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Nicole Thornton

8PUBLICATIONS
52CO-AUTHORS
Immunogenetics (incl. genetic immunology)Electroanalytical chemistryAutonomic nervous systemMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)
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Journal

Publications (8)

Sort by Publication Date:
|Jun 24, 2026
Survey of national and regional rare donor programmes regarding Immunoglobulin A deficiency.

|Jan 20, 2026
cDNA sequencing reveals an unexpected splice variation leading to weak KEL2 expression.

Bernd Schimanski, Sofia Lejon Crottet, Rahel Kräuchi

|Feb 17, 2025
Homozygosity for a novel A4GALT allele resulting in the rare p phenotype in an Indian blood donor.

Louise A Tilley, Vanja Karamatic Crew, Amy Tearle

|Aug 19, 2024
Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype.

Louise A Tilley, Vanja Karamatic Crew, Tosti J Mankelow

|Sep 19, 2022
Missense mutations in PIEZO1, which encodes the Piezo1 mechanosensor protein, define Er red blood cell antigens.

Vanja Karamatic Crew, Louise A Tilley, Timothy J Satchwell

|Mar 12, 2022
Basement membrane defects in CD151-associated glomerular disease.

Richard W Naylor, Elizabeth Watson, Samantha Williamson

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Frequent Collaborators

5 joint publications

Vanja Karamatic Crew

3 joint publications

Louise A Tilley

2 joint publications

Timothy J Satchwell

2 joint publications

Ashley M Toye

1 joint publications

Nicoletta Murciano

1 joint publications

Mark D Kilby

1 joint publications

Markus Rapedius

1 joint publications

Tosti J Mankelow

1 joint publications

Vered Yahalom

1 joint publications

Suvro Sankha Datta

Frequent Collaborators

5 joint publications

Vanja Karamatic Crew

3 joint publications

Louise A Tilley

2 joint publications

Timothy J Satchwell

2 joint publications

Ashley M Toye