Veronica Arora

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Adrenal insufficiency predicts early mortality in patients with cirrhosis

Ashish Kumar, Praveen Sharma, P. Ranjan, 2015, United European gastroenterology journal.

Hepatitis B Virus Infection can Cause Hepatocellular Carcinoma in Less Advanced Liver Cirrhosis: A Comparative Study of 142 Patients from North India.

Ashish Kumar, Praveen Sharma, P. Tyagi, 2013, Journal of clinical and experimental hepatology.

Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis.

P. Bauer, A. Bertoli-Avella, A. Rolfs, 2020, Journal of the American Society of Nephrology : JASN.

Osteopathia Striata with Cranial Sclerosis: A Face-to-Radiograph-to-Gene Diagnosis

S. Bijarnia-Mahay, Veronica Arora, K. K. Saxena, 2020, Journal of Pediatric Genetics.

Co-inheritance of pathogenic variants in PKD1 and PKD2 genes presenting as severe antenatal phenotype of autosomal dominant polycystic kidney disease.

S. Bansal, I. Verma, V. Tiwari, 2020, European journal of medical genetics.

Implications of a Genetic Etiology for Renal Transplant: Early-Onset Alport Syndrome with a Novel Mutation

R. Singh, D. Gupta, V. Tiwari, 2020, Journal of Pediatric Genetics.

Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene – A Rare But Treatable Cause of Refractory Rickets

I. Verma, S. Sandal, Veronica Arora, 2020, The Indian Journal of Pediatrics.

Iatrogenic hypervitaminosis D as an unusual cause of persistent vomiting: a case report

Ashish Kumar, Praveen Sharma, P. Tyagi, 2014, Journal of Medical Case Reports.

Looking Back at Fetal Medicine in India in 2018, and Looking Forward to 2019

I. Verma, Veronica Arora, M. Lallar, 2019, Journal of Fetal Medicine.

Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene

Veronica Arora, Renu Saxena, I. Verma, 2022, Indian Journal of Pediatrics.

Eyes See what the Mind Knows: Clues to Pattern Recognition in Single Enzyme Deficiency-Related Peroxisomal Disorders

R. Saxena, S. Bijarnia-Mahay, Veronica Arora, 2020, Molecular Syndromology.

Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome

S. Aggarwal, R. Dua-Puri, I. Verma, 2018, Molecular Syndromology.

Genetic Testing in Pediatric Kidney Disease

Veronica Arora, K. Anand, Ishwar Chander Verma, 2020, The Indian Journal of Pediatrics.

Current Status of Noninvasive Prenatal Testing and Counselling Considerations: An Indian Perspective

I. Verma, R. Puri, Veronica Arora, 2019, Journal of Fetal Medicine.

The fatal fetal tumor: a geneticist’s perspective

Seema R. Gupta, I. Verma, Veronica Arora, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

The changing scenario in prenatal diagnosis of genetic disorders: Genetics to genomics

S. Agarwal, R. Saxena, P. Paliwal, 2018, Current Medicine Research and Practice.

Genetic Testing in Pediatric Epilepsy

I. Verma, Veronica Arora, Sameer Bhatia, 2020, Indian Journal of Pediatrics.

Co-existence of CPAM with Megacystis Due to Posterior Urethral Valve and Cardiac Dysfunction in a Monozygotic Twin Pregnancy

S. Bijarnia-Mahay, I. Verma, Veronica Arora, 2019, Journal of Fetal Medicine.

Expanding the phenotypic and genotypic spectrum of Wiedemann–Steiner syndrome: First patient from India

S. Bijarnia-Mahay, I. Verma, R. Puri, 2020, American journal of medical genetics. Part A.

Neuro-Regression in a Child with Silvery Hair

I. Verma, Veronica Arora, Monika Jain, 2020, Indian Journal of Pediatrics.

Fetal valproate syndrome as a phenocopy of Kleefstra syndrome

S. Agarwal, Veronica Arora, M. Lall, 2018, Birth defects research.

Risk factors for Coronavirus disease-associated mucormycosis

S. Sinha, N. Wig, Gagandeep Singh, 2021, The Journal of Infection.

Sialidosis type II: Expansion of phenotypic spectrum and identification of a common mutation in seven patients

S. Phadke, A. Dalal, R. Saxena, 2020, Molecular Genetics and Metabolism Reports.

ANO5‐associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype

I. Verma, S. Sandal, Veronica Arora, 2020, Congenital anomalies.

ALG9 Associated Gillessen-Kaesbach–Nishimura Syndrome (GIKANIS): An Uncommon Aetiology of Enlarged Foetal Kidneys

N. Shah, S. Bijarnia-Mahay, I. Verma, 2018, Journal of Fetal Medicine.

A further case of hypotonia, ataxia, developmental delay and tooth enamel defect syndrome due to a recurrent C-terminal binding protein 1 mutation.

I. Verma, Veronica Arora, Sameer Bhatia, 2020, Clinical dysmorphology.

Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss

R. Saxena, I. Verma, R. Puri, 2020, Journal of Pediatric Genetics.

The Medical Termination of Pregnancy (Amendment) Act, 2021: A step towards liberation.

I. Verma, Veronica Arora, 2021, Indian journal of medical ethics.

Fragile X Syndrome Due to a Frameshift Deletion: A Rare Mechanism

Veronica Arora, Aashita Takkar, Praveen Kumar, 2022, Indian Journal of Pediatrics.

Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up

A. Kapoor, Veronica Arora, Tushar Kapoor, 2022, Journal of clinical imaging science.

D. Gupta, Veronica Arora, Renu Saxena, 2022, Journal of Pediatric Genetics.

A Further Case of Larsen's Syndrome: Clinical and Genotypic Challenges in Diagnosis

I. Verma, S. Pal, Veronica Arora, 2020, Journal of Pediatric Genetics.

The first case of antenatal presentation in COG8‐congenital disorder of glycosylation with a novel splice site mutation and an extended phenotype

R. Saxena, P. Bhai, S. Bijarnia-Mahay, 2019, American journal of medical genetics. Part A.

Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation

I. Verma, Kanika Singh, S. Bijarnia-Mahay, 2019, Autopsy and Case Reports.

Next Generation Clinical Practice — It’s Man Versus Artificial Intelligence!

S. Bijarnia-Mahay, Veronica Arora, 2019, Indian Pediatrics.

The molecular landscape of oculocutaneous albinism in India and its therapeutic implications.

S. Kohli, Veronica Arora, Renu Saxena, 2023, European journal of human genetics : EJHG.