WANT A PROFILE LIKE THIS?
Create my FREE Plan Or learn about other options
Safarina Malik
PeerJ Editor, Author & Reviewer
700 Points

Contributions by role

Author 270
Reviewer 30
Editor 400

Contributions by subject area

Biotechnology
Molecular Biology
Public Health
Medical Genetics
Diabetes and Endocrinology
Hematology
Bioinformatics
Genetics
Geriatrics
Metabolic Sciences
Immunology
Biochemistry
Histology
Anthropology
Biosphere Interactions
Population Biology
Epidemiology
Otorhinolaryngology

Safarina G Malik

PeerJ Editor, Author & Reviewer

Summary

Safarina G. Malik is a Principal Investigator at the Genome Diversity and Disease Division of the Mochtar Riady Institute for Nanotechnology, Tangerang, Banten, Indonesia, since January 2022. From 2011 to 2021 she lead the Lifestyle Diseases Research Group at the Eijkman Institute for Molecular Biology, Jakarta, Indonesia. Her key research topics and expertise include genetic diversity, microbiome, mitochondrial genetics and dysfunction, medical genetics, lifestyle disease association, nutrigenetics-nutrigenomics, population genetics and evolution.

Biochemistry Bioinformatics Cell Biology Diabetes & Endocrinology Ethical Issues Genetics Genomics Medical Genetics Molecular Biology Obesity Population Biology

Editorial Board Member

PeerJ - the Journal of Life & Environmental Sciences

Work details

Principal Investigator

Mochtar Riady Institute for Nanotechnology
January 2022 - January 2023
Genome Diversity and Disease Division

Websites

  • Google Scholar

PeerJ Contributions

  • Articles 2
  • Edited 2
March 22, 2022
Transcription factor 7-like 2 single nucleotide polymorphisms rs290487 and rs290481 are associated with dyslipidemia in the Balinese population
Prisca C. Limardi, Sukma Oktavianthi, Lidwina Priliani, Retno Lestari, Made Ratna Saraswati, Ketut Suastika, Safarina G. Malik
https://doi.org/10.7717/peerj.13149 PubMed 35341056
January 3, 2020
Obesity in the Balinese is associated with FTO rs9939609 and rs1421085 single nucleotide polymorphisms
Lidwina Priliani, Sukma Oktavianthi, Ria Hasnita, Hazrina T. Nussa, Rut C. Inggriani, Clarissa A. Febinia, Anom Bowolaksono, Rini Puspitaningrum, Rully A. Nugroho, Ketut Suastika, Safarina G. Malik
https://doi.org/10.7717/peerj.8327 PubMed 31915589

Academic Editor on

January 3, 2024
Evaluating the relationship between Clinical G6PD enzyme activity and gene variants
Xinyi Zhou, Zheng Qiang, Sufen Zhang, Yuqiu Zhou, Qizhi Xiao, Gongjun Tan
https://doi.org/10.7717/peerj.16554 PubMed 38188142
January 30, 2023
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia–Alania
Nika Petrova, Inna Tebieva, Vitaly Kadyshev, Zalina Getoeva, Natalia Balinova, Andrey Marakhonov, Tatyana Vasilyeva, Evgeny Ginter, Sergey Kutsev, Rena Zinchenko
https://doi.org/10.7717/peerj.14514 PubMed 36743950