Anshika Srivastava, PhD
Postdoctoral Scholar
Neurology
School of Medicine

Publications (12)

Top publication keywords:
Alternative SplicingCarrier ProteinsIntellectual DisabilitySulfonic AcidsRNA Processing, Post-TranscriptionalRNAMembrane ProteinsCHARGE SyndromeProteinsHistocompatibility Antigens Class IRNA TransportGenetic Association StudiesMalformations of Cortical DevelopmentImmunogeneticsStilbenes

• COVID-19 Vaccine Reactogenicity Marks an Innate Inflammatory Response Associated With HLA Variation and Enhanced Protection.
  Research square 2026 Srivastava A, Chatzileontiadou DSM, Adhikari A, Suseno R, Lin S, Boquett J, Tuibeo J, Yusufali T, Peyser ND, Farias TDJ, Kichula KM, Nguyen AT, Jose I, Jayasinghe D, Leong SL, Beatty A, Tarassi K, …
• An HLA Association With COVID-19 Vaccine Reactogenicity Correlates With Fewer SARS-CoV-2 Infections and Monocyte Activation.
  Research square 2025 Hollenbach J, Srivastava A, Chatzileontiadou D, Adhikari A, Suseno R, Lin S, Boquett J, Tuibeo J, Yusufali T, Peyser N, Farias T, Kichula K, Nguyen A, Jose I, Jayasinghe D, Tarassi K, Kontou E, …
• Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations.
  Cell death & disease 2024 Werren EA, Peirent ER, Jantti H, Guxholli A, Srivastava KR, Orenstein N, Narayanan V, Wiszniewski W, Dawidziuk M, Gawlinski P, Umair M, Khan A, Khan SN, Geneviève D, Lehalle D, van Gassen KLI, Giltay …
• TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.
  Nature communications 2024 Werren EA, LaForce GR, Srivastava A, Perillo DR, Li S, Johnson K, Baris S, Berger B, Regan SL, Pfennig CD, de Munnik S, Pfundt R, Hebbar M, Jimenez-Heredia R, Karakoc-Aydiner E, Ozen A, Dmytrus J, …
• In silico characterization and identification of compound heterozygous variants in H/ACA Ribonucleoprotein Assembly Factor (SHQ1) from Indian population.
  Journal of family medicine and primary care 2024 Gowda VK, Srinivasan VM, Srivastava S, Ghali N, Kinhal U, Shamnur A, Srivastava A

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• Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.
  Research square 2023 Werren E, LaForce G, Srivastava A, Perillo D, Johnson K, Berger B, Regan S, Pfennig C, Baris S, de Munnik S, Pfundt R, Hebbar M, Jimenez Heredia R, Karakoc-Aydiner E, Ozen A, Dmytrus J, Krolo A, …
• Correction to: The immunogenetics of COVID-19.
  Immunogenetics 2023 Srivastava A, Hollenbach JA
• The immunogenetics of COVID-19.
  Immunogenetics 2022 Srivastava A, Hollenbach JA
• Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations.
  Scientific reports 2021 Singh PP, Srivastava A, Sultana GNN, Khanam N, Pathak A, Suravajhala P, Singh R, Shrivastava P, van Driem G, Thangaraj K, Chaubey G
• The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations.
  Scientific reports 2021 Singh PP, Srivastava A, Sultana GNN, Khanam N, Pathak A, Suravajhala P, Singh R, Shrivastava P, van Driem G, Thangaraj K, Chaubey G
• Genotype-phenotype correlations in individuals with pathogenic RERE variants.
  Human mutation 2018 Jordan VK, Fregeau B, Ge X, Giordano J, Wapner RJ, Balci TB, Carter MT, Bernat JA, Moccia AN, Srivastava A, Martin DM, Bielas SL, Pappas J, Svoboda MD, Rio M, Boddaert N, Cantagrel V, Lewis AM, …
• Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.
  Proceedings of the National Academy of Sciences of the United States of America 2018 Bélanger C, Bérubé-Simard FA, Leduc E, Bernas G, Campeau PM, Lalani SR, Martin DM, Bielas S, Moccia A, Srivastava A, Silversides DW, Pilon N