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

Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India.

Indian pediatrics - 15 May 2021

Joshi Aditi, Sinha Aditi, Sharma Aakanksha, Shamim Uzma, Uppilli Bharathram, Sharma Pooja, Zahra Sana, Parveen Shaista, Mathur Aradhana, Chandan Monica, Tewari Prachi, Khandelwal Priyanka, Hari Pankaj, Mukerji Mitali, Faruq Mohammed, Bagga Arvind

Abstract excerpt

OBJECTIVE: Information on etiology of congenital nephrotic syndrome in non-Caucasian populations is limited. This study aimed to determine the genetic basis of congenital nephrotic syndrome in Indian patients. METHODS: In this observational, cross-sectional study, whole exome sequencing was performed on samples from all children diagnosed with congenital nephrotic syndrome, presenting at centers collaborating in...

Read the complete abstract on PubMed

Topics

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

Share to Cross-Sectional Studies
Share to High-Throughput Nucleotide Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Intracellular Signaling Peptides and Proteins

Share to Membrane Proteins

Share to Mutation

Share to Nephrotic Syndrome

Share to Phenotype

Source

Identifiers

PMID: 33980730

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India.PMID 33980730Read ↗

Congenital Nephrotic Syndrome in India in the Current Era: A Multicenter Case Series.Semantic proximity Read ↗

Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndromeSemantic proximity Read ↗

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.Semantic proximity Read ↗

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.Semantic proximity Read ↗

New insights from the genetic work-up in early onset nephrotic syndrome: report from a registry in western India.Semantic proximity Read ↗

Genetic analysis of Indian patients with steroid-resistant nephrotic syndrome in childrenSemantic proximity Read ↗

The Frequency of Genetic Mutations in Pediatric Patients Diagnosed with Nephrotic Syndrome: A Single-Center Retrospective Study in Saudi Arabia.Semantic proximity Read ↗

Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre StudySemantic proximity Read ↗

Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93.Semantic proximity Read ↗

Targeted Next-Generation Sequencing in Brazilian Children With Nephrotic Syndrome Submitted to Renal Transplant.Semantic proximity Read ↗

Gene mutation analysis in 12 Chinese children with congenital nephrotic syndromeSemantic proximity Read ↗

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