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Ankur Chaurasia

Showing results (1-10 of 10) with videos related to

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ACS Applied Bio Materials|June 26, 2025
Tribo-Mechanical and Antibacterial Performance of 3D Printed hBN/PEGDA Nanocomposites for Load-Bearing Tissue Engineering ApplicationsRaju Kumar, Jenish Patel, Avinash Parashar, et al.
Bioinformation|March 31, 2017
Net2Align: An Algorithm For Pairwise Global Alignment of Biological NetworksPriyanka Narad, Ankur Chaurasia, Gulshan Wadhwab, et al.
Physical Chemistry Chemical Physics : PCCP|November 14, 2023
Covalently bonded interface in polymer/boron nitride nanosheet composite toward enhanced mechanical and thermal behaviourAnkur Chaurasia, Kaushlendra Kumar, S P Harsha, et al.
Clinical Dysmorphology|January 14, 2025
Biallelic variants in AGRN with recurrent pregnancy losses in a family with a fetal akinesia deformation sequenceMangalore S Shravya, Ankur Chaurasia, Katta M Girisha, et al.
Bioresource Technology|September 20, 2021
Deciphering functional biomolecule potential of marine diatoms through complex network approachThomas Kiran Marella, Hina Bansal, Raya Bhattacharjya, et al.
Human Genetics|March 21, 2023
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephalyFranziska Schnabel, Elisabeth Schuler, Almundher Al-Maawali, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics|February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
ACS Applied Bio Materials|June 26, 2025
Tribo-Mechanical and Antibacterial Performance of 3D Printed hBN/PEGDA Nanocomposites for Load-Bearing Tissue Engineering ApplicationsRaju Kumar, Jenish Patel, Avinash Parashar, et al.
Bioinformation|March 31, 2017
Net2Align: An Algorithm For Pairwise Global Alignment of Biological NetworksPriyanka Narad, Ankur Chaurasia, Gulshan Wadhwab, et al.
Physical Chemistry Chemical Physics : PCCP|November 14, 2023
Covalently bonded interface in polymer/boron nitride nanosheet composite toward enhanced mechanical and thermal behaviourAnkur Chaurasia, Kaushlendra Kumar, S P Harsha, et al.
Clinical Dysmorphology|January 14, 2025
Biallelic variants in AGRN with recurrent pregnancy losses in a family with a fetal akinesia deformation sequenceMangalore S Shravya, Ankur Chaurasia, Katta M Girisha, et al.
Bioresource Technology|September 20, 2021
Deciphering functional biomolecule potential of marine diatoms through complex network approachThomas Kiran Marella, Hina Bansal, Raya Bhattacharjya, et al.
Human Genetics|March 21, 2023
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephalyFranziska Schnabel, Elisabeth Schuler, Almundher Al-Maawali, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|December 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Purvi Majethia, Karthik Nair, et al.
Clinical Genetics|February 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
Pageof 1