Muhammad Umair

University of Electronic Science and Technology of China — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

39h-index16.2kcitations291works119.12yr avg
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Research Topics

Genomics and Rare Diseases(29), Genetics and Neurodevelopmental Disorders(27), Congenital limb and hand anomalies(23), Hedgehog Signaling Pathway Studies(21), Genomic variations and chromosomal abnormalities(19)

Publications255 total

Unifying RGB, thermal infrared, infrared, and text for person re-identification: A multi-modal dataset and vision-language transformer
Information Processing & Management·2026
Nanomedicines for neurological disorders: Recent advances
Elsevier eBooks·2025
Knees on fire: Investigating the impact of knee discomfort on cardiovascular fitness among Malaysian firefighters.
PubMed·2025
NAV3 Missense Variant in a Homozygous State: Strengthening Links to Neurodevelopmental Disorder
Current Medicinal Chemistry·2025Open Access
Polymerase chain reaction and its variants in molecular diagnostics
2025
Molecular diagnostics in cardiovascular diseases
2025
Foreign direct investment, trade openness and environmental pollution in Pakistan: does renewable energy mitigate environmental degradation?
Frontiers in Environmental Science·2025· 1 citedOpen Access
Back Cover: Turning on the Heat by Cocrystal Engineering: The Rise of Organic Charge Transfer Photothermal Cocrystals as an Emerging Therapeutic Frontier in Biomedical Application
Aggregate·2025Open Access
Immediate Effect of Theragun Vs Transcutaneous Electrical Nerve Stimulation in Treating Non-Specific Neck Pain Among Young Adults
THE THERAPIST (Journal of Therapies & Rehabilitation Sciences)·2025Open Access
Behavioral and Economic Interventions to Curb Positional Consumption: Experimental Evidence from Social Networks
Physical Education Health and Social Sciences·2025Open Access
Sustainable Utilization of Invasive Alien Plant Species for Bioenergy and Fodder: A Narrative Review with Insights from Paper Mulberry
Journal of Asian Development Studies·2025· 1 citedOpen Access
Case Report: Hypomyelinating Leukodystrophy Type 20 (<scp>HLD20</scp>) With Novel <scp><i>CNP</i></scp> Gene Variant
American Journal of Medical Genetics Part A·2025Open Access
Morphological evolution of γ' and γ'' precipitation in a model superalloy: Insights from 3D phase-field simulations
Computational Materials Science·2025· 3 cited
Maternal and neonatal outcomes in placenta previa complicated by antepartum hemorrhage
Journal of Clinical and Translational Research·2025Open Access
Turning on the Heat by Cocrystal Engineering: The Rise of Organic Charge Transfer Photothermal Cocrystals as an Emerging Therapeutic Frontier in Biomedical Application
Aggregate·2025· 5 citedOpen Access
Whole exome sequencing in 33 patients revealed 4 novel variants in 11 limbs-girdle muscular dystrophy families
Gene Reports·2025· 1 cited
DENTIST AGREEMENT ON ASSESSING IMPACTED THIRD MOLARS' ANGLES VIA ORTHOPANTOMOGRAMS
2025Open Access
Gene Therapy in Rare Genetic Disorders: Current Progress and Future Perspectives
Current Genomics·2025Open Access
Immunohistochemical expression of SOX10 and GATA3 in triple negative breast carcinoma and metastatic breast carcinoma.
The Professional Medical Journal·2025Open Access
AB211. SOH25_AB_392. Incidence of neoplasms in appendix specimens across a 5-year span—a multi-centre power study
Mesentery and Peritoneum·2025Open Access
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Frequent Co-authors

Wasim Ahmad(16), Majid Alfadhel(15), Farooq Ahmad(11), Asmat Ullah(9), Safdar Abbas(7), Muhammad Bilal(6), Yusra Alyafee(6), Ahmed Alfares(5), Abeer Al Tuwaijri(5), Qamre Alam(5), Tobias B. Haack(5), Tim M. Strom(5), Thomas Meitinger(5), Abid Jan(5), Bader Almuzzaini(4), Marwan Nashabat(4), Bader Alhaddad(4), Abdulaziz Asiri(4), Amjad Khan(4), Afzal Rafique(4)