Sage Journals: Discover world-class research

Open access

Review article

First published 2016

Computational Identification of Novel Genes: Current and Future Perspectives

Steffen Klasberg, Tristan Bitard-Feildel, Ludovic Mallet

Bioinformatics and Biology Insights

Open access

Research article

First published 2023

Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation

Ayman A Bakkar, Abdulaziz Alsaedi, Naglaa M Kamal [...]

Clinical Medicine Insights: Endocrinology and Diabetes

Free access

Research article

First published 2006-06

Cell-Based Screening and Validation of Human Novel Genes Associated with Cell Viability

Lan Wang, Xia Gao, Peng Gao [...]

Journal of Biomolecular Screening

Open access

Case report

First published 2022-5

Characterization of a novel HBB:c.194dup variant of the β -globin gene combined with six alpha genes

Jungao Huang, Le Ding, Junkun Chen [...]

Journal of International Medical Research

Open access

Research article

First published 2022

Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study

Naglaa M. Kamal, Omar I. Saadah, Shahad S. Alheraiti [...]

Sage Open Chronic Disease

Retricted access

Case report

First published 2025

Spindle Cell Spindle Sarcoma Harboring a Novel RECQL::ROS1 Gene Fusion

Yuxia Gao, Haitao Deng, Yongqin Ao [...]

International Journal of Surgical Pathology

Retricted access

Other

First published 2007-07

Novel Mutation in Splicing Donor of Dystrophin Gene First Exon in a Patient With Dilated Cardiomyopathy but No Clinical Signs of Skeletal Myopathy

Shigemi Kimura, Makoto Ikezawa, Shiro Ozasa [...]

Journal of Child Neurology

Open access

Case report

First published 2025

Identification of a novel PRUNE2::NTRK2 gene fusion in soft tissue sarcoma patients—friend or foe? Case series

Klaudia Bobak, Andrzej Tysarowski, Katarzyna A. Seliga [...]

Therapeutic Advances in Medical Oncology

Retricted access

Other

First published 2009-1

Magnetic Resonance Imaging,Magnetic Resonance Spectroscopy,and Facial Dysmorphism in a Case of Lowe Syndrome with Novel OCRL1 Gene Mutation

Adnan Yuksel, Ender Karaca, M. Sait Albayram

Journal of Child Neurology

Retricted access

Research article

First published 2006-08

A Novel Genetic Algorithm Based on Gene Therapy Theory

Chao-Xue Wang, Du-Wu Cui, Ding-Sheng Wan [...]

Transactions of the Institute of Measurement and Control

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