Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Phenotype specific association of the TGFBR3 locus with nonsyndromic cryptorchidism.

The Journal of urology - 1 May 2015

Barthold Julia S, Wang Yanping, Kolon Thomas F, Kollin Claude, Nordenskjöld Agneta, Olivant Fisher Alicia, Figueroa T Ernesto, BaniHani Ahmad H, Hagerty Jennifer A, Gonzalez Ricardo, Noh Paul H, Chiavacci Rosetta M, Harden Kisha R, Abrams Debra J, Kim Cecilia E, Mateson Abigail B, Robbins Alan K, Li Jin, Akins Robert E, Hakonarson Hakon, Devoto Marcella

Abstract excerpt

PURPOSE: Based on a genome-wide association study of testicular dysgenesis syndrome showing a possible association with TGFBR3, we analyzed data from a larger, phenotypically restricted cryptorchidism population for potential replication of this signal. MATERIALS AND METHODS: We excluded samples based on strict quality control criteria, leaving 844 cases and 2,718 controls of European ancestry that were analyzed...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Phenotype
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Cryptorchidism

Share to Infant

Share to Proteoglycans

Share to Receptors, Transforming Growth Factor beta

Source

Open in PubMed Open full text

Identifiers

PMID: 25390077
DOI: 10.1016/j.juro.2014.10.097
PMCID: PMC4406821

Genes

TGFBR3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotype specific association of the TGFBR3 locus with nonsyndromic cryptorchidism.PMID 25390077Read ↗

Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.Semantic proximity Read ↗

A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation.Semantic proximity Read ↗

Genetic, Maternal, and Environmental Risk Factors for Cryptorchidism: An UpdateSemantic proximity Read ↗

Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility.Semantic proximity Read ↗

Familial bilateral cryptorchidism is caused by recessive variants in RXFP2Semantic proximity Read ↗

Associations of TGFBR1 and TGFBR2 gene polymorphisms with the risk of hypospadias: a case-control study in a Chinese population.Semantic proximity Read ↗

A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome.Semantic proximity Read ↗

Mutations of the GREAT gene cause cryptorchidismSemantic proximity Read ↗

The molecular basis of cryptorchidism.Semantic proximity Read ↗

Novel Biallelic TGFBR3 Mutation in Brothers Presenting With Craniosynostosis.Semantic proximity Read ↗

Genetic Analysis and Functional Assessment of a <i>TGFBR2</i> Variant in Micrognathia and Cleft PalateSemantic proximity Read ↗

TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.