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Current Genetic Medicine Reports

IF1.3
Papers18
Citations
Journal Papers 18
Publication Date
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"Microarray Profiling of Genetic Variants in Patients with Atrial Septal Defect from Indian population: A Case Series Report"
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-05-01
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PREAI
deleteJoshi, Radha; Murthy, Prabhatha Rashmi; Nath, Shaoni; Mandhare, Poonam; Menghal, Ruchira; Sukumaran, Rashmi; Banerjee, Moinak
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Molecular Genetic Investigation of Mucopolysaccharidosis 1 Disease in 10 Patients from Unrelated Pakistani Families
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-04-27
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PREAI
deleteBatool, Hajira; Zubaida, Bibi; Batool, Tahira; Waheed, Nadia; Cheema, Huma Arshad; Naeem, Muhammad
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Adult Diagnosis of ATN1-Related Neurodevelopmental Disorder: A Case Report of a Mild Phenotype with In-Frame Tandem Duplication in the HX Motif
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-04-27
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PREAI
deleteMcGonigle, William; Kapil, Sneha; Swols, Dayna Morel; Barbouth, Deborah
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Enrichment of CYP21A2 Promoter Variant rs150223621 in Congenital Adrenal Hyperplasia Cohorts from the 100 000 Genomes Project
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-04-27
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deleteGee, Harrison; Hearn, Timothy J.
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Comprehensive Inhibition of Breast Cancer Progression Through CD39 Targeting and Paclitaxel: Modulating Cell Proliferation, Apoptosis, and Migration
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-03-14
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deleteEslami, Sahand; Ahmadpour Youshanlui, Mahya; Baghbanzadeh, Amir; Jamali, Fereshteh; Baradaran, Behzad
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A New Chapter for Current Genetic Medicine Reports
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-02-28
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deleteFairbrother, Una L.
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Molecular Architects of Dental Caries: Genes, Proteins, and Cellular Pathway Perspectives: A Systematic Review
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-02-19
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PREAI
deleteYazdani, Reza; Mohtasham, Nooshin; Mohammadipour, Hamideh Sadat; Sadeghi, Masoumeh; Mohajertehran, Farnaz
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Charcot-Marie-Tooth 4B3 Phenotype Expansion and Confounding Factors
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-02-09
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deleteSilva, Lenia; Igreja, Liliana; Cardoso, Marcio; Samoes, Raquel; Pinto, Miguel; Marinho, Antonio; Oliveira, Jorge; Magalhaes, Marina
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The Role of LTF, ENAM, and AMELX Gene Polymorphisms in Dental Caries Susceptibility: A Meta-Analysis
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-01-30
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PREAI
deleteShojaei, Donya; Mohammadipour, Hamideh Sadat; Sekandari, Salehe; Dehghani, Mohsen; Mohajertehran, Farnaz
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Spectrum of Structural Variations in Non-Syndromic Hearing Loss in an Indian Population
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-01-12
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PREAI
deleteArdra, M.; Sindura, K. P.; Davis, P.; Padmaja, M.; Banerjee, Moinak
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Familial Cancer Predisposition Associated with Germline XPC Variant rs1450238352 in a Patient with Metastatic Prostate Cancer: A Case Report
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-01-08
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PREAI
deleteKilic, Seda; Erdogan, Ozge Sukruoglu; Demirbas, Betul Celik; Kayim, Zubeyde Yalniz; Ozgel, Merve; Tuncer, Seref Bugra
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Identification of a Novel TNNI3K Variant in a Young Patient with Complete Heart Block: Implications for Genetic Evaluation and Leadless Pacemaker Therapy
deleteCurrent Genetic Medicine Reports
IF1.3
delete2026-01-07
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PREAI
deleteRobledo, Ariadna; O'leary, Sean; Mohan, Chaitra
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Evaluation of the Sixth Exon of IL12RB1 in Patients Afflicted by the Non-Healing Form of Cutaneous Leishmaniasis
deleteCurrent Genetic Medicine Reports
IF1.3
delete2025-10-16
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PREAI
deleteMoafi, Mohammad; Rezvan, Hossien; Taleban, Roya; Mansourian, Marjan; Sokhanvari, Fatemeh; Ansari, Nazli; Sherkat, Roya
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Whole Exome Sequencing in a Pakistani Family Affected with Demyelinating Hereditary Sensorimotor Polyneuropathy with Spinocerebellar Degeneration
deleteCurrent Genetic Medicine Reports
IF1.3
delete2025-10-14
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PREAI
deleteUllah, Aman; Khan, Ranjha; Naeem, Muhammad
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Myo-Neuropathy and Congenital Bilateral Cataract Due to a GFER Variant in an Iranian Family
deleteCurrent Genetic Medicine Reports
IF1.3
delete2025-10-08
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PREAI
deleteGhasemi, Aida; Hadei, Seyed Jalaleddin; Salami, Zahra; Saffar, Hiva; Najmabadi, Hossein; Okhovat, Ali Asghar
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Pheochromocytoma in a Patient with Primarily Pulmonary and Cutaneous Manifestations of Birt-Hogg-Dubé Syndrome: A Case Report and Review of the Literature
deleteCURRENT GENETIC MEDICINE REPORTS
IF0
delete2025-09-19
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deleteDahak, Sabrina; Kunesh, Jacqueline; Greene, Adina; Patel, Sadiq S.; Laman, Susan D.
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A Rare Case of Cockayne Syndrome Type B in Bahrain: Insights from an ERCC6 Variant
deleteCURRENT GENETIC MEDICINE REPORTS
IF0
delete2025-09-19
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PREAI
deleteKhudair, Aiman D.; Alhakim, Fatima; Khudair, Ahmed D.; Marshall, Rachel A.; Kamblawi, Babaker; Hassan, Hisham Y.
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A Deleterious Frameshift Deletion Variant in Exon 5 of the CYP21A2 Gene Causes Classic Salt-Wasting Congenital Adrenal Hyperplasia
deleteCURRENT GENETIC MEDICINE REPORTS
IF0
delete2025-09-09
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PREAI
deleteMolavi, Newsha; Aghaei, Shahrzad; Hoseinzadeh, Marziyeh; Khanahmad, Hossein; Hashemipour, Mahin; Tabatabaiefar, Mohammad Amin
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