Nicole M. Thornton

Bristol, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 35 publications

Identification of a novel high-prevalence red blood cell antigen on junctional adhesion molecule-A defines a new blood group system.

Identification of a novel high-prevalence red blood cell antigen on junctional adhesion molecule-A defines a new blood group system.

Journal: Vox sanguinis
Published: June 17, 2026

Survey of national and regional rare donor programmes regarding Immunoglobulin A deficiency.

Survey of national and regional rare donor programmes regarding Immunoglobulin A deficiency.

Journal: Vox sanguinis
Published: February 07, 2026

cDNA sequencing reveals an unexpected splice variation leading to weak KEL2 expression.

cDNA sequencing reveals an unexpected splice variation leading to weak KEL2 expression.

Journal: Transfusion
Published: September 11, 2025

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Gothenburg, Barcelona and four virtual business meetings: Update on blood group systems.

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Gothenburg, Barcelona and four virtual business meetings: Update on blood group systems.

Journal: Vox sanguinis
Published: August 12, 2025

Transient suppression of high-prevalence Kell blood group antigens and concomitant development of a Kell-related antibody that appears to recognize a high-prevalence Kell antigen not previously defined.

Transient suppression of high-prevalence Kell blood group antigens and concomitant development of a Kell-related antibody that appears to recognize a high-prevalence Kell antigen not previously defined.

Journal: Immunohematology
Published: December 31, 2024

Homozygosity for a novel A4GALT allele resulting in the rare p phenotype in an Indian blood donor.

Homozygosity for a novel A4GALT allele resulting in the rare p phenotype in an Indian blood donor.

Journal: Vox sanguinis
Published: November 29, 2024

Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype.

Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype.

Journal: Blood
Published: April 22, 2024

Transfusion of incompatible blood to a patient with alloanti-Sc1.

Transfusion of incompatible blood to a patient with alloanti-Sc1.

Journal: Immunohematology
Published: July 05, 2023

The need for rare blood programs is real.

The need for rare blood programs is real.

Journal: Transfusion
Published: February 25, 2023

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems.

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems.

Journal: Vox sanguinis
Published: July 06, 2022

Missense mutations in PIEZO1, which encodes the Piezo1 mechanosensor protein, define Er red blood cell antigens.

Missense mutations in PIEZO1, which encodes the Piezo1 mechanosensor protein, define Er red blood cell antigens.

Journal: Blood
Published: March 30, 2022

A novel KEL c.1414-1G>T allele in a polish patient with anti-Ku antibody.

A novel KEL c.1414-1G>T allele in a polish patient with anti-Ku antibody.

Journal: Transfusion
Published: March 14, 2022
Showing 1-12 of 35

Last Updated: 09/26/2026