Sunita Bijarnia

486 citations

22 papers · 323 indexed · h-index 10

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 3
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics 4
Biochemistry
- Amino Acid Enzymes and Metabolism 3
Genetics
- Genomics and Rare Diseases 2
- Neurogenetic and Muscular Disorders Research 2
Endocrine and Autonomic Systems
Molecular Biology
- Mitochondrial Function and Pathology 3
Infectious Diseases
- Parvovirus B19 Infection Studies 3
Rheumatology
- Glycogen Storage Diseases and Myoclonus 2

Co-authors: I. C. Verma Veronica Wiley Bridget Wilcken Renu Saxena Ratna Dua Puri John Christodoulou Ishwar C. Verma Kevin Carpenter
Cited by: Clinical Biochemistry Pediatrics, Perinatology and Child Health Biochemistry
Partner nations: India Pakistan United States

In The Last Decade

Sunita Bijarnia

21 papers receiving 309 citations

Peers

Countries citing papers authored by Sunita Bijarnia

Since Specialization

Citations

This map shows the geographic impact of Sunita Bijarnia's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sunita Bijarnia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sunita Bijarnia more than expected).

Fields of papers citing papers by Sunita Bijarnia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sunita Bijarnia. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sunita Bijarnia. The network helps show where Sunita Bijarnia may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Sunita Bijarnia, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sunita Bijarnia Line = papers co-authored together Sunita Bijarnia links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Molecular characterization of supernumerary marker chromosomes found as unexpected chromosome abnormalities in nine prenatal and nine postnatal samples Meena Lall,Anju Joshi,Shruti Agarwal,Preeti Paliwal,Pushpa Saviour,Surbhi Mahajan,Ratna Dua Puri,Sunita Bijarnia,Ishwar C. Verma	2019	3
2	Evaluating the Utility of Next Generation Sequencing Technology in the Diagnosis and Prevention of Genetic Disorders in India, the Early Experiences Udhaya Kotecha,Ratna Dua Puri,Sunita Bijarnia,Sudha Kohli,Renu Saxena,Ishwar C. Verma	2019	1
3	Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome Veronica Arora,Shruti Aggarwal,Sunita Bijarnia,Meena Lall,Anju Joshi,Ratna Dua Puri,Umang Arora,Ishwar C. Verma	2018	0
4	Inherited metabolic disorders: prenatal diagnosis of lysosomal storage disorders Jyotsna Verma,Divya C. Thomas,Sandeepika Sharma,Geetu Jhingan,Renu Saxena,Sudha Kohli,Ratna Dua Puri,Sunita Bijarnia,Ishwar C. Verma	2015	19
5	Absent/Hypoplastic Fetal Nasal Bone and Its Association with Aneuploidies Pratima Dash,Ratna Dua Puri,Manisha Goyal,Sunita Bijarnia,Meena Lall,Udhaya Kotecha,Ishwar C. Verma	2015	1
6	Fanconi-Bickel Syndrome - Mutation in SLC2A2 Gene Mohit Kehar,Sunita Bijarnia,Sian Ellard,Jayne Houghton,Renu Saxena,I. C. Verma,Nishant Wadhwa	2014	15
7	Using Noninvasive Prenatal Testing for Aneuploidies in a Developing Country: Lessons Learnt Pratima Dash,Ratna Dua Puri,Udhaya Kotecha,Sunita Bijarnia,Meena Lall,Ishwar C. Verma	2014	7
8	Exome sequencing reveals SCO2 mutations in a family presented with fatal infantile hyperthermia Nyamkhishig Sambuughin,Xinyue Liu,Sunita Bijarnia,Tarina Wallace,Ishwar C. Verma,Susan L. Hamilton,Sheila M. Muldoon,Luke J. Tallon,Shuishu Wang	2013	6
9	Mutation Analysis of the CFTR Gene in 225 Children: Identification of Five Novel Severe and Seven Reported Severe Mutations Kabir Sachdeva,Renu Saxena,Ratna Dua Puri,Sunita Bijarnia,Sudha Kohli,Ishwar C. Verma	2012	10
10	Molecular Characterisation and Prenatal Diagnosis of Asparto-acylase Deficiency (Canavan Disease)—Report of Two Novel and Two Known Mutations from the Indian Subcontinent Sunita Bijarnia,Sudha Kohli,Ratna Dua Puri,Rintu J. Jacob,Renu Saxena,Anil Jalan,Erik A. Sistermans,Saqib Mahmood,Ishwar C. Verma	2012	5
11	Newborn screening for congenital hypothyroidism in very‐low‐birth‐weight babies: the need for a second test Sunita Bijarnia,Bridget Wilcken,Veronica Wiley	2011	55
12	Mutation studies in X-linked myotubular myopathy in three Indian families Sunita Bijarnia,Ratna Dua Puri,Monika Jain,Neelam Kler,Subimal Roy,Jon Andoni Urtizberea,Valérie Biancalana,Ishwar C. Verma	2010	3
13	Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome Sunita Bijarnia,Peter J. Shaw,Anne Vimpani,Robert O. Smith,Verity Pacey,Helen O’Grady,John Christodoulou,David Sillence	2009	9
14	Glutaric aciduria type I: outcome following detection by newborn screening Sunita Bijarnia,Veronica Wiley,Kevin Carpenter,John Christodoulou,C. J. Ellaway,Bridget Wilcken	2008	51
15	Tyrosinemia type I—Diagnostic issues and prenatal diagnosis Sunita Bijarnia,Ratna Dua Puri,Jean Ruel,George F. Gray,Linda Jenkinson,Ishwar C. Verma	2006	11
16	Leber′s hereditary optic neuropathy with molecular characterization in two Indian families IC Verma,Sunita Bijarnia,Renu Saxena,Sudha Kohli,Ratna Dua Puri,Elizabeth R. Thomas,Debashish Chowdhary,SN Jha,A. K. Grover	2005	10
17	Genetic counseling and prenatal diagnosis in India — experience at Sir Ganga Ram Hospital Ishwar C. Verma,Renu Saxena,Meena Lall,Sunita Bijarnia,Rajesh Sharma	2003	26
18	Genetic counseling in acrocallosal syndrome Sunita Bijarnia,Ashok Baijal,Ishwar C. Verma	2003	5
19	The Burden of Genetic Disorders in India and a Framework for Community Control I. C. Verma,Sunita Bijarnia	2002	72
20	Acute brucellosis of childhood: a case report with unusual features. Anil Sachdev,Rakesh Vohra,Sunita Bijarnia	2001	8

About Sunita Bijarnia

Sunita Bijarnia is a scholar working on Clinical Biochemistry, Biochemistry and Genetics, having authored 22 papers that have together received 323 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Amino Acid Enzymes and Metabolism (3 papers), Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers), Parvovirus B19 Infection Studies (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Genomics and Rare Diseases (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Clinical Biochemistry (92 citations), Pediatrics, Perinatology and Child Health (117 citations) and Biochemistry (28 citations). Sunita Bijarnia has collaborated with scholars based in India, Pakistan and United States. Frequent co-authors include I. C. Verma, Veronica Wiley, Bridget Wilcken, Renu Saxena, Ratna Dua Puri, John Christodoulou, Ishwar C. Verma, Kevin Carpenter, Ishwar C. Verma and Sudha Kohli.

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