Integrative transcriptome analysis reveals dysregulation of canonical cancer molecular pathways in placenta leading to preeclampsia
Moslehi, Roxana, Mills, James L., Signore, Caroline, Kumar, Anil, Ambroggio, Xavier, Dzutsev, Amiran
Published in Scientific reports (30.08.2013)
Published in Scientific reports (30.08.2013)
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Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects
Pangilinan, Faith, Molloy, Anne M, Mills, James L, Troendle, James F, Parle-McDermott, Anne, Signore, Caroline, O'Leary, Valerie B, Chines, Peter, Seay, Jessica M, Geiler-Samerotte, Kerry, Mitchell, Adam, VanderMeer, Julia E, Krebs, Kristine M, Sanchez, Angelica, Cornman-Homonoff, Joshua, Stone, Nicole, Conley, Mary, Kirke, Peadar N, Shane, Barry, Scott, John M, Brody, Lawrence C
Published in BMC genetics (02.08.2012)
Published in BMC genetics (02.08.2012)
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MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
Parle-McDermott, Anne, Mills, James L., Kirke, Peadar N., Cox, Christopher, Signore, Caroline C., Kirke, Sandra, Molloy, Anne M., O'Leary, Valerie B., Pangilinan, Faith J., O'Herlihy, Colm, Brody, Lawrence C., Scott, John M.
Published in American journal of medical genetics. Part A (01.02.2005)
Published in American journal of medical genetics. Part A (01.02.2005)
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Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta
MOSLEHI, Roxana, KUMAR, Anil, MILLS, James L, AMBROGGIO, Xavier, SIGNORE, Caroline, DZUTSEV, Amiran
Published in European journal of human genetics : EJHG (01.06.2012)
Published in European journal of human genetics : EJHG (01.06.2012)
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A Genome-Wide Association Study of Early Spontaneous Preterm Delivery
Zhang, Heping, Baldwin, Don A., Bukowski, Radek K., Parry, Samuel, Xu, Yaji, Song, Chi, Andrews, William W., Saade, George R., Esplin, M. Sean, Sadovsky, Yoel, Reddy, Uma M., Ilekis, John, Varner, Michael, Biggio Jr, Joseph R.
Published in Genetic epidemiology (01.03.2015)
Published in Genetic epidemiology (01.03.2015)
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