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First Trimester Noninvasive Prenatal Diagnosis of Maternally Inherited Beta-Thalassemia Mutations

Clinical chemistry (Baltimore, Md.), 2022-07, Vol.68 (8), p.1002-1004

Madgett, Tracey E

2022

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Graphene electrode modified with electrochemically reduced graphene oxide for label-free DNA detection

Biosensors & bioelectronics, 2015-10, Vol.72, p.313-319

2015

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Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle

Clinical chemistry (Baltimore, Md.), 2022-09, Vol.68 (9), p.1196-1201

2022

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The SAFE project: towards non-invasive prenatal diagnosis

Biochemical Society transactions, 2009-04, Vol.37 (Pt 2), p.460-465

2009

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Fetal Sex and RHD Genotyping with Digital PCR Demonstrates Greater Sensitivity than Real-time PCR

Clinical chemistry (Baltimore, Md.), 2015-11, Vol.61 (11), p.1399-1407

2015

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2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome

Proteome science, 2011-09, Vol.9 (1), p.56-56, Article 56

2011

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4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Haematologica (Roma), 2009-10, Vol.94 (10), p.1354-1361

2009

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Complete RHD next-generation sequencing: establishment of reference RHD alleles

Blood advances, 2018-10, Vol.2 (20), p.2713-2723

2018

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Rapid RHD Zygosity Determination Using Digital PCR

Clinical chemistry (Baltimore, Md.), 2017-08, Vol.63 (8), p.1388-1397

2017

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RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification

Transfusion (Philadelphia, Pa.), 2013-07, Vol.53 (7), p.1559-1574

2013

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Non-Invasive Screening Tools for Down's Syndrome: A Review

Diagnostics (Basel), 2013-05, Vol.3 (2), p.291-314

2013

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Next-generation sequencing of 35 RHD variants in 16 253 serologically D− pregnant women in the Finnish population

Blood advances, 2020-10, Vol.4 (20), p.4994-5001

2020

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The Bloodgen Project of the European Union, 2003–2009

Transfusion medicine and hemotherapy, 2009-01, Vol.36 (3), p.162-167

2009

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The development of a peptide SRM-based tandem mass spectrometry assay for prenatal screening of Down syndrome

Journal of proteomics, 2012-06, Vol.75 (11), p.3248-3257

2012

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Identification of new biomarkers for Down's syndrome in maternal plasma

Journal of proteomics, 2012-05, Vol.75 (9), p.2621-2628

2012

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The BloodGen project: toward mass-scale comprehensive genotyping of blood donors in the European Union and beyond

Transfusion (Philadelphia, PA), 2007-07, Vol.47 (s1), p.40S-46S

2007

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Post-genomics studies and their application to non-invasive prenatal diagnosis

Seminars in fetal & neonatal medicine, 2008-04, Vol.13 (2), p.91-98

2008

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Cell-free fetal DNA in the maternal serum and plasma: current and evolving applications

Current opinion in obstetrics & gynecology, 2009-04, Vol.21 (2), p.175-179

2009

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Molecular biology of Rh proteins and relevance to molecular medicine

Expert reviews in molecular medicine, 2006-06, Vol.8 (13), p.1-20

2006

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RHD molecular analysis—from discovery to next generation sequencing

Annals of Blood, 2023-12, Vol.8, p.36-36

2023

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4.1R-deficient human red blood cells have altered phosphatidyiserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Haematologica (Roma), 2009, Vol.94 (10), p.1354-1361

2009

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First Trimester Noninvasive Prenatal Diagnosis of Maternally Inherited Beta-Thalassemia Mutations

Graphene electrode modified with electrochemically reduced graphene oxide for label-free DNA detection

Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle

The SAFE project: towards non-invasive prenatal diagnosis

Fetal Sex and RHD Genotyping with Digital PCR Demonstrates Greater Sensitivity than Real-time PCR

2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome

4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Complete RHD next-generation sequencing: establishment of reference RHD alleles

Rapid RHD Zygosity Determination Using Digital PCR

RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification

Non-Invasive Screening Tools for Down's Syndrome: A Review

Next-generation sequencing of 35 RHD variants in 16 253 serologically D− pregnant women in the Finnish population

The Bloodgen Project of the European Union, 2003–2009

The development of a peptide SRM-based tandem mass spectrometry assay for prenatal screening of Down syndrome

Identification of new biomarkers for Down's syndrome in maternal plasma

The BloodGen project: toward mass-scale comprehensive genotyping of blood donors in the European Union and beyond

Post-genomics studies and their application to non-invasive prenatal diagnosis

Cell-free fetal DNA in the maternal serum and plasma: current and evolving applications

Molecular biology of Rh proteins and relevance to molecular medicine

RHD molecular analysis—from discovery to next generation sequencing

4.1R-deficient human red blood cells have altered phosphatidyiserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

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