ArticleThe Journal of clinical endocrinology and metabolism2013
Clinical genetic testing for Kallmann syndrome.
Article in The Journal of clinical endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
16 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Tooth agenesis and orofacial clefting: genetic brothers in arms?Human genetics · 2016Pooled it
- Nonobstructive azoospermia: an etiologic review.Asian journal of andrology · 2025Review
- Deletion in RMST lncRNA impairs hypothalamic neuronal development in a human stem cell-based model of Kallmann Syndrome.Cell death discovery · 2024Article
- X-linked recessive Kallmann syndrome: A case report.World journal of clinical cases · 2022Article
- Next-generation sequencing of patients with congenital anosmia.European journal of human genetics : EJHG · 2017Article
- Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.Fertility and sterility · 2017Article
- Genetics of Male Infertility.Current urology reports · 2016Review
- The Regulation and Function of Fibroblast Growth Factor 8 and Its Function during Gonadotropin-Releasing Hormone Neuron Development.Frontiers in endocrinology · 2016Review
- A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3.Molecular cytogenetics · 2016Article
- Diagnosis and Treatment of Hypopituitarism.Endocrinology and metabolism (Seoul, Korea) · 2015Review
- Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.Orphanet journal of rare diseases · 2015Article
- Fertility and fragrance: another cause of Kallmann syndrome.The Journal of clinical investigation · 2015Article
- Olfactory Agenesis in Kallmann Syndrome (KS).Journal of clinical and diagnostic research : JCDR · 2015Article
- Novel FGFR1 and KISS1R Mutations in Chinese Kallmann Syndrome Males with Cleft Lip/Palate.BioMed research international · 2015Article
- Functional rescue of Kallmann syndrome-associated prokineticin receptor 2 (PKR2) mutants deficient in trafficking.The Journal of biological chemistry · 2014Article
- Central hypogonadotropic hypogonadism: genetic complexity of a complex disease.International journal of endocrinology · 2014Review
Corrections and comments
- Comment on
Authors and funding
1 author.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.