Hormonal Programming Across the Lifespan

The language of covalent histone modifications

Strahl, B. D., & Allis, C. D. (2000) · Nature · doi:10.1038/47412 · Cited by 8,679 · see citing works

Epigenetic programming by maternal behavior

Weaver, I. C. G., Cervoni, N., Champagne, F. A., D'Alessio, A. C., Sharma, S., Seckl, J. R., Dymov, S., Szyf, M., & Meaney, M. J. (2004) · Nature Neuroscience · doi:10.1038/nn1276 · Cited by 6,177 · see citing works

Cloning of a novel receptor expressed in rat prostate and ovary.

Kuiper, G. G. J. M., Enmark, E., Pelto‐Huikko, M., Nilsson, S., & Gustafsson, J.-Α. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.12.5925 · Cited by 4,792 · see citing works

Genomic DNA methylation: the mark and its mediators.

Klose, R. J., & Bird, A. P. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.12.008 · Cited by 2,501 · see citing works

Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A

Green, S., Walter, P., Kumar, V., Krust, A., Bornert, J., Argos, P., & Chambon, P. (1986) · Nature · doi:10.1038/320134a0 · Cited by 2,320 · see citing works

ERβ: Identification and characterization of a novel human estrogen receptor

Mosselman, S., Polman, J., & Dijkema, R. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00782-x · Cited by 2,269 · see citing works

Distribution of androgen and estrogen receptor mRNA-containing cells in the rat brain: an in situ hybridization study

Simerly, R. B., Swanson, L. W., Chang, C., & Muramatsu, M. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902940107 · Cited by 2,118 · see citing works

Twenty-Five Years of the Nucleosome, Fundamental Particle of the Eukaryote Chromosome

Kornberg, R. D., & Lorch, Y. (1999) · Cell · doi:10.1016/s0092-8674(00)81958-3 · Cited by 1,833 · see citing works

Methylation-Induced Repression— Belts, Braces, and Chromatin

Bird, A. P., & Wolffe, A. P. (1999) · Cell · doi:10.1016/s0092-8674(00)81532-9 · Cited by 1,827 · see citing works

Atlas of estradiol‐concentrating cells in the central nervous system of the female rat

Pfaff, D. W., & Keiner, M. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901510204 · Cited by 1,494 · see citing works

Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause

Faddy, M. J., Gosden, R. G., Gougeon, A., Richardson, S. J., & Nelson, J. F. (1992) · Human Reproduction · doi:10.1093/oxfordjournals.humrep.a137570 · Cited by 1,361 · see citing works

Epigenetics: Regulation Through Repression

Wolffe, A. P., & Matzke, M. A. (1999) · Science · doi:10.1126/science.286.5439.481 · Cited by 1,241 · see citing works

Gonadal Steroid Induction of Structural Sex Differences in the Central Nervous System

Arnold, A. P., & Gorski, R. A. (1984) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.07.030184.002213 · Cited by 1,198 · see citing works

Estradiol mediates fluctuation in hippocampal synapse density during the estrous cycle in the adult rat [published erratum appears in J Neurosci 1992 Oct;12(10):following table of contents]

Woolley, C. S., & McEwen, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02549.1992 · Cited by 987 · see citing works

Cyclical DNA methylation of a transcriptionally active promoter

Métivier, R., Gallais, R., Tiffoche, C., Péron, C. L., Jurkowska, R., Carmouche, R. P., Ibberson, D., Baráth, P., Demay, F., Reid, G., et al. (2008) · Nature · doi:10.1038/nature06544 · Cited by 942 · see citing works

Estradiol and the Developing Brain

McCARTHY, M. M. (2008) · Physiological Reviews · doi:10.1152/physrev.00010.2007 · Cited by 885 · see citing works

Effects of DNA methylation on DNA-binding proteins and gene expression

Tate, P. H., & Bird, A. P. (1993) · Current Opinion in Genetics & Development · doi:10.1016/0959-437x(93)90027-m · Cited by 737 · see citing works

Age and Infertility

MENKEN, J. A., Trussell, J., & Larsen, U. (1986) · Science · doi:10.1126/science.3755843 · Cited by 705 · see citing works

Maternal Care Associated with Methylation of the Estrogen Receptor-α1b Promoter and Estrogen Receptor-α Expression in the Medial Preoptic Area of Female Offspring

Champagne, F. A., Weaver, I. C. G., Diorio, J., Dymov, S., Szyf, M., & Meaney, M. J. (2006) · Endocrinology · doi:10.1210/en.2005-1119 · Cited by 675 · see citing works

Neuronal activity modifies the DNA methylation landscape in the adult brain

Guo, J. U., Ma, D. K., Mo, H., Ball, M. P., Jang, M.-H., Bonaguidi, M. A., Balazer, J. A., Eaves, H. L., Xie, B., Ford, E., et al. (2011) · Nature Neuroscience · doi:10.1038/nn.2900 · Cited by 669 · see citing works

What does the “four core genotypes” mouse model tell us about sex differences in the brain and other tissues?

Arnold, A. P., & Chen, X. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2008.11.001 · Cited by 587 · see citing works

Androgen excess fetal programming of female reproduction: a developmental aetiology for polycystic ovary syndrome

Abbott, D. H., Barnett, D. K., Bruns, C. M., & Dumesic, D. A. (2005) · Human Reproduction Update · doi:10.1093/humupd/dmi013 · Cited by 555 · see citing works

Chromatin disruption and modification

Wolffe, A. P., & Hayes, J. J. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.3.711 · Cited by 551 · see citing works

Epigenetic mechanisms in cognition

Day, J. J., & Sweatt, J. D. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.019 · Cited by 510 · see citing works

Molecular cloning and charcterization of rat estrogen receptor cDNA

Koike, S., Sakai, M., & Muramatsu, M. (1987) · Nucleic Acids Research · doi:10.1093/nar/15.6.2499 · Cited by 489 · see citing works

The Epigenetics of Sex Differences in the Brain: Figure 1.

McCarthy, M. M., Auger, A. P., Bale, T. L., Vries, G. J. D., Dunn, G. A., Forger, N. G., Murray, E. K., Nugent, B. M., Schwarz, J. M., & Wilson, M. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3331-09.2009 · Cited by 478 · see citing works

Aromatization: Important for sexual differentiation of the neonatal rat brain

McEwen, B. S., Lieberburg, I., Chaptal, C., & Krey, L. C. (1977) · Hormones and Behavior · doi:10.1016/0018-506x(77)90060-5 · Cited by 443 · see citing works

Female reproductive ageing: current knowledge and future trends

Broekmans, F. J., Knauff, E. A. H., te Velde, E. R., Macklon, N. S., & Fauser, B. C. (2007) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2007.01.004 · Cited by 427 · see citing works

DNA methylation and histone acetylation work in concert to regulate memory formation and synaptic plasticity

Miller, C. A., Campbell, S. L., & Sweatt, J. D. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.07.016 · Cited by 417 · see citing works

Maternal serum androgens in pregnant women with polycystic ovarian syndrome: possible implications in prenatal androgenization

Sir‐Petermann, T. (2002) · Human Reproduction · doi:10.1093/humrep/17.10.2573 · Cited by 412 · see citing works

A positive autoregulatory loop of Jak-STAT signaling controls the onset of astrogliogenesis

He, F., Ge, W., Martinowich, K., Becker-Catania, S. G., Coskun, V., Zhu, W., Wu, H., Castro, D. S., Guillemot, F., Fan, G., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1440 · Cited by 398 · see citing works

Pubertal hormones modulate the addition of new cells to sexually dimorphic brain regions

Ahmed, E. I., Zehr, J. L., Schulz, K. M., Lorenz, B. H., DonCarlos, L. L., & Sisk, C. L. (2008) · Nature Neuroscience · doi:10.1038/nn.2178 · Cited by 396 · see citing works

Epigenetic mechanisms in drug addiction

Renthal, W. R., & Nestler, E. J. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2008.06.004 · Cited by 383 · see citing works

Structural Organization and Expression of the Mouse Estrogen Receptor

White, R., Lees, J. A., Needham, M., Ham, J., & Parker, M. G. (1987) · Molecular Endocrinology · doi:10.1210/mend-1-10-735 · Cited by 362 · see citing works

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes

Cooper, D. N., & Krawczak, M. (1989) · Human Genetics · doi:10.1007/bf00286715 · Cited by 349 · see citing works

Developmental time course of estradiol, testosterone, and dihydrotestosterone levels in discrete regions of male and female rat brain.

Konkle, A., & McCarthy, M. (2011) · Endocrinology · doi:10.1210/en.2010-0607 · Cited by 307 · see citing works

Alpha-fetoprotein protects the developing female mouse brain from masculinization and defeminization by estrogens

Bakker, J., De Mees, C., Douhard, Q., Balthazart, J., Gabant, P., Szpirer, J., & Szpirer, C. (2006) · Nature Neuroscience · doi:10.1038/nn1624 · Cited by 305 · see citing works

Polycystic ovary syndrome and its developmental origins

Dumesic, D. A., Abbott, D. H., & Padmanabhan, V. (2007) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-007-9046-0 · Cited by 283 · see citing works

Estrogen Receptor β (ERβ) Messenger Ribonucleic Acid (mRNA) Expression within the Human Forebrain: Distinct Distribution Pattern to ERα mRNA1

Österlund, M. K., Gustafsson, J.-Α., Keller, É., & Hurd, Y. L. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.85.10.6913 · Cited by 273 · see citing works

Metabolic and Reproductive Features before and during Puberty in Daughters of Women with Polycystic Ovary Syndrome

Sir-Petermann, T., Codner, E., Pérez, V., Echiburú, B., Maliqueo, M., Ladrón de Guevara, A., Preisler, J., Crisosto, N., Sánchez, F., Cassorla, F., et al. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-2836 · Cited by 260 · see citing works

Structure and Function of the Core Histone N-Termini: More Than Meets the Eye

Hansen, J. C., Tse, C., & Wolffe, A. P. (1998) · Biochemistry · doi:10.1021/bi982409v · Cited by 247 · see citing works

Steroid 11β- hydroxylase deficiency congenital adrenal hyperplasia

Nimkarn, S., & New, M. I. (2008) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2008.01.002 · Cited by 239 · see citing works

Sex differences in early childhood, adolescence, and adulthood on cognitive tasks that rely on orbital prefrontal cortex

Overman, W. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00279-3 · Cited by 215 · see citing works

Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia1

Cabrera, M. S., Vogiatzi, M. G., & New, M. I. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.7.7668 · Cited by 204 · see citing works

Sex differences in histone modifications in the neonatal mouse brain

Tsai, H., Grant, P. A., & Rissman, E. F. (2009) · Epigenetics · doi:10.4161/epi.4.1.7288 · Cited by 203 · see citing works

Developmental and hormone-induced epigenetic changes to estrogen and progesterone receptor genes in brain are dynamic across the life span

Schwarz, J. M., Nugent, B. M., & McCarthy, M. M. (2010) · Endocrinology · doi:10.1210/en.2010-0142 · Cited by 198 · see citing works

Roles of estrogen receptors α and β in differentiation of mouse sexual behavior

Kudwa, A. E., Michopoulos, V., Gatewood, J. D., & Rissman, E. F. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.018 · Cited by 190 · see citing works

Prenatal androgen exposure programs metabolic dysfunction in female mice

Roland, A. V., Nunemaker, C. S., Keller, S. R., & Moenter, S. M. (2010) · Journal of Endocrinology · doi:10.1677/joe-10-0217 · Cited by 184 · see citing works

Activation of ovarian sympathetic nerves in polycystic ovary syndrome

Lara, H. E., Ferruz, J. L., Luza, S., Bustamante, D. A., Borges, Y., & Ojeda, S. R. (1993) · Endocrinology · doi:10.1210/endo.133.6.7902268 · Cited by 182 · see citing works

Fetal, infant, adolescent and adult phenotypes of polycystic ovary syndrome in prenatally androgenized female rhesus monkeys

Abbott, D. H., Tarantal, A. F., & Dumesic, D. A. (2009) · American Journal of Primatology · doi:10.1002/ajp.20679 · Cited by 177 · see citing works

Anxiety and depression symptoms in women with polycystic ovary syndrome compared with controls matched for body mass index

Jedel, E., Wærn, M., Gustafson, D., Landén, M., Eriksson, E., Holm, G., Nilsson, L., Lind, A. K., Janson, P. O., & Stener‐Victorin, E. (2009) · Human Reproduction · doi:10.1093/humrep/dep384 · Cited by 177 · see citing works

Sexually dimorphic expression of estrogen receptor β in the anteroventral periventricular nucleus of the rat preoptic area: Implication in luteinizing hormone surge

Orikasa, C., Kondo, Y., Hayashi, S., McEwen, B. S., & Sakuma, Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052707299 · Cited by 176 · see citing works

Differential Modulation of Estrogen Receptors (ERs) in Ischemic Brain Injury: A Role for ERα in Estradiol-Mediated Protection against Delayed Cell Death

Dubal, D. B., Rau, S. W., Shughrue, P. J., Zhu, H., Yu, J., Cashion, A. B., Suzuki, S., Gerhold, L. M., Bottner, M. B., Dubal, S. B., et al. (2006) · Endocrinology · doi:10.1210/en.2005-1177 · Cited by 174 · see citing works

An Increased Intraovarian Synthesis of Nerve Growth Factor and Its Low Affinity Receptor Is a Principal Component of Steroid-Induced Polycystic Ovary in the Rat1

Lara, H. E., Dissen, G. A., Leyton, V., Paredes, A., Fuenzalida, H., Fiedler, J. L., & Ojeda, S. R. (2000) · Endocrinology · doi:10.1210/endo.141.3.7395 · Cited by 173 · see citing works

High prevalence of reduced fecundity in men with congenital adrenal hyperplasia

Reisch, N., Flade, L., Scherr, M., Rottenkolber, M., Pedrosa Gil, F., Bidlingmaier, M., Wolff, H., Schwarz, H.-P., Quinkler, M., Beuschlein, F., et al. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-1414 · Cited by 170 · see citing works

Histone H4 Lysine 91 Acetylation

Ye, J., Ai, X., Eugeni, E. E., Zhang, L., Carpenter, L. R., Jelinek, M. A., Freitas, M. A., & Parthun, M. R. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.02.031 · Cited by 170 · see citing works

Adrenomedullary, adrenocortical, and sympathoneural responses to stressors: a meta-analysis.

Goldstein, D. S., & Kopin, I. J. (2008) · PubMed · Cited by 169 · see citing works

Distribution patterns of estrogen receptor α and β in the human cortex and hippocampus during development and adulthood

González, M., Cabrera‐Socorro, A., Pérez‐García, C. G., Fraser, J. D., López, F. J., Alonso, R., & Meyer, G. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21419 · Cited by 167 · see citing works

Ovarian steroidal response to gonadotropins and beta-adrenergic stimulation is enhanced in polycystic ovary syndrome: role of sympathetic innervation

Barría, A., Leyton, V., Ojeda, S. R., & Lara, H. E. (1993) · Endocrinology · doi:10.1210/endo.133.6.8243293 · Cited by 160 · see citing works

Early Metabolic Derangements in Daughters of Women with Polycystic Ovary Syndrome

Sir‐Petermann, T., Maliqueo, M. A., Ethel Codner, D., Echiburú, B., Crisosto, N., Pérez, V., Pérez‐Bravo, F., & CASSORLA, F. G. (2007) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2007-1036 · Cited by 151 · see citing works

Histone Deacetylation during Brain Development Is Essential for Permanent Masculinization of Sexual Behavior

Matsuda, K., Mori, H., Nugent, B. M., Pfaff, D. W., McCarthy, M. M., & Kawata, M. (2011) · Endocrinology · doi:10.1210/en.2011-0193 · Cited by 142 · see citing works

Developmental Programming: Impact of Prenatal Testosterone Excess and Postnatal Weight Gain on Insulin Sensitivity Index and Transfer of Traits to Offspring of Overweight Females

Padmanabhan, V., Veiga‐Lopez, A., Abbott, D. H., Recabarren, S. E., & Herkimer, C. (2009) · Endocrinology · doi:10.1210/en.2009-1015 · Cited by 136 · see citing works

A previously uncharacterized role for estrogen receptor β: Defeminization of male brain and behavior

Kudwa, A. E., Bodo, C., Gustafsson, J.-Å., & Rissman, E. F. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500752102 · Cited by 135 · see citing works

Onset of the hormone‐sensitive perinatal period for sexual differentiation of the sexually dimorphic nucleus of the preoptic area in female rats

Rhees, R. W., Shryne, J. E., & Gorski, R. A. (1990) · Journal of Neurobiology · doi:10.1002/neu.480210511 · Cited by 127 · see citing works

Metabolic Profile in Sons of Women with Polycystic Ovary Syndrome

Recabarren, S. E., Smith, R., Ríos, R., Maliqueo, M. A., Echiburú, B., Ethel Codner, D., CASSORLA, F. G., Rojas, P., & Sir‐Petermann, T. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2007-2256 · Cited by 126 · see citing works

Ovarian β-Adrenergic Receptors during the Onset of Puberty: Characterization, Distribution, and Coupling to Steroidogenic Responses*

Aguado, L. I., Petrović, S. L., & Ojeda, S. R. (1982) · Endocrinology · doi:10.1210/endo-110-4-1124 · Cited by 126 · see citing works

Variation in orbitofrontal cortex volume: relation to sex, emotion regulation and affect

Welborn, B. L., Papademetris, X., Reis, D. L., Rajeevan, N., Bloise, S. M., & Gray, J. R. (2009) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsp028 · Cited by 125 · see citing works

Endocrine regulation of cognition and neuroplasticity: Our pursuit to unveil the complex interaction between hormones, the brain, and behaviour.

Galea, L. A. M., Uban, K. A., Epp, J. R., Brummelte, S., Barha, C. K., Wilson, W. L., Lieblich, S. E., & Pawluski, J. L. (2008) · Canadian Journal of Experimental Psychology/Revue canadienne de psychologie expérimentale · doi:10.1037/a0014501 · Cited by 122 · see citing works

Changes in sympathetic nerve activity of the mammalian ovary during a normal estrous cycle and in polycystic ovary syndrome: Studies on norepinephrine release

Lara, H. E., Dorfman, M. D., Venegas, M., Luza, S. M., Luna, S. L., Mayerhofer, A., Guimarães, M. A. D. B. V., Silva, A. A. M. R. E., & RAMIREZ, V. D. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10229 · Cited by 122 · see citing works

Prenatal testosterone excess programs reproductive and metabolic dysfunction in the female

Padmanabhan, V., Manikkam, M., Recabarren, S. E., & Foster, D. L. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.11.016 · Cited by 119 · see citing works

Epigenetic Regulation of Estrogen Receptor α Gene Expression in the Mouse Cortex during Early Postnatal Development

Westberry, J. M., Trout, A. L., & Wilson, M. E. (2009) · Endocrinology · doi:10.1210/en.2009-0955 · Cited by 118 · see citing works

Infants of Women with Polycystic Ovary Syndrome Have Lower Cord Blood Androstenedione and Estradiol Levels

Anderson, H., Fogel, N. R., Grebe, S. K. G., Singh, R. J., Taylor, R. L., & Dunaif, A. E. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-2651 · Cited by 118 · see citing works

Developmental Expression of Estrogen Receptor mRNA in the Rat Cerebral Cortex: A Nonisotopic in situ Hybridization Histochemistry Study

Miranda, R. C., & Toran‐Allerand, C. D. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.1.1 · Cited by 108 · see citing works

Increase in nerve fibers and loss of mast cells in polycystic and postmenopausal ovaries

Heider, U., Pedal, I., & Spanel-Borowski, K. (2001) · Fertility and Sterility · doi:10.1016/s0015-0282(01)01805-2 · Cited by 107 · see citing works

Developmental Changes in Estrogen Receptors in Mouse Cerebral Cortex between Birth and Postweaning: Studied by Autoradiography with llβ-Methoxy-16α- [¹²⁵I]Iodoestradiol*

SHUGHRUE, P. J., STUMPF, W. E., MACLUSKY, N. J., ZIELINSKI, J. E., & HOCHBERG, R. B. (1990) · Endocrinology · doi:10.1210/endo-126-2-1112 · Cited by 106 · see citing works

Effects of prenatal androgens on rhesus monkeys: A model system to explore the organizational hypothesis in primates

Thornton, J., Zehr, J. L., & Loose, M. D. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.015 · Cited by 105 · see citing works

Direct Effects of Nerve Growth Factor on Thecal Cells from Antral Ovarian Follicles**This work was supported by NIH Grants HD-24870 (to S.R.O.), HD-33372 (to M.K.S.), NICHHD/NIH through Cooperative Agreement U-54-HD-18185 as part of the Specialized Cooperative Centers Program in Reproduction Research, and RR-00163 for operation of the Oregon Regional Primate Research Center.

Dissen, G. A., Parrott, J. A., Skinner, M. K., Hill, D. F., da Costa, M. E. L. T., & Ojeda, S. R. (2000) · Endocrinology · doi:10.1210/endo.141.12.7850 · Cited by 100 · see citing works

Mecp2 organizes juvenile social behavior in a sex-specific manner

Kurian, J. R., Bychowski, M. E., Forbes-Lorman, R. M., Auger, C. J., & Auger, A. P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1345-08.2008 · Cited by 100 · see citing works

Roles of estrogen receptor α and androgen receptor in the regulation of neuronal nitric oxide synthase

Scordalakes, E. M., Shetty, S. J., & Rissman, E. F. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10413 · Cited by 100 · see citing works

Epigenetic regulation of the estrogen receptor alpha promoter in the cerebral cortex following ischemia in male and female rats

Westberry, J. M., Prewitt, A. K., & Wilson, M. E. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.01.048 · Cited by 98 · see citing works

The Human Brain Has Distinct Regional Expression Patterns of Estrogen Receptor α mRNA Isoforms Derived from Alternative Promoters

Österlund, M. K., Grandien, K., Keller, É., & Hurd, Y. L. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751390.x · Cited by 95 · see citing works

Sex Difference in Mecp2 Expression During a Critical Period of Rat Brain Development

Kurian, J. R., Forbes‐Lorman, R. M., & Auger, A. P. (2007) · Epigenetics · doi:10.4161/epi.2.3.4841 · Cited by 91 · see citing works

Of mice and rats: Key species variations in the sexual differentiation of brain and behavior

Bonthuis, P. J., Cox, K. H., Searcy, B. T., Kumar, P., Tobet, S. A., & Rissman, E. F. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.05.001 · Cited by 90 · see citing works

Chronic Intermittent Cold Stress Activates Ovarian Sympathetic Nerves and Modifies Ovarian Follicular Development in the Rat1

Dorfman, M. D., Arancibia, S., Fiedler, J. L., & Lara, H. E. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.008318 · Cited by 88 · see citing works

Rats with steroid-induced polycystic ovaries develop hypertension and increased sympathetic nervous system activity

Stener‐Victorin, E., Ploj, K., Larsson, B.-M., & Holmäng, A. B. (2005) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-3-44 · Cited by 85 · see citing works

Guanethidine-Mediated Destruction of Ovarian Sympathetic Nerves Disrupts Ovarian Development and Function in Rats*

Lara, H. E., McDonald, J., AHMED, C. E., & Ojeda, S. R. (1990) · Endocrinology · doi:10.1210/endo-127-5-2199 · Cited by 85 · see citing works

Role of Stress and Sympathetic Innervation in the Development of Polycystic Ovary Syndrome

Greiner, M., Paredes, A., Araya, V., & Lara, H. E. (2005) · Endocrine · doi:10.1385/endo:28:3:319 · Cited by 84 · see citing works

Prenatal Testosterone Excess Reduces Sperm Count and Motility

Recabarren, S. E., Rojas-Garcia, P. P., Recabarren, M. P., Alfaro, V., Smith, R., Padmanabhan, V., & Sir‐Petermann, T. (2008) · Endocrinology · doi:10.1210/en.2008-0785 · Cited by 83 · see citing works

Plasticity following Injury to the Adult Central Nervous System: Is Recapitulation of a Developmental State Worth Promoting?

Emery, D. L., Royo, N. C., Fischer, I., Saatman, K. E., & McIntosh, T. K. (2003) · Journal of Neurotrauma · doi:10.1089/089771503322686085 · Cited by 81 · see citing works

Inhibin Concentrations throughout the Menstrual Cycles of Normal, Infertile, and Older Women Compared with Those during Spontaneous Conception Cycles

Lenton, E. A., de Kretser, D., WOODWARD, A. J., & ROBERTSON, M. D. (1991) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-73-6-1180 · Cited by 76 · see citing works

Estrogen binding in the neonatal neocortex

Sheridan, P. J. (1979) · Brain Research · doi:10.1016/0006-8993(79)90101-x · Cited by 73 · see citing works

Sex differences in brain developing in the presence or absence of gonads

Büdefeld, T., Grgurevič, N., Tobet, S. A., & Majdič, G. (2008) · Developmental Neurobiology · doi:10.1002/dneu.20638 · Cited by 70 · see citing works

Estrogen receptor mRNA alterations in the developing rat hippocampus

O’Keefe, J. A., Li, Y., Burgess, L. H., & Handa, R. J. (1995) · Molecular Brain Research · doi:10.1016/0169-328x(94)00284-l · Cited by 68 · see citing works

Pituitary and Testicular Function in Sons of Women with Polycystic Ovary Syndrome from Infancy to Adulthood

Recabarren, S. E., Sir‐Petermann, T., Ríos, R., Maliqueo, M. A., Echiburú, B., Smith, R., Rojas-Garcia, P. P., Recabarren, M. P., & Rey, R. A. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-0255 · Cited by 65 · see citing works

Locus Coeruleus Mediates Cold Stress-Induced Polycystic Ovary in Rats

Bernuci, M. P., Szawka, R. E., Helena, C. V. V., Leite, C. M., Lara, H. E., & Anselmo-Franci, J. A. (2008) · Endocrinology · doi:10.1210/en.2007-1254 · Cited by 65 · see citing works

Neuroendocrine Plasticity in the Anterior Pituitary: Gonadotropin-Releasing Hormone-Mediated Movement in Vitro and in Vivo

Navratil, A. M., Knoll, J. G., Whitesell, J. D., Tobet, S. A., & Clay, C. M. (2007) · Endocrinology · doi:10.1210/en.2006-1153 · Cited by 61 · see citing works

Neonatal handling and reproductive function in female rats

Gomes, C. M., Raineki, C., de Paula, P. R., Severino, G. S., Helena, C. V. V., Anselmo-Franci, J. A., Franci, C. R., Sanvitto, G. L., & Lucion, A. B. (2005) · Journal of Endocrinology · doi:10.1677/joe.1.05907 · Cited by 58 · see citing works

Adrenergic Regulation of Ovarian Androgen Biosynthesis Is Mediated via β2-Adrenergic Theca- Interstitial Cell Recognition Sites*

Hernández, E. R., JIMENEZ, J. L., Payne, D. W., & Adashi, E. Y. (1988) · Endocrinology · doi:10.1210/endo-122-4-1592 · Cited by 58 · see citing works

Changes in estrogen receptor-alpha mRNA in the mouse cortex during development

Prewitt, A. K., & Wilson, M. E. (2007) · Brain Research · doi:10.1016/j.brainres.2006.11.069 · Cited by 57 · see citing works

Sex differences in the location of immunochemically defined cell populations in the mouse preoptic area/anterior hypothalamus

Wolfe, C. A., Doren, M. V., Walker, H. J., Seney, M. L., McClellan, K., & Tobet, S. A. (2005) · Developmental Brain Research · doi:10.1016/j.devbrainres.2005.03.001 · Cited by 54 · see citing works

The Nuclear Receptor Corepressor Has Organizational Effects within the Developing Amygdala on Juvenile Social Play and Anxiety-Like Behavior

Jessen, H. M., Kolodkin, M. H., Bychowski, M. E., Auger, C. J., & Auger, A. P. (2010) · Endocrinology · doi:10.1210/en.2009-0594 · Cited by 53 · see citing works

Sex- and hormone-dependent antigen immunoreactivity in developing rat hypothalamus.

Tobet, S. A., & Fox, T. O. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.1.382 · Cited by 52 · see citing works

Neonatal handling and the maternal odor preference in rat pups: Involvement of monoamines and cyclic AMP response element-binding protein pathway in the olfactory bulb

Raineki, C., de Souza, M. A., Szawka, R. E., Lutz, M. L., de Vasconcellos, L. F. T., Sanvitto, G. L., Izquierdo, I., Bevilaqua, L. R., Cammarota, M., & Lucion, A. B. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.12.012 · Cited by 51 · see citing works

Release of Norepinephrine from Human Ovary: Coupling to Steroidogenic Response

Lara, H. E., Arnaldo Porcile, J., Espinoza, J., Romero, C., Luza, S. M., Fuhrer, J., Miranda, C., & Roblero, L. S. (2001) · Endocrine · doi:10.1385/endo:15:2:187 · Cited by 49 · see citing works

Estrogen modulates neuronal movements within the developing preoptic area–anterior hypothalamus

Knoll, J. G., Wolfe, C. A., & Tobet, S. A. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05751.x · Cited by 48 · see citing works

Cooperation of sex chromosomal genes and endocrine influences for hypothalamic sexual differentiation

Majdič, G., & Tobet, S. A. (2011) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.02.009 · Cited by 48 · see citing works

GABA influences the development of the ventromedial nucleus of the hypothalamus

Dellovade, T., Davis, A. M., Ferguson, C., Sieghart, W., Homanics, G. E., & Tobet, S. A. (2001) · Journal of Neurobiology · doi:10.1002/neu.10011 · Cited by 47 · see citing works

Increases in norepinephrine release and ovarian cyst formation during ageing in the rat

Acuña, E., Fornes, R., Fernandois, D., Garrido, M. P., Greiner, M., Lara, H. E., & Paredes, A. H. (2009) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-7-64 · Cited by 47 · see citing works

Prenatal testosterone excess alters Sertoli and germ cell number and testicular FSH receptor expression in rams

Rojas-Garcia, P. P., Recabarren, M. P., Sarabia, L., Schön, J., Gabler, C., Einspanier, R., Maliqueo, M. A., Sir‐Petermann, T., Rey, R. A., & Recabarren, S. E. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00032.2010 · Cited by 45 · see citing works

Cold Stress Induces Metabolic Activation of Thyrotrophin‐Releasing Hormone‐Synthesising Neurones in the Magnocellular Division of the Hypothalamic Paraventricular Nucleus and Concomitantly Changes Ovarian Sympathetic Activity Parameters

Fiedler, J. L., Jara, P., Luza, S., Dorfman, M. D., Grouselle, D., Rage, F., Lara, H. E., & Arancibia, S. (2006) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01427.x · Cited by 44 · see citing works

Functional Development of the Ovarian Noradrenergic Innervation

Ricu, M. A., Paredes, A., Greiner, M., Ojeda, S. R., & Lara, H. E. (2007) · Endocrinology · doi:10.1210/en.2007-1204 · Cited by 42 · see citing works

Effects of Birth Weight on Anti-Mullerian Hormone Serum Concentrations in Infant Girls

Sir‐Petermann, T., Márquez, L., Cárcamo, M., Hitschfeld, C., Ethel Codner, D., Maliqueo, M. A., Echiburú, B., Aranda, P., Crisosto, N., & CASSORLA, F. G. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-1771 · Cited by 37 · see citing works

Release of Norepinephrine from the Rat Ovary: Local Modulation by Gonadotropins1

Ferruz, J. L., Barría, A., Galleguillos, X., & Lara, H. E. (1991) · Biology of Reproduction · doi:10.1095/biolreprod45.4.592 · Cited by 37 · see citing works

Migration of neurons containing gonadotropin releasing hormone (GnRH) in slices from embryonic nasal compartment and forebrain

Tobet, S. A., Hanna, I. K., & Schwarting, G. A. (1996) · Developmental Brain Research · doi:10.1016/s0165-3806(96)00151-4 · Cited by 35 · see citing works

Roles for γ‐aminobutyric acid in the development of the paraventricular nucleus of the hypothalamus

McClellan, K., Stratton, M. S., & Tobet, S. A. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22360 · Cited by 34 · see citing works

Do Animal Models of Polycystic Ovary Syndrome Help to Understand Its Pathogenesis and Management? Yes, but Their Limitations Should be Recognized

Franks, S. (2009) · Endocrinology · doi:10.1210/en.2009-0652 · Cited by 34 · see citing works

Polycystic ovary syndrome in post-menopausal women—marker of the metabolic syndrome

Margolin, E., Zornitzki, T., Kopernik, G., Kogan, S., Schattner, A., & Knobler, H. (2004) · Maturitas · doi:10.1016/j.maturitas.2004.09.005 · Cited by 34 · see citing works

Can Gonadal Steroids Influence Cell Position in the Developing Brain?

Tobet, S. A., Chickering, T. W., Hanna, I., Crandall, J. E., & Schwarting, G. A. (1994) · Hormones and Behavior · doi:10.1006/hbeh.1994.1028 · Cited by 32 · see citing works

Electro-Acupuncture Reverses Nerve Growth Factor Abundance in Experimental Polycystic Ovaries in the Rat

Bai, Y. H., Lim, S., Song, C. H., Bae, C. S., Jin, C. S., Choi, B. C., Jang, C. H., Lee, S. H., & Pak, S. C. (2003) · Gynecologic and Obstetric Investigation · doi:10.1159/000075382 · Cited by 27 · see citing works

Age-dependent failure of axon regeneration in organotypic culture of gerbil auditory midbrain

Hafidi, A., Lanjun, G., & Sanes, D. H. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(19991105)41:2 · Cited by 26 · see citing works

The effect of elevation of maternal plasma catecholamines on the fetus and placenta of the pregnant sheep.

Gu, W. T., & Jones, C. T. (1986) · PubMed · Cited by 24 · see citing works

Embryonic GABAB Receptor Blockade Alters Cell Migration, Adult Hypothalamic Structure, and Anxiety- and Depression-Like Behaviors Sex Specifically in Mice

Stratton, M. S., Staros, M., Büdefeld, T., Searcy, B. T., Nash, C. P., Eitel, C. M., Carbone, D. L., Handa, R. J., Majdič, G., & Tobet, S. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106015 · Cited by 23 · see citing works

Pituitary and testis responsiveness of young male sheep exposed to testosterone excess during fetal development

Recabarren, M. P., Rojas-Garcia, P. P., Einspanier, R., Padmanabhan, V., Sir‐Petermann, T., & Recabarren, S. E. (2013) · Reproduction · doi:10.1530/rep-13-0006 · Cited by 23 · see citing works

The Vasculature within the Paraventricular Nucleus of the Hypothalamus in Mice Varies as a Function of Development, Subnuclear Location, and GABA Signaling

Frahm, K., Schow, M., & Tobet, S. A. (2012) · Hormone and Metabolic Research · doi:10.1055/s-0032-1304624 · Cited by 23 · see citing works

Effects of Neonatal Handling on Central Noradrenergic and Nitric Oxidergic Systems and Reproductive Parameters in Female Rats

Raineki, C., Szawka, R. E., Gomes, C. M., Lucion, M. K., Barp, J., Belló‐Klein, A., Franci, C. R., Anselmo-Franci, J. A., Sanvitto, G. L., & Lucion, A. B. (2007) · Neuroendocrinology · doi:10.1159/000112230 · Cited by 22 · see citing works

Cold‐induced Glutamate Releasein vivofrom the Magnocellular Region of the Paraventricular Nucleus is Involved in Ovarian Sympathetic Activation

Jara, P., Rage, F., Dorfman, M. D., Grouselle, D., Barra, R., Arancibia, S., & Lara, H. E. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.02040.x · Cited by 21 · see citing works

Two neuronal cell lines expressing the myelin basic protein gene display differences in their in vitro survival and in their response to glia

Bongarzone, E. R., Foster, L. M., Byravan, S., Casaccia‐Bonnefil, P., Schonmann, V., & Campagnoni, A. T. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19981101)54:3 · Cited by 21 · see citing works

GABA regulates corticotropin releasing hormone levels in the paraventricular nucleus of the hypothalamus in newborn mice

Stratton, M. S., Searcy, B. T., & Tobet, S. A. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.01.003 · Cited by 21 · see citing works

Sympathetic pharmacological denervation in ageing rats: effects on ovulatory response and follicular population

Chávez‐Genaro, R., Lombide, P., Domı́nguez, R., Rosas, P., & Vázquez‐Cuevas, F. G. (2007) · Reproduction Fertility and Development · doi:10.1071/rd07075 · Cited by 21 · see citing works

The Contribution of Transporter-Dependent Uptake to Fetal Catecholamine Clearance

Bzoskie, L., Blount, L., Kashiwai, K., Humme, J. A., & Padbury, J. F. (2009) · Biology of the Neonate · doi:10.1159/000244403 · Cited by 20 · see citing works

Neonatal handling induces alteration in progesterone secretion after sexual behavior but not in angiotensin II receptor density in the medial amygdala: Implications for reproductive success

Gomes, C. M., Donadio, M. V. F., Anselmo-Franci, J. A., Franci, C. R., Lucion, A. B., & Sanvitto, G. L. (2005) · Life Sciences · doi:10.1016/j.lfs.2005.11.007 · Cited by 16 · see citing works

Prenatal Exposure to Androgen Excess Increases LH Pulse Amplitude During Postnatal Life in Male Sheep

Recabarren, S. E., Recabarren, M. P., Rojas-Garcia, P. P., Cordero, M., Reyes, C. D., & Sir‐Petermann, T. (2012) · Hormone and Metabolic Research · doi:10.1055/s-0032-1316291 · Cited by 9 · see citing works

Mapping Spatiotemporal Molecular Distributions Using a Microfluidic Array

Lynn, N. S., Jr., Tobet, S. A., Henry, C. S., & Dandy, D. S. (2011) · Analytical Chemistry · doi:10.1021/ac202314n · Cited by 7 · see citing works

Untitled work

(1997) · doi:10.1002/(sici)1096-9861(19971201)388:4

Untitled work

(1998) · doi:10.1002/(sici)1521-1878(199808)20:8

Clinical epidemiology of Alzheimer’s disease: assessing sex and gender differences

Mielke, M., Vemuri, P., & Rocca, W. (2014) · Clinical Epidemiology · doi:10.2147/clep.s37929 · Cited by 1,021 · see citing works

Effects of the environmental estrogenic contaminants bisphenol A and 17α-ethinyl estradiol on sexual development and adult behaviors in aquatic wildlife species

Bhandari, R. K., Deem, S. L., Holliday, D. K., Jandegian, C. M., Kassotis, C. D., Nagel, S. C., Tillitt, D. E., Saal, F. S. V., & Rosenfeld, C. S. (2014) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2014.09.014 · Cited by 298 · see citing works

Structural plasticity of the hippocampus in response to estrogens in female rodents

Sheppard, P. A. S., Choleris, E., & Galea, L. A. M. (2019) · Molecular Brain · doi:10.1186/s13041-019-0442-7 · Cited by 190 · see citing works

Sex and gender differences in the causes of dementia: A narrative review

Rocca, W. A., Mielke, M. M., Vemuri, P., & Miller, V. M. (2014) · Maturitas · doi:10.1016/j.maturitas.2014.05.008 · Cited by 186 · see citing works

Yoga- and meditation-based lifestyle intervention increases neuroplasticity and reduces severity of major depressive disorder: A randomized controlled trial

Tolahunase, M. R., Sagar, R., Faiq, M., & Dada, R. (2018) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-170810 · Cited by 167 · see citing works

The physiological roles of placental corticotropin releasing hormone in pregnancy and childbirth

Thomson, M. (2013) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-012-0227-2 · Cited by 107 · see citing works

Can ovarian aging be delayed by pharmacological strategies?

Zhang, J., Chen, Q., Du, D., Wu, T., Wen, J., Wu, M., Zhang, Y., Yan, W., Zhou, S., Li, Y., et al. (2019) · Aging · doi:10.18632/aging.101784 · Cited by 103 · see citing works

The effects of estradiol on mood and behavior in human female adolescents: a systematic review

Balzer, B. W. R., Duke, S., Hawke, C. I., & Steinbeck, K. S. (2015) · European Journal of Pediatrics · doi:10.1007/s00431-014-2475-3 · Cited by 102 · see citing works

Intestinal inflammation in a murine model of autism spectrum disorders

de Theije, C. G. M., Koelink, P. J., Korte-Bouws, G. A. H., da Silva, S. L., Korte, S. M., Olivier, B., Garssen, J., & Kraneveld, A. D. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.004 · Cited by 100 · see citing works

Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism

Mottron, L., Duret, P., Mueller, S., Moore, R. D., d’Arc, B. F., Jacquemont, S., & Xiong, L. (2015) · Molecular Autism · doi:10.1186/s13229-015-0024-1 · Cited by 97 · see citing works

Sex, stress, and epigenetics: regulation of behavior in animal models of mood disorders

Hodes, G. E. (2013) · Biology of Sex Differences · doi:10.1186/2042-6410-4-1 · Cited by 82 · see citing works

Understanding the epigenetic basis of sex differences in depression

Hodes, G. E., Walker, D. M., Labonté, B., Nestler, E. J., & Russo, S. J. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23876 · Cited by 82 · see citing works

Human Endometrial DNA Methylome Is Cycle-Dependent and Is Associated With Gene Expression Regulation

Houshdaran, S., Zelenko, Z., Irwin, J. C., & Giudice, L. C. (2014) · Molecular Endocrinology · doi:10.1210/me.2013-1340 · Cited by 80 · see citing works

Advancements in the gold standard: Measuring steroid sex hormones by mass spectrometry

Conklin, S. E., & Knezevic, C. E. (2020) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2020.03.008 · Cited by 62 · see citing works

Sex is a defining feature of neuroimaging phenotypes in major brain disorders

Salminen, L. E., Tubi, M., Bright, J. K., Thomopoulos, S., Wieand, A., & Thompson, P. (2020) · Human Brain Mapping · doi:10.1002/hbm.25438 · Cited by 58 · see citing works

Sex Hormones Regulate Cytoskeletal Proteins Involved in Brain Plasticity

Hansberg-Pastor, V., González‐Arenas, A., Piña-Medina, A. G., & Camacho‐Arroyo, I. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00165 · Cited by 58 · see citing works

Gamma power in rural Pakistani children: Links to executive function and verbal ability

Tarullo, A. R., Obradović, J., Keehn, B., Rasheed, M. A., Siyal, S., Nelson, C. A., & Yousafzai, A. K. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2017.03.007 · Cited by 57 · see citing works

Sex differences in aging, life span and spontaneous tumorigenesis in 129/Sv mice neonatally exposed to metformin

Anisimov, V. N., Popovich, I. G., Zabezhinski, M. A., Egormin, P. A., Yurova, M. N., Semenchenko, A. V., Тындык, М. Л., Панченко, А. В., Trashkov, A. P., Vasiliev, A. G., et al. (2014) · Cell Cycle · doi:10.4161/15384101.2014.973308 · Cited by 56 · see citing works

Sex Differences in Cognition Across Aging

Lee, B. H., Richard, J. E., de leon, R. G., Yagi, S., & Galea, L. A. M. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_309 · Cited by 51 · see citing works

Bisphenol A and 17α-ethinylestradiol-induced transgenerational gene expression differences in the brain–pituitary–testis axis of medaka, Oryzias latipes†

Thayil, A. J., Wang, X., Bhandari, P., Saal, F. S. V., Tillitt, D. E., & Bhandari, R. K. (2020) · Biology of Reproduction · doi:10.1093/biolre/ioaa169 · Cited by 43 · see citing works

Environmental Health Factors and Sexually Dimorphic Differences in Behavioral Disruptions

Rosenfeld, C. S., & Trainor, B. C. (2014) · Current Environmental Health Reports · doi:10.1007/s40572-014-0027-7 · Cited by 37 · see citing works

Maternal sympathetic stress impairs follicular development and puberty of the offspring

Barra, R., Cruz, G., Mayerhofer, A., Paredes, A., & Lara, H. E. (2014) · Reproduction · doi:10.1530/rep-14-0150 · Cited by 37 · see citing works

Androgen-induced epigenetic modulations in the ovary

Salinas, I., Sinha, N., & Sen, A. (2021) · Journal of Endocrinology · doi:10.1530/joe-20-0578 · Cited by 36 · see citing works

Post-translational histone modifications and their interaction with sex influence normal brain development and elaboration of neuropsychiatric disorders

Singh, G., Singh, V., & Schneider, J. S. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.10.016 · Cited by 35 · see citing works

Developmental Programming of Ovarian Functions and Dysfunctions

Puttabyatappa, M., & Padmanabhan, V. (2018) · Vitamins and hormones · doi:10.1016/bs.vh.2018.01.017 · Cited by 32 · see citing works

Regulation of Bone by Mechanical Loading, Sex Hormones, and Nerves: Integration of Such Regulatory Complexity and Implications for Bone Loss during Space Flight and Post-Menopausal Osteoporosis

Hart, D. A. (2023) · Biomolecules · doi:10.3390/biom13071136 · Cited by 31 · see citing works

Factors That Can Influence Animal Research

Baker, D. G., & Lipman, N. S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-409527-4.00033-x · Cited by 30 · see citing works

Decoding the non‐coding genome: elucidating genetic risk outside the coding genome

Barr, C. L., & Misener, V. L. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12269 · Cited by 28 · see citing works

Sex‐Specific Effects of Stress on Respiratory Control: Plasticity, Adaptation, and Dysfunction

Lopes, L. T., & Kinkead, R. (2021) · Comprehensive physiology · doi:10.1002/cphy.c200022 · Cited by 27 · see citing works

Sex-Dependent Synaptic Remodeling of the Somatosensory Cortex in Mice With Prenatal Methadone Exposure

Grecco, G. G., Huang, J.-Y., Muñoz, B., Doud, E. H., Hines, C. D., Gao, Y., Rodriguez, B., Mosley, A. L., Lu, H., & Atwood, B. K. (2022) · Advances in Drug and Alcohol Research · doi:10.3389/adar.2022.10400 · Cited by 25 · see citing works

Timing of Maternal Exposure and Foetal Sex Determine the Effects of Low‐level Chemical Mixture Exposure on the Foetal Neuroendocrine System in Sheep

Bellingham, M., Fowler, P., Macdonald, E. S., Mandon‐Pepin, B., Cotinot, C., Rhind, S. M., Sharpe, R. M., & Evans, N. P. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12444 · Cited by 25 · see citing works

Functioning and disability analysis by using WHO Disability Assessment Schedule 2.0 in older adults Taiwanese patients with dementia

Huang, S., Chang, K., Escorpizo, R. S., Chi, W., Yen, C.-F., Liao, H., Chang, F., Chiu, W., Lin, J., & Liou, T. (2015) · Disability and Rehabilitation · doi:10.3109/09638288.2015.1107636 · Cited by 24 · see citing works

Chronographic Theory of Development, Aging, and Origin of Cancer: Role of Chronomeres and Printomeres

Olovnikov, A. M. (2015) · Current Aging Science · doi:10.2174/1874609808666150422114916 · Cited by 23 · see citing works

Sex differences of brain and their implications for personalized therapy

Rezzani, R., Franco, C., & Rodella, L. F. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.01.030 · Cited by 22 · see citing works

Sex Differences in Aging and Associated Biomarkers

Thomas, N., Gurvich, C., & Kulkarni, J. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-25650-0_4 · Cited by 21 · see citing works

Sex hormones and proteins involved in brain plasticity

Camacho‐Arroyo, I., Piña-Medina, A. G., Bello‐Alvarez, C., & Zamora-Sánchez, C. J. (2020) · Vitamins and hormones · doi:10.1016/bs.vh.2020.04.002 · Cited by 21 · see citing works

On the origins of sex-based differences in respiratory disorders: Lessons and hypotheses from stress neuroendocrinology in developing rats

Rousseau, J.-P., Lopes, L. T., Baldy, C., Janes, T. A., Fournier, S., & Kinkead, R. (2017) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2017.03.013 · Cited by 20 · see citing works

Circulating preoperative testosterone level predicts unfavourable disease at radical prostatectomy in men with International Society of Urological Pathology Grade Group 1 prostate cancer diagnosed with systematic biopsies

Ferro, M., Lucarelli, G. T., COBELLI, O. D., Vartolomei, M. D., Damiano, R., Cantiello, F., Crocerossa, F., Perdonà, S., Prete, P. D., Cordima, G., et al. (2020) · World Journal of Urology · doi:10.1007/s00345-020-03368-9 · Cited by 20 · see citing works

Auditing the Editor: A Review of Key Translational Issues in Epigenetic Editing

Huerne, K., Palmour, N., Wu, A. R., Beck, S., Berner, A., Siebert, R., & Joly, Y. (2022) · The CRISPR Journal · doi:10.1089/crispr.2021.0094 · Cited by 18 · see citing works

FOXL2 is a Progesterone Target Gene in the Endometrium of Ruminants

Eozénou, C., Lesage, A., Mauffré, V., Healey, G. D., Camous, S., Bolifraud, P., Giraud‐Delville, C., Vaiman, D., Shimizu, T., Miyamoto, A., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041478 · Cited by 16 · see citing works

Transcriptomic analysis of cardiac gene expression across the life course in male and female mice

Yusifov, A., Chhatre, V. E., Koplin, E. K., Wilson, C. E., Schmitt, E. E., Woulfe, K. C., & Bruns, D. R. (2021) · Physiological Reports · doi:10.14814/phy2.14940 · Cited by 14 · see citing works

Mechanism of Progesterone Action in the Brain

Camacho‐Arroyo, I., Hansberg-Pastor, V., Vázquez-Martínez, E. R., & Cerbón, M. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803592-4.00053-5 · Cited by 14 · see citing works

Perinatal programming of the orexinergic (hypocretinergic) system in hypothalamus and anterior pituitary by testosterone

Cataldi, N. I., Lux-Lantos, V. A., & Libertun, C. (2017) · Peptides · doi:10.1016/j.peptides.2017.04.006 · Cited by 11 · see citing works

A developed HPLC-MS/MS method to quantitate 5 steriod hormones in clinical human serum by using PBS as the surrogate matrix

Liu, D., Zhao, R., Zhao, S., Wang, Z., Liu, R., Wang, F., & Gao, Y. (2021) · Journal of Chromatography B · doi:10.1016/j.jchromb.2021.123002 · Cited by 8 · see citing works

A hormonális rendszer válsága: az endokrin diszruptorok egészségügyi hatásai

Csaba, G. (2017) · Orvosi Hetilap · doi:10.1556/650.2017.30855 · Cited by 8 · see citing works

Sex and sex hormone differences in hippocampal neurogenesis and their relevance to Alzheimer’s disease

Lee, B. H., Puri, T. A., & Galea, L. A. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819344-0.00010-7 · Cited by 8 · see citing works

The Role of Brain –Pineal –Thymus System in the Determination of Lifespan: The Autoimmune Aging Theory

Csaba, G. (2017) · Advances in Neuroimmune Biology · doi:10.3233/nib-160118 · Cited by 5 · see citing works

Early-Life Stress Drives the Molecular Mechanisms Shaping the Adult Phenotype

Huber, S., Costantini, D., Houdelier, C., & Marasco, V. (2022) · Fascinating life sciences · doi:10.1007/978-3-030-90131-8_4 · Cited by 5 · see citing works

Gonadal steroid hormones as therapeutic tools for brain trauma: The time is ripe for more courageous clinical trials to get into emergency medicine

Hoffmann, S., & Beyer, C. (2014) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2014.09.002 · Cited by 4 · see citing works

Maternal Effects on Behavior

Schwabl, H. G., & Groothuis, T. G. G. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.20836-4 · Cited by 4 · see citing works

Neonatal testosterone exposure alleviates female-specific severity of formalin-induced inflammatory pain in mice

Kanaya, M., Ueta, Y., Mochizuki‐Kashio, M., Nakamura‐Ishizu, A., & Miyata, M. (2025) · Frontiers in Neural Circuits · doi:10.3389/fncir.2025.1593443 · Cited by 3 · see citing works

Sexual Dimorphism in the Functional Development of the Cochlear Amplifier in Humans

Mishra, S. K., Zambrano, S., & Rodrigo, H. (2021) · Ear and Hearing · doi:10.1097/aud.0000000000000976 · Cited by 3 · see citing works

Integrative techniques using acupuncture, Chinese herbal medicine, diet, and supplements for polycystic ovary syndrome: a case report

Ehling, D. (2013) · Journal of Chinese Integrative Medicine · doi:10.3736/jintegrmed2013055 · Cited by 3 · see citing works

Overview of CNS Organization and Development

Brown, R. E. (2023) · Springer eBooks · doi:10.1007/978-3-031-20792-1_1 · Cited by 3 · see citing works

Targeting estrogen receptors in PCOS: A receptor-specific framework for neuropsychiatric dysfunction and therapeutic modulation

Carlson, J. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.108008 · Cited by 2 · see citing works

Early Family Experiences and Neural Activity in Rural Pakistani Children: The Differential Role of Gender

Lopera‐Perez, D. C., Obradović, J., Yousafzai, A. K., Keehn, B., Siyal, S., Nelson, C. A., & Tarullo, A. R. (2024) · Developmental Psychobiology · doi:10.1002/dev.22534 · Cited by 1 · see citing works

Interplay of hormones and metabolite excretion with fern pattern prove saliva as a potent indicator of male reproductive status in Kangayam breed cattle

Ramachandran, R., Sankarganesh, D., Suriyakalaa, U., Aathmanathan, V. S., Angayarkanni, J., & Achiraman, S. (2024) · Tropical Animal Health and Production · doi:10.1007/s11250-024-03990-4 · Cited by 1 · see citing works

Ectonucleotidases in the hippocampus: Spatial distribution and expression after ovariectomy and estradiol replacement

Grković, I., Mitrović, N., & Dragić, M. (2022) · Vitamins and hormones · doi:10.1016/bs.vh.2021.11.005 · Cited by 1 · see citing works

Hipertensión arterial, menopausia y compromiso cognitivo

Sueldo, M. D., Vicario, A., Cerezo, G. H., Miranda, G., & Zilberman, J. M. (2018) · Revista Colombiana de Cardiología · doi:10.1016/j.rccar.2017.11.025 · Cited by 1 · see citing works

AXOLOTL PAEDOMORPHOSIS: A COMPARISON OF JUVENILE, METAMORPHIC, AND PAEDOMORPHIC AMBYSTOMA MEXICANUM BRAIN GENE

Johnson, C. (2013) · UKnowledge (University of Kentucky) · Cited by 1 · see citing works

Advances in Neuroendocrine Mechanisms

Mani, S. K., Lara, H. E., Romero, C., Handa, R., & Wu, T. J. (2012) · Hormone and Metabolic Research · doi:10.1055/s-0032-1316344 · Cited by 1 · see citing works

The organisational effects of adolescent gonadal hormones on behavioural development in rats

Kulbarsh, K. D. (2014) · St Andrews Research Repository (St Andrews Research Repository)

Methods for the study of behavioral neuroendocrinology

Wilkinson, M., & Brown, R. E. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781139045803.015

Environmental Pollution and Non-Perinatal Faulty Hormonal Imprinting: A Critical Review

Csaba, G. (2018) · Integrative Pediatrics and Child Care · doi:10.18314/ipcc.v1i1.1419

Sex, Gender, and the Decline of Dementia

Rocca, W. A. (2019) · ISGE series · doi:10.1007/978-3-030-11355-1_9

Unraveling the Mysteries of PCOS: A Comprehensive Investigation into Causes, Mechanisms, and Molecular Docking Analysis with Dolichos biflorus Linn.

Sharma, P., Mittal, P., & Arya, G. C. (2024) · Current Analytical Chemistry · doi:10.2174/0115734110312022240903060337

How and why your gender impacts your risk for dementia?

ZEIDAN, H. M., & ZEIDAN, I. H. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-21632-9.00004-2

Volumetric Sex Differences in Hypothalamic Volume and Associated Subunits Revealed by Automated MRI SegmentationPreprint

Ghaderi, S., Mohammadi, S., Fatehi, F., Mohammadi, M., Sisakhti, M., & Batouli, S. A. H. (2025) · Research Square · doi:10.21203/rs.3.rs-7163918/v1

Analyse du rôle du système PTH/PTHrp dans la régulation de la balance énergétique et des fonctions cognitives contrôlées par le système nerveux central

Rousseaud, A. (2018) · doi:10.70675/646b4e48z73b6z4801z94d3z20d15d31ffe7

Critical Periods During Development: Hormonal Influences on Neurobehavioral Transitions Across the Life Span

Sisk, C. L., Lonstein, J. S., & Gore, A. C. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_61 · Cited by 2 · see citing works

Sensitive Periods for Hormonal Programming of the Brain

Vries, G. J. D., Fields, C. T., Peters, N. V., Whylings, J., & Paul, M. J. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_286 · Cited by 29 · see citing works

How it’s Made: Organisational Effects of Hormones on the Developing Brain

McCarthy, M. M. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.02021.x · Cited by 138 · see citing works

Perinatal hormonal exposure and the development of neuroendocrine regulatory processes.

Gorski, R., Harlan, R. E., & Christensen, L. W. (1977) · Journal of Toxicology and Environmental Health, Part A · doi:10.1080/15287397709529551 · Cited by 101 · see citing works

Hormones and Brain Plasticity

García‐Segura, L. M. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195326611.001.0001 · Cited by 67 · see citing works