Qiliang Ding

906 total citations
18 papers, 315 citations indexed

About

Qiliang Ding is a scholar working on Genetics, Molecular Biology and Archeology. According to data from OpenAlex, Qiliang Ding has authored 18 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Archeology. Recurrent topics in Qiliang Ding's work include Forensic and Genetic Research (4 papers), Genomics and Chromatin Dynamics (4 papers) and DNA Repair Mechanisms (3 papers). Qiliang Ding is often cited by papers focused on Forensic and Genetic Research (4 papers), Genomics and Chromatin Dynamics (4 papers) and DNA Repair Mechanisms (3 papers). Qiliang Ding collaborates with scholars based in United States, China and Canada. Qiliang Ding's co-authors include Jin Li, Ya Hu, Shuhua Xu, Chuan‐Chao Wang, Jiucun Wang, Yajun Yang, Shilin Li, Yan Lü, Amnon Koren and Haiyi Lou and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Qiliang Ding

14 papers receiving 305 citations

Peers

Countries citing papers authored by Qiliang Ding

Since Specialization

Citations

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

Fields of papers citing papers by Qiliang Ding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qiliang Ding

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Rethinking the pathogenicity of intragenic DMD duplications detected by carrier screening: High prevalence of nontandem duplications revealed by long-read sequencing 2025 ·Genetics in Medicine ·Qiliang Ding, (unknown), (unknown), (unknown), Guangchao Sun, Jesse R. Walsh, Ramanath Majumdar, Eric W. Klee, Stephen J. Murphy, Devin Oglesbee, Ross Rowsey, Linda Hasadsri	0
2	Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene 2024 ·American Journal of Clinical Pathology ·Qiliang Ding, J. Fine, (unknown), (unknown), (unknown), (unknown), Nicole L. Hoppman, Cherisse A. Marcou, Ross Rowsey, Erik C. Thorland, Linnea M. Baudhuin, Ann M. Moyer, Alessia Buglioni	0
3	Accurate and Automated Genotyping of the CFTR Poly-T/TG Tract with CFTR-TIPS 2024 ·International Journal of Molecular Sciences ·Qiliang Ding, (unknown), (unknown), (unknown), (unknown), (unknown), Kandelaria M. Rumilla, Linda Hasadsri	1
4	P228: Molecular and clinical analyses of LRP1 and LRP2 variants in human congenital cardiac left-sided lesions 2024 ·SHILAP Revista de lepidopterología ·Xin Chen, Qiliang Ding, Roozbeh Manshaei, M. Schwartz, (unknown), (unknown), Raymond H. Kim, Rebekah Jobling	0
5	Congenital Myopathy Due to Pathogenic Missense Variant in the MYBPC1 Gene 2023 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·(unknown), Raymond H. Kim, Hanna Faghfoury, Josh Silver, Raymond H. Chan, Qiliang Ding, M. Schwartz, Vera Bril	1
6	Germline whole genome sequencing in adults with multiple primary tumors 2023 ·Familial Cancer ·(unknown), Qiliang Ding, Stephenie D. Prokopec, (unknown), Jeffrey P. Bruce, Selina Casalino, Jeanna McCuaig, Marta Szybowska, (unknown), Jordan Lerner‐Ellis, Trevor J. Pugh, Raymond H. Kim	0
7	The evolution of the human DNA replication timing program 2023 ·Proceedings of the National Academy of Sciences ·(unknown), (unknown), Qiliang Ding, Melissa J. Hubisz, Madison Caballero, Amnon Koren	8
8	SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing 2022 ·Human Genetics ·Qiliang Ding, (unknown), Roozbeh Manshaei, Brett Trost, Miriam S. Reuter, (unknown), (unknown), John B. A. Okello, S. Mohsen Hosseini, Eriskay Liston, Meredith Curtis, Mehdi Zarrei, Edward J. Higginbotham, Ada J. S. Chan, Worrawat Engchuan, Bhooma Thiruvahindrapuram, Stephen W. Scherer, Raymond H. Kim, Rebekah Jobling	3
9	Delayed DNA replication in haploid human embryonic stem cells 2021 ·Genome Research ·Matthew Edwards, Michael V. Zuccaro, Ido Sagi, Qiliang Ding, Dan Vershkov, Nissim Benvenisty, Dieter Egli, Amnon Koren	6
10	The genetic architecture of DNA replication timing in human pluripotent stem cells 2021 ·Nature Communications ·Qiliang Ding, Matthew Edwards, Ning Wang, Xiang Zhu, (unknown), (unknown), Ya Hu, Yao Tong, (unknown), Christine J. Charvet, Sulagna Ghosh, Robert E. Handsaker, Kevin Eggan, Florian T. Merkle, Jeannine Gerhardt, Dieter Egli, Andrew G. Clark, Amnon Koren	22
11	Positive and Negative Regulation of DNA Replication Initiation 2020 ·Trends in Genetics ·Qiliang Ding, Amnon Koren	7
12	Mutation Rate Variability across Human Y-Chromosome Haplogroups 2020 ·Molecular Biology and Evolution ·Qiliang Ding, Ya Hu, Amnon Koren, Andrew G. Clark	3
13	Ancestral Origins and Genetic History of Tibetan Highlanders 2016 ·The American Journal of Human Genetics ·Dongsheng Lu, Haiyi Lou, Kai Yuan, Xiaoji Wang, Yuchen Wang, Chao Zhang, Yan Lü, Xiong Yang, Lian Deng, Ying Zhou, Qidi Feng, Ya Hu, Qiliang Ding, Yajun Yang, Shilin Li, Jin Li, Yaqun Guan, Bing Su, Longli Kang, Shuhua Xu	149
14	Neanderthal Origin of the Haplotypes Carrying the Functional Variant Val92Met in the MC1R in Modern Humans 2014 ·Molecular Biology and Evolution ·Qiliang Ding, Ya Hu, Shuhua Xu, Chuan‐Chao Wang, Hui Li, Ruyue Zhang, Shi Yan, Jiucun Wang, Jin Li	25
15	Neanderthal Introgression at Chromosome 3p21.31 Was Under Positive Natural Selection in East Asians 2013 ·Molecular Biology and Evolution ·Qiliang Ding, Ya Hu, Shuhua Xu, Jiucun Wang, Jin Li	41
16	Late Neolithic expansion of ancient Chinese revealed by Y chromosome haplogroup O3a1c‐002611 2012 ·Journal of Systematics and Evolution ·Chuan‐Chao Wang, Shi Yan, Zhendong Qin, Yan Lü, Qiliang Ding, Lan‐Hai Wei, Shilin Li, Yajun Yang, Jin Li, Hui Li	24
17	Comment on “Phonemic Diversity Supports a Serial Founder Effect Model of Language Expansion from Africa” 2012 ·Science ·Chuan‐Chao Wang, Qiliang Ding, (unknown), Hui Li	17
18	Mapping Human Genetic Diversity on the Japanese Archipelago 2011 ·Qiliang Ding, Chuan‐Chao Wang, (unknown), Hui Li	8

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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