ISSN: 2210-7762

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Cancer genetics Q3 Unclaimed

Elsevier BV Netherlands

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Cancer genetics is a journal indexed in SJR in Molecular Biology and Genetics with an H index of 50. It has an SJR impact factor of 0,614 and it has a best quartile of Q3. It has an SJR impact factor of 0,614.

Type: Journal

Type of Copyright:

Languages:

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Cancer Research (Q3) Genetics (Q3) Molecular Biology (Q3)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,614

SJR Impact factor

50

H Index

77

Total Docs (Last Year)

223

Total Docs (3 years)

2774

Total Refs

434

Total Cites (3 years)

218

Citable Docs (3 years)

1.85

Cites/Doc (2 years)

36.03

Ref/Doc

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Aims and Scope

Best articles by citations

Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules

A translocation t(6;14) in two cases of leiomyosarcoma: Molecular cytogenetic and array-based comparative genomic hybridization characterization

Molecular targeted therapy for pancreatic adenocarcinoma: A review of completed and ongoing late phase clinical trials

An asbestos-exposed family with multiple cases of pleural malignant mesothelioma without inheritance of a predisposing BAP1 mutation

Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML

Whole Genome Copy Number Analysis of Formalin Fixed Paraffin Embedded Samples Identifies Major Genomic Aberrations in Medulloblastoma

Implementation and Routine Clinical Use of the TruSight Myeloid Sequencing Panel in Patients with Myeloid Malignancies

Clinical Validation and Implementation of a Targeted Sequencing Panel for Predisposition to Inherited Cancer

Secondary Philadelphia chromosome and erythrophagocytosis in a relapsed acute myeloid leukemia after hematopoietic cell transplantation

Petabyte-Scale Cancer Genomics in the Cloud

Recurrent Genetic Alterations in Hepatitis C-Associated Hepatocellular Carcinoma Detected by Genomic Microarray and Their correlation with Histology and Clinical Outcome

Cryptic insertion of 3'FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcoma

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Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR

Molecular Characterization of WNT5B as a Candidate Gene for Developmental Delay Associated with 12p13.13 Microdeletions

Homozygous losses detected by array comparative genomic hybridization in multiplex urothelial carcinomas of the bladder

Molecular profiling of gynecologic cancers for treatment and management of disease -demonstrating clinical significance using the AMP/ASCO/CAP guidelines for interpretation and reporting of somatic variants

Identification of the TAF15-ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12)

Enrichment of atypical hyperdiploidy and IKZF1 deletions detected by SNP-microarray in high-risk Australian AIEOP-BFM B-cell acute lymphoblastic leukaemia cohort

Acute promyelocytic leukemia with isochromosome 17q and cryptic PML-RARA successfully treated with all-trans retinoic acid and arsenic trioxide

Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia

Genome-Wide Microarray Analysis Improves Routine Diagnosis of Hematological Malignancies

Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations

Identification of gene modules and hub genes in colon adenocarcinoma associated with pathological stage based on WGCNA analysis

Multiple Segmental Chromosomal Aberrations in Low-Risk Neuroblastoma are Associated with Metastatic Relapse