Anshika Srivastava

Lucknow, UP 226014, India

Last Updated: 09/26/2026

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Found 33 publications

Generation of a hiPSC from a patient with an ITSN1-associated neurodevelopmental disorder spectrum carrying biallelic c.2893_2894insA (p.Tyr965Ter) genetic variant.

Generation of a hiPSC from a patient with an ITSN1-associated neurodevelopmental disorder spectrum carrying biallelic c.2893_2894insA (p.Tyr965Ter) genetic variant.

Journal: Stem cell research

Published: May 22, 2026

Exploring the Prognostic Significance of IL10 Variants and Their Mechanistic Regulation in Diabetic Nephropathy.

Exploring the Prognostic Significance of IL10 Variants and Their Mechanistic Regulation in Diabetic Nephropathy.

Journal: Journal of cellular and molecular medicine

Published: February 22, 2025

Uncovering the influence of nitridation on the dislocation density at atomistic scale in III-Nitrides MOCVD/MOVPE epitaxy process.

Uncovering the influence of nitridation on the dislocation density at atomistic scale in III-Nitrides MOCVD/MOVPE epitaxy process.

Journal: Scientific reports

Published: September 19, 2024

Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.

Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.

Journal: Research square

Published: September 18, 2023

Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations.

Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations.

Journal: Cell death & disease

Published: July 14, 2023

In silico characterization and identification of compound heterozygous variants in H/ACA Ribonucleoprotein Assembly Factor (SHQ1) from Indian population.

In silico characterization and identification of compound heterozygous variants in H/ACA Ribonucleoprotein Assembly Factor (SHQ1) from Indian population.

Journal: Journal of family medicine and primary care

Published: June 14, 2023

In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population.

In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population.

Journal: Cureus

Published: June 13, 2023

A novel biallelic frameshift variant in C2orf69 causing developmental regression, seizures, microcephaly, autistic features, and hypertonia.

A novel biallelic frameshift variant in C2orf69 causing developmental regression, seizures, microcephaly, autistic features, and hypertonia.

Journal: American journal of medical genetics. Part A

Published: January 11, 2023

Atomistic nonlinear carrier dynamics in Ge.

Atomistic nonlinear carrier dynamics in Ge.

Journal: Scientific reports

Published: December 30, 2022

TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.

TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.

Journal: Nature communications

Published: October 02, 2022

An innovative technique for electronic transport model of group-III nitrides.

An innovative technique for electronic transport model of group-III nitrides.

Journal: Scientific reports

Published: June 10, 2020

Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa.

Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa.

Journal: Annals of the rheumatic diseases

Published: February 06, 2018

Showing 1-12 of 33

Last Updated: 09/26/2026