The placenta in fetal growth restriction: What is going wrong?

Consensus definition of fetal growth restriction: a Delphi procedure: Consensus definition of FGR

Gordijn, S. J., Beune, I. M., Thilaganathan, B., Papageorghiou, A., Baschat, A. A., Baker, P. N., Silver, R. M., Wynia, K., & Ganzevoort, W. (2016) · Ultrasound in Obstetrics & Gynecology · doi:10.1002/uog.15884 · Cited by 1,638

Inadequate maternal vascular response to placentation in pregnancies complicated by pre‐eclampsia and by small‐for‐gestational age infants

KHONG, T. Y., DE WOLF, F., ROBERTSON, W. B., & BROSENS, I. (1986) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1986.tb07830.x · Cited by 1,591

Endovascular Trophoblast Invasion: Implications for the Pathogenesis of Intrauterine Growth Retardation and Preeclampsia

Kaufmann, P., Black, S., & Huppertz, B. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.014977 · Cited by 1,210

Rheological and Physiological Consequences of Conversion of the Maternal Spiral Arteries for Uteroplacental Blood Flow during Human Pregnancy

Burton, G. J., Woods, A., Jauniaux, E. R. M., & Kingdom, J. C. (2009) · Placenta · doi:10.1016/j.placenta.2009.02.009 · Cited by 1,190

Pathophysiology of placental-derived fetal growth restriction

Burton, G. J., & Jauniaux, E. (2018) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2017.11.577 · Cited by 1,070

Growth and function of the normal human placenta.

Gude, N., Roberts, C., Kalionis, B., & King, R. (2004) · Thrombosis Research · doi:10.1016/j.thromres.2004.06.038 · Cited by 946

DNA Repair, Genome Stability, and Aging

Lombard, D. B., Chua, K. F., Mostoslavsky, R., Franco, S., Gostissa, M., & Alt, F. W. (2005) · Cell · doi:10.1016/j.cell.2005.01.028 · Cited by 944

Human placenta and trophoblast development: key molecular mechanisms and model systems

Knöfler, M., Haider, S., Saleh, L., Pollheimer, J., Gamage, T. K. J. B., & James, J. L. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03104-6 · Cited by 818

Update on the Diagnosis and Classification of Fetal Growth Restriction and Proposal of a Stage-Based Management Protocol

Figueras, F., & Gratacós, E. (2014) · Fetal Diagnosis and Therapy · doi:10.1159/000357592 · Cited by 799

A senescent cell bystander effect: senescence‐induced senescence

Nelson, G., Wordsworth, J., Wang, C., Jurk, D., Lawless, C., Martin‐Ruiz, C., & von Zglinicki, T. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00795.x · Cited by 755

Adaptations of the human placenta to hypoxia: opportunities for interventions in fetal growth restriction

Colson, A., Sonveaux, P., Debiève, F., & Sferruzzi-Perri, A. N. (2020) · Human Reproduction Update · doi:10.1093/humupd/dmaa053 · Cited by 149

The Anti-Inflammatory and Curative Exponent of Probiotics: A Comprehensive and Authentic Ingredient for the Sustained Functioning of Major Human Organs

Virk, M. S., Virk, M. A., He, Y., Tufail, T., Gul, M., Qayum, A., Rehman, A., Rashid, A., Ekumah, J., Han, X., et al. (2024) · Nutrients · doi:10.3390/nu16040546 · Cited by 144

Temporal trends in microplastic accumulation in placentas from pregnancies in Hawaiʻi

Weingrill, R. B., Lee, M., Benny, P. A., Riel, J. M., Saiki, K., Garcia, J., Oliveira, L. F. A. D. M., Fonseca, E. J. S., de Souza, S. T., D’Amato, F. D. O. S., et al. (2023) · Environment International · doi:10.1016/j.envint.2023.108220 · Cited by 127

Microorganisms in the reproductive system and probiotic's regulatory effects on reproductive health

Feng, T., & Liu, Y. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.03.017 · Cited by 84

Hypoxia and oxidative stress induce sterile placental inflammation in vitro

Baker, B., Heazell, A. E. P., Sibley, C. P., Wright, R., Bischof, H., Beards, F., Guevara, T., Girard, S., & Jones, R. L. (2021) · Scientific Reports · doi:10.1038/s41598-021-86268-1 · Cited by 71

Microplastics caused embryonic growth retardation and placental dysfunction in pregnant mice by activating GRP78/IRE1α/JNK axis induced apoptosis and endoplasmic reticulum stress

Bai, J. Y., Wang, Y., Deng, S., Yang, Y., Chen, S., & Wu, Z. (2024) · Particle and Fibre Toxicology · doi:10.1186/s12989-024-00595-5 · Cited by 76

Altered Levels of Decidual Immune Cell Subsets in Fetal Growth Restriction, Stillbirth, and Placental Pathology

Bezemer, R. E., Schoots, M. H., Timmer, A., Scherjon, S. A., Erwich, J. J., van Goor, H., Gordijn, S. J., & Prins, J. R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01898 · Cited by 62

Fetal growth restriction and stillbirth: Biomarkers for identifying at risk fetuses

King, V. J., Bennet, L., Stone, P. R., Clark, A., Gunn, A. J., & Dhillon, S. K. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.959750 · Cited by 52

Highlighting the trajectory from intrauterine growth restriction to future obesity

Gantenbein, K. V., & Kanaka‐Gantenbein, C. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1041718 · Cited by 53

Evolving the Era of 5D Ultrasound? A Systematic Literature Review on the Applications for Artificial Intelligence Ultrasound Imaging in Obstetrics and Gynecology

Jost, E., Kosian, P., Jimenez Cruz, J., Albarqouni, S., Gembruch, U., Strizek, B., & Recker, F. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12216833 · Cited by 44

Prenatal exercise in fetal development: a placental perspective

Chae, S. A., Son, J. S., & Du, ‬. (2021) · FEBS Journal · doi:10.1111/febs.16173 · Cited by 51

Placental features of fetal vascular malperfusion and infant neurodevelopmental outcomes at 2 years of age in severe fetal growth restriction

Gardella, B., Dominoni, M., Caporali, C., Cesari, S., Fiandrino, G., Longo, S., Vito, G. B. D., Naboni, C., Tonduti, D., Perotti, G., et al. (2021) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2021.03.037 · Cited by 40

The Placental NLRP3 Inflammasome and Its Downstream Targets, Caspase-1 and Interleukin-6, Are Increased in Human Fetal Growth Restriction: Implications for Aberrant Inflammation-Induced Trophoblast Dysfunction

Alfian, I., Chakraborty, A., Yong, H. E. J., Saini, S., Lau, R. W. K., Kalionis, B., Dimitriadis, E., Alfaidy, N., Ricardo, S. D., Samuel, C. S., et al. (2022) · Cells · doi:10.3390/cells11091413 · Cited by 40

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 49

Evolutionary divergence of embryo implantation in primates

Siriwardena, D., & Boroviak, T. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2021.0256 · Cited by 38

Epigenetics Beyond Fetal Growth Restriction: A Comprehensive Overview

Salmeri, N., Carbone, I. F., Cavoretto, P. I., Farina, A., & Morano, D. (2022) · Molecular Diagnosis & Therapy · doi:10.1007/s40291-022-00611-4 · Cited by 39

From stem cells to spiral arteries: A journey through early placental development

James, J. L., Boss, A. L., Sun, C., Allerkamp, H. H., & Clark, A. R. (2021) · Placenta · doi:10.1016/j.placenta.2021.11.004 · Cited by 38

Associations of Ambient Fine Particulate Matter and Its Chemical Constituents with Birth Weight for Gestational Age in China: A Nationwide Survey

Shen, Y., Wang, C., Yu, G., Meng, X., Wang, W., Kan, H., Zhang, J., & Cai, J. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.1c08393 · Cited by 33

Maternal PlGF and umbilical Dopplers predict pregnancy outcomes at diagnosis of early-onset fetal growth restriction

Spencer, R. N., Maksym, K., Hecher, K., Maršál, K., Figueras, F., Ambler, G., Whitwell, H. J., Nene, N. R., Sebire, N. J., Hansson, S. R., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci169199 · Cited by 33

Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells

Cui, K., Chen, T.-W., Zhu, Y., Shi, Y., Guo, Y., & Qin, J. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10390 · Cited by 28

Harnessing the therapeutic potential of the stem cell secretome in neonatal diseases

Tung, S., Delavogia, E., Fernandez‐Gonzalez, A., Mitsialis, S. A., & Kourembanas, S. (2023) · Seminars in Perinatology · doi:10.1016/j.semperi.2023.151730 · Cited by 27

Identification and Characterization of Extrachromosomal Circular DNA in Human Placentas With Fetal Growth Restriction

Yang, H., He, J., Huang, S., Yang, H., Yi, Q., Tao, Y., Chen, M., Zhang, X., & Qi, H. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.780779 · Cited by 26

Bioengineering Approaches for Placental Research

Wheeler, M. L., & Oyen, M. L. (2021) · Annals of Biomedical Engineering · doi:10.1007/s10439-020-02714-7 · Cited by 25

Endothelial dysfunction in preterm infants: The hidden legacy of uteroplacental pathologies

Amelio, G. S., Provitera, L., Raffaeli, G., Tripodi, M., Amodeo, I., Gulden, S., Cortesi, V., Manzoni, F. M. P., Cervellini, G., Tomaselli, A., et al. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.1041919 · Cited by 26

Rational Design of Nanomedicine for Placental Disorders: Birthing a New Era in Women's Reproductive Health

Geisler, H. C., Safford, H. C., & Mitchell, M. J. (2023) · Small · doi:10.1002/smll.202300852 · Cited by 24

Placental treatment with insulin-like growth factor 1 via nanoparticle differentially impacts vascular remodeling factors in guinea pig sub-placenta/decidua

Davenport, B. N., Jones, H. N., & Wilson, R. L. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2022.1055234 · Cited by 23

Multi-scale Modelling of Shear Stress on the Syncytiotrophoblast: Could Maternal Blood Flow Impact Placental Function Across Gestation?

Lee, T. C., Moulvi, A., James, J. L., & Clark, A. R. (2023) · Annals of Biomedical Engineering · doi:10.1007/s10439-022-03129-2 · Cited by 22

The Role of Kisspeptin in the Pathogenesis of Pregnancy Complications: A Narrative Review

Szydełko-Gorzkowicz, M., Poniedziałek‐Czajkowska, E., Mierzyński, R., Sotowski, M., & Leszczyńska‐Gorzelak, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126611 · Cited by 25

Dissecting the Impact of Maternal Androgen Exposure on Developmental Programming through Targeting the Androgen Receptor

Lu, H., Jiang, H., Li, C., Derisoud, E., Zhao, A., Eriksson, G., Lindgren, E., Pui, H., Risal, S., Pei, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202309429 · Cited by 23

Fear Stress During Pregnancy Affects Placental m6A-Modifying Enzyme Expression and Epigenetic Modification Levels

Wang, Q., Pan, M., Zhang, T., Jiang, Y., Zhao, P., Liu, X., Gao, A., Yang, L., & Hou, J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.927615 · Cited by 20

Puerariae lobatae Radix Alleviates Pre-Eclampsia by Remodeling Gut Microbiota and Protecting the Gut and Placental Barriers

Huang, L., Liu, Z., Wu, P., Yue, X., Lian, Z., He, P., Liu, Y., Zhou, R., & Zhao, J. (2022) · Nutrients · doi:10.3390/nu14235025 · Cited by 20

Developments in functional imaging of the placenta

Clark, A. R., Flouri, D., Mufti, N., James, J. L., Clements, E., Aughwane, R., Aertsen, M., David, A. L., & Melbourne, A. (2022) · British Journal of Radiology · doi:10.1259/bjr.20211010 · Cited by 20

Placental DNA methylation analysis of selective fetal growth restriction in monochorionic twins reveals aberrant methylated CYP11A1 gene for fetal growth restriction

Shi, D., Zhou, X., Cai, L., Wei, X., Zhang, L., Sun, Q., Zhou, F., & Sun, L. (2023) · The FASEB Journal · doi:10.1096/fj.202300742r · Cited by 19

Ovarian Stimulation in Mice Resulted in Abnormal Placentation through Its Effects on Proliferation and Cytokine Production of Uterine NK Cells

Ma, R., Jin, N., Lei, H., Dong, J., Xiong, Y., Qian, C., Chen, S., & Wang, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065907 · Cited by 17

Exploration of fetal growth restriction induced by vitamin D deficiency in rats via Hippo-YAP signaling pathway

Wang, J., Qiu, F., Zhao, Y., Gu, S., Wang, J., & Zhang, H. (2022) · Placenta · doi:10.1016/j.placenta.2022.08.062 · Cited by 17

Dietary adenosine supplementation improves placental angiogenesis in IUGR piglets by up-regulating adenosine A2a receptor

Wu, Z., Nie, J., Wu, D., Huang, S., Chen, J., Liang, H., Hao, X., Feng, L., Luo, H., & Tan, C. (2023) · Animal nutrition · doi:10.1016/j.aninu.2023.02.003 · Cited by 16

The unique applicability of the human placenta to the Adverse Outcome Pathway (AOP) concept: the placenta provides fundamental insights into human organ functions at multiple levels of biological organization

Gundacker, C., & Ellinger, I. (2020) · Reproductive Toxicology · doi:10.1016/j.reprotox.2020.07.014 · Cited by 17

Understanding a Potential Role for the NLRP3 Inflammasome in Placenta‐Mediated Pregnancy Complications

Moss, C., Dilworth, M., Harris, L. K., Freeman, S., & Heazell, A. E. P. (2025) · American Journal of Reproductive Immunology · doi:10.1111/aji.70077 · Cited by 17

Matrix directs trophoblast differentiation in a bioprinted organoid model of early placental development

Richards, C., Chen, H., O’Rourke, M. B., Bannister, A., Owen, G., Volkerling, A. M., Ghosh, A., Gorrie, C. A., Gallego‐Ortega, D., Bottomley, A. L., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62996-0 · Cited by 15

Molecular regulators of defective placental and cardiovascular development in fetal growth restriction

Umapathy, A., Clark, A. R., Sehgal, A., Karanam, V. L., Rajaraman, G., Kalionis, B., Jones, H. N., James, J., & Murthi, P. (2024) · Clinical Science · doi:10.1042/cs20220428 · Cited by 15

Specialized pro-resolving mediators: key regulators in placental function and pregnancy complications

Sousa, L. G., Correia‐da‐Silva, G., Teixeira, N. A. A., & Fonseca, B. M. (2025) · Journal of Molecular Medicine · doi:10.1007/s00109-025-02561-w · Cited by 14

Impaired in vivo feto-placental development is associated with neonatal neurobehavioral outcomes

Andescavage, N. N., Bullen, T., Liggett, M., Barnett, S. D., Kapse, A., Kapse, K. J., Ahmadzia, H. K., Vézina, G., Quistorff, J. L., Lopez, C., et al. (2022) · Pediatric Research · doi:10.1038/s41390-022-02340-0 · Cited by 14

Effects of human placenta cryopreservation on molecular characteristics of placental mesenchymal stromal cells

Navakauskienė, R., Žukauskaitė, D., Borutinskaite, V. V., Bukreieva, T., Skliutė, G., Valatkaitė, E., Zentelytė, A., Piešinienė, L., & Shablii, V. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1140781 · Cited by 14

The Gut Microbiota of Pregnant Rats Alleviates Fetal Growth Restriction by Inhibiting the TLR9/MyD88 Pathway

Tang, H., Li, H., Li, D., Peng, J., Zhang, X., & Yang, W. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2304.04020 · Cited by 14

Stroke vs. Preeclampsia: Dangerous Liaisons of Hypertension and Pregnancy

Lacković, M., Nikolić, D., Janković, M. Z., Rovčanin, M., & Mihajlovic, S. (2023) · Medicina · doi:10.3390/medicina59101707 · Cited by 14

Interrelation between miRNAs Expression Associated with Redox State Fluctuations, Immune and Inflammatory Response Activation, and Neonatal Outcomes in Complicated Pregnancy, Accompanied by Placental Insufficiency

Gusar, V. A., Timofeeva, A. V., Chagovets, V., Vysokikh, M. Y., Кан, Н. Е., Manukhova, L. A., Marey, M. V., & Sukhikh, G. T. (2022) · Antioxidants · doi:10.3390/antiox12010006 · Cited by 14

Melatonin Supplementation during the Late Gestational Stage Enhances Reproductive Performance of Sows by Regulating Fluid Shear Stress and Improving Placental Antioxidant Capacity

Wang, L., Yan, L., Han, Q., Li, G., Wu, H., Ma, X., Zhao, M., Ma, W., Ji, P., Zhang, R., et al. (2023) · Antioxidants · doi:10.3390/antiox12030688 · Cited by 13

Sexually dimorphic patterns in maternal circulating microRNAs in pregnancies complicated by fetal growth restriction

Baker, B., Lui, S., Lorne, I., Heazell, A. E. P., Forbes, K. A., & Jones, R. L. (2021) · Biology of Sex Differences · doi:10.1186/s13293-021-00405-z · Cited by 12

Placental Histological Features and Neurodevelopmental Outcomes at Two Years in Very-Low-Birth-Weight Infants

Spinillo, A., Dominoni, M., Caporali, C., Olivieri, I., Piana, R. L., Longo, S., Cesari, S., Fiandrino, G., Orcesi, S., & Gardella, B. (2021) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2021.04.007 · Cited by 12

Effects of dietary supplementation of gestating sows with adenosine 5ʹ-monophosphate or adenosine on placental angiogenesis and vitality of their offspring

Wu, D., Feng, L., Hao, X., Huang, S., Wu, Z., Ma, S., Yin, Y., & Tan, C. (2022) · Journal of Animal Science · doi:10.1093/jas/skac237 · Cited by 12

The Influence of the Vanishing Twin on the Perinatal Outcome of Surviving Singleton in IVF Pregnancy

Li, J., Li, J., Zhang, Y., Hu, K., Chen, N., Gao, J., Hu, J., Cui, L., & Chen, Z. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.832665 · Cited by 12

Maternal exposure to a glyphosate-based herbicide impairs placental development through endoplasmic reticulum stress in mice

Liu, M., Lu, S., Yang, C., Zhang, D., Zhu, J., Yin, J., Zhao, H., Yang, B., & Kuang, H. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113640 · Cited by 11

FGR-associated placental insufficiency and capillary angiogenesis involves disruptions in human placental miRNAs and mRNAs

Song, W.-H., Guo, Q., Puttabyatappa, M., Elangovan, V., Wang, J., Li, F., Liu, F.-F., Bi, X., Li, H., Fu, G.-P., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28007 · Cited by 12

Morphologic development of the first-trimester utero-placental vasculature is positively associated with embryonic and fetal growth: the Rotterdam Periconception Cohort

de Vos, E. S., Mulders, A. G. M. G. J., Koning, A. H. J., Willemsen, S. P., Rousian, M., van Rijn, B. B., Steegers, E. A. P., & Steegers‐Theunissen, R. P. M. (2024) · Human Reproduction · doi:10.1093/humrep/deae056 · Cited by 11

Distribution of decidual mast cells in fetal growth restriction and stillbirth at (near) term

Schoots, M. H., Bezemer, R. E., Dijkstra, T., Timmer, B., Scherjon, S. A., Erwich, J. J., Hillebrands, J., Gordijn, S. J., van Goor, H., & Prins, J. R. (2022) · Placenta · doi:10.1016/j.placenta.2022.10.007 · Cited by 11

Evaluation of Antiaging Effect of Sheep Placenta Extract Using SAMP8 Mice

Chou, M.-Y., Yang, C.-P. O., Li, W.-C., Yang, Y.-M., Huang, Y.-J., Wang, M.-F., & Lin, W. (2022) · Processes · doi:10.3390/pr10112242 · Cited by 11

A Hybrid Model for Fetal Growth Restriction Assessment by Automatic Placental Radiomics on T2‐Weighted MRI and Multifeature Fusion

Li, R., Song, F., Zhou, Q., Wu, W., Cao, Y., Zhang, G., Qian, Z., & Wang, L. (2025) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.29399 · Cited by 10

Multimodal fusion model for classifying placenta ultrasound imaging in pregnancies with hypertension disorders

Sun, H., Jiao, J., Ren, Y., Guo, Y., & Wang, Y. (2023) · Pregnancy Hypertension · doi:10.1016/j.preghy.2022.12.003 · Cited by 10

Mechanisms of neurodevelopmental toxicity of topiramate

Steele, J., Krishnan, V., & Finnell, R. H. (2024) · Critical Reviews in Toxicology · doi:10.1080/10408444.2024.2368552 · Cited by 11

Pathologic findings of the placenta and clinical implications – recommendations for placental examination

Menter, T., Bruder, E., Hösli, I., Lapaire, O., Raio, L., Schneider, H., Höller, S., Hentschel, R., Brandt, S., Bode, P. K., et al. (2024) · Swiss Medical Weekly · doi:10.57187/s.3929 · Cited by 12

Computational modeling in pregnancy biomechanics research

Clark, A. R., Yoshida, K., & Oyen, M. L. (2022) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2022.105099 · Cited by 10

Value of placental virtual magnetic resonance elastography and intravoxel incoherent motion-based diffusion and perfusion in predicting adverse outcomes of small-for-gestational-age infants

Deng, J., Cao, Y., Lu, Y., Song, J., Zhang, A., Zhao, M., Zhou, X. Y., Mu, X., Qu, F., Wu, F., et al. (2023) · Insights into Imaging · doi:10.1186/s13244-023-01503-9 · Cited by 10

Cholic acid exposure during late pregnancy causes placental dysfunction and fetal growth restriction by reactive oxygen species‐mediated activation of placental GCN2 / eIF2α pathway

Lin, S., Ye, M., Fu, Q., Pan, C., Liu, Y., Zheng, L., Hong, Q., & Chen, Y. (2023) · The FASEB Journal · doi:10.1096/fj.202202126r · Cited by 10

Transcriptomic analysis reveals the effects of maternal selenium deficiency on placental transport, hormone synthesis, and immune response in mice

Cheng, W., Zhang, L., Sa, P., Luo, J., & Li, M. (2022) · Metallomics · doi:10.1093/mtomcs/mfac062 · Cited by 9

Health Effects and Safety Assurance of Nanoparticles in Vulnerable Generations

Higashisaka, K. (2022) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b22-00277 · Cited by 9

Placental perfusion using intravoxel incoherent motion MRI combined with Doppler findings in differentiating between very low birth weight infants and small for gestational age infants

Deng, J., Zhang, A., Zhao, M., Zhou, X., Mu, X., Qu, F., Song, J., & Chen, T. (2023) · Placenta · doi:10.1016/j.placenta.2023.02.005 · Cited by 8

Incorporating placental pathology into clinical care and research

Roberts, D. J., Aisagbonhi, O. A., & Parast, M. M. (2024) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2024.08.002 · Cited by 8

Predicting adverse perinatal outcomes in small-for-gestational-age fetuses using MRI, ultrasound, and clinical data

Rabinowich, A., Olender, A., Avisdris, N., Wexler, Y., Yehuda, B., Vanetik, S., Khawaja, J., Graziani, T., Neeman, B., Zilberman, A., et al. (2025) · Radiology Advances · doi:10.1093/radadv/umaf030 · Cited by 8

Hydrogen sulfide in placental development and pregnancy disorders: mechanisms, therapeutic potential, and translational challenges

Du, L., Zheng, R., Ren, W., Liu, Y., Zhu, X., Chang, S., & Yang, Z. (2025) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-025-01465-1 · Cited by 9

Transcriptomic mapping of the metzincin landscape in human trophoblasts

Wächter, J., Shannon, M. J., Castellana, B., Baltayeva, J., & Beristain, A. G. (2022) · Gene Expression Patterns · doi:10.1016/j.gep.2022.119283 · Cited by 8

miR-181d-5p, which is upregulated in fetal growth restriction placentas, inhibits trophoblast fusion via CREBRF

Wu, Z., Li, F., Ruan, L., Feng, Q., Zhang, S., Li, Z., Otoo, A., Tang, J., Fu, L., Liu, T., et al. (2023) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-023-02917-6 · Cited by 8

IL-27 deficiency inhibits proliferation and invasion of trophoblasts via the SFRP2/Wnt/β-catenin pathway in fetal growth restriction

Zhang, X., Qin, X., Shen, H., Liu, K., Wang, C., Peng, T., Wu, J., Zhao, S., & Li, M. (2023) · International Journal of Medical Sciences · doi:10.7150/ijms.80684 · Cited by 8

NCOA2-induced secretion of leptin leads to fetal growth restriction via the NF-κB signaling pathway

Lin, Q., Yin, Y., Yin, T., Zhang, X., Zhou, X., & Sun, L. (2023) · Annals of Translational Medicine · doi:10.21037/atm-22-6444 · Cited by 8

Impact of Co-Occurrence of Obesity and SARS-CoV-2 Infection during Pregnancy on Placental Pathologies and Adverse Birth Outcomes: A Systematic Review and Narrative Synthesis

Ferraz, T., Benton, S. J., Zareef, I., Aribaloye, O., Bloise, E., & Connor, K. L. (2023) · Pathogens · doi:10.3390/pathogens12040524 · Cited by 8

Synergistic regulation of uterine radial artery adaptation to pregnancy by paracrine and hemodynamic factors

Allerkamp, H. H., Leighton, S., Pole, T., Clark, A. R., & James, J. L. (2023) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00205.2023 · Cited by 9

Scaling the EVERREST of severe, early-onset fetal growth restriction

Su, E. J. (2023) · Journal of Clinical Investigation · doi:10.1172/jci173563 · Cited by 7

Static and dynamic responses to hyperoxia of normal placenta across gestation with T2 *‐weighted MRI sequences

Bartin, R., Melbourne, A., Bobet, L., Gauchard, G., Menneglier, A., Grévent, D., Bussières, L., Siauve, N., & Salomon, L. J. (2024) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.27609 · Cited by 9

Current understanding in deciphering trophoblast cell differentiation during human placentation

Li, Q., Wu, H., Wang, Y., & Wang, H. (2022) · Biology of Reproduction · doi:10.1093/biolre/ioac083 · Cited by 7

Characteristics of childhood-onset systemic lupus erythematosus in pregnancy and its association with pregnancy outcomes: a retrospective comparative cohort study

Li, Z.-J., Hu, H., Ding, Z., Bian, Z., Xu, Y., Wen, H., Qu, Y.-L., Wang, J.-D., Huang, X., Li, D., et al. (2022) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-022-00954-x · Cited by 7

Two dimensional shear wave elastography—Basic principles and current applications

O’Hara, S., Edwards, C. R., & Zelesco, M. (2024) · Sonography · doi:10.1002/sono.12416 · Cited by 7

miR ‐101‐3p contributes to the progression of preeclampsia by suppressing WDR5 ‐mediated proliferation and invasion of trophoblast

Zhao, X., Su, F., Kong, F., Guo, Q., Wang, X., Cui, H., Li, Q., Zhang, W., Li, L., & Li, A. (2022) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.15475 · Cited by 7

Trophoblast Side-Population Markers are Dysregulated in Preeclampsia and Fetal Growth Restriction

Wong, G. P., Hartmann, S., Simmons, D. G., Ellis, S. L., Nonn, O., Cannon, P., Nguyen, T. V., Nguyen, A., Bartho, L. A., Tong, S. Y. C., et al. (2024) · Stem Cell Reviews and Reports · doi:10.1007/s12015-024-10764-w · Cited by 7

A machine learning model based on placental magnetic resonance imaging and clinical factors to predict fetal growth restriction

Wang, J., Chen, Z., Zhang, H., Li, W., Li, K., Deng, M., & Zou, Y. (2025) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-025-07450-1 · Cited by 9

Preparation, purification and identification of antioxidant peptides from the placenta of Tibetan sheep

Ren, H., Qin, T., Zhou, Q., Pan, L., Yu, C., Wang, Y., Fan, W., Li, Z., & Zheng, Y. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105560 · Cited by 6

MORPHOMETRIC ANALYSIS OF PLACENTAL AND M1/M2 MACROPHAGES POLARIZATION IN THE DETECTION OF FETAL GROWTH RESTRICTION

Berezhna, V. A., Громова, А. М., Tv, M., Udovytska, N. O., Старченко, И. И., & Vesnina, L. E. (2021) · World of Medicine and Biology · doi:10.26724/2079-8334-2021-1-75-12-17 · Cited by 6

Immunohistochemical localization of HCA1 receptor in placenta in presence of fetal growth restriction

Kozai, A., Murakami, R., Chiba, Y., Miyai, Y., Matsumoto, K., Kanenishi, K., & Ueno, M. (2024) · Placenta · doi:10.1016/j.placenta.2024.06.013 · Cited by 6

Isolation of pure primary term human cytotrophoblasts and their differentiation into syncytiotrophoblast-like cells as an ex vivo model of the human placenta

Motomura, K., Morita, H., Yamamoto, H., Wada, S., Sago, H., Takahashi, H., Saito, H., & Matsumoto, K. (2024) · Placenta · doi:10.1016/j.placenta.2024.07.307 · Cited by 6

Association between fetal growth restriction and stillbirth in twin compared with singleton pregnancies

Martínez-Varea, A., Prasad, S., Domenech, J., Kalafat, E., Morales-Roselló, J., & Khalil, A. (2024) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.27661 · Cited by 7

Micro-haemodynamics at the maternal–fetal interface: Experimental, theoretical and clinical perspectives

Zhou, Q., Doman, E. A., Schirrmann, K., Chen, Q., Seed, E. A., Johnstone, E., Selvaganapathy, P. R., Juel, A., Jensen, O. E., Bernabéu, M. O., et al. (2022) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2022.100387 · Cited by 6

Dietary Soy Prevents Fetal Demise, Intrauterine Growth Restriction, Craniofacial Dysmorphic Features, and Impairments in Placentation Linked to Gestational Alcohol Exposure Pivotal Role of Insulin and Insulin-Like Growth Factor Signaling NetworksPreprint

Qi, W., Gündoğan, F., Gilligan, J. T., & de la Monte, S. M. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4195657 · Cited by 6

Liver X receptor activation mitigates oxysterol-induced dysfunction in fetoplacental endothelial cells

George, M., Allerkamp, H. H., Koshenov, Z., Oflaz, F. E., Tam‐Amersdorfer, C., Kolesnik, T., Rittchen, S., Lang, M., Fröhlich, E., Graier, W. F., et al. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2024.159466 · Cited by 5

The maternal body mass index and first-trimester placental (vascular) development

Schenkelaars, N., Schoenmakers, S., Faas, M. M., Willemsen, S., de Vos, E. S., & Steegers‐Theunissen, R. P. M. (2024) · Placenta · doi:10.1016/j.placenta.2024.12.015 · Cited by 7

Dicyclohexyl phthalate derails trophoblast function and lipid metabolism through NDRG1 by targeting PPARα:RXRα

Zhang, Y., Geng, Y., Zhang, Y., Ma, Y., Yin, X. H., Chen, Z., Mu, X., Gao, R., Chen, X., Li, F., et al. (2025) · Toxicology · doi:10.1016/j.tox.2025.154124 · Cited by 5

HSD17B1-mediated trophoblast differentiation lowers estrogen levels in early-onset preeclampsia

Zheng, S., Feng, W., Sun, Z., Xu, P., Dong, S., Pan, L., Shen, H., Jin, H., Chen, P., & Shu, C. (2025) · Scientific Reports · doi:10.1038/s41598-025-02490-1 · Cited by 6

Investigations of HLA‐F and HLA‐G 3′UTR Polymorphisms in Preeclampsia and Fetal Growth Restriction Indicate a Possible Role of HLA‐F‐HLA‐G Haplotypes and Diplotypes

Møller, H. I., Christiansen, C. M., Klok, F. R., Pedersen, N. H., Blauenfeldt, T., Finne, K. F., Nielsen, H. S., & Hviid, T. V. F. (2025) · HLA · doi:10.1111/tan.70293 · Cited by 5

Placental volume in pregnant women with opioid use: prenatal MRI assessment

Wise, R. L., Brown, B. P., Haas, D. M., Sparks, C., Sadhasivam, S., Zhao, Y., & Radhakrishnan, R. (2023) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2022.2157256 · Cited by 5

A genetically small fetus impairs placental adaptations near term

Sandovici, I., Knee, O., López‐Tello, J., Shreeve, N., Fowden, A. L., Sferruzzi-Perri, A. N., & Constância, M. (2024) · Disease Models & Mechanisms · doi:10.1242/dmm.050719 · Cited by 5

Biomarkers for Diagnosing and Treating Fetal Growth Restriction

Wu, M., He, J., Chen, Y., Wan, F., Tang, H., Yin, C., He, H., Yu, H., & Yuan, C. (2023) · Current Medicinal Chemistry · doi:10.2174/0109298673258444231019104656 · Cited by 5

Allicin in pregnancy diets modulates steroid metabolism in pregnant sows and placental sulphate metabolism promoting placental angiogenesis and foetal development

Peng, J., Zhang, Y., Liu, Q., Tang, Y., Zhang, W., Zheng, S., Huang, W., Yang, M., He, Y., Li, Z., et al. (2024) · animal · doi:10.1016/j.animal.2024.101224 · Cited by 5

Editorial

Carter, A. M. (2010) · Placenta · doi:10.1016/j.placenta.2009.12.005 · Cited by 1

Classics revisited: The yale embryo

Ramsey, E. M. (1991) · Placenta · doi:10.1016/0143-4004(91)90013-6 · Cited by 5

PLAC1 Regulates the Occurrence of Fetal Growth Restriction by Inhibiting the Apoptosis of Trophoblast Cells.

Sun, D., Wu, H., Ping, Z., Zhu, H. F., & Ai, L. (2021) · PubMed · Cited by 8

ПЛАЦЕНТАРНАЯ НЕДОСТАТОЧНОСТЬ И ЗАДЕРЖКА РОСТА ПЛОДА (ОБЗОР ЛИТЕРАТУРЫ)

Рахимбердиевна, Д. Р. (2022) · Research Focus International Scientific Journal · doi:10.66073/researchfocus.v1i1.1075

Fetal growth retardation – the latest molecular mechanisms (Literature review)

Степаненко, Т. О. (2024) · Reproductive health of woman · doi:10.30841/2708-8731.8.2024.320093