Ankur S. Chaurasia
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.
Journal: medRxiv : the preprint server for health sciences
Published: February 06, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.
Journal: European journal of human genetics : EJHG
Published: February 02, 2026
Biallelic variants in AGRN in a family with recurrent pregnancy losses and fetal akinesia deformation sequence.
Journal: Clinical dysmorphology
Published: January 14, 2025
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications.
Journal: Clinical genetics
Published: November 13, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.
Journal: European journal of human genetics : EJHG
Published: June 29, 2023
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly.
Journal: Human genetics
Published: September 30, 2022
"On-the-Fly" Fabrication of Highly-Ordered Interconnected Cylindrical and Spherical Porous Microparticles via Dual Polymerization Zone Microfluidics.
Journal: Langmuir : the ACS journal of surfaces and colloids
Published: August 29, 2019
Transformable bubble-filled alginate microfibers via vertical microfluidics.
Journal: Lab on a chip
Published: February 02, 2019
Flexible Asymmetric Encapsulation for Dehydration-Responsive Hybrid Microfibers.
Journal: Small (Weinheim an der Bergstrasse, Germany)
Published: February 12, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026