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Merschman, Jarret

0009-0009-5133-6800

A5129807671 | I1330342723

Mayo Clinic

Mayo Clinic

Citations 17

Characterisation of the Novel HLA‐A*03:535 Allele by Next Generation Sequencing and Oxford Nanopore Sequencing

HLA | May 22, 2026 | Volume: 107 | Issue: 5 | Pages: No page available

10.1111/tan.70761 | PMID 42170734

ABSTRACT The novel HLA‐A*03:535 allele is characterised by a single nucleotide substitution in exon 1.
Characterisation of the Novel HLA‐DQB1*03:609 Allele by Next Generation Sequencing

HLA | May 15, 2026 | Volume: 107 | Issue: 5 | Pages: No page available

10.1111/tan.70752 | PMID 42138570

ABSTRACT HLA‐DQB1*03:609 is characterised by a single nucleotide substitution in codon 132 in exon 3.
Genomic Confirmation of HLA‐C*12:68 by Next Generation Sequencing

HLA | May 6, 2026 | Volume: 107 | Issue: 5 | Pages: No page available

10.1111/tan.70740 | PMID 42089409

ABSTRACT HLA‐C*12:68 is characterised by a single nucleotide substitution in codon 62 in exon 2.
Genomic Confirmation of HLA‐B*47:14 by Next Generation Sequencing

HLA | May 5, 2026 | Volume: 107 | Issue: 5 | Pages: No page available

10.1111/tan.70737 | PMID 42083306

ABSTRACT HLA‐B*47:14 is characterised by a single nucleotide substitution in codon 97 of exon 3.
Genomic Confirmation of HLA‐DQB1*03:506:01:01 , by Next Generation Sequencing

HLA | April 21, 2026 | Volume: 107 | Issue: 4 | Pages: No page available

10.1111/tan.70726 | PMID 42059316

ABSTRACT The HLA‐DQB1*03:506:01:01 allele is characterised by a single nucleotide substitution in codon 130 in exon 3.
Genomic Confirmation of HLA‐C*14:84 , by Next Generation Sequencing

HLA | April 20, 2026 | Volume: 107 | Issue: 4 | Pages: No page available

10.1111/tan.70733 | PMID 42007826

ABSTRACT The HLA‐C*14:84 allele is characterised by a single nucleotide substitution in codon 181 in exon 3.
Genomic Extension of HLA‐C*03:31 , by Next‐Generation Sequencing

HLA | March 18, 2026 | Volume: 107 | Issue: 3 | Pages: No page available

10.1111/tan.70655 | PMID 41847913

ABSTRACT The HLA‐C*03:31 allele is characterised by a nucleotide substitution at genomic DNA position 400 in exon 2.