Publications by authors named "John Old"

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Eleven Cases of Hb J-Paris-I [: c.38C>A (or )]: A Stable α Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography.
Mohamed S M Khalil, Adele T Timbs, Shirley J Henderson, Anna Schuh, John M Old

Hemoglobin· September 2021

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Eight Cases of Hb Winnipeg [: c.226G>T (or )]: A Detailed Study.
Mohamed S M Khalil, Adele T Timbs, Shirley J Henderson, Anna Schuh, John M Old

Hemoglobin· July 2021

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Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression.
Mohamed S M Khalil, Adele T Timbs, Shirley J Henderson, Anna Schuh, John M Old

Hemoglobin· November 2020

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Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or : c.-24C>G (or ) Variants.
Mohamed S M Khalil, Adele T Timbs, Shirley J Henderson, Anna Schuh, John M Old

Hemoglobin· September 2020

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A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.
Mohamed S M Khalil, Adele T Timbs, Shirley J Henderson, Anna Schuh, Mohamed M El-Khawanky, John M Old

Hemoglobin· May 2020

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Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Shirley J Henderson, Adele T Timbs, Janice McCarthy, Alice E Gallienne, Melanie Proven, John M Old

Hemoglobin· December 2016

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Characterization of Hb Lepore variants in the UK population.
Lina Guo, Anika Kausar, John M Old, Shirley J Henderson, Alice E Gallienne

Hemoglobin· September 2015

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EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello

Eur J Hum Genet· April 2015

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IthaGenes: an interactive database for haemoglobin variations and epidemiology.
Petros Kountouris, Carsten W Lederer, Pavlos Fanis, Xenia Feleki, John Old

PLoS One· April 2015

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EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello

Eur J Hum Genet· April 2015

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A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.
Mohamed S M Khalil, Samy Marouf, David Element, Adele Timbs, Alice Gallienne, John M Old

Hemoglobin· February 2015

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Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping.
Adele T Timbs, Michelle J Rugless, Alice E Gallienne, Anna M Haywood, Shirley J Henderson, John M Old

Hemoglobin· December 2012

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Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults.
Alice E Gallienne, Hélène M P Dréau, Anna Schuh, John M Old, Shirley Henderson

Haematologica· March 2012

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Belinda Giardine, Joseph Borg, Douglas R Higgs, Kenneth R Peterson, Sjaak Philipsen, John Old

Nat Genet· March 2011

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Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.
Anna Haywood, Helene Dreau, Adele Timbs, Anna Schuh, John Old

Ann Hematol· December 2010

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Neonatal screening for hemoglobinopathies: results of a public health system in South Brazil.
Sandrine C Wagner, Simone M de Castro, Tatiana P Gonzalez, Ana Paula Santin, Carina F Zaleski, John Old

Genet Test Mol Biomarkers· August 2010

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Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
Alice E Gallienne, Nicola M Iberson, Hélène M Dréau, Helen Jackson, Patricia A Bignell, John M Old

Hemoglobin· May 2010

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Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
Rasoul Salehi, Christopher A Fisher, Patricia A Bignell, Gilda Eslami, John M Old

Hemoglobin· May 2010

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Molecular diagnostics for haemoglobinopathies.
John Old, Shirley Henderson

Expert Opin Med Diagn· May 2010

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Multiplex ligation-dependent probe amplification identification of 17 different beta-globin gene deletions (including four novel mutations) in the UK population.
Alice E Gallienne, Hélène M Dréau, Janice McCarthy, Adele T Timbs, Janet M Hampson, John M Old

Hemoglobin· March 2010

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An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
Carsten W Lederer, A Nazli Basak, Yesim Aydinok, Soteroula Christou, Amal El-Beshlawy, John Old

Hemoglobin· February 2010

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Incidence of haemoglobinopathies in various populations - the impact of immigration.
Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, John Old

Clin Biochem· December 2009

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The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position.
Mohamed S Khalil, Adele T Molyneux, Samy Marouf, Ghazy A Eldamanhory, Anna H Schuh, John M Old

Saudi Med J· September 2009

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Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.
Kamran Moradkhani, Claude Préhu, John Old, Shirley Henderson, Vera Balamitsa

Ann Hematol· June 2009

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