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Article detail · 2012 · article

InactivatingKISS1Mutation and Hypogonadotropic Hypogonadism

Journal Massachusetts Medical Society The ISSN points to another catalog journal; the name is from the YÖKSİS record.
ISSN0028-4793
YÖKSİS OpenAlex Open access · bronze Top 1%
Year2012
Citations471OpenAlex
Citations445Semantic Scholar · 17 influential
Percentile%100.0
FWCI52.461.00 = world average
Scopus (SJR)Q1
WoS (JCR)Q1

Data source split

  • YÖKSİSYÖKSİS article record
  • YÖKSİS venueMassachusetts Medical Society
  • Catalog match (ISSN)New England Journal of Medicine
  • OpenAlexOpenAlex enrichment (abstract, citations, topics)
  • Semantic Scholarcitation count (not merged with OpenAlex)

Abstract

OpenAlex English

Gonadotropin-releasing hormone (GnRH) is the central regulator of gonadotropins, which stimulate gonadal function. Hypothalamic neurons that produce kisspeptin and neurokinin B stimulate GnRH release. Inactivating mutations in the genes encoding the human kisspeptin receptor (KISS1R, formerly called GPR54), neurokinin B (TAC3), and the neurokinin B receptor (TACR3) result in pubertal failure. However, human kisspeptin loss-of-function mutations have not been described, and contradictory findings have been reported in Kiss1-knockout mice. We describe an inactivating mutation in KISS1 in a large consanguineous family that results in failure of pubertal progression, indicating that functional kisspeptin is important for puberty and reproduction in humans. (Funded by the Scientific and Technological Research Council of Turkey [TÜBİTAK] and others.).

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

471citationsOpenAlex · cited_by_count (cache / database)

51 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. 2021 Loss-of-function mutations in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 56 · OpenAlex
  2. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 56 · OpenAlex
  3. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 56 · OpenAlex
  4. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 56 · OpenAlex
  5. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 56 · OpenAlex
  6. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 55 · OpenAlex
  7. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismCitations 55 · OpenAlex
  8. 2012 Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic HypogonadismCitations 31 · OpenAlex
  9. 2012 Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic HypogonadismCitations 31 · OpenAlex
  10. 2012 Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic HypogonadismCitations 31 · OpenAlex

Authors

10
  1. ALİ KEMAL TOPALOĞLU 1
  2. Javier A. Tello 2
  3. LEMAN DAMLA KOTAN GEDİK 3
  4. MEHMET NURİ ÖZBEK MARDİN ARTUKLU ÜNİVERSİTESİ 4
  5. M. Bertan Yılmaz 5
  6. ŞEREF ERDOĞAN 6
  7. FATİH GÜRBÜZ 7
  8. FATİH TEMİZ 8
  9. Robert p. Millar 9
  10. BİLGİN YÜKSEL 10