Changlin Ding

728 total citations
12 papers, 453 citations indexed

About

Changlin Ding is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Changlin Ding has authored 12 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Nephrology. Recurrent topics in Changlin Ding's work include Genetic Syndromes and Imprinting (6 papers), Parathyroid Disorders and Treatments (5 papers) and Congenital heart defects research (3 papers). Changlin Ding is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Parathyroid Disorders and Treatments (5 papers) and Congenital heart defects research (3 papers). Changlin Ding collaborates with scholars based in United States, China and Israel. Changlin Ding's 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, Yardena Tenenbaum‐Rakover and De‐Ming Yang and has published in prestigious journals such as Journal of Clinical Investigation, Applied Physics Letters and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Changlin Ding

12 papers receiving 442 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Changlin Ding United States 9 257 249 226 80 61 12 453
Ron Krofft United States 8 213 0.8× 129 0.5× 371 1.6× 38 0.5× 30 0.5× 8 486
Jitka Štekrová Czechia 14 287 1.1× 230 0.9× 147 0.7× 31 0.4× 54 0.9× 47 504
Kamran Hamidi Asl United States 10 467 1.8× 118 0.5× 107 0.5× 48 0.6× 78 1.3× 12 504
Britta George Germany 11 277 1.1× 148 0.6× 408 1.8× 54 0.7× 22 0.4× 20 603
Naoya Morisada Japan 15 367 1.4× 205 0.8× 89 0.4× 45 0.6× 18 0.3× 46 585
Masaki Takagi Japan 14 236 0.9× 290 1.2× 43 0.2× 65 0.8× 66 1.1× 54 514
Stiina Välimäki Sweden 7 138 0.5× 190 0.8× 362 1.6× 38 0.5× 228 3.7× 7 512
Tanja Wittkampf Germany 6 180 0.7× 197 0.8× 96 0.4× 25 0.3× 23 0.4× 6 407
Francesca Giacopelli Italy 12 182 0.7× 133 0.5× 68 0.3× 53 0.7× 20 0.3× 21 415
Kohei Satoh Japan 8 162 0.6× 272 1.1× 513 2.3× 66 0.8× 200 3.3× 15 670

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-authorship network of co-authors of Changlin Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Changlin Ding. A scholar is included among the top collaborators of Changlin Ding 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 Changlin Ding. Changlin Ding is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Ding, Changlin, et al.. (2025). Quantum secure direct communication based on quantum error correction code. Applied Physics Letters. 126(2). 5 indexed citations
2.
3.
Sanchez, Janine, Erasmo M. Perera, Suzanne M. Jan de Beur, et al.. (2011). Madelung-Like Deformity in Pseudohypoparathyroidism Type 1b. The Journal of Clinical Endocrinology & Metabolism. 96(9). E1507–E1511. 26 indexed citations
4.
Lietman, Steven A., Yardena Tenenbaum‐Rakover, Tjin Shing Jap, et al.. (2009). A Novel Loss-of-Function Mutation, Gln459Arg, of the Calcium-Sensing Receptor Gene Associated with Apparent Autosomal Recessive Inheritance of Familial Hypocalciuric Hypercalcemia. The Journal of Clinical Endocrinology & Metabolism. 94(11). 4372–4379. 40 indexed citations
5.
Maret, Alexander, Changlin Ding, Sara L. Kornfield, & Michael A. Levine. (2008). Analysis of theGCM2Gene in Isolated Hypoparathyroidism: A Molecular and Biochemical Study. The Journal of Clinical Endocrinology & Metabolism. 93(4). 1426–1432. 31 indexed citations
6.
Lietman, Steven A., Changlin Ding, David W. Cooke, & Michael A. Levine. (2005). Reduction in Gs?? Induces Osteogenic Differentiation in Human Mesenchymal Stem Cells. Clinical Orthopaedics and Related Research. &NA;(434). 231–238. 37 indexed citations
7.
Lietman, Steven A., Changlin Ding, & Michael A. Levine. (2005). A HIGHLY SENSITIVE POLYMERASE CHAIN REACTION METHOD DETECTS ACTIVATING MUTATIONS OF THE GNAS GENE IN PERIPHERAL BLOOD CELLS IN MCCUNE-ALBRIGHT SYNDROME OR ISOLATED FIBROUS DYSPLASIA. Journal of Bone and Joint Surgery. 87(11). 2489–2494. 22 indexed citations
8.
Maret, Alexander, Isabelle Bourdeau, Changlin Ding, et al.. (2004). Expression of GCMB by Intrathymic Parathyroid Hormone-Secreting Adenomas Indicates Their Parathyroid Cell Origin. The Journal of Clinical Endocrinology & Metabolism. 89(1). 8–12. 26 indexed citations
9.
Beur, Suzanne M. Jan de, et al.. (2003). Discordance between Genetic and Epigenetic Defects in Pseudohypoparathyroidism Type 1b Revealed by Inconsistent Loss of Maternal Imprinting at GNAS1. The American Journal of Human Genetics. 73(2). 314–322. 35 indexed citations
10.
Ding, Changlin, Bruce A. Buckingham, & Michael A. Levine. (2001). Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB. Journal of Clinical Investigation. 108(8). 1215–1220. 101 indexed citations
11.
Ding, Changlin, Bruce A. Buckingham, & Michael A. Levine. (2001). Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB. Journal of Clinical Investigation. 108(8). 1215–1220. 120 indexed citations
12.
Ding, Changlin, et al.. (1993). The Gene for Human Phosducin (PDC), a Soluble Protein That Binds G-Protein βγ Dimers, Maps to 1q25-q31.1. Genomics. 18(2). 457–459. 4 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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