Aboulghar, M. A., Mansour, R. T., Serour, G. I., Ramzy, A. M., & Amin, Y. M. (1997). Oocyte quality in patients with severe ovarian hyperstimulation syndrome. Fertility and Sterility, 68(6), 1017–1021.

Adams, G. P., Matteri, R. L., Kastelic, J. P., Ko, J. C. H., & Ginther, O. (1992). Association between surges of follicle-stimulating hormone and the emergence of follicular waves in heifers. Reproduction, 94(1), 177–188.

Alward, K. J., Cockrum, R. R., & Ealy, A. D. (2023). Associations of antral follicle count with fertility in cattle: A review. Journal of Dairy Science Communications, 4(2), 132–137.

Barati, F., Niasari-Naslaji, A,. Bolourchi, M., Sarhaddi, F., Razavi, K., Naghzali, E., & Thatcher, W. W. (2006). Superovulatory response of Sistani cattle to three different doses of FSH during winter and summer. Theriogenology, 66(5), 1149–1155.

Bedenk, J., Vrtačnik-Bokal, E., & Virant-Klun, I. (2020). The role of anti-Müllerian hormone (AMH) in ovarian disease and infertility. Journal of Assisted Reproduction and Genetics, 37(1), 89–100.

Bezard, J., Vigier, B., Tran, D., Mauléon, P., & Josso, N. (1987). Immunocytochemical study of anti-Müllerian hormone in sheep ovarian follicles during fetal and post-natal development. Journal of reproduction and fertility, 80(2), 509–516.

Bó, G. A., Mapletoft, R. J. (2014). Historical perspectives and recent research on superovulation in cattle. Theriogenology, 81(1), 38–48.

Bó, G., & Mapletoft, R. (2013). Evaluation and classification of bovine embryos. Animal Reproduction, 10(3), 344–348.

Campbell, B. K., Clinton, M., & Webb, R. (2012). The role of anti-Müllerian hormone (AMH) during follicle development in a monovulatory species (sheep). Endocrinology, 153(9), 4533–4543.

Cate, R. L. (2022). Anti-Müllerian hormone signal transduction involved in müllerian duct regression. Frontiers in Endocrinology, 13, 905324.

Clark, Z. L, Karl, K. R., Ruebel, M. L., Latham, K. E., & Ireland, J. J. (2022). Excessive follicle-stimulating hormone during ovarian stimulation of cattle may induce premature luteinization of most ovulatory-size follicles. Biology of Reproduction, 106(5), 968–978.

Clark, Z. L., Thakur, M., Leach, R. E., & Ireland, J. J. (2021). FSH dose is negatively correlated with number of oocytes retrieved: analysis of a data set with ~650,000 ART cycles that previously identified an inverse relationship between FSH dose and live birth rate. Journal of Assisted Reproduction and Genetics, 38(7), 1787–1797.

Convissar, S., Armouti, M., Fierro, M. A., Winston, N. J., Scoccia, H., Zamah, A. M., & Stocco, C. (2017). Regulation of AMH by oocyte-specific growth factors in human primary cumulus cells. Reproduction, 154(6), 745–753.

Cory, A. T., Price, C. A., Lefebvre, R., & Palin, M. F. (2013). Identification of single nucleotide polymorphisms in the bovine follicle-stimulating hormone receptor and effects of genotypes on superovulatory response traits. Animal Genetics, 44(2), 197–201.

Deng, Q., Gao, Y., Li, C. H., Yu, X. F., Ren, J. S., Li, S. J., Chen, C. Z., Yuan, B., Ding, Y., Jiang, H., & Zhang, J. B. (2015). Effects of choice of month of treatment and parity order on bovine superovulation traits. Genetics and Molecular Research, 14(4), 15062–15072.

di Clemente, N., Goxa, B., Aemy, J. J., Cate, R. L., Jesso, N. Vigier, B., & Salesse, A. (1994). Effect of AMH upon aromalasa activity and LH receptors of granulosa calls of rat and porcile Immature ovaries. Endocrine, 2, 553–558.

Dochi, O. (2019). Direct transfer of frozen-thawed bovine embryos and its application in cattle reproduction management. Journal of Reproduction and Development, 65(5), 389–396.

Durlinger, A. L., Gruijters, M. J., Kramer, P., Karels, B., Ingraham, H. A., Nachtigal, M. W., Uilenbroek, J. T., Grootegoed, J. A., & Themmen, A. P. (2002). Anti-Mullerian hormone inhibits initiation of primordial follicle growth in the mouse ovary. Endocrinology, 143(3), 1076–1084.

Durlinger, A. L., Gruijters, M. J., Kramer, P., Karels, B., Kumar, T. R., Matzuk, M. M., Rose, U. M., de Jong, F. H., Uilenbroek, J. T., Grootegoed, J. A., & Themmen, A. P. (2001). Anti-Müllerian hormone attenuates the effects of FSH on follicle development in the mouse ovary. Endocrinology, 142(11), 4891–4899.

Durlinger, A. L., Kramer, P., Karels, B., de Jong, F. H., Uilenbroek, J. T., Grootegoed, J. A., & Themmen, A. P. (1999). Control of primordial follicle recruitment by anti-Müllerian hormone in the mouse ovary. Endocrinology, 140(12), 5789–5796.

Fushimi, Y., Okawa, H., Monniaux, D., & Takagi, M. (2020). Efficacy of a single blood anti-Müllerian hormone (AMH) concentration measurement for the selection of Japanese Black heifer embryo donors in herd breeding programs. Journal of Reproduction and Development, 66(6), 593–598.

Ghanem, N., Jin, J. I., Kim, S. S., Choi, B. H., Lee, K. L., Ha, A. N., Song. S. H., & Kong, I. K. (2016). The anti-Müllerian hormone profile is linked with the in vitro embryo production capacity and embryo viability after transfer but cannot predict pregnancy outcome. Reproduction in Domestic Animals, 51(2), 301–310.

Gigli, I., Cushman, R. A., Wahl, C. M., & Fortune, J. E. (2005). Evidence for a role for anti-Mullerian hormone in the suppression of follicle activation in mouse ovaries and bovine ovarian cortex grafted beneath the chick chorioallantoic membrane. Molecular Reproduction and Development, 71(4), 480–488.

Ginther, O. J., Bergfelt, D. R., Kulick, L. J., & Kot, K. (2000). Selection of the dominant follicle in cattle: role of two-way functional coupling between follicle-stimulating hormone and the follicles. Biology of Reproduction, 62(4), 920–927.

Gloaguen, P., Crépieux, P., Heitzler, D., Poupon, A., & Reiter, E. (2011). Mapping the follicle-stimulating hormone-induced signaling networks. Frontiers in Endocrinology (Lausanne), 2, 45.

Grossman, M. P., Nakajima, S. T., Fallat, M. E., & Siow, Y. (2008) Müllerian-inhibiting substance inhibits cytochrome P450 aromatase activity in human granulosa lutein cell culture. Fertility and Sterility, 89(5 Suppl), 1364–1370.

Grynberg, M., Pierre, A., Rey, R., Leclerc, A., Arouche, N., Hesters, L., Catteau-Jonard, S., Frydman, R., Picard, J. Y., Fanchin, R., Veitia, R., di Clemente, N., & Taieb, J. (2012). Differential regulation of ovarian anti-Müllerian hormone (AMH) by estradiol through α- and β-estrogen receptors. The Journal of Clinical Endocrinology & Metabolism, 97(9), E1649–E1657.

Hayden, C. B., Sala, R. V., Pereira, D. C., Moreno, J. F., & García-Guerra, A. (2023). Effect of use and dosage of p-follicle-stimulating hormone for ovarian superstimulation before ovum pick-up and in vitro embryo production in pregnant Holstein heifers. Journal of Dairy Science, 106(11), 8110–8121.

Hazout, A., Bouchard, P., Seifer, D. B., Aussage, P., Junca, A. M., & Cohen-Bacrie, P. (2004). Serum antimüllerian hormone/müllerian-inhibiting substance appears to be a more discriminatory marker of assisted reproductive technology outcome than follicle-stimulating hormone, inhibin B, or estradiol. Fertility and Sterility, 82(5), 1323–1329.

Hehenkamp, W. J., Looman, C. W., Themmen, A. P., de Jong, F. H., Te Velde, E. R., & Broekmans, F. J. (2006) Anti-Müllerian hormone levels in the spontaneous menstrual cycle do not show substantial fluctuation. The Journal of Clinical Endocrinology and Metabolism, 91(10), 4057–4063.

Hirayama, H., Naito, A., Fukuda, S., Fujii, T., Asada, M., Inaba, Y., Takedomi, T., Kawamata, M., Moriyasu, S., & Kageyama, S. (2017). Long-term changes in plasma anti-Müllerian hormone concentration and the relationship with superovulatory response in Japanese black cattle. The Journal of Reproduction and Development, 63(1), 95–100.

Hirayama, H., Kageyama, S., Naito, A., Fukuda, S., Fujii, T., & Minamihashi, A. (2012). Prediction of superovulatory response in Japanese Black cattle using ultrasound, plasma anti-Müllerian hormone concentrations and polymorphism in the ionotropic glutamate receptor AMPA1/GRIA1. The Journal of Reproduction and Development, 58(3), 380–383.

Hirayama, H., Naito, A., Fujii, T., Sugimoto, M., Takedomi, T., Moriyasu, S., Sakai, H., & Kageyama, S. (2019). Effects of genetic background on responses to superovulation in Japanese Black cattle. Journal of Veterinary Medical Science, 81(3), 373–378.

Hugon, J., Ouzounian, S., & Christin-Maître, S. (2010). Hormone antimüllérienne: Du gène à la protéine, sa place en clinique [Müllerian inhibitor substance: From gene to protein, its role in clinical practice]. Annales d'Endocrinologie, 71(2), 83–88 (in French).

Iliodromiti, S., Anderson, R. A., & Nelson, S. M. (2015). Technical and performance characteristics of anti-Müllerian hormone and antral follicle count as biomarkers of ovarian response. Human Reproduction Update, 21(6), 698–710.

Irshad, A. R., Sasaki, T., Kubo, T., Odashima, N., Katano, K., Osawa, T., Takahashi, T., & Izaike, Y. (2015). Development of a programmable piggyback syringe pump and four-times-a-day injection regimen for superovulation in non-lactating Holstein cows. Journal of Reproduction and Development, 61(5), 485–458.

Jaton, C., Koeck, A., Sargolzaei, M., Malchiodi, F., Price, C. A., Schenkel, F. S., & Miglior, F. (2016). Genetic analysis of superovulatory response of Holstein cows in Canada. Journal of Dairy Science, 99(5), 3612–3623.

Jayaprakasan, K., Chan, Y., Islam, R., Haoula, Z., Hopkisson, J., Coomarasamy, A., & Raine-Fenning, N. (2012). Prediction of in vitro fertilization outcome at different antral follicle count thresholds in a prospective cohort of 1,012 women. Fertility and Sterility, 98(3), 657–663.

Kanitz, W., Becker, F., Schneider, F., Kanitz, E., Leiding, C., Nohner, H. P., & Pöhland, R. (2002). Superovulation in cattle: Practical aspects of gonadotropin treatment and insemination. Reproduction Nutrition Development, 42(6), 587–599.

Karl, K. R., Jimenez-Krassel, F., Gibbings, E., Ireland, J. L. H., Clark, Z. L., Tempelman, R. J., Latham, K. E., & Ireland, J. J. (2021). Negative impact of high doses of follicle-stimulating hormone during superovulation on the ovulatory follicle function in small ovarian reserve dairy heifers. Biology of Reproduction, 104(3), 695–705.

Karl, K. R., Schall, P. Z., Clark, Z. L., Ruebel, M. L., Cibelli, J., Tempelman, R. J., Latham, K. E., & Ireland, J. J. (2023). Ovarian stimulation with excessive FSH doses causes cumulus cell and oocyte dysfunction in small ovarian reserve heifers. Molecular Human Reproduction, 29(10), gaad033.

Koca, D., Aktar, A., Turgut, A. O., Sagirkaya, H., & Alcay, S. (2024). Elecsys® AMH assay: Determination of anti-Müllerian hormone levels and evaluation of the relationship between superovulation response in Holstein dairy cows. Veterinary Medicine and Science, 10(4), e1509.

Kovpak, V. V., Kovpak, O. S., Derkach, S. S., Valchuk, O. A., Zhuk, Y. V., & Masalovych, Y. S. (2023). Influence of calcium ionophore on the fertilization of bovine oocytes and their further embryonic development. Regulatory Mechanisms in Biosystems, 14(1), 137–144.

Kovpak, V. V., Kovpak, O. S., Valchuk, O. A., Zhuk, Y. V., & Derkach, S. S. (2022). Specifics of vitrification of in vitro-produced cattle embyos at various development stages. Regulatory Mechanisms in Biosystems, 13(3), 265–271.

Kovpak, V., Kovpak, O., Babii, Y., Derkach, S., & Masalovych, Y. (2022). Influence of different environments on oocyte maturation and development of bovine embryos in vitro. Ukrainian Journal of Veterinary Sciences, 13(3), 17–24.

Kovpak, V., Kovpak, O., Derkach, S., Masalovych, Y., & Babiі, Y. (2022). The influence of platelet concentrate on the development of cattle embryos in аn in vitro system. Scientific Horizons, 25(9), 9–18.

Kwee, J., Schats, R., McDonnell, J., Themmen, A., de Jong, F., & Lambalk, C. (2008). Evaluation of anti-Müllerian hormone as a test for the prediction of ovarian reserve. Fertility and Sterility, 90(3), 737–743.

La Marca, A., & Volpe, A. (2006). Anti‐Müllerian hormone (AMH) in female reproduction: Is measurement of circulating AMH a useful tool? Clinical Endocrinology, 64(6), 603–610.

Liu, Y., Pan, Z., Wu, Y., Song, J., & Chen, J. (2023). Comparison of anti-Müllerian hormone and antral follicle count in the prediction of ovarian response: A systematic review and meta-analysis. Journal of Ovarian Research, 16(1), 117.

López-Gatius, F., López-Helguera, I., De Rensis, F., & Garcia-Ispierto, I. (2015). Effects of different five-day progesterone-based synchronization protocols on the estrous response and follicular/luteal dynamics in dairy cows. The Journal of Reproduction and Development, 61(5), 465–471.

MacLaughlin, D. T., Teixeira, J., & Donahoe, P. K. (2001). Perspective: Reproductive tract development – new discoveries and future directions. Endocrinology, 142(6), 2167–2172.

Mapletoft, R. J., & Bó, G. A. (2011). The evolution of improved and simplified superovulation protocols in cattle. Reproduction, Fertility and Development, 24(1), 278–283.

Monniaux, D., Rico, C., Larroque, H., Dalbiès-Tran, R., Médigue, C., Clément, F., & Fabre, S., (2010). L’hormone antimüllérienne, prédicteur endocrinien de la réponse à une stimulation ovarienne chez les bovins. Gynécologie Obstétrique and Fertilité, 38(7–8), 465–470.

Moore, S. G., & Hasler, J. F. (2017). A 100-year review: Reproductive technologies in dairy science. Journal of Dairy Science, 100(12), 10314–10331.

Mossa, F., & Ireland, J. J. (2019). Physiology and endocrinology symposium: Anti-Müllerian hormone: A biomarker for the ovarian reserve, ovarian function, and fertility in dairy cows. Journal of Animal Science, 97(4), 1446–1455.

Nilsson, E. E., Schindler, R., Savenkova, M. I., & Skinner, M. K. (2011). Inhibitory actions of anti-Müllerian hormone (AMH) on ovarian primordial follicle assembly. PLoS One, 6(5), e20087.

Pilsgaard, F., Grynnerup, A. G., Løssl, K., Bungum, L., & Pinborg, A. (2018). The use of anti-Müllerian hormone for controlled ovarian stimulation in assisted reproductive technology, fertility assessment and -counseling. Acta Obstetricia et Gynecologica Scandinavica, 97(9), 1105–1113.

Rajpert-De Meyts, E., Jørgensen, N., Graem, N., Müller, J., Cate, R. L., & Skakkebaek, N. E. (1999). Expression of anti-Müllerian hormone during normal and pathological gonadal development: Association with differentiation of Sertoli and granulosa cells. The Journal of Clinical Endocrinology and Metabolism, 84(10), 3836–3844.

Rey, R., Lukas-Croisier, C., Lasala, C., & Bedecarrás, P. (2003). AMH/MIS: What we know already about the gene, the protein and its regulation. Molecular and Cellular Endocrinology, 211(1–2), 21–31.

Rico, C., Drouilhet, L., Salvetti, P., Dalbiès-Tran, R., Jarrier, P., Touzé, J. L., Pillet, E., Ponsart, C., Fabre, S., & Monniaux, D. (2012). Determination of anti-Müllerian hormone concentrations in blood as a tool to select Holstein donor cows for embryo production: From the laboratory to the farm. Reproduction, Fertility and Development, 24(7), 932–944.

Rico, C., Fabre, S., Médigue, C., di Clemente, N., Clément, F., Bontoux, M., Touzé, J. L,, Dupont, M., Briant, E., Rémy, B., Beckers, J. F., & Monniaux, D. (2009). Anti-Mullerian hormone is an endocrine marker of ovarian gonadotropin-responsive follicles and can help to predict superovulatory responses in the cow. Biology of Reproductio, 80(1), 50–59.

Rico, C., Médigue, C., Fabre, S., Jarrier, P., Bontoux, M., Clément, F., & Monniaux, D. (2011). Regulation of anti-Müllerian hormone production in the cow: A multiscale study at endocrine, ovarian, follicular, and granulosa cell levels. Biology of Reproductio, 84(3), 560–571.

Rocha, J. C., Passalia, F., Matos, F. D., Maserati Jr, M. P., Alves, M. F., Almeida, T. G., Cardoso, B. L., Basso, A. C., & Nogueira, M. F. (2016). Methods for assessing the quality of mammalian embryos: How far we are from the gold standard? JBRA Assisted Reproduction, 20(3), 150–158.

Sacchi, S., D'Ippolito, G., Sena, P., Marsella, T., Tagliasacchi, D., Maggi, E., Argento, C., Tirelli, A., Giulini, S., & La Marca, A. (2016). The anti-Müllerian hormone (AMH) acts as a gatekeeper of ovarian steroidogenesis inhibiting the granulosa cell response to both FSH and LH. Journal of Assisted Reproduction and Genetics, 33(1), 95–100.

Santos, G. M. G. D., Junior, L. B., Silva-Santos, K. C., Ayres Dias, J. H., Dias, I. D. S., Seneda, M. M., & Morotti, F. (2023). Conception rate and pregnancy loss in fixed-time cattle embryo transfer programs are related to the luteal blood perfusion but not to the corpus luteum size. Theriogenology, 210, 251–255.

Santos, G. M. G. D., Silva-Santos, K. C., Barreiros, T. R. R., Morotti, F., Sanches, B. V., de Moraes. F. L. Z., Blaschi, W., & Seneda, M. M. (2016). High numbers of antral follicles are positively associated with in vitro embryo production but not the conception rate for FTAI in Nelore cattle. Animal Reproduction Science, 165, 17–21.

Saumande, J., & Chupin, D. (1996). Induction of superovulation in cyclic heifers: The inhibitory effect of large doses of PMSG. Theriogenology, 25(2), 233–247.

Son, D. S., Choe, C. Y., Cho, S. R., Choi, S. H., Kim, H. J., & Kim, I. H. (2007). The effect of reduced dose and number of treatments of FSH on superovulatory response in CIDR-treated Korean native cows. The Journal of Reproduction and Development, 53(6), 1299–1303.

Souza, A. H., Carvalho, P. D., Rozner, A. E., Vieira, L. M., Hackbart, K. S., Bender, R. W., Dresch, A. R., Verstegen, J. P., Shaver, R. D., & Wiltbank, M. C. (2015). Relationship between circulating anti-Müllerian hormone (AMH) and superovulatory response of high-producing dairy cows. Journal of Dairy Science, 98(1), 169–178.

Stalzer, A., Seybold, D., Gantt, P., Broce, M., & Cronkright, A. (2023). Anti-Müllerian hormone: A predictor of successful intrauterine insemination. The Cureus Journal of Medical Science, 15(10), e47200.

Steward, R. G., Lan, L., Shah, A. A., Yeh, J. S., Price, T. M., Goldfarb, J. M., & Muasher, S. J. (2014). Oocyte number as a predictor for ovarian hyperstimulation syndrome and live birth: An analysis of 256,381 in vitro fertilization cycles. Fertility and Sterility, 101(4), 967–973.

Sugano, M., & Watanabe, S. (1997). Use of highly purified porcine FSH preparation for superovulation in Japanese black cattle. The Journal of Veterinary Medical Science, 59(3), 223–225.

Sun, B., Ma, Y., Li, L., Hu, L., Wang, F., Zhang, Y., Dai, S., & Sun, Y. (2021). Factors associated with ovarian hyperstimulation syndrome (OHSS) severity in women with polycystic ovary syndrome undergoing IVF/ICSI. Frontiers in Endocrinology, 11, 615957.

Taneja, M., Bols, P. E., Van de Velde, A., Ju, J. C., Schreiber, D., Tripp, M. W., Levine, H., Echelard, Y., Riesen, J., & Yang, X. (2000). Developmental competence of juvenile calf oocytes in vitro and in vivo: Influence of donor animal variation and repeated gonadotropin stimulation. Biology of Reproduction, 62(1), 206–213.

Tolikas, A., Tsakos, E., Gerou, S., Prapas, Y., & Loufopoulos, A. (2011). Anti-Mullerian hormone (AMH) levels in serum and follicular fluid as predictors of ovarian response in stimulated (IVF and ICSI) cycles. Human Fertility, 14(4), 246–253.

Umer, S., Zhao, S. J., Sammad, A., Weldegebriall Sahlu, B., Yunwei, P., & Zhu, H. (2019). AMH: Could it be used as a biomarker for fertility and superovulation in domestic animals? Genes, 10(12), 1009.

Valchuk, O. A., Kovpak, V. V., Kovpak, O. S., Salizhenko, M. I., Derkach, S. S., & Mazur, V. M. (2023). Concentration of progesterone in the blood serum and size of the corpus luteum as criteria for selection of recipient cows for embryo transfer. Regulatory Mechanisms in Biosystems, 14(4), 564–569.

Viana, J. (2023). 2022 Statistics of embryo production and transfer in domestic farm animals. Embryo Technology Newsletter, 41(4), 1–25.

Visser, J. A., & Themmen, A. P. (2005). Anti-Müllerian hormone and folliculogenesis. Molecular and Cellular Endocrinology, 234(1–2), 81–86.

Visser, J. A., Durlinger, A. L., Peters, I. J., van den Heuvel, E. R., Rose, U. M., Kramer, P., de Jong, F. H., & Themmen, A. P. (2007). Increased oocyte degeneration and follicular atresia during the estrous cycle in anti-Müllerian hormone null mice. Endocrinology, 148(5), 2301–2308.

Wang, X., Jin, L., Mao, Y. D., Shi, J. Z., Huang, R., Jiang, Y. N., Zhang, C. L., & Liang, X. Y. (2021). Evaluation of ovarian reserve tests and age in the prediction of poor ovarian response to controlled ovarian stimulation – a real-world data analysis of 89.002 patients. Frontiers in Endocrinology, 12, 702061.

Zangirolamo, A. F., Morotti, F., da Silva, N. C., Sanches, T. K., & Seneda, M. M. (2018). Ovarian antral follicle populations and embryo production in cattle. Animal Reproduction, 15(3), 310–315.

Zhou, Y., Richard, S., Batchelor, N. J., Oorschot, D. E., Anderson, G. M., & Pankhurst, M. W. (2022). Anti-Müllerian hormone-mediated preantral follicle atresia is a key determinant of antral follicle count in mice. Human Reproduction, 37(11), 2635–2645.