Shrawan Kumar

1.4k citations
22 papers · 686 · h-index 14

Impact in

    • Hearing, Cochlea, Tinnitus, Genetics
  • Genetics top 10%
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
    • Congenital Ear and Nasal Anomalies

Papers in

    • Head and Neck Anomalies 15
    • Teratomas and Epidermoid Cysts 4
    • Genetic and Kidney Cyst Diseases 4
    • Genetic Syndromes and Imprinting 2

Shrawan Kumar

22 papers receiving 669 citations

Peers

Shrawan Kumar
Comparison fields: 5 of 48
  • Sensory Systems 59
  • Genetics 262
  • Surgery 307
  • Pediatrics, Perinatology and Child Health 81
  • Nephrology 30
Replace Nicolai Kohlschmidt with:
Nicolai Kohlschmidt Germany
Paola Primignani Italy
Hilmar Viđarsson Sweden
Susan J. Allen United States
Matteo Della Monica Italy
Judith B. Kenyon United States
Rosemarie Smith United States
A. David France
G Morin France
Andrea M. Oza United States
Shrawan Kumar relative to Nicolai Kohlschmidt Germany Nicolai Kohlschmidt's profile →
Citations per field
00.5×7.5×
Nicolai Kohlschmidt · 1×
Citations per year

Countries citing papers authored by Shrawan Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Shrawan Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Shrawan Kumar, 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 Shrawan Kumar Line = papers co-authored together Shrawan Kumar links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1993220
2 199251
3 200047
4 200145
5 199244
6 199842
7 199829
8 200126
9 199424
10 199924
11 200224
12 200924
13 199918
14
The genetics of cystic diseases of the kidney.
199113
15 200412
16 200211
17 199611
18 19989
19
Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.
19947
20 19912

About Shrawan Kumar

Shrawan Kumar is a scholar working on Surgery, Genetics, Molecular Biology, Nephrology and Pulmonary and Respiratory Medicine, having authored 22 papers that have together received 686 indexed citations. Recurring topics across this work include Head and Neck Anomalies (15 papers), Genetic and Kidney Cyst Diseases (4 papers), Teratomas and Epidermoid Cysts (4 papers), Renal Diseases and Glomerulopathies (3 papers), Tracheal and airway disorders (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Sensory Systems (59 citations), Genetics (262 citations), Surgery (307 citations), Pediatrics, Perinatology and Child Health (81 citations) and Nephrology (30 citations). Shrawan Kumar has collaborated with scholars based in United States, Netherlands and India. Frequent co-authors include William J. Kimberling, Cor W. R. J. Cremers, Stefan Somlo, Patricia A. Gabow, Judith B. Kenyon, Henri A. M. Marres, P.L.M. Huygen, Richard J. Smith, Karen Deffenbacher and F.B.M. Joosten. Their work appears in journals such as Genomics, Human Genetics, Human Mutation, Advances in oto-rhino-laryngology and Pediatric Nephrology.

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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