Effective August 1, 2024, this database was discontinued. All content will remain searchable and be preserved online for historical purposes only until 2029.
Precocious Puberty
What's New
Last Posted: Nov 03, 2024
- Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease.
Roberta Lattanzi, et al. Life (Basel, Switzerland) 2024 0 (10) - The rs6576457 G?>?A variant in the MKRN3 gene promoter significantly increases the risk of central precocious puberty and lung cancer in Hubei Chinese population.
Feng Wu, et al. Human molecular genetics 2024 0 - [Clinical and genetic analysis of three children with Legius syndrome due to variants of SPRED1 gene].
Xi Wang, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 0 (8) 941-946 - Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, et al. Nature genetics 2024 0 - The Genetic Etiology is a Relevant Cause of Central Precocious Puberty.
Ana Pinheiro Machado Canton, et al. European journal of endocrinology 2024 0 - Association of obesity and menarche SNPs and interaction with environmental factors on precocious puberty.
Peng Xue, et al. Pediatric research 2024 0 - Dual rare genetic diseases in five pediatric patients: insights from next-generation diagnostic methods.
Yupeng Liu, et al. Orphanet journal of rare diseases 2024 0 (1) 159 - MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations.
F Aiello, et al. Journal of endocrinological investigation 2023 0 - The functional study of a novel MKRN3 missense mutation associated with familial central precocious puberty.
Ziwei Chen, et al. American journal of medical genetics. Part A 2023 0 - A comprehensive meta-analysis to identify susceptibility genetic variants for precocious puberty.
Xiuli Gu, et al. Annals of human genetics 2023 0 - Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen.
Bonnie McCann-Crosby, et al. International journal of neonatal screening 2023 0 (3) - Clinical and genetic characterization of familial central precocious puberty.
Tinano Flávia Rezende, et al. The Journal of clinical endocrinology and metabolism 2023 0 - Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.
K?rkgöz Tar?k, et al. Journal of pediatric endocrinology & metabolism : JPEM 2023 0 - Circulating levels of DLK1 and glucose homeostasis in girls with obesity: A pilot study.
Palumbo Stefania, et al. Frontiers in endocrinology 2022 0 1033179 - Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty.
Jeong Hwal Rim, et al. Journal of pediatric endocrinology & metabolism : JPEM 2017 0 (11) 1197-1201 - MKRN3 Levels in Girls with Central Precocious Puberty during GnRHa Treatment: A Longitudinal Study.
Grandone Anna, et al. Hormone research in paediatrics 2018 0 (3) 190-195 - Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty.
Aycan Zehra, et al. Journal of clinical research in pediatric endocrinology 2018 0 (3) 223-229 - Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog.
Ramos Carolina de Oliveira, et al. Neuroendocrinology 2019 0 (7-8) 705-713 - Pioneering studies on monogenic central precocious puberty.
Canton Ana Pinheiro Machado, et al. Archives of endocrinology and metabolism 2019 0 (4) 438-444 - MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis.
Valadares Luciana Pinto, et al. Journal of the Endocrine Society 2019 0 (5) 979-995 - Genotype and clinical outcomes in children with congenital adrenal hyperplasia.
Yoon Ju Young, et al. Pediatrics international : official journal of the Japan Pediatric Society 2020 0 (6) 658-663 - Makorin RING finger protein 3 and central precocious puberty.
Maione Luigi, et al. Current opinion in endocrine and metabolic research 2020 0 152-159 - Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.
Meader Brooke N, et al. The Journal of clinical endocrinology and metabolism 2020 0 (8) 2732-9 - Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
Montenegro Luciana, et al. The Journal of clinical endocrinology and metabolism 2020 0 (10) - Relationship between growth velocity and change of levels of insulin-like growth factor-1, insulin-like growth factor binding protein-3 and, IGFBP-3 promoter polymorphism during GnRH agonist treatment.
Park Jun-Hong, et al. Annals of pediatric endocrinology & metabolism 2020 0 (4) 234-239 - Association of Polymorphisms in the Kisspeptin/GPR54 Pathway Genes With Risk of Early Puberty in Chinese Girls.
Li Di, et al. The Journal of clinical endocrinology and metabolism 2020 0 (4) - MKRN3 and KISS1R mutations in precocious and early puberty.
Pagani Sara, et al. Italian journal of pediatrics 2020 0 (1) 39 - Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty.
Neocleous Vassos, et al. Frontiers in endocrinology 2021 0 745048 - POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature.
Jadhav Swati, et al. Pituitary 2021 0 (5) 657-669 - Enrichment analyses of diseases and pathways associated with precocious puberty using PrecocityDB.
Sharma Mridula, et al. Scientific reports 2021 0 (1) 4203 - Precocious Puberty in a Boy With Bilateral Leydig Cell Tumors due to a Somatic Gain-of-Function LHCGR Variant.
Flippo Chelsi, et al. Journal of the Endocrine Society 2022 0 (10) bvac127 - Genetic causes of central precocious puberty.
Tajima Toshihiro, et al. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2022 0 (3) 101-109 - (Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.
Suzuki Erina, et al. Human genome variation 2019 0 7 - Novel DNA variation of GPR54 gene in familial central precocious puberty.
Ghaemi Nosrat, et al. Italian journal of pediatrics 2019 0 (1) 10 - Molecular screening of PROKR2 gene in girls with idiopathic central precocious puberty.
Aiello Francesca, et al. Italian journal of pediatrics 2021 0 (1) 5 - Gene Polymorphisms Associated with Central Precocious Puberty and Hormone Levels in Chinese Girls.
Li Yunwei, et al. International journal of endocrinology 2022 0 9450663 - Effects of childhood obesity and related genetic factors on precocious puberty: protocol for a multi-center prospective cohort study.
Yu Tingting, et al. BMC pediatrics 2022 5 (1) 310 - Obesity-related genetic polymorphisms are associated with the risk of early puberty in Han Chinese girls.
Li Di, et al. Clinical endocrinology 2021 11 - Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.
Lin Wei-De, et al. European journal of endocrinology 2021 7 - Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations.
Seraphim Carlos Eduardo, et al. The Journal of clinical endocrinology and metabolism 2020 12
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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