プロフィール詳細

プロジェクトを作成

★★★★★

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★★★★★

☆☆☆☆☆

Félix Julián C.に依頼

Mexico

Evidence Synthesis Specialist, Network Meta-Analysis, RoB2/ROBINS-I, Clinical Trial Data Extraction

プロフィール概要

Profile Summary I am a PhD-trained clinical researcher with 3 years of experience specializing in systematic reviews, network meta-analysis (NMA), and structured evidence synthesis for clinical and regulatory decision-making. My work bridges rigorous methodology and practical, reproducible workflows — from protocol design through data extraction, risk of bias assessment, statistical analysis, and manuscript preparation. Core expertise Systematic reviews and meta-analyses following Cochrane Handbook and PRISMA 2020 standards, including protocol registration (PROSPERO), comprehensive search strategy design, dual-reviewer screening, and GRADE certainty-of-evidence assessment. Network meta-analysis (NMA) in both frequentist and Bayesian frameworks, including assessment of transitivity, consistency, ranking (SUCRA/P-scores), and CINeMA for confidence in NMA estimates. Risk of bias assessment using RoB 2 for randomized trials and ROBINS-I for non-randomized studies, with domain-level justification and sensitivity analyses. Structured data extraction from published trials and ClinicalTrials.gov registrations, including arm-level outcome data, zero-event handling for rare outcomes, and statistical conversions (e.g., median/IQR to mean/SD using Wan et al. 2014). Reproducible analytic workflows with standardized treatment naming conventions, explicit coding of missing data (NR/NS/NE/NA), and output structured for direct ingestion into R (netmeta, meta, metafor) and Stata. Ongoing and recent projects Developing and refining a comprehensive data extraction protocol for GLP-1 receptor agonist trials, designed for full reproducibility across reviewers and sessions. Conducting trial-level data extraction on RCTs of glucose-lowering and weight-loss therapies, integrating published manuscripts with ClinicalTrials.gov outcome data. Designing NMA-ready datasets in long format (netmeta_long) with paired outcomes inventory and trial characteristics tables to support transparent re-analysis. Technical skills Statistical software: R (netmeta, meta, metafor, gemtc, tidyverse), Stata Evidence synthesis tools: Covidence, Rayyan, RevMan, EPPI-Reviewer, GRADEpro Risk of bias: RoB 2, ROBINS-I, ROBIS, AMSTAR-2 Data management: Excel (advanced), structured CSV/long-format datasets, ClinicalTrials.gov data parsing Languages Trilingual: English, Spanish, and French — enabling literature screening, data extraction, and collaboration across major bodies of clinical research literature. Education PhD — UNAM What I offer clients Whether you need a full systematic review conducted from scoping to publication, a focused data extraction effort for an existing review, an NMA built on a transparent and auditable dataset, or methodological consulting on risk of bias or evidence certainty — I deliver work that is reproducible, well-documented, and ready for peer-reviewed publication or regulatory submission.

専門分野

• ☆ Molecular Biology
• ☆ Genetics
• ☆ Statistics
• ☆ Meta-Analysis
• ☆ Medical Genetics
• ☆ Cardiovascular Disease
• ☆ Pediatric Cardiology

サービス

• Writing
• Research
• Consulting
• Data & AI

Writing Medical Writing

Research Scientific and Technical Research, Systematic Literature Review

Consulting Healthcare Consulting, Scientific and Technical Consulting

Data & AI Statistical Analysis, Data Visualization, Big Data Analytics, Data Mining, Data Cleaning, Data Processing

職務経験

Adjunct Researcher

Universidad Marista de Mérida

8月 2024 - 現在

Clinical Geneticist

Hospital General "Dr. Agustín O'Horán"

7月 2023 - 現在

Instituto Mexicano del Seguro Social Delegación Yucatán

3月 2019 - 現在

学歴

Doctor of Philosophy (Research Department, IMSS, UMAE Yucatán)

Universidad Nacional Autónoma de México

2月 2022 - 1月 2026

Master in Medical Sciences

Universidad Nacional Autonoma de Mexico

1月 2020 - 1月 2022

Clinical Geneticist

Universidad Nacional Autonoma de Mexico

3月 2010 - 2月 2013

認定資格

• Network Meta-Analysis

  Cochrane

  https://engage.cochrane.org/profiles/31760

  3月 2026 - 現在

出版物

JOURNAL ARTICLE

Delmer-Alejandro Ruiz-Martinez, Emilio-Rodrigo Vega-Peniche, Yazmin Quiñonez-Pacheco, Hugo Laviada-Molina, Carlos-Alejandro Medina-Campos, Felix-Julian Campos-Garcia (2026). Ethylmalonic encephalopathy caused by biallelic truncating variants in ETHE1: A case report . Sage Open Medical Case Reports.

Delmer-Alejandro Ruiz-Martinez, Emilio-Rodrigo Vega-Peniche, Yazmin Quiñonez-Pacheco, Hugo Laviada-Molina, Carlos-Alejandro Medina-Campos, Felix-Julian Campos-Garcia (2026). Ethylmalonic encephalopathy caused by biallelic truncating variants in ETHE1: A case report . Sage Open Medical Case Reports.

Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan C. Zenteno, Julio-Cesar Lara-Riegos, Juanita-Adriana Chuc-Chan, Ana-Isabel Velazquez-Ibarra, Paulina-Del-Carmen Cauich-Pool, Eddie-Alberto Favela-Perez, Pablo-Ysidro Pech-Gomez, et al. (2025). Genetic Burden in Congenital Anomalies of the Mitral and Tricuspid Valves: A Case–Control Study . Pediatric Cardiology.

Sandra Rodriguez-Cambranis, Addy-Manuela Castillo-Espinola, Claudia-Daniela Fuentelzas-Rosado, Paulina Salazar-Sansores, Claudia-Gabriela Nuñez-Solis, Hugo-Antonio Laviada-Molina, Aurea-Karina Zetina-Solorzano, Felix-Julian Campos-Garcia (2025). Genotype–Phenotype Correlation of EVC Variants in Ellis-Van Creveld Syndrome: A Systematic Review and Case Report . Cardiogenetics.

Sandra Rodriguez-Cambranis, Addy-Manuela Castillo-Espinola, Claudia-Daniela Fuentelzas-Rosado, Paulina Salazar-Sansores, Claudia-Gabriela Nuñez-Solis, Hugo-Antonio Laviada-Molina, Aurea-Karina Zetina-Solorzano, Felix-Julian Campos-Garcia (2025). Genotype–Phenotype Correlation of EVC Variants in Ellis-Van Creveld Syndrome: A Systematic Review and Case Report . Cardiogenetics.

Henry-Marcelo Rodriguez-Perez, Olga-Berenice Reyes-Flores, Yazmin Quiñonez-Pacheco, Yahir-Arturo Centeno-Navarrete, Cruz Gonzalez-Vazquez, Felix-Julian Campos-Garcia, Felix-Julian Campos-Garcia (2024). Dyslipidemia and hypercalciuria in a patient with pantothenate kinase 2 deficiency: A novel variant and case report . SAGE Open Medical Case Reports.

Henry-Marcelo Rodriguez-Perez, Olga-Berenice Reyes-Flores, Yazmin Quiñonez-Pacheco, Yahir-Arturo Centeno-Navarrete, Cruz Gonzalez-Vazquez, Felix-Julian Campos-Garcia (2024). Dyslipidemia and hypercalciuria in a patient with pantothenate kinase 2 deficiency: A novel variant and case report . SAGE Open Medical Case Reports.

Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan Zenteno, Julio-Cesar Lara-Riegos, Hector Rubio-Zapata, David Cruz-Robles, Ana-Isabel Velazquez-Ibarra (2022). Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1 in Patients with Conotruncal Congenital Heart Disease . Cardiogenetics.

Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan C. Zenteno, Julio-Cesar Lara-Riegos, Hector Rubio-Zapata, David Cruz-Robles, Ana-Isabel Velazquez-Ibarra (2022). Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for <i>TBX1</i> in Patients with Conotruncal Congenital Heart Disease . Cardiogenetics.

(2019). Characterization of novel GCDH pathogenic variants causing glutaric aciduria type 1 in the southeast of Mexico . Molecular Genetics and Metabolism Reports.

Ibarra-Gonz&#225;lez, I., Campos-Garcia, F.-J., Herrera-P&#233;rez, L.D.A., Mart&#237;nez-Cruz, P., Moreno-Graciano, C.-M., Contreras-Capetillo, S.-N., Le&#243;n-Burgos, V., Maldonado-Solis, F.-A., Alc&#225;ntara-Ortigoza, M.A., Del Angel, A.G., et al.(2018). Newborn cystic fibrosis screening in southeastern mexico: Birth prevalence and novel cftr gene variants . Journal of Medical Screening. 25. (3). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 119-125.

Villegas-Ruiz, V., Campos-Garcia, F.J., Contreras-Capetillo, S., Moreno-Graciano, C.M., Maldonado-Solis, F.A., Maldonado-Solis, M.A., Zenteno, J.C.(2015). Characterization and mRNA expression analysis of a novel ARG1 splicing mutation causing hyperargininemia . Clinical Biochemistry. 48. (18). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1273-1276.

CONFERENCE ABSTRACT

(2019). Follow-up of a patient with glutaric aciduria type 1 diagnosed through newborn screening in south east Mexico . Journal of Inherited Metabolic Disease.

(2017). Pyruvate Dehydrogenase E1-Alpha Deficiency, A Case Report . Journal of Inborn Errors of Metabolism and Screening.

(2015). Evolution of the first patient of Mayan ancestry with argininemia found through the expanded newborn screening program of Yucatan, Mexico . SSIEM 2015 Annual Symposium.

(2012). CARDIOVASCULAR OUTCOME AFTER FIVE YEARS OF ENZYME REPLACEMENT THERAPY IN THREE MEXICAN PATIENTS WITH HURLER SYNDROME . Annual Symposium of the SSIEM 2012.

DATA SET

Hugo, Laviada, Campos-Garcia, Felix-Julian Dataset and R Code for: Semaglutide and Risk of Completed Suicide in Adults with Obesity: A Systematic Review and Meta-analysis .

Campos-Garcia, Felix-Julian, Villas&#237;s-Keever, Miguel Angel, MEDINA ESCOBEDO, CAROLINA ELIZAABETH Whole Exome Sequencing Dataset of Patients with Congenital Mitral and Tricuspid Valve Malformations .

Campos-Garcia, Felix-Julian, Villas&#237;s-Keever, Miguel Angel, MEDINA ESCOBEDO, CAROLINA ELIZAABETH Whole Exome Sequencing VCF Dataset of Control Patients with Structurally Normal Hearts .