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Mutation databases

SWI/SNF Infobase—An exclusive information portal for SWI/SNF remodeling complex subunits

Udayakumar Mani, Alagu Sankareswaran S., Arun Goutham R. N., Suma Mohan S.

Molecular subtype specific efficacy of MEK inhibitors in pancreatic cancers

Diána Brauswetter, Bianka Gurbi, [ ... ], István Peták

Prognostic value of SRSF2 mutations in patients with de novo myelodysplastic syndromes: A meta-analysis

Xue Zheng, Zhi Zhan, [ ... ], Yuping Gong

Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype

Shoko Onodera, Akiko Saito, [ ... ], Toshifumi Azuma

Identification of a novel GJA3 mutation in a large Chinese family with congenital cataract using targeted exome sequencing

Yihua Yao, Xuedong Zheng, [ ... ], Yihua Zhu

Overall survival in EGFR mutated non-small-cell lung cancer patients treated with afatinib after EGFR TKI and resistant mechanisms upon disease progression

A. J. van der Wekken, J. L. Kuiper, [ ... ], H. J. M. Groen

Prominent features of the amino acid mutation landscape in cancer

Zachary A. Szpiech, Nicolas B. Strauli, [ ... ], Ryan D. Hernandez

MEFV M694V mutation has a role in susceptibility to ankylosing spondylitis: A meta-analysis

Linqing Zhong, Hongmei Song, [ ... ], Mingsheng Ma

DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis

Xiangyi Liu, Lipeng Yang, [ ... ], Dongsheng Fan

DNA mutation motifs in the genes associated with inherited diseases

Michal Růžička, Petr Kulhánek, [ ... ], Kamila Réblová

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia

Joel Fedida, Veronique Fressart, [ ... ], Estelle Gandjbakhch

Targeted next-generation sequencing detects novel gene–phenotype associations and expands the mutational spectrum in cardiomyopathies

Cinzia Forleo, Anna Maria D’Erchia, [ ... ], Stefano Favale

Evaluation of K-ras and p53 expression in pancreatic adenocarcinoma using the cancer genome atlas

Liming Lu, Jingchun Zeng

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