Priyanka Srivastava

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 6

Top Topics

Systematic Review

Genome Wide Association

Intellectual Disability

Top Venues

Journal of pediatric genetics

Biomarkers in medicine

Molecular biology reports

This page only lists publications with an associated author ORCID identifier.

Publications

Anupriya Kaur, Chakshu Chaudhry, Parminder Kaur, Roshan Daniel, Priyanka Srivastava
Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy. Journal of pediatric genetics 13 (1) (2022)
Ankita Singh, Amit Rawat, Anit Kaur, Anupriya Kaur, Rajni Kumrah, Nameirakpam Johnson, Himanshi Chaudhary, Rakesh Kumar Pilania, Priyanka Srivastava, Surjit Singh
Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease. Molecular biology reports 49 (8) (2022)
Priyanka Srivastava, Chitra Bamba, Seema Chopra, Kausik Mandal
Role of miRNA polymorphism in recurrent pregnancy loss: a systematic review and meta-analysis. Biomarkers in medicine 16 (2) (2022)
Anupriya Kaur, Chakshu Chaudhry, Parminder Kaur, Roshan Daniel, Priyanka Srivastava
Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy. Journal of pediatric genetics 13 (1) (2022)
Priyanka Srivastava, Parminder Kaur, Roshan Daniel, Chakshu Chaudhry, Anit Kaur, Saurabh Seth, Divya Kumari, Anupriya Kaur, Inusha Panigrahi
Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental Delay. Journal of pediatric genetics 13 (2) (2022)
Priyanka Srivastava, Parminder Kaur, Roshan Daniel, Chakshu Chaudhry, Anit Kaur, Saurabh Seth, Divya Kumari, Anupriya Kaur, Inusha Panigrahi
Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental Delay. Journal of pediatric genetics 13 (2) (2022)