| Year |
Citation |
Score |
| 2021 |
Seminara SB, Topaloglu AK. Review of human genetic and clinical studies directly relevant to GnRH signalling. Journal of Neuroendocrinology. e13080. PMID 34970798 DOI: 10.1111/jne.13080 |
0.315 |
|
| 2020 |
León S, Fergani C, Talbi R, Maguire CA, Gerutshang A, Seminara SB, Navarro VM. Tachykinin signaling is required for the induction of the preovulatory LH surge and normal LH pulses. Neuroendocrinology. PMID 32512561 DOI: 10.1159/000509222 |
0.308 |
|
| 2019 |
Barroso P, Seminara S, Chan Y. SUN-204 Transient Hypergonadotropism Upon Pubertal Entry In A Boy With Delayed Puberty And A Heterozygous Mutation In TACR3 Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Sun-204 |
0.306 |
|
| 2019 |
Delaney A, Plummer L, Burkholder A, Mericq M, Merino P, Quinton R, Lewis K, Meader B, Shaw N, Welt C, Martin K, Seminara S, Biesecker L, Bailey-Wilson J, Hall J. OR11-6 Rare Sequence Variants in GnRH-Associated Genes May Contribute to Variable Susceptibility to Environmental Stressors in Functional Hypothalamic Amenorrhea Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Or11-6 |
0.316 |
|
| 2018 |
Laisk T, Kukuškina V, Palmer D, Laber S, Chen CY, Ferreira T, Rahmioglu N, Zondervan K, Becker C, Smoller JW, Lippincott M, Salumets A, Granne I, Seminara S, Neale B, et al. Large scale meta-analysis highlights the hypothalamic-pituitary-gonadal (HPG) axis in the genetic regulation of menstrual cycle length. Human Molecular Genetics. PMID 30202859 DOI: 10.1093/Hmg/Ddy317 |
0.382 |
|
| 2018 |
Terasawa E, Garcia JP, Seminara SB, Keen KL. Role of Kisspeptin and Neurokinin B in Puberty in Female Non-Human Primates. Frontiers in Endocrinology. 9: 148. PMID 29681889 DOI: 10.3389/Fendo.2018.00148 |
0.316 |
|
| 2018 |
Lehman MN, Coolen LM, Steiner RA, Neal-Perry G, Wang L, Moenter SM, Moore AM, Goodman RL, Hwa-Yeo S, Padilla SL, Kauffman AS, Garcia J, Kelly MJ, Clarkson J, Radovick S, ... ... Seminara S, et al. The 3 World Conference on Kisspeptin, "Kisspeptin 2017: Brain and Beyond":Unresolved questions, challenges and future directions for the field. Journal of Neuroendocrinology. e12600. PMID 29656508 DOI: 10.1111/Jne.12600 |
0.435 |
|
| 2018 |
Shahab M, Lippincott M, Chan YM, Davies A, Merino PM, Plummer L, Mericq V, Seminara S. Discordance in the Dependence on Kisspeptin Signaling in Mini Puberty vs. Adolescent Puberty: Human Genetic Evidence. The Journal of Clinical Endocrinology and Metabolism. PMID 29452377 DOI: 10.1210/Jc.2017-02636 |
0.364 |
|
| 2013 |
Lippincott MF, True C, Seminara SB. Use of genetic models of idiopathic hypogonadotrophic hypogonadism in mice and men to understand the mechanisms of disease. Experimental Physiology. 98: 1522-7. PMID 23955308 DOI: 10.1113/expphysiol.2013.071910 |
0.342 |
|
| 2013 |
Popa SM, Moriyama RM, Caligioni CS, Yang JJ, Cho CM, Concepcion TL, Oakley AE, Lee IH, Sanz E, Amieux PS, Caraty A, Palmiter RD, Navarro VM, Chan YM, Seminara SB, et al. Redundancy in Kiss1 expression safeguards reproduction in the mouse. Endocrinology. 154: 2784-94. PMID 23736293 DOI: 10.1210/En.2013-1222 |
0.404 |
|
| 2013 |
Silveira LG, Latronico AC, Seminara SB. Kisspeptin and clinical disorders. Advances in Experimental Medicine and Biology. 784: 187-99. PMID 23550007 DOI: 10.1007/978-1-4614-6199-9_9 |
0.309 |
|
| 2012 |
George JT, Seminara SB. Kisspeptin and the hypothalamic control of reproduction: lessons from the human. Endocrinology. 153: 5130-6. PMID 23015291 DOI: 10.1210/en.2012-1429 |
0.344 |
|
| 2011 |
Wahab F, Quinton R, Seminara SB. The kisspeptin signaling pathway and its role in human isolated GnRH deficiency. Molecular and Cellular Endocrinology. 346: 29-36. PMID 21704672 DOI: 10.1016/j.mce.2011.05.043 |
0.32 |
|
| 2011 |
Caronia LM, Martin C, Welt CK, Sykiotis GP, Quinton R, Thambundit A, Avbelj M, Dhruvakumar S, Plummer L, Hughes VA, Seminara SB, Boepple PA, Sidis Y, Crowley WF, Martin KA, et al. A genetic basis for functional hypothalamic amenorrhea. The New England Journal of Medicine. 364: 215-25. PMID 21247312 DOI: 10.1056/NEJMoa0911064 |
0.322 |
|
| 2011 |
Martin C, Balasubramanian R, Dwyer AA, Au MG, Sidis Y, Kaiser UB, Seminara SB, Pitteloud N, Zhou QY, Crowley WF. The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations. Endocrine Reviews. 32: 225-46. PMID 21037178 DOI: 10.1210/Er.2010-0007 |
0.35 |
|
| 2010 |
Balasubramanian R, Dwyer A, Seminara SB, Pitteloud N, Kaiser UB, Crowley WF. Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons. Neuroendocrinology. 92: 81-99. PMID 20606386 DOI: 10.1159/000314193 |
0.339 |
|
| 2010 |
Sykiotis GP, Pitteloud N, Seminara SB, Kaiser UB, Crowley WF. Deciphering genetic disease in the genomic era: the model of GnRH deficiency. Science Translational Medicine. 2: 32rv2. PMID 20484732 DOI: 10.1126/Scitranslmed.3000288 |
0.317 |
|
| 2010 |
Seminara S, Nanni L, Generoso M, Mirri S, Leonardi V, Slabadzianiuk T, Vetrano ML, Buongiorno A, Losi S, Galluzzi F. Effect of Treatment with Cyproterone Acetate on Uterine Bleeding at the Beginning of GnRH Analogue Therapy in Girls with Idiopathic Central Precocious Puberty Hormone Research in Paediatrics. 73: 386-389. PMID 20389110 DOI: 10.1159/000308172 |
0.327 |
|
| 2010 |
Miura K, Miura S, Yoshiura K, Seminara S, Hamaguchi D, Niikawa N, Masuzaki H. A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1. Human Reproduction (Oxford, England). 25: 1076-80. PMID 20139426 DOI: 10.1093/Humrep/Deq006 |
0.33 |
|
| 2009 |
Chan YM, de Guillebon A, Lang-Muritano M, Plummer L, Cerrato F, Tsiaras S, Gaspert A, Lavoie HB, Wu CH, Crowley WF, Amory JK, Pitteloud N, Seminara SB. GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism. Proceedings of the National Academy of Sciences of the United States of America. 106: 11703-8. PMID 19567835 DOI: 10.1073/pnas.0903449106 |
0.329 |
|
| 2009 |
Chan YM, Broder-Fingert S, Seminara SB. Reproductive functions of kisspeptin and Gpr54 across the life cycle of mice and men. Peptides. 30: 42-8. PMID 18644412 DOI: 10.1016/j.peptides.2008.06.015 |
0.302 |
|
| 2008 |
Seminara SB, Crowley WF. Kisspeptin and GPR54: discovery of a novel pathway in reproduction. Journal of Neuroendocrinology. 20: 727-31. PMID 18601695 DOI: 10.1111/j.1365-2826.2008.01731.x |
0.307 |
|
| 2008 |
Crowley WF, Pitteloud N, Seminara S. New genes controlling human reproduction and how you find them. Transactions of the American Clinical and Climatological Association. 119: 29-37; discussion 37. PMID 18596868 |
0.317 |
|
| 2008 |
Cole LW, Sidis Y, Zhang C, Quinton R, Plummer L, Pignatelli D, Hughes VA, Dwyer AA, Raivio T, Hayes FJ, Seminara SB, Huot C, Alos N, Speiser P, Takeshita A, et al. Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum. The Journal of Clinical Endocrinology and Metabolism. 93: 3551-9. PMID 18559922 DOI: 10.1210/jc.2007-2654 |
0.314 |
|
| 2008 |
Gianetti E, Seminara S. Kisspeptin and KISS1R: a critical pathway in the reproductive system. Reproduction (Cambridge, England). 136: 295-301. PMID 18515314 DOI: 10.1530/Rep-08-0091 |
0.4 |
|
| 2008 |
Teles MG, Bianco SD, Brito VN, Trarbach EB, Kuohung W, Xu S, Seminara SB, Mendonca BB, Kaiser UB, Latronico AC. A GPR54-activating mutation in a patient with central precocious puberty. The New England Journal of Medicine. 358: 709-15. PMID 18272894 DOI: 10.1056/Nejmoa073443 |
0.35 |
|
| 2007 |
Cerrato F, Seminara SB. Human genetics of GPR54. Reviews in Endocrine & Metabolic Disorders. 8: 47-55. PMID 17334928 DOI: 10.1007/s11154-007-9027-3 |
0.304 |
|
| 2007 |
Pitteloud N, Quinton R, Pearce S, Raivio T, Acierno J, Dwyer A, Plummer L, Hughes V, Seminara S, Cheng YZ, Li WP, Maccoll G, Eliseenkova AV, Olsen SK, Ibrahimi OA, et al. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism Journal of Clinical Investigation. 117: 457-463. PMID 17235395 DOI: 10.1172/Jci29884 |
0.395 |
|
| 2006 |
Pitteloud N, Meysing A, Quinton R, Acierno JS, Dwyer AA, Plummer L, Fliers E, Boepple P, Hayes F, Seminara S, Hughes VA, Ma J, Bouloux P, Mohammadi M, Crowley WF. Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. Molecular and Cellular Endocrinology. 254: 60-9. PMID 16764984 DOI: 10.1016/J.Mce.2006.04.021 |
0.392 |
|
| 2005 |
Seminara SB. Metastin and its G protein-coupled receptor, GPR54: critical pathway modulating GnRH secretion. Frontiers in Neuroendocrinology. 26: 131-8. PMID 16309735 DOI: 10.1016/j.yfrne.2005.10.001 |
0.325 |
|
| 2005 |
Kim HG, Herrick SR, Lemyre E, Kishikawa S, Salisz JA, Seminara S, MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1. Journal of Medical Genetics. 42: 666-72. PMID 16061567 DOI: 10.1136/Jmg.2004.026989 |
0.336 |
|
| 2004 |
Meysing AU, Kanasaki H, Bedecarrats GY, Acierno JS, Conn PM, Martin KA, Seminara SB, Hall JE, Crowley WF, Kaiser UB. GNRHR mutations in a woman with idiopathic hypogonadotropic hypogonadism highlight the differential sensitivity of luteinizing hormone and follicle-stimulating hormone to gonadotropin-releasing hormone. The Journal of Clinical Endocrinology and Metabolism. 89: 3189-98. PMID 15240592 DOI: 10.1210/Jc.2003-031808 |
0.327 |
|
| 2004 |
Gottsch ML, Cunningham MJ, Smith JT, Popa SM, Acohido BV, Crowley WF, Seminara S, Clifton DK, Steiner RA. A role for kisspeptins in the regulation of gonadotropin secretion in the mouse. Endocrinology. 145: 4073-7. PMID 15217982 DOI: 10.1210/En.2004-0431 |
0.499 |
|
| 2003 |
Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS, Shagoury JK, Bo-Abbas Y, Kuohung W, Schwinof KM, Hendrick AG, Zahn D, Dixon J, Kaiser UB, Slaugenhaupt SA, Gusella JF, et al. The GPR54 gene as a regulator of puberty. The New England Journal of Medicine. 349: 1614-27. PMID 14573733 DOI: 10.1056/Nejmoa035322 |
0.376 |
|
| 2001 |
Seminara SB, Oliveira LM, Beranova M, Hayes FJ, Crowley WF. Genetics of hypogonadotropic hypogonadism. Journal of Endocrinological Investigation. 23: 560-5. PMID 11079449 DOI: 10.1007/BF03343776 |
0.344 |
|
| 2000 |
Seminara SB, Beranova M, Oliveira LM, Martin KA, Crowley WF, Hall JE. Successful use of pulsatile gonadotropin-releasing hormone (GnRH) for ovulation induction and pregnancy in a patient with GnRH receptor mutations. The Journal of Clinical Endocrinology and Metabolism. 85: 556-62. PMID 10690855 DOI: 10.1210/jcem.85.2.6357 |
0.304 |
|
| 2000 |
Seminara SB, Achermann JC, Genel M, Jameson JL, Crowley WF. X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females. The Journal of Clinical Endocrinology and Metabolism. 84: 4501-9. PMID 10599709 DOI: 10.1210/JCEM.84.12.6172 |
0.31 |
|
| 1997 |
Seminara S, Filpo A, Piccinini P, Cauza FL, Cappa M, Faedda A, Loche S. Growth hormone (GH) response to GH-releasing hormone in short children: Lack of correlation with endogenous nocturnal GH secretion Journal of Endocrinological Investigation. 20: 118-121. PMID 9186816 DOI: 10.1007/Bf03346888 |
0.332 |
|
| 1996 |
Bellone J, Aimaretti G, Valetto MR, Bellone S, Baffoni C, Arvat E, Seminara S, Camanni F, Ghigo E. Acute administration of recombinant human growth hormone inhibits the somatotrope responsiveness to growth hormone-releasing hormone in childhood. European Journal of Endocrinology. 135: 421-4. PMID 8921823 DOI: 10.1530/Eje.0.1350421 |
0.337 |
|
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