World's Best Scientists 2026 revealed!

D-Index & Metrics

Molecular Biology

D-Index
90
Citations
29904
World Ranking
736
National Ranking
59

Overview

Farida Latif is affiliated with the University of Birmingham in the United Kingdom and has contributed to research primarily in the field of Medicine. Their work encompasses several subfields, including Molecular Biology, Physiology, General Health Professions, Pediatrics, Perinatology and Child Health, and Cancer Research.

Their research topics focus on Public Health and Nutrition, Cancer-related molecular mechanisms, Epigenetics and DNA Methylation, RNA modifications in cancer, Cervical Cancer and HPV research, Molecular Biology Techniques and Applications, and Fibroblast Growth Factor research.

Frequent co-authors of Farida Latif include:

  • Nurhaedah Nurhaedah
  • Rajendra P. Pangeni
  • Ivonne Olivaries
  • David Huen
  • Vannessa C. Buzatto

Their recent papers include:

  • "Genome-wide methylation analyses identifies Non-coding RNA genes dysregulated in breast tumours that metastasise to the brain" (2022) published in Scientific Reports
  • "High frequency of HPV high-risk preventable genotypes in Ecuadorian women with invasive cervical cancer" (2024) published in Revista Panamericana de Salud Pública
  • "Significant association between FGFR1 mutation frequency and age in central giant cell granuloma" (2022) published in Pathology
  • "The Role of Mesenchymal Stem Cell Derived Exosomes versus Melatonin on Skin Wound Healing of Adult Male Albino Rats: Histological Study" (2024) published in The Egyptian Journal of Histology
  • "The effect of oral anticoagulants on the incidence of dementia in patients with atrial fibrillation: a systematic review and meta-analysis" (2024) published in European Heart Journal

Farida Latif's work has appeared in several publication venues with multiple contributions to:

  • Sahabat Sosial Jurnal Pengabdian Masyarakat
  • Scientific Reports
  • Revista Panamericana de Salud Pública
  • Pathology
  • The Egyptian Journal of Histology

Best Publications

  • Identification of the von Hippel-Lindau disease tumor suppressor gene.

    F Latif;K Tory;J Gnarra;M Yao

  • Mutations of the VHL tumour suppressor gene in renal carcinoma

    J.R. Gnarra;K. Tory;Y. Weng;L. Schmidt

  • Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

    J G Herman;F Latif;Y Weng;M I Lerman

  • Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

    Dewi Astuti;Farida Latif;Ashraf Dallol;Patricia L.M. Dahia

  • Epigenetic Inactivation of RASSF1A in Lung and Breast Cancers and Malignant Phenotype Suppression

    David G. Burbee;Eva Forgacs;Sabine Zöchbauer-Müller;Latha Shivakumar

  • Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

    Chen F;Kishida T;Yao M;Hustad T

  • Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas.

    T Shuin;K Kondo;S Torigoe;T Kishida

  • Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.

    Angelo Agathanggelou;Sofia Honorio;Donia P Macartney;Alonso Martinez

  • Role of the Ras-association domain family 1 tumor suppressor gene in human cancers.

    Angelo Agathanggelou;Wendy N. Cooper;Farida Latif

  • Germline SDHB Mutations and Familial Renal Cell Carcinoma

    Christopher Ricketts;Emma R. Woodward;Pip Killick;Mark R. Morris

  • Germline SDHD mutation in familial phaeochromocytoma

    Dewi Astuti;Fiona Douglas;Thomas W J Lennard;Irene A. Aligianis

  • Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns.

    Yoshitaka Sekido;Scott Bader;Scott Bader;Farida Latif;Jeou Yuan Chen;Jeou Yuan Chen

  • The Role of RASSF1A Methylation in Cancer

    Luke B. Hesson;Wendy N. Cooper;Farida Latif

  • Functional Properties of a New Voltage-dependent Calcium Channel α2δ Auxiliary Subunit Gene (CACNA2D2)

    Boning Gao;Yoshitaka Sekido;Anton Maximov;Mohamad Saad

  • Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

    Dewi Astuti;Mark R Morris;Mark R Morris;Wendy N Cooper;Raymond H J Staals

  • Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma.

    Mark Morris;Christopher Ricketts;Dean Gentle;Fiona McRonald

  • Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

    Carol Hardy;Farhat Khanim;Rosarelis Torres;Rosarelis Torres;Martin Scott-Brown

  • The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation

    Volker Endris;Birgit Wogatzky;Uwe Leimer;Dusan Bartsch

  • Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.

    Hiltrud Brauch;Takeshi Kishida;Damjan Glavac;Fan Chen

  • The Tumor Suppressor RASSF1A and MAP-1 Link Death Receptor Signaling to Bax Conformational Change and Cell Death

    Shairaz Baksh;Shairaz Baksh;Stella Tommasi;Sarah Fenton;Victor C. Yu

Frequent Co-Authors

Berton Zbar
Berton Zbar National Institutes of Health
Michael I. Lerman
Michael I. Lerman National Institutes of Health
Hiltrud Brauch
Hiltrud Brauch German Cancer Research Center
Eamonn R. Maher
Eamonn R. Maher University of Cambridge
William S. Modi
William S. Modi CUUR Diagnostics
John D. Minna
John D. Minna The University of Texas Southwestern Medical Center
Laura S. Schmidt
Laura S. Schmidt National Institutes of Health
Michael B. Gorin
Michael B. Gorin University of California, Los Angeles
Nabeel A. Affara
Nabeel A. Affara University of Cambridge
Ian Roberts
Ian Roberts University of Cambridge

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Pursuing a degree in Molecular Biology can open doors to a wide range of career paths in science, healthcare, and education. For those interested in combining biology with mental health support, consider exploring counseling masters programs online. These programs provide foundations in helping skills and psychological theory, which are valuable in clinical and research settings.

Another option is to pursue an online masters in clinical psychology. With this path, you can apply molecular knowledge to mental health research or clinical practice, especially in neurobiology fields.

If you are looking for flexible and accelerated education, online schools for human services offer short programs that can quickly prepare you for diverse roles supporting community and healthcare organizations.

Lastly, if you have a background in education and are considering a shift, learn more about the education required to be a speech pathologist. This rewarding field benefits from a foundation in biology and can be accessed through targeted graduate programs.

Best Scientists Citing Farida Latif

Trending Scientists

Recently Published Articles