Prolonged duration of persistent cell‐free fetal DNA from vanishing twin
Niles, K. M., Murji, A., Chitayat, D.
Published in Ultrasound in obstetrics & gynecology (01.10.2018)
Published in Ultrasound in obstetrics & gynecology (01.10.2018)
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Journal Article
NSD1 mutations generate a genome-wide DNA methylation signature
Choufani, S., Cytrynbaum, C., Chung, B. H. Y., Turinsky, A. L., Grafodatskaya, D., Chen, Y. A., Cohen, A. S. A., Dupuis, L., Butcher, D. T., Siu, M. T., Luk, H. M., Lo, I. F. M., Lam, S. T. S., Caluseriu, O., Stavropoulos, D. J., Reardon, W., Mendoza-Londono, R., Brudno, M., Gibson, W. T., Chitayat, D., Weksberg, R.
Published in Nature communications (22.12.2015)
Published in Nature communications (22.12.2015)
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Journal Article
Microarray and RASopathy‐disorder testing in fetuses with increased nuchal translucency
Sinajon, P., Chitayat, D., Roifman, M., Wasim, S., Carmona, S., Ryan, G., Noor, A., Kolomietz, E., Chong, K.
Published in Ultrasound in obstetrics & gynecology (01.03.2020)
Published in Ultrasound in obstetrics & gynecology (01.03.2020)
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Journal Article
Short‐ and long‐term outcome following thoracoamniotic shunting for fetal hydrothorax
Kelly, E. N., Seaward, G., Ye, X. Y., Windrim, R., Van Mieghem, T., Keunen, J., Abbasi, N., Chitayat, D., Ryan, G.
Published in Ultrasound in obstetrics & gynecology (01.04.2021)
Published in Ultrasound in obstetrics & gynecology (01.04.2021)
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Journal Article
OC18.01: Whole‐genome sequencing for fetal structural anomalies
Wang, Y., Greenfeld (Kolomietz), E., Marshall, C., Roifman, M., Chong, K., Chitayat, D., Stavropoulos, D.J., Noor, A.
Published in Ultrasound in obstetrics & gynecology (01.10.2021)
Published in Ultrasound in obstetrics & gynecology (01.10.2021)
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Journal Article
Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in α-Dystroglycan-Related Muscular Disorders
Talenti, G, Robson, C, Severino, M S, Alves, C A, Chitayat, D, Dahmoush, H, Smith, L, Muntoni, F, Blaser, S I, D'Arco, F
Published in American journal of neuroradiology : AJNR (01.01.2021)
Published in American journal of neuroradiology : AJNR (01.01.2021)
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Journal Article
Long‐term postnatal outcome of fetuses with prenatally suspected septo‐optic dysplasia
Shinar, S., Blaser, S., Chitayat, D., Selvanathan, T., Chau, V., Shannon, P., Agrawal, S., Ryan, G., Pruthi, V., Miller, S. P., Krishnan, P., Van Mieghem, T.
Published in Ultrasound in obstetrics & gynecology (01.09.2020)
Published in Ultrasound in obstetrics & gynecology (01.09.2020)
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Journal Article
De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype
Roifman, M., Marcelis, C.L.M., Paton, T., Marshall, C., Silver, R., Lohr, J.L., Yntema, H.G., Venselaar, H., Kayserili, H., van Bon, B., Seaward, G., Brunner, H.G., Chitayat, D.
Published in Clinical genetics (01.01.2015)
Published in Clinical genetics (01.01.2015)
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Journal Article
Diagnostic utility of microarray testing in pregnancy loss
Rosenfeld, J. A., Tucker, M. E., Escobar, L. F., Neill, N. J., Torchia, B. S., McDaniel, L. D., Schultz, R. A., Chong, K., Chitayat, D.
Published in Ultrasound in obstetrics & gynecology (01.10.2015)
Published in Ultrasound in obstetrics & gynecology (01.10.2015)
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Journal Article
Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies
Hammarsjö, A., Wang, Z., Vaz, R., Taylan, F., Sedghi, M., Girisha, K. M., Chitayat, D., Neethukrishna, K., Shannon, P., Godoy, R., Gowrishankar, K., Lindstrand, A., Nasiri, J., Baktashian, M., Newton, P. T., Guo, L., Hofmeister, W., Pettersson, M., Chagin, A. S., Nishimura, G., Yan, L., Matsumoto, N., Nordgren, A., Miyake, N., Grigelioniene, G., Ikegawa, S.
Published in Scientific reports (14.11.2017)
Published in Scientific reports (14.11.2017)
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Journal Article
Foetal "black bone" MRI: utility in assessment of the foetal spine
Robinson, A J, Blaser, S, Vladimirov, A, Drossman, D, Chitayat, D, Ryan, G
Published in British journal of radiology (01.02.2015)
Published in British journal of radiology (01.02.2015)
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Journal Article
Placental size and the prediction of severe early‐onset intrauterine growth restriction in women with low pregnancy‐associated plasma protein‐A
Proctor, L. K., Toal, M., Keating, S., Chitayat, D., Okun, N., Windrim, R. C., Smith, G. C. S., Kingdom, J. C. P.
Published in Ultrasound in obstetrics & gynecology (01.09.2009)
Published in Ultrasound in obstetrics & gynecology (01.09.2009)
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Journal Article
Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study
Roadhouse, C., Shuman, C., Anstey, K., Sappleton, K., Chitayat, D., Ignagni, E.
Published in Journal of genetic counseling (01.12.2018)
Published in Journal of genetic counseling (01.12.2018)
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Journal Article
Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies
Cizmeci, M N, Lequin, M, Lichtenbelt, K D, Chitayat, D, Kannu, P, James, A G, Groenendaal, F, Chakkarapani, E, Blaser, S, de Vries, L S
Published in American journal of neuroradiology : AJNR (01.06.2018)
Published in American journal of neuroradiology : AJNR (01.06.2018)
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Journal Article
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly
Kernohan, K.D., McBride, A., Xi, Y., Martin, N., Schwartzentruber, J., Dyment, D.A., Majewski, J., Blaser, S., Boycott, K.M., Chitayat, D.
Published in Clinical genetics (01.05.2017)
Published in Clinical genetics (01.05.2017)
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Journal Article
Prenatal diagnosis and outcome of absent pulmonary valve syndrome: contemporary single‐center experience and review of the literature
Wertaschnigg, D., Jaeggi, M., Chitayat, D., Shannon, P., Ryan, G., Thompson, M., Yoo, S. J., Jaeggi, E.
Published in Ultrasound in obstetrics & gynecology (01.02.2013)
Published in Ultrasound in obstetrics & gynecology (01.02.2013)
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Journal Article
Fetal skeletal dysplasias in a tertiary care center: radiology, pathology, and molecular analysis of 112 cases
Barkova, E., Mohan, U., Chitayat, D., Keating, S., Toi, A., Frank, J., Frank, R., Tomlinson, G., Glanc, P.
Published in Clinical genetics (01.04.2015)
Published in Clinical genetics (01.04.2015)
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Journal Article
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene
Moalem, S., Brouillard, P., Kuypers, D., Legius, E., Harvey, E., Taylor, G., Francois, M., Vikkula, M., Chitayat, D.
Published in Clinical genetics (01.04.2015)
Published in Clinical genetics (01.04.2015)
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Journal Article