Works by Felice, Alex E.

Results: 13

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.

Published in:

Nature Genetics, 2011, v. 43, n. 4, p. 295, doi. 10.1038/ng.785

By:

Giardine, Belinda;
Borg, Joseph;
Higgs, Douglas R.;
Peterson, Kenneth R.;
Philipsen, Sjaak;
Maglott, Donna;
Singleton, Belinda K.;
Anstee, David J.;
Basak, A. Nazli;
Clark, Barnaby;
Costa, Flavia C.;
Faustino, Paula;
Fedosyuk, Halyna;
Felice, Alex E.;
Francina, Alain;
Galanello, Renzo;
Gallivan, Monica V. E.;
Georgitsi, Marianthi;
Gibbons, Richard J.;
Giordano, Piero C.

Publication type:

Article

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.

Published in:

Nature Genetics, 2010, v. 42, n. 9, p. 801, doi. 10.1038/ng.630

By:

Borg, Joseph;
Papadopoulos, Petros;
Georgitsi, Marianthi;
Gutiérrez, Laura;
Grech, Godfrey;
Fanis, Pavlos;
Phylactides, Marios;
Verkerk, Annemieke J. M. H.;
van der Spek, Peter J.;
Scerri, Christian A.;
Cassar, Wilhelmina;
Galdies, Ruth;
van IJcken, Wilfred;
Özgür, Zeliha;
Gillemans, Nynke;
Hou, Jun;
Bugeja, Marisa;
Grosveld, Frank G.;
von Lindern, Marieke;
Felice, Alex E.

Publication type:

Article

Novel Polymorphisms Influencing Transcription of the Human CHRM2 Gene in Airway Smooth Muscle.

Published in:

American Journal of Respiratory Cell & Molecular Biology, 2004, v. 30, n. 5, p. 678, doi. 10.1165/rcmb.2003-0011OC

By:

Fenech, Anthony G.;
Billington, Charlotte K.;
Swan, Caroline;
Richards, Susan;
Hunter, Therese;
Ebejer, Martin J.;
Felice, Alex E.;
Ellul-Micallef, Roger;
Hall, Ian P.

Publication type:

Article

Treatment of leg ulcers with platelet-derived wound healing factor (pdwhfs) in a patient with beta thalassaemia intermedia.

Published in:

British Journal of Haematology, 2001, v. 112, n. 2, p. 528, doi. 10.1046/j.1365-2141.2001.02540-2.x

By:

Josifova, Dragana;
Gatt, Gabriella;
Aquilina, Alex;
Serafimov V, Viktor;
Vella, Adrian;
Felice, Alex E.

Publication type:

Article

Two new missense mutations (P134T and A244V) in the coagulation factor VII gene.

Published in:

Human Mutation, 1998, v. 11, p. S189, doi. 10.1002/humu.1380110161

By:

Alshinawi, Connie;
Scerri, Christian;
Galdies, Ruth;
Aquilina, Alex;
Felice, Alex E.

Publication type:

Article

A Twenty-Five Year Prospective Clinical Review and Family Studies Revealed New Globin Gene Regulators for Hb F Induction.

Published in:

2019

By:

Felice, Alex E.;
Borg, Joseph J.;
Grech, Laura;
Scerri, Christian A.;
Galdies, Ruth;
Philipsen, Sjaak

Publication type:

Abstract

Hb Valletta [β87(F3)Thr→Pro] and Hb Marseille/Long Island [β2(NA2)His→Pro; (–1)Met-(+1)Val-(+2)Pro-Leu], in a Unique Compound Heterozygote with a Normal Hemoglobin Phenotype.

Published in:

Hemoglobin, 2010, v. 34, n. 2, p. 169, doi. 10.3109/03630261003673675

By:

Galdies, Ruth;
Cassar, Wilhelmina;
Pizzuto, Monica;
Scerri, Christian A.;
Felice, Nicholas;
Cassar, Olivianne A.;
Buttigieg, George;
Felice, Alex E.

Publication type:

Article

An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project.

Published in:

Hemoglobin, 2009, v. 33, n. 3/4, p. 163, doi. 10.1080/03630260903089177

By:

Lederer, Carsten W.;
Basak, A. Nazli;
Aydinok, Yesim;
Christou, Soteroula;
El-Beshlawy, Amal;
Eleftheriou, Androulla;
Fattoum, Slaheddine;
Felice, Alex E.;
Fibach, Eitan;
Galanello, Renzo;
Gambari, Roberto;
Gavrila, Lucian;
Giordano, Piero C.;
Grosveld, Frank;
Hassapopoulou, Helen;
Hladka, Eva;
Kanavakis, Emmanuel;
Locatelli, Franco;
Old, John;
Patrinos, George P.

Publication type:

Article

A Review of Cis-Trans Interplay Between DNA Sequences 5' to the Gγ- and β-Globin Genes Among Hb F-Malta-I Heterozygotes/Homozygotes and β-Thalassemia Homozygotes/Compound Heterozygotes, and the Effects of Hydroxyurea on the Hb F/F-Erythrocyte; the Need for Large Multicenter Trials

Published in:

Hemoglobin, 2007, v. 31, n. 2, p. 279, doi. 10.1080/03630260701297261

By:

Felice, Alex E.;
Borg, Joseph;
Pizzuto, Monica;
Cassar, Wilhelmina;
Galdies, Ruth;
Bezzina Wettinger, Stephanie;
Pulis, Svetlana;
Hunter, Gary J.;
Caruana, Mary R.;
Farrugia, Mario;
Scerri, Christian A.

Publication type:

Article

Developmental Effect of the XmnI Site on Gγ-Globin Gene Expression Among Newborn Hb F-Malta-I [Gγ117(G19)Hi(s)→Arg, CA(T)→CGT] Heterozygotes and Adult β -Thalassemia Homozygotes.

Published in:

Hemoglobin, 2007, v. 31, n. 1, p. 71, doi. 10.1080/03630260601057187

By:

Pulis, Svetlana;
Scerri, Christian A.;
Schembri Wismayer, Pierre;
Galdies, Ruth;
Bezzina Wettinger, Stephanie;
Felice, Alex E.

Publication type:

Article

Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04126-6

By:

Heshusius, Steven;
Grech, Laura;
Gillemans, Nynke;
Brouwer, Rutger W. W.;
den Dekker, Xander T.;
van IJcken, Wilfred F. J.;
Nota, Benjamin;
Felice, Alex E.;
van Dijk, Thamar B.;
von Lindern, Marieke;
Borg, Joseph;
van den Akker, Emile;
Philipsen, Sjaak

Publication type:

Article

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Published in:

Human Mutation, 2011, v. 32, n. 1, p. 2, doi. 10.1002/humu.21397

By:

Patrinos, George P.;
Al Aama, Jumana;
Al Aqeel, Aida;
Al-Mulla, Fahd;
Borg, Joseph;
Devereux, Andrew;
Felice, Alex E.;
Macrae, Finlay;
Marafie, Makia J.;
Petersen, Michael B.;
Qi, Ming;
Ramesar, Rajkumar S.;
Zlotogora, Joel;
Cotton, Richard G.H.

Publication type:

Article

Genetic causes of Parkinson's disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR.

Published in:

BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0327-x

By:

Zahra, Charmaine;
Tabone, Christine;
Camilleri, Graziella;
Felice, Alex E.;
Farrugia, Rosienne;
Wettinger, Stephanie Bezzina

Publication type:

Article