Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism

The fetal and infant origins of adult disease.

Barker, D. J. (1990) · BMJ · doi:10.1136/bmj.301.6761.1111 · Cited by 2,768 · see citing works

Health: United States

Lee, J. A. H. (1986) · JAMA · doi:10.1001/jama.1986.03370120114036 · Cited by 2,252 · see citing works

Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo

Santos, F., Hendrich, B., Reik, W., & Dean, W. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0501 · Cited by 1,213 · see citing works

Influence of Metabolism on Epigenetics and Disease

Kaelin, W. G., & McKnight, S. L. (2013) · Cell · doi:10.1016/j.cell.2013.03.004 · Cited by 920 · see citing works

Review: Sex and the human placenta: Mediating differential strategies of fetal growth and survival

Clifton, V. L. (2010) · Placenta · doi:10.1016/j.placenta.2009.11.010 · Cited by 868 · see citing works

Review article: The short‐ and long‐term implications of maternal obesity on the mother and her offspring

Catalano, P., & Ehrenberg, H. M. (2006) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2006.00989.x · Cited by 828 · see citing works

Nutrition and epigenetics: an interplay of dietary methyl donors, one-carbon metabolism and DNA methylation

Anderson, O. S., Sant, K. E., & Dolinoy, D. C. (2012) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2012.03.003 · Cited by 773 · see citing works

Obesity in Pregnancy Stimulates Macrophage Accumulation and Inflammation in the Placenta

Challier, J. C., Basu, S., Bintein, T., Minium, J., Hotmire, K., Catalano, P. M., & Hauguel-de Mouzon, S. (2008) · Placenta · doi:10.1016/j.placenta.2007.12.010 · Cited by 712 · see citing works

Ten Putative Contributors to the Obesity Epidemic

McAllister, E. J., Dhurandhar, N. V., Keith, S. W., Aronne, L. J., Barger, J., Baskin, M., Benca, R. M., Biggio, J., Boggiano, M. M., Eisenmann, J. C., et al. (2009) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408390903372599 · Cited by 710 · see citing works

Overweight and obesity in mothers and risk of preterm birth and low birth weight infants: systematic review and meta-analyses

McDonald, S. D., Han, Z., Mulla, S. M., Beyene, J., & on behalf of the Knowledge Synthesis Group (2010) · BMJ · doi:10.1136/bmj.c3428 · Cited by 633 · see citing works

Epigenetics: A New Bridge between Nutrition and Health

Choi, S., & Friso, S. (2010) · Advances in Nutrition · doi:10.3945/an.110.1004 · Cited by 603 · see citing works

Boys live dangerously in the womb

Eriksson, J. G., Kajantie, E., Osmond, C., Thornburg, K., & Barker, D. J. P. (2010) · American Journal of Human Biology · doi:10.1002/ajhb.20995 · Cited by 590 · see citing works

Health, United States, 2007--With Chartbook on Trends in the Health of Americans

(2007) · PsycEXTRA Dataset · doi:10.1037/e407202008-001 · Cited by 570 · see citing works

The <i>H19</i> locus: Role of an imprinted non‐coding RNA in growth and development

Gabory, A., Jammes, H., & Dandolo, L. (2010) · BioEssays · doi:10.1002/bies.200900170 · Cited by 568 · see citing works

Placental adaptive responses and fetal programming

Myatt, L. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.104968 · Cited by 536 · see citing works

Linking prenatal maternal adversity to developmental outcomes in infants: The role of epigenetic pathways

Monk, C. E., Spicer, J., & Champagne, F. A. (2012) · Development and Psychopathology · doi:10.1017/s0954579412000764 · Cited by 458 · see citing works

Gene expression patterns in human placenta

Sood, R., Zehnder, J. L., Druzin, M. L., & Brown, P. O. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508035103 · Cited by 454 · see citing works

Aspects of Human Fetoplacental Vasculogenesis and Angiogenesis. II. Changes During Normal Pregnancy

Kaufmann, P., Mayhew, T. M., & Jones, D. S. (2003) · Placenta · doi:10.1016/j.placenta.2003.10.009 · Cited by 437 · see citing works

Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation

Lewis, A., Mitsuya, K., Umlauf, D., Smith, P., Dean, W., Walter, J., Higgins, M. J., Feil, R., & Reik, W. (2004) · Nature Genetics · doi:10.1038/ng1468 · Cited by 421 · see citing works

Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes

Umlauf, D., Goto, Y., Cao, R., Cerqueira, F., Wagschal, A., Zhang, Y., & Feil, R. (2004) · Nature Genetics · doi:10.1038/ng1467 · Cited by 416 · see citing works

Epigenetics and the placenta

Nelissen, E. C. M., van Montfoort, A. P. A., Dumoulin, J. C. M., & Evers, J. L. H. (2010) · Human Reproduction Update · doi:10.1093/humupd/dmq052 · Cited by 385 · see citing works

Placental efficiency and adaptation: endocrine regulation

Fowden, A. L., Sferruzzi-Perri, A. N., Coan, P. M., Constância, M., & Burton, G. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.173013 · Cited by 359 · see citing works

Aspects of Human Fetoplacental Vasculogenesis and Angiogenesis. I. Molecular Regulation

Jones, D. S., Kaufmann, P., & Mayhew, T. M. (2003) · Placenta · doi:10.1016/j.placenta.2003.10.004 · Cited by 359 · see citing works

Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics

Gabory, A., Roseboom, T. J., Moore, T., Moore, L. G., & Junien, C. (2013) · Biology of Sex Differences · doi:10.1186/2042-6410-4-5 · Cited by 344 · see citing works

Sex differences in developmental programming models

Aiken, C., & Ozanne, S. E. (2012) · Reproduction · doi:10.1530/rep-11-0489 · Cited by 340 · see citing works

High‐fat diet before and during pregnancy causes marked up‐regulation of placental nutrient transport and fetal overgrowth in C57/BL6 mice

Jones, H. N., Woollett, L. A., Barbour, N., Prasad, P. D., Powell, T. L., & Jansson, T. (2008) · The FASEB Journal · doi:10.1096/fj.08-116889 · Cited by 310 · see citing works

Sex determines the expression level of one third of the actively expressed genes in bovine blastocysts

Bermejo‐Álvarez, P., Rizos, D. V., Rath, D., Lonergan, P., & Gutiérrez‐Adán, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913843107 · Cited by 307 · see citing works

Activation of Placental mTOR Signaling and Amino Acid Transporters in Obese Women Giving Birth to Large Babies

Jansson, N., Rosario, F. J., Gaccioli, F., Lager, S., Jones, H. N., Roos, S., Jansson, T., & Powell, T. L. (2013) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2012-2667 · Cited by 305 · see citing works

The Role of the Placenta in Fetal Programming—A Review

Godfrey, K. M. (2002) · Placenta · doi:10.1053/plac.2002.0773 · Cited by 305 · see citing works

Placental-specific insulin-like growth factor 2 ( Igf2 ) regulates the diffusional exchange characteristics of the mouse placenta

Sibley, C. P., Coan, P. M., Ferguson‐Smith, A. C., Dean, W., Hughes, J., Smith, P., Reik, W., Burton, G. J., Fowden, A. L., & Constância, M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402508101 · Cited by 299 · see citing works

Placental structure and inflammation in pregnancies associated with obesity

Roberts, K., Riley, S. C., Reynolds, R. M., Barr, S., Evans, M., Statham, A., Hor, K., Jabbour, H. N., Norman, J. E., & Denison, F. C. (2011) · Placenta · doi:10.1016/j.placenta.2010.12.023 · Cited by 281 · see citing works

Sexual dimorphism in environmental epigenetic programming

Gabory, A., Attig, L., & Junien, C. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.02.015 · Cited by 280 · see citing works

Longitudinal Assessment of Maternal Endothelial Function and Markers of Inflammation and Placental Function throughout Pregnancy in Lean and Obese Mothers

Stewart, F. M., Freeman, D. J., Ramsay, J. E., Greer, I. A., CASLAKE, M. J., & Ferrell, W. R. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-2083 · Cited by 274 · see citing works

Increasing Maternal Body Mass Index Is Associated with Systemic Inflammation in the Mother and the Activation of Distinct Placental Inflammatory Pathways1

Aye, I. L. M. H., Lager, S., Ramirez, V. I., Gaccioli, F., Dudley, D. J., Jansson, T., & Powell, T. L. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.113.116186 · Cited by 273 · see citing works

Sex differences in sex chromosome gene expression in mouse brain

Xu, J. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.12.1409 · Cited by 269 · see citing works

Maternal High-Fat Diet Disturbs Uteroplacental Hemodynamics and Increases the Frequency of Stillbirth in a Nonhuman Primate Model of Excess Nutrition

Frias, A. E., Morgan, T. K., Evans, A. E., Rasanen, J., Oh, K. Y., Thornburg, K. L., & Grove, K. L. (2011) · Endocrinology · doi:10.1210/en.2010-1332 · Cited by 268 · see citing works

The Placenta and Intrauterine Programming

Fowden, A. L., Forhead, A. J., Coan, P. M., & Burton, G. J. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01663.x · Cited by 267 · see citing works

Contrasting effects of different maternal diets on sexually dimorphic gene expression in the murine placenta

Mao, J., Zhang, X., Sieli, P. T., Falduto, M. T., Torres, K. E., & Rosenfeld, C. S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000440107 · Cited by 261 · see citing works

Gestational diabetes mellitus epigenetically affects genes predominantly involved in metabolic diseases

Ruchat, S.-M., Houde, A.-A., Voisin, G., St‐Pierre, J., Perron, P., Baillargeon, J., Gaudet, D., Hivert, M., Brisson, D., & Bouchard, L. (2013) · Epigenetics · doi:10.4161/epi.25578 · Cited by 259 · see citing works

Metabolic Programming of MEST DNA Methylation by Intrauterine Exposure to Gestational Diabetes Mellitus

Hajj, N. E., Pliushch, G., Schneider, E., Dittrich, M. T., Müller, T., Korenkov, M., Aretz, M., Zechner, U., Lehnen, H., & Haaf, T. (2012) · Diabetes · doi:10.2337/db12-0289 · Cited by 256 · see citing works

Influence of environmental exposure on human epigenetic regulation

Marsit, C. J. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.106971 · Cited by 252 · see citing works

Review: The Placenta is a Programming Agent for Cardiovascular Disease

Thornburg, K. L. R., O'Tierney, P. F., & Louey, S. (2010) · Placenta · doi:10.1016/j.placenta.2010.01.002 · Cited by 248 · see citing works

Amino Acid (System A) Transporter Activity in Microvillous Membrane Vesicles from the Placentas of Appropriate and Small for Gestational Age Babies

Maiiendran, D., Donnai, P., Glazier, J. D., D'Souza, S. W., Boyd, R. D., & Sibley, C. P. (1993) · Pediatric Research · doi:10.1203/00006450-199311000-00019 · Cited by 247 · see citing works

Sex differences in prenatal epigenetic programing of stress pathways

Bale, T. L. (2011) · Stress · doi:10.3109/10253890.2011.586447 · Cited by 237 · see citing works

Placental Transport of Leucine and Lysine Is Reduced in Intrauterine Growth Restriction1

Jansson, T., Scholtbach, V., & Powell, T. L. (1998) · Pediatric Research · doi:10.1203/00006450-199810000-00011 · Cited by 235 · see citing works

Sex- and Diet-Specific Changes of Imprinted Gene Expression and DNA Methylation in Mouse Placenta under a High-Fat Diet

Gallou-Kabani, C., Gabory, A., Tost, J., Karimi, M., Mayeur, S., Lesage, J., Boudadi, E., Gross, M.-S., Taurelle, J., Vigé, A., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0014398 · Cited by 229 · see citing works

Regulation of Placental Nutrient Transport – A Review

Jones, H. N., Powell, T. L., & Jansson, T. (2007) · Placenta · doi:10.1016/j.placenta.2007.05.002 · Cited by 226 · see citing works

Influence of maternal size on placental, fetal and postnatal growth in the horse. I. Development in utero

Allen, W. R., Wilsher, S., Turnbull, C., Stewart, F., Ousey, J., Rossdale, P. D., & Fowden, A. L. (2002) · Reproduction · doi:10.1530/rep.0.1230445 · Cited by 223 · see citing works

Maternal cigarette smoking during pregnancy is associated with downregulation ofmiR-16,miR-21, andmiR-146ain the placenta

Maccani, M. A., Avissar-Whiting, M., Banister, C. E., McGonnigal, B., Padbury, J. F., & Marsit, C. J. (2010) · Epigenetics · doi:10.4161/epi.5.7.12762 · Cited by 206 · see citing works

Maternal Diets Trigger Sex-Specific Divergent Trajectories of Gene Expression and Epigenetic Systems in Mouse Placenta

Gabory, A., Ferry, L., Fajardy, I., Jouneau, L., Gothié, J.-D., Vigé, A., Fleur, C., Mayeur, S., Gallou-Kabani, C., Gross, M.-S., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047986 · Cited by 204 · see citing works

Maternal obesity up-regulates inflammatory signaling pathways and enhances cytokine expression in the mid-gestation sheep placenta

Zhu, M. J., Du, ‬., Nathanielsz, P. W., & Ford, S. P. (2010) · Placenta · doi:10.1016/j.placenta.2010.02.002 · Cited by 199 · see citing works

Epigenetic mechanisms linking early nutrition to long term health

Lillycrop, K. A., & Burdge, G. C. (2012) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2012.03.009 · Cited by 198 · see citing works

Placental nutrient supply and fetal growth

Desforges, M., & Sibley, C. P. (2009) · The International Journal of Developmental Biology · doi:10.1387/ijdb.082765md · Cited by 182 · see citing works

Modulation of Fatty Acid Transport and Metabolism by Maternal Obesity in the Human Full-Term Placenta1

Dubé, E., Gravel, A., Martin, C., Desparois, G., Moussa, I., Ethier-Chiasson, M., Forest, J.-C., Giguère, Y., Masse, A., & Lafond, J. (2012) · Biology of Reproduction · doi:10.1095/biolreprod.111.098095 · Cited by 180 · see citing works

The origin and evolution of genomic imprinting and viviparity in mammals

Renfree, M. B., Suzuki, S., & Kaneko‐Ishino, T. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0151 · Cited by 179 · see citing works

Global Methylation in the Placenta and Umbilical Cord Blood From Pregnancies With Maternal Gestational Diabetes, Preeclampsia, and Obesity

Nomura, Y., Lambertini, L., Rialdi, A., Lee, M., Mystal, E. Y., Grabie, M., Manaster, I., Huynh, N., Finik, J. M., Davey, M., et al. (2013) · Reproductive Sciences · doi:10.1177/1933719113492206 · Cited by 169 · see citing works

Placental weight and efficiency in relation to maternal body mass index and the risk of pregnancy complications in women delivering singleton babies

Wallace, J. M., Horgan, G. W., & Bhattacharya, S. (2012) · Placenta · doi:10.1016/j.placenta.2012.05.006 · Cited by 163 · see citing works

Developmental reprogramming of cancer susceptibility

Walker, C. L., & Ho, S. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3220 · Cited by 159 · see citing works

Epigenetic linkage of aging, cancer and nutrition

Daniel, M. G., & Tollefsbol, T. O. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.107110 · Cited by 158 · see citing works

Maternal Fructose Intake during Pregnancy and Lactation Alters Placental Growth and Leads to Sex-Specific Changes in Fetal and Neonatal Endocrine Function

Vickers, M. H., Clayton, Z. E., Yap, C., & Sloboda, D. M. (2011) · Endocrinology · doi:10.1210/en.2010-1093 · Cited by 157 · see citing works

Dietary Manipulation of Histone Structure and Function

Delage, B., & Dashwood, R. H. (2008) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.28.061807.155354 · Cited by 155 · see citing works

Developmental programming and epigenetics

Gabory, A., Attig, L., & Junien, C. (2011) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.110.000927 · Cited by 154 · see citing works

Placental angiogenesis in sheep models of compromised pregnancy

Reynolds, L. P., Borowicz, P. P., Vonnahme, K. A., Johnson, M. L., Grazul‐Bilska, A. T., Redmer, D. A., & Caton, J. S. S. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.081745 · Cited by 154 · see citing works

Placental Amino Acid Transport and Placental Leptin Resistance in Pregnancies Complicated by Maternal Obesity

Farley, D. M., Choi, J., Dudley, D. J., Li, C., Jenkins, S. L., Myatt, L., & Nathanielsz, P. W. (2010) · Placenta · doi:10.1016/j.placenta.2010.06.006 · Cited by 150 · see citing works

Blastocysts prepare for the race to be male

Mittwoch, U. (1993) · Human Reproduction · doi:10.1093/oxfordjournals.humrep.a137889 · Cited by 141 · see citing works

Obesity During Pregnancy Disrupts Placental Morphology, Cell Proliferation, and Inflammation in a Sex-Specific Manner Across Gestation in the Mouse1

Kim, D. W., Young, S. L., Grattan, D. R., & Jasoni, C. L. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.113.117259 · Cited by 138 · see citing works

Blood flows and nutrient uptakes in growth-restricted pregnancies induced by overnourishing adolescent sheep

Wallace, J. M., Bourke, D. A., Aitken, R. P., Leitch, N., & Hay, W. W. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00465.2001 · Cited by 137 · see citing works

Maternal obesity markedly increases placental fatty acid transporter expression and fetal blood triglycerides at midgestation in the ewe

Zhu, M. J., Ma, Y., Long, N. M., Du, M., & Ford, S. P. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00309.2010 · Cited by 137 · see citing works

An obesogenic diet during mouse pregnancy modifies maternal nutrient partitioning and the fetal growth trajectory

Sferruzzi‐Perri, A. N., Vaughan, O. R., Haro, M., Cooper, W. N., Musial, B., Charalambous, M., Pestana, D., Ayyar, S., Ferguson‐Smith, A. C., Burton, G. J., et al. (2013) · The FASEB Journal · doi:10.1096/fj.13-234823 · Cited by 134 · see citing works

Genomic imprinting in the placenta

Wagschal, A., & Feil, R. (2006) · Cytogenetic and Genome Research · doi:10.1159/000090819 · Cited by 130 · see citing works

Epigenetic programming of obesity and diabetes by in utero exposure to gestational diabetes mellitus

Ruchat, S.-M., Hivert, M., & Bouchard, L. (2013) · Nutrition Reviews · doi:10.1111/nure.12057 · Cited by 128 · see citing works

The fetal origins of diseases of old age.

Barker, D. J. P. (1992) · PubMed · Cited by 122 · see citing works

Maternal undernutrition during mid-pregnancy in sheep. Placental size and its relationship to calcium transfer during late pregnancy

McCrabb, G. J., Egan, A. R., & Hosking, B. J. (1991) · British Journal Of Nutrition · doi:10.1079/bjn19910077 · Cited by 116 · see citing works

Maternal obesity and gestational diabetes are associated with placental leptin DNA methylation

Lesseur, C., Armstrong, D. A., Paquette, A. G., Li, Z., Padbury, J. F., & Marsit, C. J. (2014) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2014.06.037 · Cited by 115 · see citing works

You are what you eat, and so are your children: the impact of micronutrients on the epigenetic programming of offspring

Vanhees, K., Vonhögen, I. G. C., van Schooten, F., & Godschalk, R. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1427-9 · Cited by 114 · see citing works

The sex-specific effects of famine on the association between placental size and later hypertension

van Abeelen, A. F. M., de Rooij, S. R., Osmond, C., Painter, R. C., Veenendaal, M. V. E., Bossuyt, P. M. M., Elias, S. G., Grobbee, D. E., van der Schouw, Y. T., Barker, D. J. P., et al. (2011) · Placenta · doi:10.1016/j.placenta.2011.06.012 · Cited by 114 · see citing works

Maternal undernutrition during mid-pregnancy in sheep: variable effects on placental growth

McCrabb, G. J., Egan, A. R., & Hosking, B. J. (1992) · The Journal of Agricultural Science · doi:10.1017/s002185960006809x · Cited by 114 · see citing works

Mechanisms by which maternal obesity programs offspring for obesity: evidence from animal studies

Zambrano, E., & Nathanielsz, P. W. (2013) · Nutrition Reviews · doi:10.1111/nure.12068 · Cited by 109 · see citing works

Maternal undernutrition during late gestation-induced intrauterine growth restriction in the rat is associated with impaired placental GLUT3 expression, but does not correlate with endogenous corticosterone levels

Lésage, J., Hahn, D., Léonhardt, M., Blondeau, B., Bréant, B., & Dupouy, J. (2002) · Journal of Endocrinology · doi:10.1677/joe.0.1740037 · Cited by 107 · see citing works

Effect of IL-6 and TNF-α on fatty acid uptake in cultured human primary trophoblast cells

Lager, S., Jansson, N., Olsson, A., Wennergren, M., Jansson, T., & Powell, T. L. (2010) · Placenta · doi:10.1016/j.placenta.2010.10.012 · Cited by 106 · see citing works

Feto-placental Adaptations to Maternal Obesity in the Baboon

Farley, D. R., Tejero, M. E., Comuzzie, A. G., Higgins, P. B., Cox, L. A., Werner, S. L., Jenkins, S. L., Li, C., Choi, J., Dick, E. J., et al. (2009) · Placenta · doi:10.1016/j.placenta.2009.06.007 · Cited by 105 · see citing works

The Importance of Venous Doppler Velocimetry for Evaluation of Intrauterine Growth Restriction

Kaponis, A. I., Harada, T., Makrydimas, G., Kiyama, T., Arata, K., Adonakis, G. L., Tsapanos, V., Iwabe, T., Stefos, Τ., Decavalas, G., et al. (2011) · Journal of Ultrasound in Medicine · doi:10.7863/jum.2011.30.4.529 · Cited by 91 · see citing works

Intrauterine calorie restriction affects placental DNA methylation and gene expression

Chen, P., Ganguly, A., Rubbi, L., Orozco, L. D., Morselli, M., Ashraf, D. C., Jaroszewicz, A., Feng, S., Jacobsen, S. E., Nakano, A., et al. (2013) · Physiological Genomics · doi:10.1152/physiolgenomics.00034.2013 · Cited by 90 · see citing works

Sex-specific effects of placental restriction on components of the metabolic syndrome in young adult sheep

Owens, J. A., Thavaneswaran, P., Blasio, M. J. D., McMillen, I. C., Robinson, J. S., & Gatford, K. L. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00706.2006 · Cited by 88 · see citing works

Effects of famine on placental size and efficiency

Roseboom, T. J., Painter, R. C., de Rooij, S. R., van Abeelen, A. F. M., Veenendaal, M. V. E., Osmond, C., & Barker, D. J. P. (2011) · Placenta · doi:10.1016/j.placenta.2011.03.001 · Cited by 84 · cited 1× · see citing works

Sexual Dimorphism of the Feto-Placental Phenotype in Response to a High Fat and Control Maternal Diets in a Rabbit Model

Couturier‐Tarrade, A., Rousseau‐Ralliard, D., Aubrière, M.-C., Peynot, N., Dahirel, M., Bertrand‐Michel, J., Aguirre-Lavin, T., Morel, O., Beaujean, N., Duranthon, V., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083458 · Cited by 83 · see citing works

Placental oleic acid uptake is lower in male offspring of obese women

Brass, E. P., Hanson, E., & O’Tierney-Ginn, P. F. (2013) · Placenta · doi:10.1016/j.placenta.2013.03.009 · Cited by 77 · see citing works

Early nutrition and epigenetic programming: chasing shadows

Attig, L., Gabory, A., & Junien, C. (2010) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328338aa61 · Cited by 73 · see citing works

Hyperlipidic hypercholesterolemic diet in prepubertal rabbits affects gene expression in the embryo, restricts fetal growth and increases offspring susceptibility to obesity

Picone, O., Laigre, P., Fortun‐Lamothe, L., Archilla, C., Peynot, N., Ponter, A. A. A., Berthelot, V., Cordier, A., Duranthon, V., & Chavatte‐Palmer, P. (2010) · Theriogenology · doi:10.1016/j.theriogenology.2010.08.015 · Cited by 72 · see citing works

Maternal obesity and overnutrition alter fetal growth rate and cotyledonary vascularity and angiogenic factor expression in the ewe

Ma, Y., Zhu, M. J., Zhang, L., Hein, S. M., Nathanielsz, P. W., & Ford, S. P. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00498.2009 · Cited by 70 · see citing works

Imprinting and Transgenerational Modulation of Gene Expression; Human Growth as a Model

Pembrey, M. E. (1996) · Acta geneticae medicae et gemellologiae · doi:10.1017/s0001566000001197 · Cited by 66 · see citing works

Serial Measurement of Uterine Blood Flow From Mid to Late Gestation in Growth Restricted Pregnancies Induced by Overnourishing Adolescent Sheep Dams

Wallace, J. M., Milne, J. S., MATSUZAKI, M., & Aitken, R. P. (2008) · Placenta · doi:10.1016/j.placenta.2008.05.006 · Cited by 57 · see citing works

Fetoplacental growth and vascular development in overnourished adolescent sheep at day 50, 90 and 130 of gestation

Redmer, D. A., Luther, J. S., Milne, J. S., Aitken, R. P., Johnson, M. L., Borowicz, P. P. P., Borowicz, M. A., Reynolds, L. P., & Wallace, J. M. (2009) · Reproduction · doi:10.1530/rep-08-0516 · Cited by 56 · see citing works

Effects of Sex Chromosome Dosage on Placental Size in Mice1

Ishikawa, H., Rattigan, Á., Fundele, R. H., & Burgoyne, P. S. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.012641 · Cited by 55 · see citing works

Down-Regulation of Growth Signaling Pathways Linked to a Reduced Cotyledonary Vascularity in Placentomes of Over-Nourished, Obese Pregnant Ewes

Zhu, M. J., Du, M., Nijland, M. J., Nathanielsz, P. W., Hess, B. W., Moss, G. E., & Ford, S. P. (2009) · Placenta · doi:10.1016/j.placenta.2009.02.001 · Cited by 54 · see citing works

Obesity and Health Status in Rural, Urban, and Suburban Southern Women

Ramsey, P., & Glenn, L. L. (2002) · Southern Medical Journal · doi:10.1097/00007611-200207000-00003 · Cited by 54 · see citing works

Epigenetic control of development and expression of quantitative traits

Jammes, H., Junien, C., & Chavatte‐Palmer, P. (2010) · Reproduction Fertility and Development · doi:10.1071/rd10259 · Cited by 53 · see citing works

Effect of Weight and Adiposity at Conception and Wide Variations in Gestational Dietary Intake on Pregnancy Outcome and Early Postnatal Performance in Young Adolescent Sheep1

Wallace, J. M., Milne, J. S., & Aitken, R. P. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.109.080069 · Cited by 49 · see citing works

Fetoplacental biometry and umbilical artery Doppler velocimetry in the overnourished adolescent model of fetal growth restriction

Carr, D. J., Aitken, R. P., Milne, J. S., David, A. L., & Wallace, J. M. (2012) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2012.05.008 · Cited by 47 · see citing works

Expression of the Placental Transcriptome in Maternal Nutrient Reduction in Baboons Is Dependent on Fetal Sex

Cox, L. A., Li, C., Glenn, J. P., Lange, K. J., Spradling, K. D., Nathanielsz, P. W., & Jansson, T. (2013) · Journal of Nutrition · doi:10.3945/jn.112.172148 · Cited by 47 · see citing works

Sexual Differentiation of the Brain and ADHD: What Is a Sex Difference in Prevalence Telling Us?

Waddell, J., & McCarthy, M. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2010_114 · Cited by 45 · see citing works

Maternal undernutrition and its long-term effects on the offspring

Roeder, L. M., & Chow, B. F. (1972) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/25.8.812 · Cited by 45 · see citing works

Epigenetic features of the mouse trophoblast

Rugg‐Gunn, P. J. (2012) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2012.01.012 · Cited by 38 · see citing works

What changes in DNA Methylation take Place in Individuals Exposed to Maternal Smoking in Utero ?

Suter, M., & Aagaard, K. M. (2012) · Epigenomics · doi:10.2217/epi.12.7 · Cited by 36 · see citing works

Critical periods of growth

McCance, R. A. (1976) · Proceedings of The Nutrition Society · doi:10.1079/pns19760051 · Cited by 32 · see citing works

Obesity and Health Status in Rural, Urban, and Suburban Southern Women

Ramsey, P., & Glenn, L. L. (2002) · Southern Medical Journal · doi:10.1097/00007611-200295070-00002 · Cited by 30 · see citing works

The Dysfunctional Placenta Epigenome: Causes and Consequences

Lee, S.-A., & Ding, C. (2012) · Epigenomics · doi:10.2217/epi.12.49 · Cited by 20 · see citing works

Effect of fatty acid composition of the sow diet on the innate and adaptive immunity of the piglets after weaning

Tanghe, S., Cox, E., Melkebeek, V., SMET, S. D., & Millet, S. (2014) · The Veterinary Journal · doi:10.1016/j.tvjl.2014.02.025 · Cited by 7 · see citing works

Placental Origins of Chronic Disease

Burton, G. J., Fowden, A. L., & Thornburg, K. L. (2016) · Physiological Reviews · doi:10.1152/physrev.00029.2015 · Cited by 717 · see citing works

Sex-Specific Placental Responses in Fetal Development

Rosenfeld, C. S. (2015) · Endocrinology · doi:10.1210/en.2015-1227 · Cited by 473 · see citing works

The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming

Bronson, S. L., & Bale, T. L. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.231 · Cited by 285 · see citing works

The placenta‐brain‐axis

Rosenfeld, C. S. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24603 · Cited by 280 · see citing works

Developmental Programming, a Pathway to Disease

Padmanabhan, V., Cardoso, R. C., & Puttabyatappa, M. (2016) · Endocrinology · doi:10.1210/en.2016-1003 · Cited by 234 · see citing works

The frequency and type of placental histologic lesions in term pregnancies with normal outcome

Romero, R. J., Kim, Y. M., Pacora, P., Kim, C. J., Benshalom-Tirosh, N., Jaiman, S., Bhatti, G., Kim, J.-S., Qureshi, F., Jacques, S. M., et al. (2018) · Journal of Perinatal Medicine · doi:10.1515/jpm-2018-0055 · Cited by 185 · see citing works

Male-lineage transmission of an acquired metabolic phenotype induced by grand-paternal obesity

Cropley, J. E., Eaton, S. A., Aiken, A., Young, P. E., Giannoulatou, E., Ho, J. W. K., Buckland, M. E., Keam, S. P., Hutvágner, G., Humphreys, D. T., et al. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.06.008 · Cited by 171 · see citing works

The Placental Epigenome as a Molecular Link Between Prenatal Exposures and Fetal Health Outcomes Through the DOHaD Hypothesis

Lapehn, S., & Paquette, A. G. (2022) · Current Environmental Health Reports · doi:10.1007/s40572-022-00354-8 · Cited by 166 · see citing works

Manganese in Drinking Water and Cognitive Abilities and Behavior at 10 Years of Age: A Prospective Cohort Study

Rahman, S. M., Kippler, M., Tofail, F., Bölte, S., Derakhshani Hamadani, J., & Vahter, M. (2017) · Environmental Health Perspectives · doi:10.1289/ehp631 · Cited by 133 · see citing works

Epigenetics and the Developmental Origins of Health and Disease: Parental environment signalling to the epigenome, critical time windows and sculpting the adult phenotype.

Safi-Stibler, S., & Gabory, A. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.09.008 · Cited by 127 · see citing works

SExual Epigenetic Dimorphism in The Human Placenta: Implications for Susceptibility During The Prenatal Period

Martin, E. M., Smeester, L., Bommarito, P. A., Grace, M. R., Boggess, K., Kuban, K., Karagas, M. R., Marsit, C. J., O’Shea, T. M., & Fry, R. C. (2017) · Epigenomics · doi:10.2217/epi-2016-0132 · Cited by 138 · see citing works

Mitochondrial function and glucose metabolism in the placenta with gestational diabetes mellitus: role of miR-143

Muralimanoharan, S., Maloyan, A., & Myatt, L. (2016) · Clinical Science · doi:10.1042/cs20160076 · Cited by 137 · see citing works

Maternal Lipids and Fetal Overgrowth: Making Fat from Fat

Barbour, L. A., & Hernandez, T. L. (2018) · Clinical Therapeutics · doi:10.1016/j.clinthera.2018.08.007 · Cited by 129 · see citing works

Dynamics of epigenetic phenomena: intergenerational and intragenerational phenotype ‘washout’

Burggren, W. W. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.107318 · Cited by 128 · see citing works

Female obesity increases the risk of miscarriage of euploid embryos

Cozzolino, M., García-Velasco, J. A., Meseguer, M., Pellicer, A., & Bellver, J. (2021) · Fertility and Sterility · doi:10.1016/j.fertnstert.2020.09.139 · Cited by 111 · see citing works

Manganese and Developmental Neurotoxicity

Lucchini, R. G., Placidi, D., Cagna, G., Fedrighi, C., Oppini, M., Peli, M., & Zoni, S. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-60189-2_2 · Cited by 106 · see citing works

Diet before and during Pregnancy and Offspring Health: The Importance of Animal Models and What Can Be Learned from Them

Chavatte‐Palmer, P., Couturier‐Tarrade, A., & Rousseau‐Ralliard, D. (2016) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph13060586 · Cited by 105 · see citing works

From Maternal Diet to Neurodevelopmental Disorders: A Story of Neuroinflammation

Bordeleau, M., de Cossío, L. F., Chakravarty, M. M., & Tremblay, M. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.612705 · Cited by 108 · see citing works

Long term effects of ART: What do animals tell us?

Duranthon, V., & Chavatte‐Palmer, P. (2018) · Molecular Reproduction and Development · doi:10.1002/mrd.22970 · Cited by 103 · see citing works

Maternal Obesity, Maternal Overnutrition and Fetal Programming: Effects of Epigenetic Mechanisms on the Development of Metabolic Disorders

Şanlı, E., & Kabaran, S. (2019) · Current Genomics · doi:10.2174/1389202920666191030092225 · Cited by 104 · see citing works

Metabolic Profile in Early Pregnancy Is Associated with Offspring Adiposity at 4 Years of Age: The Rhea Pregnancy Cohort Crete, Greece

Daraki, V. N., Georgiou, V., Papavasiliou, S. S., Chalkiadaki, G., Karahaliou, M., Koinaki, S., Sarri, K. O., Vassilaki, M. E., Kogevinas, M., & Chatzi, L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126327 · Cited by 92 · see citing works

The association between placental histopathology and autism spectrum disorder

Straughen, J. K., Misra, D. P., Divine, G., Shah, R., Perez, G., VanHorn, S., Onbreyt, V., Dygulska, B., Schmitt, R., Lederman, S., et al. (2017) · Placenta · doi:10.1016/j.placenta.2017.07.006 · Cited by 91 · see citing works

Impacts of bisphenol A (BPA) and phthalate exposures on epigenetic outcomes in the human placenta

Strakovsky, R. S., & Schantz, S. L. (2018) · Current Zoology · doi:10.1093/eep/dvy022 · Cited by 90 · see citing works

Leptin as a breast milk component for the prevention of obesity

Palou, M., Picó, C., & Palou, A. (2018) · Nutrition Reviews · doi:10.1093/nutrit/nuy046 · Cited by 82 · see citing works

Mechanisms for sex differences in energy homeostasis

Wang, C., & Xu, Y. (2018) · Journal of Molecular Endocrinology · doi:10.1530/jme-18-0165 · Cited by 80 · see citing works

Microglia along sex lines: From brain colonization, maturation and function, to implication in neurodevelopmental disorders

Bordeleau, M., Carrier, M., Luheshi, G. N., & Tremblay, M.-È. (2019) · Seminars in Cell &amp; Developmental Biology · doi:10.1016/j.semcdb.2019.06.001 · Cited by 75 · see citing works

Metabolic-endocrine disruption due to preterm birth impacts growth, body composition, and neonatal outcome

Möllers, L. S., Yousuf, E. I., Hamatschek, C., Morrison, K. M., Hermanussen, M., Fusch, C., & Rochow, N. (2021) · Pediatric Research · doi:10.1038/s41390-021-01566-8 · Cited by 76 · see citing works

Developmental Origins of Disease - Crisis Precipitates Change

Reichetzeder, C., Putra, S. E. D., Li, J., & Hocher, B. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000447801 · Cited by 75 · see citing works

Sex-specific differences and developmental programming for diseases in later life

Sundrani, D. P., Roy, S., Jadhav, A. T., & Joshi, S. (2017) · Reproduction Fertility and Development · doi:10.1071/rd16265 · Cited by 74 · see citing works

Nonhuman Primates and Translational Research—Cardiovascular Disease

Cox, L. A., Olivier, M., Spradling‐Reeves, K. D., Karere, G. M., Comuzzie, A. G., & VandeBerg, J. L. (2017) · ILAR Journal · doi:10.1093/ilar/ilx025 · Cited by 74 · see citing works

Cardiac remodelling in a baboon model of intrauterine growth restriction mimics accelerated ageing

Kuo, A. H., Li, C., Li, J., Huber, H. F., Nathanielsz, P. W., & Clarke, G. D. (2016) · The Journal of Physiology · doi:10.1113/jp272908 · Cited by 71 · see citing works

Excessive backfat of sows at 109 d of gestation induces lipotoxic placental environment and is associated with declining reproductive performance1

Zhou, Y., Xu, T., Cai, A., Wu, Y., Wei, H., Jiang, S., & Peng, J. (2018) · Journal of Animal Science · doi:10.1093/jas/skx041 · Cited by 72 · see citing works

Early sex-dependent differences in response to environmental stress

Pérez‐Cerezales, S., Ramos‐Ibeas, P., Rizos, D. V., Lonergan, P., Bermejo‐Álvarez, P., & Gutiérrez‐Adán, A. (2017) · Reproduction · doi:10.1530/rep-17-0466 · Cited by 67 · see citing works

Placental DNA Methylation Adaptation to Maternal Glycemic Response in Pregnancy

Cárdenas, A., Gagné‐Ouellet, V., Allard, C., Brisson, D., Perron, P., Bouchard, L., & Hivert, M. (2018) · Diabetes · doi:10.2337/db18-0123 · Cited by 62 · see citing works

Developmental programming by maternal obesity in 2015: Outcomes, mechanisms, and potential interventions

Penfold, N., & Ozanne, S. E. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.06.015 · Cited by 60 · see citing works

Maternal and pediatric health and disease: integrating biopsychosocial models and epigenetics

Rubin, L. P. (2016) · Pediatric Research · doi:10.1038/pr.2015.203 · Cited by 59 · see citing works

Lipid overload during gestation and lactation can independently alter lipid homeostasis in offspring and promote metabolic impairment after new challenge to high-fat diet

Simino, L. A. D. P., de Fante, T., Fontana, M. F., Borges, F. O., Torsoni, M. A., Milanski, M., Velloso, L. A., & Torsoni, A. S. (2017) · Nutrition & Metabolism · doi:10.1186/s12986-017-0168-4 · Cited by 63 · see citing works

Programming of mouse obesity by maternal exposure to concentrated ambient fine particles

Chen, M., Wang, X., Hu, Z., Zhou, H., Xu, Y., Qiu, L., Qin, X., Zhang, Y., & Ying, Z. (2017) · Particle and Fibre Toxicology · doi:10.1186/s12989-017-0201-9 · Cited by 59 · see citing works

Transplacental Nutrient Transport Mechanisms of Intrauterine Growth Restriction in Rodent Models and Humans

Winterhager, E., & Gellhaus, A. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00951 · Cited by 59 · see citing works

Fish Intake in Pregnancy and Child Growth

Stratakis, N., Roumeliotaki, T., Oken, E., Barros, H., Basterrechea, M., Charles, M.-A. A., Eggesbø, M. Å., Forastiere, F., Gaillard, R., Gehring, U., et al. (2016) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/jamapediatrics.2015.4430 · Cited by 55 · see citing works

Early-life nutritional exposures and lifelong health: immediate and long-lasting impacts of probiotics, vitamin D, and breastfeeding

Berti, C., Agostoni, C. V., Davanzo, R., Hyppönen, E., Isolauri, E., Meltzer, H. M., Steegers‐Theunissen, R. P. M., & Cetin, I. (2016) · Nutrition Reviews · doi:10.1093/nutrit/nuw056 · Cited by 57 · see citing works

Histone Acetylation of Immune Regulatory Genes in Human Placenta in Association with Maternal Intake of Olive Oil and Fish Consumption

Acevedo, N., Frumento, P., Harb, H., Alhamwe, B. A., Johansson, C., Eick, L., Alm, J. S., Renz, H. E., Scheynius, A., & Potaczek, D. P. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051060 · Cited by 54 · see citing works

Fetal undernutrition is associated with perinatal sex-dependent alterations in oxidative status

Rodríguez‐Rodríguez, P., de Pablo, Á. L. L., Condezo‐Hoyos, L., Martin-Cabrejas, M. A., Aguilera, Y., Ruiz‐Hurtado, G., Gutiérrez-Arzápalo, P. Y., Ramiro‐Cortijo, D., Fernández‐Alfonso, M. S., González, M. C., et al. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.08.004 · Cited by 54 · see citing works

Long term effects of fetal undernutrition on rat heart. Role of hypertension and oxidative stress

Rodríguez‐Rodríguez, P., de Pablo, Á. L. L., García‐Prieto, C. F., Somoza, B., Quintana-Villamandos, B., de Diego, J. J. G., Gutiérrez-Arzápalo, P. Y., Ramiro‐Cortijo, D., González, M. C., & Arribas, S. M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171544 · Cited by 53 · see citing works

Review shows that maternal obesity induces serious adverse neonatal effects and is associated with childhood obesity in their offspring

Mitanchez, D., & Chavatte‐Palmer, P. (2018) · Acta Paediatrica · doi:10.1111/apa.14269 · Cited by 53 · see citing works

Effects of maternal stress and nutrient restriction during gestation on offspring neuroanatomy in humans

Franke, K., den Bergh, B. R. H. V., de Rooij, S. R., Kroegel, N., Nathanielsz, P. W., Rakers, F., Roseboom, T. J., Witte, O. W., & Schwab, M. G. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.031 · Cited by 52 · see citing works

The roles of leptin and adiponectin at the fetal-maternal interface in humans

Dos Santos, E., Duval, F., Vialard, F., & Dieudonné, M.-N. (2015) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2015-0031 · Cited by 52 · see citing works

Methionine Supply During Late-Gestation Triggers Offspring Sex-Specific Divergent Changes in Metabolic and Epigenetic Signatures in Bovine Placenta

Batistel, F., Alharthi, A. S., Yambao, R. R. C. S., Elolimy, A. A., Pan, Y., Parys, C., & Loor, J. J. (2018) · Journal of Nutrition · doi:10.1093/jn/nxy240 · Cited by 50 · see citing works

Critical and Sensitive Periods in Development and Nutrition

Colombo, J. A., Gustafson, K. M., & Carlson, S. E. (2019) · Annals of Nutrition and Metabolism · doi:10.1159/000508053 · Cited by 52 · see citing works

Killing two birds with one stone: Pregnancy is a sensitive window for endocrine effects on both the mother and the fetus

Plante, I., Winn, L. M., Vaillancourt, C., Grigorova, P., & Parent, L. (2021) · Environmental Research · doi:10.1016/j.envres.2021.112435 · Cited by 50 · see citing works

Sex-Specific Neurodevelopmental Programming by Placental Insulin Receptors on Stress Reactivity and Sensorimotor Gating

Bronson, S. L., Chan, J. C., & Bale, T. L. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.12.025 · Cited by 49 · see citing works

Maternal dyslipidemia during early pregnancy and epigenetic ageing of the placenta

Shrestha, D., Workalemahu, T., & Ayele, F. T. (2019) · Epigenetics · doi:10.1080/15592294.2019.1629234 · Cited by 47 · see citing works

Effect of maternal obesity on birthweight and neonatal fat mass: A prospective clinical trial

Mitanchez, D., Jacqueminet, S., Nizard, J., Tanguy, M., Ciangura, C., Lacorte, J., Carné, C. D., Foix-L'Hélias, L., Chavatte‐Palmer, P., Charles, M.-A. A., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181307 · Cited by 46 · see citing works

Adverse Maternal Metabolic Intrauterine Environment and Placental Epigenetics: Implications for Fetal Metabolic Programming

Lesseur, C., & Chen, J. (2018) · Current Environmental Health Reports · doi:10.1007/s40572-018-0217-9 · Cited by 46 · see citing works

Placental miR-340 mediates vulnerability to activity based anorexia in mice

Schroeder, M., Jakovcevski, M., Polacheck, T., Drori, Y., Luoni, A., Röh, S., Zaugg, J., Ben‐Dor, S., Albrecht, C., & Chen, A. (2018) · Nature Communications · doi:10.1038/s41467-018-03836-2 · Cited by 44 · see citing works

Placental Malfunction, Fetal Survival and Development Caused by Sow Metabolic Disorder: The Impact of Maternal Oxidative Stress

Yang, X., Hu, R., Shi, M., Wang, L., Yan, J., Gong, J., Zhang, Q.-J., He, J., & Wu, S. (2023) · Antioxidants · doi:10.3390/antiox12020360 · Cited by 44 · see citing works

The stress of losing sleep: Sex-specific neurobiological outcomes

Wright, C. J., Milosavljevic, S., & Pocivavsek, A. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100543 · Cited by 45 · see citing works

Sex Differences in Early Embryogenesis: Inter‐Chromosomal Regulation Sets the Stage for Sex‐Biased Gene Networks

Engel, N. (2018) · BioEssays · doi:10.1002/bies.201800073 · Cited by 41 · see citing works

Maternal Nutrition and Fetal/Infant Development

Jain, S., Maheshwari, A., & Jain, S. K. (2022) · Clinics in Perinatology · doi:10.1016/j.clp.2022.02.005 · Cited by 41 · see citing works

Associations of Prenatal Exposure to Cadmium With Child Growth, Obesity, and Cardiometabolic Traits

Chatzi, L., Ierodiakonou, D., Margetaki, K., Vafeiadi, M., Chalkiadaki, G., Roumeliotaki, T., Fthenou, E., Pentheroudaki, E., McConnell, R., Kogevinas, M., et al. (2018) · American Journal of Epidemiology · doi:10.1093/aje/kwy216 · Cited by 41 · see citing works

BMI and miscarriage after IVF

Bellver, J. (2022) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0000000000000778 · Cited by 41 · see citing works

The human placenta and its role in reproductive outcomes revisited

Aye, I. L. M. H., Tong, S., Jones, D. S., & Smith, G. C. S. (2025) · Physiological Reviews · doi:10.1152/physrev.00039.2024 · Cited by 45 · see citing works

Management of the pregnant mare and long-term consequences on the offspring

Peugnet, P., Robles, M., Wimel, L., Couturier‐Tarrade, A., & Chavatte‐Palmer, P. (2016) · Theriogenology · doi:10.1016/j.theriogenology.2016.01.028 · Cited by 40 · see citing works

Epigenetic adaptation of the placental serotonin transporter gene (SLC6A4) to gestational diabetes mellitus

Blažević, S. A., Horvatiček, M., Kesić, M., Zill, P., Hranilović, D., Ivanišević, M., Desoyé, G., & Štefulj, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179934 · Cited by 40 · see citing works

Gestational sleep deprivation is associated with higher offspring body mass index and blood pressure

Ginkel, M. W. H., Ierodiakonou, D., Margetaki, K., Vafeiadi, M., Karachaliou, M., Kogevinas, M., Vrijkotte, T. G. M., & Chatzi, L. (2020) · SLEEP · doi:10.1093/sleep/zsaa110 · Cited by 40 · see citing works

The GLP-1 analog, liraglutide prevents the increase of proinflammatory mediators in the hippocampus of male rat pups submitted to maternal perinatal food restriction

Diz-Chaves, Y., Toba, L., Fandiño, J., González-Matías, L. C., García‐Segura, L. M., & Mallo, F. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1370-7 · Cited by 39 · see citing works

Differential DNA Methylation in Placenta Associated With Maternal Blood Pressure During Pregnancy

Workalemahu, T., Ouidir, M., Shrestha, D., Wu, J., Grantz, K. L., & Ayele, F. T. (2020) · Hypertension · doi:10.1161/hypertensionaha.119.14509 · Cited by 38 · see citing works

Maternal diet quality during pregnancy is associated with biomarkers of metabolic risk among male offspring

Francis, E. C., Dabelea, D., Shankar, K., & Perng, W. (2021) · Diabetologia · doi:10.1007/s00125-021-05533-0 · Cited by 36 · see citing works

Autism-Associated DNA Methylation at Birth From Multiple Tissues Is Enriched for Autism Genes in the Early Autism Risk Longitudinal Investigation

Bakulski, K. M., Dou, J., Feinberg, J. I., Aung, M. T., Ladd‐Acosta, C., Volk, H. E., Newschaffer, C. J., Croen, L., Hertz‐Picciotto, I., Levy, S. E., et al. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.775390 · Cited by 35 · see citing works

“Three Hits” Hypothesis for Developmental Origins of Health and Diseases in View of Cardiovascular Abnormalities

Li, X., Zhang, M., Pan, X., Xu, Z., & Sun, M. (2017) · Birth Defects Research · doi:10.1002/bdr2.1037 · Cited by 35 · see citing works

Maternal iron homeostasis: effect on placental development and function

Roberts, H., Bourque, S. L., & Renaud, S. J. (2020) · Reproduction · doi:10.1530/rep-20-0271 · Cited by 34 · see citing works

Placental transcriptomic signatures of prenatal exposure to Hydroxy-Polycyclic aromatic hydrocarbons

Paquette, A. G., Lapehn, S., Freije, S. L., MacDonald, J. W., Bammler, T. K., Day, D. B., Loftus, C. T., Kannan, K., Mason, W. A., Bush, N. R., et al. (2023) · Environment International · doi:10.1016/j.envint.2023.107763 · Cited by 33 · see citing works

Maternal plasma antioxidant status in the first trimester of pregnancy and development of obstetric complications

Ramiro‐Cortijo, D., Herrera, T., Rodríguez‐Rodríguez, P., de Pablo, Á. L. L., de la Calle, M., López‐Giménez, M. R., Urda, A. I. M., Gutiérrez-Arzápalo, P. Y., Rioja, R. G., Aguilera, Y., et al. (2016) · Placenta · doi:10.1016/j.placenta.2016.08.090 · Cited by 33 · see citing works

Exposure to chemical components of fine particulate matter and ozone, and placenta-mediated pregnancy complications in Tokyo: a register-based study

Michikawa, T., Morokuma, S., Yamazaki, S., Takami, A., Sugata, S., Yoshino, A., Takeda, Y., Nakahara, K., Saito, S., Hoshi, J., et al. (2021) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/s41370-021-00299-4 · Cited by 33 · see citing works

The Prenatal Hormone Milieu in Autism Spectrum Disorder

Worsham, W., Dalton, S., & Bilder, D. A. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.655438 · Cited by 29 · see citing works

Environmental risk factors in puppies and kittens for developing chronic disorders in adulthood: A call for research on developmental programming

Gaillard, V., Chastant‐Maillard, S., England, G., Forman, O. P., German, A. J., Suchodolski, J. S., Villaverde, C., Chavatte‐Palmer, P., & Péron, F. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.944821 · Cited by 31 · see citing works

Sex Differences in Placental Protein Expression and Efficiency in a Rat Model of Fetal Programming Induced by Maternal Undernutrition

Phuthong, S., Reyes‐Hernández, C. G., Rodríguez‐Rodríguez, P., Ramiro‐Cortijo, D., Gil‐Ortega, M., González‐Blázquez, R., González, M. C., de Pablo, Á. L. L., & Arribas, S. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010237 · Cited by 30 · see citing works

Maternal Iron Deficiency Alters Trophoblast Differentiation and Placental Development in Rat Pregnancy

Roberts, H., Woodman, A. G., Baines, K. J., Jeyarajah, M. J., Bourque, S. L., & Renaud, S. J. (2021) · Endocrinology · doi:10.1210/endocr/bqab215 · Cited by 30 · see citing works

DOHaD at the intersection of maternal immune activation and maternal metabolic stress: a scoping review

Goldstein, J. A., Norris, S. A., & Aronoff, D. M. (2017) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174417000010 · Cited by 30 · see citing works

Chronic maternal inflammation or high-fat-feeding programs offspring obesity in a sex-dependent manner

Dudele, A., ­Hougaard, K. S., Kjølby, M., Hokland, M., Winther, G., Elfving, B., Wegener, G., Nielsen, A. L., Larsen, A., Nøhr, M. K., et al. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.136 · Cited by 30 · see citing works

Assisted Reproductive Technologies and the Placenta: Clinical, Morphological, and Molecular Outcomes

Riesche, L., & Bartolomei, M. S. (2018) · Seminars in Reproductive Medicine · doi:10.1055/s-0038-1676640 · Cited by 30 · see citing works

Placenta as a target of trichloroethylene toxicity

Elkin, E. R., Harris, S. M., Su, A. L., Lash, L. H., & Loch-Caruso, R. K. (2020) · Environmental Science Processes & Impacts · doi:10.1039/c9em00537d · Cited by 28 · see citing works

Risk Factors for Obesity Among Children Aged 24 to 80 months in Korea: A Decision Tree Analysis

Lee, I.-S., Bang, K., Moon, H., & Kim, J. (2019) · Journal of Pediatric Nursing · doi:10.1016/j.pedn.2019.02.004 · Cited by 28 · see citing works

Maternal high-fat diet sex-specifically alters placental morphology and transcriptome in rats: Assessment by next-generation sequencing

Lin, Y., Huang, L., Tsai, C., Sheen, J., Tiao, M., Yu, H., Lin, I.-C., & Tain, Y. (2019) · Placenta · doi:10.1016/j.placenta.2019.03.004 · Cited by 28 · see citing works

The Placenta’s Role in Sexually Dimorphic Fetal Growth Strategies

Christians, J. K. (2021) · Reproductive Sciences · doi:10.1007/s43032-021-00780-3 · Cited by 28 · see citing works

The Effects of COVID-19 Pandemic and Lockdown on Pediatric Nutritional and Metabolic Diseases: A Narrative Review

Capra, M. E., Stanyevic, B., Giudice, A., Monopoli, D., Decarolis, N. M., Esposito, S., & Biasucci, G. (2022) · Nutrients · doi:10.3390/nu15010088 · Cited by 29 · see citing works

Differential expression profiles of circulating microRNAs in newborns associated to maternal pregestational overweight and obesity

Méndez‐Mancilla, A., Lima‐Rogel, V., Toro-Ortíz, J. C., Escalante-Padrón, F. J., Monsiváis-Urenda, A. E., Noyola, D. E., & Salgado‐Bustamante, M. (2017) · Pediatric Obesity · doi:10.1111/ijpo.12247 · Cited by 28 · see citing works

Maternal age at delivery, lung function and asthma in offspring: a population-based survey

Real, F. G., Burgess, J. A., Villani, S., Dratva, J., Heinrich, J., Janson, C., Jarvis, D., Koplin, J. J., Leynaert, B., Lodge, C., et al. (2018) · European Respiratory Journal · doi:10.1183/13993003.01611-2016 · Cited by 27 · see citing works

Transcriptome analysis of the effect of pyrroloquinoline quinone disodium (PQQ·Na2) on reproductive performance in sows during gestation and lactation

Zhang, B., Wang, C., Yang, W., Zhang, H., Meng, Q., Shi, B., & Shan, A. (2019) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-019-0369-y · Cited by 25 · see citing works

Mechanisms linking exposure to preeclampsia in utero and the risk for cardiovascular disease

Andraweera, P. H., Gatford, K. L., Care, A. S., Bianco‐Miotto, T., Lassi, Z. S., Dekker, G., Arstall, M. A., & Roberts, C. T. (2020) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174420000094 · Cited by 25 · see citing works

Early Pregnancy Dyslipidemia is Associated with Placental DNA Methylation at Loci Relevant for Cardiometabolic Diseases

Ouidir, M., Zeng, X., Workalemahu, T., Shrestha, D., Grantz, K. L., Mendola, P., Zhang, C., & Ayele, F. T. (2020) · Epigenomics · doi:10.2217/epi-2019-0293 · Cited by 24 · see citing works

Placental pathology predicts infantile neurodevelopment

Ueda, M., Tsuchiya, K. J., Yaguchi, C., Furuta‐Isomura, N., Horikoshi, Y., Matsumoto, M., Suzuki, M., Oda, T., Kawai, K., Itoh, T., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-06300-w · Cited by 25 · see citing works

Associations Between Maternal Lipid Blood Levels at the 13th Week of Pregnancy and Offspring’s Adiposity at Age 11-12 Years

Baas, R. E., Hutten, B. A., Henrichs, J., & Vrijkotte, T. G. M. (2022) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgac442 · Cited by 23 · see citing works

Intrinsic Sexual Dimorphism in the Placenta Determines the Differential Response to Benzene Exposure

Maxwell, A. J., Adzibolosu, N. K., Hu, A., You, Y., Stemmer, P. M., Ruden, D. M., Petriello, M. C., Sadagurski, M., Debarba, L. K., Koshko, L., et al. (2022) · iScience · doi:10.1016/j.isci.2023.106287 · Cited by 24 · see citing works

Embryo cryopreservation leads to sex-specific DNA methylation perturbations in both human and mouse placentas

Mani, S. R., Ghosh, J., Rhon‐Calderón, E. A., Lan, Y., Ord, T. S., Kalliora, C., Chan, J., Schultz, B. M., Vaughan‐Williams, E., Coutifaris, C., et al. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac138 · Cited by 24 · see citing works

Breeding animals for quality products: not only genetics

Chavatte‐Palmer, P., Couturier‐Tarrade, A., Kiefer, H., Duranthon, V., & Jammes, H. (2015) · Reproduction Fertility and Development · doi:10.1071/rd15353 · Cited by 23 · see citing works

Neurodevelopmental Disruptions in Children of Preeclamptic Mothers: Pathophysiological Mechanisms and Consequences

González, A., & Valencia, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073632 · Cited by 21 · see citing works

Unravelling the impact of epigenetic mechanisms on offspring growth, production, reproduction and disease susceptibility

Sindhu, P., Magotra, A., Sindhu, V., & Chaudhary, P. (2024) · Zygote · doi:10.1017/s0967199424000224 · Cited by 21 · see citing works

Are there sex differences in fetal growth strategies and in the long-term effects of pregnancy complications on cognitive functioning?

Christians, J. K., & Chow, N. A. (2022) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174422000204 · Cited by 21 · see citing works

Long-Term Effects of Prenatal Exposure to Undernutrition on Cannabinoid Receptor-Related Behaviors: Sex and Tissue-Specific Alterations in the mRNA Expression of Cannabinoid Receptors and Lipid Metabolic Regulators

Ramírez-López, M. T., Arco, R., Decara, J. M., Vázquez, M., Rivera, P., Blanco, R. N., Alén, F., de Heras, R. G., Suárez, J., & de Fonseca, F. R. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00241 · Cited by 21 · see citing works

Placental contribution to nutritional programming of health and diseases: ontogenesis epigenetics and sexual dimorphism

Gabory, A., Panchenko, P. E., Ferry, L., & Junien, C. (2014) · HAL

Epigenetics of sexual dimorphism under different maternal diets in mouse placenta

Gabory, A., Panchenko, P. E., Ferry, L., & Junien, C. (2013) · HAL

Male and Female Placentas Have Divergent Transcriptomic and Epigenomic Responses to Maternal Diets: Not Just Hormones

Gabory, A., Vigé, A., Ferry, L., Attig, L., Jaïs, J., Jouneau, L., & Junien, C. (2014) · Research and perspectives in endocrine interactions · doi:10.1007/978-3-319-02591-9_6 · Cited by 2 · see citing works

Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic patterns in mouse placenta

Gabory, A., Ferry, L., Jouneau, L., Vigé, A., Mayeur, S., Attig, L., Lésage, J., Vieau, D., Jaïs, J., & Junien, C. (2013) · HAL

Epigénétique et Nutrition : impacts de l’alimentation maternelle sur le développement placentaire et la santé de la descendance

Panchenko, P. E., Lemaire, M., Fneich, S., Voisin, S. A. C., Jouin, M., Junien, C., & Gabory, A. (2015) · Biologie Aujourd hui · doi:10.1051/jbio/2015021 · Cited by 14 · see citing works