Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y von Benn, P.

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Non‐invasive prenatal testing for aneuploidy: current status and future prospects von Benn, P., Cuckle, H., Pergament, E.

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Rare autosomal trisomies: comparison of detection through cell‐free DNA analysis and direct chromosome preparation of chorionic villus samples von Benn, P., Malvestiti, F., Grimi, B., Maggi, F., Simoni, G., Grati, F. R.

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Genome‐wide non‐invasive prenatal screening for all cytogenetically visible imbalances von Benn, P., Grati, F. R.

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Re: Non‐invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146 958 pregnancies. H. Zhang, Y. Gao, F. Jiang, M. Fu, Y. Yuan, Y. Guo, Z. Zhu, M. Lin, Q.... von Benn, P.

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Clinical experience with non‐invasive prenatal screening for single‐gene disorders von Mohan, P., Lemoine, J., Trotter, C., Rakova, I., Billings, P., Peacock, S., Kao, C.‐Y., Wang, Y., Xia, F., Eng, C. M., Benn, P.

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OC17.03: Correlation of SNP‐based prenatal cfDNA and clinical findings of a complete mole with a coexisting fetus von Hashimoto, K., Souter, V., Dhamankar, R., Kijacic, D., Xu, W., Benn, P.

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VP08.02: Noonan syndrome screening by non‐invasive prenatal testing for single‐gene disorders von Benn, P., Mohan, P., Krinshpun, S., Lemoine, J.

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Clinical experience with a single‐nucleotide polymorphism‐based non‐invasive prenatal test for five clinically significant microdeletions von Martin, K., Iyengar, S., Kalyan, A., Lan, C., Simon, A.L., Stosic, M., Kobara, K., Ravi, H., Truong, T., Ryan, A., Demko, Z.P., Benn, P.

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Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome von Gross, S. J., Stosic, M., McDonald‐McGinn, D. M., Bassett, A. S., Norvez, A., Dhamankar, R., Kobara, K., Kirkizlar, E., Zimmermann, B., Wayham, N., Babiarz, J. E., Ryan, A., Jinnett, K. N., Demko, Z., Benn, P.

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Fetal fraction‐based risk algorithm for non‐invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell‐free fetal DNA von McKanna, T., Ryan, A., Krinshpun, S., Kareht, S., Marchand, K., Grabarits, C., Ali, M., McElheny, A., Gardiner, K., LeChien, K., Hsu, M., Saltzman, D., Stosic, M., Martin, K., Benn, P.

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Stop Routine CD4 Monitoring in HIV-Infected Patients With Fully Suppressed Virus and CD4 ≥350 Cells/mL von Whitlock, G. G., Ahmed, N., Edwards, P. Benn, S., Waters, L.

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The "3 in 1" Study: Pooling Self-Taken Pharyngeal, Urethral, and Rectal Samples into a Single Sample for Analysis for Detection of Neisseria gonorrhoeae and Chlamydia trachomatis i... von Sultan, B, White, J A, Fish, R, Carrick, G, Brima, N, Copas, A, Robinson, A, Gilson, R, Mercey, D, Benn, P

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Thermal performance of heat pipes using nanofluids von Poplaski, Leonard M., Benn, Steven P., Faghri, Amir

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OC05.02: Clinical experience with non‐invasive prenatal screening for single gene disorders von Mohan, P., Lemoine, J., Trotter, C., Rakova, I., Billings, P., Peacock, S., Kao, C., Wang, Y., Xia, F., Eng, C., Benn, P.

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Heat pipe heat exchangers and heat sinks: Opportunities, challenges, applications, analysis, and state of the art von Shabgard, Hamidreza, Allen, Michael J., Sharifi, Nourouddin, Benn, Steven P., Faghri, Amir, Bergman, Theodore L.

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Non‐invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly von Benn, P., Cuckle, H., Pergament, E.

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Polypharmacy and potential drug–drug interactions for people with HIV in the UK from the Climate‐HIV database von Okoli, C, Schwenk, A, Radford, M, Myland, M, Taylor, S, Darley, A, Barnes, J, Fox, A, Grimson, F, Reeves, I, Munshi, S, Croucher, A, Boxall, N, Benn, P, Paice, A, Wyk, J, Khoo, S

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OC11.01: Clinical experience with carrier screening in a general population: support for a comprehensive pan‐ethnic approach von Benn, P., Westemeyer, M., Saucier, J., Prins, S., Shetty, A., Malhotra, M.M., Demko, Z., Eng, C., Weckstein, L., Boostanfar, R., Keen‐Kim, D., Billings, P.

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VP29.11: High‐positive predictive values across maternal ages in non‐invasive prenatal testing for fetal aneuploidy von Leonard, S., Benn, P., Valenti, E., Di Nonno, W., Demko, Z., Martin, K., Billings, P., Egbert, M., Zneimer, S., Keen‐Kim, D.

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