Articles published in Hereditary Genetics: Current Research have been cited by esteemed scholars and scientists all around the world. Hereditary Genetics: Current Research has got h-index 9, which means every article in Hereditary Genetics: Current Research has got 9 average citations.

Following are the list of articles that have cited the articles published in Hereditary Genetics: Current Research.

  2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012

Total published articles

10 41 30 10 11 2 6 16 20 27 20 27 17

Research, Review articles and Editorials

0 2 0 1 1 2 6 13 14 12 12 16 12

Research communications, Review communications, Editorial communications, Case reports and Commentary

10 39 30 9 10 0 0 3 6 15 8 11 5

Conference proceedings

0 0 5 8 0 0 58 0 0 0 0 0 0

Citations received as per Google Scholar, other indexing platforms and portals

18 33 84 62 43 38 47 48 90 28 17 11 2
Journal total citations count 534
Journal impact factor 1.42
Journal 5 years impact factor 2.34
Journal cite score 6.18
Journal h-index 9
Important citations

Formation and Resolution of Pial Microvascular Thrombosis in a Mouse Model of Thrombotic Thrombocytopenic Purpura

Reduced ADAMTS-13 level negatively correlates with inflammation factors in plasma of acute myeloid leukemia patients

Thrombotic Risks in Red Blood Cell Transfusions

Unconjugated bilirubin inhibits proteolytic cleavage of von Willebrand factor by ADAMTS13 protease

Tuning the endothelial response: differential release of exocytic cargos from Weibel-Palade bodies

 Division of Laboratory Medicine, Department of Pathology, The University of Alabama at Birmingham, WP-P230K, 619 19th Street South, Birmingham, AL, 35249, USA

Deep intronic variant c.5999-277G>A of F8 gene may be a hot spot mutation for mild hemophilia A patients without mutation in exonic DNA

Variant effect on splicing regulatory elements, branchpoint usage, and pseudoexonization: Strategies to enhance bioinformatic prediction using hereditary cancer genes as exemplars

Splicing mutations in human genetic disorders: examples, detection, and confirmation

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene

Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene