Hugo Hernán Abarca-Barriga

Dr. Hugo Hernán Abarca-Barriga

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 July 2017 in American Journal of Medical Genetics Part A
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Journal Article
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PKPaul Kruszka
Paul Kruszka
APAntonio R. Porras
Antonio R. Porras
YAYonit A. Addissie
Yonit A. Addissie
AMAngélica Moresco
Angélica Moresco
SMSofia Medrano
Sofia Medrano
MMMaximilian Muenke
Maximilian Muenke

23 January 2014 in Clinical Genetics
Verified
Journal Article
Closed access
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Silke LohanSilke Lohan
Silke Lohan
MSM. Spielmann
M. Spielmann
SDS.C. Doelken
S.C. Doelken
RFR. Flöttmann
R. Flöttmann
FMF. Muhammad
F. Muhammad
EKE. Klopocki
E. Klopocki

21 April 2018 in American Journal of Medical Genetics Part A
Verified
Journal Article
Closed access
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PKPaul Kruszka
Paul Kruszka
APAntonio R. Porras
Antonio R. Porras
DSDeise Helena de Souza
Deise Helena de Souza
AMAngélica Moresco
Angélica Moresco
VHVictoria Huckstadt
Victoria Huckstadt
MMMaximilian Muenke
Maximilian Muenke

1 November 2018 in Molecular Genetics & Genomic Medicine
Verified
Journal Article
Open access
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HGHEINNER GUIO
HEINNER GUIO
JPJulio A. Poterico
Julio A. Poterico
KLKelly S Levano
Kelly S Levano
Mario Cornejo-OlivasMario Cornejo-Olivas
Mario Cornejo-Olivas
PMPilar Mazzetti
Pilar Mazzetti
HAHugo Hernán Abarca-Barriga
Hugo Hernán Abarca-Barriga
Peruvians currently preserve in their DNA the history of 2.5 million years of human evolution and 150,000 years of migration from Africa to Peru or the Americas. The development of Genetics and Genomics in the clinical and academic field is shown in this review.

8 September 2018 in American Journal of Medical Genetics Part A
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Journal Article
Closed access
PDF file
HAHugo Hernán Abarca-Barriga
Hugo Hernán Abarca-Barriga
NCNathaly Caballero
Nathaly Caballero
MTMilana Trubnykova
Milana Trubnykova
MCMaría del Carmen Castro‐Mujica
María del Carmen Castro‐Mujica
JSJorge E. La Serna‐Infantes
Jorge E. La Serna‐Infantes
RHRaoul C. Hennekam
Raoul C. Hennekam

14 March 2025 in BMC Endocrine Disorders
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Journal Article
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DVDaniella Vinelli-Arzubiaga
Daniella Vinelli-Arzubiaga
CCCarmen Elizabeth Suasnabar Campos
Carmen Elizabeth Suasnabar Campos
MLMaría Cristina Laso-Salazar
María Cristina Laso-Salazar
HAHugo Hernán Abarca-Barriga
Hugo Hernán Abarca-Barriga
Neuropathy is a frequent complication of diabetes mellitus, a disease that is growing exponentially worldwide. Genetic research has emerged as an important tool for better understanding its predisposition, although a systematic synthesis of existing evidence is needed to better comprehend its association. The objective of this review was to determine the association between polymorphic variants identified through massive genomic testing and the risk of peripheral diabetic neuropathy in patients with type 2 diabetes mellitus. Inclusion criteria were case-control, cohort, and cross-sectional studies examining polymorphic variants and diabetic neuropathy (DNP) risk in type 2 diabetes, studies using GWAS, EWAS, or microarray for identifying genetic polymorphisms, studies involving adults, and articles in English or Spanish. Exclusion criteria included case reports, case series, ecological studies, editor letters, reviews, or secondary studies and conference abstracts. Exhaustive search in PubMed, Scopus, and Web of Science databases, using keywords. Risk of bias was determined through Newcastle-Ottawa scale. A qualitative synthesis of the results was performed (frequency), including meta-analysis where applicable (forest plot and funnel plot). The searching strategy identified 370 studies, from which 7 were chosen for the systematic review, included 9478 participants. The quality of the studies was mostly good, but a significant heterogeneity in methods was found. We identify a significant association between peripheral neuropathy and plenty of single nucleotide variants (SNVs). Just the SNV rs10555080 in the gene THEG5 showed a higher likelihood of neuropathy (OR:1,34; IC 95%: 1,19 − 1,49). This study faced limitations due to heterogeneity in DNP definitions, genotyping methods, and a focus on white and Arab populations, limiting generalization. Only English and Spanish articles were included, potentially excluding relevant research in other languages. Multiple SNVs were identified through genomic testing that were associated with peripheral diabetic neuropathy in patients with type 2 diabetes mellitus; however, the SNVs were not similar between studies. This research received no funding and was registered in PROSPERO (ID CRD42024505256).