Changlin Ding

720 citations
12 papers · 570 · h-index 9

Impact in

  • Nephrology top 2%
    • Parathyroid Disorders and Treatments
  • Genetics top 10%
    • Genetic Syndromes and Imprinting
    • Genomics and Rare Diseases

Papers in

    • Congenital heart defects research 2
    • Epigenetics and DNA Methylation 1
    • Bone Metabolism and Diseases 1
    • Retinal Development and Disorders 1
    • Genetic Syndromes and Imprinting 5
    • Genomics and Rare Diseases 1

Changlin Ding

11 papers receiving 518 citations

Peers

Changlin Ding
Comparison fields: 5 of 43
  • Nephrology 272
  • Genetics 274
  • Molecular Biology 255
  • Rheumatology 51
  • Surgery 98
Replace Felicia Ledgard with:
Felicia Ledgard United States
Jitka Štekrová Czechia
Zohreh Khavandgar Canada
Megan L. Noonan United States
Masaki Takagi Japan
Xue Jun Fu Japan
Minlin Liu United States
Lisa Williams‐Simons United States
P Bouloux United Kingdom
Britta George Germany
Changlin Ding relative to Felicia Ledgard United States Felicia Ledgard's profile →
Citations per field
00.5×1.5×1.9×
Felicia Ledgard · 1×
Citations per year

Countries citing papers authored by Changlin Ding

Since Specialization
Citations

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

Fields of papers citing papers by Changlin Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

12 of 12 papers shown
#Work
1 2001149
2 2001143
3 200951
4 200543
5 200342
6 200839
7 200434
8 201133
9 200526
10 20186
11 19934
12 20250

About Changlin Ding

Changlin Ding is a scholar working on Molecular Biology, Genetics, Nephrology, Genetics and Neurology, having authored 12 papers that have together received 570 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Parathyroid Disorders and Treatments (4 papers), Congenital heart defects research (2 papers), Genomics and Rare Diseases (1 paper), Epigenetics and DNA Methylation (1 paper), Retinal Diseases and Treatments (1 paper), Bone Metabolism and Diseases (1 paper) and Retinal Development and Disorders (1 paper). The work is most often cited by research in Nephrology (272 citations), Genetics (274 citations), Molecular Biology (255 citations), Rheumatology (51 citations) and Surgery (98 citations). Changlin Ding has collaborated with scholars based in United States, Switzerland and Taiwan. Frequent co-authors include Michael A. Levine, Bruce A. Buckingham, Steven A. Lietman, Alexander Maret, Suzanne M. Jan de Beur, David W. Cooke, Sara L. Kornfield, Emily L. Germain‐Lee, Isabelle Bourdeau and Tjin Shing Jap. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Clinical Investigation, APL Bioengineering, The American Journal of Human Genetics and Genomics.

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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