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An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy.
Dixon PH, Sambrotta M, Chambers J, Taylor-Harris P, Syngelaki A, Nicolaides K, Knisely AS, Thompson RJ, Williamson C.
Sci Rep 2017;7:11823. pdf -
Prognostic and mechanistic potential of progesterone sulfates in intrahepatic cholestasis of pregnancy and pruritus gravidarum.
Abu-Hayyeh S, Ovadia C, Lieu T, Jensen DD, Chambers J, Dixon PH, Lövgren-Sandblom A, Bolier R, Tolenaars D, Kremer AE, Syngelaki A, Noori M, Williams D, Marin JJ, Monte MJ, Nicolaides KH, Beuers U, Oude-Elferink R, Seed PT, Chappell L, Marschall HU, Bunnett NW.
Hepatology 2016;63:1287-98. pdf -
Embryo-fetal erythroid cell selection from celomic fluid allows earlier prenatal diagnosis of hemoglobinopathies.
Giambona A, Damiani G, Leto F, Jakil C, Renda D, Cigna V, Schillaci G, Picciotto F, Nicolaides KH, Passarello C, Makrydimas G, Maggio A.
Prenat Diagn 2016;36:375-81. pdf -
Maternal and pregnancy characteristics affect plasma fibrin monomer complexes and D-dimer reference ranges for venous thromboembolism in pregnancy.
Grossman KB, Arya R, Peixoto AB, Akolekar R, Staboulidou I, Nicolaides KH.
Am J Obstet Gynecol 2016;215:466.e1-8. pdf -
A comprehensive analysis of common genetic variation around six candidate loci for intrahepatic cholestasis of pregnancy.
Dixon PH, Wadsworth CA, Chambers J, Donnelly J, Cooley S, Buckley R, Mannino R, Jarvis S, Syngelaki A, Geenes V, Paul P, Sothinathan M, Kubitz R, Lammert F, Tribe RM, Ch'ng CL, Marschall HU0, Glantz A, Khan SA, Nicolaides K, Whittaker J, Geary M, Williamson C.
Am J Gastroenterol 2014;109:76-84. pdf -
Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis.
Giambona A, Makrydimas G, Leto F, Damiani G, Jakil MC, Picciotto F, Renda D, Fiorino R, Renda MC, Schillaci G, Gueli-Alletti D, Nicolaides KH, Maggio A.
Br J Haematol 2011;153:268-72. -
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variation.
Gerovassili A, Nicolaides KH, Thein SL, Rees DC.
Br J Haematol 2006;135:738-41. -
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS alpha2gammabetaS) in sickle cell disease.
Ofori-Acquah SF, Green BN, Davies SC, Nicolaides KH, Serjeant GR, Layton DM.
Anal Biochem 2001;298:76-82. -
Audit of prenatal diagnosis for hemoglobin disorders in the United Kingdom The first twenty years.
Modell B, Petrou M, Layton M, Varnavides L, Moisely C, Ward RH, Rodeck C, Nicolaides K, Fitches A, Old J.
Ann N Y Acad Sci 1998;850:420-2. -
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: The first 20 years.
Modell B, Petrou M, Layton M, Varnavides L, Slater C, Ward R H, Rodeck C, Nicolaides KH, Gibbons S, Fitches A, Old J.
BMJ 1997;315:779-84.