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RH genotyping by nonspecific quantitative next‐generation sequencing

Transfusion (Philadelphia, Pa.), 2020-11, Vol.60 (11), p.2691-2701

2020

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Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles

Transfusion (Philadelphia, Pa.), 2023-12, Vol.63 (12), p.E59-E61

2023

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Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression

Transfusion (Philadelphia, Pa.), 2023-04, Vol.63 (4), p.E12-E14

2023

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Four novel ABOAW alleles associated with weak antigen expression

Transfusion (Philadelphia, Pa.), 2022-12, Vol.62 (12), p.E76-E78

2022

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An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype

Transfusion (Philadelphia, Pa.), 2022-02, Vol.62 (2), p.E14-E16

2022

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Novel KEL02N allele in Saudi Arabia encoding a Kell null (K0) phenotype

Transfusion (Philadelphia, Pa.), 2021-07, Vol.61 (7), p.E49-E50

2021

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A GYPB variant encoding an altered leader peptide leads to a weak S phenotype

Transfusion (Philadelphia, Pa.), 2019-07, Vol.59 (7), p.2461-2462

2019

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Two new RHD alleles with deletions spanning multiple exons

Transfusion (Philadelphia, Pa.), 2021-03, Vol.61 (3), p.682-686

2021

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Effect on gene expression of three allelic variants in GATA motifs of ABO, RHD, and RHCE regulatory elements

Transfusion (Philadelphia, Pa.), 2017-11, Vol.57 (11), p.2804-2808

2017

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The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families

Frontiers in neuroscience, 2024-09, Vol.18, p.1408105

2024

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Three new alleles encoding an apparent Kellnull phenotype

Transfusion (Philadelphia, Pa.), 2017-01, Vol.57 (1), p.221-222

2017

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FYA silencing by the GATA-motif variant FYA(−69C) in a Caucasian family

Transfusion (Philadelphia, Pa.), 2015-11, Vol.55 (11), p.2616-2619

2015

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Three novel Er blood group system alleles and insights from protein modeling

Transfusion (Philadelphia, Pa.), 2024-07, Vol.64 (9), p.1633-1639

2024

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Real-World Feasibility of RH Genotype-Matched Red Blood Cells for Chronically Transfused Patients with Sickle Cell Disease

Blood, 2023-11, Vol.142 (Supplement 1), p.1291-1291

2023

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Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies

Transfusion (Philadelphia, Pa.), 2016-06, Vol.56 (6), p.1413-1418

2016

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Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor

Transfusion (Philadelphia, Pa.), 2017-09, Vol.57 (9), p.2281-2283

2017

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New RHD variant alleles

Transfusion (Philadelphia, Pa.), 2015-02, Vol.55 (2), p.427-429

2015

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Three new alleles encoding an apparent Kell null phenotype

Transfusion (Philadelphia, Pa.), 2017-01, Vol.57 (1), p.221-222

2017

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New RHCE variant alleles encoding the D- - phenotype

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.3018-3023

2013

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Identification of six new RHCE variant alleles in individuals of diverse racial origin

Transfusion (Philadelphia, Pa.), 2016-01, Vol.56 (1), p.244-248

2016

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Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping

Prenatal diagnosis, 2014-01, Vol.34 (1), p.56-62

2014

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Rh-null phenotype caused by a complete RHAG deletion

Transfusion (Philadelphia, Pa.), 2015-01, Vol.55 (1), p.197-198

2015

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DNA Reference Reagents for Genotyping RH Variants

The Journal of molecular diagnostics : JMD, 2024-06, Vol.26 (6), p.456-466

2024

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Resolving variable maternal D typing using serology and genotyping in selected prenatal patients

Transfusion (Philadelphia, Pa.), 2016-12, Vol.56 (12), p.2980-2985

2016

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Gene expression patterns related to osteogenic differentiation of bone marrow-derived mesenchymal stem cells during ex vivo expansion

Tissue engineering. Part C, Methods, 2010-06, Vol.16 (3), p.511-524

2010

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Sequence Analysis, Dna
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RH genotyping by nonspecific quantitative next‐generation sequencing

Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles

Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression

Four novel ABOAW alleles associated with weak antigen expression

An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype

Novel KEL02N allele in Saudi Arabia encoding a Kell null (K0) phenotype

A GYPB variant encoding an altered leader peptide leads to a weak S phenotype

Two new RHD alleles with deletions spanning multiple exons

Effect on gene expression of three allelic variants in GATA motifs of ABO, RHD, and RHCE regulatory elements

The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families

Three new alleles encoding an apparent Kellnull phenotype

FYA silencing by the GATA-motif variant FYA(−69C) in a Caucasian family

Three novel Er blood group system alleles and insights from protein modeling

Real-World Feasibility of RH Genotype-Matched Red Blood Cells for Chronically Transfused Patients with Sickle Cell Disease

Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies

Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor

New RHD variant alleles

Three new alleles encoding an apparent Kell null phenotype

New RHCE variant alleles encoding the D- - phenotype

Identification of six new RHCE variant alleles in individuals of diverse racial origin

Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping

Rh-null phenotype caused by a complete RHAG deletion

DNA Reference Reagents for Genotyping RH Variants

Resolving variable maternal D typing using serology and genotyping in selected prenatal patients

Gene expression patterns related to osteogenic differentiation of bone marrow-derived mesenchymal stem cells during ex vivo expansion

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