Anshika Srivastava, PhD
Postdoctoral Scholar
Neurology
School of Medicine

Publications (7)

Top publication keywords:
Tumor Suppressor ProteinsCarrier ProteinsIntellectual DisabilityNeurodevelopmental DisordersSulfonic AcidsRNA Processing, Post-TranscriptionalRNAMembrane ProteinsMammalsHistocompatibility Antigens Class IRNA TransportGenetic Association StudiesMalformations of Cortical DevelopmentStilbenesImmunogenetics

• 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, …
• 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
• 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, …