Priyanka Srivastava

11PUBLICATIONS
23CO-AUTHORS
Haematological tumoursObstetrics and gynaecologyNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)
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Publications (11)

|Jul 10, 2026
Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants.

|Apr 10, 2026
Quantitative proteomic profiling of placental extracellular vesicles in recurrent pregnancy loss reveals their role in feto-maternal crosstalk.

Chitra Bhardwaj, Priyanka Srivastava, Ravi Pratap Singh Bhadoriya

|May 14, 2025
NR3C1 variants and glucocorticoid response in childhood nephrotic syndrome in North India.

Sarranya Paranthaman, Priyanka Srivastava, Anu Kumari

|Nov 07, 2024
Developmental and Epileptic Encephalopathies: Need for Bridging the Gaps Between Clinical Syndromes and Underlying Genetic Etiologies.

Priyanka Srivastava, Chitra Bhardwaj, Kausik Mandal

|May 09, 2024
Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental Delay.

Priyanka Srivastava, Parminder Kaur, Roshan Daniel

|Apr 03, 2024
Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy.

Anupriya Kaur, Chakshu Chaudhry, Parminder Kaur

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Frequent Collaborators

3 joint publications

Chitra Bhardwaj

3 joint publications

Anupriya Kaur

3 joint publications

Devi Dayal

2 joint publications

Kausik Mandal