CrossRef Cited-by Linking Search Results

This Article:

has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking:

  • Exosomal miR-10a derived from amniotic fluid stem cells preserves ovarian follicles after chemotherapy
    Guan-Yu Xiao, Chun-Chun Cheng, Yih-Shien Chiang, Winston Teng-Kuei Cheng, I-Hsuan Liu, and Shinn-Chih Wu
    Scientific Reports (2016) 6 :
  • The transcription factor GATA4 is required for follicular development and normal ovarian function
    Evgeni Efimenko, Maria B. Padua, Nikolay L. Manuylov, Shawna C. Fox, Deborah A. Morse, and Sergei G. Tevosian
    Developmental Biology (2013) 381 :144
  • MicroRNA-125a-5p induces mouse granulosa cell apoptosis by targeting signal transducer and activator of transcription 3
    Chaojun Wang, Donghua Li, Suyun Zhang, Yan Xing, Yingchun Gao, and Jie Wu
    Menopause (2016) 23 :100
  • Hyaluronic Acid Promotes the Expression of Progesterone Receptor Membrane Component 1 via Epigenetic Silencing of miR-139-5p in Human and Rat Granulosa Cells1
    Guangfeng Zhao, Xue Zhou, Ting Fang, Yayi Hou, and Yali Hu
    Biology of Reproduction (2014) 91 :
  • Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency
    Shidou Zhao, Guangyu Li, Raymond Dalgleish, Svetlana Vujovic, Xue Jiao, Jin Li, Joe Leigh Simpson, Yingying Qin, Maja Ivanisevic, Miomira Ivovic, Milina Tancic, Farook Al-Azzawi, and Zi-Jiang Chen
    Fertility and Sterility (2015) 103 :548
  • Single nucleotide polymorphisms in premature ovarian failure‑associated genes in a Chinese�Hui population
    Lili Ma, Yan Chen, Si Mei, Chunlian Liu, Xiaohong Ma, Yongli Li, Yinzhi Jiang, Lingxia Ha, and Xian Xu
    Molecular Medicine Reports (2015) :
  • Genetics of primary ovarian insufficiency: a review
    Cristina Fortuño and Elena Labarta
    Journal of Assisted Reproduction and Genetics (2014) 31 :1573
  • Association between fragile X premutation and premature ovarian failure: a case–control study and meta-analysis
    Durgadatta Tosh, K. Lakshmi Rao, H. Surekha Rani, D. Anupama Deenadayal, U. S. N. Murty, and Paramjit Grover
    Archives of Gynecology and Obstetrics (2014) 289 :1255
  • Positive cross talk between FOXL2 and antimüllerian hormone regulates ovarian reserve
    Mira Park, Dae-Shik Suh, Kangseok Lee, and Jeehyeon Bae
    Fertility and Sterility (2014) 102 :847
  • Relationship between inhibin-α gene polymorphisms and premature ovarian failure in Korean women
    Hoon Kim, Sungwook Chun, Bon Seon Gu, Seung-Yup Ku, Seok Hyun Kim, and Jung Gu Kim
    Menopause (2011) 18 :1232
  • Reductions in the number of mid-sized antral follicles are associated with markers of premature ovarian senescence in dairy cows
    Silvia C. Modina, Irene Tessaro, Valentina Lodde, Federica Franciosi, Davide Corbani, and Alberto M. Luciano
    Reproduction, Fertility and Development (2014) 26 :235
  • AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency
    B. Alvaro Mercadal, R. Imbert, I. Demeestere, C. Gervy, A. De Leener, Y. Englert, S. Costagliola, and A. Delbaere
    Human Reproduction (2015) 30 :1196
  • Mutational analysis of theFSTgene in Chinese women with idiopathic premature ovarian failure
    L. Liu, R. Tan, J. Liu, Y. Cui, J. Liu, and J. Wu
    Climacteric (2013) 16 :469
  • Genetic defects of ovarian TGF-β-like factors and premature ovarian failure
    L. Persani, R. Rossetti, C. Cacciatore, and S. Fabre
    Journal of Endocrinological Investigation (2011) 34 :244
  • Insufficienza ovarica primaria: elementi per una gestione up-to-date
    Luca Persani, Marco Bonomi, and Raffaella Rossetti
    L'Endocrinologo (2015) 16 :45
  • Impaired protein stability and nuclear localization ofNOBOXvariants associated with premature ovarian insufficiency
    Ilaria Ferrari, Justine Bouilly, Isabelle Beau, Fabiana Guizzardi, Alberto Ferlin, Marzia Pollazzon, Mariacarolina Salerno, Nadine Binart, Luca Persani, and Raffaella Rossetti
    Human Molecular Genetics (2016) :ddw342
  • Mutational analysis of the FIGLA gene in women with idiopathic premature ovarian failure
    Durgadatta Tosh, Hanumanth Surekha Rani, Upadhyayula Suryanarayana Murty, Anupama Deenadayal, and Paramjit Grover
    Menopause (2015) 22 :520
  • Genetic association studies in female reproduction: from candidate-gene approaches to genome-wide mapping
    Han Zhao and Zi-Jiang Chen
    MHR: Basic science of reproductive medicine (2013) 19 :644
  • Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency
    L. Leng, Y. Tan, F. Gong, L. Hu, Q. Ouyang, Y. Zhao, G. Lu, and G. Lin
    Human Reproduction (2015) 30 :737
  • Genetics of primary ovarian insufficiency
    R. Rossetti, I. Ferrari, M. Bonomi, and L. Persani
    Clinical Genetics (2017) 91 :183
  • An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report
    Tse-Ya Yu, Huan-Sheng Lin, Pei-Lung Chen, and Tien-Shang Huang
    Journal of the Formosan Medical Association (2015) 114 :77
  • CITED2 mutations potentially cause idiopathic premature ovarian failure
    Dora Janeth Fonseca, Diego Ojeda, Besma Lakhal, Rim Braham, Stefanie Eggers, Erin Turbitt, Stefan White, Sonia Grover, Garry Warne, Margaret Zacharin, Alexandra Nevin Lam, Hanène Landolsi, Hatem Elghezal, Ali Saâd, Carlos Martín Restrepo, Marc Fellous, Andrew Sinclair, Peter Koopman, and Paul Laissue
    Translational Research (2012) 160 :384
  • Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform
    A. Norling, A.L. Hirschberg, K.A. Rodriguez-Wallberg, E. Iwarsson, A. Wedell, and M. Barbaro
    Human Reproduction (2014) 29 :1818
  • The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders
    L. Persani, R. Rossetti, E. Di Pasquale, C. Cacciatore, and S. Fabre
    Human Reproduction Update (2014) 20 :869
  • Association study of five functional polymorphisms in matrix metalloproteinase-2, -3, and -9 genes with risk of primary ovarian insufficiency in Korean women
    Young Ran Kim, Young Joo Jeon, Hyun Seok Kim, Jung O Kim, Myoung Jin Moon, Eun Hee Ahn, Woo Sik Lee, and Nam Keun Kim
    Maturitas (2015) 80 :192
  • Mutant Cohesin in Premature Ovarian Failure
    Sandrine Caburet, Valerie A. Arboleda, Elena Llano, Paul A. Overbeek, Jose Luis Barbero, Kazuhiro Oka, Wilbur Harrison, Daniel Vaiman, Ziva Ben-Neriah, Ignacio García-Tuñón, Marc Fellous, Alberto M. Pendás, Reiner A. Veitia, and Eric Vilain
    New England Journal of Medicine (2014) 370 :943
  • Evolutionary Origin of Bone Morphogenetic Protein 15 and Growth and Differentiation Factor 9 and Differential Selective Pressure Between Mono- and Polyovulating Species1
    Olivier Monestier, Bertrand Servin, Sylvain Auclair, Thomas Bourquard, Anne Poupon, Géraldine Pascal, and Stéphane Fabre
    Biology of Reproduction (2014) 91 :
  • Involvement of FoxO1 in the effects of follicle-stimulating hormone on inhibition of apoptosis in mouse granulosa cells
    M Shen, Z Liu, B Li, Y Teng, J Zhang, Y Tang, S-C Sun, and H Liu
    Cell Death and Disease (2014) 5 :e1475
  • Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency
    Anna Murray, Minouk J. Schoemaker, Claire E. Bennett, Sarah Ennis, James N. Macpherson, Michael Jones, Danielle H. Morris, Nick Orr, Alan Ashworth, Patricia A. Jacobs, and Anthony J. Swerdlow
    Genetics in Medicine (2014) 16 :19
  • XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription
    David Zangen, Yotam Kaufman, Sharon Zeligson, Shira Perlberg, Hila Fridman, Moein Kanaan, Maha Abdulhadi-Atwan, Abdulsalam Abu Libdeh, Ayal Gussow, Irit Kisslov, Liran Carmel, Paul Renbaum, and Ephrat Levy-Lahad
    The American Journal of Human Genetics (2011) 89 :572
  • Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing
    Paul Laissue
    Molecular and Cellular Endocrinology (2015) 411 :243
  • Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure
    Nouha Bouali, Dorra Hmida, Soumaya Mougou, Jérôme Bouligand, Besma Lakhal, Sarra Dimessi, Bruno Francou, Ghada Saad, Saoussen Trabelsi, Monia Zaouali, Moez Gribaa, Molka Chaieb, Mouhamed Bibi, Anne Guiochon-Mantel, and Ali Saad
    Annales d'Endocrinologie (2015) 76 :671
  • Age-associated up-regulation of EGR1 promotes granulosa cell apoptosis during follicle atresia in mice through the NF-κB pathway
    Suzhen Yuan, Jingyi Wen, Jing Cheng, Wei Shen, Su Zhou, Wei Yan, Lu Shen, Aiyue Luo, and Shixuan Wang
    Cell Cycle (2016) 15 :2895
  • A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis–ptosis–epicanthus inversus syndrome
    Nikolaos Settas, Margarita Anapliotou, Emmanuel Kanavakis, Helen Fryssira, Christalena Sofocleous, Catherine Dacou-Voutetakis, George P. Chrousos, and Antonis Voutetakis
    Menopause (2015) 22 :1264
  • The impact of FMR1 gene mutations on human reproduction and development: a systematic review
    Vincenzo Noto, Conor Harrity, David Walsh, and Kevin Marron
    Journal of Assisted Reproduction and Genetics (2016) 33 :1135
  • Boy or Girl’s Mendelian Genetics with “Precious” Families
    Marc Fellous
    Journal of Molecular Neuroscience (2014) 54 :586
  • Anti-Müllerian hormone: an ovarian reserve marker in primary ovarian insufficiency
    Jenny A. Visser, Izaäk Schipper, Joop S. E. Laven, and Axel P. N. Themmen
    Nature Reviews Endocrinology (2012) :
  • Gene variation and premature ovarian failure: a meta-analysis
    D. Pu, Y. Xing, Y. Gao, L. Gu, and J. Wu
    European Journal of Obstetrics & Gynecology and Reproductive Biology (2014) 182 :226
  • Oocyte–somatic cell interactions in the human ovary—novel role of bone morphogenetic proteins and growth differentiation factors
    Hsun-Ming Chang, Jie Qiao, and Peter C.K. Leung
    Human Reproduction Update (2016) 23 :1
  • Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases
    O. Tšuiko, M. Nõukas, O. Žilina, K. Hensen, J.S. Tapanainen, R. Mägi, M. Kals, P.A. Kivistik, K. Haller-Kikkatalo, A. Salumets, and A. Kurg
    Human Reproduction (2016) 31 :1913
  • Interference of Steroidogenesis by Gold Nanorod Core/Silver Shell Nanostructures: Implications for Reproductive Toxicity of Silver Nanomaterials
    Xiumei Jiang, Liming Wang, Yinglu Ji, Jinglong Tang, Xin Tian, Mingjing Cao, Jingxuan Li, Shuying Bi, Xiaochun Wu, Chunying Chen, and Jun-Jie Yin
    Small (2017) 13 :1602855
  • Germ cell-specific Atg7 knockout results in primary ovarian insufficiency in female mice
    Z-H Song, H-Y Yu, P Wang, G-K Mao, W-X Liu, M-N Li, H-N Wang, Y-L Shang, C Liu, Z-L Xu, Q-Y Sun, and W Li
    Cell Death and Disease (2015) 6 :e1589
  • Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policyEuropean Society of Human Genetics and European Society of Human Reproduction and Embryology
    Joyce C Harper, Joep Geraedts, Pascal Borry, Martina C Cornel, Wybo Dondorp, Luca Gianaroli, Gary Harton, Tanya Milachich, Helena Kääriäinen, Inge Liebaers, Michael Morris, Jorge Sequeiros, Karen Sermon, Françoise Shenfield, Heather Skirton, Sirpa Soini, Claudia Spits, Anna Veiga, Joris Robert Vermeesch, Stéphane Viville, Guido de Wert, and Milan Macek
    European Journal of Human Genetics (2013) 21 :S1
  • Induction of Estrogen-Sensitive Epithelial Cells Derived from Human-Induced Pluripotent Stem Cells to Repair Ovarian Function in a Chemotherapy-Induced Mouse Model of Premature Ovarian Failure
    Te Liu, Wenxing Qin, Yongyi Huang, Yanhui Zhao, and Jiejun Wang
    DNA and Cell Biology (2013) 32 :685
  • Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy
    J. Harper, J. Geraedts, P. Borry, M. C. Cornel, W. J. Dondorp, L. Gianaroli, G. Harton, T. Milachich, H. Kaariainen, I. Liebaers, M. Morris, J. Sequeiros, K. Sermon, F. Shenfield, H. Skirton, S. Soini, C. Spits, A. Veiga, J. R. Vermeesch, S. Viville, G. de Wert, and M. Macek
    Human Reproduction (2014) 29 :1603
  • The Bologna criteria for poor ovarian response; has the job been accomplished?
    J. S. Younis
    Human Reproduction (2012) 27 :1874
  • Mutations in inhibin and activin genes associated with human disease
    Andrew N. Shelling
    Molecular and Cellular Endocrinology (2012) 359 :113
  • Homozygous Inactivating Mutation inNANOS3in Two Sisters with Primary Ovarian Insufficiency
    Mariza G. Santos, Aline Z. Machado, Conceição N. Martins, Sorahia Domenice, Elaine M. F. Costa, Mirian Y. Nishi, Bruno Ferraz-de-Souza, Soraia A. C. Jorge, Carlos A. Pereira, Fernanda C. Soardi, Maricilda P. de Mello, Andrea T. Maciel-Guerra, Gil Guerra-Junior, and Berenice B. Mendonca
    BioMed Research International (2014) 2014 :1
  • Role of androgens in normal and pathological ovarian function
    K. A. Walters
    Reproduction (2015) 149 :R193
  • Investigating the Role of Tbx4 in the Female Germline in Mice1
    Nataki C. Douglas, Ripla Arora, Cayla Yiyu Chen, Mark V. Sauer, and Virginia E. Papaioannou
    Biology of Reproduction (2013) 89 :
  • Germline development from human pluripotent stem cells toward disease modeling of infertility
    Yohei Hayashi, Mitinori Saitou, and Shinya Yamanaka
    Fertility and Sterility (2012) 97 :1250
  • GAPO syndrome: a new syndromic cause of premature ovarian insufficiency
    C. L. Benetti-Pinto, V. Ferreira, L. Andrade, D. A. Yela, and M. P. De Mello
    Climacteric (2016) 19 :594
  • Current concepts in premature ovarian insufficiency
    Kate Maclaran and Nick Panay
    Women's Health (2015) 11 :169
  • Primary Ovarian Insufficiency
    Rodney J. Baber and Michele Kwik
    Current Obstetrics and Gynecology Reports (2014) 3 :223
  • Ovarian aging
    Johnny S. Younis
    Current Opinion in Obstetrics and Gynecology (2011) 23 :427
  • Environmentally Induced Epigenetic Transgenerational Inheritance of Ovarian Disease
    Eric Nilsson, Ginger Larsen, Mohan Manikkam, Carlos Guerrero-Bosagna, Marina I. Savenkova, Michael K. Skinner, and Toshi Shioda
    PLoS ONE (2012) 7 :e36129
  • Primary ovarian insufficiency in the adolescent
    Valerie L. Baker
    Current Opinion in Obstetrics and Gynecology (2013) 25 :375
  • Genetic associations with diminished ovarian reserve: a systematic review of the literature
    Alexis D. Greene, George Patounakis, and James H. Segars
    Journal of Assisted Reproduction and Genetics (2014) 31 :935
  • Fertility treatment in women with premature ovarian failure
    Zeev Blumenfeld
    Expert Review of Obstetrics & Gynecology (2011) 6 :321
  • Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations
    Mariana Moysés-Oliveira, Roberta dos Santos Guilherme, Anelisa Gollo Dantas, Renata Ueta, Ana Beatriz Perez, Mauro Haidar, Rosane Canonaco, Vera Ayres Meloni, Nadezda Kosyakova, Thomas Liehr, Gianna Maria Carvalheira, and Maria Isabel Melaragno
    Fertility and Sterility (2015) 103 :1289
  • A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing
    Matthew S. Bramble, Ellen H. Goldstein, Allen Lipson, Tuck Ngun, Ascia Eskin, Jason E. Gosschalk, Lara Roach, Neerja Vashist, Hayk Barseghyan, Eric Lee, Valerie A. Arboleda, Daniel Vaiman, Zafer Yuksel, Marc Fellous, and Eric Vilain
    Human Reproduction (2016) 31 :905
  • Transplantation of Human Menstrual Blood Stem Cells to Treat Premature Ovarian Failure in Mouse Model
    Te Liu, Yongyi Huang, Jian Zhang, Wenxing Qin, Huiying Chi, Jiulin Chen, Zhihua Yu, and Chuan Chen
    Stem Cells and Development (2014) 23 :1548
  • DSDs: genetics, underlying pathologies and psychosexual differentiation
    Valerie A. Arboleda, David E. Sandberg, and Eric Vilain
    Nature Reviews Endocrinology (2014) 10 :603
  • Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation
    Rita Genesio, Angela Mormile, Maria Rosaria Licenziati, Daniele De Brasi, Graziella Leone, Sara Balzano, Antonella Izzo, Ferdinando Bonfiglio, Anna Conti, Gennaro Fioretti, Selvaggia Lenta, Maria Rita Poggiano, Paolo Siani, and Lucio Nitsch
    Molecular Cytogenetics (2015) 8 :
  • Comparative cytogenetic analysis in two tissues with different lineage in Turner’s syndrome patients: correlation with phenotype
    Cristina Ros, Anna Serra, Juan Balasch, Ester Margarit, and Camil Castelo-Branco
    Gynecological Endocrinology (2014) 30 :282
  • The prevalence and phenotypic characteristics of spontaneous premature ovarian failure: a general population registry-based study
    K. Haller-Kikkatalo, R. Uibo, A. Kurg, and A. Salumets
    Human Reproduction (2015) 30 :1229
  • NOBOXis a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency
    N. Bouali, B. Francou, J. Bouligand, B. Lakhal, I. Malek, M. Kammoun, J. Warszawski, S. Mougou, A. Saad, and A. Guiochon-Mantel
    Clinical Genetics (2016) 89 :608
  • The Insectan Apes
    Bernard Crespi
    Human Nature (2014) 25 :6
  • Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure
    Yardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, Orit Lobel, Hasan Eideh, Suleyman Gulsuner, Dvir Dahary, Amal Abu-Rayyan, Moien Kanaan, Ephrat Levy-Lahad, Dani Bercovich, and David Zangen
    Journal of Medical Genetics (2015) 52 :391