Sudha Kohli

443 total citations
28 papers, 264 citations indexed

About

Sudha Kohli is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sudha Kohli has authored 28 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Genetics. Recurrent topics in Sudha Kohli's work include Metabolism and Genetic Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Sudha Kohli is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Sudha Kohli collaborates with scholars based in India, Pakistan and Japan. Sudha Kohli's co-authors include Renu Saxena, Ishwar C. Verma, Ratna Dua Puri, Dinesh Goyal, Sunita Bijarnia‐Mahay, Jyotsna Verma, Sunita Bijarnia, Elizabeth R. Thomas, Seiji Yamaguchi and Yosuke Shigematsu and has published in prestigious journals such as SHILAP Revista de lepidopterología, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Sudha Kohli

26 papers receiving 252 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sudha Kohli India 11 114 69 58 56 50 28 264
Lina Ghaloul‐Gonzalez United States 10 131 1.1× 17 0.2× 52 0.9× 16 0.3× 58 1.2× 29 254
Suzanne K. Cordovado United States 11 93 0.8× 19 0.3× 52 0.9× 35 0.6× 155 3.1× 23 391
Yvonne Mark United States 7 111 1.0× 21 0.3× 12 0.2× 31 0.6× 51 1.0× 11 293
Mika Ishige Japan 8 148 1.3× 10 0.1× 155 2.7× 16 0.3× 28 0.6× 24 264
A. Bou� France 9 134 1.2× 22 0.3× 41 0.7× 122 2.2× 155 3.1× 11 388
J Starup Denmark 13 89 0.8× 14 0.2× 11 0.2× 38 0.7× 70 1.4× 41 417
M. B. Coleman United States 10 62 0.5× 344 5.0× 7 0.1× 71 1.3× 38 0.8× 17 377
R Balducci Italy 11 200 1.8× 10 0.1× 14 0.2× 48 0.9× 90 1.8× 23 512
Agnès Choiset France 11 96 0.8× 8 0.1× 14 0.2× 181 3.2× 150 3.0× 20 390
Engela Honey South Africa 9 65 0.6× 21 0.3× 24 0.4× 16 0.3× 38 0.8× 25 168

Countries citing papers authored by Sudha Kohli

Since Specialization
Citations

This map shows the geographic impact of Sudha Kohli'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 Sudha Kohli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sudha Kohli more than expected).

Fields of papers citing papers by Sudha Kohli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sudha Kohli. 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 Sudha Kohli. The network helps show where Sudha Kohli may publish in the future.

Co-authorship network of co-authors of Sudha Kohli

This figure shows the co-authorship network connecting the top 25 collaborators of Sudha Kohli. A scholar is included among the top collaborators of Sudha Kohli based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sudha Kohli. Sudha Kohli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kohli, Sudha, et al.. (2023). The molecular landscape of oculocutaneous albinism in India and its therapeutic implications. European Journal of Human Genetics. 32(10). 1267–1277.
2.
Singh, Kanika, Ratna Dua Puri, Sunita Bijarnia‐Mahay, et al.. (2022). Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India. Indian Pediatrics. 59(6). 463–466. 1 indexed citations
3.
Verma, Ishwar C., et al.. (2020). Carrier screening of spinal muscular atrophy in North Indian population and its public health implications. Clinical Genetics. 98(2). 198–199. 4 indexed citations
4.
Kohli, Sudha, Renu Saxena, Elizabeth R. Thomas, et al.. (2020). Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy. The Indian Journal of Pediatrics. 87(7). 495–504. 10 indexed citations
5.
Singh, Kanika, Sunita Bijarnia‐Mahay, Vedam L. Ramprasad, et al.. (2020). NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study. BMC Medical Genetics. 21(1). 216–216. 15 indexed citations
6.
Ramachandran, Vijaya, Arndt Rolfs, Oliver Brandau, et al.. (2019). Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD. Journal of Human Genetics. 64(5). 409–419. 5 indexed citations
7.
Bijarnia‐Mahay, Sunita, Johannes Häberle, Anil Jalan, et al.. (2018). Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing. Orphanet Journal of Rare Diseases. 13(1). 174–174. 22 indexed citations
8.
Bijarnia‐Mahay, Sunita, Sudha Kohli, Renu Saxena, et al.. (2016). Seventeen Novel Mutations in PCCA and PCCB Genes in Indian Propionic Acidemia Patients, and Their Outcomes. Genetic Testing and Molecular Biomarkers. 20(7). 373–382. 10 indexed citations
9.
Sondhi, Vishal, Biswaroop Chakrabarty, Atin Kumar, et al.. (2016). RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathy. Brain and Development. 38(10). 937–942. 10 indexed citations
10.
Soni, Jai Prakash, Ratna Dua Puri, Gandham SriLakshmi Bhavani, et al.. (2016). Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among “Malis (Farmers)” in Jodhpur. The Indian Journal of Pediatrics. 83(11). 1341–1345. 3 indexed citations
11.
Ramachandran, Vijaya, et al.. (2016). NOS3 gene Glu298Asp polymorphism and severity of disease in patients of ADPKD from North India. Meta Gene. 11. 75–80.
12.
Bijarnia‐Mahay, Sunita, Renu Saxena, Sudha Kohli, et al.. (2015). Identification of mutations, genotype–phenotype correlation and prenatal diagnosis of maple syrup urine disease in Indian patients. European Journal of Medical Genetics. 58(9). 471–478. 24 indexed citations
13.
Saxena, Renu, et al.. (2012). Mutation Analysis of the CFTR Gene in 225 Children: Identification of Five Novel Severe and Seven Reported Severe Mutations. Genetic Testing and Molecular Biomarkers. 16(7). 798–801. 10 indexed citations
14.
Bijarnia, Sunita, Sudha Kohli, Ratna Dua Puri, et al.. (2012). Molecular Characterisation and Prenatal Diagnosis of Asparto-acylase Deficiency (Canavan Disease)—Report of Two Novel and Two Known Mutations from the Indian Subcontinent. The Indian Journal of Pediatrics. 80(1). 26–31. 5 indexed citations
15.
Verma, I. C., Renu Saxena, & Sudha Kohli. (2012). Hemoglobinopathies in India—Clinical and Laboratory Aspects. Clinics in Laboratory Medicine. 32(2). 249–262. 7 indexed citations
16.
Verma, Ishwar C., Renu Saxena, & Sudha Kohli. (2011). Past, present & future scenario of thalassaemic care & control in India.. PubMed. 134. 507–21. 51 indexed citations
17.
Ranjan, Piyush, Sudha Kohli, Renu Saxena, & Seema Thakur. (2011). Mutation Analysis in Crigler-Najjar Syndrome Type II—Case Report and Literature Review. Journal of Clinical and Experimental Hepatology. 1(3). 204–206. 4 indexed citations
18.
Kohli, Sudha & Dinesh Goyal. (2010). EFFECT OF FLY ASH APPLICATION ON SOME SOIL PHYSICAL PROPERTIES AND MICROBIAL ACTIVITIES. Acta Agrophysica. 16(16). 18 indexed citations
19.
20.
Bijarnia, Sunita, Renu Saxena, Sudha Kohli, et al.. (2005). Leber′s hereditary optic neuropathy with molecular characterization in two Indian families. Indian Journal of Ophthalmology. 53(3). 167–167. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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