Bianchi, Diana W.

Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum

Bianchi, D. W., Zickwolf, G. K., Weil, G. J., Sylvester, S., & DeMaria, M. A. (1996) · Proceedings of the National Academy of Sciences

Prenatal Screening and DiagnosticsReproductive System and Pregnancy

Cited by 1,264

The conception of the ABCD study: From substance use to a broad NIH collaboration

Volkow, N. D., Koob, G. F., Croyle, R. T., Bianchi, D. W., Gordon, J. A., Koroshetz, W. J., Pérez-Stable, E. J., Riley, W. T., Bloch, M. H., Conway, K., et al. (2018) · Developmental Cognitive Neuroscience

Neural and Behavioral Psychology StudiesSubstance Abuse Treatment and Outcomes

Cited by 970

Down syndrome

Antonarakis, S. E., Skotko, B. G., Rafii, M. S., Strydom, A., Pape, S. E., Bianchi, D. W., Sherman, S. L., & Reeves, R. H. (2020) · Nature Reviews Disease Primers

Down syndrome and intellectual disability researchWilliams Syndrome Research

Cited by 964

Noninvasive Fetal Sex Determination Using Cell-Free Fetal DNA: A Systematic Review and Meta-analysis

Devaney, S. A., Palomaki, G. E., Scott, J. A., & Bianchi, D. W. (2011) · JAMA

Prenatal Screening and DiagnosticsDemographic Trends and Gender Preferences

Cited by 247

Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome

Aziz, N. M., Guedj, F., Pennings, J. L. A., Olmos-Serrano, J. L., Siegel, A., Haydar, T. F., & Bianchi, D. W. (2018) · Disease Models & Mechanisms

Down syndrome and intellectual disability researchGenetics and Neurodevelopmental Disorders

Cited by 118

Absence of Prenatal Forebrain Defects in the Dp(16)1Yey/+ Mouse Model of down Syndrome.

Goodliffe, J. W., Olmos-Serrano, J. L., Aziz, N. M., Pennings, J. L. A., Guedj, F., Bianchi, D. W., & Haydar, T. F. (2016) · The Journal of Neuroscience

Down syndrome and intellectual disability researchGenetics and Neurodevelopmental Disorders

Cited by 65

Redefining the progeroid form of ehlers–danlos syndrome: Report of the fourth patient with B4GALT7 deficiency and review of the literature

Guo, M. H., Stoler, J., Lui, J., Nilsson, O., Bianchi, D. W., Hirschhorn, J. N., & Dauber, A. (2013) · American Journal of Medical Genetics Part A

Connective tissue disorders researchProteoglycans and glycosaminoglycans research

Cited by 52

Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome

Massingham, L. J., Johnson, K. L., Scholl, T. M., Slonim, D. K., Wick, H. C., & Bianchi, D. W. (2014) · Human Genetics

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 52

Quantitative MRI Analyses of Regional Brain Growth in Living Fetuses with Down Syndrome

Tarui, T., Im, K., Madan, N., Madankumar, R., Skotko, B. G., Schwartz, A., Sharr, C., Ralston, S. J., Kitano, R., Akiyama, S., et al. (2020) · Cerebral Cortex

Down syndrome and intellectual disability researchFetal and Pediatric Neurological Disorders

Cited by 50

Regional Alterations in Cortical Sulcal Depth in Living Fetuses with Down Syndrome

Yun, H. J., Perez, J. D. R., Sosa, P., Valdés, J. A., Madan, N., Kitano, R., Akiyama, S., Skotko, B. G., Feldman, H. A., Bianchi, D. W., et al. (2021) · Cerebral Cortex

Down syndrome and intellectual disability researchFetal and Pediatric Neurological Disorders

Cited by 33