Qurratulain Hasan

Kamineni Hospitals — India

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index2.9kcitations146works0.32yr avg
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Research Topics

Mitochondrial Function and Pathology(12), BRCA gene mutations in cancer(10), Endometriosis Research and Treatment(10), Epigenetics and DNA Methylation(9), Genetic Neurodegenerative Diseases(9)

Publications146 total

Correlation Between Asprosin and Irisin in Iraqi Patients with Type 2 Diabetes or High Blood Pressure
Baghdad Science Journal·2025Open Access
A novel variant in the ALDH3A2 gene causative of Sjögren–Larsson syndrome evaluated in silico aids in proper genetic counseling and planning management
Academia molecular biology and genomics.·2025Open Access
Genetic counselling of disorders of sex development (DSD) in low middle income country (LMIC): case studies
Egyptian Journal of Medical Human Genetics·2025Open Access
6P vAO - Variant Annotator for OncoKB: A simplified interface to identify targeted therapies for somatic tumors
ESMO Open·2025Open Access
Streamlined Analysis of Exome Sequencing Data for Identifying Common Variants: An Interface Tool for Enhancing Diagnostic Yield
SSRN Electronic Journal·2025Open Access
Enhancing Diagnostic Yield in Exome Sequencing with vDBS: Streamlined Cohort-Based Variant Analysis from 200+ Exomes
SSRN Electronic Journal·2025Open Access
Consanguinity in the genomic era—Requirement of focused counseling
Elsevier eBooks·2024
Contributors
Elsevier eBooks·2024Open Access
EVALUATION OF GENE POLYMORPHISMS FOR PERSONALIZING ANTIPLATELET AND ANTICOAGULANT THERAPY
GLOBAL JOURNAL FOR RESEARCH ANALYSIS·2024
Awareness Regarding Screening Programs in General Population to Improve Health Indicators: Genetic Counselors as Facilitators
International Journal of Innovative Science and Research Technology (IJISRT)·2024· 1 citedOpen Access
Short-Term Clinical Results of Single-Injection Autologous Bone Marrow Aspirate Concentrate (BMAC) as a Therapeutic Option/Tool in Knee Osteoarthritis
Biologics·2024· 2 citedOpen Access
Bibliometric analysis of genetic counseling publications in Asia: Insights and implications
Genetics in Medicine Open·2024· 1 citedOpen Access
The landscape of actionable genomic alterations in lung adenocarcinomas in India
Frontiers in Genetics·2023· 6 citedOpen Access
Frequency of dihydropyrimidine dehydrogenase and UDP-glucuronosyltransferase 1A1 variants in cancer patients requiring chemotherapy: A single-center study in southern India
Yādgār.·2023· 1 citedOpen Access
Quantitative phase imaging of biological cells using lensless inline holographic microscopy through sparsity-assisted iterative phase retrieval algorithm
Journal of Applied Physics·2022· 19 cited
Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer
Frontiers in Genetics·2022· 4 citedOpen Access
Identifying Molecular Aetiology of Syndromic and Non syndromic Renal Disorders using Exome Analysis
2022Open Access
Utility of next-generation sequencing in genetic testing and counseling of disorders involving the musculoskeletal system—trends observed from a single genetic unit
Journal of Orthopaedic Surgery and Research·2022· 4 citedOpen Access
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries
Genetics in Medicine·2022· 12 citedOpen Access
Tumour Necrosis Factor Alpha Serum Levels and its Gene Polymorphism 850 C/T (rs1799724) as Prognostic Markers of Traumatic Brain Injury Outcome
International Journal of Anatomy Radiology and Surgery·2022· 1 citedOpen Access
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Frequent Co-authors

Imran Ali Khan(10), Parveen Jahan(9), Pragna Rao(8), Noor Ahmad Shaik(8), Vijayalakshmi Kodati(7), Beate M. Rüger(6), Sireesha Movva(6), Kiran Kumar Vattam(6), Sujatha Govindan(6), K. Prabhakar Rao(6), Bhavani Vedicherla(5), Yog Raj Ahuja(5), Paul F. Davis(4), Vasavi Mohan(4), Srinivas Chava(4), Syeda Zubeda(4), Madhavi Latha(4), Sambasivan Venkatasubramanian(4), T J Neale(3), Ravindra V. Alluri(3)