Daniel B Bellissimo
Overview
Explore the profile of Daniel B Bellissimo including associated specialties, affiliations and a list of published articles.
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17
Citations
799
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Recent Articles
1.
Deignan J, Aggarwal V, Bale A, Bellissimo D, Booker J, Cao Y, et al.
Genet Med Open
. 2024 Aug;
2.
PMID: 39175871
Purpose: The specialty of Laboratory Genetics and Genomics (LGG) was created in 2017 in an effort to reflect the increasing convergence in technologies and approaches between clinical molecular genetics and...
2.
Sadler B, Christopherson P, Perry C, Bellissimo D, Haberichter S, Haller G, et al.
Res Pract Thromb Haemost
. 2023 Dec;
7(7):102232.
PMID: 38077814
Background: Genetic analysis for von Willebrand disease (VWD) commonly utilizes DNA sequencing to identify variants in the von Willebrand factor () gene; however, this technique cannot always detect copy-number variants...
3.
Christopherson P, Haberichter S, Flood V, Perry C, Sadler B, Bellissimo D, et al.
J Thromb Haemost
. 2022 Mar;
20(7):1576-1588.
PMID: 35343054
Background: Type 3 von Willebrand Disease (VWD) is a rare and severe form of VWD characterized by the absence of von Willebrand factor (VWF). Objectives: As part of the Zimmerman...
4.
Megy K, Downes K, Simeoni I, Bury L, Morales J, Mapeta R, et al.
J Thromb Haemost
. 2019 Jun;
17(8):1253-1260.
PMID: 31179617
No abstract available.
5.
Flood V, Johnsen J, Kochelek C, Slobodianuk T, Christopherson P, Haberichter S, et al.
Res Pract Thromb Haemost
. 2018 Jul;
2(2):390-398.
PMID: 30046743
Background: Genetic variation in the gene is associated with von Willebrand factor (VWF) and factor VIII (FVIII) levels in healthy individuals. Objectives: We hypothesized that sequence variants associated with higher...
6.
Simeoni I, Stephens J, Hu F, Deevi S, Megy K, Bariana T, et al.
Blood
. 2016 Apr;
127(23):2791-803.
PMID: 27084890
Inherited bleeding, thrombotic, and platelet disorders (BPDs) are diseases that affect ∼300 individuals per million births. With the exception of hemophilia and von Willebrand disease patients, a molecular analysis for...
7.
Flood V, Christopherson P, Gill J, Friedman K, Haberichter S, Bellissimo D, et al.
Blood
. 2016 Feb;
127(20):2481-8.
PMID: 26862110
von Willebrand disease (VWD) is the most common inherited bleeding disorder, and type 1 VWD is the most common VWD variant. Despite its frequency, diagnosis of type 1 VWD remains...
8.
Flood V, Schlauderaff A, Haberichter S, Slobodianuk T, Jacobi P, Bellissimo D, et al.
Blood
. 2015 Feb;
125(14):2297-304.
PMID: 25662333
Von Willebrand factor (VWF) contains binding sites for platelets and for vascular collagens to facilitate clot formation at sites of injury. Although previous work has shown that VWF can bind...
9.
Bellissimo D, Christopherson P, Flood V, Gill J, Friedman K, Haberichter S, et al.
Blood
. 2011 Dec;
119(9):2135-40.
PMID: 22197721
Diagnosis and classification of VWD is aided by molecular analysis of the VWF gene. Because VWF polymorphisms have not been fully characterized, we performed VWF laboratory testing and gene sequencing...
10.
Flood V, Gill J, Friedman K, Bellissimo D, Haberichter S, Montgomery R
Semin Thromb Hemost
. 2011 Nov;
37(5):528-34.
PMID: 22102196
Von Willebrand disease (VWD) is a common bleeding disorder with prevalence in the United States of 0.01 to 1% and a prevalence in the region around Milwaukee, Wisconsin, of at...