Prenatal maternal depressive symptoms are associated with neonatal left amygdala microstructure in a sex‐dependent way
Open accessAbstract
Exposures to prenatal maternal depressive symptoms (PMDS) may lead to neurodevelopmental changes in the offspring in a sex‐dependent way. Although a connection between PMDS and infant brain development has been established by earlier studies, the relationship between PMDS exposures measured at various prenatal stages and microstructural alterations in fundamental subcortical structures such as the amygdala remains unknown. In this study, we investigated the associations between PMDS measured during gestational weeks 14, 24 and 34 and infant amygdala microstructural properties using diffusion tensor imaging. We explored amygdala mean diffusivity (MD) alterations in response to PMDS in infants aged 11 to 54 days from birth. PMDS had no significant main effect on the amygdala MD metrics. However, there was a significant interaction effect for PMDS and infant sex in the left amygdala MD. Compared with girls, boys exposed to greater PMDS during gestational week 14 showed significantly higher left amygdala MD. These results indicate that PMDS are linked to infants' amygdala microstructure in boys. These associations may be relevant to later neuropsychiatric outcomes in the offspring. Further research is required to better understand the mechanisms underlying these associations and to develop effective interventions to counteract any potential adverse consequences.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Male offspring exposed to greater maternal depressive symptoms at 14 GW show higher left amygdala mean diffusivity (MD) compared with females.
“Compared with females, male offspring exposed to greater maternal depressive symptoms at 14 GW show higher left amygdala mean diffusivity (MD) [17].”
From Brain structural and functional outcomes in the offspring of women experiencing psychological distress during pregnancy (2024) · cites this paper as [17]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works
Detection of Postnatal Depression: Development of the 10-item Edinburgh Postnatal Depression Scale
Cox, J. L., Holden, J. M., & Sagovsky, R. (1987) · British Journal of Psychiatry · doi:10.1192/bjp.150.6.782 · Cited by 14,183 · see citing works
Jenkinson, M., Beckmann, C. F., Behrens, T. E. J., Woolrich, M. W., & Smith, S. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.015 · Cited by 11,314 · see citing works
Fast robust automated brain extraction
Smith, S. M. (2002) · Human Brain Mapping · doi:10.1002/hbm.10062 · Cited by 10,496 · see citing works
Yushkevich, P. A., Piven, J., Hazlett, H. C., Smith, R. G., Ho, S., Gee, J. C., & Gerig, G. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.015 · Cited by 8,868 · cited 1× · see citing works
“Figures were created using ParaView, ITK-SNAP and FSLeyes software (Ayachit, 2015; Jenkinson et al., 2012; Yushkevich et al., 2006).”
MethodEffects of stress throughout the lifespan on the brain, behaviour and cognition
Lupien, S. J., McEwen, B. S., Gunnar, M. R., & Heim, C. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2639 · Cited by 6,256 · see citing works
Andersson, J., & Sotiropoulos, S. N. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.019 · Cited by 3,439 · see citing works
Maternal Depression and Child Psychopathology: A Meta-Analytic Review
Goodman, S. H., Rouse, M. H., Connell, A. M., Broth, M. R., Hall, C. M., & Heyward, D. (2011) · Clinical Child and Family Psychology Review · doi:10.1007/s10567-010-0080-1 · Cited by 2,621 · cited 1× · see citing works
“Exposures to prenatal maternal depressive symptoms (PMDS) may predict the risk of developing long-term adverse physical and mental health outcomes in children (Bennett et al., 2004; Douros et al., 2017; Goodman et al., 2011; Lupien et al., 2009; Nazzari et al., 2019; Sidebottom et al., 2021).”
BackgroundUnbiased average age-appropriate atlases for pediatric studies
Fonov, V., Evans, A. C., Botteron, K., Almli, C. R., McKinstry, R. C., & Collins, D. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.033 · Cited by 2,290 · see citing works
Self-citationPrevalence of Depression During Pregnancy: Systematic Review
Bennett, H. A., Einarson, A., Taddio, A., Koren, G., & Einarson, T. R. (2004) · Obstetrics & Gynecology · doi:10.1097/01.aog.0000116689.75396.5f · Cited by 1,725 · see citing works
The ParaView Guide: A Parallel Visualization Application
Ayachit, U. (2015) · Cited by 1,254 · see citing works
Jeurissen, B., Leemans, A., Tournier, J., Jones, D. K., & Sijbers, J. (2013) · Human Brain Mapping · doi:10.1002/hbm.22099 · Cited by 1,088 · see citing works
Handy, D. E., Castro, R., & Loscalzo, J. (2011) · Circulation · doi:10.1161/circulationaha.110.956839 · Cited by 1,080 · see citing works
Maternal antenatal anxiety and children's behavioural/emotional problems at 4 years
O'Connor, T. G., Heron, J., Golding, J., Beveridge, M., & Glover, V. (2002) · British Journal of Psychiatry · doi:10.1192/bjp.180.6.502 · Cited by 1,070 · see citing works
Review: Sex and the human placenta: Mediating differential strategies of fetal growth and survival
Clifton, V. L. (2010) · Placenta · doi:10.1016/j.placenta.2009.11.010 · Cited by 868 · see citing works
Tamnes, C. K., Østby, Y., Fjell, A. M., Westlye, L. T., Due-Tønnessen, P., & Walhovd, K. B. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp118 · Cited by 779 · see citing works
Jones, D. K. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20033 · Cited by 776 · see citing works
Sex differences and stress across the lifespan
Bale, T. L., & Epperson, C. N. (2015) · Nature Neuroscience · doi:10.1038/nn.4112 · Cited by 751 · see citing works
Diffusion MRI : from quantitative measurement to in vivo neuroanatomy
Johansen‐Berg, H., & Behrens, T. E. J. (2014) · doi:10.1016/b978-0-12-374709-9.x0001-6 · Cited by 703 · see citing works
Prenatal stress and the programming of the HPA axis
Glover, V., O’Connor, T. G., & O’Donnell, K. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.11.008 · Cited by 567 · see citing works
Placental 11β‐hydroxysteroid dehydrogenase: a key regulator of fetal glucocorticoid exposure
Benediktsson, R., Calder, A. A., Edwards, C. R. W., & Seckl, J. R. (1997) · Clinical Endocrinology · doi:10.1046/j.1365-2265.1997.1230939.x · Cited by 536 · see citing works
Perinatal Risks of Untreated Depression during Pregnancy
Bonari, L., Pinto, N., Ahn, E., Einarson, A., Steiner, M. S., & Koren, G. (2004) · The Canadian Journal of Psychiatry · doi:10.1177/070674370404901103 · Cited by 524 · see citing works
Regional Gray Matter Growth, Sexual Dimorphism, and Cerebral Asymmetry in the Neonatal Brain
Gilmore, J. H., Lin, W., Prastawa, M. W., Looney, C. B., Vetsa, Y. S. K., Knickmeyer, R. C., Evans, D. D., Smith, J. K., Hamer, R. M., Lieberman, J. A., et al. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3339-06.2007 · Cited by 465 · see citing works
Mukherjee, P., Miller, J. H., Shimony, J. S., Philip, J. V., Nehra, D., Snyder, A. Z., Conturo, T. E., Neil, J. J., & McKinstry, R. C. (2002) · PubMed Central · Cited by 445 · see citing works
Prenatal stress and risk for autism
KINNEY, D., MUNIR, K., CROWLEY, D., & MILLER, A. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.06.004 · Cited by 440 · see citing works
Uematsu, A., Matsui, M., Tanaka, C., Takahashi, T., Noguchi, K., Suzuki, M., & Nishijo, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046970 · Cited by 378 · see citing works
Dubois, J., Dehaene‐Lambertz, G., Perrin, M., Mangin, J., Cointepas, Y., Duchesnay, É., Bihan, D. L., & Hertz‐Pannier, L. (2007) · Human Brain Mapping · doi:10.1002/hbm.20363 · Cited by 374 · see citing works
Radial diffusivity predicts demyelination in ex vivo multiple sclerosis spinal cords
Klawiter, E. C., Schmidt, R. E., Trinkaus, K., Liang, H.-F., Budde, M. D., Naismith, R. T., Song, S.-K., Cross, A. H., & Benzinger, T. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.007 · Cited by 364 · see citing works
Diffusion tensor imaging: serial quantitation of white matter tract maturity in premature newborns
Partridge, S. C., Mukherjee, P., Henry, R. G., Miller, S. P., Berman, J., Jin, H., Lü, Y., Glenn, O. A., Ferriero, D. M., Barkovich, A. J., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.02.038 · Cited by 328 · see citing works
Prenatal Maternal Stress Associated with ADHD and Autistic Traits in early Childhood
Ronald, A., Pennell, C. E., & Whitehouse, A. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2010.00223 · Cited by 289 · see citing works
Adouard, F., Glangeaud-Freudenthal, N. M. C., & Golse, B. (2005) · Archives of Women’s Mental Health · doi:10.1007/s00737-005-0077-9 · Cited by 285 · see citing works
Prenatal maternal depression alters amygdala functional connectivity in 6-month-old infants
Qiu, A., Anh, T. T., Li, Y., Chen, H., Rifkin-Graboi, A., Broekman, B. F. P., Kwek, K., Saw, S.-M., Chong, Y.-S., Gluckman, P. D., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.3 · Cited by 282 · see citing works
Prenatal depression restricts fetal growth
Diego, M., Field, T. M., Hernandez‐Reif, M., Schanberg, S. M., Kuhn, C. M., & González-Quintero, V. H. (2008) · Early Human Development · doi:10.1016/j.earlhumdev.2008.07.002 · Cited by 277 · see citing works
Prenatal stress: Role in psychotic and depressive diseases
Markham, J. A., & Koenig, J. I. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2035-0 · Cited by 274 · see citing works
Untreated prenatal maternal depression and the potential risks to offspring: a review
Davalos, D. B., Yadon, C. A., & Tregellas, H. C. (2012) · Archives of Women s Mental Health · doi:10.1007/s00737-011-0251-1 · Cited by 268 · see citing works
DTIPrep: quality control of diffusion-weighted images
Oğuz, İ., Farzinfar, M., Matsui, J., Budin, F., Liu, Z., Gerig, G., Johnson, H. J., & Styner, M. A. (2014) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2014.00004 · Cited by 261 · see citing works
Prenatal maternal depression associates with microstructure of right amygdala in neonates at birth.
Rifkin-Graboi, A., Bai, J., Chen, H., Hameed, W. B., Sim, L. W., Tint, M. T., Leutscher-Broekman, B., Chong, Y.-S., Gluckman, P. D., Fortier, M. V., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.06.019 · Cited by 258 · see citing works
Cohort Profile: The FinnBrain Birth Cohort Study (FinnBrain)
Karlsson, L., Tolvanen, M., Scheinin, N. M., Uusitupa, H., Korja, R., Ekholm, E. M. K., Tuulari, J. J., Pajulo, M., Huotilainen, M., Paunio, T., et al. (2017) · International Journal of Epidemiology · doi:10.1093/ije/dyx173 · Cited by 256 · see citing works
Self-citationDWI predicts future progression to Alzheimer disease in amnestic mild cognitive impairment
Kantarci, K., Petersen, R. C., Boeve, B. F., Knopman, D. S., Weigand, S. D., O’Brien, P. C., Shiung, M. M., Smith, G. E., Ivnik, R. J., Tangalos, E. G., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000153076.46126.e9 · Cited by 251 · see citing works
Amygdala and hippocampus volumes in pediatric major depression
Rosso, I. M., Cintron, C. M., Steingard, R. J., Renshaw, P. F., Young, A. D., & Yurgelun-Todd, D. A. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.10.027 · Cited by 239 · see citing works
Transfer of maternal psychosocial stress to the fetus
Rakers, F., Rupprecht, S., Dreiling, M., Bergmeier, C., Witte, O. W., & Schwab, M. G. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.019 · Cited by 231 · see citing works
Gousias, I. S., Edwards, A. D., Rutherford, M., Counsell, S. J., Hajnal, J. V., Rueckert, D., & Hammers, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.083 · Cited by 219 · see citing works
Gender differences in human cortical synaptic density
Alonso‐Nanclares, L., González‐Soriano, J., Rodríguez, J., & DeFelipe, J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803652105 · Cited by 210 · see citing works
Age-related regional variations of the corpus callosum identified by diffusion tensor tractography
Lebel, C., Caverhill-Godkewitsch, S., & Beaulieu, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.072 · Cited by 209 · see citing works
Roalf, D. R., Quarmley, M., Elliott, M. A., Satterthwaite, T. D., Vandekar, S. N., Ruparel, K., Gennatas, E. D., Calkins, M. E., Moore, T. M., Hopson, R., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.068 · Cited by 199 · see citing works
Time-Trend Analysis of Plasma Cortisol Concentrations in the Fetal Sheep in Relation to Parturition*
MAGYAR, D. M., FRIDSHAL, D., ELSNER, C. W., GLATZ, T., ELIOT, J., KLEIN, A. H., LOWE, K. C., BUSTER, J. E., & NATHANIELSZ, P. W. (1980) · Endocrinology · doi:10.1210/endo-107-1-155 · Cited by 189 · see citing works
Wen, D. J., Poh, J. S., Ni, S. N., Chong, Y.-S., Chen, H., Kwek, K., Shek, L. P., Gluckman, P. D., Fortier, M. V., Meaney, M. J., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.74 · Cited by 186 · cited 4× · see citing works
“PMDS exposures have been observed to associate with the amygdala in a sex-specific manner (Acosta, Kantojärvi, et al., 2020; Acosta, Tuulari, et al., 2020; Lehtola et al., 2020; Wen et al., 2017).”
BackgroundResultInfluentialReduced Intrinsic Connectivity of Amygdala in Adults with Major Depressive Disorder
Ramasubbu, R., Konduru, N., Cortese, F., Bray, S., Gaxiola‐Valdez, I., & Goodyear, B. G. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00017 · Cited by 178 · see citing works
Complex Trajectories of Brain Development in the Healthy Human Fetus
Andescavage, N. N., du Plessis, A., McCarter, R., Serag, A., Evangelou, I., Vezina, G., Robertson, R., & Limperopoulos, C. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw306 · Cited by 163 · see citing works
The development of the human amygdala during early embryonic life
Humphrey, T. (1968) · Journal of Comparative Neurology · doi:10.1002/cne.901320108 · Cited by 160 · see citing works
Murphy, V. E., & Clifton, V. L. (2003) · Placenta · doi:10.1016/s0143-4004(03)00103-6 · Cited by 155 · see citing works
Diffusion tensor imaging of normal brain development
Yoshida, S., Oishi, K., Faria, A., & Mori, S. (2013) · Pediatric Radiology · doi:10.1007/s00247-012-2496-x · Cited by 145 · see citing works
Sidebottom, A., Vacquier, M., LaRusso, E., Erickson, D., & Hardeman, R. (2021) · Archives of Women's Mental Health · doi:10.1007/s00737-020-01035-x · Cited by 141 · see citing works
Ontogeny of the Human Amygdala
Ulfig, N., Setzer, M., & Böhl, J. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07068.x · Cited by 138 · see citing works
DeepDTI: High-fidelity six-direction diffusion tensor imaging using deep learning
Tian, Q., Bilgiç, B., Fan, Q., Liao, C., Ngamsombat, C., Hu, Y., Witzel, T., Setsompop, K., Polimeni, J. R., & Huang, S. Y. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117017 · Cited by 137 · see citing works
Maternal prenatal stress and infant emotional reactivity six months postpartum
Nolvi, S., Karlsson, L., Bridgett, D. J., Korja, R., Huizink, A. C., Kataja, E., & Karlsson, H. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.04.020 · Cited by 135 · see citing works
Self-citationGérardin, P., Wendland, J., Bodeau, N., Galin, A., Bialobos, S., Tordjman, S., Mazet, P., Darbois, Y., Nizard, J., Dommergues, M., et al. (2010) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.09m05724blu · Cited by 131 · see citing works
Indicators of subjective social status: Differential associations across race and sex
Shaked, D., Williams, M., Evans, M. K., & Zonderman, A. B. (2016) · SSM - Population Health · doi:10.1016/j.ssmph.2016.09.009 · Cited by 129 · see citing works
Cherubini, A., Péran, P., Spoletini, I., Di Paola, M., Di Iulio, F., Hagberg, G. E., Sancesario, G., Gianni, W., Bossù, P., Caltagirone, C., et al. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-091186 · Cited by 123 · cited 3× · see citing works
“…have been associated with a reduction in neuron size and synapse loss, along with alterations in the cytoarchitecture that lead to neurofibrillary changes and an increase in the extracellular space (Cherubini et al., 2010; De Gennaro et al., 2011; Gillespie et al., 2017; Kantarci et al., 2005).”
BackgroundLugo-Candelas, C. I., Cha, J., Hong, S. N., Bastidas, V., Weissman, M. M., Fifer, W. P., Myers, M. D., Talati, A., Bansal, R., Peterson, B. S., et al. (2018) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/jamapediatrics.2017.5227 · Cited by 122 · see citing works
Sexton, C. E., Mackay, C. E., Lonie, J. A., Bastin, M. E., Terrière, E., O’Carroll, R. E., & Ebmeier, K. P. (2010) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2010.07.005 · Cited by 120 · see citing works
An afferent white matter pathway from the pulvinar to the amygdala facilitates fear recognition
McFadyen, J., Mattingley, J. B., & Garrido, M. I. (2019) · eLife · doi:10.7554/elife.40766 · Cited by 115 · see citing works
Pohl, K. M., Sullivan, E. V., Rohlfing, T., Chu, W., Kwon, D., Nichols, B. N., Zhang, Y., Brown, S. A., Tapert, S. F., Cummins, K., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.061 · Cited by 85 · see citing works
Acosta, H., Tuulari, J. J., Scheinin, N. M., Hashempour, N., Rajasilta, O., Lavonius, T. I., Pelto, J., Saunavaara, V., Parkkola, R., Lähdesmäki, T., et al. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00175 · Cited by 80 · see citing works
Self-citationAmygdala and hippocampus volumetry and diffusivity in relation to dreaming
De Gennaro, L., Cipolli, C., Cherubini, A., Assogna, F., Cacciari, C., Marzano, C., Curcio, G., Ferrara, M., Caltagirone, C., & Spalletta, G. (2011) · Human Brain Mapping · doi:10.1002/hbm.21120 · Cited by 79 · see citing works
Sandman, C. A., Wadhwa, P. D., Dunkel‐Schetter, C., Chicz-DeMet, A., Belman, J., Porto, M., Murata, Y., Garite, T. J., & Crinella, F. M. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb19822.x · Cited by 79 · see citing works
Beyond the HPA-axis: Exploring maternal prenatal influences on birth outcomes and stress reactivity
Nazzari, S., Fearon, P. R. M., Rice, F. J., Dottori, N., Ciceri, F., Molteni, M., & Frigerio, A. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.11.018 · Cited by 79 · see citing works
Straub, J., Metzger, C., Plener, P. L., Kölch, M. G., Groen, G., & Abler, B. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.11.024 · Cited by 68 · see citing works
Stoye, D. Q., Blesa, M., Sullivan, G., Galdi, P., Lamb, G. J., Black, G. S., Quigley, A. J., Thrippleton, M. J., Bastin, M. E., Reynolds, R. M., et al. (2020) · eLife · doi:10.7554/elife.60729 · Cited by 66 · see citing works
Aeby, A., Liu, Y., Tiège, X. D., Denolin, V., David, P., Balériaux, D., Kavec, M., Metens, T., & Bogaert, P. V. (2009) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1660 · Cited by 63 · see citing works
Taki, Y., Thyreau, B., Hashizume, H., Sassa, Y., Takeuchi, H., Wu, K., Kotozaki, Y., Nouchi, R., Asano, M., Asano, K., et al. (2012) · Human Brain Mapping · doi:10.1002/hbm.22027 · Cited by 62 · see citing works
Associations of age and sex with brain volumes and asymmetry in 2–5-week-old infants
Lehtola, S. J., Tuulari, J. J., Karlsson, L., Parkkola, R. K., Merisaari, H., Saunavaara, J. P., Lähdesmäki, T., Scheinin, N. M., & Karlsson, H. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1787-x · Cited by 62 · see citing works
Self-citationTest-retest reliability of Diffusion Tensor Imaging metrics in neonates
Merisaari, H., Tuulari, J. J., Karlsson, L., Scheinin, N. M., Parkkola, R. K., Saunavaara, J. P., Lähdesmäki, T., Lehtola, S. J., Keskinen, M., Lewis, J. D., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.04.067 · Cited by 53 · see citing works
Self-citationPrenatal Maternal Stress and the Risk of Asthma in Children
Douros, K., Moustaki, M., Tsabouri, S., Papadopoulou, A., Papadopoulos, M., & Priftis, K. Ν. (2017) · Frontiers in Pediatrics · doi:10.3389/fped.2017.00202 · Cited by 52 · see citing works
Neural correlates of prenatal stress in young women
Favaro, A., Tenconi, E., Degortes, D., Manara, R., & Santonastaso, P. (2015) · Psychological Medicine · doi:10.1017/s003329171500046x · Cited by 51 · see citing works
Lehtola, S. J., Tuulari, J. J., Scheinin, N. M., Karlsson, L., Parkkola, R., Merisaari, H., Lewis, J. D., Fonov, V. S., Louis Collins, D., Evans, A., et al. (2020) · NeuroImage: Clinical · doi:10.1016/j.nicl.2020.102380 · Cited by 51 · see citing works
Self-citationThe amygdaloid complex and the medial and lateral ventricular eminences in staged human embryos
Müller, F., & O’Rahilly, R. (2006) · Journal of Anatomy · doi:10.1111/j.1469-7580.2006.00553.x · Cited by 46 · see citing works
A Novel Approach for Manual Segmentation of the Amygdala and Hippocampus in Neonate MRI
Hashempour, N., Tuulari, J. J., Merisaari, H., Lidauer, K., Luukkonen, I., Saunavaara, J. P., Parkkola, R. K., Lähdesmäki, T., Lehtola, S. J., Keskinen, M., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01025 · Cited by 40 · see citing works
Self-citationSalo, R. A., Belevich, I. N., Manninen, E., Jokitalo, E., Gröhn, O. H. J., & Sierra, A. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.01.087 · Cited by 39 · see citing works
Yrondi, A., Nemmi, F., Billoux, S., Giron, A., Sporer, M., Taïb, S., Salles, J., Pierre, D., Thalamas, C., Schmitt, L., et al. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00694 · Cited by 36 · see citing works
Acosta, H., Kantojärvi, K., Hashempour, N., Pelto, J., Scheinin, N. M., Lehtola, S. J., Lewis, J. D., Fonov, V. S., Collins, D. L., Evans, A., et al. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa158 · Cited by 34 · see citing works
Self-citationMoura, L. M., Kempton, M. J., Barker, G. J., Salum, G. A., Gadelha, A., Pan, P. M., Hoexter, M. Q., Aquilla, M. A. G. D., Picon, F. A., Anés, M., et al. (2015) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2015.12.021 · Cited by 33 · see citing works
Highly Accurate Segmentation of Brain Tissue and Subcortical Gray Matter from Newborn MRI
Weisenfeld, N. I., Mewes, A. U. J., & Warfield, S. K. (2006) · Lecture notes in computer science · doi:10.1007/11866565_25 · Cited by 32 · see citing works
Mean diffusivity in the amygdala correlates with anxiety in pediatric TBI
Juranek, J. J., Johnson, C. P., Prasad, M. R., Kramer, L. A., Saunders, A. E., Filipek, P. A., Swank, P. R., Cox, C. S., & Ewing‐Cobbs, L. (2011) · Brain Imaging and Behavior · doi:10.1007/s11682-011-9140-5 · Cited by 31 · see citing works
Structural and diffusional brain abnormality related to relatively low level alcohol consumption
Sasaki, H., Abe, O., Yamasue, H., Fukuda, R., Yamada, H., Takei, K., Suga, M., Takao, H., Kasai, K., Aoki, S., et al. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.007 · Cited by 29 · see citing works
Cortical and subcortical T1 white/gray contrast, chronological age, and cognitive performance
Lewis, J. D., Fonov, V., Collins, D. L., Evans, A. C., Tohka, J., & for the Brain Development Cooperative Group, A. T. P. I. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.04.022 · Cited by 26 · see citing works
Self-citationBao, Y., He, R., Zeng, Q., et al. (2018) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2017.12.002 · Cited by 24 · see citing works
Diffusion Tensor Imaging in the Study of Aging and Age-Associated Neural Disease
Salat, D. H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00012-3 · Cited by 21 · see citing works
Genetic and Environmental Influences on Mean Diffusivity and Volume in Subcortical Brain Regions
Gillespie, N., Neale, M., Hagler, D., Eyler, L., Fennema-Notestine, C., Franz, C., Lyons, M., McEvoy, L., Dale, A., Panizzon, M., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23544 · Cited by 21 · see citing works
Empathizing associates with mean diffusivity
Takeuchi, H., Taki, Y., Nouchi, R., Yokoyama, R., Kotozaki, Y., Nakagawa, S., Sekiguchi, A., Iizuka, K., Yamamoto, Y., Hanawa, S., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45106-1 · Cited by 21 · see citing works
H, A., JJ, T., NM, S., N, H., O, R., TI, L., J, P., V, S., R, P., T, L., et al. (2020) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2020.111153 · Cited by 20 · see citing works
Alterations of white matter fractional anisotropy in unmedicated obsessive–compulsive disorder
Tao, J., Wang, X., Zhong, Z., Han, H., Liu, S., Wen, S., Guan, N., & Li, L. (2016) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s123669 · Cited by 12 · see citing works
Diffusion Tensor Imaging in Parkinson’s Disease
Stebbins, G. T. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374105-9.00020-4 · Cited by 8 · see citing works
Hay, R. E., Reynolds, J. E., Grohs, M., Paniukov, D., Giesbrecht, G. F., Letourneau, N., Dewey, D., & Lebel, C. (2019) · doi:10.1101/692335 · Cited by 7 · see citing works
Stoye, D. Q., Blesa, M., Sullivan, G., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.16.154922 · Cited by 6 · see citing works
Pervolaraki, E., Tyson, A. L., Pibiri, F., Poulter, S. L., Reichelt, A. C., Rodgers, R. J., Clapcote, S. J., Lever, C., Andreae, L. C., & Dachtler, J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/300806 · Cited by 2 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- tb02031.x · DOI · Paper page
Cited by
Sorted by citations
Wu, Y., De Asis-Cruz, J., & Limperopoulos, C. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02449-0 · Cited by 124 · see citing works
- Authors
- Hashempour, N., Tuulari, J. J., Merisaari, H., Acosta, H., Lewis, J. D., Pelto, J., Scheinin, N. M., Fonov, V. S., Collins, D. L., Lehtola, S. J., Saunavaara, J., Lähdesmäki, T., Parkkola, R., Karlsson, L., & Karlsson, H.
- Affiliations
- University of Turku (FI)
- Montreal Neurological Institute and Hospital (CA)
- Turku University Hospital (FI)
- FinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine University of Turku Turku Finland
- Corresponding author
- Hashempour, Niloofar
- ORCID
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2023-05
- Volume
- 57
- Issue
- 10
- Pages
- 1671-1688
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W4365135202
- Cited by
- 20
- References
- 96
- Citations by year
- 2026: 8 · 2025: 4 · 2024: 7 · 2023: 1
- FWCI
- 5.10
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- European Journal of Neuroscience (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- UTUPub (University of Turku) (submittedVersion)
- Funders
- Turun yliopiston tutkijakoulu
- Orionin Tutkimussäätiö
- Emil Aaltosen Säätiö
- Juho Vainion Säätiö
- Jane ja Aatos Erkon Säätiö
- Canadian Institutes of Health Research
- Natural Sciences and Engineering Research Council of Canada
- Signe ja Ane Gyllenbergin Säätiö
- Academy of Finland (134950, 253270, 264363 (HK), 308176 (LK), 26080983 (HM))
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Maternal Mental Health During Pregnancy and Postpartum
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Substance Exposure Effects
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Keywords
- left amygdala, sex differences, mean diffusivity, infant brain development, gestational age, prenatal stress, neurodevelopmental outcomes
- MeSH terms
- Amygdala, Brain, Depression, Female, Humans, Infant, Infant, Newborn, Male, Pregnancy, Diffusion Magnetic Resonance Imaging, Diffusion Tensor Imaging, White Matter
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review