Screening for trisomy 21 in monochorionic twins by measurement of fetal nuchal translucency thickness von Vandecruys, H., Faiola, S., Auer, M., Sebire, N., Nicolaides, K. H.

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Analysis of cell‐free DNA in maternal blood in screening for fetal aneuploidies: updated meta‐analysis von Gil, M. M., Quezada, M. S., Revello, R., Akolekar, R., Nicolaides, K. H.

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Large loop excision of transformation zone and cervical length in the prediction of spontaneous preterm delivery von Poon, LCY, Savvas, M, Zamblera, D, Skyfta, E, Nicolaides, KH

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Prevention of perinatal death and adverse perinatal outcome using low‐dose aspirin: a meta‐analysis von Roberge, S., Nicolaides, K. H., Demers, S., Villa, P., Bujold, E.

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Screening for trisomies by cell‐free DNA testing of maternal blood: consequences of a failed result von Revello, R., Sarno, L., Ispas, A., Akolekar, R., Nicolaides, K. H.

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Fetal fraction in maternal plasma cell‐free DNA at 11–13 weeks' gestation: relation to maternal and fetal characteristics von Ashoor, G., Syngelaki, A., Poon, L. C. Y., Rezende, J. C., Nicolaides, K. H.

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Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities von Nicolaides, Kypros H.

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Serum placental growth factor in the three trimesters of pregnancy: effects of maternal characteristics and medical history von Tsiakkas, A., Duvdevani, N., Wright, A., Wright, D., Nicolaides, K. H.

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Birth weight in live births and stillbirths von Poon, L. C. Y., Tan, M. Y., Yerlikaya, G., Syngelaki, A., Nicolaides, K. H.

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Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y von Nicolaides, K. H., Syngelaki, A., Gil, M., Atanasova, V., Markova, D.

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Vaginal progesterone is as effective as cervical cerclage to prevent preterm birth in women with a singleton gestation, previous spontaneous preterm birth, and a short cervix: upda... von Conde-Agudelo, Agustin, Romero, Roberto, Da Fonseca, Eduardo, O’Brien, John M., Cetingoz, Elcin, Creasy, George W., Hassan, Sonia S., Erez, Offer, Pacora, Percy, Nicolaides, Kypros H.

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Prospective first‐trimester screening for trisomies by cell‐free DNA testing of maternal blood in twin pregnancy von Sarno, L., Revello, R., Hanson, E., Akolekar, R., Nicolaides, K. H.

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Clinical implementation of routine screening for fetal trisomies in the UK NHS: cell‐free DNA test contingent on results from first‐trimester combined test von Gil, M. M., Revello, R., Poon, L. C., Akolekar, R., Nicolaides, K. H.

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A unified approach to risk assessment for fetal aneuploidies von Wright, D., Wright, A., Nicolaides, K. H.

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Meta‐analysis of second‐trimester markers for trisomy 21 von Agathokleous, M., Chaveeva, P., Poon, L. C. Y., Kosinski, P., Nicolaides, K. H.

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Evaluation of the RCOG guideline for the prediction of neonates that are small for gestational age and comparison with the competing risks model von Papastefanou, I, Nowacka, U, Buerger, O, Akolekar, R, Wright, D, Nicolaides, KH

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First‐trimester contingent screening for trisomy 21 by biomarkers and maternal blood cell‐free DNA testing von Nicolaides, K. H., Wright, D., Poon, L. C., Syngelaki, A., Gil, M. M.

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Prediction of small‐for‐gestational‐age neonates: screening by fetal biometry at 30–34 weeks von Bakalis, S., Silva, M., Akolekar, R., Poon, L. C., Nicolaides, K. H.

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Implementation of maternal blood cell‐free DNA testing in early screening for aneuploidies von Gil, M. M., Quezada, M. S., Bregant, B., Ferraro, M., Nicolaides, K. H.

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Screening for trisomies 21, 18 and 13 by cell‐free DNA analysis of maternal blood at 10–11 weeks' gestation and the combined test at 11–13 weeks von Quezada, M. S., Gil, M. M., Francisco, C., Oròsz, G., Nicolaides, K. H.

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