Increased glucose and placental GLUT-1 in large infants of obese nondiabetic mothers

Hyperglycemia and adverse pregnancy outcomes

(2008) · New England Journal of Medicine · doi:10.1056/nejmoa0707943 · Cited by 5,563 · see citing works

Metabolic Syndrome in Childhood: Association With Birth Weight, Maternal Obesity, and Gestational Diabetes Mellitus

Boney, C. M., Verma, A., Tucker, R., & Vohr, B. R. (2005) · Pediatrics · doi:10.1542/peds.2004-1808 · Cited by 2,303 · see citing works

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

Donovan, A., Brownlie, A., Zhou, Y., Shepard, J., Pratt, S. J., Moynihan, J., Paw, B. H., Drejer, A., Barut, B., Zapata, A., et al. (2000) · Nature · doi:10.1038/35001596 · Cited by 1,667 · 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

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

Fetuses of obese mothers develop insulin resistance in utero

Catalano, P. M., Presley, L., Minium, J., & Hauguel-de Mouzon, S. (2009) · Diabetes Care · doi:10.2337/dc08-2077 · Cited by 655 · see citing works

WEIGHT AND LENGTH AT BIRTH OF INFANTS OF DIABETIC MOTHERS

Pedersen, J. (1954) · European Journal of Endocrinology · doi:10.1530/acta.0.0160330 · Cited by 495 · see citing works

Management of Obesity in Pregnancy

Catalano, P. M. (2007) · Obstetrics and Gynecology · doi:10.1097/01.aog.0000253311.44696.85 · Cited by 373 · see citing works

Glucose transporter protein expression in human placenta throughout gestation and in intrauterine growth retardation.

Jansson, T., Wennergren, M., & Illsley, N. P. (1993) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.77.6.8263141 · Cited by 320 · see citing works

Identification and Characterization of Human Glucose Transporter-like Protein-9 (GLUT9)

Augustin, R., Carayannopoulos, M. O., Dowd, L. O., Phay, J. E., Moley, J. F., & Moley, K. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312226200 · Cited by 284 · 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

Glucose Transport and System A Activity in Syncytiotrophoblast Microvillous and Basal Plasma Membranes in Intrauterine Growth Restriction

Jansson, T., Ylvén, K., Wennergren, M., & Powell, T. L. (2002) · Placenta · doi:10.1053/plac.2002.0826 · Cited by 218 · see citing works

Placental glucose transport and GLUT 1 expression in insulin-dependent diabetes

Jansson, T., Wennergren, M., & Powell, T. L. (1999) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(99)70169-9 · Cited by 166 · see citing works

Should we always choose a nonparametric test when comparing two apparently nonnormal distributions?

Skovlund, E., & Fenstad, G. U. (2001) · Journal of Clinical Epidemiology · doi:10.1016/s0895-4356(00)00264-x · Cited by 163 · see citing works

Diabetes Alters the Expression and Activity of the Human Placental GLUT1 Glucose Transporter¹

Gaither, K., Quraishi, A. N., & Illsley, N. P. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.2.5438 · Cited by 149 · see citing works

Simultaneous preparation of paired, syncytial, microvillous and basal membranes from human placenta

Illsley, N. P., Wang, Z.-Q., Gray, A., Sellers, M. C., & Jacobs, M. M. (1990) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(90)90157-j · Cited by 140 · see citing works

Localisation of proteins of iron metabolism in the human placenta and liver

Bastin, J. M., Drakesmith, H., REES, M. C. P., Sargent, I. L., & Townsend, A. (2006) · British Journal of Haematology · doi:10.1111/j.1365-2141.2006.06216.x · Cited by 130 · see citing works

Protein Nitration in Placenta – Functional Significance

Webster, R. P., Roberts, V. H. J., & Myatt, L. (2008) · Placenta · doi:10.1016/j.placenta.2008.09.003 · Cited by 114 · see citing works

Localization of erythrocyte/HepG2-type glucose transporter (GLUT1) in human placental villi

Takata, K., Kasahara, T., Kasahara, M., Ezaki, O., & Hirano, H. (1992) · Cell and Tissue Research · doi:10.1007/bf00319362 · Cited by 109 · see citing works

Birth weight for gestational age of Mexican American infants born in the United States

Overpeck, M. D. (1999) · Obstetrics and Gynecology · doi:10.1016/s0029-7844(98)00553-5 · Cited by 91 · see citing works

Maternal BMI, glucose tolerance, and adverse pregnancy outcomes

Stuebe, A., Landon, M., Lai, Y., Spong, C., Carpenter, M., Ramin, S., Casey, B., Wapner, R., Varner, M., Rouse, D., et al. (2012) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2012.04.035 · Cited by 81 · see citing works

Transepithelial Glucose Transport and Metabolism in BeWo Choriocarcinoma Cells

Vardhana, P. A., & Illsley, N. P. (2002) · Placenta · doi:10.1053/plac.2002.0857 · Cited by 78 · see citing works

Glucose transport across the basal plasma membrane of human placental syncytiotrophoblast

Johnson, L. W., & Smith, C. H. (1985) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(85)90472-9 · Cited by 77 · see citing works

Stability of reference proteins in human placenta: General protein stains are the benchmark

Lanoix, D., St‐Pierre, J., Lacasse, A., Viau, M., Lafond, J., & Vaillancourt, C. (2012) · Placenta · doi:10.1016/j.placenta.2011.12.008 · Cited by 74 · see citing works

Influence of gestational age and fetal iron status on IRP activity and iron transporter protein expression in third-trimester human placenta

Bradley, J. L., Leibold, E. A., Harris, Z. L., Wobken, J. D., Clarke, S. L., Zumbrennen‐Bullough, K. B., Eisenstein, R. S., & Georgieff, M. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00525.2003 · Cited by 74 · see citing works

ATLANTIC-DIP: Raised Maternal Body Mass Index (BMI) Adversely Affects Maternal and Fetal Outcomes in Glucose-Tolerant Women According to International Association of Diabetes and Pregnancy Study Groups (IADPSG) Criteria

Dennedy, M. C., Avalos, G., O’Reilly, M., O'Sullivan, E. P., Gaffney, G., & Dunne, F. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-2674 · Cited by 63 · see citing works

Metabolism of the Human Placenta Perfused in Vitro: Glucose Transfer and Utilization, O2 Consumption, Lactate and Ammonia Production

Mouzon, S. H., Challier, J.-C., Cedard, L., & Olivé, G. (1983) · Pediatric Research · doi:10.1203/00006450-198309000-00009 · Cited by 62 · see citing works

Asymmetric Syncytial Expression of GLUT9 Splice Variants in Human Term Placenta and Alterations in Diabetic Pregnancies

Bibee, K., Illsley, N. P., & Moley, K. H. (2010) · Reproductive Sciences · doi:10.1177/1933719110380276 · Cited by 53 · see citing works

Increase in normal placental weights related to increase in maternal body mass index

Swanson, L. D., Bewtra, C., Swanson, L. D., & Bewtra, C. (2008) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767050701866963 · Cited by 52 · see citing works

Asymmetrical Transport of Glucose Across the In Vitro Perfused Human Placenta

Schneider, H., Reiber, W., Sager, R., & Malek, A. (2002) · Placenta · doi:10.1053/plac.2002.0869 · Cited by 48 · see citing works

The association of maternal and fetal glucose homeostasis with fetal adiposity and birthweight

Walsh, J., Mahony, R., Byrne, J., Foley, M., & McAuliffe, F. M. (2011) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2011.09.022 · Cited by 47 · see citing works

Reduced Placental Taurine Transporter (TauT) Activity in Pregnancies Complicated by Pre-eclampsia and Maternal Obesity

Desforges, M., Ditchfield, A., Hirst, C., Pegorie, C., Martyn-Smith, K., Sibley, C. P., & Greenwood, S. L. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-6093-0_9 · Cited by 43 · see citing works

Glucose Production by the Human Placenta in Vivo

Prendergast, C. H., Parker, K. H., Gray, R., Venkatesan, S., Bannister, P. A., Castro-Soares, J., Murphy, K. W., Beard, R. W., Regan, L., Robinson, S., et al. (1999) · Placenta · doi:10.1053/plac.1999.0419 · Cited by 26 · see citing works

Glucose transport from mother to fetus—A theoretical study

Barta, E., & Drugan, A. (2009) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2009.12.010 · Cited by 25 · see citing works

Influence of Maternal Obesity on the Long-Term Health of Offspring

Godfrey, K. M., Reynolds, R. M., Prescott, S. L., Nyirenda, M., Jaddoe, V. W. V., Eriksson, J. G., & Broekman, B. F. P. (2017) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(16)30107-3 · Cited by 1,059 · 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

Developmental origins of metabolic diseases

Hoffman, D. J., Powell, T. L., Barrett, E. S., & Hardy, D. B. (2020) · Physiological Reviews · doi:10.1152/physrev.00002.2020 · Cited by 483 · see citing works

Effects of maternal obesity on placental function and fetal development

Howell, K. R., & Powell, T. L. (2016) · Reproduction · doi:10.1530/rep-16-0495 · Cited by 354 · see citing works

Placental Function in Maternal Obesity

Kelly, A. C., Powell, T. L., & Jansson, T. (2020) · Clinical Science · doi:10.1042/cs20190266 · Cited by 227 · see citing works

Metabolic landscape in cardiac aging: insights into molecular biology and therapeutic implications

Xie, S., Xu, S., Deng, W., & Tang, Q. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01378-8 · Cited by 185 · see citing works

Adiponectin supplementation in pregnant mice prevents the adverse effects of maternal obesity on placental function and fetal growth

Aye, I. L. M. H., Rosario, F. J., Powell, T. L., & Jansson, T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515484112 · Cited by 163 · see citing works

Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring

Helle, E., & Priest, J. R. (2020) · Journal of the American Heart Association · doi:10.1161/jaha.119.011541 · Cited by 151 · see citing works

Δ9-tetrahydrocannabinol exposure during rat pregnancy leads to symmetrical fetal growth restriction and labyrinth-specific vascular defects in the placenta

Natale, B. V., Gustin, K., Lee, K., Holloway, A. C., Laviolette, S. R., Natale, D. R. C., & Hardy, D. B. (2020) · Scientific Reports · doi:10.1038/s41598-019-57318-6 · Cited by 125 · see citing works

Large for gestational age and macrosomia in singletons born after frozen/thawed embryo transfer (FET) in assisted reproductive technology (ART)

Berntsen, S., & Pinborg, A. B. (2018) · Birth Defects Research · doi:10.1002/bdr2.1219 · Cited by 116 · see citing works

Placental Function and the Development of Fetal Overgrowth and Fetal Growth Restriction

Dumolt, J. H., Powell, T. L., & Jansson, T. (2021) · Obstetrics and Gynecology Clinics of North America · doi:10.1016/j.ogc.2021.02.001 · Cited by 106 · see citing works

Maternal-fetal cross-talk via the placenta: influence on offspring development and metabolism

Kramer, A. C., Jansson, T., Bale, T. L., & Powell, T. L. (2023) · Development · doi:10.1242/dev.202088 · Cited by 110 · see citing works

Review: Placental transport and metabolism of energy substrates in maternal obesity and diabetes

Gallo, L. A., Barrett, H. L., & Nitert, M. D. (2016) · Placenta · doi:10.1016/j.placenta.2016.12.006 · Cited by 88 · see citing works

Exercise prevents the adverse effects of maternal obesity on placental vascularization and fetal growth

Son, J. S., Liu, X., Tian, Q., Zhao, L., Chen, Y., Hu, Y., Chae, S. A., de Avila, J. M., Zhu, M. J., & Du, ‬. (2019) · The Journal of Physiology · doi:10.1113/jp277698 · Cited by 86 · see citing works

Expression and functional characterisation of System L amino acid transporters in the human term placenta

Gaccioli, F., Aye, I. L. M. H., Roos, S., Lager, S., Ramirez, V. I., Kanai, Y., Powell, T. L., & Jansson, T. (2015) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-015-0054-8 · Cited by 85 · see citing works

Let-7a-5p inhibits triple-negative breast tumor growth and metastasis through GLUT12-mediated warburg effect

Shi, Y., Zhang, Y., Ran, F., Liu, J., Lin, J., Hao, X., Ding, L., & Ye, Q. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.09.012 · Cited by 83 · see citing works

Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice

Panchenko, P. E., Voisin, S. A. C., Jouin, M., Jouneau, L., Prézelin, A., Lecoutre, S., Breton, C., Jammes, H., Junien, C., & Gabory, A. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0188-3 · Cited by 77 · see citing works

Protein expression of fatty acid transporter 2 is polarized to the trophoblast basal plasma membrane and increased in placentas from overweight/obese women

Lager, S., Ramirez, V. I., Gaccioli, F., Jang, B., Jansson, T., & Powell, T. L. (2016) · Placenta · doi:10.1016/j.placenta.2016.02.010 · Cited by 78 · see citing works

Impact of pre-gestational and gestational diabetes mellitus on the expression of glucose transporters GLUT-1, GLUT-4 and GLUT-9 in human term placenta

Stanirowski, P. J., Szukiewicz, D., Pyźlak, M., Abdalla, N., Sawicki, W., & Cendrowski, K. (2016) · Endocrine · doi:10.1007/s12020-016-1202-4 · Cited by 75 · see citing works

Curcumin ameliorates high glucose-induced neural tube defects by suppressing cellular stress and apoptosis

Wu, Y., Wang, F., Reece, E. A., & Yang, P. (2015) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2015.01.017 · Cited by 74 · see citing works

Uteroplacental Glucose Uptake and Fetal Glucose Consumption: A Quantitative Study in Human Pregnancies

Michelsen, T. M., Holme, A. M., Holm, M. B., Roland, M. C. P., Haugen, G. N., Powell, T. L., Jansson, T., & Henriksen, T. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-01154 · Cited by 74 · see citing works

Complex, coordinated and highly regulated changes in placental signaling and nutrient transport capacity in IUGR

Chassen, S. S., & Jansson, T. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.12.024 · Cited by 66 · see citing works

Adipokines underlie the early origins of obesity and associated metabolic comorbidities in the offspring of women with pregestational obesity

Arroyo‐Jousse, V., Jaramillo, A., Castaño‐Moreno, E., Lépez, M., Carrasco‐Negüe, K., & Casanello, P. C. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2019.165558 · Cited by 68 · see citing works

Effects of Maternal Obesity and Gestational Diabetes Mellitus on the Placenta: Current Knowledge and Targets for Therapeutic Interventions

Bedell, S., Hutson, J. R., de Vrijer, B., & Eastabrook, G. D. M. (2020) · Current Vascular Pharmacology · doi:10.2174/1570161118666200616144512 · Cited by 94 · see citing works

Lower risk of adverse perinatal outcomes in natural versus artificial frozen–thawed embryo transfer cycles: a systematic review and meta-analysis

Moreno-Sepulveda, J. A., Espinós, J. J., & Checa, M. Á. (2021) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2021.03.002 · Cited by 61 · see citing works

Milk consumption during pregnancy increases birth weight, a risk factor for the development of diseases of civilization

Melnik, B. C., John, S. M., & Schmitz, G. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-014-0377-9 · Cited by 56 · see citing works

Insulin Stimulates GLUT4 Trafficking to the Syncytiotrophoblast Basal Plasma Membrane in the Human Placenta

James‐Allan, L. B., Arbet, J., Teal, S. B., Powell, T. L., & Jansson, T. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-02778 · Cited by 55 · see citing works

Persistent influence of maternal obesity on offspring health: Mechanisms from animal models and clinical studies

Wankhade, U. D., Thakali, K. M., & Shankar, K. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.07.001 · Cited by 48 · see citing works

Maternal obesity influences placental nutrient transport, inflammatory status and morphology in human term placenta.

Nogues, P., Santos, E. D., Couturier-Tarrade, A., Berveiller, P., Arnould, L., Lamy, E., Grassin-Delyle, S., Vialard, F., & Dieudonné, M. (2020) · Journal of Clinical Endocrinology and Metabolism · doi:10.1210/clinem/dgaa660 · Cited by 42 · see citing works

Placental Expression of Glucose Transporter Proteins in Pregnancies Complicated by Gestational and Pregestational Diabetes Mellitus

Stanirowski, P. J., Szukiewicz, D., Pazura, M., Sawicki, W., & Cendrowski, K. (2017) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2017.04.008 · Cited by 45 · see citing works

Maternal obesity causes fetal cardiac hypertrophy and alters adult offspring myocardial metabolism in mice

Vaughan, O. R., Rosario, F. J., Chan, J., Cox, L. A., Ferchaud‐Roucher, V., Berry, K. A. Z., Reusch, J. E. B., Keller, A. C., Powell, T. L., & Jansson, T. (2022) · The Journal of Physiology · doi:10.1113/jp282462 · Cited by 44 · see citing works

Pre-pregnancy underweight and obesity are positively associated with small-for-gestational-age infants in a Chinese population

Chen, Y. H., Li, L., Chen, W., Liu, Z. B., Ma, L., Gao, X., He, J. L., Wang, H., Zhao, M., Yang, Y., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-52018-7 · Cited by 43 · see citing works

Impact of pregravid obesity on maternal and fetal immunity: Fertile grounds for reprogramming

Sureshchandra, S., Marshall, N., & Messaoudi, I. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ri0619-181r · Cited by 38 · see citing works

Docosahexaenoic Acid Supplementation in Pregnancy Modulates Placental Cellular Signaling and Nutrient Transport Capacity in Obese Women

Lager, S., Ramirez, V. I., Acosta, O. M., Meireles, C. L., Miller, E., Gaccioli, F., Rosario, F. J., Gelfond, J. A. L., Hakala, K. W., Weintraub, S. T., et al. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-01384 · Cited by 39 · see citing works

The impact of maternal obesity in pregnancy on placental glucocorticoid and macronutrient transport and metabolism

Johns, E. C., Denison, F. C., & Reynolds, R. M. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.12.025 · Cited by 41 · see citing works

Fetomaternal Expression of Glucose Transporters (GLUTs)—Biochemical, Cellular and Clinical Aspects

Sibiak, R., Ożegowska, K., Wender-Ożegowska, E., Gutaj, P., Mozdziak, P. E., & Kempisty, B. (2022) · Nutrients · doi:10.3390/nu14102025 · Cited by 40 · see citing works

Modulation of fetoplacental growth, development and reproductive function by endocrine disrupters

Basak, S., Varma, S., & Duttaroy, A. K. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1215353 · Cited by 39 · see citing works

Role of Placental Glucose Transporters in Determining Fetal Growth

Joshi, N. P., Mane, A. R., Sahay, A. S., Sundrani, D. P., Joshi, S., & Yajnik, C. S. (2021) · Reproductive Sciences · doi:10.1007/s43032-021-00699-9 · Cited by 38 · see citing works

Independent factors influencing large-for-gestation birth weight in singletons born after in vitro fertilization

Korošec, S., Frangež, H. B., Steblovnik, L., Verdenik, I., & Bokal, E. V. (2015) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-015-0601-4 · Cited by 37 · see citing works

Normalizing adiponectin levels in obese pregnant mice prevents adverse metabolic outcomes in offspring

Paulsen, M. E., Rosario, F. J., Wesolowski, S. R., Powell, T. L., & Jansson, T. (2018) · The FASEB Journal · doi:10.1096/fj.201801015r · Cited by 35 · see citing works

Normalisation of circulating adiponectin levels in obese pregnant mice prevents cardiac dysfunction in adult offspring

Vaughan, O. R., Rosario, F. J., Powell, T. L., & Jansson, T. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0374-4 · Cited by 32 · see citing works

Analysis of correlations between the placental expression of glucose transporters GLUT-1, GLUT-4 and GLUT-9 and selected maternal and fetal parameters in pregnancies complicated by diabetes mellitus

Stanirowski, P. J., Szukiewicz, D., Pyźlak, M., Abdalla, N., Sawicki, W., & Cendrowski, K. (2017) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2017.1387897 · Cited by 32 · see citing works

HTLV-1 targets human placental trophoblasts in seropositive pregnant women

Tezuka, K., Fuchi, N., Okuma, K., Tsukiyama, T., Miura, S., Hasegawa, Y., Nagata, A., Komatsu, N., Hasegawa, H., Sasaki, D., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci135525 · Cited by 31 · see citing works

Changes in Placental Nutrient Transporter Protein Expression and Activity Across Gestation in Normal and Obese Women

James‐Allan, L. B., Teal, S. B., Powell, T. L., & Jansson, T. (2020) · Reproductive Sciences · doi:10.1007/s43032-020-00173-y · Cited by 30 · see citing works

Elevated body mass index during pregnancy and gestational weight gain in HIV‐infected and HIV‐uninfected women in Cape Town, South Africa: association with adverse birth outcomes

Madlala, H. P., Malaba, T. R., Newell, M., & Myer, L. (2020) · Tropical Medicine & International Health · doi:10.1111/tmi.13387 · Cited by 29 · see citing works

Maternal High Linoleic Acid Alters Placental Fatty Acid Composition

Shrestha, N., Holland, O. J., Kent, N. L., Perkins, A. V., McAinch, A. J., Cuffe, J. S. M., & Hryciw, D. H. (2020) · Nutrients · doi:10.3390/nu12082183 · Cited by 28 · see citing works

Maternal body mass index impacts fetal-placental size at birth and umbilical cord oxygen values with implications for regulatory mechanisms

Richardson, B. S., Ruttinger, S., Brown, H. K., Regnault, T. R. H., & de Vrijer, B. (2017) · Early Human Development · doi:10.1016/j.earlhumdev.2017.06.009 · Cited by 27 · see citing works

Placenta nutrient transport-related gene expression: the impact of maternal obesity and excessive gestational weight gain

Brett, K., Ferraro, Z. M., Holčı́k, M., & Adamo, K. B. (2015) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2015.1049522 · Cited by 26 · see citing works

First trimester mechanisms of gestational sac placental and foetal teratogenicity: a framework for birth cohort studies

Adibi, J. J., Layden, A. J., Birru, R. L., Miragaia, A. S., Xun, X., Smith, M. C., Yin, Q., Millenson, M. E., O’Connor, T. G., Barrett, E. S., et al. (2020) · Human Reproduction Update · doi:10.1093/humupd/dmaa063 · Cited by 26 · see citing works

No evidence of attenuation of placental insulin-stimulated Akt phosphorylation and amino acid transport in maternal obesity and gestational diabetes mellitus

Castillo‐Castrejón, M., Jansson, T., & Powell, T. L. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00196.2019 · Cited by 25 · see citing works

Effect of type 2 diabetes mellitus on placental expression and activity of nutrient transporters and their association with birth weight and neonatal adiposity

Castillo‐Castrejón, M., Yamaguchi, K., Rodel, R. L., Erickson, K., Kramer, A. W., Hirsch, N. M., Rolloff, K. P., Jansson, T., Barbour, L. A., & Powell, T. L. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111319 · Cited by 24 · see citing works

Expression of placental glucose transporter proteins in pregnancies complicated by fetal growth disorders

Stanirowski, P. J., Lipa, M., Bomba-Opon, D. A., & Wielgoś, M. (2020) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2019.12.003 · Cited by 24 · see citing works

Characterization of Visceral and Subcutaneous Adipose Tissue Transcriptome and Biological Pathways in Pregnant and Non-Pregnant Women: Evidence for Pregnancy-Related Regional-Specific Differences in Adipose Tissue

Mazaki‐Tovi, S., Vaisbuch, E., Tarca, A. L., Kusanovic, J. P., Than, N. G., Chaiworapongsa, T., Dong, Z., Hassan, S. S., & Romero, R. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0143779 · Cited by 23 · see citing works

Associations between maternal body mass index and diet composition with placental DNA methylation at term

Thakali, K. M., Zhong, Y., Cleves, M., Andres, A., & Shankar, K. (2020) · Placenta · doi:10.1016/j.placenta.2020.02.018 · Cited by 26 · see citing works

Maternal health around pregnancy and autism risk: a diagnosis-wide, population-based study

Kodesh, A., Levine, S. Z., Khachadourian, V., Rahman, R., Schlessinger, A., O’Reilly, P. F., Grove, J., Schendel, D., Buxbaum, J. D., Croen, L., et al. (2021) · Psychological Medicine · doi:10.1017/s0033291721001021 · Cited by 22 · see citing works

Placental Nutrient Transporters and Maternal Fatty Acids in SGA, AGA, and LGA Newborns From Mothers With and Without Obesity

García-Santillán, J.-A., Lazo-de-la-Vega-Monroy, M.-L., Rodriguez-Saldaña, G.-C., Solís‐Barbosa, M. A., Corona-Figueroa, M.-A., Gónzalez-Domínguez, M.-I., Gomez-Zapata, H.-M., Malacara, J. M., & Barbosa‐Sabanero, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.822527 · Cited by 24 · see citing works

Differential Expression of Glucose Transporter Proteins GLUT-1, GLUT-3, GLUT-8 and GLUT-12 in the Placenta of Macrosomic, Small-for-Gestational-Age and Growth-Restricted Foetuses

Stanirowski, P. J., Szukiewicz, D., Majewska, A., Wątroba, M., Pyźlak, M., Bomba-Opon, D. A., & Wielgoś, M. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10245833 · Cited by 19 · see citing works

The unexplored role of sedentary time and physical activity in glucose and lipid metabolism‐related placental mRNAs in pregnant women who are obese: the DALI lifestyle randomised controlled trial

Acosta‐Manzano, P., Leopold‐Posch, B., Simmons, D. S., Devlieger, R., Galjaard, S., Corcoy, R., Adelantado, J. M., Dunne, F., Harreiter, J., Kautzky‐Willer, A., et al. (2021) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.16945 · Cited by 18 · see citing works

Maternal prepregnancy weight as an independent risk factor for congenital heart defect: systematic review and meta‐analysis stratified by subtype and severity of defect

Salmeri, N., Seidenari, A., Cavoretto, P. I., Papale, M., Candiani, M., & Farina, A. (2024) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.27659 · Cited by 18 · see citing works

Made in the Womb: Maternal Programming of Offspring Cardiovascular Function by an Obesogenic Womb

Diniz, M. S., Grilo, L. F., Tocantins, C., Falcão‐Pires, I., & Pereira, S. P. (2023) · Metabolites · doi:10.3390/metabo13070845 · Cited by 17 · see citing works

Insulin-dependent, glucose transporter 1 mediated glucose uptake and tube formation in the human placental first trimester trophoblast cells

Basak, S., Vilasagaram, S., Naidu, K., & Duttaroy, A. K. (2018) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-018-3396-7 · Cited by 15 · see citing works

FGF15/FGF19 alleviates insulin resistance and upregulates placental IRS1/GLUT expression in pregnant mice fed a high-fat diet

Zhao, S., Wang, D., Li, Z., Xu, S., Chen, H., Ding, W., Yang, J., Zhao, W., Sun, B., & Wang, Z. (2021) · Placenta · doi:10.1016/j.placenta.2021.07.286 · Cited by 15 · see citing works

Differential Effects of Post-Weaning Diet and Maternal Obesity on Mouse Liver and Brain Metabolomes

Safi-Stibler, S., Thévenot, E., Jouneau, L., Jouin, M., Seyer, A., Jammes, H., Rousseau‐Ralliard, D., Baly, C., & Gabory, A. (2020) · Nutrients · doi:10.3390/nu12061572 · Cited by 14 · see citing works

The early life exposome and autism risk: a role for the maternal microbiome?

Gesù, C. M. D., & Buffington, S. A. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2385117 · Cited by 16 · see citing works

Placental Glucose Transporters and Response to Bisphenol A in Pregnancies from of Normal and Overweight Mothers

Ermini, L., Nuzzo, A. M., Ietta, F., Romagnoli, R., Moretti, L., Masturzo, B., Paulesu, L. R., & Rolfo, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126625 · Cited by 14 · see citing works

Hyperglycemia in Pregnancy-Associated Oxidative Stress Augments Altered Placental Glucose Transporter 1 Trafficking via AMPKα/p38MAPK Signaling Cascade

Wang, S., Ning, J., Huai, J., & Yang, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158572 · Cited by 13 · see citing works

Maternal diet modulates placental nutrient transporter gene expression in a mouse model of diabetic pregnancy

Kappen, C., Krüger, C., Jones, S., Herion, N. J., & Salbaum, J. M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0224754 · Cited by 13 · see citing works

Sex hormone‐binding globulin regulates glucose metabolism in human placental trophoblasts via cAMP/PKA/CREB1

Chi, X., Feng, C., Wang, X., & Jin, Z. (2020) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.14429 · Cited by 13 · see citing works

Mouse models of preeclampsia with preexisting comorbidities

Waker, C. A., Hwang, A. E., Bowman-Gibson, S., Chandiramani, C. H., Linkous, B., Stone, M. L., Keoni, C., Kaufman, M. R., & Brown, T. L. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1137058 · Cited by 12 · see citing works

Chlorpyrifos and Δ9 Tetrahydrocannabinol exposure and effects on parameters associated with the endocannabinoid system and risk factors for obesity

Silva, M. H. (2021) · Current Research in Toxicology · doi:10.1016/j.crtox.2021.08.002 · Cited by 12 · see citing works

Histone modifications as molecular drivers of cardiac aging: Metabolic alterations, epigenetic mechanisms, and emerging therapeutic strategies

Alrumaihi, F., Al-Doaiss, A. A., Ullah, F., Alwanian, W. M., Alharbi, H. O., Alassaf, F. S., Alfifi, S. M., Alshabrmi, F. M., Alkhayl, F. F. A., & Alatawi, E. A. (2025) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2025.103056 · Cited by 10 · see citing works

Isthmin-1 Improves Aging-Related Cardiac Dysfunction in Mice through Enhancing Glycolysis and SIRT1 Deacetylase Activity

Hu, M., Zhang, X., Gao, Y.-P., Hu, Y., Teng, T., Wang, S., & Tang, Q. (2024) · Aging and Disease · doi:10.14336/ad.2024.0113 · Cited by 9 · see citing works

Adiponectin Deficiency Alters Placenta Function but Does Not Affect Fetal Growth in Mice

Shrestha, M. M., Wermelin, S., Stener‐Victorin, E., Asterholm, I. W., & Benrick, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094939 · Cited by 9 · see citing works

Characterization of visceral and subcutaneous adipose tissue transcriptome in pregnant women with and without spontaneous labor at term: implication of alternative splicing in the metabolic adaptations of adipose tissue to parturition

Mazaki‐Tovi, S., Tarca, A. L., Vaisbuch, E., Kusanovic, J. P., Than, N. G., Chaiworapongsa, T., Dong, Z., Hassan, S. S., & Romero, R. J. (2016) · Journal of Perinatal Medicine · doi:10.1515/jpm-2015-0259 · Cited by 8 · see citing works

Synthesis of phospholipids in human placenta

Powell, T. L., Ferchaud‐Roucher, V., Madi, L., Uhlson, C. L., Berry, K. A. Z., Kramer, A. C., Erickson, K., Palmer, C. E., Chassen, S. S., & Castillo‐Castrejón, M. (2024) · Placenta · doi:10.1016/j.placenta.2024.01.007 · Cited by 9 · see citing works

The impact of obesity on placental vascular development and function

Ramanlal, I., James, J. L., & Boss, A. L. (2026) · Molecular Human Reproduction · doi:10.1093/molehr/gaag002 · Cited by 7 · see citing works

Maternal obesity-related placental dysfunction: From peri-conception to late gestation

Amabebe, E., Ikumi, N. M., Pillay, K., Matjila, M. J., & Anumba, D. O. C. (2023) · Placenta and Reproductive Medicine · doi:10.54844/prm.2023.0361 · Cited by 6 · see citing works

AMPK–mTORC1 pathway mediates hepatic IGFBP-1 phosphorylation in glucose deprivation: a potential molecular mechanism of hypoglycemia-induced impaired fetal growth

Kakadia, J. H., Khalid, M. U., Heinemann, I. U., & Han, V. K. M. (2024) · Journal of Molecular Endocrinology · doi:10.1530/jme-23-0137 · Cited by 5 · see citing works

Maternal obesity attenuates PPARγ nuclear migration impairing offspring adipogenesis

de Sousa, É., & Rodrigues, A. C. (2023) · Journal of Molecular Endocrinology · doi:10.1530/jme-23-0050 · Cited by 5 · see citing works

d-Glucose and its derivatives labeled with radioactive carbon and hydrogen: key tools for investigating biological processes and molecular mechanisms

Bayat, F. (2025) · EJNMMI Radiopharmacy and Chemistry · doi:10.1186/s41181-025-00346-7 · Cited by 4 · see citing works

Placental expression of GLUT ‐1, GLUT ‐3, and GLUT ‐4 mRNA and transcriptome profiling in pregnant women with diabetes

Sibiak, R., Gutaj, P., Mantaj, U., Adamczak, Ł., Blatkiewicz, M., Ruciński, M., & Wender-Ożegowska, E. (2024) · Journal of Diabetes Investigation · doi:10.1111/jdi.14369 · Cited by 4 · see citing works

Expression of glucose transporters in the human amnion derived mesenchymal stromal cells under normoglycemic and hyperglycemic conditions

Ünek, G., Çetinkaya, B. D., Doğru, S., Dogum, K., Molbay, M., Özmen, A., Yanar, K., Kipmen‐Korgun, D., Köksoy, S., Sakıncı, M., et al. (2019) · Biologia · doi:10.2478/s11756-019-00350-8 · Cited by 3 · see citing works

Insulin like growth factor 1 (IGF-1) and IGF binding proteins in obese pregnant women and their babies: Potential effects on placental function and fetal growth

Soliman, A. T., Hamed, N., Alyafei, F., Alaaraj, N., Ahmad, S., Itani, M., & Soliman, N. A. (2023) · World Journal of Advanced Research and Reviews · doi:10.30574/wjarr.2023.17.2.0222 · Cited by 2 · see citing works

Ferrous–sucrose complex supplementation regulates maternal plasma metabolism and the fecal microbiota composition and improves neonatal immunity and placental glucose transportation by activating the EGF/PI3K/AKT signaling pathways in sows

Dong, Z., Liu, H., Wan, D., Wu, X., & Yin, Y. (2023) · Food & Function · doi:10.1039/d3fo03733a · Cited by 2 · see citing works

Association between changes in glycosylated hemoglobin during the second and third trimesters and adverse pregnancy outcomes among women without hyperglycemia in pregnancy

Hu, M., Liang, S., Wu, Q., Lee, C. S., Lu, J., Bao, S., Wu, C., & Liang, Z. (2024) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2024.111841 · Cited by 2 · see citing works

Gene expression profiles in placenta and their association with anesthesia, delivery mode and maternal diabetes

Aljani, B., Garbe, A. I., Sedlmeier, E., Lickert, R., Rost, F., Ziegler, A., Bonifacio, E. E., & Eugster, A. (2024) · Placenta · doi:10.1016/j.placenta.2024.10.008 · Cited by 2 · see citing works

The Potential Impact of Maternal Milk Consumption During Pregnancy on mTORC1-Driven Fetal Growth

Melnik, B. C. (2016) · Springer eBooks · doi:10.1007/978-3-319-14874-8_18 · Cited by 2 · see citing works

Placental Nutrient Transport

James‐Allan, L. B., Powell, T. L., & Jansson, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64683-4 · Cited by 2 · see citing works

Gestational High-Fat Diet Drives Premature Differentiation of Orexigenic Neurons and Reactivity of Astrocytes in the Fetal Rat Lateral Hypothalamus

Galindo-Solano, N., Trejo-Villarreal, X., Díaz-Olivares, G., Rea-Palomino, G., Montes-Aguirre, D., Villagrán-Santa-Cruz, M., & Gutiérrez‐Ospina, G. (2025) · Brain Sciences · doi:10.3390/brainsci16010052 · Cited by 1 · see citing works

Maternal nutrition as a key determinant of placental and developing blood–brain barrier xenobiotic protective functions

Connor, K. L., Souza, N. I. S., dos Anjos, B. G., Matthews, S. G., & Bloise, E. (2026) · The Journal of Physiology · doi:10.1113/jp289627 · Cited by 1 · see citing works

Glucose and Amino Acid and Their Roles in Placentation

Duttaroy, A. K., & Basak, S. (2016) · Springer eBooks · doi:10.1007/978-3-319-38804-5_3 · Cited by 1 · see citing works

Carbohydrate Metabolism During Pregnancy

Chu, A., & Devaskar, S. U. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00040-8

Studies of the human placenta in vivo -The role of the placenta in glucose transfer and secretion of anti-angiogenic factors

Holme, A. M. (2018) · NORA - Norwegian Open Research Archives

Obésité et perte de poids maternelle chez la souris : effets métaboliques olfactifs et epigénétiques sur la descendance mâle et femelle

Junien, C., Panchenko, P. E., Lacroix, M. C., Jouin, M., Badonnel, K., Lemaire, M., Meunier, N., Safi-Stibler, S., Jammes, H., Breton, C., et al. (2020) · Bulletin de l Académie Nationale de Médecine · doi:10.1016/j.banm.2020.09.042

Physical activity during pregnancy alters gene expression in neonatal tissue

Reynolds, L. J., Vsevolozhskaya, O. A., Rice, B. B., Chavan, N. R., Dugan, A. J., Maddox, H. F., Preston, J. D., DeHoff, L. B., O’Brien, J., & Pearson, K. J. (2021) · Physiology International · doi:10.1556/2060.2021.00003

Placental Nutrient Transport

James‐Allan, L. B., Powell, T. L., & Jansson, T. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-21477-6.00085-7 · Cited by 1 · see citing works

Placental dysfunction in maternal obesity is a key mechanism of fetal programming of metabolic syndrome

Galagudza, M. M., Uspensky, Y. P., Fominykh, Y. A., Butko, D. Y., & Komar, V. V. (2025) · Translational Medicine · doi:10.18705/2311-4495-2025-12-3-268-282

ДИСФУНКЦИЯ ПЛАЦЕНТЫ ПРИ МАТЕРИНСКОМ ОЖИРЕНИИ — КЛЮЧЕВОЙ МЕХАНИЗМ ФЕТАЛЬНОГО ПРОГРАММИРОВАНИЯ МЕТАБОЛИЧЕСКОГО СИНДРОМА У ПЛОДА

Komar, V. V., Galagudza, M. M., Успенский, Ю. П., & Насыров, Р. А. (2025) · University therapeutic journal · doi:10.56871/utj.2025.49.25.002

Mémoire épigénétique des trajectoires pondérales maternelles préconceptionnelles au cours du développement et à long terme

Panchenko, P. E. (2015) · doi:10.70675/1c8455acza5c1z427fzb7c6z5b17ad36641e

Maternal glucagon-like peptide-1 is positively associated with fetal growth in pregnancies complicated with obesity

Dumolt, J. H., Rosario, F. J., Kramer, A. C., Horwitz, S., Powell, T. L., & Jansson, T. (2023) · Clinical Science · doi:10.1042/cs20220890 · Cited by 17 · see citing works

Inverse relationship between gestational weight gain and glucose uptake in human placenta from female foetuses

Walker, S. P., Ugoni, A. M., Lim, R., & Lappas, M. (2013) · Pediatric Obesity · doi:10.1111/j.2047-6310.2013.00206.x · Cited by 10 · see citing works

Insulin Stimulates GLUT4 Trafficking to the Syncytiotrophoblast Basal Plasma Membrane in the Human Placenta

James‐Allan, L. B., Arbet, J., Teal, S. B., Powell, T. L., & Jansson, T. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-02778 · Cited by 55 · see citing works

Placental hormones and maternal glucose metabolism. A study of fetal growth in normal pregnancy

Langhoff‐Roos, J., Lindmark, G., Wibell, L. B., & GEBRE‐MEDHIN, M. (1989) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1989.tb02392.x · Cited by 21 · see citing works

Uteroplacental Glucose Uptake and Fetal Glucose Consumption: A Quantitative Study in Human Pregnancies

Michelsen, T. M., Holme, A. M., Holm, M. B., Roland, M. C. P., Haugen, G. N., Powell, T. L., Jansson, T., & Henriksen, T. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-01154 · Cited by 74 · see citing works