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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 779 · see citing works

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 · see citing works

Oxygen measurements in endometrial and trophoblastic tissues during early pregnancy.

Rodesch, F., Simon, P., Donner, C., & Jauniaux, E. R. M. (1992) · PubMed · Cited by 753 · see citing works

Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches

Jansson, T., & Powell, T. L. (2007) · Clinical Science · doi:10.1042/cs20060339 · Cited by 542 · see citing works

Trophoblastic Oxidative Stress in Relation to Temporal and Regional Differences in Maternal Placental Blood Flow in Normal and Abnormal Early Pregnancies

Jauniaux, E., Hempstock, J., Greenwold, N., & Burton, G. J. (2003) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63803-5 · Cited by 511 · see citing works

Increased apoptosis in the syncytiotrophoblast in human term placentas complicated by either preeclampsia or intrauterine growth retardation

Ishihara, N., Matsuo, H., Murakoshi, H., Laoag‐Fernandez, J. B., Samoto, T., & Maruo, T. (2002) · American Journal of Obstetrics and Gynecology · doi:10.1067/mob.2002.119176 · Cited by 509 · see citing works

Maternal–Fetal Nutrient Transport in Pregnancy Pathologies: The Role of the Placenta

Brett, K., Ferraro, Z. M., Yockell‐Lelièvre, J., Gruslin, A., & Adamo, K. B. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150916153 · Cited by 459 · see citing works

Regulation of Nutrient Transport across the Placenta

Lager, S., & Powell, T. L. (2012) · Journal of Pregnancy · doi:10.1155/2012/179827 · Cited by 456 · see citing works

From Ancient Pathways to Aging Cells—Connecting Metabolism and Cellular Senescence

Wiley, C. D., & Campisi, J. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.010 · Cited by 440 · 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

Intrauterine growth restriction with absent end-diastolic flow velocity in the umbilical artery is associated with maldevelopment of the placental terminal villous tree

Krebs, C., Macara, L., Leiser, R., BOWMAN, A. W., Greer, I. A., & Kingdom, J. C. (1996) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(96)70103-5 · Cited by 427 · see citing works

Placental apoptosis in normal human pregnancy

SMITH, S. C. H., Baker, P. N., & SYMONDS, E. M. (1997) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(97)70438-1 · Cited by 400 · see citing works

Evidence of Placental Translation Inhibition and Endoplasmic Reticulum Stress in the Etiology of Human Intrauterine Growth Restriction

Yung, H.-W., Calabrese, S., Hynx, D., Hemmings, B. A., Cetin, I., Charnock-Jones, D. S., & Burton, G. J. (2008) · The American Journal of Pathology · doi:10.2353/ajpath.2008.071193 · Cited by 388 · see citing works

Regulation of vascular growth and function in the human placenta

Burton, G. J., Jones, D. S., & Jauniaux, E. (2009) · Reproduction · doi:10.1530/rep-09-0092 · Cited by 362 · see citing works

The pattern of interstitial trophoblasticinvasion of the myometrium in early human pregnancy

Pijnenborg, R., Bland, J. M., Robertson, W. B., Dixon, G., & Brosens, I. A. (1981) · Placenta · doi:10.1016/s0143-4004(81)80027-6 · Cited by 354 · see citing works

Structural analysis of placental terminal villi from growth-restricted pregnancies with abnormal umbilical artery doppler waveforms

Macara, L., Kingdom, J. C., Kaufmann, P., Kohnen, G., Hair, J., More, I. A. R., Lyall, F., & Greer, I. A. (1996) · Placenta · doi:10.1016/s0143-4004(05)80642-3 · Cited by 352 · 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

The influence of the intrauterine environment on human placental development

Burton, G. J., Jauniaux, E., & Charnock-Jones, D. S. (2010) · The International Journal of Developmental Biology · doi:10.1387/ijdb.082764gb · Cited by 307 · see citing works

Placental Adaptation: What Can We Learn from Birthweight:Placental Weight Ratio?

Hayward, C. E., Lean, S. C., Sibley, C. P., Jones, R. L., Wareing, M., Greenwood, S. L., & Dilworth, M. R. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00028 · Cited by 286 · see citing works

Stereological Investigation of Placental Morphology in Pregnancies Complicated by Pre-eclampsia with and without Intrauterine Growth Restriction

Mayhew, T. M., Ohadike, C., Baker, P. N., Crocker, I. P., Mitchell, C. A., & Ong, S. S. (2003) · Placenta · doi:10.1053/plac.2002.0900 · Cited by 278 · see citing works

Apoptosis in the Trophoblast—Role of Apoptosis in Placental Morphogenesis

Huppertz, B., & Kingdom, J. C. P. (2004) · Journal of the Society for Gynecologic Investigation · doi:10.1016/j.jsgi.2004.06.002 · Cited by 262 · see citing works

Umbilical amino acid concentrations in normal and growth-retarded fetuses sampled in utero by cordocentesis

Cetin, I., Corbetta, C., Sereni, L. P., Marconi, A. M., Bozzetti, P., Pardi, G., & Battaglia, F. C. (1990) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(90)90860-a · Cited by 259 · see citing works

Placental Phenotypes of Intrauterine Growth

Sibley, C. P., Turner, M. A., Cetin, I., Ayuk, P. T.-Y., Boyd, C. A. R., D'Souza, S. W., Glazier, J. D., Greenwood, S. L., Jansson, T., & Powell, T. L. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000181381.82856.23 · Cited by 250 · see citing works

Metabolic analysis of senescent human fibroblasts reveals a role for AMP in cellular senescence

Zwerschke, W., Mazurek, S., Stöckl, P., Hütter, E., EIGENBRODT, E., & Jansen‐Dürr, P. (2003) · Biochemical Journal · doi:10.1042/bj20030816 · 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

Vasculogenesis and angiogenesis in the early human placenta

Demir, R., Seval, Y., & Huppertz, B. (2007) · Acta Histochemica · doi:10.1016/j.acthis.2007.02.008 · Cited by 241 · see citing works

Placenta and Fetal Growth Restriction

SALAFIA, C. M., CHARLES, A. K., & MAAS, E. M. (2006) · Clinical Obstetrics and Gynecology · doi:10.1097/00003081-200606000-00007 · Cited by 235 · 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

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

Differences in Apoptotic Susceptibility of Cytotrophoblasts and Syncytiotrophoblasts in Normal Pregnancy to Those Complicated with Preeclampsia and Intrauterine Growth Restriction

Crocker, I. P., Cooper, S., Ong, S. S., & Baker, P. N. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63857-6 · Cited by 215 · see citing works

Customised birthweight centiles predict SGA pregnancies with perinatal morbidity

McCowan, L. M. E., Harding, J. E., & Stewart, A. W. (2005) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2005.00656.x · Cited by 209 · see citing works

Malaria and Pregnancy: Placental Cytokine Expression and Its Relationship to Intrauterine Growth Retardation

Moormann, A. M., Sullivan, A. D., Rochford, R. A., Chensue, S. W., Bock, P. J., Nyirenda, T. E., & Meshnick, S. R. (1999) · The Journal of Infectious Diseases · doi:10.1086/315135 · Cited by 208 · see citing works

Human placentation from nidation to 5 weeks of gestation. Part I: What do we know about formative placental development following implantation?

James, J. L., Carter, A. M., & Chamley, L. (2012) · Placenta · doi:10.1016/j.placenta.2012.01.020 · Cited by 204 · see citing works

Formation of Syncytial Knots is Increased by Hyperoxia, Hypoxia and Reactive Oxygen Species

Heazell, A. E. P., Moll, S. J., Jones, C. J. P., Baker, P. N., & Crocker, I. P. (2007) · Placenta · doi:10.1016/j.placenta.2006.10.007 · Cited by 204 · see citing works

Review: Trophoblast-Vascular Cell Interactions in Early Pregnancy: How to Remodel a Vessel

Harris, L. K. (2010) · Placenta · doi:10.1016/j.placenta.2009.12.012 · Cited by 203 · see citing works

Apoptotic changes occur in syncytiotrophoblast of human placental villi where fibrin type fibrinoid is deposited at discontinuities in the villous trophoblast

Nelson, D. M. (1996) · Placenta · doi:10.1016/s0143-4004(96)90019-3 · Cited by 194 · see citing works

Fetal growth restriction, catch-up growth and the early origins of insulin resistance and visceral obesity

Morrison, J. L., Duffield, J. A., Mühlhäusler, B. S., Gentili, S., & McMillen, I. C. (2009) · Pediatric Nephrology · doi:10.1007/s00467-009-1407-3 · Cited by 190 · see citing works

Screening for pre‐eclampsia and fetal growth restriction by uterine artery Doppler and PAPP‐A at 11–14 weeks' gestation

Pilalis, A., Souka, A. P., Antsaklis, P. J., Daskalakis, G., Papantoniou, N., Mesogitis, S. A., & Antsaklis, A. J. (2007) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.3881 · Cited by 188 · see citing works

Divergent trophoblast invasion and apoptosis in placental bed spiral arteries from pregnancies complicated by maternal anemia and early-onset preeclampsia/intrauterine growth restriction

Kadyrov, M., Kingdom, J. C., & Huppertz, B. (2006) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2005.07.035 · Cited by 188 · see citing works

Consensus Based Definition of Growth Restriction in the Newborn

Beune, I. M., Bloomfield, F. H., Ganzevoort, W., Embleton, N. D., Rozance, P. J., Leemhuis, A. G., Wynia, K., & Gordijn, S. J. (2018) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2017.12.059 · Cited by 180 · see citing works

Proliferation of villous trophoblast of the human placenta in normal and abnormal pregnancies

Arnholdt, H., Meisel, F., Fandrey, K., & Löhrs, U. (1991) · Virchows Archiv B Cell Pathology Including Molecular Pathology · doi:10.1007/bf02899568 · Cited by 178 · see citing works

FETAL GROWTH RETARDATION AND THE MATERNAL ARTERIAL SUPPLY OF THE HUMAN PLACENTA IN THE ABSENCE OF SUSTAINED HYPERTENSION

Wolf, F. D., Brosens, I. A., & Renaer, M. (1980) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1980.tb04601.x · Cited by 173 · see citing works

Imaging tumour hypoxia with oxygen-enhanced MRI and BOLD MRI

O’Connor, J. P. B., Robinson, S. P., & Waterton, J. C. (2018) · British Journal of Radiology · doi:10.1259/bjr.20180642 · Cited by 170 · see citing works

Morphometric evidence that villous development and fetoplacental angiogenesis are compromised by intrauterine growth restriction but not by pre-eclampsia

Mayhew, T. M., Wijesekara, J., Baker, P. N., & Ong, S. S. (2004) · Placenta · doi:10.1016/j.placenta.2004.04.011 · Cited by 168 · see citing works

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

Jansson, T. (1993) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.77.6.1554 · Cited by 162 · see citing works

Decreased vascularization and cell proliferation in placentas of intrauterine growth–restricted fetuses with abnormal umbilical artery flow velocity waveforms

Chen, C.-P., Bajoria, R., & Aplin, J. (2002) · American Journal of Obstetrics and Gynecology · doi:10.1067/mob.2002.125243 · Cited by 161 · see citing works

Reconciling the distinct roles of angiogenic/anti-angiogenic factors in the placenta and maternal circulation of normal and pathological pregnancies

Umapathy, A., Chamley, L., & James, J. L. (2019) · Angiogenesis · doi:10.1007/s10456-019-09694-w · Cited by 161 · see citing works

Early first trimester uteroplacental flow and the progressive disintegration of spiral artery plugs: new insights from contrast-enhanced ultrasound and tissue histopathology

Roberts, V. H. J., Morgan, T. K., Bednarek, P. H., Morita, M., Burton, G. J., Lo, J. O.-T., & Frias, A. E. (2017) · Human Reproduction · doi:10.1093/humrep/dex301 · Cited by 159 · see citing works

Quantitative description of the elaboration and maturation of villi from 10 weeks of gestation to term

Jackson, M., Mayhew, T. M., & Boyd, P. A. (1992) · Placenta · doi:10.1016/0143-4004(92)90060-7 · Cited by 158 · see citing works

Impact of cerebral redistribution on neurodevelopmental outcome in small-for-gestational-age or growth-restricted babies: a systematic review

Meher, S., Hernandez‐Andrade, E. A., Basheer, S. N., & Lees, C. C. (2015) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.14818 · Cited by 158 · see citing works

Mitochondrial – Endoplasmic reticulum interactions in the trophoblast: Stress and senescence

Burton, G. J., Yung, H. W., & Murray, A. J. (2016) · Placenta · doi:10.1016/j.placenta.2016.04.001 · Cited by 155 · see citing works

Placental size and the prediction of severe early‐onset intrauterine growth restriction in women with low pregnancy‐associated plasma protein‐A

Proctor, L., Toal, M., Keating, S. J., Chitayat, D. A., Okun, N. B., Windrim, R. C., Smith, G. C. S., & Kingdom, J. C. (2009) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.7308 · Cited by 151 · see citing works

Is there a role for placental senescence in the genesis of obstetric complications and fetal growth restriction?

Sultana, Z., Maiti, K., Dedman, L., & Smith, R. (2017) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2017.11.567 · Cited by 148 · see citing works

Short telomeres may play a role in placental dysfunction in preeclampsia and intrauterine growth restriction

Biron‐Shental, T., Halevy, R. S., Sharon, Y. A. M. V., Goldberg-Bittman, L., Kidron, D., Fejgin, M. D., & Amiel, A. (2010) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2010.01.036 · Cited by 146 · see citing works

Shunting the intervillous space: new concepts in human uteroplacental vascularization

Schaaps, J.-P., Tsatsaris, V., Goffin, F., Brichant, J.-F., Delbecque, K., Tebache, M., Collignon, L., Retz, M. C., & Foidart, J.-M. (2005) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2004.06.066 · Cited by 142 · see citing works

Comparison between three‐dimensional placental volume at 12 weeks and uterine artery impedance/notching at 22 weeks in screening for pregnancy‐induced hypertension, pre‐eclampsia and fetal growth restriction in a low‐risk population

Hafner, E., Metzenbauer, M., Höfinger, D., Stonek, F., Schuchter, K., Waldhör, T., & Philipp, K. (2006) · Ultrasound in Obstetrics & Gynecology · doi:10.1002/uog.2641 · Cited by 137 · see citing works

Cellular senescence, ageing and disease

Burton, D. G. A. (2008) · AGE · doi:10.1007/s11357-008-9075-y · Cited by 135 · see citing works

Villous trophoblast apoptosis is elevated and restricted to cytotrophoblasts in pregnancies complicated by preeclampsia, IUGR, or preeclampsia with IUGR

Longtine, M. S., Chen, B., Odibo, A. O., Zhong, Y., & Nelson, D. M. (2012) · Placenta · doi:10.1016/j.placenta.2012.01.017 · Cited by 134 · see citing works

Trophoblast interaction with fibrin matrix. Epithelialization of perivillous fibrin deposits as a mechanism for villous repair in the human placenta.

Nelson, D. M., Crouch, E. C., Curran, E. M., & Farmer, D. R. (1990) · Europe PMC (PubMed Central) · Cited by 133 · see citing works

Placental villous stroma as a model system for myofibroblast differentiation

Kohnen, G., Kertschanska, S., Demir, R., & Kaufmann, P. (1996) · Histochemistry and Cell Biology · doi:10.1007/bf01457655 · Cited by 129 · see citing works

Oxygen delivery and fetal-placental growth: Beyond a question of supply and demand?

Murray, A. J. (2012) · Placenta · doi:10.1016/j.placenta.2012.06.006 · Cited by 129 · see citing works

The Placenta in Pre-eclampsia and Intrauterine Growth Restriction: Studies on Exchange Surface Areas, Diffusion Distances and Villous Membrane Diffusive Conductances

Mayhew, T. M., Manwani, R., Ohadike, C., Wijesekara, J., & Baker, P. N. (2006) · Placenta · doi:10.1016/j.placenta.2006.02.011 · Cited by 128 · see citing works

Placental Growth from the First to the Second Trimester of Pregnancy in SGA-foetuses and Pre-eclamptic Pregnancies Compared to Normal Foetuses

Hafner, E., Metzenbauer, M., Höfinger, D., Münkel, M., Gassner, R., Schuchter, K., Dillinger‐Paller, B., & Philipp, K. (2003) · Placenta · doi:10.1053/plac.2002.0918 · Cited by 127 · see citing works

Evidence of oxidative stress-induced senescence in mature, post-mature and pathological human placentas

Cindrova-Davies, T., Fogarty, N. M. E., Jones, C. J. P., Kingdom, J., & Burton, G. J. (2018) · Placenta · doi:10.1016/j.placenta.2018.06.307 · Cited by 127 · see citing works

Placental surface shape, function, and effects of maternal and fetal vascular pathology

Salafia, C. M., Yampolsky, M., Misra, D. P., Shlakhter, O., Haas, D., Eucker, B., & Thorp, J. M. (2010) · Placenta · doi:10.1016/j.placenta.2010.09.005 · Cited by 126 · see citing works

Intrauterine growth restriction: comparison of American College of Obstetricians and Gynecologists practice bulletin with other national guidelines

Chauhan, S. P., Gupta, L. M., Hendrix, N. W., & Berghella, V. (2009) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2008.11.025 · Cited by 125 · see citing works

Trophoblast Invasion of Spiral Arteries: a Novel In Vitro Model

Cartwright, J. E., Kenny, L. C., Dash, P. R., Crocker, I. P., Aplin, J., Baker, P. N., & Whitley, G. S. J. (2002) · Placenta · doi:10.1053/plac.2001.0760 · Cited by 111 · see citing works

Pre-eclampsia and Fetal Growth Restriction: How Morphometrically Different is the Placenta?

Egbor, M., Ansari, T., Morris, N., Green, C. J., & Sibbons, P. D. (2005) · Placenta · doi:10.1016/j.placenta.2005.06.002 · Cited by 109 · see citing works

Reference values for the weight of freshly delivered term placentas and for placental weight–birth weight ratios

Burkhardt, T., Schäffer, L., Schneider, C., Zimmermann, R., & Kurmanavičius, J. (2005) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2005.10.032 · Cited by 103 · see citing works

Villous trophoblast of human placenta: a coherent view of its turnover, repair and contributions to villous development and maturation.

Mayhew, T. M. (2001) · PubMed · doi:10.14670/hh-16.1213 · Cited by 102 · see citing works

Trophoblast plugs: impact on utero-placental haemodynamics and spiral artery remodelling

James, J. L., Saghian, R., Perwick, R. D., & Clark, A. R. (2018) · Human Reproduction · doi:10.1093/humrep/dey225 · Cited by 102 · see citing works

Diagnosis of IUGR: traditional biometry

Platz, E., & Newman, R. (2008) · Seminars in Perinatology · doi:10.1053/j.semperi.2008.02.002 · Cited by 94 · see citing works

Placental MRI in Intrauterine Fetal Growth Restriction

Damodaram, M. S., Story, L., Eixarch, E., Patel, A., McGuinness, A., Allsop, J. M., Wyatt‐Ashmead, J., Kumar, S., & Rutherford, M. (2010) · Placenta · doi:10.1016/j.placenta.2010.03.001 · Cited by 93 · see citing works

Intra-uterine growth restriction is associated with increased apoptosis and altered expression of proteins in the p53 pathway in villous trophoblast

Heazell, A. E. P., Sharp, A. N., Baker, P. N., & Crocker, I. P. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0551-3 · Cited by 92 · see citing works

An evaluation of fetal glucogenesis in intrauterine growth-retarded pregnancies

Marconi, A. M., Cetin, I., Davoli, E., Baggiani, A., Fanelli, R., Fennessey, P. V., Battaglia, F. C., & Pardi, G. (1993) · Metabolism · doi:10.1016/0026-0495(93)90060-2 · Cited by 92 · see citing works

Understanding placental nutrient transfer – why bother? New biomarkers of fetal growth

Sibley, C. P. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.172403 · Cited by 92 · see citing works

Placental glucose transporter 3 (GLUT3) is up-regulated in human pregnancies complicated by late-onset intrauterine growth restriction

Janzen, C., Lei, M. Y. Y., Cho, J., Sullivan, P., Shin, B., & Devaskar, S. U. (2013) · Placenta · doi:10.1016/j.placenta.2013.08.010 · Cited by 91 · see citing works

Placental Volume at 11–13 Weeks’ Gestation in the Prediction of Birth Weight Percentile

Plasencia, W., Akolekar, R., Dagklis, T., Veduta, A., & Nicolaides, K. H. (2011) · Fetal Diagnosis and Therapy · doi:10.1159/000324318 · Cited by 86 · see citing works

Understanding abnormal uterine artery Doppler waveforms: a novel computational model to explore potential causes within the utero-placental vasculature

Clark, A. R., James, J. L., Stevenson, G. N., & Collins, S. L. (2018) · Placenta · doi:10.1016/j.placenta.2018.05.001 · Cited by 86 · see citing works

Aberrations in Placental Cytokine mRNA Related to Intrauterine Growth Retardation

Hahn‐Zoric, M., Hagberg, H., Kjellmer, I., Ellis, J., Wennergren, M., & Hanson, L. Å. (2002) · Pediatric Research · doi:10.1203/00006450-200202000-00013 · Cited by 85 · see citing works

Fetoplacental vascular alterations associated with fetal growth restriction

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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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

A Hybrid Model for Fetal Growth Restriction Assessment by Automatic Placental Radiomics on <scp>T2</scp>‐Weighted <scp>MRI</scp> 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 · see citing works

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 · see citing works

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 10 · see citing works

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 10 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 8 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 5 · see citing works

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 · see citing works

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 5 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Editorial

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

Classics revisited: The yale embryo

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

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 · see citing works

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