fresno, Cristobal, Walss-Bass, Consuelo, et al. | 2020 | SCHIZOPHRENIA BULLETIN | WoS-id: 000537751800379
| 0 | 0 |
| 18 | The anti-aging effects of lithium in lymphoblastoid cell lines from patients with bipolar disorder and controls | Coautor: Monroy-Jaramillo N., Fries G.R., Zamzow M.J., Colpo G.D., et al. | 2020 | JOURNAL OF PSYCHIATRIC RESEARCH | WoS-id: 000541924200007
Scopus-id: 2-s2.0-85085761194
| 8 | 11 |
| 19 | X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient | Coautor: Monroy-Jaramillo, Nancy, 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 |
| 20 | First report of pathogenic SGCE variants in Mexican patients with myoclonus dystonia: A five-year follow-up study | Coautor: Monroy-Jaramillo N., Dávila-Ortiz de Montellano D.J., González-del Rincón M.D.L., Abundes-Corona A., et al. | 2020 | PARKINSONISM & RELATED DISORDERS | WoS-id: 000581932600022
Scopus-id: 2-s2.0-85090581243
| 0 | 0 |
| 21 | High prevalence of CYP2D6 ultrarapid metabolizers in a mestizo Colombian population in relation to Hispanic mestizo populations | Coautor: Monroy-Jaramillo, Nancy, Sarmiento, Alba P., Dorado, Pedro, Borbon, Angelica, et al. | 2020 | Pharmacogenomics | WoS-id: 000584494200001
Scopus-id: 2-s2.0-85096947039
| 0 | 1 |
| 22 | High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia | Coautor: Monroy-Jaramillo N., García-Delgado C., Noriega-Juárez M., Cervantes A., et al. | 2020 | DERMATOLOGICA SINICA | WoS-id: 000601214900006
Scopus-id: 2-s2.0-85091512458
| 0 | 0 |
| 23 | BRAIN GENE EXPRESSION-DNA METHYLATION CORRELATION IN SUICIDE COMPLETERS: PRELIMINARY RESULTS | Coautor: Monroy-Jaramillo, Nancy, Cabrera-Mendoza, Brenda, Martinez-Magana, Jose J., Genis-Mendoza, Alma D., et al. | 2020 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000613899600004
Scopus-id: 2-s2.0-85103348030
| 6 | 6 |
| 24 | Displasia ectodérmica hipohidrótica ligada al cromosoma X de novo por variante recurrente en un paciente mexicano | Coautor: Monroy-Jaramillo N., 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 |
| 25 | Dear Editor | 1ᵉʳ autor: Monroy-Jaramillo N., Cerón A., León E., Rivas V., et al. | 2019 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-85065803489
| 0 | 0 |
| 26 | BACE1-deficient mice exhibit alterations in immune system pathways | Coautor: Monroy-Jaramillo N., Stertz L., Contreras-Shannon V., Sun J., et al. | 2018 | MOLECULAR NEUROBIOLOGY | WoS-id: 000424702600063
Scopus-id: 2-s2.0-85050472965
| 9 | 8 |
| 27 | Phenotypic variability in a Mexican Mestizo family with retinal vasculopathy with cerebral leukodystrophy and trex1 mutation P.V235GFSâ??6 | 1ᵉʳ autor: Monroy-Jaramillo N., Cerón A., León E., Rivas V., et al. | 2018 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000432756800002
Scopus-id: 2-s2.0-85049383685
| 9 | 10 |
| 28 | Interethnic variability in CYP2D6, CYP2C9, and CYP2C19 genes and predicted drug metabolism phenotypes among 6060 ibero-and native Americans: RIBEF-CEIBA consortium report on population pharmacogenomics | Coautor: Monroy-Jaramillo N., Naranjo M.-E.G., Rodrigues-Soares F., Peñas-Lledó E.M., et al. | 2018 | OMICS | WoS-id: 000444386700001
Scopus-id: 2-s2.0-85053861167
| 28 | 33 |
| 29 | Telomere length in psychiatric disorders: Is it more than an ageing marker? | 1ᵉʳ autor: Monroy-Jaramillo N., Dyukova E., Walss-Bass C. | 2018 | WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY | WoS-id: 000453922200002
Scopus-id: 2-s2.0-85010690624
| 27 | 26 |
| 30 | Leukocyte telomere length in Hispanic schizophrenia patients under treatment with olanzapine | 1ᵉʳ autor: Monroy-Jaramillo N., Rodríguez-Agudelo Y., Aviña-Cervantes L.C., Roberts D.L., et al. | 2017 | JOURNAL OF PSYCHIATRIC RESEARCH | WoS-id: 000404198400004
Scopus-id: 2-s2.0-85013108576
| 12 | 11 |
| 31 | Analyzing leukocyte telomere length in bipolar disorder | 1ᵉʳ autor y autor de correspondencia: Monroy-Jaramillo N. | 2017 | BRAZILIAN JOURNAL OF PSYCHIATRY | WoS-id: 000407800600014
Scopus-id: 2-s2.0-85027523460
| 2 | 2 |
| 32 | Distinct lithium-induced gene expression effects in lymphoblastoid cell lines from patients with bipolar disorder | Coautor: Monroy-Jaramillo N., Fries G.R., Colpo G.D., Zhao J., et al. | 2017 | EUROPEAN NEUROPSYCHOPHARMACOLOGY | Scopus-id: 2-s2.0-85029552170
| 0 | 15 |
| 33 | Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico | Coautor: Monroy-Jaramillo N., Sesar A., Cacheiro P., López-López M., et al. | 2016 | JOURNAL OF THE NEUROLOGICAL SCIENCES | WoS-id: 000372558400063
Scopus-id: 2-s2.0-84962280645
| 14 | 14 |
| 34 | Relevance of the ancestry for the variability of the Drug-Metabolizing Enzymes CYP2C9, CYP2C19 and CYP2D6 polymorphisms in a multiethnic Costa Rican population | Coautor: Monroy-Jaramillo N., Céspedes-Garro C., Rodrigues-Soares F., Jiménez-Arce G., et al. | 2016 | REVISTA DE BIOLOGIA TROPICAL | Scopus-id: 2-s2.0-84978983285
| 0 | 11 |
| 35 | Genetic mutations in early-onset Parkinson's disease mexican patients: Molecular testing implications | 1ᵉʳ autor: Monroy-Jaramillo N., Guerrero-Camacho J.L., Rodríguez-Violante M., Boll-Woehrlen M.-C., et al. | 2014 | AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | WoS-id: 000333835100005
Scopus-id: 2-s2.0-84897525289
| 16 | 15 |
| 36 | Pharmacogenetic potential biomarkers for carbamazepine adverse drug reactions and clinical response | 1ᵉʳ autor: Jaramillo N.M., Galindo I.F., Vázquez A.O., Cook H.J., et al. | 2014 | Drug Metabolism and Drug Interactions | Scopus-id: 2-s2.0-84904208935
| 0 | 17 |
| 37 | Interethnic differences in UGT1A4 genetic polymorphisms between Mexican Mestizo and Spanish populations | Coautor: Monroy N., López M., Dorado P., Ortega A., et al. | 2013 | MOLECULAR BIOLOGY REPORTS | WoS-id: 000316221100047
Scopus-id: 2-s2.0-84877993138
| 14 | 21 |
| 38 | The L444P GBA mutation is associated with early-onset Parkinson's disease in Mexican Mestizos | 2ᵒ autor: Jaramillo, NM, Gonzalez-del Rincon, MD, Martinez, AIS, Gomez, PY, et al. | 2013 | CLINICAL GENETICS | WoS-id: 000324297800016
Scopus-id: 2-s2.0-84883771008
| 19 | 19 |
| 39 | Pharmacogenetics in Latin American populations: Regulatory aspects, application to herbal medicine, cardiovascular and psychiatric disorders | Coautor: Monroy-Jaramillo N., Rodeiro I., Remírez-Figueredo D., García-Mesa M., et al. | 2012 | Drug Metabolism and Drug Interactions | Scopus-id: 2-s2.0-84860531136
| 0 | 16 |
| 40 | Pharmacogenetics of the antiepileptic drugs phenytoin and lamotrigine | Coautor: Monroy N., López M., Dorado P., ElisaAlonso M., et al. | 2011 | Drug Metabolism and Drug Interactions | Scopus-id: 2-s2.0-79956340310
| 0 | 25 |
| 41 | Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease | Coautor: Monroy N., Yescas P., López M., Boll, MC, et al. | 2010 | NEUROSCIENCE LETTERS | WoS-id: 000283704300001
Scopus-id: 2-s2.0-77957347508
| 27 | 28 |
| 42 | Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) in two Mexican brothers harboring a novel mutation in the ECGF1 gene | 1ᵉʳ autor: Monroy N., Kauffer, LRM, Mutchinick O.M. | 2008 | EUROPEAN JOURNAL OF MEDICAL GENETICS | WoS-id: 000257199100008
Scopus-id: 2-s2.0-43149088948
| 15 | 23 |
| 43 | A novel PtdIns3P and PtdIns(3,5)P2 phosphatase with an inactivating variant in centronuclear myopathy | Coautor: Monroy N., Tosch V., Rohde H.M., Tronchère H., et al. | 2006 | HUMAN MOLECULAR GENETICS | WoS-id: 000241430000002
Scopus-id: 2-s2.0-33750219395
| 104 | 117 |
| 44 | Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype | Coautor: Monroy N., Zafra De La Rosa G., Venegas-Vega C.A., Contreras-Bucio G., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230288400006
Scopus-id: 2-s2.0-22044437226
| 9 | 9 |
| 45 | Microsatellite analysis in Turner syndrome: Parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes | 1ᵉʳ autor: Monroy N., López M., Cervantes A., García-Cruz D., et al. | 2002 | AM J MED GENET | WoS-id: 000173116600001
Scopus-id: 2-s2.0-0037154032
| 16 | 22 |
| 46 | New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia | 2ᵒ autor: Monroy-Jaramillo N., Machuca-Tzili L., González-del Angel A., Kofman-Alfaro S. | 2002 | CLINICAL GENETICS | Scopus-id: 2-s2.0-0036590210
| 9 | 16 |
| 47 | PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype | Coautor: Monroy N., Cervantes A., Guevara-Yáñez R., López M., et al. | 2001 | CLINICAL GENETICS | WoS-id: 000172475000014
Scopus-id: 2-s2.0-0035184239
| 6 | 10 |
| 48 | Del Xq23 in a mosaic Turner female: Molecular and cytogenetic studies | Coautor: Monroy-Jaramillo N., Mesa-Cornejo V.M., García-Cruz D., Vásquez A.I., et al. | 2001 | ANN GENET-PARIS | WoS-id: 000172999400002
Scopus-id: 2-s2.0-0035662872
| 2 | 2 |
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